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Impurity profile study of capecitabine

Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
Five new peaks of potential impurities, ranging from 0.05 to 0.12% on an area-percent basis, have been observed in reversed-phase high-performance liquid chromatography of capecitabine drug substance. On the basis of comparison of relative retention times and mass values two of the impurities were identified as intermediates in the process used for synthesis of capecitabine and were characterized as (2-(4-amino-5-fluoro-2-oxopyrimidin-1(2 H )-yl)-5-methyltetrahydrofuran-3,4-diyl diacetate and 2-(5-fluoro-2-oxo-4-(pentyloxycarbonylamino)pyrimidin-1(2 H )-yl)-5-methyl tetrahydrofuran-3,4-diyl diacetate. The area percentages of two of the other peaks increased substantially when the drug was treated with acid and base. The three compounds other than the two intermediates were isolated by preparative HPLC with gradient elution and were characterized by use of spectroscopic techniques, viz. MS-MS, FTIR, and NMR ( 1 H, 13 C and DEPT). On the basis of the spectral data, the structures 5?-deoxy-5-fluorocytidine, 5?-deoxy-5-fluorouridine, and 2-(4-(bis(pentyloxycarbonyl)amino)-5-fluoro-2-oxopyrimidin-(2 H )-yl)-5-methyltetrahydrofuran-3,4-diyl diacetate were proposed for the three impurities.
Rocznik
Strony
609--624
Opis fizyczny
Bibliogr. 17 poz., rys., tab.
Twórcy
autor
  • University of Mysore Department of Chemistry Manasagangothri, Mysore 570006 Karnataka India, hiriyannag@gmail.com
Bibliografia
  • [1] A.A. Adjei, Br. J. Clin. Pharmacol., 48 , 265–277 (1999)
  • [2] L. Zufia, A. Aldaz, and J. Giraldez, J. Chromatogr. B, 809 , 51–58 (2004)
  • [3] R. Diasio, Drugs, 58 ,Supplement 3, 119–126 (1999)
  • [4] F.G.A. Jansman, M.J. Postma, D.V. Hartskamp, P.H.B. Willemse, and J.R.B.J. Brouwers, Clin. Ther., 26 , 579–589 (2004)
  • [5] B. Reigner, J. Verweij, L. Dirix, J. Cassidy, C. Twelves, D. Allman, E. Weidekamm, B. Roos, L. Banken, M. Utoh, and B. Osterwalder, Clin. Cancer Res., 4 , 941–948 (1998)
  • [6] W. Scheithauer, J. McKendrick, S. Begbie, M. Borner, W.I. Burns, H.A. Burris, J. Cassidy, D. Jodrell, P. Koralewski, E.L. Levine, N. Marschner, J. Maroun, P. Garcia-Alfonso, J. Tujakowski, G. Van Hazel, A. Wong, J. Zaluski, and C. Twelves, Ann. Oncol., 14 , 1735–1743 (2003)
  • [7] W. Scheithauer, G.V. Kornek, M. Raderer, B. Schull, K. Schmid, E. Kovats, B. Schneeweiss, F. Lang, A. Lenauer, and D. Depisch, J. Clin. Oncol., 21 , 1307–1312 (2003)
  • [8] S.M. Guichard, I. Mayer, and D.I. Jodrell, J. Chromatogr. B, 826 , 232–237 (2005)
  • [9] M.R. Dhananjeyan, J. Liu, C. Bykowski, J.A. Trendel, J.G. Sarver, H. Ando, and P.W. Erhardt, J. Chromatogr. A, 1138 , 101–108 (2007)
  • [10] X.U. Yan and J.L. Grem, J. Chromatogr. B, 783 , 273–285 (2003)
  • [11] A. Salvador, L. Millerioux, and A. Renou, Chromatographia 63 , 609–615 (2006)
  • [12] F. Desmoulin, V. Gilard, R. Martino, and M. Malet-Martino, J. Chromatogr. B, 792 , 323–332 (2003)
  • [13] R. Martino, V. Gilard, F. Desmoulin, and M. Malet-Martino, J. Pharm. Biomed. Anal., 38 , 871–891 (2005)
  • [14] M. Malet-Martino, V. Gilard, F. Desmoulin, and R. Martino, Clin. Chim. Acta, 366 , 61–73 (2006)
  • [15] International Conference on Harmonization, Draft Revised Guidance on Impurities in New Drug Substances. Q3A(R). Federal Register, 65 , 45085–45090 (2000)
  • [16] ICH Draft Guidelines on Validation of Analytical Procedures: Definitions and Terminology, IFPMA, Switzerland, Federal Register, 60 , 11260 (1995)
  • [17] M. Arasaki, H. Ishitsuka, I. Kuruma, M. Miwa, C. Murasaki, N. Shimma, and I. Umeda, United States Patent 5472949, Dec. 5, 1995.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-article-BATE-0001-0046
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