Department of Laboratory Medicine and Genetics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.
Department of Laboratory Medicine, Kangbuk Samsung Hospital, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.
J Pharm Biomed Anal. 2019 Apr 15;167:161-165. doi: 10.1016/j.jpba.2019.02.001. Epub 2019 Feb 4.
Teicoplanin is a glycopeptide antibiotic used for treatment of severe Gram-positive bacterial infection. The aim of this study was to develop and validate a liquid chromatography-tandem mass spectrometry (LC-MS/MS) method for therapeutic drug monitoring (TDM) of teicoplanin and to review our clinical experience. We established an LC-MS/MS method to analyze serum concentration of teicoplanin using simple protein precipitation with a 5 min run time for each sample. The linearity, lower limit of quantitation, detection accuracy, precision, carryover, matrix effect, and extraction recovery were evaluated. From September 2014 to June 2017, a total of 421 serum teicoplanin concentrations was measured in 223 patients. We collected demographic and clinical data, medication history, and laboratory findings through retrospective review of medical records. The LC-MS/MS method was linear for serum teicoplanin concentrations in the range of 12.0-89.0 μg/mL. The intra- and inter-assay precisions were below CV 7.5%. The accuracy was less than ±10% bias. The lower limit of quantification was 0.2 μg/mL. The extraction recovery ranged from 88.8% to 96.6%. Of 421 measurements, 87 (20.7%) were subtherapeutic (< 10 μg/mL), and four (0.9%) were above the toxic threshold (≥ 60 μg/mL). Serum teicoplanin concentration was measured once in 140 patients (63%), and multiple measurements were completed for the others (83 patients, 37%). Intra-patient variability in teicoplanin concentration was found (CV 33%, range 2-94%). Our simple and rapid LC-MS/MS method was successfully applied in TDM of teicoplanin in clinical practice. Such TDM of teicoplanin may be useful for individualized dose adjustment.
替考拉宁是一种糖肽类抗生素,用于治疗严重的革兰氏阳性细菌感染。本研究旨在开发和验证替考拉宁的治疗药物监测(TDM)的液相色谱-串联质谱(LC-MS/MS)方法,并回顾我们的临床经验。我们建立了一种 LC-MS/MS 方法,使用简单的蛋白质沉淀,每个样品的运行时间为 5 分钟,分析替考拉宁的血清浓度。评价了线性、定量下限、检测准确性、精密度、携带、基质效应和提取回收率。从 2014 年 9 月至 2017 年 6 月,对 223 例患者的 421 例血清替考拉宁浓度进行了测量。我们通过回顾病历收集了人口统计学和临床数据、药物史和实验室发现。LC-MS/MS 方法在血清替考拉宁浓度 12.0-89.0μg/mL 范围内呈线性。日内和日间精密度均低于 7.5%的 CV。准确度小于 10%的偏差。定量下限为 0.2μg/mL。提取回收率为 88.8%至 96.6%。在 421 次测量中,87 次(20.7%)为治疗性(<10μg/mL),4 次(0.9%)高于毒性阈值(≥60μg/mL)。140 例患者(63%)单次测量血清替考拉宁浓度,其余患者(83 例,37%)完成多次测量。发现替考拉宁浓度的个体内变异性(CV 33%,范围 2-94%)。我们的简单快速 LC-MS/MS 方法已成功应用于临床实践中的替考拉宁 TDM。这种替考拉宁的 TDM 可能有助于个体化剂量调整。