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Development and validation of a stability-indicating HPTLC method for analysis of nebivolol hydrochloride and hydrochlorothiazide in the bulk material and in pharmaceutical dosage forms

Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
An accurate, sensitive, rapid, and precise stability-indicating high-performance thin-layer chromatographic (HPTLC) method for analysis of nebivolol hydrochloride and hydrochlorothiazide as the bulk drug and in tablets has been developed and validated. Optimum separation was achieved on silica gel 60 F 254 plates with ethyl acetate-methanol-acetic acid 6.5:1:0.5 ( υ/υ ) as mobile phase. Detection and quantification were performed at 280 and 270 nm for nebivolol hydrochloride and hydrochlorothiazide, respectively. The drugs get resolved with R F 0.46 ± 0.02 and 0.78 ± 0.02 for nebivolol hydrochloride and hydrochlorothiazide, respectively. The drugs were subjected to hydrolysis under acidic, basic, and neutral conditions, oxidation, heat, and photolysis as stress conditions. Peaks of degradation products were observed when the drugs were subjected to oxidative stress. Acidic conditions were also found to affect the tablet sample substantially. The degradation products resulting from stress conditions did not interfere with the drug peak. The method can be used for stability testing of these drugs during stability studies.
Rocznik
Strony
433--443
Opis fizyczny
Bibliogr. 20 poz., rys., tab.
Twórcy
autor
  • AISSMS College of Pharmacy Pharmaceutical Chemistry Department Kennedy Road, Near RTO Pune 411001 Maharashtra India
autor
  • AISSMS College of Pharmacy Pharmaceutical Chemistry Department Kennedy Road, Near RTO Pune 411001 Maharashtra India
  • AISSMS College of Pharmacy Pharmaceutical Chemistry Department Kennedy Road, Near RTO Pune 411001 Maharashtra India
Bibliografia
  • [1] S. Budavari, The Merck Index, Merck & Co., INC., New Jersey, 2001
  • [2] Indian Pharmacopoeia 2007 edn., Volume II. The controller of Publication, Delhi 151 , 1194
  • [3] British Pharmacopoeia 2009 edn., Volume I & II, accessed soft copy
  • [4] The United States Pharmacopoeia 2007 edn. (USP-30 NF-25), Asian edition, Rockville, MD: USP Convention Rockville, MD, USP Convention Inc, pp. 2288
  • [5] F. Belal, I.A. Al-Zaagi, E.A. Gadkariem, and M.A. Abounassif, J. Pharm. Biomed. Anal, 24 , 335 (2001)
  • [6] D.L. Hertzog, J.F. McCafferty, X. Fang, R.J. Tyrrell, and R.A. Reed, J. Pharm. Biomed. Anal., 30 , 747 (2002)
  • [7] S.L. Daniels and A.J. Vanderwielen, J. Pharm Sci., 70 , 211 (1981)
  • [8] I.L. Bebawy and E.N. Kousy, Anal. Lett., 30 , 1379 (1997)
  • [9] N. Chheta, S.P. Gandhi, and S.J. Rajput, Int. J. ChemTech Res., 1 , 654 (2009)
  • [10] P. Rathee, S. Rathee, D. Rathee, H. Chaudhary, Eurasian J. Anal. Chem., 4 , 1 (2009)
  • [11] M.P. Tagliari, H.K. Stulzer, F.S. Murakami, G. Kuminek, B. Valente, P.R. Oliveira, and M.A. Segatto Silva, Chromatographia, 67 , 647 (2008)
  • [12] D.D. Rao, N.V. Satyanarayana, S.S. Sait, Y.R. Reddy, and K. Mukkanti, Chromatographia, 70 , 647 (2009)
  • [13] M. Lusina, T. Cindric, J. Tomaic, M. Peko, L. Pozaic, and N. Musulin, Int. J. Pharm., 291 , 127 (2005)
  • [14] D.A. Shah, K.K. Bhatt, R.S. Mehta, S.L. Baldania, and T.R. Gandhi, Ind. J. Pharm. Sci., 5 , 591 (2008)
  • [15] P.K. Kachhadia, A.S. Doshi, and H.S. Joshi, J. AOAC Int., 91 , 557 (2008)
  • [16] S.P. Senthamil, G.K. Veeran, U. Mandal, W.D.S. Solomon, and T.K. Pal, J. Chromatogr, B, 858 , 143 (2007)
  • [17] N.V.S. Ramakrishna, K.N. Vishwottam, M. Koteshwara, S. Manoj, M. Santosh, and D.P. Verma, J. Pharm. Biomed. Anal., 39 , 1006 (2005)
  • [18] L.J. Patel, B.N. Suhagia, and P.B. Shah, Indian J. Pharm. Sci., 69 , 594 (2007)
  • [19] ICH, Q2(R1): Validation of Analytical Procedures: Text and Methodology, Geneva, (2005)
  • [20] ICH, Q1A(R2): Stability Testing of New Drug Substances and Products (Second revision), Geneva, (2003)
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-825293a8-5997-4efd-aa83-0dd24ab8cbd4
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