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Volumn 93, Issue 5, 2010, Pages 1462-1467

Simple and rapid RP-HPLC method for simultaneous determination of acyclovir and zidovudine in human plasma

Author keywords

[No Author keywords available]

Indexed keywords

DRUG DOSAGE; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HIGH PRESSURE LIQUID CHROMATOGRAPHY; ORTHOPHOSPHORIC ACID; PARTICLE SIZE; PRECIPITATION (CHEMICAL); VIRUSES;

EID: 78651477669     PISSN: 10603271     EISSN: None     Source Type: Journal    
DOI: 10.1093/jaoac/93.5.1462     Document Type: Article
Times cited : (12)

References (18)
  • 1
    • 0004074875 scopus 로고    scopus 로고
    • 33rd Ed., S.C. Sweetmann (Ed.), The Pharmaceutical Press, London, UK
    • Martindale: The Complete Drug Reference (2002) 33rd Ed., S.C. Sweetmann (Ed.), The Pharmaceutical Press, London, UK
    • (2002) Martindale: The Complete Drug Reference
  • 2
    • 78651506585 scopus 로고    scopus 로고
    • The Controller of Publications, New Delhi, India
    • Indian Pharmacopoeia-Addendum (2002) The Controller of Publications, New Delhi, India
    • (2002) Indian Pharmacopoeia-Addendum
  • 3
    • 0003986004 scopus 로고    scopus 로고
    • 4th Ed., Jaypee Brothers Medical Publishers, New Delhi, India
    • Tripathi, K.D. (1999) Essentials of Medical Pharmacology, 4th Ed., Jaypee Brothers Medical Publishers, New Delhi, India
    • (1999) Essentials of Medical Pharmacology
    • Tripathi, K.D.1
  • 4
    • 38949098548 scopus 로고    scopus 로고
    • The Department of Health, Social Services, and Public Safety, London, UK
    • British Pharmacopoeia (2003) The Department of Health, Social Services, and Public Safety, London, UK
    • (2003) British Pharmacopoeia
  • 17
    • 0035950020 scopus 로고    scopus 로고
    • Guidance for Industry, Bioanalytical Method Validation, U.S. Food and Drug Administration
    • Guidance for Industry, Bioanalytical Method Validation (2001) U.S. Food and Drug Administration, Fed. Regist. 66, 49028-49029
    • (2001) Fed. Regist. , vol.66 , pp. 49028-49029
  • 18
    • 33646551011 scopus 로고    scopus 로고
    • The European Agency for the Evaluation of Medicinal Products, Committee for Proprietary Medicinal Products, CPMP/EWP/QWP/1401/98
    • Guidance on the Investigation of Bioavailability and Bioequivalence (2001) The European Agency for the Evaluation of Medicinal Products, Committee for Proprietary Medicinal Products, CPMP/EWP/QWP/1401/98
    • (2001) Guidance on the Investigation of Bioavailability and Bioequivalence


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.