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胶束变形和场放大样品堆积在毛细管电泳中用于动物源性食品中甲氧苄啶和磺胺甲噁唑的测定。

Combination of micelle collapse and field-amplified sample stacking in capillary electrophoresis for determination of trimethoprim and sulfamethoxazole in animal-originated foodstuffs.

机构信息

Guangdong Provincial Key Laboratory of New Drug Screening, School of Pharmaceutical Sciences, Southern Medical University, Guangzhou 510515, China.

Guangdong Provincial Key Laboratory of New Drug Screening, School of Pharmaceutical Sciences, Southern Medical University, Guangzhou 510515, China.

出版信息

Food Chem. 2017 Mar 15;219:7-12. doi: 10.1016/j.foodchem.2016.09.118. Epub 2016 Sep 19.

Abstract

An on-line preconcentration method combining micelle to solvent stacking (MSS) with field-amplified sample stacking (FASS) was employed for the analysis of trimethoprim (TMP) and sulfamethoxazole (SMZ) by capillary zone electrophoresis (CZE). The optimized experimental conditions were as followings: (1) sample matrix, 10.0mM SDS-5% (v/v) methanol; (2) trapping solution (TS), 35mM HPO-60% acetonitrile (CHCN); (3) running buffer, 30mM NaHPO (pH=7.3); (4) sample solution volume, 168nL; TS volume, 168nL; and (5) 9kV voltage, 214nm UV detection. Under the optimized conditions, the limits of detection (LODs) for SMZ and TMP were 7.7 and 8.5ng/mL, and they were 301 and 329 times better compared to a typical injection, respectively. The contents of TMP and SMZ in animal foodstuffs such as dairy products, eggs and honey were analyzed, too. Recoveries of 80-104% were acquired with relative standard deviations of 0.5-5.4%.

摘要

采用胶束电动毛细管色谱在线浓缩结合胶束增稳堆积(MSS)与场放大样品堆积(FASS)技术,建立了同时测定甲氧苄啶(TMP)和磺胺甲噁唑(SMZ)的毛细管电泳分析方法。优化实验条件如下:(1)样品基质,10.0mM SDS-5%(v/v)甲醇;(2)堆积液(TS),35mM HPO-60%乙腈(CHCN);(3)运行缓冲液,30mM NaHPO(pH=7.3);(4)样品溶液进样量,168nL;TS 进样量,168nL;(5)9kV 电压,214nm 紫外检测。在优化的实验条件下,SMZ 和 TMP 的检出限(LODs)分别为 7.7ng/mL 和 8.5ng/mL,与典型进样相比,灵敏度分别提高了 301 倍和 329 倍。对乳制品、禽蛋和蜂蜜等动物食品中 TMP 和 SMZ 的含量进行了分析,回收率为 80%-104%,相对标准偏差为 0.5%-5.4%。

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