Development and Validation of a High-Performance Liquid Chromatography-Ultraviolet Spectrometry Method for Ampicillin and its Application in Routine Therapeutic Drug Monitoring of Intensive Care Patients.

IF 2.8 4区 医学 Q2 MEDICAL LABORATORY TECHNOLOGY Therapeutic Drug Monitoring Pub Date : 2024-09-18 DOI:10.1097/FTD.0000000000001253
Benedict Morath, Linda Schultes, Otto Roman Frey, Anka Christa Röhr, Hannes Christow, Torsten Hoppe-Tichy, Alexander Brinkmann, Ute Chiriac
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Abstract

Background: Ampicillin/sulbactam, a combination of a β-lactam and β-lactamase inhibitor, is widely used in clinical settings. However, therapeutic drug monitoring (TDM) of ampicillin is not commonly performed, particularly in intensive care units (ICUs). The purpose of this study was to develop and validate a rapid and cost-effective high-performance liquid chromatography (HPLC)-ultraviolet spectrometry method to quantify ampicillin in human serum and evaluate its clinical application in ICU patients.

Methods: Sample cleanup included a protein precipitation protocol, followed by chromatographic separation on a C18 reverse-phase HPLC column within 12.5 minutes using gradient elution of the mobile phase. The assay was validated according to the German Society of Toxicology and Forensic Chemistry criteria. Clinical applications involved the retrospective analysis of TDM data from ICU patients receiving continuous infusion of ampicillin/sulbactam, including the attainment of target ranges and individual predicted and observed pharmacokinetics.

Results: The method was robust, with linear relations between the peak area responses and drug concentrations in the range of 2-128 mg/L. The coefficient of variation for precision and the bias for accuracy (both interday and intraday) were less than 10%. Clinical application revealed variable pharmacokinetics of ampicillin in ICU patients (clearance of 0.5-31.2 L/h). TDM-guided dose adjustments achieved good therapeutic drug exposure, with 92.9% of the samples being within the optimal (16-32 mg/L) or quasioptimal (8-48 mg/L) range.

Conclusions: This method provides a practical solution for the routine TDM of ampicillin, facilitating individualized dosing strategies to ensure adequate therapeutic drug exposure. Given its simplicity, cost-effectiveness, and clinical relevance, HPLC-ultraviolet spectrometry holds promise for broad implementation in hospital pharmacies and clinical laboratories.

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氨苄西林高效液相色谱-紫外光谱法的开发与验证及其在重症监护患者常规治疗药物监测中的应用
背景:氨苄西林/舒巴坦是β-内酰胺与β-内酰胺酶抑制剂的复方制剂,在临床上广泛使用。然而,氨苄西林的治疗药物监测(TDM)并不常见,尤其是在重症监护病房(ICU)。本研究旨在开发和验证一种快速、经济的高效液相色谱-紫外光谱法,用于定量检测人血清中的氨苄西林,并评估其在重症监护室患者中的临床应用:方法:样品清理包括蛋白质沉淀程序,然后使用流动相梯度洗脱,在 12.5 分钟内在 C18 反相高效液相色谱柱上进行色谱分离。该检测方法根据德国毒理学和法医化学学会的标准进行了验证。临床应用包括对连续输注氨苄西林/舒巴坦的重症监护室患者的 TDM 数据进行回顾性分析,包括目标范围的实现情况以及个体预测和观察到的药代动力学:该方法稳健可靠,峰面积反应与药物浓度在 2-128 mg/L 范围内呈线性关系。精确度的变异系数和准确度的偏差(日间和日内)均小于 10%。临床应用表明,ICU 患者的氨苄西林药代动力学各不相同(清除率为 0.5-31.2 L/h)。TDM指导下的剂量调整取得了良好的治疗药物暴露效果,92.9%的样本在最佳(16-32 mg/L)或准最佳(8-48 mg/L)范围内:该方法为氨苄西林的常规 TDM 提供了一个实用的解决方案,有助于制定个体化用药策略,确保足够的治疗药物暴露。高效液相色谱-紫外光谱法简便易行、成本效益高且与临床相关,有望在医院药房和临床实验室广泛应用。
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来源期刊
Therapeutic Drug Monitoring
Therapeutic Drug Monitoring 医学-毒理学
CiteScore
5.00
自引率
8.00%
发文量
213
审稿时长
4-8 weeks
期刊介绍: Therapeutic Drug Monitoring is a peer-reviewed, multidisciplinary journal directed to an audience of pharmacologists, clinical chemists, laboratorians, pharmacists, drug researchers and toxicologists. It fosters the exchange of knowledge among the various disciplines–clinical pharmacology, pathology, toxicology, analytical chemistry–that share a common interest in Therapeutic Drug Monitoring. The journal presents studies detailing the various factors that affect the rate and extent drugs are absorbed, metabolized, and excreted. Regular features include review articles on specific classes of drugs, original articles, case reports, technical notes, and continuing education articles.
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