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Volumn 877, Issue 5-6, 2009, Pages 471-476

Remediation of undesirable secondary interactions encountered in hydrophilic interaction chromatography during development of a quantitative LC-MS/MS assay for a dipeptidyl peptidase IV (DPP-IV) inhibitor in monkey serum

Author keywords

Bioanalysis; Dipeptidyl peptidase IV (DPP IV) inhibitor; HILIC; Hydrophilic interaction chromatography; LC MS MS

Indexed keywords

BODY FLUIDS; CHROMATOGRAPHIC ANALYSIS; CHROMATOGRAPHY; ETHYLENE; ETHYLENE GLYCOL; EXTRACTION; GLYCOLS; HYDROPHILICITY; MILITARY ENGINEERING; SUGAR (SUCROSE);

EID: 59249105097     PISSN: 15700232     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jchromb.2008.11.048     Document Type: Article
Times cited : (12)

References (24)
  • 15
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    • ACD/pKa DB, ACD/Labs Release: 9.00, Product Version 9.04, Advanced Chemistry Development, Inc., Copyright © 1997-2005.
    • ACD/pKa DB, ACD/Labs Release: 9.00, Product Version 9.04, Advanced Chemistry Development, Inc., Copyright © 1997-2005.
  • 16
    • 59249094846 scopus 로고    scopus 로고
    • ACD/LogD, ACD/Labs Release 9.00, Product Version 9.03, Advanced Chemistry Development, Inc., Copyright © 1997-2005.
    • ACD/LogD, ACD/Labs Release 9.00, Product Version 9.03, Advanced Chemistry Development, Inc., Copyright © 1997-2005.
  • 17
    • 59249084102 scopus 로고    scopus 로고
    • Guidance for Industry, Bioanalytical Method Validation, U.S. Food and Drug Administration, May 2001.
    • Guidance for Industry, Bioanalytical Method Validation, U.S. Food and Drug Administration, May 2001.
  • 21
    • 23144465464 scopus 로고    scopus 로고
    • N. Seedher, S. Bhatia, AAPS PharmSci Tech. 2003 4 (2004) (issue 3) Article 33.
    • N. Seedher, S. Bhatia, AAPS PharmSci Tech. 2003 4 (2004) (issue 3) Article 33.
  • 23
    • 59249100126 scopus 로고    scopus 로고
    • Center for Drug Evaluation and Research, U.S. Food and Drug Administration, Reviewer Guidance, Validation of Chromatographic Methods, FDA, Rockville, MD, November 1994.
    • Center for Drug Evaluation and Research, U.S. Food and Drug Administration, Reviewer Guidance, Validation of Chromatographic Methods, FDA, Rockville, MD, November 1994.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.