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羊水和母血中齐多夫定、拉米夫定及奈非那韦的浓度。

Zidovudine, lamivudine, and nelfinavir concentrations in amniotic fluid and maternal serum.

作者信息

Bennetto-Hood Chantelle, Bryson Yvonne J, Stek Alice, King Jennifer R, Mirochnick Mark, Acosta Edward P

机构信息

Division of Clinical Pharmacology, University of Alabama at Birmingham School of Medicine, Birmingham, AL 35294-0019, USA.

出版信息

HIV Clin Trials. 2009 Jan-Feb;10(1):41-7. doi: 10.1310/hct1001-041.

Abstract

PURPOSE

The objective of this study was to examine lamivudine (3TC), zidovudine (ZDV), nelfinavir (NFV), and its active nelfinavir metabolite (M8) concentrations in paired maternal plasma and amniotic fluid samples to determine antiretroviral penetration or accumulation in the fetal compartment.

METHOD

Ten paired amniotic fluid and maternal plasma samples were obtained during caesarian section for pharmacokinetic analysis. Antiretroviral concentrations were measured in both matrices using high-performance liquid chromatography (HPLC) and mass spectrometry (LC/MS) methodologies.

RESULTS

Median maternal plasma concentrations for NFV, M8, 3TC, and ZDV were 456, 244, 176, and 794 ng/mL, respectively, while median amniotic fluid concentrations were 118, 21, 2537, and 1483 ng/mL, respectively. The median NFV amniotic fluid to maternal plasma ratio was 0.44; the median M8 ratio was 0.11. Median 3TC and ZDV amniotic fluid to plasma ratios were 11.9 and 1.5, respectively.

CONCLUSIONS

NFV and M8 exhibited partial drug transfer and/or accumulation in the amniotic compartment, whereas ZDV and 3TC concentrations mostly exceeded that in maternal plasma. Overall, all drugs achieved exposures in the amniotic fluid in excess of their wild-type viral susceptibilities. Amniotic fluid is an important compartment in the prevention of mother-to-child transmission; a further understanding of protease inhibitor and other antiretroviral drug penetration into amniotic fluid is warranted.

摘要

目的

本研究的目的是检测拉米夫定(3TC)、齐多夫定(ZDV)、奈非那韦(NFV)及其活性代谢产物奈非那韦(M8)在配对的母体血浆和羊水样本中的浓度,以确定抗逆转录病毒药物在胎儿体内的渗透或蓄积情况。

方法

剖宫产时获取10对羊水和母体血浆样本用于药代动力学分析。使用高效液相色谱(HPLC)和质谱(LC/MS)方法测定两种基质中的抗逆转录病毒药物浓度。

结果

NFV、M8、3TC和ZDV的母体血浆中位数浓度分别为456、244、176和794 ng/mL,而羊水中位数浓度分别为118、21、2537和1483 ng/mL。NFV羊水与母体血浆的中位数比值为0.44;M8的中位数比值为0.11。3TC和ZDV羊水与血浆的中位数比值分别为11.9和1.5。

结论

NFV和M8在羊膜腔中表现出部分药物转移和/或蓄积,而ZDV和3TC的浓度大多超过母体血浆中的浓度。总体而言,所有药物在羊水中的暴露量均超过其对野生型病毒的敏感性。羊水是预防母婴传播的重要部位;有必要进一步了解蛋白酶抑制剂和其他抗逆转录病毒药物在羊水中的渗透情况。

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