메뉴 건너뛰기




Volumn 3, Issue 5, 2011, Pages 550-564

In vitro-in vivo correlation: Application in pharmaceutical development of various dosages forms

Author keywords

Bcs; Convolution; Correlation; Deconvolution; Dissolution

Indexed keywords

CONTROLLED RELEASE FORMULATION; CORRELATION ANALYSIS; DISSOLUTION; DRUG BIOAVAILABILITY; DRUG DELIVERY SYSTEM; DRUG DIFFUSION; DRUG DOSAGE FORM; DRUG INDUSTRY; DRUG MANUFACTURE; DRUG MARKETING; DRUG RELEASE; IN VITRO IN VIVO CORRELATION; IN VITRO STUDY; IN VIVO STUDY; MATHEMATICAL MODEL; PREDICTION; REVIEW;

EID: 80053496805     PISSN: None     EISSN: 09757384     Source Type: Journal    
DOI: None     Document Type: Review
Times cited : (8)

References (72)
  • 1
    • 80053463560 scopus 로고    scopus 로고
    • U.S. Department of Health and Human Services. Guidance for industrial. Extended release oral dosage forms: Development, evaluation and application of In vitro/In vivo correlations. Food and Drug Administration, Center for Drug Evaluation and Research (CDER). Rockville, MD
    • U.S. Department of Health and Human Services. Guidance for industrial. Extended release oral dosage forms: Development, evaluation and application of In vitro/In vivo correlations. Food and Drug Administration, Center for Drug Evaluation and Research (CDER). Rockville, MD, 1997.
    • (1997)
  • 3
    • 80053496946 scopus 로고    scopus 로고
    • In vitro and In vivo Evaluation of Dosage Forms. In USP 26-NF 21; United States Pharmacopeial Convention, Inc.: Rockville, MD
    • In vitro and In vivo Evaluation of Dosage Forms. In USP 26-NF 21; United States Pharmacopeial Convention, Inc.: Rockville, MD, 2002, 1088.
    • (2002) , pp. 1088
  • 4
    • 80053468710 scopus 로고    scopus 로고
    • In vitro Release Testing and In vivo Bioequivalence Documentation; Guidance for Industry; U.S. Department of Health and Human Services, Food and Drug Administration, Centre for Drug Evaluation and Research (CDER),U.S. Government Printing Office: Washington, DC
    • In vitro Release Testing and In vivo Bioequivalence Documentation; Guidance for Industry; U.S. Department of Health and Human Services, Food and Drug Administration, Centre for Drug Evaluation and Research (CDER),U.S. Government Printing Office: Washington, DC, 1997.
    • (1997)
  • 5
    • 80053502941 scopus 로고    scopus 로고
    • Note for Guidance on Development Pharmaceutics; European Agency for the Evaluation of Medicinal Products, Human Medicines Evaluation Unit, Committee for Proprietary Medicinal Products, CPMP/QWP/155/96, London, U.K
    • Note for Guidance on Development Pharmaceutics; European Agency for the Evaluation of Medicinal Products, Human Medicines Evaluation Unit, Committee for Proprietary Medicinal Products, CPMP/QWP/155/96, London, U.K., 1998.
    • (1998)
  • 6
    • 80053543208 scopus 로고    scopus 로고
    • Note for Guidance on Modified Release Oral and Transdermal Dosage Forms: Section II (Pharmacokinetic and Clinical Evaluation); European Agency for the Evaluation of Medicinal Products, Human Medicines Evaluation Unit, Committee for Proprietary Medicinal Products, CPMP/EWP/280/96, London, U.K
    • Note for Guidance on Modified Release Oral and Transdermal Dosage Forms: Section II (Pharmacokinetic and Clinical Evaluation); European Agency for the Evaluation of Medicinal Products, Human Medicines Evaluation Unit, Committee for Proprietary Medicinal Products, CPMP/EWP/280/96, London, U.K., 1999.
    • (1999)
  • 10
    • 0017807805 scopus 로고
    • Mathematical basis of point-area de-convolution method for determining in vivo input functions
    • D.P. Vaughan, M. Dennis, Mathematical basis of point-area de-convolution method for determining in vivo input functions, J. Pharm. Sci. 67 (1978) 663-665.
    • (1978) J. Pharm. Sci , vol.67 , pp. 663-665
    • Vaughan, D.P.1    Dennis, M.2
  • 11
    • 0018190102 scopus 로고
    • Numerical de-convolution by least squares: Use of prescribed input functions
    • D.J. Cutler, Numerical de-convolution by least squares: use of prescribed input functions, J. Pharmacokin. Biopharm. 6 (1978) 227-241.
    • (1978) J. Pharmacokin. Biopharm. , vol.6 , pp. 227-241
    • Cutler, D.J.1
  • 12
    • 0017823608 scopus 로고
    • Use of polynomials to represent the input function
    • D. J. Cutler, Use of polynomials to represent the input function, Ibid 6(1978) 243-263.
    • (1978) J. Pharmacokin. Biopharm. , vol.6 , pp. 243-263
    • Cutler, D.J.1
  • 29
    • 80053498863 scopus 로고
    • USP23/NF18, k1088l. In vitro and in vivo evaluations of dosage forms
    • USP23/NF18, k1088l. In vitro and in vivo evaluations of dosage forms, 1995, 924-929.
    • (1995) , pp. 924-929
  • 30
    • 84962087263 scopus 로고    scopus 로고
    • FDA. Guidance for Industry: extended release oral dosage forms: development, evaluation and application of in vitro/in vivo correlations, Diss. Technol
    • FDA. Guidance for Industry: extended release oral dosage forms: development, evaluation and application of in vitro/in vivo correlations, Diss. Technol., 1997, 23-32.
    • (1997) , pp. 23-32
  • 35
    • 80053517958 scopus 로고    scopus 로고
    • Encyclopaedia of Controlled Drug Delivery
    • E Mathiowitz. Encyclopaedia of Controlled Drug Delivery. John Wiley & Sons., 1999, 1, 425-434.
    • (1999) John Wiley & Sons , vol.1 , pp. 425-434
    • Mathiowitz, E.1
  • 49
    • 33744544180 scopus 로고
    • R Kopelman. Science, 1988, 241, 1620-1626.
    • (1988) Science , vol.241 , pp. 1620-1626
    • Kopelman, R.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.