Suppr超能文献

通过在线分子印迹固相萃取结合液相色谱/质谱法对尿液样本中的β受体阻滞剂药物进行直接掺杂分析。

Direct doping analysis of beta-blocker drugs from urinary samples by on-line molecularly imprinted solid-phase extraction coupled to liquid chromatography/mass spectrometry.

作者信息

Santos Mariane Gonçalves, Tavares Isabela Maria Campos, Boralli Vanessa Bergamin, Figueiredo Eduardo Costa

机构信息

Toxicants and Drugs Analysis Laboratory - LATF, Faculty of Pharmaceutical Sciences, Federal University of Alfenas - Unifal-MG, 700 Gabriel Monteiro da Silva Street, 37130-000, Alfenas, MG, Brazil.

出版信息

Analyst. 2015 Apr 21;140(8):2696-703. doi: 10.1039/c4an02066a. Epub 2015 Feb 13.

Abstract

The use of beta-blockers to enhance performance in some sports is forbidden. Based on this regulation, there is a demand for dynamic analytical procedures for analyzing these compounds quickly and without manual sample preparation. Therefore, the use of a molecularly imprinted polymer (MIP) in a multidimensional liquid chromatographic system coupled to a mass spectrometer provides a good alternative for improving the selectivity and practicality of the beta-blocker analyses, as described in this paper. A water-compatible MIP for oxprenolol was synthesized by the precipitation method, using methacrylic acid as a functional monomer and 2-hydroxyethyl methacrylate and glycerol dimethacrylate as hydrophilic monomers. A column filled with MIP was coupled to an LC-MS/MS instrument under the multidimensional configuration, with 10.0 mmol L(-1) ammonium formate buffer (pH 5.0) as the loading and reconditioning mobile phase and a 0.01% formic acid aqueous solution-methanol (30 : 70 v : v) as the elution mobile phase. The system was used for on-line extraction and quantization of oxprenolol (from 1.0 to 75.0 μg L(-1)), atenolol, propranolol, nadolol, pindolol, labetalol and metoprolol (all from 3.0 to 50 μg L(-1)) simultaneously, from urine samples. The correlation coefficient was higher than 0.99 for all the analytes. Suitable precision and accuracy were obtained.

摘要

在某些运动中使用β受体阻滞剂来提高成绩是被禁止的。基于这一规定,需要有动态分析程序来快速分析这些化合物且无需手动样品制备。因此,如本文所述,在与质谱联用的多维液相色谱系统中使用分子印迹聚合物(MIP)为提高β受体阻滞剂分析的选择性和实用性提供了一个很好的选择。采用沉淀法,以甲基丙烯酸为功能单体,甲基丙烯酸2 - 羟乙酯和二甲基丙烯酸甘油酯为亲水性单体,合成了一种与水相容的氧烯洛尔分子印迹聚合物。在多维配置下,将填充有MIP的色谱柱与液相色谱 - 串联质谱仪联用,以10.0 mmol L⁻¹甲酸铵缓冲液(pH 5.0)作为加载和再平衡流动相,以0.01%甲酸水溶液 - 甲醇(30∶70 v∶v)作为洗脱流动相。该系统用于从尿液样品中同时在线萃取和定量氧烯洛尔(浓度范围为1.0至75.0 μg L⁻¹)、阿替洛尔、普萘洛尔、纳多洛尔、吲哚洛尔、拉贝洛尔和美托洛尔(浓度范围均为3.0至50 μg L⁻¹)。所有分析物的相关系数均高于0.99。获得了合适的精密度和准确度。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验