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Volumn 877, Issue 8-9, 2009, Pages 680-688

Stability evaluation and sensitive determination of antiviral drug, valacyclovir and its metabolite acyclovir in human plasma by a rapid liquid chromatography-tandem mass spectrometry method

Author keywords

Acyclovir; Bench top stability; High throughput; LC ESI MS MS; Solid phase extraction; Valacyclovir

Indexed keywords

CHROMATOGRAPHIC ANALYSIS; ELECTROSPRAY IONIZATION; EXTRACTION; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HIGH PRESSURE LIQUID CHROMATOGRAPHY; LIQUIDS; MASS SPECTROMETERS; MASS SPECTROMETRY; METHANOL; ORGANIC ACIDS; PLASMA (HUMAN); PLASMAS; SPECTRUM ANALYSIS; THROUGHPUT;

EID: 61349201634     PISSN: 15700232     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jchromb.2009.01.042     Document Type: Article
Times cited : (43)

References (38)
  • 31
    • 61349110250 scopus 로고    scopus 로고
    • Guidance for Industry: Bioanalytical Method Validation, U.S. Department of Health and Human Services, Food and Drug Administration Centre for Drug Evaluation and Research (CDER), Centre for Veterinary Medicine (CVM) 2001.
    • Guidance for Industry: Bioanalytical Method Validation, U.S. Department of Health and Human Services, Food and Drug Administration Centre for Drug Evaluation and Research (CDER), Centre for Veterinary Medicine (CVM) 2001.
  • 33
    • 39549088409 scopus 로고    scopus 로고
    • FDA Guidance for Industry:, U.S. Department of Health and Human Services, Food and Drug Administration Centre for Drug Evaluation and Research CEDR
    • FDA Guidance for Industry: Bioavailability Studies for Orally Administered Drug Products-General Considerations, U.S. Department of Health and Human Services, Food and Drug Administration Centre for Drug Evaluation and Research (CEDR), 2000.
    • (2000) Bioavailability Studies for Orally Administered Drug Products-General Considerations


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.