Department of Clinical Biochemistry and Metabolic Medicine, Royal Liverpool and Broadgreen University Hospital, 4th floor Duncan Building, Liverpool L7 8XP, UK.
Ann Clin Biochem. 2012 Sep;49(Pt 5):475-81. doi: 10.1258/acb.2012.011257. Epub 2012 Aug 8.
Teicoplanin is an antibiotic used for the treatment of endocarditis, osteomyelitis, septic arthritis and methicillin-resistant Staphylococcus aureus. Teicoplanin is emerging as a suitable alternative antibiotic to vancomycin, where their trough serum levels are monitored by immunoassay routinely. This is the first report detailing the development of a liquid chromatography-tandem mass spectrometry (LC-MS/MS) method for measuring teicoplanin in patients' serum.
An Acquity™ UPLC (ultra-pressure liquid chromatography) tandem mass spectrometer was used to measure teicoplanin concentrations in samples from patients, quality assurance schemes and quality control preparations. Ristocetin was successfully implemented as a suitable internal standard. Ion suppression, linearity, stability, matrix effects, recovery, imprecision, lower limits of quantification and detection, interference and method comparison against immunoassay were all assessed.
Teicoplanin and ristocetin had elution times of 1.39 and 1.24 min, respectively. Ion suppression was shown to be negligible, and linear calibration curves (0-200 μg/mL) were consistently reproduced to have r(2) values >0.99. Postextraction stability was achieved up to 20 h, while matrix effects were minimal coupled with sample recovery of >93%. The lower limit of quantification was 1 μg/mL, and 0.2 μg/mL was the lower limit of detection. Interference with other antibiotics was dependent on the combination of drugs present in patients' serum. A method comparison between immunoassay and LC-MS/MS suggested a negative bias for tandem mass spectrometry.
This novel method of teicoplanin determination by LC-MS/MS is proven to be a robust protocol that is consistent and reproducible. Clinicians searching for alternatives in therapeutic drug monitoring may have an additional option that is potentially more accurate and specific.
替考拉宁是一种用于治疗心内膜炎、骨髓炎、脓毒性关节炎和耐甲氧西林金黄色葡萄球菌感染的抗生素。替考拉宁作为万古霉素的替代抗生素正在逐渐兴起,其血药谷浓度通常通过免疫分析法进行监测。本研究首次详细报告了一种用于测量患者血清中替考拉宁浓度的液相色谱-串联质谱(LC-MS/MS)方法的建立。
采用 Acquity UPLC(超高压液相色谱)串联质谱仪测量来自患者样本、质量保证方案和质控品的替考拉宁浓度。成功地将瑞斯托霉素作为合适的内标物进行了应用。评估了离子抑制、线性、稳定性、基质效应、回收率、精密度、定量下限和检测限、干扰以及与免疫分析法的方法比较。
替考拉宁和瑞斯托霉素的洗脱时间分别为 1.39 和 1.24 分钟。结果表明离子抑制可忽略不计,线性校准曲线(0-200μg/ml)具有一致的重现性,相关系数(r²)均大于 0.99。提取后稳定性可长达 20 小时,而基质效应最小,样品回收率大于 93%。定量下限为 1μg/ml,检测下限为 0.2μg/ml。与其他抗生素的干扰取决于患者血清中存在的药物组合。免疫分析法和 LC-MS/MS 之间的方法比较表明,串联质谱法存在负偏倚。
本研究建立的 LC-MS/MS 测定替考拉宁的新方法是一种可靠且可重现的方法。在寻找治疗药物监测替代方法的临床医生可能会有一个潜在更准确和更特异的选择。