Mitesh Patel, Ph.D.
Affiliations: | 2014 | Pharmaceutical Science | University of Missouri - Kansas City, USA |
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Sign in to add mentorAshim K. Mitra | grad student | 2014 | University of Missouri - Kansas City | |
(Prodrug approach to improve oral and brain absorption of HIV protease inhibitor, lopinavir.) |
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Publications
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Zamek-Gliszczynski MJ, Patel M, Yang X, et al. (2020) Intestinal P-gp and Putative Hepatic OATP1B Induction: ITC Perspective on Drug Development Implications. Clinical Pharmacology and Therapeutics |
Patel M, Eberl HC, Wolf A, et al. (2019) Mechanistic basis of cabotegravir-glucuronide disposition in humans. The Journal of Pharmacology and Experimental Therapeutics |
Patel M, Johnson M, Sychterz CJ, et al. (2018) Hepatobiliary disposition of atovaquone: A case of mechanistically unusual biliary clearance. The Journal of Pharmacology and Experimental Therapeutics |
Patel M, Taskar KS, Zamek-Gliszczynski MJ. (2016) Importance of Hepatic Transporters in Clinical Disposition of Drugs and Their Metabolites. Journal of Clinical Pharmacology. 56: S23-S39 |
Mandal A, Patel M, Sheng Y, et al. (2015) Design of lipophilic prodrugs to improve drug delivery and efficacy. Current Drug Targets |
Patel M, Sheng Y, Mandava NK, et al. (2014) Dipeptide prodrug approach to evade efflux pumps and CYP3A4 metabolism of lopinavir. International Journal of Pharmaceutics. 476: 99-107 |
Patel A, Patel M, Yang X, et al. (2014) Recent advances in protein and Peptide drug delivery: a special emphasis on polymeric nanoparticles. Protein and Peptide Letters. 21: 1102-20 |
Patel M, Mandava N, Gokulgandhi M, et al. (2014) Amino Acid Prodrugs: An Approach to Improve the Absorption of HIV-1 Protease Inhibitor, Lopinavir. Pharmaceuticals (Basel, Switzerland). 7: 433-52 |
Vadlapatla RK, Patel M, Paturi DK, et al. (2014) Clinically relevant drug-drug interactions between antiretrovirals and antifungals. Expert Opinion On Drug Metabolism & Toxicology. 10: 561-80 |
Patel M, Mandava NK, Pal D, et al. (2014) Amino acid prodrug of quinidine: an approach to circumvent P-glycoprotein mediated cellular efflux. International Journal of Pharmaceutics. 464: 196-204 |