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采用电子捕获检测法通过气相色谱法测定人和犬血浆中的甲氟喹。

Gas chromatographic determination of mefloquine in human and dog plasma using electron-capture detection.

作者信息

Dadgar D, Climax J, Lambe R, Darragh A

出版信息

J Chromatogr. 1985 Jan 11;337(1):47-54. doi: 10.1016/0378-4347(85)80006-2.

Abstract

A sensitive and selective gas-liquid chromatographic method for the determination of plasma levels of mefloquine in human and dog plasma is described. The drug and internal standard were extracted from plasma at pH 9.0 into isopropyl acetate. After evaporation of the solvent, the residue was taken up in toluene and derivatised with heptafluorobutyrylimidazole. The derivative was quantified by gas-liquid chromatography on a 3% GC GE-SE30 column with electron-capture detection. The limit of detection for mefloquine in plasma was 10 ng/ml. The mean overall recovery from plasma was 102.7 +/- 3.3%. The method was shown to be specific for mefloquine without any interference from endogenous compounds in plasma or from the drugs pyrimethamine and sulfadoxine (compounds often administered in combination with mefloquine). The assay described was successfully applied to the determination of plasma levels of mefloquine in man and dog following oral and intravenous administration, respectively.

摘要

本文描述了一种灵敏且具选择性的气液色谱法,用于测定人和犬血浆中氯喹酮的血浆浓度。药物和内标在pH 9.0条件下从血浆中萃取至乙酸异丙酯中。溶剂蒸发后,残留物用甲苯溶解并用七氟丁酰咪唑衍生化。衍生物通过在3% GC GE-SE30柱上进行气液色谱并采用电子捕获检测进行定量。血浆中氯喹酮的检测限为10 ng/ml。血浆的平均总回收率为102.7 +/- 3.3%。该方法对氯喹酮具有特异性,不受血浆中内源性化合物或药物乙胺嘧啶和磺胺多辛(常与氯喹酮联合使用的化合物)的干扰。所描述的测定法分别成功应用于口服和静脉给药后人及犬血浆中氯喹酮血浆浓度的测定。

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