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Fast and Sensitive RP-HPLC—Fluorescence Method for the Quantitative Analysis of Moxifloxacin in Rat Plasma and Its Application to a Preclinical Pharmacokinetic Study

Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
A fast, simple, and sensitive reversed-phase high-performance liquid chromatography (RP-HPLC) method has been developed and fully validated for the determination of moxifloxacin (MXF) in rat plasma. MXF and gatifloxacin (internal standard, I.S.) were extracted from plasma by single-step protein precipitation with acidified acetonitrile. Chromatographic separation was accomplished in less than 8 min on an Atlantis ® T3 column with 0.4% aqueous triethylamine–methanol–acetonitrile (60:35:5, v/v/v) solution as mobile phase. Detection was achieved by fluorescence (λexcitation = 295 nm, λemission = 500 nm), and the calibration curves were found to be linear over the plasma concentration range of 10–2,500 ng mL−1 with a mean correlation coefficient (r) of 0.9946 (n = 6). The intra- and inter-assay imprecision (% CV) was less than 2.4 and 3.3%, respectively, and the accuracy was >90%. The mean extraction recoveries for MXF and I.S. from plasma were 77 and 82%, respectively. The method was also validated for specificity, sensitivity, and stability; all the results were within the acceptable range. The proposed method was then successfully applied to the quantitative analysis of MXF in rat plasma samples, being a valuable and high-throughput assay to support ongoing pharmacokinetic studies on this promising anti-infective agent.
Słowa kluczowe
Rocznik
Strony
175--191
Opis fizyczny
Bibliogr. 24 poz., rys., tab.
Twórcy
  • Bioanalytical Facility, College of Pharmacy, Federal University of Rio Grande do Sul, Av. Ipiranga 2752, 90610-000 Porto Alegre, RS, Brazil
autor
  • Bioanalytical Facility, College of Pharmacy, Federal University of Rio Grande do Sul, Av. Ipiranga 2752, 90610-000 Porto Alegre, RS, Brazil
autor
  • Bioanalytical Facility, College of Pharmacy, Federal University of Rio Grande do Sul, Av. Ipiranga 2752, 90610-000 Porto Alegre, RS, Brazil
autor
  • Bioanalytical Facility, College of Pharmacy, Federal University of Rio Grande do Sul, Av. Ipiranga 2752, 90610-000 Porto Alegre, RS, Brazil
Bibliografia
  • [1] K. Drlica and X. Zhao, Microbiol. Mol. Biol. Rev., 61, 377 (1997)
  • [2] G. Perletti, F. Wagenlehner, K. Naber, and V. Magrid, Int. J. Antimicrob. Agents, 33, 206 (2009)
  • [3] G. Jain, N. Jain, S. Pathan, S. Akhter, S. Talegaonkar, P. Chander, R. Khar, and F. Ahmad, J. Pharm. Biomed. Anal., 52, 110 (2010)
  • [4] J. Moller, H. Stass, R. Heinig, and G. Blaschke, J. Chromatogr. B, 716, 325 (1998)
  • [5] K. Vishwanathan, M. Bartlett, and J. Stewart, J. Pharm. Biomed. Anal., 30, 961 (2002)
  • [6] J. De Smet, K. Boussery, K. Colpaer, P. De Sutter, P. De Paepe, J. Decruyenaere, and J. Van Bocxlaer, J. Chromatogr. B: Anal. Technol. Biomed. Life Sci., 877, 961 (2009)
  • [7] K. Chan, K. Chu, W. Lai, K. Choy, C. Wang, D. Lam, and C. Pang, Anal. Biochem., 353, 30 (2006)
  • [8] N. Srinivas, L. Narasu, B.P. Shankar, and R. Mullangi, Biomed. Chromatogr., 22, 1288 (2008)
  • [9] Y. Xu, D. Li, X. Liu, Y. Li, and J. Lu, J. Chromatogr. B: Anal. Technol. Biomed. Life Sci., 878, 3437 (2010)
  • [10] T. Lemoine, D. Breilh, D. Ducint, J. Dubrez, J. Jougon, J.F. Velly, and M.C. Saux, J. Chromatogr. B: Biomed. Sci. Appl., 742, 247 (2000)
  • [11] E. Nemutlu, S. Kir, O. Ozyuncu, and M. Beksac, Chromatographia, 66, S15 (2007)
  • [12] H.A. Nguyen, J. Grellet, B.B. Ba, C. Quentin, and M.C. Saux, J. Chromatogr. B: Anal. Technol. Biomed. Life Sci., 810, 77 (2004)
  • [13] H. Stass and A. Dalhoff, J. Chromatogr. B: Biomed. Sci. Appl., 702, 163 (1997)
  • [14] S. Schulte, T. Ackermann, N. Bertram, T. Sauerbruch, and W.D. Paar, J. Chromatogr. Sci., 44, 205 (2006)
  • [15] L. Baietto, A. D'Avolio, F.G. De Rosa, S. Garazzino, S. Patanella, M. Siccardi, M. Sciandra, and G. Di Perri, Ther. Drug Monit., 31, 104 (2009)
  • [16] A.K. Hemanth Kumar and G. Ramachandran, J. Chromatogr. B: Anal. Technol. Biomed. Life Sci., 877, 1205 (2009)
  • [17] A. Laban-Djurdjevic, M. Jelikic-Stankov, and P. Djurdjevic, J. Chromatogr. B: Anal. Technol. Biomed. Life Sci., 844, 104 (2006)
  • [18] S. Bansal and A. DeStefano, AAPS J., 9, E109 (2007)
  • [19] R. Causon, J. Chromatogr. B: Biomed. Sci. Appl., 689, 175 (1997)
  • [20] U.S. Food and Drug Administration (FDA), 2001. Guidance for Industry: Bioanalytical Method Validation. Available at: http://www.fda.gov/downloads/Drugs/Guidances/ucm070107.pdf
  • [21] J. Gonzalez, M. Mochon, and F. de la Rosa, Talanta, 52, 1149 (2000)
  • [22] F.K. Hurtado, B. Weber, H. Derendorf, G. Hochhaus, and T. Dalla Costa, Antimicrob. Agents Chemother., 58, 678 (2014)
  • [23] H.M. Siefert, A. Domdey-Bette, K. Henninger, F. Hucke, C. Kohlsdorfer, and H.H. Stass, J. Antimicrob. Chemother., 43, 69 (1999)
  • [24] J. Sousa, G. Alves, A. Fortuna, and A. Falcão, Anal. Bioanal. Chem., 403, 93 (2012)
Uwagi
PL
Opracowanie ze środków MNiSW w ramach umowy 812/P-DUN/2016 na działalność upowszechniającą naukę.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-e0019b46-7cb3-471c-9965-a3c3f7d288da
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