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采用高效液相色谱法测定血浆和尿液中的匹克隆朵。

Determination of pirlindole in plasma and urine by high-performance liquid chromatography.

作者信息

Ostrowski J, Theumer J, Gärtner W, Resag K, Passing H

出版信息

J Chromatogr. 1984 Jul 13;309(1):115-23. doi: 10.1016/0378-4347(84)80011-0.

Abstract

A high-performance liquid chromatographic method is described for the analysis of pirlindole [2,3,3a,4,5,6-hexahydro-8-methyl-1H-pyrazino(3,2,1-jk)carbazole hydrochloride], a new antidepressive drug. The drug was extracted from plasma into dichloromethane, and the analysis was carried out on a reversed-phase column, the effluent being monitored by fluorescence detection. The method is selective and sensitive (limit of detection 1-2 ng/ml plasma). Urine analysis was done by direct injection of the diluted sample. The method was applied to the analysis of plasma and urine samples of eight healthy male volunteers who received a 75-mg oral dose of a tablet formulation of pirlindole. The method was also applied to a study in three beagle dogs which received pirlindole (1 mg/kg) by infusion (0.1 mg/kg/min) and orally (10 mg/kg) to estimate the absolute bioavailability of the drug.

摘要

本文描述了一种用于分析新型抗抑郁药物匹吲哚[2,3,3a,4,5,6-六氢-8-甲基-1H-吡嗪并(3,2,1-jk)咔唑盐酸盐]的高效液相色谱法。该药物从血浆中萃取到二氯甲烷中,分析在反相柱上进行,流出物通过荧光检测进行监测。该方法具有选择性和灵敏性(检测限为1 - 2 ng/ml血浆)。尿液分析通过直接进样稀释后的样品进行。该方法应用于8名健康男性志愿者的血浆和尿液样本分析,这些志愿者口服了75 mg匹吲哚片剂制剂。该方法还应用于一项对3只比格犬的研究,这些比格犬通过输注(0.1 mg/kg/min)和口服(10 mg/kg)接受匹吲哚(1 mg/kg),以评估该药物的绝对生物利用度。

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