[超高效液相色谱-串联质谱法测定猪尿液中的 12 种违禁兽药残留]。

Jian-Chun Wan, Ying Han, Xin-Xin Ma, Shi-Xiang Li, Hua-Wen Wu, Li-Hua Ji, Zhi-Wei Deng, Chun-Rui Zhan
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引用次数: 0

摘要

建立了同时检测猪尿液中12种违禁兽药的方法,包括β2-受体激动剂、硝基呋喃类代谢物、硝基咪唑类、氯丙嗪和氯霉素。样品经酶解、酸水解/脱活化、液液萃取结合固相萃取进行预处理。检测采用超高效液相色谱-串联质谱法(UHPLC-MS/MS)。向样品中加入醋酸铵溶液(0.2 mol/L,4.5 mL)和β-葡糖醛酸酶/芳基硫酸酯酶(40 μL),然后在 37 ℃ 下酶解 2 小时。混合物在 37 ℃ 温育 16 h,然后用 8 mL 乙酸乙酯液-液萃取法萃取分析物。萃取后得到的下层水相使用混合阳离子交换固相萃取柱进行萃取和净化。合并萃取液,用氮气吹干萃取液,重新溶解残留物进行测定。样品在正负电喷雾多重反应监测模式下进行分析,并采用同位素内标法进行定量。12 种化合物的相关系数(r)均大于 0.99。氯霉素的检出限(LOD)和定量限(LOQ)分别为 0.05 和 0.1 μg/L,其他化合物的检出限(LOD)和定量限(LOQ)分别为 0.25 和 0.5 μg/L。在1、2和10倍LOQ下的平均回收率和RSD分别为83.6%~115.3%和2.20%~12.34%。该方法灵敏度高、稳定性好、定量准确,适用于猪尿液中12种禁用兽药残留的同时测定。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Determination of 12 prohibited veterinary drug residues in pig urine by ultra high performance liquid chromatography-tandem mass spectrometry].

A method was established for the simultaneous detection of 12 prohibited veterinary drugs, including β2-receptor agonists, nitrofuran metabolites, nitroimidazoles, chlorpromazine, and chloramphenicol, in pig urine. The sample was pretreated by enzymolysis, acid hydrolysis/derivatization, and liquid-liquid extraction combined with solid-phase extraction. Detection was performed using ultra high performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS). Ammonium acetate solution (0.2 mol/L, 4.5 mL) and β-glucuronidase/aryl sulfatase (40 μL) were added to the sample, which was subsequently enzymolized at 37 ℃ for 2 h. Then, 1.5 mL of 1.0 mol/L hydrochloric acid solution and 100 μL of 0.1 mol/L o-nitrobenzaldehyde solution were added to the sample. The mixture was incubated at 37 ℃ for 16 h, and the analytes were extracted with 8 mL of ethyl acetate by liquid-liquid extraction. The lower aqueous phase obtained after extraction was extracted and purified using a mixed cation-exchange solid-phase extraction column. The extracts were combined, the extraction solution was blow-dried with nitrogen, and the residue was redissolved for determination. The samples were analyzed under multiple-reaction monitoring mode with both positive and negative electrospray ionization, and quantified using an isotope internal standard method. The correlation coefficients (r) of the 12 compounds were >0.99. The limits of detection (LODs) and quantification (LOQs) of chloramphenicol were 0.05 and 0.1 μg/L, respectively, and the LODs and LOQs of the other compounds were 0.25 and 0.5 μg/L, respectively. The mean recoveries and RSDs at 1, 2, and 10 times the LOQ were 83.6%-115.3% and 2.20%-12.34%, respectively. The proposed method has the advantages of high sensitivity, good stability, and accurate quantification; thus, it is suitable for the simultaneous determination of the 12 prohibited veterinary drug residues in pig urine.

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