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采用离子对萃取法,以丙酮萃取环境水样和肉样中的头孢菌素,萃取液经毛细管液相色谱分离分析。

Ion-paired extraction of cephalosporins in acetone prior to their analysis by capillary liquid chromatography in environmental water and meat samples.

机构信息

Department of Analytical Chemistry, University of Granada, Campus Fuentenueva, s/n,E-18071 Granada, Spain.

出版信息

Talanta. 2013 Oct 15;115:943-9. doi: 10.1016/j.talanta.2013.07.008. Epub 2013 Jul 10.

DOI:10.1016/j.talanta.2013.07.008
PMID:24054686
Abstract

Ion-pair extraction of cephalosporins from aqueous solution into acetone by the addition of ammonium sulfate to a 1:2 (v/v) acetone-water solvent was carried out followed by their determination using reversed-phase capillary liquid chromatography. The analytes included are cephoperazone, cefquinome, cephalexin, cephapirin, cephaloniun, cephamandole, cephazolin and cephadroxile. In order to form the ion-pair, hexadecyltrimethylammonium bromide (CTAB) was selected as cationic ion-pairing agent at a concentration of 0.9 mM using 10mM phosphate buffer at pH 8 as the optimum condition for the aqueous solution. The applied methodology, named salting-out assisted liquid/liquid extraction (SALLE) involves the use of 1.25 g of ammonium sulfate as salting-out agent. The separation of cephalosporins using a Luna C18 (150 mm × 0.3mm, 5 µm, 100 Å) column was achieved under the following conditions: a gradient program combining solvent A (0.1% formic acid in water, pH 4) and solvent B (acetonitrile-methanol (50:50, v/v)), at a flow rate of 20 µl min(-1), column temperature 35°C and injection volume 7 µl with UV detection at 250 nm. The limits of quantification for the studied compounds were between 4.3 and 22.7 μg/L for water samples and 4.1 and 73.3 μg/kg in the case of beef samples, lower than the maximum residue limits permitted by the EU for this kind of food. The developed methodology has demonstrated its suitability for the analysis of these widely applied antibiotics in environmental water and meat samples, including beef and pork muscle, with high sensitivity, precision and satisfactory recoveries.

摘要

采用正相毛细管液相色谱法,通过向 1:2(v/v)丙酮-水溶液中添加硫酸铵,从水溶液中萃取头孢菌素形成离子对,然后对其进行测定。分析物包括头孢哌酮、头孢喹肟、头孢氨苄、头孢匹林、头孢尼西、头孢孟多、头孢唑林和头孢羟氨苄。为了形成离子对,选择十六烷基三甲基溴化铵(CTAB)作为阳离子离子对试剂,浓度为 0.9mM,使用 10mM 磷酸盐缓冲液(pH8)作为水溶液的最佳条件。所采用的方法,称为盐析辅助液/液萃取(SALLE),涉及使用 1.25g 硫酸铵作为盐析剂。采用 Luna C18(150mm×0.3mm,5µm,100Å)柱,在以下条件下实现头孢菌素的分离:采用溶剂 A(水中 0.1%甲酸,pH4)和溶剂 B(乙腈-甲醇(50:50,v/v))的梯度程序,流速为 20µl min(-1),柱温 35°C,进样量 7µl,在 250nm 处进行紫外检测。对于水样,所研究化合物的定量限在 4.3 和 22.7μg/L 之间,对于牛肉样品,在 4.1 和 73.3μg/kg 之间,低于欧盟对此类食品允许的最大残留限量。所开发的方法已证明其适用于分析环境水中和肉类样品中这些广泛应用的抗生素,包括牛肉和猪肉肌肉,具有高灵敏度、精密度和令人满意的回收率。

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