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首页> 外文期刊>Therapeutic Drug Monitoring >Semen quality and drug concentrations in seminal plasma of patients using a didanosine or didanosine plus tenofovir containing antiretroviral regimen.
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Semen quality and drug concentrations in seminal plasma of patients using a didanosine or didanosine plus tenofovir containing antiretroviral regimen.

机译:使用含二羟肌苷或二羟肌苷加替诺福韦的抗逆转录病毒疗法的患者精液中精液质量和药物浓度。

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Data on the concentrations of didanosine (ddI) and tenofovir (TFV) in seminal plasma are sparse. Subtherapeutic drug concentrations within the lumen of the male genital tract may have implications for selection and transmission of drug-resistant HIV strains. On the other hand, sufficient penetration of these drugs into the male genital tract has potential toxic effects on the spermatozoa and their precursors. In the current study, the authors obtained paired semen and blood samples at variable time points after drug intake from 30 HIV-1-infected patients using a ddI (n = 15) or ddI + TFV (n = 15) containing an antiretroviral regimen. Didanosine and TFV concentrations were measured in seminal and blood plasma and semen quality was assessed. Both ddI and TFV penetrated well into seminal plasma. Whereas blood plasma ddI concentrations dropped to near or below the lower limit of quantification of 0.017 microg/mL 9 hours after drug intake, the ddI concentration in seminal plasma remained detectable during the whole dosing interval with a median of 0.20 and 0.21 microg/mL in the ddI and ddI + TFV groups, respectively. Tenofovir was detectable during the whole dosing interval in both blood and seminal plasma with a median concentration of 0.12 and 0.25 microg/mL, respectively, and a median seminal-to-blood-plasma ratio of 3.3. Semen quality was within the normal range according to the criteria of the World Health Organization, except for the percentage of progressively motile sperm, which was low in both groups of patients. The authors conclude that ddI and TFV penetrate well into seminal plasma and that the reduced sperm motility deserves further study.
机译:精浆中双羟肌苷(ddI)和替诺福韦(TFV)浓度的数据稀疏。男性生殖道管腔内的亚治疗药物浓度可能会对耐药性HIV菌株的选择和传播产生影响。另一方面,这些药物充分渗透到男性生殖道对精子及其前体具有潜在的毒性作用。在当前研究中,作者使用包含抗逆转录病毒疗法的ddI(n = 15)或ddI + TFV(n = 15)从30名感染HIV-1的患者中,在吸毒后的不同时间点获得了配对的精液和血液样本。在精液和血浆中测量去羟肌苷和TFV的浓度,并评估精液质量。 ddI和TFV都能很好地渗透到精浆中。药物摄入后9小时血浆ddI浓度降至或低于定量下限0.017 microg / mL,而精浆中ddI浓度在整个给药间隔期间仍可检测到,血浆中ddI浓度中位数为0.20和0.21 microg / mL。 ddI和ddI + TFV组。在整个给药间隔期间,在血液和精浆中均可检测到替诺福韦,其中位数浓度分别为0.12和0.25 microg / mL,中位精浆与血浆的比例为3.3。根据世界卫生组织的标准,精液质量在正常范围内,除了精子逐渐活动的百分比在两组患者中均较低。作者得出的结论是,ddI和TFV可以很好地渗透到精浆中,精子活力的降低值得进一步研究。

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