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A gadolinium-based magnetic ionic liquid for supramolecular dispersive liquid-liquid microextraction followed by HPLC/UV for the determination of favipiravir in human plasma.
Abdallah, Inas A; Hammad, Sherin F; Bedair, Alaa; Abdelaziz, Mohamed A; Danielson, Neil D; Elshafeey, Ahmed H; Mansour, Fotouh R.
  • Abdallah IA; Department of Analytical Chemistry, Faculty of Pharmacy, University of Sadat City, Sadat City, Egypt.
  • Hammad SF; Department of Pharmaceutical Analytical Chemistry, Faculty of Pharmacy, Tanta University, Tanta, Egypt.
  • Bedair A; Department of Analytical Chemistry, Faculty of Pharmacy, University of Sadat City, Sadat City, Egypt.
  • Abdelaziz MA; Department of Pharmaceutical Analytical Chemistry, Faculty of Pharmacy, Kafrelsheikh University, Kafrelsheikh, Egypt.
  • Danielson ND; Department of Chemistry and Biochemistry, Miami University, Oxford, OH, USA.
  • Elshafeey AH; Department of Chemistry and Biochemistry, Miami University, Oxford, OH, USA.
  • Mansour FR; Pharmaceutics and Industrial Pharmacy Department, Faculty of Pharmacy, Cairo University, Cairo, Egypt.
Biomed Chromatogr ; 36(6): e5365, 2022 Jun.
Article in English | MEDLINE | ID: covidwho-1739127
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 × 105  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.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Ionic Liquids / Liquid Phase Microextraction / COVID-19 Type of study: Clinical Practice Guide Limits: Humans Language: English Journal: Biomed Chromatogr Year: 2022 Document Type: Article Affiliation country: Bmc.5365

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Ionic Liquids / Liquid Phase Microextraction / COVID-19 Type of study: Clinical Practice Guide Limits: Humans Language: English Journal: Biomed Chromatogr Year: 2022 Document Type: Article Affiliation country: Bmc.5365