Nanda K. Mandava, Ph.D.
Affiliations: | 2013 | Pharmaceutical Science | University of Missouri - Kansas City, USA |
Area:
Pharmacy, BiochemistryGoogle:
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Parents
Sign in to add mentor| Ashim K. Mitra | grad student | 2013 | University of Missouri - Kansas City | |
| (Evasion of efflux and enhancing bioavailability of Amprenavir by prodrug derivatization.) | ||||
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Publications
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| 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 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 |
| 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 |
| Patel M, Mandava NK, Vadlapatla RK, et al. (2013) Recent patents and emerging therapeutics for HIV infections: a focus on protease inhibitors. Pharmaceutical Patent Analyst. 2: 513-38 |
| Minocha M, Mandava NK, Kwatra D, et al. (2011) Effect of short term and chronic administration of Sutherlandia frutescens on pharmacokinetics of nevirapine in rats. International Journal of Pharmaceutics. 413: 44-50 |
| Mandava N, Oberoi R, Minocha M, et al. (2010) Transporter targeted drug delivery Journal of Drug Delivery Science and Technology. 20: 89-99 |
| Jain R, Agarwal S, Mandava NK, et al. (2008) Interaction of dipeptide prodrugs of saquinavir with multidrug resistance protein-2 (MRP-2): evasion of MRP-2 mediated efflux. International Journal of Pharmaceutics. 362: 44-51 |
| Jain R, Duvvuri S, Kansara V, et al. (2007) Intestinal absorption of novel-dipeptide prodrugs of saquinavir in rats. International Journal of Pharmaceutics. 336: 233-40 |
| Luo S, Kansara VS, Zhu X, et al. (2006) Functional characterization of sodium-dependent multivitamin transporter in MDCK-MDR1 cells and its utilization as a target for drug delivery. Molecular Pharmaceutics. 3: 329-39 |