Laboratory of Clinical Pharmacology, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland; Service of Clinical Pharmacology, Department of Laboratory Medicine and Pathology, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.
Laboratory of Clinical Pharmacology, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland; Service of Clinical Pharmacology, Department of Laboratory Medicine and Pathology, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.
J Chromatogr B Analyt Technol Biomed Life Sci. 2020 Nov 10;1157:122160. doi: 10.1016/j.jchromb.2020.122160. Epub 2020 May 17.
Unpredictable pharmacokinetics of antibiotics in patients with life-threatening bacterial infections is associated with drug under- or overdosing. Therapeutic drug monitoring (TDM) may guide dosing adjustment aimed at maximizing antibacterial efficacy and minimizing toxicity. Rapid and accurate analytical methods are key for real-time TDM. Our objective was to develop a robust high-performance liquid chromatography-tandem mass spectrometry method (HPLC-MS/MS) for multiplex quantification of plasma concentrations of 12 antibiotics: imipenem/cilastatin, meropenem, ertapenem, cefepime, ceftazidime, ceftriaxone, piperacillin/tazobactam, amoxicillin, flucloxacillin, rifampicin, daptomycin.
A single extraction procedure consisting in methanol plasma protein precipitation and HO dilution was used for all analytes. After chromatographic separation on an Acquity UPLC HSS-T3 2.1 × 50 mm, 1.8 µm (Waters®) column, quantification was performed by electro-spray ionisation-triple quadrupole mass spectrometry with selected reaction monitoring detection. Antibiotics were divided in two pools of calibration according to the frequency of analyses requests in the hospital routine antibiotic TDM program. Stable isotopically-labelled analogues were used as internal standards. A single analytical run lasted less than 9 min.
The method was validated based on FDA recommendations, including assessment of extraction yield (96-113.8%), matrix effects, and analytical recovery (86.3-99.6%). The method was sensitive (lower limits of quantification 0.02-0.5 µg/mL), accurate (intra/inter-assay bias -11.3 to +12.7%) and precise (intra/inter-assay CVs 2.1-11.5%) over the clinically relevant plasma concentration ranges (upper limits of quantification 20-160 µg/mL). The application of the TDM assay was illustrated with clinical cases that highlight the impact on patients' management of an analytical assay providing information with short turn-around time on antibiotic plasma concentration.
This simple, robust high-throughput multiplex HPLC-MS/MS assay for simultaneous quantification of plasma concentrations of 12 daily used antibiotics is optimally suited for clinically efficient real-time TDM.
危及生命的细菌感染患者的抗生素药代动力学不可预测,与药物剂量不足或过量有关。治疗药物监测(TDM)可能有助于指导剂量调整,旨在最大限度地提高抗菌疗效和最小化毒性。快速准确的分析方法是实时 TDM 的关键。我们的目标是开发一种稳健的高效液相色谱-串联质谱法(HPLC-MS/MS),用于同时定量测定 12 种抗生素的血浆浓度:亚胺培南/西司他丁、美罗培南、厄他培南、头孢吡肟、头孢他啶、头孢曲松、哌拉西林/他唑巴坦、阿莫西林、氟氯西林、利福平、达托霉素。
采用甲醇血浆蛋白沉淀和 HO 稀释的单一提取程序,用于所有分析物。在 Acquity UPLC HSS-T3 2.1×50mm,1.8μm(Waters®)柱上进行色谱分离后,通过电喷雾电离-三重四极杆质谱法进行定量分析,采用选择反应监测检测。根据医院常规抗生素 TDM 程序中分析请求的频率,将抗生素分为两个校准池。使用稳定同位素标记的类似物作为内标。单个分析运行时间不到 9 分钟。
该方法基于 FDA 建议进行了验证,包括评估提取效率(96-113.8%)、基质效应和分析回收率(86.3-99.6%)。该方法具有较高的灵敏度(定量下限 0.02-0.5μg/mL)、准确性(日内/间偏差-11.3%至+12.7%)和精密度(日内/间 CVs 2.1%-11.5%),涵盖了临床相关的血浆浓度范围(定量上限 20-160μg/mL)。通过临床病例说明了 TDM 检测的应用,这些病例突出了分析检测对患者管理的影响,该检测提供了具有较短周转时间的抗生素血浆浓度信息。
该简单、稳健的高通量 HPLC-MS/MS 测定法可同时定量测定 12 种日常使用的抗生素的血浆浓度,非常适合临床高效的实时 TDM。