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Volumn 7, Issue 1, 2010, Pages 25-36

Rapid, sensitive and validated ultra-performance liquid chromatography/mass spectrometric method for the determination of fenofibric acid and its application to human pharmacokinetic study

Author keywords

Fenofibric acid; LC MS MS; Lipid regulating agent; Pharmacokinetics; Validation

Indexed keywords


EID: 77649319341     PISSN: None     EISSN: 09734945     Source Type: Journal    
DOI: 10.1155/2010/726124     Document Type: Article
Times cited : (4)

References (15)
  • 7
    • 85036776813 scopus 로고    scopus 로고
    • Guidance for Industry: Bioavailability and Bioequivalence Studies for Orally Administered Drug Products-General Considerations, 2003
    • Guidance for Industry: Bioavailability and Bioequivalence Studies for Orally Administered Drug Products-General Considerations, 2003.
  • 8
    • 85036783374 scopus 로고    scopus 로고
    • Method Validation for Extemporaneous Pediatric Formulation Prototypes of Quinapril Hydrochloride/ Assay and Stability Method. Pfizer Global Research and Development, Ann Arbor, Michigan, November, 2001
    • Method Validation for Extemporaneous Pediatric Formulation Prototypes of Quinapril Hydrochloride/ Assay and Stability Method. Pfizer Global Research and Development, Ann Arbor, Michigan, November, 2001.
  • 9
    • 85036772989 scopus 로고    scopus 로고
    • Validation of Analytical Procedures: Methodology, ICH-Q2B, International Conference on Harmonization of Technical Requirements for the Registration of Pharmaceuticals for Human Use, Geneva, Switzerland, 1996
    • Validation of Analytical Procedures: Methodology, ICH-Q2B, International Conference on Harmonization of Technical Requirements for the Registration of Pharmaceuticals for Human Use, Geneva, Switzerland, 1996.
  • 10
    • 85036780450 scopus 로고    scopus 로고
    • Guidance for Industry: Analytical Procedures and Method Validation, U.S. Food and Drug Administration, Center for Drug Evaluation and Research, Rockville, Maryland, 2000
    • Guidance for Industry: Analytical Procedures and Method Validation, U.S. Food and Drug Administration, Center for Drug Evaluation and Research, Rockville, Maryland, 2000.
  • 11
    • 85036787236 scopus 로고    scopus 로고
    • Validation of Analytical Methods for Drug Products, Pfizer Global Research and Development, Ann Arbor, Michigan, 2001
    • Validation of Analytical Methods for Drug Products, Pfizer Global Research and Development, Ann Arbor, Michigan, 2001.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.