Mansoor A Khan

发表

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.

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.

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

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

Absorption enhancers in pulmonary protein delivery.

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

Focused beam reflectance measurement to monitor nimodipine precipitation process.

Akhtar Siddiqui, Mansoor A Khan, Xiaoming Xu, 2013, International journal of pharmaceutics.

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 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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

Physicochemical and mechanical properties of carbamazepine cocrystals with saccharin

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

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.