Hsyu P H, Pritchard J F, Bozigian H P, Gooding A E, Griffin R H, Mitchell R, Bjurstrom T, Panella T L, Huang A T, Hansen L A
Glaxo Research Institute, Research Triangle Park, NC 27709.
J Clin Pharmacol. 1994 Jul;34(7):767-73. doi: 10.1002/j.1552-4604.1994.tb02038.x.
The effect of a typical 5-day chemotherapy treatment with cisplatin (20-40 mg/m2 per day) and 5-fluorouracil (5-FU, 1 gm/m2 per day) on the pharmacokinetics of ondansetron was investigated. Twenty cancer patients received 8 mg of ondansetron in three periods, including an oral tablet on day 1, an intravenous infusion on day 4, and an oral tablet on day 5. Absolute bioavailability after the oral dosing on day 1 was 87.5 +/- 31.3%, and on day 5 was 85.2 +/- 22.1% (P > .05). Mean values of AUC, Cmax, Tmax, and half life on days 1 and 5 were 399 +/- 275 and 381 +/- 222 ng.hour/mL, 53.3 +/- 26.8 and 43.6 +/- 21.7 ng/mL, 1.9 +/- 1.4 and 2 +/- 1.4 hours, and 5.21 +/- 1.78 and 6.19 +/- 1.99 hours, respectively. These values were not significantly different (P > .05). In summary, this study showed that cisplatin and 5-FU did not significantly alter the pharmacokinetics of oral ondansetron in cancer patients during the 5 days of chemotherapy. Oral bioavailability of ondansetron appeared to be greater in cancer patients than in healthy subjects.
研究了顺铂(每天20 - 40mg/m²)和5-氟尿嘧啶(5-FU,每天1g/m²)进行的为期5天的典型化疗对昂丹司琼药代动力学的影响。20名癌症患者在三个时间段接受8mg昂丹司琼,包括第1天口服片剂、第4天静脉输注以及第5天口服片剂。第1天口服给药后的绝对生物利用度为87.5±31.3%,第5天为85.2±22.1%(P>0.05)。第1天和第5天的AUC、Cmax、Tmax和半衰期的平均值分别为399±275和381±222ng·小时/mL、53.3±26.8和43.6±21.7ng/mL、1.9±1.4和2±1.4小时以及5.21±1.78和6.19±1.99小时。这些值无显著差异(P>0.05)。总之,本研究表明,在化疗的5天期间,顺铂和5-FU未显著改变癌症患者口服昂丹司琼的药代动力学。癌症患者中昂丹司琼的口服生物利用度似乎高于健康受试者。