Araştırma Makalesi
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Yıl 2022, Cilt: 12 Sayı: 3, 648 - 652, 28.09.2022
https://doi.org/10.33808/clinexphealthsci.992869

Öz

Kaynakça

  • [1] Ibraam EM, Heba E, Fathalla B, Adel EI. Green micellar solvent- free HPLC and spectrofluorimetric determination of favipiravir as one of COVID-19 antiviral regimens Microchemical Journal 2021;165 (2021): 106189.
  • [2] Wiersinga WJ, Rhodes A, Cheng AC, Peacock SJ, Prescott HC. Pathophysiology, transmission, diagnosis, and treatment of coronavirus disease, (COVID-19): A review. JAMA 2020; 324 (2019): 782–793.
  • [3] Acquavia A, Foti L, Pascale R, Nicolo A, Brancaleone V, Cataldi TR. Detection and quantification of Covid-19 antiviral drugs in biological fluids and tissues. Talanta. 2021; 224 (2021):121862.
  • [4] Delang L; Abdelnabi R, Neyts J. Favipiravir as a potential countermeasure against neglected and emerging RNA viruses. Antiviral Res. 2018; 153: 85–94.
  • [5] China patent (CN104914185A). HPLC method for measuring related substances in Favipiravir. 16.09.2015.
  • [6] Madelain JG, Nguyen THT, Jacquot F, Oestereich L, Kadota T. Favipiravir pharmacokinetics in nonhuman primates and insights for future efficacy studies of hemorrhagic fever viruses, Antimicrob. Agents Chemother.2017; 61 (1): (2017), https://doi.org/10.1128/AAC.01305-16.
  • [7] Smee DF, Hurst BL, Egawa H, Takahashi, K, Kadota T, Furuta Y. Intracellular metabolism of favipiravir (T-705) in uninfected and influenza A (H5N1) virusinfected cells, J. Antimicrob. Chemother. 2009;64 (2009): 741–746.
  • [8] Nguyen THT, Guedj J, Anglaret X, Laou´enan C, Madelain V, Taburet AM. Favipiravir pharmacokinetics in Ebola-Infected patients of the JIKI trial reveals concentrations lower than targeted, PLoS Negl. Trop. Dis. 2017;11 (2): e0005389.
  • [9] Gowen BB, Sefing EJ, Westover JB, Smee, DF, Hagloch J, Furuta Y, et al., Alterations in favipiravir (T-705) pharmacokinetics and biodistribution in a hamster model of viral hemorrhagic fever. Antiviral Res. 2015;121 (2015): 132–137.
  • [10] Safa MM, Ahmed A H, Sherin F H, Amira H. Kamal Experimental design approach for development of spectrofluorimetric method for determination of favipiravir; a potential therapeutic agent against COVID-19 virus: Application to spiked human plasma Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy.2021; 249 (2021): 119241
  • [11] Nguyen THT, Guedj J, Anglaret X, Laou´enan C, Madelain V, Taburet AM. Favipiravir pharmacokinetics in Ebola-Infected patients of the JIKI trial reveals concentrations lower than targeted, PLoS Negl. Trop. Dis. 2017;11 (2): e0005389.
  • [12] A kind of Favipiravir has the HPLC assay method of related substance, Google Patents, CN104914185B (2015) Chinese article.
  • [13] Bulduk I. HPLC-UV method for quantification of favipiravir in pharmaceutical formulations, Acta Chromatographica. 2020; 1-7, DOI: 10.1556/1326.2020.00828.
  • [14] ICH Topic Q 2 (R1) Validation of Analytical Procedures: Text and Methodology.; 2018 July 7. Available from: http://www. ema.europa.eu/docs/en_GB/document_library /Scientific_ guideline/2009/09/WC500002662.pdf [Website].

Development and Validation of a Rapid HPLC-DAD Method for Determination of Favipiravir in Pharmaceutical Formulation

Yıl 2022, Cilt: 12 Sayı: 3, 648 - 652, 28.09.2022
https://doi.org/10.33808/clinexphealthsci.992869

Öz

Objective: The aim of this work was to develop and validate a rapid and simple high-performance liquid chromatography method with a diode- array detector (HPLC-DAD) for determination of favipiravir in bulk and tablet formulations.

Methods: The chromatographic analysis was performed at 30 °C with a Poroshell 120EC-C18 column (4.6 x 50 mm, 2.7 µm). The mobile phase was a mixture of 0.1% formic acid in water and 0.1% formic acid in acetonitrile (90:10, v/v). The run time was 5 min at a flow rate of 0.5 mL/min.

Results: The proposed method was successfully validated in terms of precision, accuracy, linearity, robustness, limits of detection (LOD) and quantification (LOQ) parameters. The calibration plot was linear over a concentration range of 10-100 µg/mL. The LOD and LOQ values were found to be 0.58 µg/mL and 2.03 µg/mL, respectively. The average recovery values were found to vary from 99.45 percent to 104.29 percent.

Conclusion: As a result, it was concluded that the developed method can be used successfully in the determination of favipiravir in pharmaceutical preparations.

Kaynakça

  • [1] Ibraam EM, Heba E, Fathalla B, Adel EI. Green micellar solvent- free HPLC and spectrofluorimetric determination of favipiravir as one of COVID-19 antiviral regimens Microchemical Journal 2021;165 (2021): 106189.
  • [2] Wiersinga WJ, Rhodes A, Cheng AC, Peacock SJ, Prescott HC. Pathophysiology, transmission, diagnosis, and treatment of coronavirus disease, (COVID-19): A review. JAMA 2020; 324 (2019): 782–793.
  • [3] Acquavia A, Foti L, Pascale R, Nicolo A, Brancaleone V, Cataldi TR. Detection and quantification of Covid-19 antiviral drugs in biological fluids and tissues. Talanta. 2021; 224 (2021):121862.
  • [4] Delang L; Abdelnabi R, Neyts J. Favipiravir as a potential countermeasure against neglected and emerging RNA viruses. Antiviral Res. 2018; 153: 85–94.
  • [5] China patent (CN104914185A). HPLC method for measuring related substances in Favipiravir. 16.09.2015.
  • [6] Madelain JG, Nguyen THT, Jacquot F, Oestereich L, Kadota T. Favipiravir pharmacokinetics in nonhuman primates and insights for future efficacy studies of hemorrhagic fever viruses, Antimicrob. Agents Chemother.2017; 61 (1): (2017), https://doi.org/10.1128/AAC.01305-16.
  • [7] Smee DF, Hurst BL, Egawa H, Takahashi, K, Kadota T, Furuta Y. Intracellular metabolism of favipiravir (T-705) in uninfected and influenza A (H5N1) virusinfected cells, J. Antimicrob. Chemother. 2009;64 (2009): 741–746.
  • [8] Nguyen THT, Guedj J, Anglaret X, Laou´enan C, Madelain V, Taburet AM. Favipiravir pharmacokinetics in Ebola-Infected patients of the JIKI trial reveals concentrations lower than targeted, PLoS Negl. Trop. Dis. 2017;11 (2): e0005389.
  • [9] Gowen BB, Sefing EJ, Westover JB, Smee, DF, Hagloch J, Furuta Y, et al., Alterations in favipiravir (T-705) pharmacokinetics and biodistribution in a hamster model of viral hemorrhagic fever. Antiviral Res. 2015;121 (2015): 132–137.
  • [10] Safa MM, Ahmed A H, Sherin F H, Amira H. Kamal Experimental design approach for development of spectrofluorimetric method for determination of favipiravir; a potential therapeutic agent against COVID-19 virus: Application to spiked human plasma Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy.2021; 249 (2021): 119241
  • [11] Nguyen THT, Guedj J, Anglaret X, Laou´enan C, Madelain V, Taburet AM. Favipiravir pharmacokinetics in Ebola-Infected patients of the JIKI trial reveals concentrations lower than targeted, PLoS Negl. Trop. Dis. 2017;11 (2): e0005389.
  • [12] A kind of Favipiravir has the HPLC assay method of related substance, Google Patents, CN104914185B (2015) Chinese article.
  • [13] Bulduk I. HPLC-UV method for quantification of favipiravir in pharmaceutical formulations, Acta Chromatographica. 2020; 1-7, DOI: 10.1556/1326.2020.00828.
  • [14] ICH Topic Q 2 (R1) Validation of Analytical Procedures: Text and Methodology.; 2018 July 7. Available from: http://www. ema.europa.eu/docs/en_GB/document_library /Scientific_ guideline/2009/09/WC500002662.pdf [Website].
Toplam 14 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Konular Sağlık Kurumları Yönetimi
Bölüm Articles
Yazarlar

Duygu Taşkın 0000-0002-5279-0900

Yayımlanma Tarihi 28 Eylül 2022
Gönderilme Tarihi 8 Eylül 2021
Yayımlandığı Sayı Yıl 2022 Cilt: 12 Sayı: 3

Kaynak Göster

APA Taşkın, D. (2022). Development and Validation of a Rapid HPLC-DAD Method for Determination of Favipiravir in Pharmaceutical Formulation. Clinical and Experimental Health Sciences, 12(3), 648-652. https://doi.org/10.33808/clinexphealthsci.992869
AMA Taşkın D. Development and Validation of a Rapid HPLC-DAD Method for Determination of Favipiravir in Pharmaceutical Formulation. Clinical and Experimental Health Sciences. Eylül 2022;12(3):648-652. doi:10.33808/clinexphealthsci.992869
Chicago Taşkın, Duygu. “Development and Validation of a Rapid HPLC-DAD Method for Determination of Favipiravir in Pharmaceutical Formulation”. Clinical and Experimental Health Sciences 12, sy. 3 (Eylül 2022): 648-52. https://doi.org/10.33808/clinexphealthsci.992869.
EndNote Taşkın D (01 Eylül 2022) Development and Validation of a Rapid HPLC-DAD Method for Determination of Favipiravir in Pharmaceutical Formulation. Clinical and Experimental Health Sciences 12 3 648–652.
IEEE D. Taşkın, “Development and Validation of a Rapid HPLC-DAD Method for Determination of Favipiravir in Pharmaceutical Formulation”, Clinical and Experimental Health Sciences, c. 12, sy. 3, ss. 648–652, 2022, doi: 10.33808/clinexphealthsci.992869.
ISNAD Taşkın, Duygu. “Development and Validation of a Rapid HPLC-DAD Method for Determination of Favipiravir in Pharmaceutical Formulation”. Clinical and Experimental Health Sciences 12/3 (Eylül 2022), 648-652. https://doi.org/10.33808/clinexphealthsci.992869.
JAMA Taşkın D. Development and Validation of a Rapid HPLC-DAD Method for Determination of Favipiravir in Pharmaceutical Formulation. Clinical and Experimental Health Sciences. 2022;12:648–652.
MLA Taşkın, Duygu. “Development and Validation of a Rapid HPLC-DAD Method for Determination of Favipiravir in Pharmaceutical Formulation”. Clinical and Experimental Health Sciences, c. 12, sy. 3, 2022, ss. 648-52, doi:10.33808/clinexphealthsci.992869.
Vancouver Taşkın D. Development and Validation of a Rapid HPLC-DAD Method for Determination of Favipiravir in Pharmaceutical Formulation. Clinical and Experimental Health Sciences. 2022;12(3):648-52.

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