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使用液相色谱-串联质谱法同时定量测定人血清中的七种抗真菌药物。

Simultaneous Quantification of Seven Antifungal Agents in Human Serum Using Liquid Chromatography-Tandem Mass Spectrometry.

作者信息

Li Wenjing, Li Yang, Cai Junlong, Wang Yue, Liu Yanan, Hu Hankun, Liu Liang

机构信息

Department of Pharmacy, Zhongnan Hospital of Wuhan University, 169 Donghu Road, Wuhan 430071, China.

Department of Blood Transfusion, Zhongnan Hospital of Wuhan University, Wuhan 430071, China.

出版信息

Pharmaceuticals (Basel). 2023 Oct 30;16(11):1537. doi: 10.3390/ph16111537.

Abstract

Systemic antifungal agents are essential for high-risk patients undergoing immunosuppressive therapy or cancer chemotherapy because of the rapid increase in opportunistic fungal infections. Therapeutic drug monitoring is crucial to ensuring the efficacy and safety of antifungal agents owing to their pharmacokinetic variability. In the present study, we developed and validated a quantitative method for the simultaneous detection of seven commonly used antifungal drugs (amphotericin B, isavuconazole, voriconazole, fluconazole, posaconazole, caspofungin, and micafungin) using liquid chromatography-tandem mass spectrometry. Methanol (containing 0.1% formic acid) was used for protein precipitation and only 50 μL of serum was required for the analysis. Chromatographic separation was conducted using a Waters Acquity UPLC C8 column, and one stable isotope-labeled agent and two analogs were used as internal standards. The calibration curves ranged from 0.1 to 50 μg/mL for all agents, and the correlation coefficient (R) for all calibration curves was above 0.9835. The intra-day precision (1.2-11.2%), inter-day precision (2.4-13.2%), and mean bias values (-10.9 to 13.6%) were within an acceptable range of ±15%. Successful implementation of the developed method in clinical practice would facilitate the effective monitoring of these antifungal agents.

摘要

由于机会性真菌感染迅速增加,全身用抗真菌药物对于接受免疫抑制治疗或癌症化疗的高危患者至关重要。由于抗真菌药物的药代动力学变异性,治疗药物监测对于确保其疗效和安全性至关重要。在本研究中,我们开发并验证了一种使用液相色谱 - 串联质谱同时检测七种常用抗真菌药物(两性霉素B、艾沙康唑、伏立康唑、氟康唑、泊沙康唑、卡泊芬净和米卡芬净)的定量方法。使用甲醇(含0.1%甲酸)进行蛋白沉淀,分析仅需50μL血清。使用沃特世Acquity UPLC C8柱进行色谱分离,并使用一种稳定同位素标记剂和两种类似物作为内标。所有药物的校准曲线范围为0.1至50μg/mL,所有校准曲线的相关系数(R)均高于0.9835。日内精密度(1.2 - 11.2%)、日间精密度(2.4 - 13.2%)和平均偏差值(-10.9至13.6%)在±15%的可接受范围内。所开发方法在临床实践中的成功实施将有助于对这些抗真菌药物进行有效监测。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66d4/10675106/5d53d562cb8b/pharmaceuticals-16-01537-g001.jpg

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