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Ion spray liquid chromatography/tandem mass spectrometry for the confirmation of aminoglycoside antibiotic residues in bovine kidney.

机译:离子喷雾液相色谱/串联质谱法用于确认牛肾脏中氨基糖苷类抗生素残留。

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In order to regulate aminoglycoside antibiotic residues in edible tissues of livestock, the FDA requires confirmatory methods based on mass spectrometry (MS). In this work a method is presented for the multi-residue confirmation of the following 6 priority aminoglycosides in bovine kidney: spectinomycin, hygromycin B, streptomycin, dihydrostreptomycin, gentamicin C complex, and neomycin B. FDA levels of concern in bovine kidney range from 0.02 ppm for hygromycin B to 0.5 ppm for streptomycin and dihydrostreptomycin. Because of the thermal lability and/or nonvolatility of these compounds ion spray HPLC/MS/MS was investigated.; Ion spray mass spectra of all compounds exhibited little fragmentation and base peaks were doubly-protonated doubly-charged molecules except for spectinomycin, which was singly-charged. HPLC/MS conditions were optimized with respect to ion-pairing agent, its concentration, and type of organic modifier. A 17-min gradient separation was developed with mobile phases consisting of aqueous 20 mM pentafluoropropionic acid and acetonitrile using a 2-mm i.d. YMCbasic column at a flow of 0.2 mL/min. With several modifications, an existing matrix solid-phase dispersion (MSPD) method was employed for tissue extraction. Protonated molecules served as precursor ions for collision-induced dissociation (CID) and 3 product ions were selected for selected reaction monitoring (SRM) where possible.; Validation of the confirmatory method was conducted through SRM HPLC/MS/MS analysis of negative control, fortified and incurred bovine kidney samples on two different days. All of the samples could be confirmed with ion ratios within 15% of the daily mean of fortified standards and 90% of the samples had ion ratios within 10%. Absolute retention time data of samples were all within 1% of a consecutively injected fortified standard except for dihydrostreptomycin, which displayed 3% variability. Use of retention time relative to the internal standard tobramycin provides for even better agreement in all cases except dihydrostreptomycin. All compounds except spectinomycin could be detected (while monitoring 3 ions by SRM) in bovine kidney tissue at or below the level of concern. MSPD recoveries were acceptable with the exception of the 27% value observed for spectinomycin.
机译:为了调节牲畜可食组织中的氨基糖苷类抗生素残留,FDA要求基于质谱法(MS)的确认方法。在这项工作中,提出了一种方法来对牛肾中的以下6种优先氨基糖苷进行多残留确认:壮观霉素,潮霉素B,链霉素,二氢链霉素,庆大霉素C复合物和新霉素B。FDA对牛肾的关注水平为0.02潮霉素B的ppm为链霉素和二氢链霉素的0.5 ppm。由于这些化合物的热不稳定性和/或不挥发性,因此对离子喷雾HPLC / MS / MS进行了研究。所有化合物的离子喷雾质谱图均显示出很少的碎裂,并且碱基峰是双质子化的双电荷分子,但壮观霉素是单电荷的。 HPLC / MS条件针对离子配对剂,其浓度和有机改性剂类型进行了优化。用2-mm i.d用流动相进行17分钟的梯度分离,该流动相由20 mM五氟丙酸水溶液和乙腈组成。 YMCbasic柱,流速为0.2 mL / min。经过一些修改,现有的基质固相分散(MSPD)方法用于组织提取。质子化的分子用作碰撞诱导离解(CID)的前体离子,并在可能的情况下选择3种产物离子用于选定的反应监测(SRM)。通过SRM HPLC / MS / MS分析阴性对照,强化和摄取的牛肾样品在两天之内进行验证方法的验证。可以确认所有样品的离子比率均在强化标准品日均含量的15%以内,而90%的样品离子比率均在10%以内。样品的绝对保留时间数据都在连续注入的强化标准品的1%以内,除了二氢链霉素显示3%的变异性。使用相对于内标妥布霉素的保留时间可在除二氢链霉素以外的所有情况下提供更好的一致性。可以在牛肾组织中检测到或低于关注水平的物质(壮观霉素除外)(同时通过SRM监测3个离子)。 MSPD回收率是可接受的,但壮观霉素的值只有27%。

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