School of Pharmacy, Xi'an Jiaotong University, Xi'an 710061, PR China.
School of Pharmacy, Xi'an Jiaotong University, Xi'an 710061, PR China.
J Chromatogr B Analyt Technol Biomed Life Sci. 2020 Sep 1;1152:122201. doi: 10.1016/j.jchromb.2020.122201. Epub 2020 Jun 11.
Fluconazole and voriconazole are the two broad-spectrum triazole antifungals. The present work described the fabrication method for the synthesis of the amino-modified magnetic metal-organic framework. This material was applied as a pre-sample treatment sorbent for the selective extraction of fluconazole and voriconazole in rat plasma samples. The material was fabricated by the chemical bonding approach method and was characterized by different parameters. The factors which affect the extraction efficiency of the sorbent material were also optimized in this study. Due to the optimization of solid-phase extraction conditions, the nonspecific interaction was reduced and the extraction recoveries of target drugs were increased in plasma samples. The extraction method was combined with the HPLC-UV method for the analysis. Excellent linearity (0.1-25 µg/mL), detections (0.02, 0.03 µg/mL) and quantification limits (0.04, 0.05 µg/mL) were resulted for fluconazole and voriconazole respectively. The maximum recoveries from spiked plasma samples of fluconazole and voriconazole were 86.8% and 78.6% and relative standard deviation were 0.9-2.8% and 2.2-3.6% respectively. Moreover, this sorbent material was used multiple times which was an improvement over single-use commercial sorbent materials. This validated method has practical potential for the simultaneous determination of these drugs in therapeutic drug monitoring studies as well as for routine pharmacokinetic evaluations.
氟康唑和伏立康唑是两种广谱三唑类抗真菌药物。本工作描述了合成氨基修饰的磁性金属有机骨架的制备方法。该材料被用作大鼠血浆样品中氟康唑和伏立康唑的选择性提取的预样品处理吸附剂。该材料通过化学键合方法制备,并通过不同参数进行了表征。本研究还优化了影响吸附剂材料萃取效率的因素。由于固相萃取条件的优化,减少了非特异性相互作用,提高了血浆样品中目标药物的提取回收率。该提取方法与 HPLC-UV 法相结合进行分析。氟康唑和伏立康唑分别得到了优异的线性(0.1-25μg/mL)、检测限(0.02、0.03μg/mL)和定量限(0.04、0.05μg/mL)。氟康唑和伏立康唑从加标血浆样品中的最大回收率分别为 86.8%和 78.6%,相对标准偏差分别为 0.9-2.8%和 2.2-3.6%。此外,该吸附剂材料可多次使用,优于一次性商业吸附剂材料。该验证方法在治疗药物监测研究中以及常规药代动力学评估中同时测定这些药物具有实际潜力。