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氟苯尼考及其代谢物氟苯尼考胺在鸡蛋中的残留消除情况。

Depletion of florfenicol and florfenicol amine residues in chicken eggs.

作者信息

Filazi A, Sireli U T, Yurdakok B, Aydin F G, Kucukosmanoglu A G

机构信息

a Department of Pharmacology and Toxicology, Faculty of Veterinary Medicine , Ankara University , Diskapi-Ankara , Turkey.

出版信息

Br Poult Sci. 2014;55(4):460-5. doi: 10.1080/00071668.2014.935701. Epub 2014 Sep 3.

DOI:10.1080/00071668.2014.935701
PMID:24945307
Abstract
  1. The aim of this study was to develop a suitable method for the analysis of florfenicol (FF) and its metabolite florfenicol amine (FFA) in chicken eggs and to determine FF and FFA residue depletion in eggs of laying hens. 2. The analytes were extracted from yolk, albumen and whole egg by phosphate buffer and ethyl acetate. Following purification, samples were analysed by high-performance liquid chromatography. 3. Fifty laying hens were divided into 5 groups, and each hen received doses of 20 mg/kg FF: Group 1 (received a single oral dose by gavage); Group 2 (a single intramuscular dose); Group 3 (a single subcutaneous dose); Group 4 (multiple oral doses for 3 d) and Group 5 (multiple oral doses for 5 d). 4. Limits of detection and of quantitation values were 1.94 and 6.45 g/10(9) g (ppb) for FF, respectively, and 0.48 and 1.58 ppb for FFA, respectively. Relative standard deviation values of intra-day and inter-day variation below 11% also confirmed the usefulness of the method for analysing FF and FFA in eggs. 5. From the first day of both oral and parenteral administration, FF and FFA were detected at 0.1% and 0.08% of dosage, respectively, and 57% of the drugs were eliminated from the egg yolk. Elimination time of FF was 8 d in Groups 1, 2 and 3; 9 d in Group 4 and 10 d in Group 5.
摘要
  1. 本研究的目的是开发一种适用于分析鸡蛋中氟苯尼考(FF)及其代谢物氟苯尼考胺(FFA)的方法,并测定产蛋母鸡鸡蛋中FF和FFA残留的消除情况。2. 用磷酸盐缓冲液和乙酸乙酯从蛋黄、蛋清和全蛋中提取分析物。纯化后,采用高效液相色谱法对样品进行分析。3. 将50只产蛋母鸡分为5组,每只母鸡接受20mg/kg FF的剂量:第1组(经口单次灌胃给药);第2组(单次肌肉注射);第3组(单次皮下注射);第4组(连续3天多次经口给药)和第5组(连续5天多次经口给药)。4. FF的检测限和定量限分别为1.94和6.45μg/10⁹g(ppb),FFA的检测限和定量限分别为0.48和1.58 ppb。日内和日间变异的相对标准偏差值均低于11%,这也证实了该方法用于分析鸡蛋中FF和FFA的有效性。5. 从口服和非肠道给药的第一天起,分别在剂量的0.1%和0.08%处检测到FF和FFA,57%的药物从蛋黄中消除。第1、2和3组中FF的消除时间为8天;第4组为9天,第5组为10天。

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