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双脱氧肌苷在猪尾猕猴体内的经胎盘药代动力学

Transplacental pharmacokinetics of dideoxyinosine in pigtailed macaques.

作者信息

Pereira C M, Nosbisch C, Winter H R, Baughman W L, Unadkat J D

机构信息

Department of Pharmaceutics, University of Washington, Seattle 98195.

出版信息

Antimicrob Agents Chemother. 1994 Apr;38(4):781-6. doi: 10.1128/AAC.38.4.781.

Abstract

To determine whether dideoxyinosine is actively transported across the placenta, four pregnant macques (Macaca nemestrina) near term and their fetuses were infused intravenously in random order with simultaneous doses of dideoxyinosine (42.5 micrograms/min/kg of body weight) and antipyrine (41.7 micrograms/min/kg) for 30 h. The infusions took place after the dams had been chronically catheterized at 128 +/- 0.8 days of gestation. In a third infusion, the dams alone received a higher dosage of dideoxyinosine (425 micrograms/min/kg) and the same dosage of antipyrine (41.7 micrograms/min/kg). Samples of maternal and fetal blood and amniotic fluid were collected at intervals for up to 30 h. The concentrations of dideoxyinosine and antipyrine were determined by high-performance liquid chromatography. The transplacental maternal-fetal drug clearances were compared by the paired Student's t test. The ratio (mean +/- standard deviation) of the steady-state plasma dideoxyinosine concentration in the fetus to that in the dam was 0.49 +/- 0.10 at the low dideoxyinosine infusion rate and 0.51 +/- 0.00 at the high dideoxyinosine infusion rate. The clearance associated with maternal-fetal transfer of the drug, CLdf (0.38 +/- 0.21 ml/min/kg), was not significantly different (P > 0.05) from the clearance associated with fetal-maternal transfer of the drug, CLfd (0.56 +/- 0.27 ml/min/kg). Also, CLdf was not significantly different (P > 0.05) from CLfd when normalized with respect to the corresponding transplacental clearance of antipyrine (0.07 +/- 0.04 CLdf versus 0.09 +/- 0.04 CLfd). ur data indicate that passage of dideoxyinosine across the placenta in pregnant M. nemestrina near term is passive and constant over the dosage range studied.

摘要

为确定双脱氧肌苷是否能主动转运穿过胎盘,对4只接近足月的怀孕食蟹猴(食蟹猕猴)及其胎儿按随机顺序静脉输注同时剂量的双脱氧肌苷(42.5微克/分钟/千克体重)和安替比林(41.7微克/分钟/千克),持续30小时。输注在妊娠128±0.8天时对母猴进行长期插管后进行。在第三次输注中,仅母猴接受更高剂量的双脱氧肌苷(425微克/分钟/千克)和相同剂量的安替比林(41.7微克/分钟/千克)。在长达30小时的时间内定期采集母血、胎儿血和羊水样本。通过高效液相色谱法测定双脱氧肌苷和安替比林的浓度。采用配对t检验比较经胎盘的母胎药物清除率。在低双脱氧肌苷输注速率下,胎儿与母猴稳态血浆双脱氧肌苷浓度之比(平均值±标准差)为0.49±0.10,在高双脱氧肌苷输注速率下为0.51±0.00。与药物母胎转运相关的清除率CLdf(0.38±0.21毫升/分钟/千克)与与药物胎母转运相关的清除率CLfd(0.56±0.27毫升/分钟/千克)无显著差异(P>0.05)。此外,当以安替比林相应的经胎盘清除率进行标准化时,CLdf与CLfd也无显著差异(P>0.05)(0.07±0.04CLdf对0.09±0.04CLfd)。我们的数据表明,在接近足月的怀孕食蟹猕猴中,双脱氧肌苷在研究的剂量范围内经胎盘的转运是被动且恒定的。

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本文引用的文献

1
Transfer and metabolism of dideoxyinosine by the perfused human placenta.
J Acquir Immune Defic Syndr (1988). 1993 Jan;6(1):2-6.
2
2',3'-Dideoxyinosine is not metabolized in human placenta.
Drug Metab Dispos. 1993 May-Jun;21(3):544-6.

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