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高效液相色谱-电喷雾电离质谱联用法测定猪和牛组织中的庆大霉素

Determination of gentamicin in swine and calf tissues by high-performance liquid chromatography combined with electrospray ionization mass spectrometry.

作者信息

Cherlet M, Baere S D, Backer P D

机构信息

Ghent University, Faculty of Veterinary Medicine, Department of Pharmacology, Pharmacy and Toxicology, Salisburylaan 133, B-9820 Merelbeke, Belgium.

出版信息

J Mass Spectrom. 2000 Nov;35(11):1342-50. doi: 10.1002/1096-9888(200011)35:11<1342::AID-JMS71>3.0.CO;2-Y.

Abstract

Gentamicin is a broad-spectrum aminoglycoside antibiotic widely used in veterinary medicine for the treatment of serious infections. The purpose of this study was to develop and validate a method to determine gentamicin residues in edible tissues of swine and calf. Extraction of gentamicin was performed using a liquid extraction with phosphate buffer containing trichloroacetic acid, followed by a solid-phase clean-up procedure on a CBA weak cation-exchange column. Tobramycin was used as the internal standard. After drying of the eluate, the residue was redissolved and further analyzed by reversed-phase liquid chromatography/electrospray ionization tandem mass spectrometry (MS/MS). Chromatographic separation of the internal standard tobramycin and the gentamicin components was achieved on a Nucleosil (5 microm) column using a mixture of 10 mM pentafluoropropionic acid in water and acetonitrile as the mobile phase. The gentamicin components C1a, C2 + C2a and C1 could be identified with the MS/MS detection, and subsequently quantified. The method was validated according to the requirements of the EC at the maximum residue limit (MRL) (100 ng g(-1) for muscle and fat, 200 ng g(-1) for liver and 1000 ng g(-1) for kidney), half the MRL and double the MRL levels. Calibration graphs were prepared for all tissues and good linearity was achieved over the concentration ranges tested (r > 0.99 and goodness of fit <10%). Limits of quantification of 25.0 ng g(-1) were obtained for the determination of gentamicin in muscle, fat, liver and kidney tissues of swine and calf, which correspond in all cases to at least half the MRLs. Limits of detection ranged between 0.5 and 2.5 ng g(-1) for the tissues. The within-day and between-day precisions (RSD) and the results for accuracy fell within the ranges specified. The method was successfully used for the determination of gentamicin in tissue samples of swines and calves medicated with gentamicin by intramuscular injection.

摘要

庆大霉素是一种广谱氨基糖苷类抗生素,在兽医学中广泛用于治疗严重感染。本研究的目的是开发并验证一种测定猪和小牛可食用组织中庆大霉素残留量的方法。庆大霉素的提取采用含三氯乙酸的磷酸盐缓冲液进行液液萃取,随后在CBA弱阳离子交换柱上进行固相净化程序。妥布霉素用作内标。洗脱液干燥后,残留物重新溶解,再通过反相液相色谱/电喷雾电离串联质谱(MS/MS)进一步分析。使用10 mM五氟丙酸水溶液和乙腈的混合物作为流动相,在内径5微米的Nucleosil柱上实现了内标妥布霉素和庆大霉素各组分的色谱分离。通过MS/MS检测可鉴定庆大霉素组分C1a、C2 + C2a和C1,随后进行定量。该方法根据欧盟委员会在最大残留限量(MRL)(肌肉和脂肪为100 ng g⁻¹,肝脏为200 ng g⁻¹,肾脏为1000 ng g⁻¹)、MRL的一半和两倍MRL水平的要求进行了验证。针对所有组织制备了校准曲线,在所测试的浓度范围内实现了良好的线性(r > 0.99且拟合优度<10%)。猪和小牛肌肉、脂肪、肝脏和肾脏组织中庆大霉素测定的定量限为25.0 ng g⁻¹,在所有情况下均至少相当于MRL的一半。各组织的检测限在0.5至2.5 ng g⁻¹之间。日内和日间精密度(RSD)以及准确度结果均在规定范围内。该方法成功用于测定通过肌肉注射用庆大霉素治疗的猪和小牛的组织样品中的庆大霉素。

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