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采用溶胶-凝胶衍生的甲基丙烯酸丁酯/硅胶纤维,结合固相微萃取与毛细管电泳法测定水和尿液中的麻黄碱衍生物。

Solid-phase microextraction coupled with capillary electrophoresis to determine ephedrine derivatives in water and urine using a sol-gel derived butyl methacrylate/silicone fiber.

作者信息

Fang Huaifang, Liu Mingming, Zeng Zhaorui

机构信息

Department of Chemistry, Wuhan University, Wuhan, China.

出版信息

Talanta. 2006 Jan 15;68(3):979-86. doi: 10.1016/j.talanta.2005.06.062. Epub 2005 Aug 10.

Abstract

A sensitive method for determination of ephedrine derivatives using headspace solid-phase microextraction (SPME) with a novel fiber followed by capillary electrophoresis has been developed. The co-poly(butyl methacrylate/hydroxy-terminated silicone oil) (BMA/OH-TSO) was used as stationary phases with the aid of gamma-methacryloxypropyltrimethoxysilane (KH-570) as bridge in SPME using sol-gel-coating method and cross-linking technology. It has high extraction efficiency for ephedrine derivatives in comparison with commercial poly(dimethylsiloxane) and poly(acrylate)-coated fiber. The coating exhibits good thermal and solvent stability as well as long lifetime. A simple and flexible device for desorption of analytes after headspace SPME was constructed. The effect of various experimental parameters for SPME (temperature, time, pH, ionic strength, desorption solvent, etc.) were discussed. Field amplified sample injection (FASI) was applied for on-line sample concentration and a sensitivity enhancement of two orders of magnitude was achieved. Linear ranges were found to be 20-5000 ng/ml. The detection limits for (1R,2S)-ephedrine, (1R,2R)-pseudoephedrine and (1S,2S)-pseudoephedrine were 3, 5 and 5ng/ml, respectively. Relative standard deviation (n=6) was found to be 4.96-7.57%. The method was successfully applied to the analysis of ephedrine derivatives in human urine.

摘要

已开发出一种灵敏的方法,用于测定麻黄碱衍生物。该方法采用顶空固相微萃取(SPME)结合新型纤维,随后进行毛细管电泳。在溶胶 - 凝胶涂层法和交联技术的SPME中,以γ-甲基丙烯酰氧基丙基三甲氧基硅烷(KH - 570)为桥梁,将共聚(甲基丙烯酸丁酯/羟基封端的硅油)(BMA/OH - TSO)用作固定相。与商用聚二甲基硅氧烷和聚丙烯酸酯涂层纤维相比,它对麻黄碱衍生物具有较高的萃取效率。该涂层表现出良好的热稳定性和溶剂稳定性以及较长的使用寿命。构建了一种简单灵活的装置,用于顶空SPME后分析物的解吸。讨论了SPME各种实验参数(温度、时间、pH值、离子强度、解吸溶剂等)的影响。采用场放大进样(FASI)进行在线样品浓缩,灵敏度提高了两个数量级。线性范围为20 - 5000 ng/ml。(1R,2S)-麻黄碱、(1R,2R)-伪麻黄碱和(1S,2S)-伪麻黄碱的检测限分别为3、5和5 ng/ml。相对标准偏差(n = 6)为4.96 - 7.57%。该方法已成功应用于人体尿液中麻黄碱衍生物的分析。

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