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采用磁固相萃取和毛细管电泳联用技术测定牛奶样品中的喹诺酮类药物。

Determination of quinolones in milk samples using a combination of magnetic solid-phase extraction and capillary electrophoresis.

机构信息

Centro de Investigaciones Químicas, Universidad Autónoma del Estado de Hidalgo, Pachuca, Hgo, Mexico.

出版信息

Electrophoresis. 2012 Jul;33(13):2041-8. doi: 10.1002/elps.201100559.

Abstract

A magnetic solid-phase extraction (MSPE) method combined with capillary electrophoresis for the simultaneous determination of seven quinolones (QNs) (danofloxacin, ciprofloxacin, marbofloxacin, enrofloxacin, difloxacin, oxolinic acid, and flumequine), using (S)-(+)-6-methoxy-α-methyl-2-naphthaleneacetic acid as internal standard, in milk samples was developed. The variables involved in the preconcentration magnetic procedure were: the composition of the magnetic support composition, the sample pH, and the weight of magnetic adsorbent used. The variables were optimized using a simplex-lattice design. Different magnetite covered with octyl-phenyl silica adsorbents were synthesized by varying the molar ratio of phenyltrimethylsilane and octyltrimethoxysilane; the solids were evaluated for QN preconcentration. Under optimal conditions, a linear range was obtained from 27 to 1000 μg L(-1) with limits of detection ranging from 9 to 12 μg L(-1) for the seven QNs. The absolute recoveries of the seven QNs at three different spiked levels (40, 150, and 400 μg L(-1) ) ranged from 74% to 98% with a relative standard deviation less than 10% in all cases. The proposed method was applied to analyze 20 whole milk samples of different brands. All samples were positive for the presence of QN residues; in some cases, extract dilution was required. The concentrations found are in the range from 31.1 to 5047.3 μg L(-1) . Marbofloxacin was the most frequently found. The method proposed offers advantages in terms of simplicity, sensitivity, efficiency, cost, and analysis time making it an alternative for the analysis of QNs in whole milk samples.

摘要

建立了一种结合毛细管电泳同时测定牛奶中 7 种喹诺酮类药物(丹诺沙星、环丙沙星、马波沙星、恩诺沙星、二氟沙星、恶喹酸和氟甲喹)的磁固相萃取(MSPE)方法,以(S)-(+)-6-甲氧基-α-甲基-2-萘乙酸为内标。在预浓缩磁过程中,优化了变量:磁载体组成、样品 pH 值和使用的磁性吸附剂的重量。使用单纯形格子设计优化了变量。通过改变苯基三甲基硅烷和辛基三甲氧基硅烷的摩尔比,合成了不同的覆盖有辛基-苯基硅烷的磁铁矿,用于 QN 预浓缩。在最佳条件下,7 种 QN 的线性范围为 27-1000μg/L,检测限范围为 9-12μg/L。在三个不同的加标水平(40、150 和 400μg/L)下,7 种 QN 的绝对回收率在 74%-98%之间,所有情况下相对标准偏差均小于 10%。该方法用于分析 20 种不同品牌的全脂牛奶样品。所有样品均呈 QN 残留阳性;在某些情况下,需要对提取物进行稀释。发现的浓度范围为 31.1-5047.3μg/L。马波沙星是最常见的。该方法具有简单、灵敏、高效、经济和分析时间短的优点,是全脂牛奶样品中 QN 分析的一种替代方法。

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