Quantification of cefuroxime and flucloxacillin in synovial tissue and bone using ultra-performance convergence chromatography-tandem mass spectrometry

IF 2.8 3区 医学 Q2 BIOCHEMICAL RESEARCH METHODS Journal of Chromatography B Pub Date : 2024-05-26 DOI:10.1016/j.jchromb.2024.124169
S. Bahmany , A. Holst , M.H. Hoogendoorn , M. Oosterhoff , J. van Oldenrijk , P.K. Bos , E.S. Veltman , B.C.P. Koch
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Abstract

After a revision surgery, approximately 1–2 % of patients will develop a periprosthetic joint infection (PJI). During the revision surgery, the infected prosthesis is removed, a debridement is performed and a new or temporary spacer is placed. Additionally, patients are treated with antibiotics during and after the surgery. Adequate exposure of the administered antibiotic to the pathogen is of crucial importance during the treatment of any infection. Inadequately low concentrations are associated with an increase in antibiotic resistance, antibiotic related side effects, treatment failures and prolonged infections. While high concentrations may lead to serious adverse events and potential lasting damage. Despite the importance of optimal dosing, there is a lack of knowledge with respect to the correlation between the plasma concentrations and target site concentrations of the antibiotics. Two of the commonly administered antimicrobial agents during the arthroplasty exchange are cefuroxime and flucloxacillin. Therefore, an accurate, specific, and sensitive quantification method is required in order to assess pharmacokinetics of cefuroxime and flucloxacillin in synovial tissue and bone. The aim of this study is to develop and validate a quantification method for the measurement of cefuroxime and flucloxacillin in human synovial tissue and bone using the UPC2-MS/MS conform Food and Drug Administration guidelines. The method was found linear for both compounds in both matrices (r2 > 0.990) from 1 µg/g to 20 µg/g, except for cefuroxime in bone, which was validated from 1 µg/g to 15 µg/g. We developed and validated a quantification method for cefuroxime and flucloxacillin in synovial tissue and bone using a simple sample preparation and a short analysis run time of 5.0 min, which has been already successfully applied in a clinical study. To our knowledge, no methods have been described earlier for the simultaneous quantification of cefuroxime and flucloxacillin in synovial tissue and bone.

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利用超高效聚合色谱-串联质谱法对滑膜组织和骨骼中的头孢呋辛和氟氯西林进行定量分析
翻修手术后,约有 1-2% 的患者会发生假体周围感染(PJI)。在翻修手术中,会移除受感染的假体,进行清创,并放置一个新的或临时的垫片。此外,患者还需在手术期间和术后接受抗生素治疗。在治疗任何感染的过程中,抗生素与病原体的充分接触至关重要。浓度过低会导致抗生素耐药性、抗生素相关副作用、治疗失败和感染时间延长。而高浓度则可能导致严重的不良反应和潜在的持久损害。尽管最佳剂量非常重要,但人们对抗生素的血浆浓度与靶点浓度之间的相关性还缺乏了解。关节置换术中常用的两种抗菌药物是头孢呋辛和氟氯西林。因此,需要一种准确、特异、灵敏的定量方法来评估滑膜组织和骨骼中头孢呋辛和氟氯西林的药代动力学。本研究的目的是开发并验证一种定量方法,利用 UPC2-MS/MS 方法测定人体滑膜组织和骨骼中的头孢呋辛和氟氯西林,该方法符合食品和药物管理局的指导方针。该方法对两种基质中的两种化合物在1微克/克至20微克/克的范围内均呈线性关系(r2 > 0.990),只有骨中的头孢呋辛的线性范围为1微克/克至15微克/克。我们开发并验证了滑膜组织和骨骼中头孢呋辛和氟氯西林的定量方法,样品制备简单,分析时间短,仅需 5.0 分钟。据我们所知,此前还没有人描述过同时定量检测滑膜组织和骨骼中头孢呋辛和氟氯西林的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Chromatography B
Journal of Chromatography B 医学-分析化学
CiteScore
5.60
自引率
3.30%
发文量
306
审稿时长
44 days
期刊介绍: The Journal of Chromatography B publishes papers on developments in separation science relevant to biology and biomedical research including both fundamental advances and applications. Analytical techniques which may be considered include the various facets of chromatography, electrophoresis and related methods, affinity and immunoaffinity-based methodologies, hyphenated and other multi-dimensional techniques, and microanalytical approaches. The journal also considers articles reporting developments in sample preparation, detection techniques including mass spectrometry, and data handling and analysis. Developments related to preparative separations for the isolation and purification of components of biological systems may be published, including chromatographic and electrophoretic methods, affinity separations, field flow fractionation and other preparative approaches. Applications to the analysis of biological systems and samples will be considered when the analytical science contains a significant element of novelty, e.g. a new approach to the separation of a compound, novel combination of analytical techniques, or significantly improved analytical performance.
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