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通过固相萃取与毛细管电泳的自动在线联用测定生物流体中的非甾体抗炎药。

Determination of nonsteroidal anti-inflammatory drugs in biological fluids by automatic on-line integration of solid-phase extraction and capillary electrophoresis.

作者信息

Mardones C, Ríos A, Valcárcel M

机构信息

Analytical Chemistry Division, University of Córdoba, Spain.

出版信息

Electrophoresis. 2001 Feb;22(3):484-90. doi: 10.1002/1522-2683(200102)22:3<484::AID-ELPS484>3.0.CO;2-X.

Abstract

A new, automatic method for the clean-up, preconcentration, separation, and quantitation of nonsteroidal anti-inflammatory drugs (NSAIDs) in biological samples (human urine and serum) using solid-phase extraction coupled on-line to capillary electrophoresis is proposed. Automatic pretreatment is carried out by using a continuous flow system operating simultaneously with the capillary electrophoresis equipment, to which it is linked via a laboratory-made mechanical arm. This integrated system is controlled by an electronic interface governed via a program developed in GWBasic. Capillary electrophoresis is conducted by using a separation buffer consisting of 20 mM NaHPO4, 20 mM beta-cyclodextrin and 50 mM SDS at pH 9.0, an applied potential of 20 kV and a temperature of 20 degrees C. The analysis time is 10 min and the detection limits were between 0.88 and 1.71 microg mL(-1). Automatic clean-up and preconcentration is accomplished by using a C-18 minicolumn and 75% methanol as eluent. The limit of detection of NSAIDs can be up to 400-fold improved when using sample clean-up. The extraction efficiency for these compounds is between 71.1 and 109.7 microg mL(-1) (RSD 2.0-7.7%) for urine samples and from 77.2 to 107.1 microg mL(-1) (RSD 3.5-7.1%) for serum samples.

摘要

提出了一种新的自动方法,用于使用与毛细管电泳在线联用的固相萃取技术,对生物样品(人尿液和血清)中的非甾体抗炎药(NSAIDs)进行净化、预浓缩、分离和定量分析。自动预处理通过使用与毛细管电泳设备同时运行的连续流动系统进行,该系统通过自制的机械臂与毛细管电泳设备相连。这个集成系统由一个通过GWBasic开发的程序控制的电子接口进行控制。毛细管电泳采用由20 mM NaHPO4、20 mM β-环糊精和50 mM SDS组成的分离缓冲液,pH值为9.0,施加电压为20 kV,温度为20℃。分析时间为10分钟,检测限在0.88至1.71 μg mL(-1)之间。自动净化和预浓缩通过使用C-18微型柱和75%甲醇作为洗脱剂来完成。使用样品净化时,NSAIDs的检测限可提高多达400倍。这些化合物在尿液样品中的萃取效率在71.1至109.7 μg mL(-1)之间(相对标准偏差2.0 - 7.7%),在血清样品中的萃取效率在77.2至107.1 μg mL(-1)之间(相对标准偏差3.5 - 7.1%)。

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