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首页> 外文期刊>Electrophoresis: The Official Journal of the International Electrophoresis Society >Validation of a procedure to quantify oxolinic acid, danofloxacin, ciprofloxacin and enrofloxacin in selected meats by micellar liquid chromatography according to EU Commission Decision 2002/657/EC
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Validation of a procedure to quantify oxolinic acid, danofloxacin, ciprofloxacin and enrofloxacin in selected meats by micellar liquid chromatography according to EU Commission Decision 2002/657/EC

机译:验证通过胶束液相色谱法测定量化草胆酸,丹氟氯嘧嘧啶,环丙沙星和瑞西沙星的胶片液相传,根据欧盟委员会决定2002/657 / EC

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摘要

The suitability of an analytical method to determine oxolinic acid, danofloxacin, ciprofloxacin and enrofloxacin in edible tissues, based on micellar liquid chromatography coupled with fluorescence detection, to be applied in chicken, turkey, duck, lamb, goat, rabbit and horse muscle, is described. The method was fully matrix-matched in-lab revalidated, for each antimicrobial drug and meat, following the guidelines of the EU Commission Decision 2002/657/EC. The permitted limits were the maximum residue limits stated by the EU Commission Regulation 37/2010. The results obtained for the studied validation parameters were in agreement with the guidelines: selectivity (the antibiotics were resolved), linearity (r(2)>0.995), limit of detection (0.004-0.02mg/kg), limits of quantification (0.01-0.05mg/kg), calibration range (up to 0.5mg/kg), recovery (89.5-105.0%), precision (<8.3%), decision limit, detection capability, ruggedness, stability and application to incurred samples. The method was found to be able to provide reliable concentrations with low uncertainty within a large interval, including the maximum residue limits, and then was useful to find out prohibited contaminated samples. The method did not require to be adapted for these matrices, and then it maintained its interesting advantages: short-time, eco-friendly, safe, inexpensive, easy-to-conduct, minimal manipulation and useful for routine analysis.
机译:的分析方法的适用性,以确定在动物组织奥索利酸,达氟沙星,环丙沙星和恩诺沙星,基于加上荧光检测,在鸡,火鸡,鸭,羊,山羊,兔和马肌施加胶束液相色谱法,是描述。该方法完全实验室重新验证基质匹配,每个抗菌药物的肉,继欧盟委员会决议六百五十七分之二千零二/ EC的准则。在允许的范围是由欧盟委员会条例二千零十分之三十七规定的最大残留限量。对于所研究的验证参数获得的结果与准则协议:选择性(抗生素得到解决),线性关系(r(2)> 0.995),检测限(0.004-0.02mg / kg)的,定量限(0.01 -0.05mg / kg)的,校准范围(高达0.5毫克/公斤),恢复(89.5-105.0%),精密(<8.3%),决定限,检测能力,耐用性,稳定性和应用到所产生的样品。该方法被认为是能够在大间隔内提供可靠的浓度低的不确定性,包括的最大残留限量,然后是有用找出禁止污染的样品。该方法并不需要进行调整对于这些矩阵,然后将它保持了有趣的优势:短时,环境友好,安全,廉价,易于开展,最小操纵和有用的常规分析。

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