HR job title
- Dean - Faculty
- Contact Info
- 9794360562
Khan, Mansoor Professor and Vice Dean
Positions
- Regents Professor and Presidential Impact Fellow, Center for Microencapsulation and Drug Delivery, School of Medicine
Dr. Mansoor A. Khan serves as a professor and Vice Dean of the Texas A&M University Rangel College of Pharmacy at College Station, Texas. Prior to joining Texas A&M in 2015, he served as the Director of Product Quality Research and a Senior Biomedical Research Scientist (SBRS) at CDER in US Food and Drug Administration for over eleven years. In FDA, he led the research and review teams to promote manufacturing science, and served as a founding member of the FDA Emerging Technology Team. Dr. Khan received his Ph.D. degree in industrial pharmacy form St. Johns University in NY. He has published over 335 peer-reviewed manuscripts in pharmaceutical formulations and manufacturing sciences, and delivered over 300 presentations world-wide. Dr. Khan's research, currently supported by the NIH and FDA, spans drug delivery and formulations, and he has received over ten million dollars in funding as a principal investigator.
Dr. Khan has held leadership positions at the AAPS including elected chair of formulations design and development (FDD) section. He serves on the editorial board of Pharmaceutical Technology, International Journal of Pharmaceutics, AAPSPharmsciTech, and the Drug Delivery and Translational Research. He has received about 20 FDA/CDER review, research, and exemplary achievement awards, outstanding alumni award at St. Johns University College of Pharmacy, Excellence Award in Texas A&M University. He received the 2012 AAPS Research Achievement Award in Formulations Design and Development. He is also an AAPS and AAiPS Fellow. Dr. Khan served as FDA representative to the World Health Organization (WHO), United States Pharmacopoeia (USP), European Medicine Agency (EMA), DARPA, NIH, National Institute of Pharmaceutical Technology and Education (NIPTE), and International Pharmaceutical Federation (FIP). He is also a member of the European Union Academy of Sciences.
Dr. Khan has held leadership positions at the AAPS including elected chair of formulations design and development (FDD) section. He serves on the editorial board of Pharmaceutical Technology, International Journal of Pharmaceutics, AAPSPharmsciTech, and the Drug Delivery and Translational Research. He has received about 20 FDA/CDER review, research, and exemplary achievement awards, outstanding alumni award at St. Johns University College of Pharmacy, Excellence Award in Texas A&M University. He received the 2012 AAPS Research Achievement Award in Formulations Design and Development. He is also an AAPS and AAiPS Fellow. Dr. Khan served as FDA representative to the World Health Organization (WHO), United States Pharmacopoeia (USP), European Medicine Agency (EMA), DARPA, NIH, National Institute of Pharmaceutical Technology and Education (NIPTE), and International Pharmaceutical Federation (FIP). He is also a member of the European Union Academy of Sciences.
- Overview
- Publications
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Overview
Publications
selected publications
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academic article
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Kayalar, C., Helal, N., Mohamed, E. M., Dharani, S., Khuroo, T., Kuttolamadom, M. A., Rahman, Z., & Khan, M. A.
(2024).
In Vitro and In Vivo testing of 3D-Printed Amorphous Lopinavir Printlets by SelectiveLaser Sinitering: Improved Bioavailability of a Poorly Soluble Drug. AAPS PharmSciTech.
25(1), 20.
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Dharani, S., Mohamed, E. M., Rahman, Z., & Khan, M. A.
(2024).
Patient In-Use Stability Testing of FDA-Approved Metformin Combination Products for N-Nitrosamine Impurity. AAPS PharmSciTech.
25(1), 19.
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Kayalar, C., Rahman, Z., Mohamed, E. M., Dharani, S., Khuroo, T., Helal, N., Kuttolamadom, M. A., & Khan, M. A.
(2023).
Preparation and Characterization of 3D-Printed Dose-Flexible Printlets of Tenofovir Disoproxil Fumarate. AAPS PharmSciTech.
24(6), 171.
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Mohamed, E. M., Dharani, S., Khuroo, T., Hamed, R., Khan, M. A., & Rahman, Z.
(2023).
In Vitro and In Vivo Characterization of the Transdermal Gel Formulation of Desloratadine for Prevention of Obesity and Metabolic Syndrome. Pharmaceuticals.
16(4), 578-578.
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Rahman, Z., Khuroo, T., Mohamed, E. M., Dharani, S., Kayalar, C., Kuttolamadom, M. A., Sangar, L. O., & Khan, M. A.
(2023).
Pyrimethamine 3D printlets for pediatric toxoplasmosis: design, pharmacokinetics, and anti-toxoplasma activity. 20(2), 301-311.
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Charoo, N. A., Dharani, S., Khan, M. A., & Rahman, Z.
(2023).
Nitroso Impurities in Drug Products: An Overview of Risk Assessment, Regulatory Milieu, and Control Strategy. AAPS PharmSciTech.
24(2), 60.
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Charoo, N. A., Khan, M. A., & Rahman, Z.
(2023).
Data integrity issues in pharmaceutical industry: Common observations, challenges and mitigations strategies. International Journal of Pharmaceutics.
631, 122503-122503.
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Dharani, S., Mohamed, E. M., Khuroo, T., Rahman, Z., & Khan, M. A.
(2022).
Formulation Characterization and Pharmacokinetic Evaluation of Amorphous Solid Dispersions of Dasatinib. Pharmaceutics.
14(11), 2450-2450.
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Doke, M., McLaughlin, J. P., Cai, J. J., Pendyala, G., Kashanchi, F., Khan, M. A., & Samikkannu, T.
(2022).
HIV-1 Tat and cocaine impact astrocytic energy reservoirs and epigenetic regulation by influencing the LINC01133-hsa-miR-4726-5p-NDUFA9 axis. Molecular Therapy : Nucleic Acids.
29, 243-258.
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Khuroo, T., Mohamed, E. M., Dharani, S., Immadi, S., Nutan, M., Lu, D., ... Rahman, Z.
(2022).
In-Situ Implant Formulation of Laurate and Myristate Prodrugs of Dolutegravir for Ultra-Long Delivery. Journal of Pharmaceutical Sciences.
111(8), 2312-2321.
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Khuroo, T., Mohamed, E. M., Dharani, S., Kayalar, C., Ozkan, T., Kuttolamadom, M. A., Rahman, Z., & Khan, M. A.
(2022).
Very-Rapidly Dissolving Printlets of Isoniazid Manufactured by SLS 3D Printing: In Vitro and In Vivo Characterization. Molecular Pharmaceutics.
19(8), 2937-2949.
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Dharani, S., Mohamed, E. M., Khuroo, T., Ali, H. I., Reddy, I. K., Rahman, Z., & Khan, M. A.
(2022).
In-use stability assessment of FDA approved metformin immediate release and extended release products for N-Nitrosodimethylamine and dissolution quality attributes. International Journal of Pharmaceutics.
623, 121923-121923.
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Rahman, Z., Mohamed, E. M., Dharani, S., Khuroo, T., Young, M., Feng, C., Cecil, T., & Khan, M. A.
(2022).
Development and Validation Of A Discriminatory Dissolution Method for Portioned Moist Snuff and Snus. Journal of Pharmaceutical Sciences.
111(6), 1700-1708.
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Doke, M., Kashanchi, F., Khan, M. A., & Samikkannu, T.
(2022).
HIV-1 Tat and cocaine coexposure impacts piRNAs to affect astrocyte energy metabolism. Epigenomics.
14(5), 261-278.
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Dharani, S., Sediri, K., Cook, P., Arunagiri, R., Khan, M. A., & Rahman, Z.
(2021).
Preparation and Characterization of Stable Amorphous Glassy Solution of BCS II and IV Drugs. AAPS PharmSciTech.
23(1), 35.
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Seko, I., Tonbul, H., Tavukuolu, E., ahin, A., Akbas, S., Yank, H., ... Capan, Y.
(2021).
Development of curcumin and docetaxel co-loaded actively targeted PLGA nanoparticles to overcome blood brain barrier. Journal of Drug Delivery Science and Technology.
66, 102867-102867.
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Doke, M., Kashanchi, F., Khan, M. A., & Samikkannu, T.
(2021).
HIV-1 Tat and cocaine impact astrocytic energy reservoir influence on miRNA epigenetic regulation. Genomics.
113(6), 3461-3475.
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Sivalingam, K., Doke, M., Khan, M. A., & Samikkannu, T.
(2021).
Influence of psychostimulants and opioids on epigenetic modification of class III histone deacetylase (HDAC)-sirtuins in glial cells. Scientific Reports.
11(1), 21335.
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Khuroo, T., Dharani, S., Mohamed, E. M., Immadi, S., Wu, Z., Khan, M. A., ... Rahman, Z.
(2021).
Ultra-long acting prodrug of dolutegravir and delivery system - Physicochemical, pharmacokinetic and formulation characterizations. International Journal of Pharmaceutics.
607, 120889-120889.
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Hamed, R., Mohamed, E. M., Sediri, K., Khan, M. A., & Rahman, Z.
(2021).
Development of stable amorphous solid dispersion and quantification of crystalline fraction of lopinavir by spectroscopic-chemometric methods. International Journal of Pharmaceutics.
602, 120657-120657.
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Hamideh, A., Rahman, Z., Dharani, S., Khuroo, T., Mohamed, E. M., Nutan, M., Reddy, I. K., & Khan, M. A.
(2021).
Preparation and characterization of dicarboxylic acids salt of aripiprazole with enhanced physicochemical properties. PHARMACEUTICAL DEVELOPMENT AND TECHNOLOGY.
26(4), 455-463.
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Khuroo, T., Mohamed, E. M., Dharani, S., Afrooz, H., Barakh Ali, S. F., Cook, P., Khan, M. A., & Rahman, Z.
(2021).
Coating characterization by hyperspectroscopy and predictive dissolution models of tablets coated with blends of cellulose acetate and cellulose acetate phthalate. AAPS PharmSciTech.
22(3), 122.
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Charoo, N. A., Funkhouser, C., Kuttolamadom, M. A., Khan, M., & Rahman, Z.
(2021).
Opportunities and Challenges of Selective Laser Sintering 3D Printing in Personalized Pharmaceutical Manufacturing. American Pharmaceutical Review.
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Yce, M., Sert, F., Torabfam, M., Parlar, A., Grel, B., akr, N., ... apan, Y.
(2021).
Fractionated charge variants of biosimilars: A review of separation methods, structural and functional analysis. Analytica Chimica Acta.
1152, 238189-238189.
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Rahman, Z., Dharani, S., Khuroo, T., & Khan, M. A.
(2021).
Potential Application of USP Paddle and Basket Dissolution Methods in Discriminating for Portioned Moist Snuff and Snus Smokeless Tobacco Products. AAPS PharmSciTech.
22(1), 51.
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Afrooz, H., Mohamed, E. M., Barakh Ali, S. F., Dharani, S., Nutan, M., Khan, M. A., & Rahman, Z.
(2021).
Salt Engineering of Aripiprazole with Polycarboxylic Acids to Improve Physicochemical Properties. AAPS PharmSciTech.
22(1), 31.
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Hamed, R., Mohamed, E. M., Rahman, Z., & Khan, M. A.
(2021).
3D-printing of lopinavir printlets by selective laser sintering and quantification of crystalline fraction by XRPD-chemometric models. International Journal of Pharmaceutics.
592, 120059-120059.
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Dharani, S., Barakh Ali, S. F., Afrooz, H., Khan, M. A., & Rahman, Z.
(2020).
Studying effect of glyceryl palmitostearate amount, manufacturing method and stability on polymorphic transformation and dissolution of rifaximin tablets. International Journal of Pharmaceutics.
589(Ind. Eng. Chem. Res. 54 2015), 119785-119785.
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Mohamed, E. M., Khuroo, T., Afrooz, H., Dharani, S., Sediri, K., Cook, P., ... Rahman, Z.
(2020).
Development of a Multivariate Predictive Dissolution Model for Tablets Coated with Cellulose Ester Blends. Pharmaceuticals.
13(10), 311-311.
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Mohamed, E. M., Barakh Ali, S. F., Rahman, Z., Dharani, S., Ozkan, T., Kuttolamadom, M. A., & Khan, M. A.
(2020).
Formulation Optimization of Selective Laser Sintering 3D-Printed Tablets of Clindamycin Palmitate Hydrochloride by Response Surface Methodology. AAPS PharmSciTech.
21(6), 232.
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Charoo, N. A., Barakh Ali, S. F., Mohamed, E. M., Kuttolamadom, M. A., Ozkan, T., Khan, M. A., & Rahman, Z.
(2020).
Selective laser sintering 3D printing - an overview of the technology and pharmaceutical applications. 46(6), 869-877.
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Caban-Toktas, S., Sahin, A., Lule, S., Esendagli, G., Vural, I., Karl Oguz, K., ... Capan, Y.
(2020).
Combination of Paclitaxel and R-flurbiprofen loaded PLGA nanoparticles suppresses glioblastoma growth on systemic administration. International Journal of Pharmaceutics.
578, 119076-119076.
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Rahman, Z., Dharani, S., Barakh Ali, S. F., Nutan, M., & Khan, M. A.
(2020).
Effects of Diluents on Physical and Chemical Stability of Phenytoin and Phenytoin Sodium. AAPS PharmSciTech.
21(3), 104.
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Barakh Ali, S. F., Dharani, S., Afrooz, H., Mohamed, E. M., Cook, P., Khan, M. A., & Rahman, Z.
(2020).
Development of Abuse-Deterrent Formulations Using Sucrose Acetate Isobutyrate. AAPS PharmSciTech.
21(3), 99.
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Dharani, S., Barakh Ali, S. F., Afrooz, H., Mohamed, E. M., Cook, P., Khan, M. A., & Rahman, Z.
(2020).
Development of Methamphetamine Abuse-Deterrent Formulations Using Sucrose Acetate Isobutyrate. Journal of Pharmaceutical Sciences.
109(3), 1338-1346.
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Barakh Ali, S. F., Dharani, S., Afrooz, H., Khan, M. A., Mohamed, E. M., Kohli, K., & Rahman, Z.
(2019).
Application of salt engineering to reduce/mask bitter taste of clindamycin. 45(12), 1871-1878.
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Dharani, S., Barakh Ali, S. F., Afrooz, H., Khan, M. A., & Rahman, Z.
(2019).
Univariate and Multivariate Models for Determination of Prasugrel Base in the Formulation of Prasugrel Hydrochloride Using XRPD Method. Journal of Pharmaceutical Sciences.
108(11), 3575-3581.
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Barakh Ali, S. F., Mohamed, E. M., Ozkan, T., Kuttolamadom, M. A., Khan, M. A., Asadi, A., & Rahman, Z.
(2019).
Understanding the effects of formulation and process variables on the printlets quality manufactured by selective laser sintering 3D printing. International Journal of Pharmaceutics.
570, 118651-118651.
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Faustino, P. J., Brown, A., Lowry, B., Yang, Y., Wang, Y., Khan, M. A., Dunbar, K. R., & Mohammad, A.
(2019).
Quantitative evaluation of the thallium binding of soluble and insoluble Prussian blue hexacyanoferrate analogs: A scientific comparison based on their critical quality attributes. International Journal of Pharmaceutics.
569, 118600-118600.
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Ali, S., Afrooz, H., Hampel, R., Mohamed, E. M., Bhattacharya, R., Cook, P., Khan, M. A., & Rahman, Z.
(2019).
Blend of cellulose ester and enteric polymers for delayed and enteric coating of core tablets of hydrophilic and hydrophobic drugs. International Journal of Pharmaceutics.
567, 118462-118462.
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Xu, X., Siddiqui, A., Srinivasan, C., Mohammad, A., Rahman, Z., Korang-Yeboah, M., ... Ashraf, M.
(2019).
Evaluation of Abuse-Deterrent Characteristics of Tablets Prepared via Hot-Melt Extrusion. AAPS PharmSciTech.
20(6), 230.
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Dharani, S., Barakh Ali, S. F., Afrooz, H., Khan, M. A., & Rahman, Z.
(2019).
Development and Validation of a Discriminatory Dissolution Method for Rifaximin Products. Journal of Pharmaceutical Sciences.
108(6), 2112-2118.
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Dharani, S., Barakh Ali, S. F., Afrooz, H., Bhattacharya, R., Khan, M. A., & Rahman, Z.
(2019).
Quality and In-Use Stability Comparison of Brand and Generics of Extended-Release Phenytoin Sodium Capsules. Journal of Pharmaceutical Sciences.
108(5), 1808-1817.
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Barakh Ali, S. F., Rahman, Z., Dharani, S., Afrooz, H., & Khan, M. A.
(2019).
Chemometric Models for Quantification of Carbamazepine Anhydrous and Dihydrate Forms in the Formulation. Journal of Pharmaceutical Sciences.
108(3), 1211-1219.
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Martinez, M. N., Bhoopathy, S., Carlert, S., Cirit, M., Fahmy, R., Flanagan, T., ... Vertzoni, M.
(2019).
Workshop Report: USP Workshop on Exploring the Science of Drug Absorption. Dissolution Technologies.
26(3), 38-66.
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Rahman, Z., Dharani, S., Barakh Ali, S. F., Afrooz, H., Reddy, I. K., & Khan, M. A.
(2018).
Effect of processing parameters and controlled environment storage on the disproportionation and dissolution of extended-release capsule of phenytoin sodium. International Journal of Pharmaceutics.
550(1-2), 290-299.
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Rahman, Z., Barakh Ali, S. F., Ozkan, T., Charoo, N. A., Reddy, I. K., & Khan, M. A.
(2018).
Additive Manufacturing with 3D Printing: Progress from Bench to Bedside. AAPS Journal.
20(6), 101.
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Dharani, S., Rahman, Z., Barakh Ali, S. F., Afrooz, H., & Khan, M. A.
(2018).
Quantitative estimation of phenytoin sodium disproportionation in the formulations using vibration spectroscopies and multivariate methodologies. International Journal of Pharmaceutics.
539(1-2), 65-74.
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Rahman, Z., Akhtar, S., Siddiqui, A., Ciavarella, A. B., Nguyenpho, A., Faustino, P. J., & Khan, M. A.
(2018).
A headspace-gas chromatography method for isopropanol determination in warfarin sodium products as a measure of drug crystallinity. Acta Pharmaceutica.
68(1), 31-46.
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Sahin, A., Esendagli, G., Yerlikaya, F., Caban-Toktas, S., Yoyen-Ermis, D., Horzum, U., ... Capan, Y.
(2017).
A small variation in average particle size of PLGA nanoparticles prepared by nanoprecipitation leads to considerable change in nanoparticles' characteristics and efficacy of intracellular delivery. Artificial cells, nanomedicine, and biotechnology.
45(8), 1657-1664.
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Krishnaiah, Y., Pavurala, N., Yang, Y., Manda, P., Katragadda, U., Yang, Y., ... Khan, M. A.
(2017).
In Vitro Drug Transfer Due to Drug Retention in Human Epidermis Pretreated with Application of Marketed Estradiol Transdermal Systems. AAPS PharmSciTech.
18(6), 2131-2140.
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Spinks, C. B., Zidan, A. S., Khan, M. A., Habib, M. J., & Faustino, P. J.
(2017).
Pharmaceutical characterization of novel tenofovir liposomal formulations for enhanced oral drug delivery: in vitro pharmaceutics and Caco-2 permeability investigations. Clinical Pharmacology: Advances and Applications.
9, 29-38.
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Rahman, Z., Zidan, A. S., Korang-Yeboah, M., Yang, Y., Siddiqui, A., Shakleya, D., ... Ashraf, M.
(2017).
Effects of excipients and curing process on the abuse deterrent properties of directly compressed tablets. International Journal of Pharmaceutics.
517(1-2), 303-311.
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Norman, J., Madurawe, R. D., Moore, C., Khan, M. A., & Khairuzzaman, A.
(2017).
A new chapter in pharmaceutical manufacturing: 3D-printed drug products. Advanced Drug Delivery Reviews.
108, 39-50.
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Ciavarella, A. B., Khan, M. A., Gupta, A., & Faustino, P. J.
(2016).
Dose Uniformity of Scored and Unscored Tablets: Application of the FDA Tablet Scoring Guidance for Industry. Journal of pharmaceutical science and technology : the official journal of PDA.
70(6), 523-532.
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Stegemann, S., Ternik, R. L., Onder, G., Khan, M. A., & van Riet-Nales, D. A.
(2016).
Defining Patient Centric Pharmaceutical Drug Product Design. AAPS Journal.
18(5), 1047-1055.
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Khan, S. R., Mohammad, A., Khan, M. A., & Faustino, P. J.
(2016).
Critical Importance and Quality Evaluation of Drug Delivery Autoinjectors in the FDA-DOD Shelf Life Extension Program (SLEP). AAPS Journal.
18(4), 801-803.
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Ciavarella, A. B., Khan, M. A., Gupta, A., & Faustino, P. J.
(2016).
Dose Uniformity of Scored and Unscored Tablets: Application of the FDA Tablet Scoring Guidance for Industry. Journal of pharmaceutical science and technology : the official journal of PDA.
70(6), 523-532.
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Rahman, Z., Yang, Y., Korang-Yeboah, M., Siddiqui, A., Xu, X., Ashraf, M., & Khan, M. A.
(2016).
Assessing impact of formulation and process variables on in-vitro performance of directly compressed abuse deterrent formulations. International Journal of Pharmaceutics.
502(1-2), 138-150.
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Korang-Yeboah, M., Akhtar, S., Siddiqui, A., Rahman, Z., & Khan, M. A.
(2016).
Application of NIR chemometric methods for quantification of the crystalline fraction of warfarin sodium in drug product. 42(4), 584-594.
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Moolchandani, V., Augsburger, L. L., Gupta, A., Khan, M. A., Langridge, J., & Hoag, S. W.
(2016).
To investigate the influence of machine operating variables on formulations derived from lactose types in capsule filling: part 2. 42(4), 624-635.
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Xu, X., Gupta, A., Al-Ghabeish, M., Calderon, S. N., & Khan, M. A.
(2016).
Risk based in vitro performance assessment of extended release abuse deterrent formulations. International Journal of Pharmaceutics.
500(1-2), 255-267.
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Korang-Yeboah, M., Rahman, Z., Shah, D., Mohammad, A., Wu, S., Siddiqui, A., & Khan, M. A.
(2016).
Impact of formulation and process variables on solid-state stability of theophylline in controlled release formulations. International Journal of Pharmaceutics.
499(1-2), 20-28.
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Yang, Y., Mohammad, A., Berendt, R. T., Carlin, A., Khan, M. A., & Faustino, P. J.
(2016).
Evaluation of the In Vitro Efficacy of Sevelamer Hydrochloride and Sevelamer Carbonate. Journal of Pharmaceutical Sciences.
105(2), 864-875.
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Costa, A. P., Xu, X., Khan, M. A., & Burgess, D. J.
(2016).
Liposome Formation Using a Coaxial Turbulent Jet in Co-Flow. Pharmaceutical Research.
33(2), 404-416.
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Chavez, B. K., Agarabi, C. D., Read, E. K., Boyne, M. T., Khan, M. A., & Brorson, K. A.
(2016).
Improved Stability of a Model IgG3 by DoE-Based Evaluation of Buffer Formulations. 2016, 2074149-8.
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Korang-Yeboah, M., Rahman, Z., Shah, D. A., & Khan, M. A.
(2016).
Spectroscopic-Based Chemometric Models for Quantifying Low Levels of Solid-State Transitions in Extended Release Theophylline Formulations. Journal of Pharmaceutical Sciences.
105(1), 97-105.
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Rahman, Z., Mohammad, A., Siddiqui, A., & Khan, M. A.
(2015).
Comparison of Univariate and Multivariate Models of C SSNMR and XRPD Techniques for Quantification of Nimodipine Polymorphs. AAPS PharmSciTech.
16(6), 1368-1376.
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Nguyenpho, A., Ciavarella, A. B., Siddiqui, A., Rahman, Z., Akhtar, S., Hunt, R., Korang-Yeboah, M., & Khan, M. A.
(2015).
Evaluation of In-Use Stability of Anticoagulant Drug Products: Warfarin Sodium. Journal of Pharmaceutical Sciences.
104(12), 4232-4240.
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Al-Ghabeish, M., Xu, X., Krishnaiah, Y., Rahman, Z., Yang, Y., & Khan, M. A.
(2015).
Influence of drug loading and type of ointment base on the in vitro performance of acyclovir ophthalmic ointment. International Journal of Pharmaceutics.
495(2), 783-791.
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Rathore, A. S., Kumar Singh, S., Pathak, M., Read, E. K., Brorson, K. A., Agarabi, C. D., & Khan, M.
(2015).
Fermentanomics: Relating quality attributes of a monoclonal antibody to cell culture process variables and raw materials using multivariate data analysis. 31(6), 1586-1599.
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Xu, X., Al-Ghabeish, M., Krishnaiah, Y., Rahman, Z., & Khan, M. A.
(2015).
Kinetics of drug release from ointments: Role of transient-boundary layer. International Journal of Pharmaceutics.
494(1), 31-39.
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Siddiqui, A., Rahman, Z., Korang-Yeboah, M., & Khan, M. A.
(2015).
Development and validation of X-ray diffraction method for quantitative determination of crystallinity in warfarin sodium products. International Journal of Pharmaceutics.
493(1-2), 1-6.
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Xu, X., Al-Ghabeish, M., Rahman, Z., Krishnaiah, Y., Yerlikaya, F., Yang, Y., ... Khan, M. A.
(2015).
Formulation and process factors influencing product quality and in vitro performance of ophthalmic ointments. International Journal of Pharmaceutics.
493(1-2), 412-425.
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Moolchandani, V., Augsburger, L. L., Gupta, A., Khan, M., Langridge, J., & Hoag, S. W.
(2015).
Characterization and selection of suitable grades of lactose as functional fillers for capsule filling: part 1. 41(9), 1452-1463.
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irat, Y., Adil, M., Patrick, J. F., Mansoor, A. K., & Saeed, R. K.
(2015).
A Comparative Evaluation of Polystyrene Divinylbenzene Copolymer HPLC Columns on the Chromatographic Performance of the Compendial Method for Doxycycline Hyclate Capsules: Implications for Method Implementation of a Medical Countermeasure Medication. Journal of Analytical Sciences, Methods and Instrumentation.
05(03), 23-34.
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Wu, H., Read, E., White, M., Chavez, B., Brorson, K., Agarabi, C., & Khan, M.
(2015).
Real time monitoring of bioreactor mAb IgG3 cell culture process dynamics via Fourier transform infrared spectroscopy: Implications for enabling cell culture process analytical technology. Frontiers of Chemical Science and Engineering.
9(3), 386-406.
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Rahman, Z., Mohammad, A., Akhtar, S., Siddiqui, A., Korang-Yeboah, M., & Khan, M. A.
(2015).
Chemometric Model Development and Comparison of Raman and (13)C Solid-State Nuclear Magnetic Resonance-Chemometric Methods for Quantification of Crystalline/Amorphous Warfarin Sodium Fraction in the Formulations. Journal of Pharmaceutical Sciences.
104(8), 2550-2558.
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Yang, Y., Manda, P., Pavurala, N., Khan, M. A., & Krishnaiah, Y.
(2015).
Development and validation of in vitro-in vivo correlation (IVIVC) for estradiol transdermal drug delivery systems. Journal of Controlled Release.
210, 58-66.
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Awotwe-Otoo, D., Agarabi, C., Read, E. K., Lute, S., Brorson, K. A., & Khan, M. A.
(2015).
Product and process understanding to relate the effect of freezing method on glycation and aggregation of lyophilized monoclonal antibody formulations. International Journal of Pharmaceutics.
490(1-2), 341-350.
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Cantor, S. L., Khan, M. A., & Gupta, A.
(2015).
Development and optimization of taste-masked orally disintegrating tablets (ODTs) of clindamycin hydrochloride. 41(7), 1156-1164.
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Yu, L. X., Baker, J., Berlam, S. C., Boam, A., Brandreth, E. J., Buhse, L., ... Vaithiyalingam, S.
(2015).
Advancing Product Quality: a Summary of the Inaugural FDA/PQRI Conference. AAPS Journal.
17(4), 1011-1018.
-
Agarabi, C. D., Schiel, J. E., Lute, S. C., Chavez, B. K., Boyne, M. T., Brorson, K. A., Khan, M., & Read, E. K.
(2015).
Bioreactor process parameter screening utilizing a Plackett-Burman design for a model monoclonal antibody. Journal of Pharmaceutical Sciences.
104(6), 1919-1928.
-
Wu, H., Lyon, R. C., Khan, M. A., Voytilla, R. J., & Drennen, J. K.
(2015).
Integration of Near-Infrared Spectroscopy and Mechanistic Modeling for Predicting Film-Coating and Dissolution of Modified Release Tablets. Industrial & Engineering Chemistry Research.
54(22), 6012-6023.
-
Siddiqui, A., Rahman, Z., & Khan, M. A.
(2015).
Application of chemometric methods to differential scanning calorimeter (DSC) to estimate nimodipine polymorphs from cosolvent system. 41(6), 995-999.
-
Rahman, Z., Bykadi, S., Siddiqui, A., & Khan, M. A.
(2015).
Comparison of X-ray powder diffraction and solid-state nuclear magnetic resonance in estimating crystalline fraction of tacrolimus in sustained-release amorphous solid dispersion and development of discriminating dissolution method. Journal of Pharmaceutical Sciences.
104(5), 1777-1786.
-
Srinivasan, C., Siddiqui, A., Korang-Yeboah, M., & Khan, M. A.
(2015).
Stability characterization and appearance of particulates in a lyophilized formulation of a model peptide hormone-human secretin. International Journal of Pharmaceutics.
481(1-2), 104-113.
-
Mohammad, A., Yang, Y., Khan, M. A., & Faustino, P. J.
(2015).
Long-term stability study of Prussian blue-A quality assessment of water content and cyanide release. 53(2), 102-107.
-
Gupta, A., Chidambaram, N., & Khan, M. A.
(2015).
An index for evaluating difficulty of Chewing Index for chewable tablets. 41(2), 239-243.
-
Mohammad, A., Yang, Y., Khan, M. A., & Faustino, P. J.
(2015).
A long-term stability study of Prussian blue: A quality assessment of water content and cesium binding. JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS.
103, 85-90.
-
Wu, H., Dong, Z., Li, H., & Khan, M.
(2015).
An Integrated Process Analytical Technology (PAT) Approach for Pharmaceutical Crystallization Process Understanding to Ensure Product Quality and Safety: FDA Scientists Perspective. Organic Process Research and Development.
19(1), 89-101.
-
Wu, H., White, M., & Khan, M.
(2015).
An Integrated Process Analytical Technology (PAT) Approach for Process Dynamics-Related Measurement Error Evaluation and Process Design Space Development of a Pharmaceutical Powder Blending Bed. Organic Process Research and Development.
19(1), 215-226.
-
Simon, L. L., Pataki, H., Marosi, G., Meemken, F., Hungerbuhler, K., Baiker, A., ... Chiu, M.
(2015).
Assessment of Recent Process Analytical Technology (PAT) Trends: A Multiauthor Review. Organic Process Research and Development.
19(1), 3-62.
-
Oka, S., Kapar, O., Tokrov, V., Sowrirajan, K., Wu, H., Khan, M., ... Ramachandran, R.
(2015).
A quantitative study of the effect of process parameters on key granule characteristics in a high shear wet granulation process involving a two component pharmaceutical blend. Advanced Powder Technology.
26(1), 315-322.
-
Wu, H., Kurtyka, B., Wu, G., Maguire, J. A., Madurawe, R., Moore, C., ... Yu, L.
(2015).
Monitoring, understanding and assessing pharmaceutical process and product quality. European Pharmaceutical Review.
20(6), 50-56.
-
Krishnaiah, Y., Yang, Y., Hunt, R. L., & Khan, M. A.
(2014).
Cold flow of estradiol transdermal systems: influence of drug loss on the in vitro flux and drug transfer across human epidermis. International Journal of Pharmaceutics.
477(1-2), 73-80.
-
Mohammad, A., Faustino, P. J., Khan, M. A., & Yang, Y.
(2014).
Long-term stability study of Prussian blue - a quality assessment of water content and thallium binding. International Journal of Pharmaceutics.
477(1-2), 122-127.
-
Rahman, Z., Siddiqui, A., Bykadi, S., & Khan, M. A.
(2014).
Determination of tacrolimus crystalline fraction in the commercial immediate release amorphous solid dispersion products by a standardized X-ray powder diffraction method with chemometrics. International Journal of Pharmaceutics.
475(1-2), 462-470.
-
Krishnaiah, Y., Xu, X., Rahman, Z., Yang, Y., Katragadda, U., Lionberger, R., ... Khan, M. A.
(2014).
Development of performance matrix for generic product equivalence of acyclovir topical creams. International Journal of Pharmaceutics.
475(1-2), 110-122.
-
Siddiqui, A., Rahman, Z., Khan, S. R., Awotwe-Otoo, D., & Khan, M. A.
(2014).
Root cause evaluation of particulates in the lyophilized indomethacin sodium trihydrate plug for parenteral administration. International Journal of Pharmaceutics.
473(1-2), 545-551.
-
Krishnaiah, Y., Yang, Y., Bykadi, S., Sayeed, V. A., & Khan, M. A.
(2014).
Comparative evaluation of in vitro efficacy of colesevelam hydrochloride tablets. 40(9), 1173-1179.
-
Siddiqui, A., Rahman, Z., Bykadi, S., & Khan, M. A.
(2014).
Chemometric methods for the quantification of crystalline tacrolimus in solid dispersion by powder X-ray diffractrometry. Journal of Pharmaceutical Sciences.
103(9), 2819-2828.
-
Woodcock, J., & Khan, M. A.
(2014).
FDA Analysis of Atorvastatin Products Refutes Report of Methyl Ester Impurities. 48(5), 554-556.
-
Rahman, Z., Siddiqui, A., Bykadi, S., & Khan, M. A.
(2014).
Near-infrared and fourier transform infrared chemometric methods for the quantification of crystalline tacrolimus from sustained-release amorphous solid dispersion. Journal of Pharmaceutical Sciences.
103(8), 2376-2385.
-
Yu, L. X., Amidon, G., Khan, M. A., Hoag, S. W., Polli, J., Raju, G. K., & Woodcock, J.
(2014).
Understanding pharmaceutical quality by design. AAPS Journal.
16(4), 771-783.
-
Awotwe Otoo, D., Agarabi, C., & Khan, M. A.
(2014).
An integrated process analytical technology (PAT) approach to monitoring the effect of supercooling on lyophilization product and process parameters of model monoclonal antibody formulations. Journal of Pharmaceutical Sciences.
103(7), 2042-2052.
-
Gandhi, S. V., Rodriguez, W., Khan, M., & Polli, J. E.
(2014).
Considerations for a Pediatric Biopharmaceutics Classification System (BCS): application to five drugs. AAPS PharmSciTech.
15(3), 601-611.
-
Khan, S. R., Kona, R., Faustino, P. J., Gupta, A., Taylor, J. S., Porter, D. A., & Khan, M.
(2014).
United States Food and Drug Administration and Department of Defense shelf-life extension program of pharmaceutical products: progress and promise. Journal of Pharmaceutical Sciences.
103(5), 1331-1336.
-
Krishnaiah, Y., Katragadda, U., & Khan, M. A.
(2014).
Stereomicroscopic imaging technique for the quantification of cold flow in drug-in-adhesive type of transdermal drug delivery systems. Journal of Pharmaceutical Sciences.
103(5), 1433-1442.
-
Shah, R. B., Yang, Y., Khan, M. A., Raw, A., Yu, L. X., & Faustino, P. J.
(2014).
Pharmaceutical characterization and thermodynamic stability assessment of a colloidal iron drug product: iron sucrose. International Journal of Pharmaceutics.
464(1-2), 46-52.
-
Chaudhury, A., Wu, H., Khan, M., & Ramachandran, R.
(2014).
A mechanistic population balance model for granulation processes: Effect of process and formulation parameters. Chemical Engineering Science.
107, 76-92.
-
Rahman, Z., Xu, X., Katragadda, U., Krishnaiah, Y., Yu, L., & Khan, M. A.
(2014).
Quality by design approach for understanding the critical quality attributes of cyclosporine ophthalmic emulsion. Molecular Pharmaceutics.
11(3), 787-799.
-
Madhavarao, C. N., Agarabi, C. D., Wong, L., Mller-Loennies, S., Braulke, T., Khan, M., Anderson, H., & Johnson, G. R.
(2014).
Evaluation of butyrate-induced production of a mannose-6-phosphorylated therapeutic enzyme using parallel bioreactors. BIOTECHNOLOGY AND APPLIED BIOCHEMISTRY.
61(2), 184-192.
-
Cantor, S. L., Gupta, A., & Khan, M. A.
(2014).
Analytical methods for the evaluation of melamine contamination. Journal of Pharmaceutical Sciences.
103(2), 539-544.
-
Wu, H., White, M., Berendt, R., Foringer, R. D., & Khan, M.
(2014).
Integrated Process Analytical Technology Approach for Nucleation Induction Time Measurement and Nucleation Mechanism Assessment for a Dynamic Multicomponent Pharmaceutical Antisolvent Crystallization System. Industrial & Engineering Chemistry Research.
53(4), 1688-1701.
-
Zidan, A. S., Spinks, C. B., Habib, M. J., & Khan, M. A.
(2013).
Formulation and transport properties of tenofovir loaded liposomes through Caco-2 cell model. Journal of Liposome Research.
23(4), 318-326.
-
Rahman, Z., Siddiqui, A., & Khan, M. A.
(2013).
Characterization of a nonribosomal peptide antibiotic solid dispersion formulation by process analytical technologies sensors. Journal of Pharmaceutical Sciences.
102(12), 4337-4346.
-
Gupta, A., & Khan, M. A.
(2013).
Challenges of pediatric formulations: a FDA science perspective. International Journal of Pharmaceutics.
457(1), 346-348.
-
Xu, X., Siddiqui, A., & Khan, M. A.
(2013).
Focused beam reflectance measurement to monitor nimodipine precipitation process. International Journal of Pharmaceutics.
456(2), 353-356.
-
Rahman, Z., & Khan, M. A.
(2013).
Hunter screening design to understand the product variability of solid dispersion formulation of a peptide antibiotic. International Journal of Pharmaceutics.
456(2), 572-582.
-
Siddiqui, A., Rahman, Z., Sayeed, V. A., & Khan, M. A.
(2013).
Chemometric evaluation of near infrared, fourier transform infrared, and Raman spectroscopic models for the prediction of nimodipine polymorphs. Journal of Pharmaceutical Sciences.
102(11), 4024-4035.
-
Rahman, Z., Siddiqui, A., & Khan, M. A.
(2013).
Orally disintegrating tablet of novel salt of antiepileptic drug: formulation strategy and evaluation. European Journal of Pharmaceutics and Biopharmaceutics.
85(3 Pt B), 1300-1309.
-
Kimchi-Sarfaty, C., Schiller, T., Hamasaki-Katagiri, N., Khan, M. A., Yanover, C., & Sauna, Z. E.
(2013).
Building better drugs: developing and regulating engineered therapeutic proteins. Trends in Pharmacological Sciences.
34(10), 534-548.
-
Rahman, Z., Siddiqui, A., & Khan, M. A.
(2013).
Assessing the impact of nimodipine devitrification in the ternary cosolvent system through quality by design approach. International Journal of Pharmaceutics.
455(1-2), 113-123.
-
Yerlikaya, F., Ozgen, A., Vural, I., Guven, O., Karaagaoglu, E., Khan, M. A., & Capan, Y.
(2013).
Development and evaluation of paclitaxel nanoparticles using a quality-by-design approach. Journal of Pharmaceutical Sciences.
102(10), 3748-3761.
-
Zajicek, A., Fossler, M. J., Barrett, J. S., Worthington, J. H., Ternik, R., Charkoftaki, G., ... MacLaren, D. D.
(2013).
A report from the pediatric formulations task force: perspectives on the state of child-friendly oral dosage forms. AAPS Journal.
15(4), 1072-1081.
-
Xu, X., Gupta, A., Faustino, P., Sathe, P. M., Sayeed, V. A., & Khan, M. A.
(2013).
Development and validation of a HPLC method for dissolution and stability assay of liquid-filled cyclosporine capsule drug products. AAPS PharmSciTech.
14(3), 959-967.
-
Awotwe-Otoo, D., Agarabi, C., Read, E. K., Lute, S., Brorson, K. A., Khan, M. A., & Shah, R. B.
(2013).
Impact of controlled ice nucleation on process performance and quality attributes of a lyophilized monoclonal antibody. International Journal of Pharmaceutics.
450(1-2), 70-78.
-
Siddiqui, A., Shah, R. B., & Khan, M. A.
(2013).
Oseltamivir phosphate-amberlite(TM) IRP 64 ionic complex for taste masking: preparation and chemometric evaluation. Journal of Pharmaceutical Sciences.
102(6), 1800-1812.
-
Xu, X., Gupta, A., Sayeed, V. A., & Khan, M. A.
(2013).
Process analytical technology to understand the disintegration behavior of alendronate sodium tablets. Journal of Pharmaceutical Sciences.
102(5), 1513-1523.
-
Yang, Y., Bykadi, S., Carlin, A. S., Shah, R. B., Yu, L. X., & Khan, M. A.
(2013).
Comparative evaluation of the in vitro efficacy of lanthanum carbonate chewable tablets. Journal of Pharmaceutical Sciences.
102(4), 1370-1381.
-
Yang, Y., Shah, R. B., Yu, L. X., & Khan, M. A.
(2013).
In vitro bioequivalence approach for a locally acting gastrointestinal drug: lanthanum carbonate. Molecular Pharmaceutics.
10(2), 544-550.
-
Mirza, T., Bykadi, S. A., Ellison, C. D., Yang, Y., Davit, B. M., & Khan, M. A.
(2013).
Use of in vitro-in vivo correlation to predict the pharmacokinetics of several products containing a BCS class 1 drug in extended release matrices. Pharmaceutical Research.
30(1), 179-190.
-
Wu, G. K., Gupta, A., Khan, M. A., & Faustino, P. J.
(2013).
Development and Application of a Validated HPLC Method for the Determination of Clindamycin Palmitate Hydrochloride in Marketed Drug Products: An Optimization of the Current USP Methodology for Assay. Journal of Analytical Sciences, Methods and Instrumentation.
2013(04), 202-211.
-
Woodcock, J., Khan, M., & Yu, L. X.
(2012).
Withdrawal of generic budeprion for nonbioequivalence. NEW ENGLAND JOURNAL OF MEDICINE.
367(26), 2463-2465.
-
Awotwe-Otoo, D., Agarabi, C., Wu, G. K., Casey, E., Read, E., Lute, S., ... Shah, R. B.
(2012).
Quality by design: impact of formulation variables and their interactions on quality attributes of a lyophilized monoclonal antibody. International Journal of Pharmaceutics.
438(1-2), 167-175.
-
Rahman, Z., Zidan, A. S., Khan, S. R., Reddy, I. K., & Khan, M. A.
(2012).
Cholorpheniramine tannate complexes: physicochemical, chemometric, and taste masking evaluation. International Journal of Pharmaceutics.
436(1-2), 582-592.
-
Krishnaiah, Y., & Khan, M. A.
(2012).
Strategies of targeting oral drug delivery systems to the colon and their potential use for the treatment of colorectal cancer. PHARMACEUTICAL DEVELOPMENT AND TECHNOLOGY.
17(5), 521-540.
-
Xu, X., Costa, A. P., Khan, M. A., & Burgess, D. J.
(2012).
Application of quality by design to formulation and processing of protein liposomes. International Journal of Pharmaceutics.
434(1-2), 349-359.
-
Awotwe-Otoo, D., Agarabi, C., Keire, D., Lee, S., Raw, A., Yu, L., ... Shah, R. B.
(2012).
Physicochemical characterization of complex drug substances: evaluation of structural similarities and differences of protamine sulfate from various sources. AAPS Journal.
14(3), 619-626.
-
Rahman, Z., Zidan, A. S., Samy, R., Sayeed, V. A., & Khan, M. A.
(2012).
Improvement of physicochemical properties of an antiepileptic drug by salt engineering. AAPS PharmSciTech.
13(3), 793-801.
-
Berendt, R. T., Samy, R., Carlin, A. S., Pendse, A., Schwartz, P., Khan, M. A., & Faustino, P. J.
(2012).
Spontaneous carbonate formation in an amorphous, amine-rich, polymeric drug substance: sevelamer HCl product quality. Journal of Pharmaceutical Sciences.
101(8), 2681-2685.
-
Rahman, Z., Samy, R., Sayeed, V. A., & Khan, M. A.
(2012).
Physicochemical and mechanical properties of carbamazepine cocrystals with saccharin. PHARMACEUTICAL DEVELOPMENT AND TECHNOLOGY.
17(4), 457-465.
-
Wu, H., & Khan, M.
(2012).
THz spectroscopy: An emerging technology for pharmaceutical development and pharmaceutical Process Analytical Technology (PAT) applications. JOURNAL OF MOLECULAR STRUCTURE.
1020, 112-120.
-
Hamid, M., Khan, M. A., Khatri, A., & Akhtar, I.
(2012).
Effectiveness of premedication at the time of separation from parent and mask induction in paediatric patients coming for congenital heart disease surgery. Journal of the College of Physicians and Surgeons--Pakistan : JCPSP.
22(5), 280-284.
-
Xu, X., Khan, M. A., & Burgess, D. J.
(2012).
A two-stage reverse dialysis in vitro dissolution testing method for passive targeted liposomes. International Journal of Pharmaceutics.
426(1-2), 211-218.
-
Zidan, A. S., Rahman, Z., & Khan, M. A.
(2012).
Chemometric evaluation of brompheniramine-tannate complexes. Journal of Pharmaceutical Sciences.
101(4), 1450-1461.
-
Awotwe-Otoo, D., Agarabi, C., Faustino, P. J., Habib, M. J., Lee, S., Khan, M. A., & Shah, R. B.
(2012).
Application of quality by design elements for the development and optimization of an analytical method for protamine sulfate. JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS.
62, 61-67.
-
Xu, X., Khan, M. A., & Burgess, D. J.
(2012).
A quality by design (QbD) case study on liposomes containing hydrophilic API: II. Screening of critical variables, and establishment of design space at laboratory scale. International Journal of Pharmaceutics.
423(2), 543-553.
-
Zidan, A. S., Rahman, Z., Sayeed, V., Raw, A., Yu, L., & Khan, M. A.
(2012).
Crystallinity evaluation of tacrolimus solid dispersions by chemometric analysis. International Journal of Pharmaceutics.
423(2), 341-350.
-
Xu, X., Khan, M. A., & Burgess, D. J.
(2012).
Predicting hydrophilic drug encapsulation inside unilamellar liposomes. International Journal of Pharmaceutics.
423(2), 410-418.
-
Rahman, Z., Zidan, A. S., Berendt, R. T., & Khan, M. A.
(2012).
Tannate complexes of antihistaminic drug: sustained release and taste masking approaches. International Journal of Pharmaceutics.
422(1-2), 91-100.
-
Khan, S. R., Tawakkul, M., Sayeed, V. A., Faustino, P., & Khan, M. A.
(2012).
Stability Characterization, Kinetics and Mechanism of Degradation of Dantrolene in Aqueous Solution: Effect of pH and Temperature. Pharmacology & Pharmacy.
2012(03), 281-290.
-
Mockus, L. N., Paul, T. W., Pease, N. A., Harper, N. J., Basu, P. K., Oslos, E. A., ... Nail, S. L.
(2011).
Quality by design in formulation and process development for a freeze-dried, small molecule parenteral product: a case study. PHARMACEUTICAL DEVELOPMENT AND TECHNOLOGY.
16(6), 549-576.
-
Xu, X., Khan, M. A., & Burgess, D. J.
(2011).
A quality by design (QbD) case study on liposomes containing hydrophilic API: I. Formulation, processing design and risk assessment. International Journal of Pharmaceutics.
419(1-2), 52-59.
-
Asafu-Adjaye, E. B., Carlin, A. S., Jefferson, E. H., Bryant, A. R., Rothman, B., Khan, M. A., & Faustino, P. J.
(2011).
Comparative stability study of unit-dose repackaged furosemide tablets. Clinical Research and Regulatory Affairs.
28(2), 38-48.
-
Rahman, Z., Agarabi, C., Zidan, A. S., Khan, S. R., & Khan, M. A.
(2011).
Physico-mechanical and stability evaluation of carbamazepine cocrystal with nicotinamide. AAPS PharmSciTech.
12(2), 693-704.
-
Wu, H., & Khan, M. A.
(2011).
Quality-by-design: an integrated process analytical technology approach to determine the nucleation and growth mechanisms during a dynamic pharmaceutical coprecipitation process. Journal of Pharmaceutical Sciences.
100(5), 1969-1986.
-
Cantor, S. L., Hoag, S. W., Ellison, C. D., Khan, M. A., & Lyon, R. C.
(2011).
NIR spectroscopy applications in the development of a compacted multiparticulate system for modified release. AAPS PharmSciTech.
12(1), 262-278.
-
Mockus, L., LeBlond, D., Basu, P. K., Shah, R. B., & Khan, M. A.
(2011).
A QbD case study: Bayesian prediction of lyophilization cycle parameters. AAPS PharmSciTech.
12(1), 442-448.
-
Wu, H., White, M., & Khan, M. A.
(2011).
Quality-by-Design (QbD): An integrated process analytical technology (PAT) approach for a dynamic pharmaceutical co-precipitation process characterization and process design space development. International Journal of Pharmaceutics.
405(1-2), 63-78.
-
Collier, J. W., Shah, R. B., Bryant, A. R., Habib, M. J., Khan, M. A., & Faustino, P. J.
(2011).
Development and application of a validated HPLC method for the analysis of dissolution samples of levothyroxine sodium drug products. JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS.
54(3), 433-438.
-
Zhao, N. a., Zidan, A., Tawakkul, M., Sayeed, V. A., & Khan, M.
(2010).
Tablet splitting: Product quality assessment of metoprolol succinate extended release tablets. International Journal of Pharmaceutics.
401(1-2), 25-31.
-
Rahman, Z., Zidan, A. S., & Khan, M. A.
(2010).
Risperidone solid dispersion for orally disintegrating tablet: its formulation design and non-destructive methods of evaluation. International Journal of Pharmaceutics.
400(1-2), 49-58.
-
Shah, R. B., Collier, J. S., Sayeed, V. A., Bryant, A., Habib, M. J., & Khan, M. A.
(2010).
Tablet splitting of a narrow therapeutic index drug: a case with levothyroxine sodium. AAPS PharmSciTech.
11(3), 1359-1367.
-
Rahman, Z., Zidan, A. S., & Khan, M. A.
(2010).
Non-destructive methods of characterization of risperidone solid lipid nanoparticles. European Journal of Pharmaceutics and Biopharmaceutics.
76(1), 127-137.
-
Zidan, A. S., Rahman, Z., & Khan, M. A.
(2010).
Online monitoring of PLGA microparticles formation using Lasentec focused beam reflectance (FBRM) and particle video microscope (PVM). AAPS Journal.
12(3), 254-262.
-
Collier, J. W., Shah, R. B., Gupta, A., Sayeed, V., Habib, M. J., & Khan, M. A.
(2010).
Influence of formulation and processing factors on stability of levothyroxine sodium pentahydrate. AAPS PharmSciTech.
11(2), 818-825.
-
Zidan, A. S., Spinks, C., Fortunak, J., Habib, M., & Khan, M. A.
(2010).
Near-infrared investigations of novel anti-HIV tenofovir liposomes. AAPS Journal.
12(2), 202-214.
-
Rahman, Z., Zidan, A. S., & Khan, M. A.
(2010).
Formulation and evaluation of a protein-loaded solid dispersions by non-destructive methods. AAPS Journal.
12(2), 158-170.
-
Rahman, Z., Zidan, A. S., Habib, M. J., & Khan, M. A.
(2010).
Understanding the quality of protein loaded PLGA nanoparticles variability by Plackett-Burman design. International Journal of Pharmaceutics.
389(1-2), 186-194.
-
Samy, R., Faustino, P. J., Adams, W., Yu, L., Khan, M. A., & Yang, Y.
(2010).
Development and validation of an ion chromatography method for the determination of phosphate-binding of lanthanum carbonate. JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS.
51(5), 1108-1112.
-
Wu, H., & Khan, M. A.
(2010).
Quality-by-Design (QbD): an integrated process analytical technology (PAT) approach for real-time monitoring and mapping the state of a pharmaceutical coprecipitation process. Journal of Pharmaceutical Sciences.
99(3), 1516-1534.
-
Tawakkul, M. A., Faustino, P. J., Sayeed, V. A., Khan, M. A., & Khan, S. R.
(2010).
Development and application of a validated stability-indicating Ultra-Performance Liquid Chromatography (UPLC) method for the determination of dantrolene and its related impurities. Clinical Research and Regulatory Affairs.
27(1), 21-29.
-
Zidan, A. S., Rahman, Z., Habib, M. J., & Khan, M. A.
(2010).
Spectral and spatial characterization of protein loaded PLGA nanoparticles. Journal of Pharmaceutical Sciences.
99(3), 1180-1192.
-
Lee, A., McVey, J., Faustino, P., Lute, S., Sweeney, N., Pawar, V., ... Hussong, D.
(2010).
Use of Hydrogenophaga pseudoflava penetration to quantitatively assess the impact of filtration parameters for 0.2-micrometer-pore-size filters. 76(3), 695-700.
-
Yang, Y., Gupta, A., Carlin, A. S., Faustino, P. J., Lyon, R. C., Ellison, C. D., Rothman, B., & Khan, M. A.
(2010).
Comparative stability of repackaged metoprolol tartrate tablets. International Journal of Pharmaceutics.
385(1-2), 92-97.
-
Yang, Y., Shah, R. B., Faustino, P. J., Raw, A., Yu, L. X., & Khan, M. A.
(2010).
Thermodynamic stability assessment of a colloidal iron drug product: sodium ferric gluconate. Journal of Pharmaceutical Sciences.
99(1), 142-153.
-
Shah, R. B., Tawakkul, M. A., Sayeed, V. A., & Khan, M. A.
(2009).
Complexation between risperidone and amberlite resin by various methods of preparation and binding study. 35(12), 1409-1418.
-
Jameel, F., & Khan, M.
(2009).
Quality-by-design as applied to the development and manufacturing of a lyophilized protein product. American Pharmaceutical Review.
12(7), 20-24.
-
Wu, H., & Khan, M. A.
(2009).
Quality-by-design (QbD): an integrated approach for evaluation of powder blending process kinetics and determination of powder blending end-point. Journal of Pharmaceutical Sciences.
98(8), 2784-2798.
-
Tawakkul, M. A., Shah, R. B., Zidan, A., Sayeed, V. A., & Khan, M. A.
(2009).
Complexation of risperidone with a taste-masking resin: novel application of near infra-red and chemical imaging to evaluate complexes. PHARMACEUTICAL DEVELOPMENT AND TECHNOLOGY.
14(4), 409-421.
-
Gupta, A., Ciavarella, A. B., Rothman, B., Faustino, P. J., & Khan, M. A.
(2009).
Stability of gabapentin 300-mg capsules repackaged in unit dose containers. American Journal of Health-System Pharmacy.
66(15), 1376-1380.
-
Gupta, A., Hamad, M. L., Tawakkul, M., Sayeed, V. A., & Khan, M. A.
(2009).
Difference in the lubrication efficiency of bovine and vegetable-derived magnesium stearate during tabletting. AAPS PharmSciTech.
10(2), 500-504.
-
Gupta, A., Hunt, R. L., Shah, R. B., Sayeed, V. A., & Khan, M. A.
(2009).
Disintegration of highly soluble immediate release tablets: a surrogate for dissolution. AAPS PharmSciTech.
10(2), 495-499.
-
Shah, R. B., Tawakkul, M. A., Sayeed, V. A., & Khan, M. A.
(2009).
Complexation between risperidone and amberlite resin by various methods of preparation and binding study. 090526005142032-090526005142019.
-
Wu, H., Tawakkul, M., White, M., & Khan, M. A.
(2009).
Quality-by-design (QbD): an integrated multivariate approach for the component quantification in powder blends. International Journal of Pharmaceutics.
372(1-2), 39-48.
-
Xiang, D., Berry, J., Buntz, S., Gargiulo, P., Cheney, J., Joshi, Y., ... Khan, M. A.
(2009).
Robust calibration design in the pharmaceutical quantitative measurements with near-infrared (NIR) spectroscopy: Avoiding the chemometric pitfalls. Journal of Pharmaceutical Sciences.
98(3), 1155-1166.
-
Yang, Y., Carlin, A. S., Faustino, P. J., Motta, M., Hamad, M. L., He, R., ... Khan, M. A.
(2009).
Participation of women in clinical trials for new drugs approved by the food and drug administration in 2000-2002. Journal of Women's Health.
18(3), 303-310.
-
Sulub, Y., Wabuyele, B., Gargiulo, P., Pazdan, J., Cheney, J., Berry, J., ... Khan, M.
(2009).
Real-time on-line blend uniformity monitoring using near-infrared reflectance spectrometry: a noninvasive off-line calibration approach. JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS.
49(1), 48-54.
-
Xiang, D., LoBrutto, R., Cheney, J., Wabuyele, B. W., Berry, J., Lyon, R., ... Hussain, A. S.
(2009).
Evaluation of transmission and reflection modalities for measuring content uniformity of pharmaceutical tablets with near-infrared spectroscopy. APPLIED SPECTROSCOPY.
63(1), 33-47.
-
Hamad, M. L., Gupta, A., Shah, R. B., Lyon, R. C., Sayeed, V. A., & Khan, M. A.
(2008).
Functionality of magnesium stearate derived from bovine and vegetable sources: dry granulated tablets. Journal of Pharmaceutical Sciences.
97(12), 5328-5340.
-
Gupta, A., Hunt, R. L., & Khan, M. A.
(2008).
Influence of tablet characteristics on weight variability and weight loss in split tablets. American Journal of Health-System Pharmacy.
65(24), 2326-2328.
-
Xie, L., Wu, H., Shen, M., Augsburger, L. L., Lyon, R. C., Khan, M. A., Hussain, A. S., & Hoag, S. W.
(2008).
Quality-by-design (QbD): effects of testing parameters and formulation variables on the segregation tendency of pharmaceutical powder measured by the ASTM D 6940-04 segregation tester. Journal of Pharmaceutical Sciences.
97(10), 4485-4497.
-
Zidan, A. S., Habib, M. J., & Khan, M. A.
(2008).
Process analytical technology: nondestructive evaluation of cyclosporine A and phospholipid solid dispersions by near infrared spectroscopy and imaging. Journal of Pharmaceutical Sciences.
97(8), 3388-3399.
-
Shah, R. B., Bryant, A., Collier, J., Habib, M. J., & Khan, M. A.
(2008).
Stability indicating validated HPLC method for quantification of levothyroxine with eight degradation peaks in the presence of excipients. International Journal of Pharmaceutics.
360(1-2), 77-82.
-
Volpe, D. A., Asafu-Adjaye, E. B., Ellison, C. D., Doddapaneni, S., Uppoor, R. S., & Khan, M. A.
(2008).
Effect of ethanol on opioid drug permeability through caco-2 cell monolayers. AAPS Journal.
10(2), 360-362.
-
Faustino, P. J., Yang, Y., Progar, J. J., Brownell, C. R., Sadrieh, N., May, J. C., ... Lyon, R. C.
(2008).
Quantitative determination of cesium binding to ferric hexacyanoferrate: Prussian blue. JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS.
47(1), 114-125.
-
Zidan, A. S., Sammour, O. A., Hammad, M. A., Megrab, N. A., Habib, M. J., & Khan, M. A.
(2008).
Process analytical technology: non-destructive assessment of anastrozole entrapment within PLGA microparticles by near infrared spectroscopy and chemical imaging. Journal of Microencapsulation.
25(3), 145-153.
-
Shah, R. B., Yang, Y., Khan, M. A., & Faustino, P. J.
(2008).
Molecular weight determination for colloidal iron by Taguchi optimized validated gel permeation chromatography. International Journal of Pharmaceutics.
353(1-2), 21-27.
-
Yang, Y., Faustino, P. J., Progar, J. J., Brownell, C. R., Sadrieh, N., May, J. C., ... Lyon, R. C.
(2008).
Quantitative determination of thallium binding to ferric hexacyanoferrate: Prussian blue. International Journal of Pharmaceutics.
353(1-2), 187-194.
-
Shah, R. B., Tawakkul, M. A., & Khan, M. A.
(2008).
Comparative evaluation of flow for pharmaceutical powders and granules. AAPS PharmSciTech.
9(1), 250-258.
-
Volpe, D. A., Gupta, A., Ciavarella, A. B., Faustino, P. J., Sayeed, V. A., & Khan, M. A.
(2008).
Comparison of the stability of split and intact gabapentin tablets. International Journal of Pharmaceutics.
350(1-2), 65-69.
-
Wu, H., Heilweil, E. J., Hussain, A. S., & Khan, M. A.
(2008).
Process analytical technology (PAT): quantification approaches in terahertz spectroscopy for pharmaceutical application. Journal of Pharmaceutical Sciences.
97(2), 970-984.
-
Shah, R. B., Prasanna, H. R., Rothman, B., & Khan, M. A.
(2008).
Stability of ranitidine syrup re-packaged in unit-dose containers. American Journal of Health-System Pharmacy.
65(4), 325-329.
-
Agarwal, V., Khan, M. A., & Nazzal, S.
(2008).
Polymethacrylate based microparticulates of insulin for oral delivery, part II: solid state characterization. Die Pharmazie: an international journal of pharmaceutical sciences.
63(2), 122-128.
-
Gupta, A., Ciavarella, A. B., Sayeed, V. A., Khan, M. A., & Faustino, P. J.
(2008).
Development and application of a validated HPLC method for the analysis of dissolution samples of gabapentin drug products. JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS.
46(1), 181-186.
-
Agarwal, V., Nazzal, S., & Khan, M. A.
(2008).
Optimization and in vivo evaluation of an oral dual controlled-release tablet dosage form of insulin and duck ovomucoid. PHARMACEUTICAL DEVELOPMENT AND TECHNOLOGY.
13(4), 291-298.
-
Hamad, M. L., Ellison, C. D., Khan, M. A., & Lyon, R. C.
(2007).
Drug product characterization by macropixel analysis of chemical images. Journal of Pharmaceutical Sciences.
96(12), 3390-3401.
-
Wu, H., Heilweil, E. J., Hussain, A. S., & Khan, M. A.
(2007).
Process analytical technology (PAT): effects of instrumental and compositional variables on terahertz spectral data quality to characterize pharmaceutical materials and tablets. International Journal of Pharmaceutics.
343(1-2), 148-158.
-
Zidan, A. S., Sammour, O. A., Hammad, M. A., Megrab, N. A., Habib, M. J., & Khan, M. A.
(2007).
Quality by design: understanding the product variability of a self-nanoemulsified drug delivery system of cyclosporine A. Journal of Pharmaceutical Sciences.
96(9), 2409-2423.
-
Martinez, M. N., Bonate, P., Chapman, R. L., De Groot, A., D'Souza, S., Ghilazi, N., ... Zahn, M.
(2007).
Corrigendum: 2007 highlights of advances in the pharmaceutical sciences: An American Association of Pharmaceutical Scientists (AAPS) perspective. AAPS Journal.
9(3), e328-e328.
-
Shah, R. B., Zidan, A. S., Funck, T., Tawakkul, M. A., Nguyenpho, A., & Khan, M. A.
(2007).
Quality by design: characterization of self-nano-emulsified drug delivery systems (SNEDDs) using ultrasonic resonator technology. International Journal of Pharmaceutics.
341(1-2), 189-194.
-
Shah, R. B., & Khan, M. A.
(2007).
The evolution of FDA's role in ensuring product quality. Pharmaceutical Technology.
31(7), 52-58.
-
Martinez, M. N., Bonate, P., Chapman, R. L., De Groot, A., D'Souza, S., Ghilazi, N., ... Zahn, M.
(2007).
2007 highlights of advances in the pharmaceutical sciences: An American Association of Pharmaceutical Scientists (AAPS) perspective. AAPS Journal.
9(2), e219-e226.
-
Shah, R. B., Tawakkul, M. A., & Khan, M. A.
(2007).
Process analytical technology: chemometric analysis of Raman and near infra-red spectroscopic data for predicting physical properties of extended release matrix tablets. Journal of Pharmaceutical Sciences.
96(5), 1356-1365.
-
Ciavarella, A. B., Gupta, A., Sayeed, V. A., Khan, M. A., & Faustino, P. J.
(2007).
Development and application of a validated HPLC method for the determination of gabapentin and its major degradation impurity in drug products. JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS.
43(5), 1647-1653.
-
Zidan, A. S., Sammour, O. A., Hammad, M. A., Megrab, N. A., Habib, M. J., & Khan, M. A.
(2007).
Quality by design: understanding the formulation variables of a cyclosporine A self-nanoemulsified drug delivery systems by Box-Behnken design and desirability function. International Journal of Pharmaceutics.
332(1-2), 55-63.
-
Wu, H., Khan, M. A., & Hussain, A. S.
(2007).
PROCESS CONTROL PERSPECTIVE FOR PROCESS ANALYTICAL TECHNOLOGY: INTEGRATION OF CHEMICAL ENGINEERING PRACTICE INTO SEMICONDUCTOR AND PHARMACEUTICAL INDUSTRIES. Chemical Engineering Communications.
194(6), 760-779.
-
Nutan, M., Vaithiyalingam, S. R., & Khan, M. A.
(2007).
Controlled release multiparticulate beads coated with starch acetate: material characterization, and identification of critical formulation and process variables. PHARMACEUTICAL DEVELOPMENT AND TECHNOLOGY.
12(3), 307-320.
-
Sharpless, K. E., Anderson, D. L., Betz, J. M., Butler, T. A., Capar, S. G., Cheng, J., ... Ziobro, G. C.
(2006).
Preparation and characterization of a suite of ephedra-containing standard reference materials. Journal of AOAC International.
89(6), 1483-1495.
-
Motlekar, N., Khan, M. A., & Youan, B. C.
(2006).
Preparation and characterization of genistein containing poly(ethylene glycol) microparticles. Journal of Applied Polymer Science.
101(3), 2070-2078.
-
Zidan, A. S., Sammour, O. A., Hammad, M. A., Megrab, N. A., Hussain, M. D., Khan, M. A., & Habib, M. J.
(2006).
Formulation of anastrozole microparticles as biodegradable anticancer drug carriers. AAPS PharmSciTech.
7(3), 61-e46.
-
Nazzal, S., & Khan, M. A.
(2006).
Controlled release of a self-emulsifying formulation from a tablet dosage form: stability assessment and optimization of some processing parameters. International Journal of Pharmaceutics.
315(1-2), 110-121.
-
Shah, R. B., Hullahalli, P. R., Tawakkul, M. A., Faustino, P. J., Nguyenpho, A., & Khan, M. A.
(2006).
Development of a Validated Stability Indicating HPLC Method for Ranitidine Hydrochloride Syrup. Clinical Research and Regulatory Affairs.
23(1), 35-51.
-
Zaghloul, A., Mustafa, F., Siddiqui, A., & Khan, M.
(2006).
Response surface methodology to obtain beta-estradiol biodegradable microspheres for long-term therapy of osteoporosis. PHARMACEUTICAL DEVELOPMENT AND TECHNOLOGY.
11(3), 377-387.
-
Shah, R. B., & Khan, M. A.
(2005).
Oral delivery of salmon calcitonin with ovomudoids. American Pharmaceutical Review.
8(1), 45-47.
-
Zaghloul, A., Mustafa, F., Siddiqu, A., & Khan, M.
(2005).
Biodegradable microparticulates of beta-estradiol: preparation and in vitro characterization. 31(8), 803-811.
-
Nutan, M., Soliman, M. S., Taha, E. I., & Khan, M. A.
(2005).
Optimization and characterization of controlled release multi-particulate beads coated with starch acetate. International Journal of Pharmaceutics.
294(1-2), 89-101.
-
Soliman, M. S., & Khan, M. A.
(2005).
Preparation and in vitro characterization of a semi-solid dispersion of flurbiprofen with Gelucire 44/14 and Labrasol. Die Pharmazie: an international journal of pharmaceutical sciences.
60(4), 288-293.
-
Palamakula, A., Soliman, M., & Khan, M.
(2005).
Regional permeability of coenzyme Q10 in isolated rat gastrointestinal tracts. Die Pharmazie: an international journal of pharmaceutical sciences.
60(3), 212-214.
-
Taha, E. I., Samy, A. M., Kassem, A. A., & Khan, M. A.
(2005).
Response surface methodology for the development of self-nanoemulsified drug delivery system (SNEDDS) of all-trans-retinol acetate. PHARMACEUTICAL DEVELOPMENT AND TECHNOLOGY.
10(3), 363-370.
-
Taha, E. I., Al-Saidan, S., Samy, A. M., & Khan, M. A.
(2004).
Preparation and in vitro characterization of self-nanoemulsified drug delivery system (SNEDDS) of all-trans-retinol acetate. International Journal of Pharmaceutics.
285(1-2), 109-119.
-
Mondal, A., Li, Y., Khan, M. A., Ross, J. H., & Houser, R. P.
(2004).
Supramolecular copper hydroxide tennis balls: self-assembly, structures, and magnetic properties of octanuclear [Cu(8)L(8)(OH)(4)](4+) clusters (HL = N-(2-pyridylmethyl)acetamide). Inorganic Chemistry.
43(22), 7075-7082.
-
Shah, R. B., & Khan, M. A.
(2004).
Regional permeability of salmon calcitonin in isolated rat gastrointestinal tracts: Transport mechanism using Caco-2 cell monolayer. AAPS Journal.
6(4),
-
Shah, R. B., & Khan, M. A.
(2004).
Regional permeability of salmon calcitonin in isolated rat gastrointestinal tracts: transport mechanism using Caco-2 cell monolayer. AAPS Journal.
6(4), e31-40.
-
Palamakula, A., Soliman, M., Reddy, I. K., & Khan, M. A.
(2004).
Preparation and in vitro characterization of self-nanoemulsified drug delivery systems of coenzyme Q10 using chiral essential oil components. Pharmaceutical Technology.
28(10), 74-88.
-
Taha, E. I., Zaghloul, A. A., Samy, A. M., Al-Saidan, S., Kassem, A. A., & Khan, M. A.
(2004).
Bioavailability assessment of salbutamol sulfate suppositories in human volunteers. International Journal of Pharmaceutics.
279(1-2), 3-7.
-
Palamakula, A., Nutan, M., & Khan, M. A.
(2004).
Response surface methodology for optimization and characterization of limonene-based coenzyme Q10 self-nanoemulsified capsule dosage form. AAPS PharmSciTech.
5(4), e66-121.
-
Shah, R. B., Palamakula, A., & Khan, M. A.
(2004).
Cytotoxicity evaluation of enzyme inhibitors and absorption enhancers in Caco-2 cells for oral delivery of salmon calcitonin. Journal of Pharmaceutical Sciences.
93(4), 1070-1082.
-
Palamakula, A., & Khan, M. A.
(2004).
Evaluation of cytotoxicity of oils used in coenzyme Q10 Self-emulsifying Drug Delivery Systems (SEDDS). International Journal of Pharmaceutics.
273(1-2), 63-73.
-
Mustafa, F., Yang, T., Khan, M. A., & Ahsan, F.
(2004).
Chain length-dependent effects of alkylmaltosides on nasal absorption of enoxaparin. Journal of Pharmaceutical Sciences.
93(3), 675-683.
-
Shah, R. B., & Khan, M. A.
(2004).
Protection of salmon calcitonin breakdown with serine proteases by various ovomucoid species for oral drug delivery. Journal of Pharmaceutical Sciences.
93(2), 392-406.
-
Hussain, A., Arnold, J. J., Khan, M. A., & Ahsan, F.
(2004).
Absorption enhancers in pulmonary protein delivery. Journal of Controlled Release.
94(1), 15-24.
-
Shah, R. B., Nutan, M., Reddy, I. K., & Khan, M. A.
(2004).
A Dual Controlled Gastrointestinal Therapeutic System of Salmon Calcitonin. II. Screening of Process and Formulation Variables. Clinical Research and Regulatory Affairs.
21(3-4), 231-238.
-
Shah, R. B., Nutan, M., & Khan, M. A.
(2004).
An Enteric DualControlled Gastrointestinal Therapeutic System of Salmon CalcitoninI: Preparation, Characterization, and Preclinical Bioavailability in Rats. Clinical Research and Regulatory Affairs.
21(1), 81-96.
-
Vuppugalla, R., Agarwal, V., & Khan, M. A.
(2003).
A simple HPLC method for the simultaneous analysis of insulin and ovomucoid. Die Pharmazie: an international journal of pharmaceutical sciences.
58(11), 793-795.
-
Shah, R. B., Siddiqui, A., Shah, G., & Khan, M. A.
(2003).
A validated HPLC assay for simultaneous analysis of salmon calcitonin and duck ovomucoid. Die Pharmazie: an international journal of pharmaceutical sciences.
58(9), 620-622.
-
Afouna, M. I., Fincher, T. K., Khan, M. A., & Reddy, I. K.
(2003).
Percutaneous permeation of enantiomers and racemates of chiral drugs and prediction of their flux ratios using thermal data: a pharmaceutical perspective. Chirality: the pharmacological, biological, and chemical consequences of molecular asymmetry.
15(5), 456-465.
-
Zaghloul, A., Hussain, A., Khan, M. A., & Ahsan, F.
(2003).
Development of a HPLC method for the determination of cyclosporin-A in rat blood and plasma using naproxen as an internal standard. JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS.
31(6), 1101-1107.
-
Motlekar, N. A., Shah, R. B., Reddy, I. K., Keller, W. J., & Khan, M. A.
(2003).
Permeation of genistein through human skin. Pharmaceutical Technology.
27(3), 140-148.
-
Taha, E. I., Zaghloul, A., Kassem, A. A., & Khan, M. A.
(2003).
Salbutamol sulfate suppositories: influence of formulation on physical parameters and stability. PHARMACEUTICAL DEVELOPMENT AND TECHNOLOGY.
8(1), 21-30.
-
Hutak, C. M., Kavanagh, M. E., Agarwal, V., Afouna, M. I., Khan, M. A., & Reddy, I. K.
(2003).
Use of SIRC Rabbit Corneal Cell Lines Grown on Polycarbonate- or Polyester-Based Filters to Assess the In Vitro Corneal Transport/Toxicity Screening Using Pilocarpine With or Without Benzalkonium Chloride. Cutaneous and Ocular Toxicology.
22(1-2), 101-114.
-
Zaghloul, A., Gurley, B., Khan, M., Bhagavan, H., Chopra, R., & Reddy, I.
(2002).
Bioavailability assessment of oral coenzyme Q10 formulations in dogs. 28(10), 1195-1200.
-
Vaithiyalingam, S. R., Tuliani, P., Wilber, W., Reddy, I. K., & Khan, M. A.
(2002).
Formulation and stability evaluation of ketoprofen sustained-release tablets prepared by fluid bed granulation with Carbopol 971P solution. 28(10), 1231-1240.
-
Shah, R. B., Ahsan, F., & Khan, M. A.
(2002).
Oral delivery of proteins: progress and prognostication. Critical Reviews in Therapeutic Drug Carrier Systems.
19(2), 135-169.
-
Nazzal, S., Zaghloul, A. A., & Khan, M. A.
(2002).
Effect of extragranular microcrystalline cellulose: On compaction, surface roughness, and in vitro dissolution of a self-nanoemulsified solid dosage form of ubiquinone. Pharmaceutical Technology North America.
26(4), 86-98.
-
Nazzal, S., Nutan, M., Palamakula, A., Shah, R., Zaghloul, A. A., & Khan, M. A.
(2002).
Optimization of a self-nanoemulsified tablet dosage form of Ubiquinone using response surface methodology: effect of formulation ingredients. International Journal of Pharmaceutics.
240(1-2), 103-114.
-
Vaithiyalingam, S., Nutan, M., Reddy, I., & Khan, M.
(2002).
Preparation and characterization of a customized cellulose acetate butyrate dispersion for controlled drug delivery. Journal of Pharmaceutical Sciences.
91(6), 1512-1522.
-
Nazzal, S., Smalyukh, I. I., Lavrentovich, O. D., & Khan, M. A.
(2002).
Preparation and in vitro characterization of a eutectic based semisolid self-nanoemulsified drug delivery system (SNEDDS) of ubiquinone: mechanism and progress of emulsion formation. International Journal of Pharmaceutics.
235(1-2), 247-265.
-
Vaithiyalingam, S., & Khan, M. A.
(2002).
Optimization and characterization of controlled release multi-particulate beads formulated with a customized cellulose acetate butyrate dispersion. International Journal of Pharmaceutics.
234(1-2), 179-193.
-
Nazzal, S., & Khan, M. A.
(2002).
Response surface methodology for the optimization of ubiquinone self-nanoemulsified drug delivery system. AAPS PharmSciTech.
3(1), E3-31.
-
Ahsan, F., Rivas, I. P., Khan, M. A., & Torres Suarez, A. I.
(2002).
Targeting to macrophages: role of physicochemical properties of particulate carriers--liposomes and microspheres--on the phagocytosis by macrophages. Journal of Controlled Release.
79(1-3), 29-40.
-
Lockman, P. R., Mumper, R. J., Khan, M. A., & Allen, D. D.
(2002).
Nanoparticle technology for drug delivery across the blood-brain barrier. 28(1), 1-13.
-
Nazzal, S., Guven, N., Reddy, I. K., & Khan, M. A.
(2002).
Preparation and characterization of coenzyme Q10-Eudragit solid dispersion. 28(1), 49-57.
-
Agarwal, V., Reddy, I. K., & Khan, M. A.
(2001).
Polymethyacrylate based microparticulates of insulin for oral delivery: preparation and in vitro dissolution stability in the presence of enzyme inhibitors. International Journal of Pharmaceutics.
225(1-2), 31-39.
-
Agarwal, V., Nazzal, S., Reddy, I. K., & Khan, M. A.
(2001).
Transport studies of insulin across rat jejunum in the presence of chicken and duck ovomucoids. Journal of Pharmacy and Pharmacology.
53(8), 1131-1138.
-
Reddy, I. K., Vaithiyalingam, S. R., Khan, M. A., & Bodor, N. S.
(2001).
Design, in vitro stability, and ocular hypotensive activity of t-butalone chemical delivery systems. Journal of Pharmaceutical Sciences.
90(8), 1026-1033.
-
Zaghloul, A. A., el-Shattawy, H. H., Kassem, A. A., Ibrahim, E. A., Reddy, I. K., & Khan, M. A.
(2001).
Honey, a prospective antibiotic: extraction, formulation, and stability. Die Pharmazie: an international journal of pharmaceutical sciences.
56(8), 643-647.
-
Nazzal, S., Zaghloul, A. A., Reddy, I. K., & Khan, M. A.
(2001).
Analysis of ubidecarenone (CoQ10) aqueous samples using reversed phase liquid chromatography. Die Pharmazie: an international journal of pharmaceutical sciences.
56(5), 394-396.
-
Vaithiyalingam, S., Reddy, I. K., Khan, M. A., & Guven, N.
(2001).
Aqueous-Based Cellulose Acetate Butyrate Dispersion: Screening of Process and Formulation Variables to Obtain Verapamil HCl-Controlled Release Beads. Particulate Science and Technology: an international journal.
19(2), 131-144.
-
Vaithiyalingam, S. R., Agarwal, V., Reddy, I. K., Ashraf, M., & Khan, M. A.
(2001).
Formulation Development and Stability Evaluation: Of a Multicomponent Nutritional Supplement. Pharmaceutical Technology.
25(4), 38-48.
-
Zaghloul, A. A., Faltinek, J., Vaithiyalingam, S. R., Reddy, I. K., & Khan, M. A.
(2001).
Naproxen-Eudragit microspheres: screening of process and formulation variables for the preparation of extended release tablets. Die Pharmazie: an international journal of pharmaceutical sciences.
56(4), 321-324.
-
Reddy, I. K., Vaithiyalingam, S. R., Khan, M. A., & Bodor, N. S.
(2001).
Intraocular pressure-lowering activity and in vivo disposition of dipivalyl terbutalone in rabbits. 27(2), 137-141.
-
Kommuru, T. R., Gurley, B., Khan, M. A., & Reddy, I. K.
(2001).
Self-emulsifying drug delivery systems (SEDDS) of coenzyme Q10: formulation development and bioavailability assessment. International Journal of Pharmaceutics.
212(2), 233-246.
-
Agarwal, V., & Khan, M. A.
(2001).
Current status of the oral delivery of insulin. Pharmaceutical Technology.
25(10), 76-90.
-
Vaithiyalingam, S. R., Sastry, S. V., Dehon, R. H., Reddy, I. K., & Khan, M. A.
(2001).
Long-term stability characterization of a controlled release gastrointestinal therapeutic system coated with a cellulose acetate pseudolatex. Die Pharmazie: an international journal of pharmaceutical sciences.
56(1), 66-69.
-
Zaghloul, A. A., Vaithiyalingam, S. R., Faltinek, J., Reddy, I. K., & Khan, M. A.
(2001).
Response surface methodology to obtain naproxen controlled release tablets from its microspheres with Eudragit L100-55. Journal of Microencapsulation.
18(5), 651-662.
-
Reddy, I. K., Kommuru, T. R., Zaghloul, A. A., & Khan, M. A.
(2000).
Chirality and its implications in transdermal drug development. Critical Reviews in Therapeutic Drug Carrier Systems.
17(4), 285-325.
-
Vaithiyalingam, S., Zaghloul, A. A., Reddy, I. K., & Khan, M. A.
(2000).
Artificial neural network and simplex optimization for mixing of aqueous-coated beads to obtain controlled-release formulations. Pharmaceutical Technology.
24(6), 60-72.
-
AGARWAL, V., REDDY, I. K., & KHAN, M. A.
(2000).
Oral Delivery of Proteins: Effect of Chicken and Duck Ovomucoid on the Stability of Insulin in the Presence of Chymotrypsin and Trypsin. Journal of Pharmacy and Pharmacology.
6(5), 223-227.
-
Khan, M. A., Sastry, S. V., Vaithiyalingam, S. R., Agarwal, V., Nazzal, S., & Reddy, I. K.
(2000).
Captopril gastrointestinal therapeutic system coated with cellulose acetate pseudolatex: evaluation of main effects of several formulation variables. International Journal of Pharmaceutics.
193(2), 147-156.
-
Khan, M. A., Karnachi, A. A., Agarwal, V., Vaithiyalingam, S. R., Nazzal, S., & Reddy, I. K.
(2000).
Stability characterization of controlled release coprecipitates and solid dispersions. Journal of Controlled Release.
63(1-2), 1-6.
-
Goskonda, V. R., Hill, R. A., Khan, M. A., & Reddy, I. K.
(2000).
Permeability of chemical delivery systems across rabbit corneal (SIRC) cell line and isolated corneas: a comparative study. PHARMACEUTICAL DEVELOPMENT AND TECHNOLOGY.
5(3), 409-416.
-
Shojaei, A. H., Khan, M., Lim, G., & Khosravan, R.
(1999).
Transbuccal permeation of a nucleoside analog, dideoxycytidine: effects of menthol as a permeation enhancer. International Journal of Pharmaceutics.
192(2), 139-146.
-
Kommuru, T. R., Khan, M. A., & Reddy, I. K.
(1999).
Effect of chiral enhancers on the permeability of optically active and racemic metoprolol across hairless mouse skin. 11(7), 536-540.
-
Kommuru, T. R., Ashraf, M., Khan, M. A., & Reddy, I. K.
(1999).
Stability and bioequivalence studies of two marketed formulations of coenzyme Q10 in beagle dogs. Chemical and Pharmaceutical Bulletin.
47(7), 1024-1028.
-
Ross, W. H., Lawrence, L. W., Reddy, I. K., Dick, R. M., Roane, D. S., Schulte, M. K., ... Sponberg, L. A.
(1999).
Implementation of a New Course with a Focus on Active Learning Through Integrated Curricular Approach: Pharmacy Care Laboratory I. Journal of Pharmacy Teaching.
7(2), 15-34.
-
Agarwal, V., Singh, S. K., Reddy, I. K., Durrani, M. J., & Khan, M. A.
(1999).
Cataplasm-based controlled drug delivery: development and optimization of a novel formulation. 25(5), 659-665.
-
Goskonda, V. R., Khan, M. A., Bodor, N. S., & Reddy, I. K.
(1999).
Chemical delivery systems: evaluation of physicochemical properties and enzymatic stability of phenylephrone derivatives. PHARMACEUTICAL DEVELOPMENT AND TECHNOLOGY.
4(2), 189-198.
-
Khan, M. A., Shojaei, A. H., Karnachi, A. A., & Reddy, I. K.
(1999).
Comparative evaluation of controlled-release solid oral dosage forms prepared with solid dispersions and coprecipitates. Pharmaceutical Technology.
23(5), 58-74.
-
Goskonda, V. R., Khan, M. A., Hutak, C. M., & Reddy, I. K.
(1999).
Permeability characteristics of novel mydriatic agents using an in vitro cell culture model that utilizes SIRC rabbit corneal cells. Journal of Pharmaceutical Sciences.
88(2), 180-184.
-
Sastry, S. V., & Khan, M. A.
(1998).
Aqueous-based polymeric dispersion: face-centered cubic design for the development of atenolol gastrointestinal therapeutic system. PHARMACEUTICAL DEVELOPMENT AND TECHNOLOGY.
3(4), 423-432.
-
Zahir, A., Kunta, J. R., Khan, M. A., & Reddy, I. K.
(1998).
Effect of menthol on permeability of an optically active and racemic propranolol across guinea pig skin. 24(9), 875-878.
-
Sastry, S. V., & Khan, M. A.
(1998).
Aqueous based polymeric dispersion: Plackett--Burman design for screening of formulation variables of atenolol gastrointestinal therapeutic system. Pharmaceutica acta Helvetiae.
73(2), 105-112.
-
Kommuru, T. R., Khan, M. A., & Reddy, I. K.
(1998).
Racemate and enantiomers of ketoprofen: phase diagram, thermodynamic studies, skin permeability, and use of chiral permeation enhancers. Journal of Pharmaceutical Sciences.
87(7), 833-840.
-
Goskonda, V. R., Reddy, I. K., Durrani, M. J., Wilber, W., & Khan, M. A.
(1998).
Solid-state stability assessment of controlled release tablets containing Carbopol 971P. Journal of Controlled Release.
54(1), 87-93.
-
Sastry, S. V., Wilber, W., Reddy, I. K., & Khan, M. A.
(1998).
Aqueous-based polymeric dispersion: preparation and characterization of cellulose acetate pseudolatex. International Journal of Pharmaceutics.
165(2), 175-189.
-
Kommuru, T. R., Khan, M. A., Ashraf, M., Kattenacker, R., & Reddy, I. K.
(1998).
A simplified chromatographic method for quantitative determination of coenzyme Q10 in dog plasma. JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS.
16(6), 1037-1040.
-
Khan, M. A., & Reddy, I. K.
(1997).
Controlled drug delivery Development of solid oral dosage forms with acrylate polymers. Journal of Drug Delivery Science and Technology.
7(6), 483-490.
-
Kunta, J. R., Goskonda, V. R., Brotherton, H. O., Khan, M. A., & Reddy, I. K.
(1997).
Effect of menthol and related terpenes on the percutaneous absorption of propranolol across excised hairless mouse skin. Journal of Pharmaceutical Sciences.
86(12), 1369-1373.
-
Naidu, S. V., Sastry, S. V., Maxie, C. S., & Khan, M. A.
(1997).
Effect of plasticizer on free volume and permeability in cellulose acetate pseudolatex membranes studied by positron annihilation and tracer diffusion methods. Materials Science Forum.
255-257, 333-335.
-
Sastry, S. V., Reddy, I. K., & Khan, M. A.
(1997).
Atenolol gastrointestinal therapeutic system: optimization of formulation variables using response surface methodology. Journal of Controlled Release.
45(2), 121-130.
-
Sastry, S. V., Degennaro, M. D., Reddy, L. K., & Khan, M. A.
(1997).
Atenolol Gastrointestinal Therapeutic System. I. Screening of Formulation Variables. 23(2), 157-165.
-
Karnachi, A. A., Reddy, I. K., Degennaro, M. D., & Khan, M. A.
(1997).
Comparative evaluation of the severity of gastric ulceration by solid dispersions and coprecipitates of indomethacin. 4(5), 297-301.
-
Singh, S. K., & Khan, M. A.
(1997).
Ibuprofen Release from Beads Coated with an Experimental Latex: Effect of Certain Variables. 23(2), 145-155.
-
Reddy, I. K., & Khan, M. A.
(1996).
Drug delivery system. U.S. Pharmacist.
21(2),
-
Singh, S. K., Durrani, M. J., Reddy, I. K., & Khan, M. A.
(1996).
Effect of permeation enhancers on the release of ketoprofen through transdermal drug delivery systems. Die Pharmazie: an international journal of pharmaceutical sciences.
51(10), 741-744.
-
Singh, S. K., Reddy, I. K., & Khan, M. A.
(1996).
Optimization and characterization of controlled release pellets coated with an experimental latex: II. Cationic drug. International Journal of Pharmaceutics.
141(1-2), 179-195.
-
Karnachi, A. A., & Khan, M. A.
(1996).
Box-behnken design for the optimization of formulation variables of indomethacin coprecipitates with polymer mixtures. International Journal of Pharmaceutics.
131(1), 9-17.
-
Singh, S. K., Roane, D. S., Reddy, L. K., Durrani, M. J., & Khan, M. A.
(1996).
Effect of Additives on the Diffusion of Ketoprofen Through Human Skin. 22(5), 471-474.
-
Reddy, I. K., Khan, M. A., Wu, W. M., & Bodor, N. S.
(1996).
Permeability of a soft steroid, loteprednol etabonate, through an excised rabbit cornea. Journal of Ocular Pharmacology and Therapeutics.
12(2), 159-167.
-
Khan, M. A., Dib, J., & Reddy, L. K.
(1996).
Statistical Optimization of Ketoprofen-Eudragit S100 Coprecipitates to Obtain Controlled-Release Tablets. 22(2), 135-141.
-
Khan, M. A., Karnachi, A. A., Singh, S. K., Sastry, S. V., Kislalioglu, S. M., & Bolton, S.
(1995).
Controlled release coprecipitates: formulation considerations. Journal of Controlled Release.
37(1-2), 131-141.
-
Singh, S. K., Dodge, J., Durrani, M. J., & Khan, M. A.
(1995).
Optimization and characterization of controlled release pellets coated with an experimental latex: I. Anionic drug. International Journal of Pharmaceutics.
125(2), 243-255.
-
Karnachi, A. A., De Hon, R. A., & Khan, M. A.
(1995).
Compression of Indomethacin Coprecipitates with Polymer Mixtures: Effect of Preparation Methodology. 21(12), 1473-1483.
-
Karnachi, A. A., Dehon, R. A., & Khan, M. A.
(1995).
Plackett-Burman screening of micromatrices with polymer mixtures for controlled drug delivery. Die Pharmazie: an international journal of pharmaceutical sciences.
50(8), 550-553.
-
Tammara, V. K., Narurkar, M. M., Crider, A. M., & Khan, M. A.
(1994).
Morpholinoalkyl ester prodrugs of diclofenac: synthesis, in vitro and in vivo evaluation. Journal of Pharmaceutical Sciences.
83(5), 644-648.
-
Khan, M. A., Bolton, S., & Kislalioglu, M. S.
(1994).
Optimization of process variables for the preparation of ibuprofen coprecipitates with eudragit S100. International Journal of Pharmaceutics.
102(1-3), 185-192.
-
Tammara, V. K., Narurkar, M. M., Crider, A. M., & Khan, M. A.
(1993).
Synthesis and evaluation of morpholinoalkyl ester prodrugs of indomethacin and naproxen. Pharmaceutical Research.
10(8), 1191-1199.
-
Kislalioglu, M. S., Khan, M. A., Blount, C., Goettsch, R. W., & Bolton, S.
(1991).
Physical characterization and dissolution properties of ibuprofen: Eudragit coprecipitates. Journal of Pharmaceutical Sciences.
80(8), 799-804.
-
Balasubbramanian, D., Dharani, S., Tauseef, M., Khan, M. A., Rahman, Z., & Mitchell, B. M.
High Dose Vardenafil Blunts the Hypertensive Effects of Toll-Like Receptor 3 Activation During Pregnancy. 1, 780298.
-
Kayalar, C., Helal, N., Mohamed, E. M., Dharani, S., Khuroo, T., Kuttolamadom, M. A., Rahman, Z., & Khan, M. A.
(2024).
In Vitro and In Vivo testing of 3D-Printed Amorphous Lopinavir Printlets by SelectiveLaser Sinitering: Improved Bioavailability of a Poorly Soluble Drug. AAPS PharmSciTech.
25(1), 20.
-
book
-
Reddy, I. K., & Khan, M. A.
(2017).
Essential Math and Calculations for Pharmacy Technicians. Taylor & Francis.
-
Kahn, M. A., & Reddy, I. K.
(2000).
Pharmaceutical and Clinical Calculations, 2nd Edition. CRC Press.
-
Reddy, I. K., & Khan, M. A.
(2017).
Essential Math and Calculations for Pharmacy Technicians. Taylor & Francis.
-
chapter
-
Charoo, N. A., Mohamed, E. M., Kuttolamadom, M., Khan, M. A., & Rahman, Z.
(2023).
Binder Jetting Powder Bed 3D Printing for the Fabrication of Drug Delivery System. Nano- and Microfabrication Techniques in Drug Delivery.
(pp. 137-172).
Springer Nature.
-
Rahman, Z., Charoo, N. A., Kuttolamadom, M., Asadi, A., & Khan, M. A.
(2020).
Chapter 46 Printing of personalized medication using binder jetting 3D printer. Precision Medicine for Investigators, Practitioners and Providers.
(pp. 473-481).
Elsevier.
-
Charoo, N. A., Rahman, Z., & Khan, M. A.
(2019).
Chapter 11 Nanoparticles for improvement in oral bioavailability. Nanoarchitectonics in Biomedicine.
(pp. 371-410).
Elsevier.
-
Awotwe-Otoo, D., & Khan, M.
(2019).
Regulatory Aspects of Freeze-Drying. Lyophilization of Pharmaceuticals and Biologicals.
(pp. 173-192).
Springer Nature.
-
Rahman, Z., Charoo, N. A., Akhter, S., Beg, S., Reddy, I. K., & Khan, M. A.
(2018).
Chapter 16 Nanotechnology-based drug products Science and regulatory considerations. Nanoscale Fabrication, Optimization, Scale-Up and Biological Aspects of Pharmaceutical Nanotechnology.
(pp. 619-655).
Elsevier.
-
Mockus, L., LeBlond, D., Reklaitis, G. V., Basu, P. K., Paul, T., Pease, N., Nail, S. L., & Khan, M. A.
(2017).
Design Space Definition. Reklaitis, G. V., Seymour, C., & Garcia-Munoz, S. (Eds.),
Comprehensive Quality by Design for Pharmaceutical Product Development and Manufacture.
(pp. 301-318).
Wiley.
-
Wu, H., & Khan, M. A.
(2017).
Quality by Design. Reklaitis, G. V., Seymour, C., & Garcia-Munoz, S. (Eds.),
Comprehensive Quality by Design for Pharmaceutical Product Development and Manufacture.
(pp. 235-256).
Wiley.
-
Wu, H., Xie, L., Hoag, S. W., Augsburger, L. L., & Khan, M.
(2017).
Quality-by-design (QbD) for capsule formulation and process development regulatory science relevance, scientific case studies, and future challenges. Pharmaceutical Dosage Forms: Capsules.
(pp. 393-413).
-
Khan, S. R., Berendt, R. T., Ellison, C. D., Ciavarella, A. B., Asafu-Adjaye, E., Khan, M. A., & Faustino, P. J.
(2016).
Bupropion Hydrochloride. Profiles of drug substances, excipients, and related methodology.
Brittain, H. G. (Eds.),
Profiles of Drug Substances, Excipients and Related Methodology.
(pp. 1-30).
Elsevier.
-
Xu, X., & Khan, M. A.
(2016).
Regulatory Perspective on the Development of Polymer Nanomaterials. Vauthier, C., & Ponchel, G. (Eds.),
Polymer Nanoparticles for Nanomedicines.
(pp. 615-633).
Springer Nature.
-
Awotwe-Otoo, D., & Khan, M. A.
(2015).
Lyophilization of Biologics: An FDA Perspective. Varshney, D., & Singh, M. (Eds.),
Lyophilized Biologics and Vaccines.
(pp. 341-359).
Springer Nature.
-
Gupta, A., Rahman, Z., & Khan, M. A.
(2015).
Scientific and Regulatory Considerations in Product Development. Pharmaceutical Sciences Encyclopedia.
(pp. 1-17).
Wiley.
-
Agarabi, C., Khan, M. A., & Shah, R. B.
(2015).
Challenges and Opportunities for Biotech Quality by Design. Jameel, F., Hershenson, S., Khan, M. A., & Martin-Moe, S. (Eds.),
Quality by Design for Biopharmaceutical Drug Product Development.
(pp. 1-15).
Springer Nature.
-
Shah, R., & Khan, M.
(2014).
Regulatory Aspects of Nanomaterial Applications in Pharmaceutical Industry. Yin, S., & Wei, A. (Eds.),
Nanomaterials for Pharmaceutical Scientists.
JOhn Wiley & Sons.
-
Rahman, Z., Siddiqui, A., Gupta, A., & Khan, M.
(2014).
Regulatory Considerations in Development of Amorphous Solid Dispersions. Shah, N., Sandhu, H., Choi, D. S., Chokshi, H., & Malick, A. W. (Eds.),
AMORPHOUS SOLID DISPERSIONS: THEORY AND PRACTICE.
(pp. 545-563).
Springer Nature.
-
Gupta, A., Rahmna, Z., & Khan, M.
(2014).
Scientific and Regulatory Considerations in Product Development. Newman, A. (Eds.),
Pharmaceutical Amorphous Solid Dispersions.
(pp. 398-414).
Wiley and Sons.
-
Rahman, Z., Zidan, A., & Khan, M. A.
(2013).
Tacrolimus properties and formulations: Potential impact of product quality on safety and efficacy. Tacrolimus: Effectiveness, Safety and Drug Interactions.
(pp. 1-39).
-
Gupta, A., & Khan, M. A.
(2013).
Consistency of Pharmaceutical Products: An FDA Perspective on Hot-Melt Extrusion Process. Repka, M. A., Langley, N., & DiNunzio, J. (Eds.),
Melt Extrusion.
(pp. 435-445).
Springer Nature.
-
Gupta, A., & Khan, M. A.
(2012).
HotMelt Extrusion: An FDA Perspective on Product and Process Understanding. HotMelt Extrusion: Pharmaceutical Applications.
(pp. 323-331).
Wiley.
-
Martinez, M. N., & Khan, M. A.
(2012).
Regulatory Issues and Challenges Associated with the Development of Performance Specifications for Modified Release Parenteral Products. Long Acting Injections and Implants.
(pp. 505-535).
Springer Nature.
-
Shah, R., Brorson, K., Read, E., Park, J., Watts, C., & Khan, M.
(2011).
Scientific and Regulatory Overview of Process Analytical Technology in Bioprocesses. Undey, C., Low, D., Menezes, J. C., & Koch, M. (Eds.),
PAT Applied in Biopharmaceutical Process Development And Manufacturing.
(pp. 1-8).
Taylor & Francis.
-
Shah, R. B., & Khan, M. A.
(2010).
The Science and Regulatory Perspectives of Emerging Controlled Release Dosage Forms. Oral Controlled Release Formulation Design and Drug Delivery.
(pp. 337-349).
Wiley.
-
Shah, R. B., Park, J. T., Read, E. K., Khan, M. A., & Brorson, K.
(2010).
Quality by Design (QbD), Biopharmaceutical Manufacture. Encyclopedia of Industrial Biotechnology.
(pp. 1-36).
Wiley.
-
Khan, M. A.
(2010).
Stability of Repackaged Products. Huynh-Ba, K. (Eds.),
Pharmaceutical Stability Testing to Support Global Markets.
(pp. 123-133).
Springer Nature.
-
Sayeed, V. A., Gupta, A., & Khan, M. A.
(2010).
Stability of Split Tablets. Huynh-Ba, K. (Eds.),
Pharmaceutical Stability Testing to Support Global Markets.
(pp. 153-160).
Springer Nature.
-
Gupta, A., Sayeed, V. A., & Khan, M. A.
(2010).
The Science and Regulatory Perspectives of Pharmaceutical Suspensions. Pharmaceutical Suspensions.
(pp. 265-283).
Springer Nature.
-
Shah, R. B., & Khan, M. A.
(2009).
Nanopharmaceuticals: Challenges and Regulatory Perspective. de Villiers, M. M., Aramwit, P., & Kwon, G. S. (Eds.),
Nanotechnology in Drug Delivery.
(pp. 621-646).
Springer Nature.
-
Vaddi, H. K., Khan, M., & Reddy, I. K.
(2007).
Ocular, Nasal, and Otic Drug Delivery. Lee, M., & Desai, A. (Eds.),
Gibaldi's Drug Delivery Systems in Pharmaceutical Care.
(pp. 59-78).
ASHP.
-
Ahsan, F., & Khan, M.
(2005).
Formulation and Route of AdministrationInfluencing Drug Permeability and Absorption. Preclinical Drug Development.
(pp. 221-250).
Taylor & Francis.
-
Khan, M. A., & Reddy, I. K.
(1998).
Calcium Phosphate in Pharmaceutical Product Development. Amjad, Z. (Eds.),
Calcium Phosphates in Biological and Industrial Systems.
(pp. 303-323).
Springer Nature.
-
Khan, M., & Durrani, M. J.
(1995).
Polymers in Ophthalmic Drug Delivery Systems. Reddy, I. K. (Eds.),
Ocular Theraputics and Drug Delivery.
(pp. 405-440).
CRC Press.
-
Charoo, N. A., Mohamed, E. M., Kuttolamadom, M., Khan, M. A., & Rahman, Z.
(2023).
Binder Jetting Powder Bed 3D Printing for the Fabrication of Drug Delivery System. Nano- and Microfabrication Techniques in Drug Delivery.
(pp. 137-172).
Springer Nature.
-
conference paper
-
Funkhouser, C., Ali, S., Richardson, L., Rahman, Z., Khan, M., & Kuttolamadom, M.
(2020).
THERMAL INFLUENCE ON PRINTLET QUALITY IN THE SELECTIVE LASER SINTERING OF PHARMACEUTICAL FORMULATIONS
-
Mohammed, E., Hamed, R., Barakh Ali, S. F., Khan, M. A., Ozkan, T., Kuttolamadom, M., & Rahman, Z.
(2020).
Chemometric Assisted X-Ray Powder Diffractometry Method for Crystalline Lopinavir Quantification in 3D Printlets Manufactured by Selective Laser Sintering
-
Wu, H., White, M., Foringer, R., & Khan, M.
(2012).
An integrated Process Analytical Technology (PAT) approach to examine the effect of temperature on nucleation kinetics of a dynamic pharmaceutical co-precipitation process
-
Wu, H., & Khan, M.
(2012).
Scientific validation of THz spectroscopic measurement and its pharmaceutical process analytical technology (PAT) applications: Case studies of first principles modeling approach
-
Khan, M. A., Wu, K., & Gupta, A.
(2012).
FDA: contribution to developing pediatric formulations and transatlantic collaboration. International Journal of Pharmaceutics.
146-148.
-
Wu, H., White, M., Foringer, R., & Khan, M.
(2012).
An integrated process analytical technology (PAT) approach to examine the effect of temperature on nucleation kinetics of a dynamic pharmaceutical coprecipitation process. 59-67.
-
Wu, H., & Khan, M.
(2012).
Scientific validation of THz spectroscopic measurement and its pharmaceutical process analytical technology (PAT) Applications: Case studies of first principles modeling approach. 18-35.
-
Wu, H., & Khan, M.
(2011).
Challenges, opportunities, and scientific aspects of implementing PAT in biopharmaceuticals
-
Wu, H., White, M., & Khan, M.
(2011).
Process QbD case study: An integrated PAT approach for a dynamic pharmaceutical co-precipitation process characterization and process design space development
-
Zidan, A. S., Rahman, Z., & Khan, M. A.
(2011).
Product and process understanding of a novel pediatric anti-HIV tenofovir niosomes with a high-pressure homogenizer. European Journal of Pharmaceutical Sciences.
93-102.
-
Wu, H., & Khan, M.
(2011).
Challenges, opportunities, and scientific aspects of implementing PAT in biopharmaceuticals. 119-127.
-
Wu, H., & Khan, M.
(2011).
Challenges, opportunities, and scientific aspects of implementing pat in biopharmaceuticals. 1030-1038.
-
Wu, H., White, M., & Khan, M.
(2011).
Process QbD case study: An integrated PAT approach for a dynamic pharmaceutical coprecipitation process characterization and process design space development. 32-46.
-
Wu, H., White, M., & Khan, M.
(2011).
Process QbD case study: An integrated PAT approach for a dynamic pharmaceutical coprecipitation process characterization and process design space development. 262-276.
-
Mockus, L., Basu, P. K., Khan, M. A., Harper, N. J., Nail, S. L., Pease, N., ... LeBlond, D.
(2009).
Application of quality by design principles to development of freeze-dried parenteral dosage forms
-
Wu, H., White, M., & Khan, M. A.
(2009).
Quality-by-Design (QbD): Examining the impact of process variables on particle size distribution for a pharmaceutical co-precipitation process using real-time Lasentec FBRM and PVM process monitoring and design of experiments (DOE) approach
-
Wu, H., & Khan, M. A.
(2009).
Quality-by-design (QbD): Process trajectory development for a pharmaceutical co-precipitation process based on an integrated real-time process monitoring strategy
-
Wu, H., & Khan, M. A.
(2008).
Quality-by-Design (QbD) case study: Powder blending process kinetics evaluation
-
Wu, H., Xie, L., Shen, M., Khan, M. A., Lyon, R. C., Augsburger, L., & Hoag, S. W.
(2007).
A Quality by Design (QbD) approach for pharmaceutical capsule filling unit operation: Identifying critical process variables and detecting possible interactions
-
Wu, H., Tawakkul, M., & Khan, M. A.
(2007).
An integrated Quality-by-Design (QbD) approach for pharmaceutical powder blending unit operation: Process monitoring, endpoint determination, and concentration quantification
-
Wu, H., Shen, M., Wheelock, T. D., & Khan, M. A.
(2006).
Engineering considerations on modeling for pharmaceutical process analytical technology (PAT) applications
-
Wu, H., & Khan, M. A.
(2006).
Mapping the state of a pharmaceutical Co-precipitation process: An integrated process analytical technology (PAT) approach
-
Khan, M. A.
(2005).
Pharmaceutical coating operations: Challenges and opportunities in the changing regulatory paradigm. 8497.
-
Khan, M. A., Vaithiyalingam, S. R., Agarwal, V., Nazzal, S., Reddy, I. K., & Sastry, S. V.
(1999).
Effect of temperature and humidity on long term storage of atenolol gastro-intestinal therapeutic system. Proceedings of the International Symposium on Controlled Release of Bioactive Materials.
982-983.
-
Khan, M. A., Agarwal, V., Vaithiyalingam, S., Nazzal, S., Reddy, I. K., & Sastry, S. V.
(1999).
Osmotically-controlled oral dosage form of a dipeptide: Screening of formulation variables. Proceedings of the International Symposium on Controlled Release of Bioactive Materials.
980-981.
-
Singh, S. K., Karnachi, A. A., Dorrani, M. J., Dodge, J., & Khan, M. A.
(1995).
Application of a novel latex on ibuprofen pellets. Proceedings of the International Symposium on Controlled Release of Bioactive Materials.
270-271.
-
Karnachi, A. A., Singh, S. K., Sastry, S. V., Reddy, I. K., & Khan, M. A.
(1995).
Characterization and in vivo ulcerogenicity study of oral extended release preparations. Proceedings of the International Symposium on Controlled Release of Bioactive Materials.
296-297.
-
Funkhouser, C., Ali, S., Richardson, L., Rahman, Z., Khan, M., & Kuttolamadom, M.
(2020).
THERMAL INFLUENCE ON PRINTLET QUALITY IN THE SELECTIVE LASER SINTERING OF PHARMACEUTICAL FORMULATIONS
editor of
-
book
-
Jameel, F., Hershenson, S., Khan, M. A., & Martin-Moe, S.
(2015).
Quality by Design for Biopharmaceutical Drug Product Development
Jameel, F., Hershenson, S., Khan, M. A., & Martin-Moe, S. (Eds.),
Springer.
-
Jameel, F., Hershenson, S., Khan, M. A., & Martin-Moe, S.
(2015).
Quality by Design for Biopharmaceutical Drug Product Development
Jameel, F., Hershenson, S., Khan, M. A., & Martin-Moe, S. (Eds.),
Springer.
Research
principal investigator on
Teaching
teaching activities
- PHAR642 Pharmaceutics I Instructor
- PHAR713 Ipt Iv: Neurology Pain Mgmt Instructor
- PHAR765 Pediatric Pharmacotherapy Instructor
- PHAR785 Independent Study Instructor
- PHSC611 Drug Delvery & Formulations Instructor
- PHSC613 Laboratory Rotations Coordinator
- PHSC685 Directed Studies Instructor
- PHSC689 Sptp: Industrial Pharmac Instructor
- PHSC691 Research Instructor
Background
education and training
- Ph.D. in Pharmaceutics (focus on Industrial Pharmacy and Biopharmaceutics), St. John's University - (New York, New York, United States) 1992
- M.S. in Pharmaceutics (focus on Physical Pharmacy and Drug Delivery System), Idaho State University - (Pocatello, Idaho, United States) 1988
- M.S. in Pharmaceutical Technology, Andhra University - (Visakhapatnam, Andhra Pradesh, India) 1984
- B.S. in Pharmacy, Kakatiya University - (Warangal, India) 1982
awards and honors
- Regents Professor Award, conferred by Texas A&M University - (College Station, Texas, United States), 2021
- Excellence Award, conferred by Center for Drug Evaluation and Research - (Silver Spring, Maryland, United States), 2015
- Team Excellence Award, conferred by Center for Drug Evaluation and Research - (Silver Spring, Maryland, United States), 2015
- Team Excellence Award, conferred by Center for Drug Evaluation and Research - (Silver Spring, Maryland, United States), 2015
- AAPS Excellence in Ligand Binding Assays, conferred by American Association of Pharmaceutical Scientists - (Arlington, Virginia, United States), 2005
Contact
first name
- Mansoor
has last name
- Khan
mailing address
-
206 Olsen BLVD, Reynolds Medical building
College Station, TX
USA
Other
- mkhan@tamu.edu