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在对富马酸替诺福韦二吡呋酯具有良好依从性的成年人中停止治疗后,替诺福韦的血浆药代动力学和尿排泄。

Plasma pharmacokinetics and urinary excretion of tenofovir following cessation in adults with controlled levels of adherence to tenofovir disoproxil fumarate.

机构信息

PHPT/IRD UMI 174, Faculty of Associated Medical Sciences, Chiang Mai University, Chiang Mai, Thailand; Department of Immunology and Infectious Diseases, Boston, Harvard T.H. Chan School of Public Health, Boston, MA, USA; Department of Molecular and Clinical Pharmacology, University of Liverpool, Liverpool, UK.

Sanpatong Hospital, Chiang Mai, Thailand.

出版信息

Int J Infect Dis. 2020 Aug;97:365-370. doi: 10.1016/j.ijid.2020.06.037. Epub 2020 Jun 14.

Abstract

OBJECTIVES

The aim was to fully characterize the plasma and urine washout pharmacokinetics of tenofovir (TFV) in adults following 6 weeks of controlled levels of tenofovir disoproxil fumarate (TDF) adherence, in order to inform the utility of clinic-based adherence testing.

DESIGN

This was a three-arm, randomized, open-label study in adult volunteers. Participants were randomized to receive TDF 300 mg/emtricitabine (FTC) 200 mg as (1) 7 doses/week (perfect adherence), (2) 4 doses/week (moderate adherence), or (3) 2 doses/week (low adherence). Plasma and urine samples were collected regularly during the 6-week dosing phase and for 4 weeks following drug cessation.

RESULTS

Twenty-eight adults were included in this analysis. Median (range) age was 33 (20-49) years. No differences in TFV pharmacokinetic parameters during the washout were observed across the study arms. Small differences in TFV plasma concentrations occurred across arms between 4 and 10 h post-dose. The cumulative amount of TFV excreted in urine was not different at 24 h post-dose, but at 148 h it was 24.8 mg, 21.0 mg, and 17.2 mg for the perfect, moderate, and low adherence arms, respectively (p = 0.043).

CONCLUSIONS

Among adults with different TDF adherence patterns, relative differences in plasma concentrations and cumulative urine extraction of TFV were minor following cessation. TFV measurement in plasma or urine is more indicative of last drug ingestion, rather than prior dose patterns.

摘要

目的

旨在全面描述成人在经过 6 周的富马酸替诺福韦二吡呋酯(TDF)控制水平的依从性后,替诺福韦(TFV)的血浆和尿液洗脱药代动力学特征,以便为临床依从性检测的应用提供信息。

设计

这是一项三臂、随机、开放标签的成人志愿者研究。参与者被随机分为每周接受 TDF 300 mg/恩曲他滨(FTC)200 mg 治疗:(1)7 剂/周(完全依从)、(2)4 剂/周(中等依从)或(3)2 剂/周(低依从)。在 6 周的给药阶段和停药后 4 周内,定期采集血浆和尿液样本。

结果

本分析纳入了 28 名成年人。中位(范围)年龄为 33(20-49)岁。在洗脱期,研究臂之间未观察到 TFV 药代动力学参数的差异。在给药后 4 至 10 小时,各研究臂之间的 TFV 血浆浓度存在微小差异。在给药后 24 小时,TFV 在尿液中的累积排泄量没有差异,但在 148 小时时,完全、中等和低依从性组分别为 24.8mg、21.0mg 和 17.2mg(p=0.043)。

结论

在 TDF 依从性模式不同的成年人中,停药后血浆浓度和 TFV 累积尿液提取的相对差异较小。TFV 在血浆或尿液中的测量更能反映最后一次药物摄入,而不是之前的剂量模式。

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