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采用固相萃取和高效液相色谱法测定人血浆和尿液中的血栓素合成酶抑制剂6-(1-咪唑基甲基)-5,6,7,8-四氢萘-2-羧酸(DP-1904)。

Determination of the thromboxane synthetase inhibitor 6-(1-imidazolylmethyl)-5,6,7,8-tetrahydronaphthalene-2-carboxylic acid (DP-1904) in human plasma and urine using solid-phase extraction and high-performance liquid chromatography.

作者信息

Tanaka M, Ono K, Takegoshi T

机构信息

Drug Metabolism Research Centre, Daiichi Seiyaku Co. Ltd., Tokyo, Japan.

出版信息

J Chromatogr. 1988 Apr 8;426(1):111-9. doi: 10.1016/s0378-4347(00)81932-5.

Abstract

A high-performance liquid chromatographic method for the determination of 6-(1-imidazolylmethyl)-5,6,7,8-tetrahydronaphthalene-2-carboxylic acid hydrochloride hemihydrate (DP-1904), a potent and long-acting thromboxane synthetase inhibitor, in human plasma and urine has been developed. DP-1904 and an internal standard were extracted from plasma and urine by means of a Sep-Pak C18 cartridge. The methanol eluate was evaporated and the residue was chromatographed on a reversed-phase column using tetrahydrofuran-0.5% potassium dihydrogen phosphate solution (pH 3.0) (1:16) as the mobile phase at a flow-rate of 1.2 ml/min. Ultraviolet detection at 240 nm resulted in limits of detection of 50 ng/ml for plasma and 1.0 microgram/ml for urine. The method showed satisfactory accuracy and precision. The method was applied to the determination of DP-1904 in plasma and urine samples from a normal human volunteer who had received a 200-mg oral dose of the drug. DP-1904 was rapidly absorbed from the gastrointestinal tract and had a half-life of ca. 30 min. The primary route of elimination was renal, with ca. 60% of the dose being excreted in the urine in the unchanged form within 48 h.

摘要

已开发出一种高效液相色谱法,用于测定人血浆和尿液中的6-(1-咪唑基甲基)-5,6,7,8-四氢萘-2-羧酸盐酸盐半水合物(DP-1904),一种强效长效的血栓素合成酶抑制剂。通过Sep-Pak C18柱从血浆和尿液中提取DP-1904和内标物。甲醇洗脱液蒸发后,残留物在反相柱上进行色谱分析,使用四氢呋喃-0.5%磷酸二氢钾溶液(pH 3.0)(1:16)作为流动相,流速为1.2 ml/min。在240 nm处进行紫外检测,血浆的检测限为50 ng/ml,尿液的检测限为1.0 μg/ml。该方法具有令人满意的准确度和精密度。该方法应用于测定一名口服200 mg该药物的正常人类志愿者的血浆和尿液样本中的DP-1904。DP-1904从胃肠道迅速吸收,半衰期约为30分钟。主要消除途径是肾脏,约60%的剂量在48小时内以原形从尿液中排出。

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