三替康唑在大鼠尿液和粪便中的排泄立体选择性

Jing Nie, P. Yaro, Kaifeng He, Hai-hong Hu, S. Zeng
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引用次数: 5

摘要

摘要本研究旨在研究三替康唑对映体在大鼠尿液和粪便中的排泄立体选择性。雄性Sprague-Dawley (SD)大鼠6只,给药50 mg/kg曲康唑。在0-3、3-6、6-9、9-12、12-24、24-36、36-48 h分别定量收集大鼠尿液和粪便。粪便样品在含有0.2% DMSO的水溶液中按1 g: 40 mL的比例均质。取100 μL大鼠尿液或粪便匀浆,加入6.0 μL 1.00 μg/mL氟咪唑作为内标。样品制备后,采用高效液相色谱-质谱联用法测定尿液和粪便中的曲康唑对映体。除3 ~ 6 h外,各组尿液中对映体的排泄量差异均有统计学意义(P < 0.05)。R-(−)-和S-(+)-三替康唑的尿累积排泄率(xu→24)分别为26.43±0.08%和37.58±0.11%,具有较高的对映体选择性(P < 0.001)。R-(−)-和S-(+)-三替康唑的累积排泄率(Xu0→72)分别为6.93±0.03%和6.77±0.03%,差异无统计学意义。结果表明:大鼠尿液和粪便中三替康唑对映体总累积百分比分别为64.00±0.13%和13.70±0.32%,R-(−)-和S-(+)-三替康唑排泄差异显著,S-(+)-三替康唑优先排泄。然而,对映体的粪便排泄没有差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Excretion stereoselectivity of triticonazole in rat urine and faeces
Abstract The purpose of this study was to study the excretion stereoselectivity of triticonazole enantiomers in rat urine and faeces. Six male Sprague-Dawley (SD) rats were administrated 50 mg/kg rac-triticonazole. Rats urine and faeces were separately and quantitatively collected at the following intervals: 0–3, 3–6, 6–9, 9–12, 12–24, 24–36 and 36–48 h. The faeces samples were homogenized in an aqueous solution containing 0.2% DMSO at the ratio of 1 g: 40 mL. An aliquot of 100 μL rats urine or faeces homogenate was spiked and mixed with 6.0 μL of 1.00 μg/mL flusilazole as an internal standard. The triticonazole enantiomers in urine and faeces were determined by using an HPLC/MS–MS after samples preparation. The excreted amounts of enantiomers in the urine showed a significant difference (P < 0.05) except for 3–6 h. The cumulative excretion rate (Xu0→24) in urine was 26.43 ± 0.08% and 37.58 ± 0.11% for R-(−)- and S-(+)-triticonazole, respectively, indicating high enantioselectivity (P < 0.001). The cumulative excretion rate (Xu0→72) in faeces was 6.93 ± 0.03% and 6.77 ± 0.03% for R-(−)- and S-(+)-triticonazole, respectively, without a difference. The results showed that the total cumulative percentage of triticonazole enantiomers accounted for in urine and faeces was 64.00 ± 0.13% and 13.70 ± 0.32%, the urinary excretion of R-(−)- and S-(+)-triticonazole were significantly different and S-(+)-triticonazole was preferentially excreted. However, the faecal excretion of the enantiomers showed no difference.
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