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Determination of emamectin residues in the tissues of Atlantic salmon(Salmo salar L.) using HPLC with fluorescence detection

机译:高效液相色谱-荧光检测法测定大西洋鲑(Salmo salar L.)组织中的依蒙菌素残留

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An accurate, reliable, and reproducible assay for the determination of residual concentrations of emamectin B-1a in muscle, skin, and intact muscle/skin in natural proportions from Atlantic salmon treated with SCH 58854 (emamectin benzoate) is described. The determinative method was developed and validated using fortified control tissues at five levels over a range of 50-800 ng/g as well as tissues containing incurred levels in the same range. Incurred tissues were obtained from a metabolism study of [H-3]emamectin benzoate in Atlantic salmon. The assay employs processing of a tissue ethyl acetate extract on a propylsulfonic acid solid phase extraction cartridge, followed by derivatization with trifluoroacetic anhydride in the presence of N-methylimidazole. Following separation using reversed phase HPLC, the amount of derivatized emamectin B-1a is determined by fluorescence detection. The theoretical limits of detection were determined from the analysis of control tissue matrices to be 2.6, 3.3, and 3.8 ng/g as emamectin B-1a for muscle, skin, and intact muscle/skin, respectively. Likewise, the theoretical limits of quantitation (LOQ) were determined to be 6.9, 8.1, and 9.5 ng/g as emamectin Bla for muscle, skin, and intact muscle/skin, respectively. The lowest fortification level used for method validation was 50 ng/g,which served as the effective LOQ for the method. The overall percent recoveries (+/-% CV) were 94.4 +/- 6.89% (n = 25) for muscle, 88.4 +/- 5.35% (n = 25) for skin, and 88.0 +/- 3.73% for intact muscle/skin (n = 25). Accuracy, precision, linearity, selectivity, and ruggedness were demonstrated. The structure of the final fluorescent derivative of emamectin B-1a free base was identified by ESI(+)/LC-MS. The frozen storage stability of [H-3]emamectin Bla in tissues with incurred residues was demonstrated for similar to 15 months by radiometric analysis and for an additional similar to 13 months by fluorometric analysis for a total of similar to 28 months.
机译:描述了一种准确,可靠且可重现的测定方法,用于测定以SCH 58854处理的大西洋鲑鱼(阿马菌素苯甲酸酯)中自然比例的肌肉,皮肤和完整肌肉/皮肤中Emamectin B-1a的残留浓度。开发了确定性方法,并使用了浓度在50-800 ng / g范围内的五个水平的强化对照组织以及在相同范围内发生水平的组织进行了验证。从大西洋鲑中[H-3]阿马菌素苯甲酸酯的代谢研究中获得了引起的组织。该测定方法是在丙磺酸固相萃取柱上处理组织乙酸乙酯萃取物,然后在N-甲基咪唑存在下用三氟乙酸酐衍生化。使用反相HPLC分离后,通过荧光检测确定衍生的阿曼菌素B-1a的量。根据对肌肉,皮肤和完整肌肉/皮肤的依莫菌素B-1a的对照组织基质的分析,确定的理论检测极限分别为2.6 ng / g,3.3 ng / g和3.8 ng / g。同样,定量测定的理论极限(LOQ)为Emamectin Bla,分别针对肌肉,皮肤和完整的肌肉/皮肤,分别为6.9、8.1和9.5 ng / g。用于方法验证的最低强化水平为50 ng / g,可作为该方法的有效LOQ。肌肉的总回收率(+ /-%CV)为94.4 +/- 6.89%(n = 25),皮肤为88.4 +/- 5.35%(n = 25)和完整肌肉为88.0 +/- 3.73% /皮肤(n = 25)。证明了准确性,精密度,线性,选择性和坚固性。通过ESI(+)/ LC-MS鉴定了Emamectin B-1a游离碱最终荧光衍生物的结构。通过放射分析表明[H-3]阿马菌素Bla在具有残留物的组织中的冷冻储存稳定性类似于15个月,而通过荧光分析表明又类似于13个月,总共类似于28个月。

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