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5-氟尿嘧啶和丝裂霉素C腹腔化疗的药代动力学特征

Pharmacokinetic characteristics of 5-fluorouracil and mitomycin C in intraperitoneal chemotherapy.

作者信息

Kuzuya T, Yamauchi M, Ito A, Hasegawa M, Hasegawa T, Nabeshima T

机构信息

Department of Hospital Pharmacy, Nagoya University School of Medicine, Japan.

出版信息

J Pharm Pharmacol. 1994 Aug;46(8):685-9. doi: 10.1111/j.2042-7158.1994.tb03883.x.

Abstract

Eight patients with malignancies confined to the peritoneal space participated in this study. Five hundred milligrams 5-fluorouracil or 10 mg mitomycin C was diluted in 1 L saline. The mixed solution was injected intraperitoneally through the semi-permanent peritoneal catheter. Blood and peritoneal fluid were collected after injection. 5-Fluorouracil concentrations in the peritoneal fluid were 1000 times those in serum, while mitomycin C concentrations were 100 times those in serum. Areas under the concentration vs time curve (AUC) were calculated by the trapezoidal method with extrapolation to infinity. The ratio of peritoneal fluid AUC to serum AUC was about 1400 for 5-fluorouracil and 80 for mitomycin C. Patterns for the absorption and elimination from systemic circulation were similar for both compounds. Drug concentrations in the peritoneal fluid and serum were analysed according to the compartment model. The half-life in the peritoneal fluid (t1/2p) and the rate constant from the peritoneal fluid to the systemic circulation (ka) were nearly equal for both 5-fluorouracil and mitomycin C (t1/2p, 1.0 h for 5-fluorouracil and 1.3 h for mitomycin C; ka 0.71 h-1 for 5-fluorouracil and 0.68 h-1 for mitomycin C), although the apparent volume of distribution (Vds/F) and clearance in the peritoneal cavity (CLp) for mitomycin C (78 L m-2 and 1.8 L h-1 m-2) were about twice the values for 5-fluorouracil (149 L m-2 and 0.8 L h-1 m-2).

摘要

八名腹膜腔内局限存在恶性肿瘤的患者参与了本研究。将500毫克5-氟尿嘧啶或10毫克丝裂霉素C稀释于1升生理盐水中。通过半永久性腹膜导管将混合溶液经腹腔注射。注射后采集血液和腹膜液。腹膜液中5-氟尿嘧啶的浓度是血清中的1000倍,而丝裂霉素C的浓度是血清中的100倍。浓度-时间曲线下面积(AUC)采用梯形法并外推至无穷大来计算。5-氟尿嘧啶的腹膜液AUC与血清AUC之比约为1400,丝裂霉素C为80。两种化合物从体循环的吸收和消除模式相似。根据房室模型分析腹膜液和血清中的药物浓度。5-氟尿嘧啶和丝裂霉素C在腹膜液中的半衰期(t1/2p)以及从腹膜液到体循环的速率常数(ka)几乎相等(5-氟尿嘧啶的t1/2p为1.0小时,丝裂霉素C为1.3小时;5-氟尿嘧啶的ka为0.71 h-1,丝裂霉素C为0.68 h-1),尽管丝裂霉素C的表观分布容积(Vds/F)和腹膜腔清除率(CLp)(分别为78 L m-2和1.8 L h-1 m-2)约为5-氟尿嘧啶(分别为149 L m-2和0.8 L h-1 m-2)的两倍。

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