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一种基于钆的磁性离子液体,用于超分子分散液液微萃取,随后采用高效液相色谱/紫外检测法测定人血浆中的法匹拉韦。

A gadolinium-based magnetic ionic liquid for supramolecular dispersive liquid-liquid microextraction followed by HPLC/UV for the determination of favipiravir in human plasma.

作者信息

Abdallah Inas A, Hammad Sherin F, Bedair Alaa, Abdelaziz Mohamed A, Danielson Neil D, Elshafeey Ahmed H, Mansour Fotouh R

机构信息

Department of Analytical Chemistry, Faculty of Pharmacy, University of Sadat City, Sadat City, Egypt.

Department of Pharmaceutical Analytical Chemistry, Faculty of Pharmacy, Tanta University, Tanta, Egypt.

出版信息

Biomed Chromatogr. 2022 Jun;36(6):e5365. doi: 10.1002/bmc.5365. Epub 2022 Mar 19.

Abstract

Favipiravir is a potential antiviral medication that has been recently licensed for Covid-19 treatment. In this work, a gadolinium-based magnetic ionic liquid was prepared and used as an extractant in dispersive liquid-liquid microextraction (DLLME) of favipiravir in human plasma. The high enriching ability of DLLME allowed the determination of favipiravir in real samples using HPLC/UV with sufficient sensitivity. The effects of several variables on extraction efficiency were investigated, including type of extractant, amount of extractant, type of disperser and disperser volume. The maximum enrichment was attained using 50 mg of the Gd-magnetic ionic liquid (MIL) and 150 μl of tetrahydrofuran. The Gd-based MIL could form a supramolecular assembly in the presence of tetrahydrofuran, which enhanced the extraction efficiency of favipiravir. The developed method was validated according to US Food and Drug Administration bioanalytical method validation guidelines. The coefficient of determination was 0.9999, for a linear concentration range of 25 to 1.0 × 10  ng/ml. The percentage recovery (accuracy) varied from 99.83 to 104.2%, with RSD values (precision) ranging from 4.07 to 11.84%. The total extraction time was about 12 min and the HPLC analysis time was 5 min. The method was simple, selective and sensitive for the determination of favipiravir in real human plasma.

摘要

法匹拉韦是一种潜在的抗病毒药物,最近已被批准用于治疗新冠肺炎。在这项工作中,制备了一种基于钆的磁性离子液体,并将其用作人血浆中法匹拉韦分散液液微萃取(DLLME)的萃取剂。DLLME的高富集能力使得能够使用高效液相色谱/紫外检测法以足够的灵敏度测定实际样品中的法匹拉韦。研究了几个变量对萃取效率的影响,包括萃取剂类型、萃取剂用量、分散剂类型和分散剂体积。使用50毫克钆磁性离子液体(MIL)和150微升四氢呋喃可实现最大富集。基于钆的MIL在四氢呋喃存在下可形成超分子聚集体,从而提高了法匹拉韦的萃取效率。根据美国食品药品监督管理局生物分析方法验证指南对所建立的方法进行了验证。在25至1.0×10纳克/毫升的线性浓度范围内,测定系数为0.9999。回收率(准确度)百分比在99.83%至104.2%之间,相对标准偏差值(精密度)在4.07%至11.84%之间。总萃取时间约为12分钟,高效液相色谱分析时间为5分钟。该方法对于测定实际人血浆中的法匹拉韦而言简单、具有选择性且灵敏。

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