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Short Communication: Specimen Processing Impacts Tissue Tenofovir Pharmacokinetic Measurements

机译:简短交流:标本处理影响组织替诺福韦的药代动力学测量

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摘要

Antiretroviral drug concentrations at sites of HIV exposure are important drivers that influence the development of HIV pre-exposure chemoprophylaxis strategies and regimens. We assessed the effect of collection method—in the presence or absence of tissue culture medium—on tenofovir (TFV) and tenofovir diphosphate (TFV-DP) concentrations in colonic biopsies. We find significant baseline interbiopsy variation in TFV (38% CV) and TFV-DP (33% CV) concentrations. Incubation in medium leads to a fluid absorption-driven twofold increase in tissue weight with a concomitant 75% decrease in weight-adjusted tissue TFV concentrations 120 min post-incubation. In contrast, adjusted TFV-DP concentrations decrease by only 25% during the same period, with this difference not achieving statistical significance. Although colonic biopsies should be collected in the absence of medium for accurate TFV concentrations, the presence of medium does not significantly impact TFV-DP-dependent pharmacokinetic or pharmacodynamic assays. Appropriate assessment of tissue drug concentrations should account for biopsy collection method and drug mechanism of action.
机译:HIV暴露部位的抗逆转录病毒药物浓度是影响HIV暴露前化学预防策略和治疗方案发展的重要驱动力。我们评估了收集方法(在存在或不存在组织培养基的情况下)对结肠活检中替诺福韦(TFV)和替诺福韦二磷酸(TFV-DP)浓度的影响。我们发现TFV(38%CV)和TFV-DP(33%CV)浓度存在明显的基线活检变化。在培养基中温育会导致液体吸收,使组织重量增加两倍,而在温育后120分钟,重量调整后的组织TFV浓度降低75%。相反,调整后的TFV-DP浓度在同一时期仅降低了25%,这种差异没有达到统计学意义。尽管应在无培养基的情况下收集结肠活检标本以准确测定TFV浓度,但培养基的存在不会显着影响TFV-DP依赖性药代动力学或药效学测定。组织药物浓度的适当评估应考虑活检的收集方法和药物作用机理。

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