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固定在沃特曼纤维素纸上的抗可待因适配体,用于从尿液中对可待因进行薄膜微萃取,随后进行电喷雾电离离子迁移谱分析。

Anticodeine aptamer immobilized on a Whatman cellulose paper for thin-film microextraction of codeine from urine followed by electrospray ionization ion mobility spectrometry.

作者信息

Hashemian Zahra, Khayamian Taghi, Saraji Mohammad

机构信息

Department of Chemistry, Isfahan University of Technology, Isfahan, 84156-83111, Iran.

出版信息

Anal Bioanal Chem. 2015 Feb;407(6):1615-23. doi: 10.1007/s00216-014-8392-5. Epub 2014 Dec 19.

DOI:10.1007/s00216-014-8392-5
PMID:25524232
Abstract

A combination of thin-film microextaction based on an aptamer immobilized on modified Whatman cellulose paper followed by electrospray ionization ion mobility spectrometry has been developed for the analysis of codeine in urine samples. The immobilization is based on the covalent linking of an amino-modified anticodeine aptamer to aldehyde groups of the oxidized cellulose paper. The covalent bonds were examined by infrared spectroscopy and elemental analysis. The effect of the extraction parameters, including the elution conditions (solvent type and volume), extraction time, and extraction temperature, on the extraction efficiency were investigated. Under the optimized conditions, the linear dynamic range was found to be 10-300 ng/mL with a detection limit of 3.4 ng/mL for codeine in urine. The relative standard deviation was 6.8% for three replicate measurements of codeine at 100 ng/mL in urine. Furthermore, the samples were analyzed with a standard method for the analysis of codeine using high-performance liquid chromatography with ultraviolet detection. The comparison of the results validates the accuracy of the proposed method as an alternative method for the analysis of codeine in urine samples.

摘要

基于固定在改性沃特曼纤维素纸上的适体的薄膜微萃取,随后结合电喷雾电离离子迁移谱,已被开发用于尿液样本中可待因的分析。固定是基于氨基修饰的抗可待因适体与氧化纤维素纸醛基的共价连接。通过红外光谱和元素分析检测共价键。研究了包括洗脱条件(溶剂类型和体积)、萃取时间和萃取温度在内的萃取参数对萃取效率的影响。在优化条件下,尿液中可待因的线性动态范围为10 - 300 ng/mL,检测限为3.4 ng/mL。尿液中100 ng/mL可待因的三次重复测量的相对标准偏差为6.8%。此外,使用高效液相色谱 - 紫外检测的可待因标准分析方法对样品进行分析。结果比较验证了所提出方法作为尿液样本中可待因分析替代方法的准确性。

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