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通过自动固相萃取和手性柱液相色谱法对手性新苯甲酰胺衍生物氨磺必利在人血浆和尿液中的立体特异性测定及其在药代动力学中的应用

Stereospecific determination of amisulpride, a new benzamide derivative, in human plasma and urine by automated solid-phase extraction and liquid chromatography on a chiral column. application to pharmacokinetics.

作者信息

Ascalone V, Ripamonti M, Malavasi B

机构信息

Department of Chemical and Pharmaceutical Development, Clinical Pharmacokinetics Group of Milan, Italy.

出版信息

J Chromatogr B Biomed Appl. 1996 Feb 9;676(1):95-105. doi: 10.1016/0378-4347(95)00418-1.

Abstract

Amisulpride, a drug belonging to the benzamide series, demonstrates antischizophrenic and antidepressant (antidysthymic) properties in man. For the pharmacokinetic studies of the racemic drug in man, a method of determination based on solid-phase extraction (SPE) from plasma and HPLC on a stereoselective column was developed. For this aim, one millilitre of plasma, after the addition of the internal standard, tiapride or metoclopramide, is diluted with a borate buffer at pH 9, then automatically loaded onto a SPE C18 100-mg column. The column is washed with different solvents, then eluted with 0.5 ml of methanol. After evaporation of the eluted fraction, the residue is reconstituted in 0.25 ml of eluent mixture. An aliquot is injected onto the HPLC column, a Chiralpak AS, equilibrated with an eluent mixture constituted by n-hexane-ethanol, (67:33, v/v) containing 0.2% (v/v) of diethylamine (DEA) or n-heptane-ethanol, (70:29.8, v/v) containing 0.2% of DEA and connected to a UV detector set at 280 nm or to a fluorimetric detector set at lambda ex = 280 nm and lambda cm = 370 nm. The limit of quantitation (LOQ) in human plasma is 2.5 ng ml-1 for both S-(-)- and R-(+)-amisulpride isomers with both detection methods. The method has been demonstrated to be linear in the range 2.5-320 ng ml-1 for both R-(+)- and S-(-)-amisulpride in human plasma with both UV and fluorescence detection. Absolute recovery of S-(-)- and R-(+)-amisulpride enantiomers from human plasma, as well as selectivity, precision and accuracy have been demonstrated to be satisfactory for pharmacokinetics in man and equivalent for both the proposed methods that have been cross-validated on real dosed human plasma samples. The methods have been used for clinical pharmacokinetic studies allowing pharmacokinetic parameters for amisulpride enantiomers in agreement with those obtained for the racemate to be obtained. After dilution with water, urinary samples from subjects treated with amisulpride racemate can be analysed according to the method used for plasma.

摘要

氨磺必利是一种苯甲酰胺类药物,对人体具有抗精神分裂和抗抑郁(抗心境恶劣)特性。为了研究外消旋氨磺必利在人体内的药代动力学,开发了一种基于血浆固相萃取(SPE)和在立体选择性柱上进行高效液相色谱(HPLC)的测定方法。为此,在加入内标替加色罗或甲氧氯普胺后,将1毫升血浆用pH 9的硼酸盐缓冲液稀释,然后自动加载到100毫克的SPE C18柱上。该柱先用不同溶剂冲洗,然后用0.5毫升甲醇洗脱。洗脱液蒸发后,残渣用0.25毫升洗脱液混合物复溶。取一份注入HPLC柱,即Chiralpak AS柱,该柱用由正己烷 - 乙醇(67:33,v/v)含0.2%(v/v)二乙胺(DEA)或正庚烷 - 乙醇(70:29.8,v/v)含0.2% DEA组成的洗脱液混合物平衡,并连接到设置在280纳米的紫外检测器或设置在激发波长λex = 280纳米和发射波长λem = 370纳米的荧光检测器上。两种检测方法对人血浆中S - (-)-和R - (+)-氨磺必利异构体的定量限(LOQ)均为2.5纳克/毫升。该方法已证明在人血浆中,对于R - (+)-和S - (-)-氨磺必利,在2.5 - 320纳克/毫升范围内,采用紫外和荧光检测均呈线性。从人血浆中回收S - (-)-和R - (+)-氨磺必利对映体的绝对回收率以及选择性、精密度和准确度,已证明对人体药代动力学而言是令人满意的,并且对于在实际给药的人血浆样本上进行交叉验证的两种方法来说是等效的。这些方法已用于临床药代动力学研究,从而获得与外消旋体所得结果一致的氨磺必利对映体药代动力学参数。用水稀释后,服用外消旋氨磺必利的受试者的尿液样本可按照用于血浆的方法进行分析。

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