99
Views
1
CrossRef citations to date
0
Altmetric
Articles

Eco-friendly micellar electrokinetic capillary chromatographic method for the simultaneous determination of newly developed antiviral agents in pharmaceutical formulations

, &

References

  • WHO. Global Health Sector Strategy on Viral Hepatitis 2016-2021 [Internet].World Health Organization. 2016 [cited 19 April 2017]. Available from: http://apps.who.int/iris/bitstream/10665/246177/1/WHO-HIV-2016.06-eng.pdf?ua=1
  • Li, H.; Lo, S. Hepatitis C Virus: Virology, Diagnosis and Treatment. World J. Hepatol. 2015, 7(10), 1377–1389.
  • EASL. EASL Recommendations on Treatment of Hepatitis C. J. Hepatol. 2015, 63(1), 199–236.
  • Gutierrez, J.; Lawitz, E.; Poordad, F. Interferon-Free, Direct-Acting Antiviral Therapy for Chronic Hepatitis C. J. Viral Hepat. 2015, 22(11), 861–870.
  • Jack, K. Advances in Treatments for Hepatitis C. British J. Healthcare Manage. 2015, 21(9), 408–412.
  • Majumdar, A.; Kitson, M.; Roberts, S. Treatment of Hepatitis C in Patients with Cirrhosis: Remaining Challenges for Direct-Acting Antiviral Therapy. Drugs. 2015, 75(8), 823–834.
  • Zhang, X. Direct Anti-HCV Agents. Acta Pharm. Sin B. 2016, 6(1), 26–31.
  • Asselah, T.; Boyer, N.; Saadoun, D.; Martinot-Peignoux, M.; Marcellin, P. Direct-Acting Antivirals for the Treatment of Hepatitis C Virus Infection: Optimizing Current IFN-Free Treatment and Future Perspectives. Liver Int. 2016, 36(Suppl 1), 47–57.
  • Wang, Y.; Lv, Z.; Chu, Y. HIV Protease Inhibitors: A Review of Molecular Selectivity and Toxicity. HIV AIDS. 2015, 7(1), 95–104.
  • Hussaini, T. Paritaprevir/Ritonavir-Ombitasvir and Dasabuvir, the 3D Regimen for the Treatment of Chronic Hepatitis C Virus Infection: A Concise Review. HIV AIDS. 2016, 8(1), 61–68.
  • A 4-Drug Combination (Viekira Pak) for Hepatitis C. JAMA. 2015, 313(18), 1857–1858. doi:10.1001/jama.2015.4562.
  • US.FDA. FDA Approves Viekira Pak to Treat Hepatitis C 2014 [cited 2016 Sep.26]. Available from: http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm427530.htm.
  • US.FDA. FDA Approves Technivie for Treatment of Chronic Hepatitis C Genotype 4. 2015 [cited 2016 Sep.26]. Available from: http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm455857.htm.
  • Bonfilio, R.; Araujo, M.; Salgado, H. Recent Applications of Analytical Techniques for Quantitative Pharmaceutical Analysis: A Review. WSEAS Trans. Biol. Biomed. 2010, 7(4), 316–338.
  • Gutleben, W.; Tuan, N.; Stoiber, H.; Dierich, M.; Sarcletti, M.; Zemann, A. Capillary Electrophoretic Separation of Protease Inhibitors Used in Human Immunodeficiency Virus Therapy. J. Chromatogr. A. 2001, 922(1-2), 313–320.
  • Pereira, E.; Micke, G.; Tavares, M. Determination of Antiretroviral Agents in Human Serum by Capillary Electrophoresis. J. Chromatogr A. 2005, 1091(1-2), 169–176.
  • Fan, B.; Stewart, J. Determinations of Zidovudine/Didanosine/Nevirapine and Zidovudine/Didanosine/Ritonavir in Human Serum by Micellarelectrokinetic Chromatography. J. Pharmaceut Biomed. 2002, 30(4), 955–960.
  • Carvalho, A.; El-Attug, M.; Zayed, S.; Hove, E.; Duppen, J.; Hoogmartens J.; Schepdael, A. Micellarelectrokinetic Chromatography Method Development for Determination of Impurities in Ritonavir. J. Pharmaceut. Biomed. 2010, 53(5), 1210–1216.
  • Gutleben, W.; Scherer, K.; Tuan, N.; Stoiber, H.; Dierich, M.; Zemann, A. Simultaneous Separation of 11 Protease and Reverse Transcriptase Inhibitors for Human Immunodeficiency Virus Therapy by Co-Electroosmotic Capillary Zone Electrophoresis. J. Chromatogr. A. 2002, 982(1), 153–161.
  • Rao, B.; Vidyadhara, S.; Babu, R.; Kumar, B.; Kumar, G. Analytical Method Development and Validation for Simultaneous Estimation of Lopinavir and Ritonavir by RP-HPLC. IJRDPL. 2014, 3(4), 1074–1079.
  • Pabolu, H.; Binginapalli, B.; Konidala, S. New Validated RP-HPLC Method for the Determination of Ritonavir in Bulk and Pharmaceutical Dosage Form. Int. J. Pharm. Pharm. Sci. 2013, 5(4), 556–559.
  • Kumar, K.; Sudhakar, M.; Reddy, Y.; Malleshwari, P.; Hafeez, S. RP-HPLC Method Development and Validation for Simultaneous Estimation of Lopinavir and Ritonavir in Dosage Form and in Plasma. Int. J. Pharma Res. Rev. 2014, 3(9), 1–8.
  • Hiremath, S.; Bhirud, C. Development and Validation of a Stability Indicating HPLC Method for the Simultaneous Analysis of Lopinavir and Ritonavir in Fixed-Dose Combination Tablets. J. TaibahUniv. Sci. 2015, 10(3), 271–277.
  • Usami, Y.; Oki, T.; Nakai, M.; Sagisaka, M.; Kaneda, T. A Simple HPLC Method for Simultaneous Determination of Lopinavir, Ritonavir and Efavirenz. Chem. Pharm. Bull. 2003, 51(6), 715–718.
  • Chiranjeevi, K.; Channabasavaraj, K. Development and Validation of RP-HPLC Method for Quantitative Estimation of Ritonavir in Bulk and Pharmaceutical Dosage Forms. Int. J. Pharm. Sci. Res. 2011, 2(3), 596–600.
  • Killi, G.; Maddinapudi, R.; Dinakaran, S.; Harani A. A Novel Validated UPLC Method for Quantitation of Lopinavir and Ritonavir in Bulk Drug and Pharmaceutical Formulation with Its Impurities. Braz. J. Pharm. Sci. 2014, 50(2), 301–308.
  • Huang, J.; Gautam, N.; Bathena, S.; Roy, U.; McMillan, J.; Gendelman, H.; Alnouti, Y. UPLC–MS/MS Quantification of Nanoformulated Ritonavir, Indinavir, Atazanavir, and Efavirenz in Mouse Serum and Tissues. J. Chromatogr. B. 2011, 879(23), 2332–2338.
  • Venugopal, N.; VijayaBhaskar Reddy, A.; Madhavi, G. Development and Validation of a Systematic UPLC–MS/MS Method for Simultaneous Determination of Three Phenol Impurities in Ritonavir. J. Pharm. and Biomed. Anal. 2014, 90(1), 127–133.
  • Mishra, T.; Shrivastav, P. Validation of Simultaneous Quantitative Method of HIV Protease Inhibitors Atazanavir, Darunavir and Ritonavir in Human Plasma by UPLC-MS/MS. Sci. World J. 2014, 2014(1), 1–12.
  • Mishra, T.; Kurani, H.; Singhal, P.; Shrivastav, P. Simultaneous Quantitation of HIV-Protease Inhibitors Ritonavir, Lopinavir and Indinavir in Human Plasma by UPLC-ESI-MS-MS. J. Chromatogr. Sci. 2012, 50(7), 625–635.
  • Koppala, S.; Panigrahi, B.; Raju, S.; Padmaja Reddy, K.; Ranga Reddy, V.; Anireddy, J. Development and Validation of a Simple, Sensitive, Selective and Stability-Indicating RP-UPLC Method for the Quantitative Determination of Ritonavir and Its Related Compounds. J. Chromatogr. Sci. 2014, 53(5), 662–675.
  • Hendrikx. J.; Hillebrand, M.; Thijssen, B.; Rosing, H.; Schinkel, A.; Schellens, J.; et al. A Sensitive Combined Assay for the Quantification of Paclitaxel, Docetaxel and Ritonavir in Human Plasma Using Liquid Chromatography Coupled with Tandem Mass Spectrometry. J. Chromatogr. B. 2011, 879(28), 2984–2990.
  • Rezk, N.; White, N.; Bridges, A.; Abdel-Megeed, M.; Mohamed, T.; Moselhy, S.; Kashuba, A. Studies on Antiretroviral Drug Concentrations in Breast Milk: Validation of a Liquid Chromatography-Tandem Mass Spectrometric Method for the Determination of 7 Anti-Human Immunodeficiency Virus Medications. Ther Drug Monit. 2008, 30(5), 611–619.
  • Yao, Y.; Sun, J.; Chen, J.; Liu, X.; Lu, H.; Zhang, L. LC-MS/MS Method for Simultaneous Quantification of Lopinavir and Ritonavir in Human Plasma. Yao XueXueBao. 2010, 45(2), 279–282.
  • Rao, R.; Ramachandra, B.; Vali, R.; Raju, S. LC–MS/MS Studies of Ritonavir and Its Forced Degradation Products. J. Pharmaceut. Biomed. 2010, 53(4), 833–842.
  • Damaramadugu, R.; Inamadugu, J.; Kanneti, R.; Polagani, S.; Ponneri, V. Simultaneous Determination of Ritonavir and Lopinavir in Human Plasma After Protein Precipitation and LC-MS-MS. Chromatographia. 2010, 71(9-10), 815–824.
  • Koehn, J.; Ho, R. Novel Liquid Chromatography-Tandem Mass Spectrometry Method for Simultaneous Detection of Anti-HIV Drugs Lopinavir, Ritonavir, and Tenofovir in Plasma. Antimicrob. Agents Ch. 2014, 58(5), 2675–2680.
  • Burugula, L.; Pilli, N.; Makula, A.; Lodagala, D.; Kandhagatla, R. Simultaneous Determination of Ritonavir and Atazanavir in Human Plasma by LC - MS/MS and Its Pharmacokinetic Application. Am. J. Pharm. Tech. Res. 2012, 2(4), 559–571.
  • Abdelhay, M.; Gazy, A.; Shaalan, R.; Ashour, H. Validated Stability-Indicating HPLC and HPTLC Methods for the Determination of Ritonavir in Bulk Powder and in Capsules. J. Food Drug Anal. 2012, 20(4), 963–973.
  • Patil, P.; Wankhede, S.; Chaudhari, P. Stability-Indicating HPTLC Method for Simultaneous Determination of Lopinavir and Ritonavir in Bulk and Pharmaceutical Dosage Form. WJPPS. 2014, 3(6), 1613–1629.
  • Al-zoman, N. Z.; Maher, H. M.; Al-subaie, A. Simultaneous Determination of Newly Developed Antiviral Agents in Pharmaceutical Formulations by HPLC-DAD. Chem. Cent. J. 2017, 11, 1.1–8.
  • Ariaudo, A.; Favata, F.; De Nicolò, A.; Simiele, M.; Paglietti, L.; Boglione, L.; Cardellino, C. S.; Carcieri, C.; Di Perri, G.; D’Avolio, A. A UHPLC–MS/MS Method for the Quantification of Direct Antiviral Agents Simeprevir, Daclatasvir, Ledipasvir, Sofosbuvir/GS-331007, Dasabuvir, Ombitasvir and Paritaprevir, Together with Ritonavir, in Human Plasma. J. Pharm. Biomed. Anal. 2016, 125(1), 369–375.
  • Ocque, A.; Hagler, C.; Difrancesco, R.; Woolwine-Cunningham, Y.; Bednasz, C.; Morse, G.; Talal, A. Development and Validation of a UPLC–MS/MS Method for the Simultaneous Determination of Paritaprevir and Ritonavir in Rat Liver. Bioanalysis. 2016, 8(13), 1353–1363.
  • Sultan, M.; Maher, H.; Alzoman, N.; Alshehri, M.; Rizk, M.; Elshahed, M.; Olah, IV. Capillary Electrophoretic Determination of Antimigraine Formulations Containing Caffeine, Ergotamine, Paracetamol and Domperidone or Metoclopramide. J. Chromatogr. Sci. 2012, 51(6), 502–510.
  • Haj-Ali, D.; Hamdan, I. Development of a Capillary Electrophoresis Method for the Determination of Orphenadrine Citrate in Tablets in the Presence of Paracetamol. Saudi Pharm. J. 2010, 18(4), 233–237.
  • Azhagvuel, S.; Sekar, R. Method Development and Validation for the Simultaneous Determination of Cetirizine Dihydrochloride, Paracetamol, and Phenylpropanolamine Hydrochloride in Tablets by Capillary Zone Electrophoresis. J. Pharm. Biomed. Anal. 2007, 43(3), 873–878.
  • ICH. Q2(R1): Validation of Analytical Procedure: Text and Methodology [Internet]. ICH Guideline. 2005 [cited 14 April 2017]. Available from: https://www.ich.org/fileadmin/Public_Web_Site/ICH_Products/Guidelines/Quality/Q2_R1/Step4/Q2_R1__Guideline.pdf
  • Miller, J. N.; Miller, J. C. Statistics and Chemometrics for Analytical Chemistry. 5th ed. Pearson Prentice Hall: Harlow, England; New York, 2005.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.