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Volumn 877, Issue 8-9, 2009, Pages 791-798

Development and validation of a high throughput and robust LC-MS/MS with electrospray ionization method for simultaneous quantitation of diltiazem and its two metabolites in human plasma: Application to a bioequivalence study

Author keywords

Acquity; Diltiazem; Human plasma; LC MS MS; N desmethylediltiazem; O desacetylediltiazem; UPLC

Indexed keywords

ACETONITRILE; AMMONIUM COMPOUNDS; BIOMOLECULES; CHROMATOGRAPHIC ANALYSIS; ETHERS; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HIGH PRESSURE LIQUID CHROMATOGRAPHY; IONIZATION; LIQUIDS; MASS SPECTROMETRY; METABOLISM; METABOLITES; PLASMA (HUMAN); PLASMAS; SOLVENT EXTRACTION; THROUGHPUT;

EID: 61549099282     PISSN: 15700232     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jchromb.2009.02.016     Document Type: Article
Times cited : (20)

References (16)
  • 13
    • 61549093101 scopus 로고    scopus 로고
    • Guidance for Industry, Bioanalytical Method Validation, US Department of Health and Human Services Food and Drug Administration, Center for Drug Evaluation and Research (CDER), 2001 Center for Veterinary
    • May
    • Guidance for Industry, Bioanalytical Method Validation, US Department of Health and Human Services Food and Drug Administration, Center for Drug Evaluation and Research (CDER), 2001 Center for Veterinary Medicine (CV), May 2001. http://www/fda.gov/cder/guidance/index.htm.
    • (2001) Medicine , vol.105


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.