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Volumn 22, Issue 6, 2008, Pages 645-653

Development and validation of a sensitive LC-MS/MS method with electrospray ionization for quantitation of zafirlukast, a selective leukotriene antagonist in human plasma: Application to a clinical pharmacokinetic study

Author keywords

Human plasma; LC MS MS; Pharmacokinetics; Validation; Zafirlukast

Indexed keywords

PHARMACOKINETICS; PLASMA (HUMAN);

EID: 46949106905     PISSN: 02693879     EISSN: 10990801     Source Type: Journal    
DOI: 10.1002/bmc.983     Document Type: Article
Times cited : (15)

References (10)
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    • Determination of zafirlukast, a selective leukotriene antagonist, human plasma by normal-phase high-performance liquid chromatography with fluorescence detection
    • Bui KH, Kennedy CM, Azumaya CT and Birmingham BK. Determination of zafirlukast, a selective leukotriene antagonist, human plasma by normal-phase high-performance liquid chromatography with fluorescence detection. Journal of Chromatography B 1997; 696: 131-136.
    • (1997) Journal of Chromatography B , vol.696 , pp. 131-136
    • Bui, K.H.1    Kennedy, C.M.2    Azumaya, C.T.3    Birmingham, B.K.4
  • 2
    • 0142195729 scopus 로고    scopus 로고
    • Matrix effect in bio-analysis of illicit drugs with LC-MS/MS: Influence of ionization type, sample preparation, and biofluid
    • Dams R, Huestis MA, Lambert WE and Murphy CM. Matrix effect in bio-analysis of illicit drugs with LC-MS/MS: influence of ionization type, sample preparation, and biofluid. Journal of the American Society for Mass Spectrometry 2003; 14: 1290-1294.
    • (2003) Journal of the American Society for Mass Spectrometry , vol.14 , pp. 1290-1294
    • Dams, R.1    Huestis, M.A.2    Lambert, W.E.3    Murphy, C.M.4
  • 6
    • 85165064198 scopus 로고    scopus 로고
    • Hubert Ph, Chiap P, Crommen J, Boulanger B, Chapuzet E, Mercier N, Bervoas-Martin S, Chevalier P, Grandjean D, Lagorce P, Lallier M, Laparra MC, Laurentie M and Nivet JC. The SFSTP guide on the validation of chromatographic methods for drug bioanalysis Washington conférence to the laboratory. Analytica Chimica Acta 1999; 391: 135-148.
    • Hubert Ph, Chiap P, Crommen J, Boulanger B, Chapuzet E, Mercier N, Bervoas-Martin S, Chevalier P, Grandjean D, Lagorce P, Lallier M, Laparra MC, Laurentie M and Nivet JC. The SFSTP guide on the validation of chromatographic methods for drug bioanalysis Washington conférence to the laboratory. Analytica Chimica Acta 1999; 391: 135-148.
  • 8
    • 33845794814 scopus 로고    scopus 로고
    • A reversed-phase high-performance liquid chromatographic method for the determination of zafirlukast in pharmaceutical formulations and human plasma
    • Suslu I and Altinoz S. A reversed-phase high-performance liquid chromatographic method for the determination of zafirlukast in pharmaceutical formulations and human plasma. Journal of AOAC International 2006; 89: 1557-1564.
    • (2006) Journal of AOAC International , vol.89 , pp. 1557-1564
    • Suslu, I.1    Altinoz, S.2
  • 9
    • 34047248373 scopus 로고    scopus 로고
    • Optimisation, validation and application of a capillary electrophoretic method for the determination of zafirlukast in pharmaceutical formulations
    • Suslu I, Demircan S, Altinoz S and Kir S. Optimisation, validation and application of a capillary electrophoretic method for the determination of zafirlukast in pharmaceutical formulations. Journal of Pharmaceutical and Biomedical Analysis 2007; 44: 16-22.
    • (2007) Journal of Pharmaceutical and Biomedical Analysis , vol.44 , pp. 16-22
    • Suslu, I.1    Demircan, S.2    Altinoz, S.3    Kir, S.4
  • 10
    • 85165017405 scopus 로고    scopus 로고
    • US DHHS, FDA, CDER. Guidance for Industry: Bioanalytical Method Validation. US Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research, Center for Veterinary Medicine, 2001. Available at: www/fda.gov/cder/guidance/ index.htm
    • US DHHS, FDA, CDER. Guidance for Industry: Bioanalytical Method Validation. US Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research, Center for Veterinary Medicine, 2001. Available at: www/fda.gov/cder/guidance/ index.htm


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.