A general framework for multi-compartmental analysis of drug chemotherapy dynamics in human immunodeficiency virus type-1 infected individuals

被引:6
|
作者
Joly, Marcel [1 ,2 ]
Pinto, Jose M. [1 ,3 ]
机构
[1] Univ Sao Paulo, Dept Chem Engn, BR-05508900 Sao Paulo, Brazil
[2] Petrobras Petr Brasileiro SA, BR-20031915 Rio De Janeiro, RJ, Brazil
[3] Polytech Univ, Metrotech Ctr 6, Othmer Jacobs Dept Chem & Biol Engn, Brooklyn, NY USA
基金
巴西圣保罗研究基金会;
关键词
HIV; AIDS; Chemotherapy; Pharmacokinetics; Computational simulation; MULTIPLE-DOSE PHARMACOKINETICS; MATHEMATICAL-ANALYSIS; LYMPHOID-TISSUE; T-CELL; COMBINATION; ZIDOVUDINE; CD4; SUSCEPTIBILITY; ZALCITABINE; SAQUINAVIR;
D O I
10.1016/j.apm.2012.01.042
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
An optimal control strategy for the highly active antiretroviral therapy associated to the acquired immunodeficiency syndrome should be designed regarding a comprehensive analysis of the drug chemotherapy behavior in the host tissues, from major viral replication sites to viral sanctuary compartments. Such approach is critical in order to efficiently explore synergistic, competitive and prohibitive relationships among drugs and, hence, therapy costs and side-effect minimization. In this paper, a novel mathematical model for HIV-1 drug chemotherapy dynamics in distinct host anatomic compartments is proposed and theoretically evaluated on fifteen conventional anti-retroviral drugs. Rather than interdependence between drug type and its concentration profile in a host tissue, simulated results suggest that such profile is importantly correlated with the host tissue under consideration. Furthermore, the drug accumulative dynamics are drastically affected by low patient compliance with pharmacotherapy, even when a single dose lacks. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:5830 / 5843
页数:14
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