Tanaka M, Ono K, Takegoshi T
Drug Metabolism Research Centre, Daiichi Seiyaku Co. Ltd., Tokyo, Japan.
J Chromatogr. 1988 Apr 8;426(1):111-9. doi: 10.1016/s0378-4347(00)81932-5.
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.
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。