Literature DB >> 19649922

Pharmacokinetic enhancers for HIV drugs.

Lianhong Xu1, Manoj C Desai.   

Abstract

The HIV protease inhibitor (PI) ritonavir is a potent, mechanism-based inhibitor of cytochrome P450 CYP3A4, an enzyme that is responsible for metabolizing most HIV PIs. Ritonavir is therefore able to enhance the effectiveness of PI treatment by reducing the pill burden, simplifying dosing regimens and improving therapy adherence. Ritonavir coadministration improves the pharmacokinetic (PK) profiles of concomitant PIs, and represents a cornerstone of PI-containing regimens. However, ritonavir is associated with undesirable side effects, such as gastrointestinal problems and lipid disturbances. This review summarizes salient features and limitations associated with the use of ritonavir as a PK enhancer, and briefly describes novel PK enhancers that are in development.

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Year:  2009        PMID: 19649922

Source DB:  PubMed          Journal:  Curr Opin Investig Drugs        ISSN: 1472-4472


  19 in total

1.  Nanoformulated antiretroviral drug combinations extend drug release and antiretroviral responses in HIV-1-infected macrophages: implications for neuroAIDS therapeutics.

Authors:  Ari S Nowacek; JoEllyn McMillan; Reagan Miller; Alec Anderson; Barrett Rabinow; Howard E Gendelman
Journal:  J Neuroimmune Pharmacol       Date:  2010-03-17       Impact factor: 4.147

Review 2.  Correlating structure and function of drug-metabolizing enzymes: progress and ongoing challenges.

Authors:  Eric F Johnson; J Patrick Connick; James R Reed; Wayne L Backes; Manoj C Desai; Lianhong Xu; D Fernando Estrada; Jennifer S Laurence; Emily E Scott
Journal:  Drug Metab Dispos       Date:  2013-10-15       Impact factor: 3.922

3.  Inhibition of Human CYP3A4 by Rationally Designed Ritonavir-Like Compounds: Impact and Interplay of the Side Group Functionalities.

Authors:  Eric R Samuels; Irina Sevrioukova
Journal:  Mol Pharm       Date:  2017-12-12       Impact factor: 4.939

4.  Structure-Based Inhibitor Design for Evaluation of a CYP3A4 Pharmacophore Model.

Authors:  Parminder Kaur; A Richard Chamberlin; Thomas L Poulos; Irina F Sevrioukova
Journal:  J Med Chem       Date:  2015-09-24       Impact factor: 7.446

5.  Cobicistat (GS-9350): A Potent and Selective Inhibitor of Human CYP3A as a Novel Pharmacoenhancer.

Authors:  Lianhong Xu; Hongtao Liu; Bernard P Murray; Christian Callebaut; Melody S Lee; Allen Hong; Robert G Strickley; Luong K Tsai; Kirsten M Stray; Yujin Wang; Gerry R Rhodes; Manoj C Desai
Journal:  ACS Med Chem Lett       Date:  2010-05-17       Impact factor: 4.345

6.  Differential effects of ethanol on spectral binding and inhibition of cytochrome P450 3A4 with eight protease inhibitors antiretroviral drugs.

Authors:  Santosh Kumar; Anil Kumar
Journal:  Alcohol Clin Exp Res       Date:  2011-06-17       Impact factor: 3.455

7.  Interaction of human cytochrome P4503A4 with ritonavir analogs.

Authors:  Irina F Sevrioukova; Thomas L Poulos
Journal:  Arch Biochem Biophys       Date:  2012-03-05       Impact factor: 4.013

8.  Structure and mechanism of the complex between cytochrome P4503A4 and ritonavir.

Authors:  Irina F Sevrioukova; Thomas L Poulos
Journal:  Proc Natl Acad Sci U S A       Date:  2010-10-11       Impact factor: 11.205

9.  Pyridine-substituted desoxyritonavir is a more potent inhibitor of cytochrome P450 3A4 than ritonavir.

Authors:  Irina F Sevrioukova; Thomas L Poulos
Journal:  J Med Chem       Date:  2013-04-26       Impact factor: 7.446

10.  An increase in side-group hydrophobicity largely improves the potency of ritonavir-like inhibitors of CYP3A4.

Authors:  Eric R Samuels; Irina F Sevrioukova
Journal:  Bioorg Med Chem       Date:  2020-01-31       Impact factor: 3.641

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