Kelley J A, Litterst C L, Roth J S, Vistica D T, Poplack D G, Cooney D A, Nadkarni M, Balis F M, Broder S, Johns D G
Laboratory of Pharmacology and Experimental Therapeutics, National Cancer Institute, Bethesda, MD 20892.
Drug Metab Dispos. 1987 Sep-Oct;15(5):595-601.
The pharmacokinetics and metabolism of the anti-human T-lymphotrophic virus type III/lymphadenopathy-associated virus agent 2',3-dideoxycytidine have been examined in BDF1 mice and rhesus monkeys, with ancillary enzyme studies carried out on tissue derived from both the latter species and also from human subjects. For the pharmacokinetic studies, 2',3-dideoxycytidine and its catabolic product 2',3-dideoxyuridine have been separated and measured in plasma, urine, and cerebrospinal fluid by a reverse HPLC method. For metabolic studies, tritium-labeled drug (labeled in the 5- and 6-positions of the pyrimidine ring) has been employed, utilizing an ion exchange HPLC analytical method suitable for the separation of the parent nucleoside from its mono-, di-, and triphosphates in cell extracts and in tissue homogenates. The drug is rapidly cleared from plasma in a biphasic manner (terminal t 1/2 in BDF1 mice and rhesus monkeys of 67 min and 109 min, respectively) following an iv bolus dose of 325 mg/m2. This two-compartment open model is predictive of plasma concentrations during long term ip infusions in mice. Dideoxycytidine is predominantly excreted in the urine as unchanged parent compound, although a minor urinary metabolite (2,3-dideoxyuridine) is detected in the monkey but not in the mouse. Oral absorption of 2',3'-dideoxycytidine is rapid, with plasma levels approaching those seen after iv administration within 45 min in the mouse. Entry to the central nervous system is also rapid, but the cerebrospinal fluid to plasma AUC ratio after iv administration is only 0.026-0.040 in rhesus monkeys.(ABSTRACT TRUNCATED AT 250 WORDS)
已在BDF1小鼠和恒河猴中研究了抗人III型T淋巴细胞白血病病毒/淋巴结病相关病毒药物2',3-双脱氧胞苷的药代动力学和代谢情况,并对来自后一物种以及人类受试者的组织进行了辅助酶研究。对于药代动力学研究,采用反相高效液相色谱法在血浆、尿液和脑脊液中分离并测定了2',3-双脱氧胞苷及其分解代谢产物2',3-双脱氧尿苷。对于代谢研究,使用了在嘧啶环的5位和6位标记有氚的药物,采用一种离子交换高效液相色谱分析方法,该方法适用于在细胞提取物和组织匀浆中从其一磷酸、二磷酸和三磷酸中分离母体核苷。静脉推注剂量为325mg/m2后,药物以双相方式从血浆中迅速清除(BDF1小鼠和恒河猴的终末t1/2分别为67分钟和109分钟)。这种二室开放模型可预测小鼠长期腹腔注射期间的血浆浓度。双脱氧胞苷主要以未改变的母体化合物形式经尿液排泄,尽管在猴子尿液中检测到少量代谢产物(2,3-双脱氧尿苷),但在小鼠中未检测到。2',3'-双脱氧胞苷的口服吸收迅速,在小鼠中45分钟内血浆水平接近静脉给药后的水平。进入中枢神经系统也很快,但恒河猴静脉给药后脑脊液与血浆的AUC比值仅为0.026 - 0.040。(摘要截短至250字)