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A validated densitometric TLC method for analysis of cefuroxime axetil and potassium clavulanate in combined tablet dosage forms

Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
A simple, specific, accurate, and precise high-performance thin-layer chromatographic method for analysis of cefuroxime axetil and potassium clavulanate in a combined tablet dosage form is reported. The compounds were separated on aluminium foil plates precoated with silica gel 60 F 254 , with chloroform-methanol-toluene 4:3:3 ( v / v ) as mobile phase. Densitometric evaluation of the separated bands was performed at 225 nm. The two drugs were satisfactorily separated with R F 0.77 ± 0.0114 and 0.29 ± 0.0114 for cefuroxime axetil and potassium clavulanate, respectively. Response was a linear function of amount over the calibration ranges 500–2500 and 2000–10 000 ng per band, respectively. The method was successfully validated and used for analysis of the drugs in a pharmaceutical formulation. Recovery was 100.05 ± 0.98% for cefuroxime axetil and 99.94 ± 0.538% for potassium clavulanate (mean ± RSD).
Rocznik
Strony
91--97
Opis fizyczny
Bibliogr. 14 poz., rys., tab.
Twórcy
autor
  • A.I.S.S.M.S. College of Pharmacy Department of Pharmaceutical Analysis Kennedy Road Pune 411001 India
autor
  • A.I.S.S.M.S. College of Pharmacy Department of Pharmaceutical Analysis Kennedy Road Pune 411001 India
autor
  • A.I.S.S.M.S. College of Pharmacy Department of Pharmaceutical Analysis Kennedy Road Pune 411001 India
autor
  • A.I.S.S.M.S. College of Pharmacy Department of Pharmaceutical Analysis Kennedy Road Pune 411001 India
  • A.I.S.S.M.S. College of Pharmacy Department of Pharmaceutical Analysis Kennedy Road Pune 411001 India
Bibliografia
  • [1] http://www.rxlist.com/cgi/generic/cefurox.htm accessed on 20.09.08
  • [2] S.M. Foroutan, A. Zarghi, A. Shafaati, A. Khoddamc, H. Movahed, J. Pharm. Biomed. Anal., 45 , 531 (2007)
  • [3] S.V. Chaudhary, A. Karnik, A. Adhikary, R.S. Tandale, P.R. Vavia, Indian J. Pharm. Sci., 68 , 59 (2006)
  • [4] N.J. Shah, S.K. Shah, V.F. Patel, N.M. Patel, Indian J. Pharm. Sci., 69 , 140 (2007)
  • [5] J. Krzekand, M.D. Browska-Tylka, Chromatographia, 58 , 231 (2003)
  • [6] J. Ivana, Z. Ljiljana, Z. Mira, J. Chromatogr. A, 1119 , 209 (2006)
  • [7] O.C. Nafiz, A. Goksel, Y. Hassan, A. Aboul-Enein, E. Gindy, Anal. Chim. Acta, 576 , 246 (2006)
  • [8] M.T. Rosseel, R. Peleman, H.V. Hoorebeke, R.A. Pauwels, J. Chromatogr. B, 689 , 438 (1997)
  • [9] G. Hoizey, D. Lamiable, C. Frances, T. Trenque, M. Kaltenbach, J. Denis, H. Millart, J. Pharm. Biomed. Anal., 30 , 661 (2002)
  • [10] L. Valvo, L. Manna, R. Alimenti, S. Alimonti, P. Bertocchi, E. Ciranni, J. Pharm. Biomed. Anal., 21 , 9 (1999)
  • [11] S.M. Foroutan, A. Zarghi, A. Shafaati, A. Khoddamc, H. Movahed, J. Pharm. Biomed. Anal., 45 , 531 (2007)
  • [12] T. Tsou, J. Wu, C. Young, T. Wang, J. Pharm. Biomed. Anal., 15 , 1197 (1997)
  • [13] A.J. Shah, M.W. Adlard, J.D. Stride, J. Pharm. Biomed. Anal., 8 , 437 (1990)
  • [14] ICH harmonised tripartite guideline, Q2 (R1), Validation of analytical procedures: Text and Methodology, Geneva, Nov, 2005
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-ba32aee6-5eee-4d82-8e1c-5c46b0a7698f
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