PL EN


Preferencje help
Widoczny [Schowaj] Abstrakt
Liczba wyników
Tytuł artykułu

Computer-assisted optimization of liquid-liquid extraction for HPLC analysis of domperidone and pantoprazole in human plasma

Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
This paper deals with optimization of a liquid-liquid extraction procedure for simultaneous HPLC analysis of domperidone and pantoprazole in human plasma. Central composite design and Derringer’s desirability function were used to optimize the concentration of KOH and the volume of ethyl acetate as the main factors affecting the liquid-liquid extraction procedure. After extraction, the analytes were separated quantitatively on a C 18 column with 10 mM pH 7.0 phosphate buffer-methanol-acetonitrile 48.46:20:31.54 ( υ / υ ) as mobile phase at a flow rate of 1.20 mL min -1 and with UV detection at 285 nm. It was concluded that extraction recovery of both the analytes was affected by KOH concentration and that recovery of pantoprazole was affected by ethyl acetate (extraction solvent) volume. Extraction recovery under optimum extraction conditions was 93.52% for domperidone and 92.72% for pantoprazole. The optimized extraction method was validated. Linearity was established for six levels in the ranges 10–1000 ng mL -1 for pantoprazole and 15–1000 ng mL -1 for domperidone. The lower limit of quantitation (LLOQ) and detection (LOD) were estimated as 9.84 and 5.91 ng mL -1 , respectively, for pantoprazole and 14.56 and 8.79 ng mL -1 for domperidone. The optimized method was linear, specific, accurate, and precise; the high recovery (>92%) and low relative standard deviation (<2.5%) enable reliable quantification of these analytes in spiked human plasma.
Rocznik
Strony
549--562
Opis fizyczny
Bibliogr. 27 poz., rys., tab.
Twórcy
autor
autor
  • Annamalai University Department of Pharmacy, Faculty of Engineering and Technology Annamalainagar, Tamil Nadu 608 002 India, kvalliappan@gmail.com
Bibliografia
  • [1] Fitton and L. Wiseman, Drugs, 51 , 460 (1995)
  • [2] J.A. Barone, Ann. Pharmacother., 33 , 429 (1999)
  • [3] R. Huber, W. Muller, M.C. Banks, S.J. Rogers, P.C. Norwood, and E. Doyle, J. Chromatogr., 529 , 389 (1990)
  • [4] N.V.S. Ramakrishna, K.N. Vishwottam, S. Wishu, and M. Koteshwara, J. Chromatogr. B, 822 , 326 (2005)
  • [5] M. Tanaka and H. Yamazaki, Anal, Chem., 68 , 1513 (1996)
  • [6] Q.B. Cass, A.L.G. Degani, N.M. Cassiano, and J. Pedrazolli Jr, J. Chromatogr. B, 766 , 153 (2001)
  • [7] O. Peres, C.H. Oliveira, A.R.E. Barrientos, V.M. Rezende, and G. de-Nucci, Arzneimittelforschung, 54 , 314 (2004)
  • [8] I. Heykants, R. Hendriks, W. Meuldermans, M. Michiels, H. Scheygrond, and H. Reyntjens, Eur. J. Drug Metab. Pharmacokinet., 6 , 61 (1981)
  • [9] Y.C. Huang, J.L. Colaizzi, R.H. Bierman, R. Woestenborghs, and J.J. Heykants, J. Clin. Pharmacol., 26 , 628 (1986)
  • [10] W. Meuldermans, R. Hurkmans, E. Swysen, J. Hendricks, M. Michiels, W. Lauwers, and J. Heykants, Eur. J. Drug Metab. Pharmacokinet., 6 , 49 (1981)
  • [11] M. Michiels, R. Hendriks, and J. Heykants, Eur. J. Drug Metab. Pharmacokinet., 6 , 37 (1981)
  • [12] K. Yamamoto, M. Hagino, H. Kotaki, and T. Iga, J. Chromatogr. B, 720 , 251(1998)
  • [13] M. Kobylinska and K. Kobylinska, J. Chromatogr. B, 744 , 207 (2000)
  • [14] A.P. Zavitsanos, C. MacDonald, E. Bassoob, and D. Gopaul, J. Chromatogr. B, 730 , 9 (1999)
  • [15] M.J. Smit, F.C.W. Sutherland, H.K.L. Hundt, K.J. Swart, A.F. Hundt, and J. Els, J. Chromatogr. A, 949 , 65 (2002)
  • [16] M.J. Sáiz-Abajo, J.M. González-Sáiz, and C. Pizarro, Anal. Chim. Acta, 528 , 63 (2005)
  • [17] T. Sivakumar, R. Manavalan, and K. Valliappan, Acta Chromatogr., 19 , 29 (2007)
  • [18] T. Sivakumar, R. Manavalan, C. Muralidharan, and K. Valliappan, J. Sep. Sci., 30 , 3143 (2007)
  • [19] T. Sivakumar, R. Manavalan, C. Muralidharan, and K. Valliappan, J. Pharm. Biomed. Anal., 43 , 1842 (2007)
  • [20] FDA-Center for Drug Evaluation and Research (CDER): Guidance for industry, Bioanalytical method validation, 2001
  • [21] S. Mitra (Ed.) Sample Preparation Techniques in Analytical Chemistry, John Wiley and Sons, Hoboken, New Jersey, 2003, pp. 37–138
  • [22] A. Jadoul and V. Préat, Int. J. Pharm., 154 , 229 (1997)
  • [23] K. Florey (Ed.) Analytical Profiles of Drug Substances and Excipients, Elsevier Science, New York, 2002, pp. 213–259
  • [24] T. Lundstedt, E. Seifert, L. Abramo, B. Thelin, Å. Nyström, J. Pettersen, and R. Bergman, Chemom. Intell. Lab. Syst., 42 , 3 (1998)
  • [25] Q. Beg, V. Sahai, and R. Gupta, Process Biochem., 39 , 203 (2003)
  • [26] G. Derringer and R. Suich, J. Qual. Technol., 12 , 214 (1980)
  • [27] P. Wester, J. Gottfries, K. Johansson, F. Klintebäck, and B. Winblad, J. Chromatogr., 415 , 261 (1987).
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-article-BATE-0001-0041
JavaScript jest wyłączony w Twojej przeglądarce internetowej. Włącz go, a następnie odśwież stronę, aby móc w pełni z niej korzystać.