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Simultaneous TLC-densitometric analysis of atenolol and lercanidipine hydrochloride in tablets

Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
A new simple, precise, accurate, and selective thin-layer chromatographic (TLC) method has been developed for simultaneous analysis of atenolol and lercanidipine hydrochloride in a tablet dosage form. Chromatographic separation was achieved on aluminum foil plates precoated with silica gel 60F 254 , with toluene-methanoltriethylamine 3.5:1.5:0.1 (v/v) as mobile phase. Detection was performed densitometrically at 275 nm. The R F of atenolol and lercanidipine hydrochloride were 0.24 and 0.68, respectively. The reliability of the method was assessed by evaluation of linearity (2000-12000 ng per band for atenolol and 400-2400 ng per band for lercanidipine hydrochloride), accuracy (98.94 š 0.30% for atenolol and 99.75 š 0.69% for lercanidipine hydrochloride), and specificity, in accordance with ICH guidelines. The method can be used for routine simultaneous analysis of atenolol and lercanidipine hydrochloride in pharmaceutical formulations.
Rocznik
Strony
463--473
Opis fizyczny
Bibliogr. 17 poz., rys., tab.
Twórcy
autor
autor
Bibliografia
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  • [2] Indian Pharmacopoeia, Government of India, Ministry of Health and Family Welfare, Controller of Publications, Delhi, 1996, pp. 72–73
  • [3] British Pharmacopoeia, Vol. I, The stationary office, London, 2005, pp. 179–181
  • [4] United States Pharmacopeia, 28th edn, The United States Pharmacopeial Convention, Rockville, MD, 2005, p. 193
  • [5] A.V. Kasture and M. Ramteke, Indian J. Pharm. Sci., 68 (3), 394 (2006)
  • [6] S.M. Al-Ghannam, J. Pharm. Biomed. Anal., 40 , 151 (2006)
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  • [8] R.K. Barman, M.A. Islam, M. Ahmad, M.I. Ibnewahed, R. Islam, A. Khan, M.B. Hossain, and B.M. Rahman, Pak. J. Pharm. Sci., 20 (4), 274 (2007)
  • [9] L.R.P. de Abreu, S.A.C. de Castro, and J. Pedrazzoli Jr., AAPS Pharm. Sci. 5 (2), article 21 (2003)
  • [10] A.P. Argekar and S.G. Powar, J. Pharm. Biomed. Anal., 21 (6), 1137 (2000)
  • [11] S.R. Sathe and S.B. Bari, Acta Chromatogr., 19 , 270 (2007)
  • [12] S.C. Sweetman (Ed.) Martindale — The Complete Drug Reference, Vol. I, Pharmaceutical Press, 2007, p. 1189
  • [13] A.A. Shirkhedkar, P.V. Deore, and S.J. Surana, Biosci. Biotech. Res. Asia, 4 (2), 753 (2007)
  • [14] S. Mihaljica, D. Radulovic, and J. Trbojevic, Chromatographia, 61 (1/2), 25 (2005)
  • [15] A. Alvarez-Lueje, S. Pujol, J.A. Squella, and L.J. Nunez-Vergara, J. Pharm. Biomed. Anal., 31 , 1 (2003)
  • [16] I.I. Salem, J. Idrees, J.I. Al Tamimi, and P. Farina, J. Chromatogr. B, 803 , 201 (2004)
  • [17] ICH Guidelines Q2B, Validation of Analytical Procedures — Methodology, 1996.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-article-BATE-0001-0036
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