M. Khan

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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

F. Muzzio, S. Oka, O. Kašpar, 2015 .

Quality by design: impact of formulation variables and their interactions on quality attributes of a lyophilized monoclonal antibody.

M. Khan, D. Awotwe-Otoo, C. Agarabi, 2012, International journal of pharmaceutics.

Scientific and Regulatory Overview of Process Analytical Technology in Bioprocesses

Jun Park, Kurt Brorson, Christopher Watts, 2011 .

Process analytical technology: Non-destructive assessment of anastrozole entrapment within PLGA microparticles by near infrared spectroscopy and chemical imaging

M. Khan, A. Zidan, O. Sammour, 2008 .

Assessment of Recent Process Analytical Technology (PAT) Trends: A Multiauthor Review

Richard D. Braatz, Yannick Maret, Niklas Sandler, 2015 .

Process analytical technology (PAT): quantification approaches in terahertz spectroscopy for pharmaceutical application.

H. Wu, M. Khan, E. Heilweil, 2008, Journal of pharmaceutical sciences.

Quality-by-Design (QbD): An integrated process analytical technology (PAT) approach for a dynamic pharmaceutical co-precipitation process characterization and process design space development.

H. Wu, M. Khan, Maury White, 2011, International journal of pharmaceutics.

Quality-by-design: an integrated process analytical technology approach to determine the nucleation and growth mechanisms during a dynamic pharmaceutical coprecipitation process.

H. Wu, M. Khan, Huiquan Wu, 2011, Journal of pharmaceutical sciences.

Quality-by-design (QbD): an integrated approach for evaluation of powder blending process kinetics and determination of powder blending end-point.

H. Wu, M. Khan, Huiquan Wu, 2009, Journal of pharmaceutical sciences.

Chemometric methods for the quantification of crystalline tacrolimus in solid dispersion by powder X-ray diffractrometry.

M. Khan, A. Siddiqui, Ziyaur Rahman, 2014, Journal of pharmaceutical sciences.

Integrated Process Analytical Technology Approach for Nucleation Induction Time Measurement and Nucleation Mechanism Assessment for a Dynamic Multicomponent Pharmaceutical Antisolvent Crystallization System

H. Wu, M. Khan, Maury White, 2014 .

THz spectroscopy: An emerging technology for pharmaceutical development and pharmaceutical Process Analytical Technology (PAT) applications

H. Wu, M. Khan, Huiquan Wu, 2012 .

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

H. Wu, M. Khan, Maury White, 2015 .

Process analytical technology (PAT): effects of instrumental and compositional variables on terahertz spectral data quality to characterize pharmaceutical materials and tablets.

H. Wu, M. Khan, E. Heilweil, 2007, International journal of pharmaceutics.

A mechanistic population balance model for granulation processes: Effect of process and formulation parameters

H. Wu, M. Khan, R. Ramachandran, 2014 .

Salt Engineering of Aripiprazole with Polycarboxylic Acids to Improve Physicochemical Properties

M. Khan, Ziyaur Rahman, Hamideh Afrooz, 2021, AAPS PharmSciTech.

Online Monitoring of PLGA Microparticles Formation Using Lasentec Focused Beam Reflectance (FBRM) and Particle Video Microscope (PVM)

Ziyaur Rahman, M. Khan, Ziyaur Rahman, 2010, The AAPS Journal.

Combination of Paclitaxel and R-flurbiprofen loaded PLGA nanoparticles suppresses glioblastoma growth on systemic administration.

M. Khan, F. Söylemezoğlu, G. Esendagli, 2020, International journal of pharmaceutics.

In Vitro Drug Transfer Due to Drug Retention in Human Epidermis Pretreated with Application of Marketed Estradiol Transdermal Systems

M. Khan, R. Shah, Guodong Fang, 2016, AAPS PharmSciTech.

A new chapter in pharmaceutical manufacturing: 3D‐printed drug products☆, ☆☆

M. Khan, C. M. Moore, James Norman, 2017, Advanced drug delivery reviews.

A QbD Case Study: Bayesian Prediction of Lyophilization Cycle Parameters

L. Mockus, M. Khan, R. Shah, 2011, AAPS PharmSciTech.

NIR Spectroscopy Applications in the Development of a Compacted Multiparticulate System for Modified Release

Stuart L. Cantor, M. Khan, S. Hoag, 2011, AAPS PharmSciTech.

Development and optimization of taste-masked orally disintegrating tablets (ODTs) of clindamycin hydrochloride

Stuart L. Cantor, M. Khan, Abhay Gupta, 2015, Drug development and industrial pharmacy.

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.

H. Wu, M. Khan, S. Hoag, 2008, Journal of pharmaceutical sciences.

Real time monitoring of bioreactor mAb IgG3 cell culture process dynamics via Fourier transform infrared spectroscopy: Implications for enabling cell culture process analytical technology

H. Wu, M. Khan, C. Agarabi, 2015, Frontiers of Chemical Science and Engineering.

Characterization of a nonribosomal peptide antibiotic solid dispersion formulation by process analytical technologies sensors.

M. Khan, A. Siddiqui, Ziyaur Rahman, 2013, Journal of pharmaceutical sciences.

Formulation and Evaluation of a Protein-loaded Solid Dispersions by Non-destructive Methods

M. Khan, Ziyaur Rahman, A. Zidan, 2010, The AAPS Journal.

Evaluation of Abuse-Deterrent Characteristics of Tablets Prepared via Hot-Melt Extrusion

M. Khan, A. Siddiqui, Ziyaur Rahman, 2019, AAPS PharmSciTech.

Pharmaceutical characterization of novel tenofovir liposomal formulations for enhanced oral drug delivery: in vitro pharmaceutics and Caco-2 permeability investigations

Patrick J Faustino, M. Khan, M. Habib, 2017, Clinical pharmacology : advances and applications.

Risperidone solid dispersion for orally disintegrating tablet: its formulation design and non-destructive methods of evaluation.

M. Khan, Ziyaur Rahman, A. Zidan, 2010, International journal of pharmaceutics.

Targeting to macrophages: role of physicochemical properties of particulate carriers--liposomes and microspheres--on the phagocytosis by macrophages.

M. Khan, F. Ahsan, I. P. Rivas, 2002, Journal of controlled release : official journal of the Controlled Release Society.

Regulatory Perspective on the Development of Polymer Nanomaterials

M. Khan, Xiaoming Xu, 2016 .

Real-time on-line blend uniformity monitoring using near-infrared reflectance spectrometry: a noninvasive off-line calibration approach.

Abhay Gupta, Huiquan Wu, James Pazdan, 2009, Journal of pharmaceutical and biomedical analysis.

Physicochemical and mechanical properties of carbamazepine cocrystals with saccharin

Ziyaur Rahman, Vilayat A Sayeed, M. Khan, 2012, Pharmaceutical development and technology.

Comparison of raloxifene and bisphosphonates based on adherence and treatment satisfaction in postmenopausal Asian women

M. Khan, D. Thiebaud, A. Kung, 2007, Journal of Bone and Mineral Metabolism.

Preparation and Characterization of Coenzyme Q10–Eudragit® Solid Dispersion

M. Khan, S. Nazzal, N. Gũven, 2002, Drug development and industrial pharmacy.

Development of a HPLC method for the determination of cyclosporin-A in rat blood and plasma using naproxen as an internal standard.

M. Khan, F. Ahsan, A. Hussain, 2003, Journal of pharmaceutical and biomedical analysis.

Root cause evaluation of particulates in the lyophilized indomethacin sodium trihydrate plug for parenteral administration.

M. Khan, D. Awotwe-Otoo, A. Siddiqui, 2014, International journal of pharmaceutics.

Semi‐fluorinated polyarylenes: Microwave‐assisted synthesis and structure–property relationships

S. T. Iacono, M. Khan, S. Budy, 2020 .

Controlled release coprecipitates : formulation considerations

Sanford Bolton, M. Khan, S. Singh, 1995 .

CALCIUM PHOSPHATE IN PHARMACEUTICAL PRODUCT DEVELOPMENT

M. Khan, I. Reddy, 1998 .

Chemometric evaluation of near infrared, fourier transform infrared, and Raman spectroscopic models for the prediction of nimodipine polymorphs.

M. Khan, A. Siddiqui, Ziyaur Rahman, 2013, Journal of pharmaceutical sciences.

Difference in the Lubrication Efficiency of Bovine and Vegetable-Derived Magnesium Stearate During Tabletting

M. Khan, M. Tawakkul, Abhay Gupta, 2009, AAPS PharmSciTech.

Defining Patient Centric Pharmaceutical Drug Product Design

Graziano Onder, Sven Stegemann, M. Khan, 2016, The AAPS Journal.

Current Status of the Oral Delivery of Insulin

M. Khan, V. Agarwal, 2001 .

Understanding effect of formulation and manufacturing variables on the critical quality attributes of warfarin sodium product.

M. Khan, A. Siddiqui, Ziyaur Rahman, 2015, International journal of pharmaceutics.

Ibuprofen Release from Beads Coated with an Experimental Latex: Effect of Certain Variables

M. Khan, S. Singh, 1997 .

Univariate and multivariate models for determination of prasugrel base in the formulation of prasugrel hydrochloride using XRPD method.

M. Khan, Ziyaur Rahman, Hamideh Afrooz, 2019, Journal of pharmaceutical sciences.

Quality by Design for Biopharmaceutical Drug Product Development

M. Khan, F. Jameel, S. Hershenson, 2015, AAPS Advances in the Pharmaceutical Sciences Series.

Chemometric evaluation of brompheniramine-tannate complexes.

M. Khan, Ziyaur Rahman, A. Zidan, 2012, Journal of pharmaceutical sciences.

Quality by design: understanding the product variability of a self-nanoemulsified drug delivery system of cyclosporine A.

M. Khan, O. Sammour, N. A. Megrab, 2007, Journal of pharmaceutical sciences.

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

M. Khan, P. Couvreur, G. Esendagli, 2017, Artificial cells, nanomedicine, and biotechnology.

Considerations for a Pediatric Biopharmaceutics Classification System (BCS): Application to Five Drugs

M. Khan, J. Polli, W. Rodriguez, 2014, AAPS PharmSciTech.

Chain length-dependent effects of alkylmaltosides on nasal absorption of enoxaparin.

M. Khan, F. Ahsan, Tianzhi Yang, 2004, Journal of pharmaceutical sciences.

Assessing impact of formulation and process variables on in-vitro performance of directly compressed abuse deterrent formulations.

M. Khan, A. Siddiqui, Ziyaur Rahman, 2016, International journal of pharmaceutics.

Influence of drug loading and type of ointment base on the in vitro performance of acyclovir ophthalmic ointment.

M. Khan, Ziyaur Rahman, Y. Krishnaiah, 2015, International journal of pharmaceutics.

Oral delivery of proteins: progress and prognostication.

M. Khan, R. Shah, F. Ahsan, 2002, Critical reviews in therapeutic drug carrier systems.

Manufacturing Engineering Challenges of Pharmaceutical 3D Printing for on-Demand Drug Delivery

M. Khan, T. Ozkan, Ienina, 2018 .

Tannate complexes of antihistaminic drug: sustained release and taste masking approaches.

M. Khan, Ziyaur Rahman, A. Zidan, 2012, International journal of pharmaceutics.

Synthesis of graphene oxide doped poly(2-acrylamido-2-methyl propane sulfonic acid) [GO@p(AMPS)] composite hydrogel with pseudo-plastic thixotropic behavior

M. Khan, L. Shah, T. Rehman, 2019, Polymer Bulletin.

Colorimetric acetone sensor based on ionic liquid functionalized drug-mediated silver nanostructures.

M. Khan, N. Muhammad, Amir Badshah, 2022, Journal of pharmaceutical and biomedical analysis.

Analytical methods for the evaluation of melamine contamination.

Stuart L. Cantor, M. Khan, Abhay Gupta, 2014, Journal of pharmaceutical sciences.

Application of NIR chemometric methods for quantification of the crystalline fraction of warfarin sodium in drug product

M. Khan, S. Akhtar, A. Siddiqui, 2016, Drug development and industrial pharmacy.

Quality and In-Use Stability Comparison of Brand and Generics of Extended-Release Phenytoin Sodium Capsules.

M. Khan, Ziyaur Rahman, Hamideh Afrooz, 2019, Journal of pharmaceutical sciences.

Evaluation of the In Vitro Efficacy of Sevelamer Hydrochloride and Sevelamer Carbonate.

M. Khan, R. T. Berendt, Yongsheng Yang, 2016, Journal of pharmaceutical sciences.

Comparative evaluation of the in vitro efficacy of lanthanum carbonate chewable tablets.

Lawrence X. Yu, M. Khan, R. Shah, 2013, Journal of pharmaceutical sciences.

Development and validation of an ion chromatography method for the determination of phosphate-binding of lanthanum carbonate.

Lawrence X. Yu, M. Khan, Yongsheng Yang, 2010, Journal of pharmaceutical and biomedical analysis.

Design Space Definition

G. Reklaitis, L. Mockus, M. Khan, 2017 .

Quantitative determination of cesium binding to ferric hexacyanoferrate: Prussian blue.

M. Khan, A. Hussain, N. Sadrieh, 2008, Journal of pharmaceutical and biomedical analysis.

Nickel Oxide-incorporated Polyaniline/Polyvinyl Alcohol Composite for Enhanced Antibacterial Activity

M. Khan, G. Rahman, M. S. Khan, 2019, Zeitschrift für Physikalische Chemie.

Vortex assisted magnetic solid phase extraction of lead(II) and cobalt(II) on silica coated magnetic multiwalled carbon nanotubes impregnated with 1-(2-pyridylazo)-2-naphthol

M. Khan, M. Soylak, E. Yılmaz, 2016 .

Adsorption and recovery of hexavalent chromium from tannery wastewater over magnetic max phase composite

M. Khan, F. Hussain, W. Ahmad, 2020, Separation Science and Technology.

Removal and recovery of cadmium from aqueous solutions using magnetic nanoparticle-modified sawdust: kinetics and adsorption isotherm studies

M. Khan, J. Shah, M. R. Jan, 2016 .

Bioavailability Assessment of Oral Coenzyme Q10 Formulations in Dogs

M. Khan, A. Zaghloul, B. Gurley, 2002, Drug development and industrial pharmacy.

Development of a Multivariate Predictive Dissolution Model for Tablets Coated with Cellulose Ester Blends

M. Khan, Ziyaur Rahman, Hamideh Afrooz, 2020, Pharmaceuticals.

Non-enzymatic colorimetric biosensor for hydrogen peroxide using lignin-based silver nanoparticles tuned with ionic liquid as a peroxidase mimic

M. Khan, N. Muhammad, A. Rahim, 2021 .

A long-term stability study of Prussian blue: A quality assessment of water content and cesium binding.

M. Khan, Yongsheng Yang, A. Mohammad, 2015, Journal of pharmaceutical and biomedical analysis.

Long-term stability study of Prussian blue - a quality assessment of water content and thallium binding.

M. Khan, Yongsheng Yang, A. Mohammad, 2014, International journal of pharmaceutics.

Blend of cellulose ester and enteric polymers for delayed and enteric coating of core tablets of hydrophilic and hydrophobic drugs.

M. Khan, Ziyaur Rahman, Hamideh Afrooz, 2019, International journal of pharmaceutics.

Effect of Additives on the Diffusion of Ketoprofen Through Human Skin

M. Khan, S. Singh, D. Roane, 1996 .

Preparation and characterization of magnetic allylamine modified graphene oxide-poly(vinyl acetate-co-divinylbenzene) nanocomposite for vortex assisted magnetic solid phase extraction of some metal ions.

M. Khan, M. Soylak, E. Yılmaz, 2016, Talanta.

Formulation Optimization of Selective Laser Sintering 3D-Printed Tablets of Clindamycin Palmitate Hydrochloride by Response Surface Methodology

M. Khan, Ziyaur Rahman, Mathew Kuttolamadom, 2020, AAPS PharmSciTech.

Development and application of a validated stability-indicating Ultra-Performance Liquid Chromatography (UPLC) method for the determination of dantrolene and its related impurities

M. Khan, M. Tawakkul, V. Sayeed, 2010 .

Comparative Evaluation of Flow for Pharmaceutical Powders and Granules

M. Khan, R. Shah, M. Tawakkul, 2008, AAPS PharmSciTech.

Oseltamivir phosphate-amberlite(TM) IRP 64 ionic complex for taste masking: preparation and chemometric evaluation.

M. Khan, R. Shah, A. Siddiqui, 2013, Journal of pharmaceutical sciences.

Fabrication of stable superabsorbent hydrogels for successful removal of crystal violet from waste water

M. Khan, A. Khan, L. Shah, 2019, RSC advances.

Implementation of a New Course with a Focus on Active Learning Through Integrated Curricular Approach: Pharmacy Care Laboratory I

William H. Ross, M. Khan, L. Lawrence, 1999 .

Effect of Extragranular Microcrystalline Cellulose on Compaction, Surface Roughness, and In Vitro Dissolution of a Self-Nanoemulsified Solid Dosage Form of Ubiquinone

M. Khan, S. Nazzal, A. Zaghloul, 2002 .

Building better drugs: developing and regulating engineered therapeutic proteins.

Chen Yanover, Chava Kimchi-Sarfaty, Tal Schiller, 2013, Trends in pharmacological sciences.

Product and process understanding of a novel pediatric anti-HIV tenofovir niosomes with a high-pressure homogenizer.

M. Khan, Ziyaur Rahman, A. Zidan, 2011, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Physico-mechanical and Stability Evaluation of Carbamazepine Cocrystal with Nicotinamide

M. Khan, C. Agarabi, Ziyaur Rahman, 2011, AAPS PharmSciTech.

PROCESS CONTROL PERSPECTIVE FOR PROCESS ANALYTICAL TECHNOLOGY: INTEGRATION OF CHEMICAL ENGINEERING PRACTICE INTO SEMICONDUCTOR AND PHARMACEUTICAL INDUSTRIES

Mansoor A. Khan, Huiquan Wu, Ajaz S. Hussain, 2007 .

Zwitterionic superabsorbent polymer hydrogels for efficient and selective removal of organic dyes

M. Khan, L. Shah, T. Rehman, 2019, RSC advances.

Development and application of a validated HPLC method for the analysis of dissolution samples of gabapentin drug products.

M. Khan, Abhay Gupta, V. Sayeed, 2008, Journal of pharmaceutical and biomedical analysis.

Development and application of a validated HPLC method for the determination of gabapentin and its major degradation impurity in drug products.

M. Khan, Abhay Gupta, V. Sayeed, 2007, Journal of pharmaceutical and biomedical analysis.

Improvement of Physicochemical Properties of an Antiepileptic Drug by Salt Engineering

M. Khan, Ziyaur Rahman, A. Zidan, 2012, AAPS PharmSciTech.

Influence of Formulation and Processing Factors on Stability of Levothyroxine Sodium Pentahydrate

M. Khan, R. Shah, M. Habib, 2010, AAPS PharmSciTech.

Complexation of risperidone with a taste-masking resin: Novel application of near infra-red and chemical imaging to evaluate complexes

M. Khan, R. Shah, A. Zidan, 2009, Pharmaceutical development and technology.

Stability Characterization, Kinetics and Mechanism of Degradation of Dantrolene in Aqueous Solution: Effect of pH and Temperature

M. Khan, M. Tawakkul, V. Sayeed, 2012 .

Quantitative evaluation of the thallium binding of soluble and insoluble Prussian blue hexacyanoferrate analogs: A scientific comparison based on their critical quality attributes.

M. Khan, Andrew J. Brown, Yongsheng Yang, 2019, International journal of pharmaceutics.

Quantitative determination of thallium binding to ferric hexacyanoferrate: Prussian blue.

Lawrence X. Yu, M. Khan, N. Sadrieh, 2008, International journal of pharmaceutics.

Switchable solvent based liquid phase microextraction of mercury from environmental samples: a green aspect

M. Khan, M. Soylak, 2016 .

Switchable solvent based liquid phase microextraction of uranium in environmental samples: a green approach

M. Khan, M. Soylak, E. Yılmaz, 2016 .

Development and validation of in vitro-in vivo correlation (IVIVC) for estradiol transdermal drug delivery systems.

M. Khan, Y. Krishnaiah, Naresh Pavurala, 2015, Journal of controlled release : official journal of the Controlled Release Society.

Understanding the quality of protein loaded PLGA nanoparticles variability by Plackett-Burman design.

Ziyaur Rahman, M. Khan, M. Habib, 2010, International journal of pharmaceutics.

Understanding Pharmaceutical Quality by Design

G. K. Raju, Lawrence X. Yu, Mansoor A. Khan, 2014, The AAPS Journal.

Atenolol gastrointestinal therapeutic system: optimization of formulation variables using response surface methodology

Indra K. Reddy, M. Khan, Mansoor A. Khan, 1997 .

Preparation and in vitro characterization of a eutectic based semisolid self-nanoemulsified drug delivery system (SNEDDS) of ubiquinone: mechanism and progress of emulsion formation.

M. Khan, O. Lavrentovich, I. Smalyukh, 2002, International journal of pharmaceutics.

Evaluation of cytotoxicity of oils used in coenzyme Q10 Self-emulsifying Drug Delivery Systems (SEDDS).

M. Khan, A. Palamakula, Anitha Palamakula, 2004, International journal of pharmaceutics.

Crystallinity evaluation of tacrolimus solid dispersions by chemometric analysis.

Lawrence X. Yu, M. Khan, Ziyaur Rahman, 2012, International journal of pharmaceutics.

An index for evaluating difficulty of Chewing Index for chewable tablets

M. Khan, Abhay Gupta, Nallaperumal Chidambaram, 2015, Drug development and industrial pharmacy.

Coating characterization by hyperspectroscopy and predictive dissolution models of tablets coated with blends of cellulose acetate and cellulose acetate phthalate

M. Khan, Ziyaur Rahman, Hamideh Afrooz, 2021, AAPS PharmSciTech.

Response surface methodology for the optimization of ubiquinone self-nanoemulsified drug delivery system

M. Khan, S. Nazzal, 2008, AAPS PharmSciTech.

Controlled release of a self-emulsifying formulation from a tablet dosage form: stability assessment and optimization of some processing parameters.

Sami Nazzal, M. Khan, S. Nazzal, 2006, International journal of pharmaceutics.

Development of performance matrix for generic product equivalence of acyclovir topical creams.

John R. Peters, M. Khan, Ziyaur Rahman, 2014, International journal of pharmaceutics.

Effect of processing parameters and controlled environment storage on the disproportionation and dissolution of extended‐release capsule of phenytoin sodium

M. Khan, Ziyaur Rahman, Hamideh Afrooz, 2018, International journal of pharmaceutics.

A quality by design (QbD) case study on liposomes containing hydrophilic API: I. Formulation, processing design and risk assessment.

Diane J Burgess, M. Khan, D. Burgess, 2011, International journal of pharmaceutics.

Formulation and process factors influencing product quality and in vitro performance of ophthalmic ointments.

M. Khan, Ziyaur Rahman, Y. Krishnaiah, 2015, International journal of pharmaceutics.

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.

Diane J Burgess, M. Khan, D. Burgess, 2012, International journal of pharmaceutics.

Optimization and In Vivo Evaluation of an Oral Dual Controlled-Release Tablet Dosage Form of Insulin and Duck Ovomucoid

M. Khan, S. Nazzal, V. Agarwal, 2008, Pharmaceutical development and technology.

Protection of salmon calcitonin breakdown with serine proteases by various ovomucoid species for oral drug delivery.

M. Khan, R. Shah, 2004, Journal of pharmaceutical sciences.

Oral Delivery of Proteins: Effect of Chicken and Duck Ovomucoid on the Stability of Insulin in the Presence of α‐Chymotrypsin and Trypsin

M. Khan, I. Reddy, V. Agarwal, 2000 .

Nanoparticles for improvement in oral bioavailability

Naseem A. Charoo, M. Khan, Ziyaur Rahman, 2019, Nanoarchitectonics in Biomedicine.

Impact of controlled ice nucleation on process performance and quality attributes of a lyophilized monoclonal antibody.

Scott Lute, Cyrus Agarabi, David Awotwe-Otoo, 2013, International journal of pharmaceutics.

Supramolecular solvent based liquid–liquid microextraction of aluminum from water and hair samples prior to UV-visible spectrophotometric detection

M. Khan, M. Soylak, 2015 .

Application of quality by design elements for the development and optimization of an analytical method for protamine sulfate.

Cyrus Agarabi, Sau Lee, David Awotwe-Otoo, 2012, Journal of pharmaceutical and biomedical analysis.

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

M. Khan, Saeed R. Khan, A. Mohammad, 2015 .

Absorption enhancers in pulmonary protein delivery.

Fakhrul Ahsan, M. Khan, F. Ahsan, 2004, Journal of controlled release : official journal of the Controlled Release Society.

Improved Stability of a Model IgG3 by DoE-Based Evaluation of Buffer Formulations

Cyrus D. Agarabi, Erik K. Read, M. Khan, 2016, BioMed research international.

Product and process understanding to relate the effect of freezing method on glycation and aggregation of lyophilized monoclonal antibody formulations.

Kurt A Brorson, Erik K Read, Scott Lute, 2015, International journal of pharmaceutics.

An integrated process analytical technology (PAT) approach to monitoring the effect of supercooling on lyophilization product and process parameters of model monoclonal antibody formulations.

Cyrus Agarabi, M. Khan, C. Agarabi, 2014, Journal of pharmaceutical sciences.

Application of quality by design to formulation and processing of protein liposomes.

Antonio P. Costa, Diane J Burgess, M. Khan, 2012, International journal of pharmaceutics.

Controlled Release Multiparticulate Beads Coated with Starch Acetate: Material Characterization, and Identification of Critical Formulation and Process Variables

M. Khan, M. Nutan, S. Vaithiyalingam, 2007, Pharmaceutical development and technology.

Transport studies of insulin across rat jejunum in the presence of chicken and duck ovomucoids

M. Khan, S. Nazzal, I. Reddy, 2001, The Journal of pharmacy and pharmacology.

A Report from the Pediatric Formulations Task Force: Perspectives on the State of Child-Friendly Oral Dosage Forms

M. Khan, J. Breitkreutz, J. Barrett, 2013, The AAPS Journal.

An Enteric Dual‐Controlled Gastrointestinal Therapeutic System of Salmon Calcitonin‐I: Preparation, Characterization, and Preclinical Bioavailability in Rats

M. Khan, R. Shah, M. Nutan, 2004 .

Atenolol Gastrointestinal Therapeutic System. I. Screening of Formulation Variables

M. Khan, Mansoor A. Khan, Lndra K. Reddy, 1997 .

An Integrated Process Analytical Technology (PAT) Approach for Pharmaceutical Crystallization Process Understanding to Ensure Product Quality and Safety: FDA Scientist’s Perspective

Haitao Li, Huiquan Wu, Zedong Dong, 2015 .

Quality-by-Design (QbD): an integrated process analytical technology (PAT) approach for real-time monitoring and mapping the state of a pharmaceutical coprecipitation process.

Mansoor A. Khan, Huiquan Wu, M. Khan, 2010, Journal of pharmaceutical sciences.

Preparation and in vitro characterization of self-nanoemulsified drug delivery system (SNEDDS) of all-trans-retinol acetate.

M. Khan, A. Samy, E. Taha, 2004, International journal of pharmaceutics.

Development and Validation of a HPLC Method for Dissolution and Stability Assay of Liquid-Filled Cyclosporine Capsule Drug Products

M. Khan, Abhay Gupta, V. Sayeed, 2013, AAPS PharmSciTech.

Optimization and characterization of controlled release multi-particulate beads formulated with a customized cellulose acetate butyrate dispersion.

M. Khan, Mansoor A Khan, Siva Vaithiyalingam, 2002, International journal of pharmaceutics.

Nanopharmaceuticals: Challenges and Regulatory Perspective

M. Khan, R. Shah, 2009 .

Comparison of the stability of split and intact gabapentin tablets.

M. Khan, Abhay Gupta, V. Sayeed, 2008, International journal of pharmaceutics.

Intraocular Pressure-Lowering Activity and In Vivo Disposition of Dipivalyl Terbutalone in Rabbits

M. Khan, I. Reddy, S. Vaithiyalingam, 2001, Drug development and industrial pharmacy.

Permeability of Chemical Delivery Systems Across Rabbit Corneal (SIRC) Cell Line and Isolated Corneas: A Comparative Study

M. Khan, M. A. Khan, R. A. Hill, 2000, Pharmaceutical development and technology.

A two-stage reverse dialysis in vitro dissolution testing method for passive targeted liposomes.

M. Khan, D. Burgess, Xiaoming Xu, 2012, International journal of pharmaceutics.

Preparation and characterization of dicarboxylic acids salt of aripiprazole with enhanced physicochemical properties

M. Khan, Ziyaur Rahman, E. Mohamed, 2021, Pharmaceutical development and technology.

Considerations for a Pediatric Biopharmaceutics Classification System (BCS): Application to Five Drugs

M. Khan, J. Polli, W. Rodriguez, 2014, AAPS PharmSciTech.

Risk based in vitro performance assessment of extended release abuse deterrent formulations.

M. Khan, Abhay Gupta, Xiaoming Xu, 2016, International journal of pharmaceutics.

Development of Stable Amorphous Solid Dispersion and Quantification of Crystalline Fraction of Lopinavir by Spectroscopic-chemometric Methods.

M. Khan, Ziyaur Rahman, E. Mohamed, 2021, International journal of pharmaceutics.

Influence of tablet characteristics on weight variability and weight loss in split tablets.

M. Khan, Abhay Gupta, Robert L Hunt, 2008, American Journal of Health-System Pharmacy.

Complexation between risperidone and amberlite resin by various methods of preparation and binding study

M. Khan, R. Shah, M. Tawakkul, 2009, Drug development and industrial pharmacy.

Process analytical technology: chemometric analysis of Raman and near infra-red spectroscopic data for predicting physical properties of extended release matrix tablets.

M. Khan, R. Shah, M. Tawakkul, 2007, Journal of pharmaceutical sciences.

Cholorpheniramine tannate complexes: physicochemical, chemometric, and taste masking evaluation.

M. Khan, Ziyaur Rahman, A. Zidan, 2012, International journal of pharmaceutics.

Quality by design: understanding the formulation variables of a cyclosporine A self-nanoemulsified drug delivery systems by Box-Behnken design and desirability function.

M. Khan, O. Sammour, N. A. Megrab, 2007, International journal of pharmaceutics.

Chemometric Models for Quantification of Carbamazepine Anhydrous and Dihydrate Forms in the Formulation.

M. Khan, Ziyaur Rahman, Hamideh Afrooz, 2019, Journal of pharmaceutical sciences.

Use of In Vitro–In Vivo Correlation to Predict the Pharmacokinetics of Several Products Containing a BCS Class 1 Drug in Extended Release Matrices

M. Khan, S. Bykadi, Yongsheng Yang, 2012, Pharmaceutical Research.

Box-behnken design for the optimization of formulation variables of indomethacin coprecipitates with polymer mixtures

M. Khan, Mansoor A. Khan, Anees Abdulquadar Karnachi, 1996 .

Disintegration of Highly Soluble Immediate Release Tablets: A Surrogate for Dissolution

M. Khan, R. Shah, Abhay Gupta, 2009, AAPS PharmSciTech.

Development Of Methamphetamine Abuse-Deterrent Formulations Using Sucrose Acetate Isobutyrate.

M. Khan, Ziyaur Rahman, Hamideh Afrooz, 2019, Journal of pharmaceutical sciences.

Response Surface Methodology for the Development of Self-Nanoemulsified Drug Delivery System (SNEDDS) of All-Trans-Retinol Acetate

M. Khan, A. Samy, E. Taha, 2005, Pharmaceutical development and technology.

Effects of Diluents on Physical and Chemical Stability of Phenytoin and Phenytoin Sodium

M. Khan, Ziyaur Rahman, Sogra F. Barakh Ali, 2020, AAPS PharmSciTech.

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.

M. Khan, S. Akhtar, A. Siddiqui, 2015, Journal of pharmaceutical sciences.

Aqueous-based polymeric dispersion: preparation and characterization of cellulose acetate pseudolatex

M. Khan, I. Reddy, S. Sastry, 1998 .

Compression of Indomethacin Coprecipitates with Polymer Mixtures: Effect of Preparation Methodology

M. Khan, R. D. Hon, A. Karnachi, 1995 .

Hunter screening design to understand the product variability of solid dispersion formulation of a peptide antibiotic.

Ziyaur Rahman, M. Khan, Ziyaur Rahman, 2013, International journal of pharmaceutics.

Response surface methodology for optimization and characterization of limonene-based coenzyme Q10 self-nanoemulsified capsule dosage form

Mohammad T. H. Nutan, M. Khan, M. Nutan, 2004, AAPS PharmSciTech.

Formulation and transport properties of tenofovir loaded liposomes through Caco-2 cell model

M. Khan, M. Habib, A. Zidan, 2013, Journal of liposome research.

Tablet Splitting of a Narrow Therapeutic Index Drug: A Case with Levothyroxine Sodium

Vilayat A. Sayeed, Rakhi B. Shah, M. Khan, 2010, AAPS PharmSciTech.

Process analytical technology: nondestructive evaluation of cyclosporine A and phospholipid solid dispersions by near infrared spectroscopy and imaging.

M. Khan, M. Habib, A. Zidan, 2008, Journal of pharmaceutical sciences.

Orally disintegrating tablet of novel salt of antiepileptic drug: formulation strategy and evaluation.

Ziyaur Rahman, Akhtar Siddiqui, M. Khan, 2013, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Response Surface Methodology to Obtain β-Estradiol Biodegradable Microspheres for Long-Term Therapy of Osteoporosis

M. Khan, A. Zaghloul, F. Mustafa, 2006, Pharmaceutical development and technology.

Biodegradable Microparticulates of Beta-Estradiol: Preparation and In Vitro Characterization

M. Khan, A. Zaghloul, F. Mustafa, 2005, Drug development and industrial pharmacy.

Non-destructive methods of characterization of risperidone solid lipid nanoparticles.

M. Khan, Ziyaur Rahman, A. Zidan, 2010, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Pyrimethamine 3D printlets for pediatric toxoplasmosis: design, pharmacokinetics, and anti-toxoplasma activity

M. Khan, Ziyaur Rahman, Mathew Kuttolamadom, 2023, Expert opinion on drug delivery.

Printing of personalized medication using binder jetting 3D printer

Mansoor A. Khan, Ziyaur Rahman, Mathew Kuttolamadom, 2020 .

Dose Uniformity of Scored and Unscored Tablets: Application of the FDA Tablet Scoring Guidance for Industry

M. Khan, Abhay Gupta, P. Faustino, 2016, PDA Journal of Pharmaceutical Science and Technology.

Dose uniformity of scored and unscored tablets: Application of the FDA Tablet Scoring Guidance for Industry.

M. Khan, Abhay Gupta, P. Faustino, 2016, PDA journal of pharmaceutical science and technology.

Tablet splitting: Product quality assessment of metoprolol succinate extended release tablets.

M. Khan, A. Zidan, M. Tawakkul, 2010, International journal of pharmaceutics.

Strategies of targeting oral drug delivery systems to the colon and their potential use for the treatment of colorectal cancer

M. Khan, Y. Krishnaiah, 2012, Pharmaceutical development and technology.

Salbutamol Sulfate Suppositories: Influence of Formulation on Physical Parameters and Stability

M. Khan, E. Taha, A. Zaghloul, 2003, Pharmaceutical development and technology.

Synthesis of physically cross-linked gum Arabic-based polymer hydrogels with enhanced mechanical, load bearing and shape memory behavior

M. Khan, A. Khan, L. Shah, 2020, Iranian Polymer Journal.

Synthesis and Rheological Survey of Xanthan Gum Based Terpolymeric Hydrogels

M. Khan, L. Shah, Ijaz Ali, 2020 .

Pharmaceutical characterization and thermodynamic stability assessment of a colloidal iron drug product: iron sucrose.

Lawrence X. Yu, M. Khan, R. Shah, 2014, International journal of pharmaceutics.

Fermentanomics: Relating quality attributes of a monoclonal antibody to cell culture process variables and raw materials using multivariate data analysis

Anurag S Rathore, Kurt A Brorson, Sumit Kumar Singh, 2015, Biotechnology progress.

Development of High Temperature High Pressure (HTHP) Water Based Drilling Mud using Synthetic Polymers, and Nanoparticles

M. Khan, H. S. Al-Salim, Leila Niloofar Arsanjani, 2018 .

A Study On Thyroxine and Thyroid Stimulating Hormone in Women During Pregnancy

M. Khan, A. Habib, .. M.T.Javed, 1999 .

Characterization and selection of suitable grades of lactose as functional fillers for capsule filling: part 1

M. Khan, S. Hoag, L. Augsburger, 2015, Drug development and industrial pharmacy.

Optimization and characterization of controlled release pellets coated with an experimental latex: II. Cationic drug

M. Khan, S. Singh, Mansoor A. Khan, 1995 .

To investigate the influence of machine operating variables on formulations derived from lactose types in capsule filling: part 2

M. Khan, S. Hoag, L. Augsburger, 2016, Drug development and industrial pharmacy.

Effects of excipients and curing process on the abuse deterrent properties of directly compressed tablets.

Celia N. Cruz, M. Khan, A. Siddiqui, 2017, International journal of pharmaceutics.

Nitroso Impurities in Drug Products: An Overview of Risk Assessment, Regulatory Milieu, and Control Strategy

Naseem A. Charoo, M. Khan, Ziyaur Rahman, 2023, AAPS PharmSciTech.

Development of a Validated Stability Indicating HPLC Method for Ranitidine Hydrochloride Syrup

M. Khan, R. Shah, M. Tawakkul, 2006 .

Regulatory Considerations in Development of Amorphous Solid Dispersions

Abhay Gupta, Mansoor A. Khan, Ziyaur Rahman, 2014 .

In-Situ Implant Formulation of Laurate and Myristate Prodrugs of Dolutegravir for Ultra-Long Delivery.

Hamed I. Ali, M. Khan, Ziyaur Rahman, 2022, Journal of pharmaceutical sciences.

Predicting hydrophilic drug encapsulation inside unilamellar liposomes.

M. Khan, D. Burgess, Xiaoming Xu, 2012, International journal of pharmaceutics.

Preparation and characterization of a customized cellulose acetate butyrate dispersion for controlled drug delivery.

M. Khan, M. Nutan, I. Reddy, 2002, Journal of pharmaceutical sciences.

Development and Validation of a Discriminatory Dissolution Method for Portioned Moist Snuff and Snus.

M. Khan, Ziyaur Rahman, E. Mohamed, 2021, Journal of pharmaceutical sciences.

Preparation and in vitro characterization of self-nanoemulsified drug delivery systems of coenzyme Q10 using chiral essential oil components

M. Khan, M. Soliman, I. Reddy, 2004 .

Impact of formulation and process variables on solid-state stability of theophylline in controlled release formulations.

M. Khan, A. Siddiqui, Ziyaur Rahman, 2016, International journal of pharmaceutics.

Spectroscopic-Based Chemometric Models for Quantifying Low Levels of Solid-State Transitions in Extended Release Theophylline Formulations.

M. Khan, Ziyaur Rahman, Maxwell Korang-Yeboah, 2016, Journal of pharmaceutical sciences.

Thermodynamic stability assessment of a colloidal iron drug product: sodium ferric gluconate.

Lawrence X. Yu, M. Khan, R. Shah, 2010, Journal of pharmaceutical sciences.

Use of In Vitro–In Vivo Correlation to Predict the Pharmacokinetics of Several Products Containing a BCS Class 1 Drug in Extended Release Matrices

M. Khan, S. Bykadi, Yongsheng Yang, 2012, Pharmaceutical Research.

Fractionated charge variants of biosimilars: A review of separation methods, structural and functional analysis.

M. Khan, Y. Capan, Meral Yüce, 2021, Analytica chimica acta.

Preparation and Characterization of Stable Amorphous Glassy Solution of BCS II and IV Drugs

M. Khan, Ziyaur Rahman, S. Dharani, 2021, AAPS PharmSciTech.

Preparation and characterization of genistein containing poly(ethylene glycol) microparticles

M. Khan, B. Youan, Nusrat A. Motlekar, 2006 .

Defining Patient Centric Pharmaceutical Drug Product Design

M. Khan, G. Onder, S. Stegemann, 2016, The AAPS Journal.

Quality-by-design (QbD): an integrated multivariate approach for the component quantification in powder blends.

Huiquan Wu, Maury White, M. Khan, 2009, International journal of pharmaceutics.

Quality by design approach for understanding the critical quality attributes of cyclosporine ophthalmic emulsion.

Lawrence X. Yu, M. Khan, Ziyaur Rahman, 2014, Molecular Pharmaceutics.

Cytotoxicity evaluation of enzyme inhibitors and absorption enhancers in Caco-2 cells for oral delivery of salmon calcitonin.

M. Khan, R. Shah, A. Palamakula, 2004, Journal of pharmaceutical sciences.

Supramolecular solvent microextraction of uranium at trace levels from water and soil samples

M. Khan, M. Soylak, E. Yılmaz, 2017 .

Potential Application of USP Paddle and Basket Dissolution Methods in Discriminating for Portioned Moist Snuff and Snus Smokeless Tobacco Products

M. Khan, Ziyaur Rahman, S. Dharani, 2021, AAPS PharmSciTech.

Understanding the effects of formulation and process variables on the printlets quality manufactured by selective laser sintering 3D printing.

M. Khan, Ziyaur Rahman, Mathew Kuttolamadom, 2019, International journal of pharmaceutics.

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

M. Khan, Geoffrey K. Wu, Abhay Gupta, 2013 .

ALENDRONATE A PROMISING / MULTI ASPECT DRUG IN THE MANAGEMENT OF OSTOEOPOROSIS

M. Khan, S. S. Noor, S. Shaheen, 2011 .

Comparative stability of repackaged metoprolol tartrate tablets.

M. Khan, Abhay Gupta, Yongsheng Yang, 2010, International journal of pharmaceutics.

Stability of gabapentin 300-mg capsules repackaged in unit dose containers.

M. Khan, Abhay Gupta, P. Faustino, 2009, American journal of health-system pharmacy : AJHP : official journal of the American Society of Health-System Pharmacists.

3D-printing of lopinavir printlets by selective laser sintering and quantification of crystalline fraction by XRPD-chemometric models.

M. Khan, Ziyaur Rahman, E. Mohamed, 2020, International journal of pharmaceutics.

Selective laser sintering 3D printing – an overview of the technology and pharmaceutical applications

Mathew A Kuttolamadom, Naseem A Charoo, Sogra F Barakh Ali, 2020, Drug development and industrial pharmacy.

Spontaneous carbonate formation in an amorphous, amine-rich, polymeric drug substance: sevelamer HCl product quality.

M. Khan, R. T. Berendt, P. Schwartz, 2012, Journal of pharmaceutical sciences.

Very-Rapidly Dissolving Printlets of Isoniazid Manufactured by SLS 3D Printing: In Vitro and In Vivo Characterization.

M. Khan, Ziyaur Rahman, Mathew Kuttolamadom, 2022, Molecular pharmaceutics.

Regional permeability of salmon calcitonin in isolated rat gastrointestinal tracts: Transport mechanism using Caco-2 cell monolayer

M. Khan, R. Shah, 2004, AAPS Journal.

Drug product characterization by macropixel analysis of chemical images.

Mansoor A Khan, Mazen L Hamad, Christopher D Ellison, 2007, Journal of pharmaceutical sciences.

Cold flow of estradiol transdermal systems: influence of drug loss on the in vitro flux and drug transfer across human epidermis.

M. Khan, Y. Krishnaiah, Yang Yang, 2014, International journal of pharmaceutics.

Kinetics of drug release from ointments: Role of transient-boundary layer.

M. Khan, Ziyaur Rahman, Y. Krishnaiah, 2015, International journal of pharmaceutics.

High Dose Vardenafil Blunts the Hypertensive Effects of Toll-Like Receptor 3 Activation During Pregnancy

M. Khan, Ziyaur Rahman, S. Dharani, 2021, Frontiers in Virology.

Application of chemometric methods to differential scanning calorimeter (DSC) to estimate nimodipine polymorphs from cosolvent system

M. Khan, A. Siddiqui, Ziyaur Rahman, 2015, Drug development and industrial pharmacy.

Assessing the impact of nimodipine devitrification in the ternary cosolvent system through quality by design approach.

Ziyaur Rahman, Akhtar Siddiqui, M. Khan, 2013, International journal of pharmaceutics.

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.

M. Khan, A. Siddiqui, Ziyaur Rahman, 2015, Journal of pharmaceutical sciences.

Quality by Design (QbD), Biopharmaceutical Manufacture

Kurt Brorson, Mansoor A. Khan, Rakhi B. Shah, 2010 .

Regulatory Issues and Challenges Associated with the Development of Performance Specifications for Modified Release Parenteral Products

Marilyn N. Martinez, Mansoor A. Khan, M. Khan, 2012 .

United States Food and Drug Administration and Department of Defense shelf-life extension program of pharmaceutical products: progress and promise.

Abhay Gupta, Ravikanth Kona, Patrick J Faustino, 2014, Journal of pharmaceutical sciences.

Near-Infrared Investigations of Novel Anti-HIV Tenofovir Liposomes

M. Khan, M. Habib, A. Zidan, 2010, The AAPS Journal.

Development of Abuse-Deterrent Formulations Using Sucrose Acetate Isobutyrate

M. Khan, Ziyaur Rahman, Hamideh Afrooz, 2020, AAPS PharmSciTech.

Quantitative estimation of phenytoin sodium disproportionation in the formulations using vibration spectroscopies and multivariate methodologies.

M. Khan, Ziyaur Rahman, Hamideh Afrooz, 2018, International journal of pharmaceutics.

Pharmaceutical and Clinical Calculations

M. Khan, I. Reddy, 2000 .

Optimization and characterization of controlled release multi-particulate beads coated with starch acetate.

M. Khan, M. Nutan, M. Soliman, 2005, International journal of pharmaceutics.

Quality by design in formulation and process development for a freeze-dried, small molecule parenteral product: a case study

Gregory A Sacha, Lisa M. Hardwick, Elizabeth A. Oslos, 2011, Pharmaceutical development and technology.

Challenges of pediatric formulations: a FDA science perspective.

M. Khan, Abhay Gupta, 2013, International journal of pharmaceutics.

Additive Manufacturing with 3D Printing: Progress from Bench to Bedside

Naseem A. Charoo, M. Khan, Ziyaur Rahman, 2018, The AAPS Journal.

Determination of tacrolimus crystalline fraction in the commercial immediate release amorphous solid dispersion products by a standardized X-ray powder diffraction method with chemometrics.

M. Khan, A. Siddiqui, Ziyaur Rahman, 2014, International journal of pharmaceutics.

Comparison of Univariate and Multivariate Models of 13C SSNMR and XRPD Techniques for Quantification of Nimodipine Polymorphs

M. Khan, A. Siddiqui, Ziyaur Rahman, 2015, AAPS PharmSciTech.

Studying effect of glyceryl palmitostearate amount, manufacturing method and stability on polymorphic transformation and dissolution of rifaximin tablets.

M. Khan, Ziyaur Rahman, Hamideh Afrooz, 2020, International journal of pharmaceutics.

Synthesis and Evaluation of Morpholinoalkyl Ester Prodrugs of Indomethacin and Naproxen

M. Khan, A. Crider, M. Narurkar, 1993, Pharmaceutical Research.

Spectral and spatial characterization of protein loaded PLGA nanoparticles.

M. Khan, M. Habib, Ziyaur Rahman, 2010, Journal of pharmaceutical sciences.

Optimization of process variables for the preparation of ibuprofen coprecipitates with Eudragit S100

Sanford Bolton, M. Khan, M. Kislalioglu, 1994 .

Consistency of Pharmaceutical Products: An FDA Perspective on Hot-Melt Extrusion Process

Abhay Gupta, Mansoor A. Khan, M. Khan, 2013 .

Development and evaluation of paclitaxel nanoparticles using a quality-by-design approach.

Ergun Karaagaoglu, Firat Yerlikaya, Yilmaz Capan, 2013, Journal of pharmaceutical sciences.

Development and Validation of a Discriminatory Dissolution Method for Rifaximin Products.

M. Khan, Ziyaur Rahman, Hamideh Afrooz, 2019, Journal of pharmaceutical sciences.

Potential Application of USP Paddle and Basket Dissolution Methods in Discriminating for Portioned Moist Snuff and Snus Smokeless Tobacco Products

M. Khan, Ziyaur Rahman, S. Dharani, 2021, AAPS PharmSciTech.

Percutaneous permeation of enantiomers and racemates of chiral drugs and prediction of their flux ratios using thermal data: a pharmaceutical perspective.

M. Khan, I. Reddy, M. Afouna, 2003, Chirality.

Effect of Ethanol on Opioid Drug Permeability Through Caco-2 Cell Monolayers

M. Khan, R. Uppoor, C. D. Ellison, 2008, The AAPS Journal.

In vitro bioequivalence approach for a locally acting gastrointestinal drug: lanthanum carbonate.

Lawrence X. Yu, M. Khan, R. Shah, 2013, Molecular pharmaceutics.

Solid phase extraction of uranium(VI) on phosphorus-containing polymer grafted 4-aminoantipyrine

M. Khan, M. Soylak, M. R. Jan, 2016, Journal of Radioanalytical and Nuclear Chemistry.

Development and Validation of a HPLC Method for Dissolution and Stability Assay of Liquid-Filled Cyclosporine Capsule Drug Products

M. Khan, Abhay Gupta, V. Sayeed, 2013, AAPS PharmSciTech.

Formulation Characterization and Pharmacokinetic Evaluation of Amorphous Solid Dispersions of Dasatinib

M. Khan, Ziyaur Rahman, E. Mohamed, 2022, Pharmaceutics.

Functionality of magnesium stearate derived from bovine and vegetable sources: dry granulated tablets.

M. Khan, R. Shah, Abhay Gupta, 2008, Journal of pharmaceutical sciences.

Stability of ranitidine syrup re-packaged in unit-dose containers.

M. Khan, R. Shah, Hullahalli R. Prasanna, 2008, American journal of health-system pharmacy : AJHP : official journal of the American Society of Health-System Pharmacists.

Transbuccal permeation of a nucleoside analog, dideoxycytidine: effects of menthol as a permeation enhancer.

M. Khan, R. Khosravan, A. Shojaei, 1999, International journal of pharmaceutics.

Statistical Optimization of Ketoprofen-Eudragit® S100 Coprecipitates to Obtain Controlled-Release Tablets

M. Khan, Mansoor A. Khan, Jean Dib, 1996 .

Effects of Diluents on Physical and Chemical Stability of Phenytoin and Phenytoin Sodium

M. Khan, Ziyaur Rahman, Sogra F. Barakh Ali, 2020, AAPS PharmSciTech.

Evaluation of In-Use Stability of Anticoagulant Drug Products: Warfarin Sodium.

M. Khan, S. Akhtar, A. Siddiqui, 2015, Journal of Pharmacy and Science.

A headspace-gas chromatography method for isopropanol determination in warfarin sodium products as a measure of drug crystallinity

M. Khan, S. Akhtar, A. Siddiqui, 2018, Acta pharmaceutica.

Development and validation of X-ray diffraction method for quantitative determination of crystallinity in warfarin sodium products.

M. Khan, A. Siddiqui, Ziyaur Rahman, 2015, International journal of pharmaceutics.