Chromatographic determination of oxytetracycline in milk product samples using liquid-liquid microextraction procedure.

IF 2.3 3区 农林科学 Q2 CHEMISTRY, APPLIED
Ilona Kiszkiel-Taudul, Martyna Skorupska
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引用次数: 0

Abstract

Miniaturized procedures for chemical analysis give the possibility of a significant reduction in quantities of organic solvents used during isolation and determination processes. Liquid-liquid microextraction (LLME) using butanol as an extractant was investigated to selectively isolate oxytetracycline (OTC) antibiotic residues from dairy products. The optimal conditions of LLME were established after deproteinization of the samples. The isolation procedure for OTC was performed using 700 µL of butanol. The extracts were analysed by HPLC-UV and LC-MS/MS. A satisfactory analyte recovery was achieved in the range 97.6%-98.9%. The concentration of the linearity range of the studied antibiotic should allow its determination at the level of MRL values. The limit of detection during HPLC-UV and LC-MS/MS determination of OTC in milk samples was 9.9·10-8 mol L-1 (47.85 µg kg-1) and 5.7·10-9 mol L-1 (2.75 µg kg-1), respectively. The precision (1.7%-8.6%) of the methods using LLME isolation of OTC varied depending on the kind of sample and the chromatographic technique used. The developed methods were applied to the analysis of milk and cottage cheese to estimate the presence and detection of OTC content.

利用液-液微萃取程序色谱法测定奶制品样品中的土霉素。
微型化的化学分析程序可以大大减少分离和测定过程中有机溶剂的用量。研究人员使用丁醇作为萃取剂进行液液微萃取(LLME),以选择性地分离乳制品中的土霉素(OTC)抗生素残留。在对样品进行脱蛋白处理后,确定了 LLME 的最佳条件。OTC 的分离过程使用 700 µL 丁醇进行。提取物通过 HPLC-UV 和 LC-MS/MS 进行分析。分析回收率在 97.6%-98.9% 之间,结果令人满意。所研究的抗生素在线性范围内的浓度应能达到最高残留限量值的水平。牛奶样品中 OTC 的 HPLC-UV 和 LC-MS/MS 检测限分别为 9.9-10-8 mol L-1 (47.85 µg kg-1)和 5.7-10-9 mol L-1 (2.75 µg kg-1)。使用 LLME 分离 OTC 的方法的精密度(1.7%-8.6%)因样品种类和色谱技术的不同而不同。所开发的方法被应用于牛奶和松软干酪的分析,以估计 OTC 的存在和检测其含量。
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来源期刊
CiteScore
7.40
自引率
6.90%
发文量
136
审稿时长
3 months
期刊介绍: Food Additives & Contaminants: Part A publishes original research papers and critical reviews covering analytical methodology, occurrence, persistence, safety evaluation, detoxification and regulatory control of natural and man-made additives and contaminants in the food and animal feed chain. Papers are published in the areas of food additives including flavourings, pesticide and veterinary drug residues, environmental contaminants, plant toxins, mycotoxins, marine biotoxins, trace elements, migration from food packaging, food process contaminants, adulteration, authenticity and allergenicity of foods. Papers are published on animal feed where residues and contaminants can give rise to food safety concerns. Contributions cover chemistry, biochemistry and bioavailability of these substances, factors affecting levels during production, processing, packaging and storage; the development of novel foods and processes; exposure and risk assessment.
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