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Analytical method validation on simultaneous estimation of Ozenoxacin and Benzoic acid in pharmaceutical formulation

Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
In this study, an accurate, simple, economical and precise Reversed-Phase High Pressure Liquid Chromatography (RP-HPLC) method was developed for the simultaneous estimation of Ozenoxacin and Benzoic Acid in a pharmaceutical cream formulation, according to the International Conference on Harmonisation (ICH) guidelines. Chromatographic separation was achieved by gradient elution, on RP-HPLC Instrument, equipped with column C8 (150 mm × 4.6 mm, 5 μm particle size) using Ultra Violet (UV) detector at 235 nm wavelength, by using Mobile Phase A: triethylamine, trifloroacetic acid and water (1:1:1000) and Mobile Phase B: methanol and Diluent: water, acetonitrile and triethylamine (500:500:1), at flow rate 0.8 mL min⁻¹; injection volume of 20 μL; column oven temperature 45 °C and sample temperature: 25 °C; Run time: 15 min. All the validation parameters were within the acceptance criteria, as per ICH requirements, for Ozenoxacin and Benzoic acid. Consequently, this method has found to be validated, simple, rapid and successfully applicable, to the simultaneous estimation of Ozenoxacin and Benzoic acid by RP-HPLC, for routine analytical testing in quality control, with a run time of 15 min and for future research studies. Forced degradation of Ozenoxacin cream 1% w/w formulation was performed and found that validated method has stability indicating potential that needs to be further studied.
Słowa kluczowe
Rocznik
Strony
278--285
Opis fizyczny
Bibliogr. 27 poz., rys., tab., wykr.
Twórcy
  • Department of Pharmaceutical Sciences, Jawaharlal Nehru Technological University Anantapur (JNTUA), Ananthapuramu, Andhra Pradesh, 515002, India
  • Chemical Engineering, JNTUA College of Engineering (Autonomous), Jawaharlal Nehru Technological University Anantapur (JNTUA), Ananthapuramu, Andhra Pradesh, 515002, India
Bibliografia
  • 1. Wren, C.; Bell, E.; Eiland, L. S. Ozenoxacin: a novel topical quinolone for impetigo. Ann. Pharmacother. 2018, 52(12), 1233–7. https://doi.org/10.1177/1060028018786510.
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  • 3. Rosen, T.; Albareda, N.; Rosenberg, N.; García Alonso, F.; Roth, S.; Zsolt, I. Efficacy and safety of Ozenoxacin cream for treatment of adult and pediatric patients with impetigo: a randomized clinical trial. JAMA Dermatol. 2018, 154(7), 806–13. https://doi.org/10.1001/jamadermatol.2018.1103.
  • 4. Dagan, R. Impetigo in childhood: changing epidemiology and new treatments. Pediatr. Ann. 1993, 22, 235–40. https://doi.org/10.3928/0090-4481-19930401-07.
  • 5. Bruijnzeels, M. A.; van Suijlekom-Smit, L. W. A.; van der Velden, J.; van der Wouden, J. C. The Child in General Practice. Dutch National Survey of Morbidity and Interventions in General Practice; Erasmus University Rotterdam: Rotterdam, 1993.
  • 6. Hlady, W. G.; Middaugh, J. P. An epidemic of bullous impetigo in a newborn nursery due to Staphylococcus aureus: epidemiology and control measures. Alaska Med. 1986, 28, 99–103.
  • 7. López, Y.; Tato, M.; Espinal, P.; Garcia-Alonso, F.; Gargallo-Viola, D.; Cantón, R.; Vila, J. In vitro activity of Ozenoxacin against quinolone-susceptible and quinolone-resistant gram-positive bacteria. Antimicrob. Agents Chemother. 2013, 57(12), 6389–92. https://doi.org/10.1128/AAC.01509-13.
  • 8. https://www.accessdata.fda.gov/drugsatfda_docs/label/2017/208945lbl.pdf (accessed Apr 21, 2022).
  • 9. https://pubchem.ncbi.nlm.nih.gov/compound/Ozenoxacin (accessed Mar 13, 2022).
  • 10. https://www.gattefosse.com/pharmaceuticals-products/labrafil-m-1944-cs (accessed Apr 21, 2022).
  • 11. https://www.gattefosse.com/pharmaceuticals-products/tefose-63 (accessed Apr 21, 2022).
  • 12. https://pubchem.ncbi.nlm.nih.gov/compound/Benzoic-acid (accessed Apr 21, 2022).
  • 13. Sam, T.; Ernest, T. B.; Walsh, J.; Williams, J. L. European Paediatric Formulation Initiative (EuPFI). A benefit/risk approach towards selecting appropriate pharmaceutical dosage forms - an application for paediatric dosage form selection. Int. J. Pharm. 2012, 435(2), 115–23. https://doi.org/10.1016/j.ijpharm.2012.05.024 (Epub 2012 May 22. PMID: 22626885).
  • 14. JibenRoy (2011). The stability of medicines. An introduction to pharmaceutical sciences - production, chemistry, techniques and technology. p. 170.
  • 15. Kar, M.; Chourasiya, Y.; Maheshwari, R.; Tekade, R. K. Current developments in excipient science: implication of quantitative selection of each excipient in product development. In Basic Fundamentals of Drug Delivery. A Volume in Advances in Pharmaceutical Product Development and Research; 2019, pp 29–83.
  • 16. Santos, B.; Ortiz, J.; Gropper, S. In vitro percutaneous absorption and metabolism of Ozenoxacin in excised human skin. Future Microbiol. 2014, 9(8s), S3–9. https://doi.org/10.2217/fmb.14.81.
  • 17. Gupta, V. D. Quantitative determination of benzoic acid and salicylic acid in ointments by high-pressure liquid chromatography. J. Pharm. Sci. 1977, 66(1), 110–1. https://doi.org/10.1002/jps.2600660128.
  • 18. Cheng, Z.; Qin, R.; Liu, J.; Deng, X.; Qiu, H.; Jia, Z.; Su, X. Rapid determination for benzoic acid, sorbic acid, phenyllactic acid, phenylalanine, and saccharin sodium in vinegar by high-performance liquid chromatography–UV. Food Anal. Method. 2020, 13, 1673–80. https://doi.org/10.1007/s12161-020-01784-6.
  • 19. Kubota, K.; Horai, Y.; Kushida, K.; Ishizaki, T. Determination of benzoic acid and hippuric acid in human plasma and urine by high-performance liquid chromatography. J. Chromatogr. 1988, 425(1), 67–75. https://doi.org/10.1016/0378-4347(88)80007-0.
  • 20. Heinanen, M.; Barbas, C. Validation of an HPLC method for the quantification of ambroxol hydrochloride and benzoic acid in a syrup as pharmaceutical form stress test for stability evaluation. J. Pharm. Biomed. Anal. 2001, 24(5–6), 1005–10. https://doi.org/10.1016/s0731-7085(00)00533-1.
  • 21. Kulikov, A. U.; Verushkin, A. G. Simultaneous determination of paracetamol, caffeine, guaifenesin and preservatives in syrups by micellar LC. Chromatographia 2008, 67, 347–55. https://doi.org/10.1365/s10337-007-0510-5.
  • 22. Mansour, A. M.; Ibrahiem, M. M. Simultaneous determination of azelaic and benzoic acids in topical preparations by liquid chromatography. Chromatographia 2002, 55, 435–7. https://doi.org/10.1007/BF02492273.
  • 23. Kokya, T. A.; Farhadi, K.; Kalhori, A. A. Optimized dispersive liquid–liquid microextraction and determination of sorbic acid and benzoic acid in beverage samples by gas chromatography. Food Anal. Methods 2012, 5, 351–8. https://doi.org/10.1007/s12161-011-9245-x.
  • 24. Zhang, X.; Xu, S.; Sun, Y.; Wang, Y.; Wang, C. Simultaneous determination of benzoic acid and sorbic acid in food products by CE after on-line preconcentration by dynamic pH junction. Chromatographia 2011, 73, 1217–21. https://doi.org/10.1007/s10337-011-2009-3.
  • 25. Validation of analytical procedures: text and methodology Q2(R1). https://www.ich.org/page/quality-guidelines (accessed Mar 13, 2022).
  • 26. https://www.chromatographyonline.com/view/chromatography-fundamentals-part-viii-meaning-and-significance-chromatographic-resolution (accessed Aug 09, 2022).
  • 27. Reviewer Guidance Validation of chromatographic methods. https://www.fda.gov/regulatory-information/search-fda-guidance-documents/reviewer-guidance-validation-chromatographic-methods (accessed Mar 13, 2022).
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-8921d64e-3c05-45d5-afc4-6a10f3c18910
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