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一种高效液相色谱法的开发与验证,用于定量测定血浆和微透析液中伏立康唑,反映一个重要的靶位点。

Development and validation of an efficient HPLC method for quantification of voriconazole in plasma and microdialysate reflecting an important target site.

作者信息

Simmel Franziska, Soukup Jens, Zoerner Alexander, Radke Joachim, Kloft Charlotte

机构信息

Department of Clinical Pharmacy, Institute of Pharmacy, Martin-Luther-Universitaet Halle-Wittenberg, Wolfgang-Langenbeck-Str. 4, 06120, Halle, Germany.

出版信息

Anal Bioanal Chem. 2008 Oct;392(3):479-88. doi: 10.1007/s00216-008-2286-3. Epub 2008 Aug 3.

Abstract

Voriconazole is a very potent antifungal agent used to treat serious fungal infections (candidiasis); it is also the therapy of choice for aspergillosis. After standard dosing, several factors affect exposure of voriconazole, resulting in large variability and demanding further elucidation of drug distribution. For measurements at the site of action, microdialysis is considered to be an outstanding minimally invasive method. For determination of voriconazole in microdialysate and human plasma a new, efficient, reliable, and robust HPLC assay using UV detection at 254 nm has been developed and validated. After simple sample preparation using acetonitrile for plasma and for microdialysate, 20 microL were injected and separated on an RP-18 column. The chromatographic run time was less than 4 min. Overall, the assay showed high precision (CV 93.9 to 99.5%) and accuracy (RE -96.7 to +107%) for both matrices. Of the 36 drug products typically co-administered with voriconazole, none except ambroxol interfered with its peak signal, and this interference was successfully managed. In summary, the method is highly suitable for application in (pre)clinical microdialysis studies, e.g., of critically ill patients with invasive mycoses.

摘要

伏立康唑是一种强效抗真菌药物,用于治疗严重的真菌感染(念珠菌病);它也是曲霉病的首选治疗药物。标准给药后,有几个因素会影响伏立康唑的暴露量,导致差异很大,需要进一步阐明药物分布情况。对于作用部位的测量,微透析被认为是一种出色的微创方法。为了测定微透析液和人血浆中的伏立康唑,已开发并验证了一种新的、高效、可靠且稳健的HPLC测定法,该方法使用254nm的紫外检测。使用乙腈对血浆和微透析液进行简单的样品制备后,进样20μL,并在RP - 18柱上进行分离。色谱运行时间不到4分钟。总体而言,该测定法对两种基质均显示出高精度(CV为93.9%至99.5%)和准确度(RE为 - 96.7%至 + 107%)。在通常与伏立康唑联合使用的36种药品中,除氨溴索外,没有其他药物干扰其峰信号,并且这种干扰得到了成功处理。总之,该方法非常适合应用于(临床前)微透析研究,例如侵袭性真菌病的重症患者。

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