Department of Pharmacy, Cancer Hospital of China Medical University, Liaoning Cancer Hospital & Institute, Number 44 Xiaoheyan Road, Dadong District, Shenyang 110042, Liaoning, PR China.
Department of Pharmacy, Cancer Hospital of China Medical University, Liaoning Cancer Hospital & Institute, Number 44 Xiaoheyan Road, Dadong District, Shenyang 110042, Liaoning, PR China.
J Pharm Biomed Anal. 2022 Oct 25;220:114964. doi: 10.1016/j.jpba.2022.114964. Epub 2022 Jul 26.
Linezolid, vancomycin, teicoplanin, tigecycline, imipenem, meropenem, voriconazole, and micafungin are eight special-grade antimicrobials commonly used for patients with severe infections. Changes in the pharmacodynamics and pharmacokinetics of critically ill patients severely affect the efficacy of antimicrobial drugs. Therefore, conventional or standard dosing regimens do not achieve satisfactory anti-infective effects. In the current study a simple and specific ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) method was developed and validated for simultaneously determining the concentrations of the above-mentioned eight antimicrobials in human plasma only 3 min after one-step magnetic solid phase extraction pre-treatment. Multiple-reaction monitoring and positive ion modes were used for detection. The calibration curves were established over a concentration range of 0.1-25.0 μg/mL for teicoplanin, linezolid, micafungin, voriconazole, imipenem, igecyclin, and meropenem, and 0.2-50.0 μg/mL for vancomycin; the coefficient of correlation was > 0.9971 for all the compounds. The inter- and intra-day coefficients of variation were < 6.88% at the lower limit of quantification and quality control (QC) levels (low concentration-QC, medium concentration-QC, and high-concentration QC). The UPLC-MS/MS method was successfully used for clinical therapeutic drug monitoring of linezolid, vancomycin, teicoplanin, tigecycline, imipenem, meropenem, voriconazole, and micafungin for critically ill patients.
利奈唑胺、万古霉素、替考拉宁、替加环素、亚胺培南、美罗培南、伏立康唑和米卡芬净是常用于严重感染患者的八种特殊级别的抗菌药物。危重症患者的药效学和药代动力学变化严重影响抗菌药物的疗效。因此,常规或标准剂量方案无法达到令人满意的抗感染效果。在本研究中,开发并验证了一种简单而特异的超高效液相色谱-串联质谱法(UPLC-MS/MS),仅需一步磁固相萃取预处理,3 分钟内即可同时测定人血浆中上述八种抗菌药物的浓度。采用多反应监测和正离子模式进行检测。替考拉宁、利奈唑胺、米卡芬净、伏立康唑、亚胺培南、替加环素和美罗培南的校准曲线浓度范围为 0.1-25.0 μg/mL,万古霉素的校准曲线浓度范围为 0.2-50.0 μg/mL;所有化合物的相关系数均>0.9971。在定量下限和质控(QC)水平(低浓度 QC、中浓度 QC 和高浓度 QC)下,日内和日间变异系数均<6.88%。UPLC-MS/MS 方法成功用于危重症患者的临床治疗药物监测,包括利奈唑胺、万古霉素、替考拉宁、替加环素、亚胺培南、美罗培南、伏立康唑和米卡芬净。