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Development and Validation of a Confirmatory HPLC Method for Simultaneous Determination of Sudan Dyes in Animal Tissues and Eggs

机译:同时测定动物组织和卵中苏丹红的验证性HPLC方法的建立和验证

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摘要

A simple and sensitive high-performance liquid chromatography(HPLC) analytical method for the simultaneous determination of six Sudan dyes (Sudan Red G, Sudan I, Sudan II, Sudan III, Sudan Red 7B, Sudan IV) in animal tissues and eggs was developed. Samples were extracted with acetonitrile followed by a cleanup using a C18 solid-phase extraction column. Chromatographic separation was achieved on a Zorbax SB-C18 column under gradient conditions. The analytes were detected at 510 nm by HPLC with diode array detection. Specificity, decision limit (CCα), detection capacity (CCβ), accuracy, and precision were determined during validation process. Recoveries for six Sudan dyes from three animal tissues and eggs were 77.2–98.0% with excellent relative standard deviations. CCα and CCβ were in the range of 7.7–9.0 μg/kg and 9.1–10.3 μg/kg, respectively. The limits of quantitations were between 12.8 μg/kg and 15.0 μg/kg.
机译:建立了同时测定动物组织和卵中六种苏丹红(苏丹红G,苏丹I,苏丹II,苏丹III,苏丹红7B,苏丹IV)的简单灵敏的高效液相色谱分析方法。 。样品用乙腈萃取,然后使用C18固相萃取柱进行净化。在梯度条件下在Zorbax SB-C18色谱柱上完成色谱分离。通过具有二极管阵列检测的HPLC在510nm处检测分析物。在验证过程中确定特异性,决策极限(CCα),检测能力(CCβ),准确性和精确度。从三个动物组织和卵中检出的六种苏丹红的回收率为77.2–98.0%,相对标准偏差极好。 CCα和CCβ的范围分别为7.7–9.0μg/ kg和9.1–10.3μg/ kg。定量限在12.8μg/ kg和15.0μg/ kg之间。

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