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人静脉注射和腹腔注射后,用高效液相色谱法测定血浆和腹水中的卡波醌。

Determination of carboquone in plasma and ascites by high performance liquid chromatography after intravenous and intraperitoneal administration in man.

作者信息

Hisaoka M, Morioka T, Yagita A

出版信息

Gan. 1982 Apr;73(2):161-6.

PMID:7117751
Abstract

A new method for the determination of carboquone (CQ) in human plasma and ascites by high performance liquid chromatography has been developed. The method is sensitive enough to determine levels as low as 1.0 ng per 1.0 ml of plasma or ascites. The average recovery of CQ from these samples was 89.3 +/- 0.9% (n = 5, mean +/- SD). The method consists of 2 steps, 1) extracting CQ from human body fluids with chloroform and 2) quantization of CQ by chromatography using a mu-Bondapak C18 column, monitored at 340 nm, 2,5-Diethyleneimino-3,6-dimethylbenzoquinone was used as the internal standard. Using this analytical method, the concentration-time profiles of CQ in human body fluids after intravenous and intraperitoneal administrations were obtained. It was recognized that intraperitoneal administration of CQ was advantagenous for the treatment of peritonitis carcinomatosa since an effective concentration could be maintained in ascites for about 6 hr.

摘要

已开发出一种通过高效液相色谱法测定人血浆和腹水中卡波醌(CQ)的新方法。该方法灵敏度足够高,能够测定低至每1.0毫升血浆或腹水1.0纳克的水平。这些样品中CQ的平均回收率为89.3±0.9%(n = 5,平均值±标准差)。该方法包括两个步骤:1)用氯仿从人体体液中提取CQ;2)使用μ-Bondapak C18柱通过色谱法对CQ进行定量,在340纳米处进行监测,使用2,5-二乙撑亚氨基-3,6-二甲基苯醌作为内标。使用这种分析方法,获得了静脉注射和腹腔注射后人体体液中CQ的浓度-时间曲线。人们认识到,腹腔注射CQ对治疗癌性腹膜炎是有利的,因为在腹水中可以维持约6小时的有效浓度。

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