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Tytuł artykułu

Development and validation of stability-indicating high-performance thin-layer chromatography method for estimation of repaglinide in bulk and in pharmaceutical formulation

Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
A simple, selective, precise, and stability-indicating high-performance thin-layer chromatographic method for analysis of repaglinide both in a bulk and in pharmaceutical formulation has been developed and validated. The method employed high-performance thin-layer chromatography (HPTLC) aluminum plates precoated with silica gel 60 RP-18 F254 as the stationary phase. The solvent system consisted of chloroform-methanol-ammonia (4.5:0.8:0.05, v/v). The system was found to give compact spot for repaglinide (RF value of 0.55 ± 0.03). Densitometric analysis of repaglinide was carried out in the absorbance mode at 288 nm. The linear regression analysis data for the calibration plots showed good linear relationship with r2 = 0.998 ± 0.0015 with respect to peak area in the concentration range 600–1600 ng per spot. The mean value ± SD of slope and intercept were 3.38 ± 1.47 and 986.9 ± 108.78, with respect to peak area. The method was validated for precision, recovery, and robustness. The limits of detection and quantification were 22.64 and 68.84 ng per spot, respectively. Repaglinide was subjected to acid and alkali hydrolysis, oxidation, and thermal degradation. The drug undergoes degradation under acidic and basic conditions. This indicates that the drug is susceptible to acid and base. The degraded product was well resolved from the pure drug with significantly different RF value. Statistical analysis proves that the method is repeatable, selective, and accurate for the estimation of investigated drug. The proposed developed HPTLC method can be applied for identification and quantitative determination of repaglinide in bulk drug and pharmaceutical formulation.
Słowa kluczowe
Rocznik
Strony
531--544
Opis fizyczny
Bibliogr. 17 poz., rys., tab.
Twórcy
autor
  • R. C. Patel Institute of Pharmaceutical Education and Research Karwand Naka, Shirpur, Dist. Dhule 425 405 (M. S.) India
autor
  • R. C. Patel Institute of Pharmaceutical Education and Research Karwand Naka, Shirpur, Dist. Dhule 425 405 (M. S.) India
autor
  • R. C. Patel Institute of Pharmaceutical Education and Research Karwand Naka, Shirpur, Dist. Dhule 425 405 (M. S.) India
Bibliografia
  • [1] ICH, Stability testing of new drug substances and products Q1A (R2), International Conference on Harmonization, IFPMA, Geneva, 2003
  • [2] Martindale, The Complete drug reference, 33rd edn., Council of Royal Pharmaceutical Society of Great Britain, 2007, pp. 334
  • [3] Budavari, The Merck Index, 13th edn., Merck and Co. Inc., White House station, NJ, 2001, pp. 790
  • [4] United States Pharmacopeia, Asian edn., USP Convention Inc., Rockville, MD, 2003, pp. 623
  • [5] A.B. Ruzilawati, M.S. Wahab, A. Imran, Z. Ismail, and S.H. Gan, J. Pharm. Biomed. Anal., 43, 1831–1835 (2007)
  • [6] M. Gandhimathi, T.K. Ravi, and S.K. Renu, Anal. Sci., 19, 1675–1677 (2003)
  • [7] R.H. Khan, S. Talegaonkar, R.M. Singh, S.C. Mathur, R. Shiv, and G.N. Singh, Indian Drugs, 44, 428–433 (2007)
  • [8] A. Goyal and I. Singhavi, Indian J. Pharm. Sci., 68, 656–657 (2006)
  • [9] Gumieniczek, A. Berecka, and H. HopkaŁa, J. Planar Chromatogr., 18, 155–159 (2005)
  • [10] G.Y. Swamy, K. Ravikumar, and L.K. Wadhwa, Acta Cryst., 61, 3608–3610 (2005)
  • [11] P.D. Sethi, High Performance Thin Layer Chromatography (Quantitative Analysis of Pharmaceutical Formulations), CBS Publishers, New Delhi, 1996, 56–63
  • [12] M. Bakshi and S. Singh, J. Pharm. Biomed. Anal., 28, 1011–1040 (2002)
  • [13] S. Singh and M. Bakshi, Pharm. Tech., 24, 1–14 (2000)
  • [14] ICH, Guidance on Analytical Method Validation, in: Proceedings of the International Convention on Quality for the Pharmaceutical Industry, Toronto, September 2002
  • [15] ICH, Q2A Validation of Analytical Procedure, in: Methodology, International Conference on Harmonization, Geneva, October 1994
  • [16] ICH Harmonised Tripartite Guideline: Validation of Analytical Procedures: Text and Methodology, Q2(R1) Geneva, 2005
  • [17] M.C. Sharma and S. Sharma, Int. J. Chem. Tech. Res., 3, 210–216 (2011)
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-2b371f11-de8f-44b0-8891-a4010837cfed
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