S. Pathak

发表

IMI – Oral biopharmaceutics tools project – Evaluation of bottom‐up PBPK prediction success part 3: Identifying gaps in system parameters by analysing In Silico performance across different compound classes

Amitava Mitra, Jian Lin, Mai Anh Nguyen, 2017, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

IMI – Oral biopharmaceutics tools project – Evaluation of bottom‐up PBPK prediction success part 2: An introduction to the simulation exercise and overview of results

Amitava Mitra, Jian Lin, Mai Anh Nguyen, 2017, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

IMI – oral biopharmaceutics tools project – evaluation of bottom‐up PBPK prediction success part 1: Characterisation of the OrBiTo database of compounds

Xavier Pepin, Leon Aarons, Hans Lennernäs, 2017, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Biopharmaceutic IVIVE-Mechanistic Modeling of Single- and Two-Phase In Vitro Experiments to Obtain Drug-Specific Parameters for Incorporation Into PBPK Models.

M. Jamei, D. Turner, S. Pathak, 2019, Journal of pharmaceutical sciences.

Model-Based Analysis of Biopharmaceutic Experiments To Improve Mechanistic Oral Absorption Modeling: An Integrated in Vitro in Vivo Extrapolation Perspective Using Ketoconazole as a Model Drug.

N. Patel, M. Jamei, E. Kostewicz, 2017, Molecular pharmaceutics.

Pre‐clinical evidence of enhanced oral bioavailability of the P‐glycoprotein substrate talinolol in combination with morin

N. Udupa, S. Pathak, 2010, Biopharmaceutics & drug disposition.

IMI - Oral biopharmaceutics tools project - Evaluation of bottom-up PBPK prediction success part 4: Prediction accuracy and software comparisons with improved data and modelling strategies.

M. Jamei, L. Aarons, M. Bolger, 2020, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Establishment of in vitro–in vivo equivalence of highly variable drugs – a generic product development perspective

D. Aggarwal, S. Pathak, V. Venkateswarlu, 2014, Pharmaceutical development and technology.

Evaluation of chemical interactions of maleic acid with sodium hypochlorite and chlorhexidine gluconate.

Syed sajjad Hussen, N. Ballal, S. Pathak, 2011, Journal of endodontics.

A simple and rapid high performance liquid chromatographic method with fluorescence detection for the estimation of fexofenadine in rat plasma--application to preclinical pharmacokinetics.

N. Udupa, P. Musmade, S. Pathak, 2008, Talanta.

Critical attributes of transdermal drug delivery system (TDDS) – a generic product development review

D. Aggarwal, S. Pathak, P. K. Ruby, 2014, Drug development and industrial pharmacy.

In Silico Modeling Approach for the Evaluation of Gastrointestinal Dissolution, Supersaturation, and Precipitation of Posaconazole.

Amitava Mitra, Bart Hens, Bo Liu, 2017, Molecular pharmaceutics.

Practical and operational considerations related to paediatric oral drug formulation: an industry survey.

P. Augustijns, J. Brouwers, H. Batchelor, 2022, International journal of pharmaceutics.

A Population-based PBPK Model for the Prediction of Time-Variant Bile Salt Disposition within GI Luminal Fluids.

L. Marciani, D. Turner, S. Pathak, 2020, Molecular pharmaceutics.

The Regional-Specific Relative and Absolute Expression of Gut Transporters in Adult Caucasians: A Meta-Analysis

Sibylle Neuhoff, S. Neuhoff, M. Harwood, 2019, Drug Metabolism and Disposition.

Novel liquid chromatographic method for simultaneous estimation of pioglitazone and glimepiride in rat plasma by solid phase extraction: application to preclinical pharmacokinetic studies

N. Udupa, P. Musmade, S. Pathak, 2011, Arzneimittelforschung.

In Vitro and In Vivo Equivalence Testing of Nanoparticulate Intravenous Formulations

D. Aggarwal, S. Pathak, P. K. Ruby, 2013, Drug Research.

Validated HPLC method for quantitative determination of talinolol in rat plasma and application to a preclinical pharmacokinetic study.

N. Udupa, P. Musmade, S. Pathak, 2010, Bioanalysis.

Best Practices in the Development and Validation of Physiologically Based Biopharmaceutics Modeling. A Workshop Summary Report.

Talia Flanagan, Amitava Mitra, Sandra Suarez-Sharp, 2020, Journal of pharmaceutical sciences.

Enhanced oral absorption of saquinavir with Methyl-Beta-Cyclodextrin-Preparation and in vitro and in vivo evaluation.

N. Udupa, P. Musmade, S. Pathak, 2010, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Comment on "In Silico Modeling of Gastrointestinal Drug Absorption: Predictive Performance of Three Physiologically-Based Absorption Models".

N. Patel, M. Jamei, S. Polak, 2017, Molecular pharmaceutics.

Development and validation of a reversed-phase liquid chromatographic method with fluorescence detection for the study of Saquinavir pharmacokinetics in rat plasma.

N. Udupa, S. Pathak, A. R. Kumar, 2007, Analytica chimica acta.

Establishment of Inherent Stability of Saquinavir Under Various Conditions Using a Stability-Indicating High-Performance Liquid Chromatographic Assay with Photodiode Array (PDA) Detection

N. Udupa, P. Musmade, S. Pathak, 2009 .