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Volumn 5, Issue 4, 1998, Pages 5-11

Dissolution tests for ER products

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BIOEQUIVALENCE; DRUG BIOAVAILABILITY; DRUG FORMULATION; DRUG INDUSTRY; DRUG RELEASE; DRUG SOLUBILITY; EXTENDED RELEASE FORMULATION; FOOD DRUG INTERACTION; FOOD INTAKE; MEAN DISSOLUTION TIME; PH; QUALITY CONTROL; ROTATION; SIMULATION;

EID: 33644594819     PISSN: 1521298X     EISSN: None     Source Type: Journal    
DOI: 10.14227/DT050498P5     Document Type: Article
Times cited : (7)

References (21)
  • 1
    • 0001319970 scopus 로고
    • Per cent absorbed time plots derived from blood level and/or urinary excretion data
    • J. G. Wagner and E. Nelson. Per cent absorbed time plots derived from blood level and/or urinary excretion data. J. Pharm. Sci. 52 (6): 610-611 (1963).
    • (1963) J. Pharm. Sci , vol.52 , Issue.6 , pp. 610-611
    • Wagner, J.G.1    Nelson, E.2
  • 2
    • 0342702115 scopus 로고
    • Effect of dosage form on drug absorption - A frequent variable in clinical pharmacology
    • G. Levy. Effect of dosage form on drug absorption - A frequent variable in clinical pharmacology. Arch. Int. Pharmacodyn. 152 (1-2) 59-68 (1964).
    • (1964) Arch. Int. Pharmacodyn , vol.152 , Issue.1-2 , pp. 59-68
    • Levy, G.1
  • 3
    • 0014297946 scopus 로고
    • New method for calculating the intrinsic absorption rate of drugs
    • J. C. K. Loo and S. Riegelman. New method for calculating the intrinsic absorption rate of drugs. J. Pharm. Sci. 57 (6) 918-928 (1968).
    • (1968) J. Pharm. Sci , vol.57 , Issue.6 , pp. 918-928
    • Loo, J.C.K.1    Riegelman, S.2
  • 4
    • 84962091810 scopus 로고
    • Dissolution
    • Dissolution, USP 18, 934-935 (1970).
    • (1970) USP , vol.18 , pp. 934-935
  • 5
    • 0001419666 scopus 로고
    • Joint Report of the Section for Control Laboratories and the Section of Industrial Pharmacists of FIP: Guidelines for dissolution testing of solid oral products
    • Joint Report of the Section for Control Laboratories and the Section of Industrial Pharmacists of FIP: Guidelines for dissolution testing of solid oral products. Pharm. Ind. 43 334-343 (1981).
    • (1981) Pharm. Ind , vol.43 , pp. 334-343
  • 6
    • 0020400710 scopus 로고
    • Numerical convolution/deconvolution as a tool for correlating in vitro with in vivo drug availability
    • F. Langenbucher. Numerical convolution/deconvolution as a tool for correlating in vitro with in vivo drug availability. Pharm. Ind. 44 (11) 1166-1172 (1982).
    • (1982) Pharm. Ind , vol.44 , Issue.11 , pp. 1166-1172
    • Langenbucher, F.1
  • 8
    • 0002915214 scopus 로고
    • In vitro / in vivo correlation for extended release oral dosage forms. Pharm
    • USP Subcommittee on Biopharmaceutics
    • USP Subcommittee on Biopharmaceutics. In vitro / in vivo correlation for extended release oral dosage forms. Pharm. Forum 14 (4) 4160-4161 (1988)
    • (1988) Forum , vol.14 , Issue.4 , pp. 4160-4161
  • 9
    • 1842491883 scopus 로고
    • Importance of assessing 'food effects' in evaluating controlled-release formulations
    • A. Yacobi and E. Halperin-Walega (eds), Pergamon Press New York
    • A. Karim. Importance of assessing 'food effects' in evaluating controlled-release formulations. In: A. Yacobi and E. Halperin-Walega (eds). Oral sustained release formulations: Design and evaluations. Pergamon Press New York (1988)
    • (1988) Oral Sustained Release Formulations: Design and Evaluations
    • Karim, A.1
  • 10
    • 84935556756 scopus 로고
    • A novel approach to the specification of in vitro dissolution boundaries based on regulatory requirements for once-daily administration
    • V. E. Steinijans, R. Dietrich, H. Trautmann, R. Sauter and G. Benedikt. A novel approach to the specification of in vitro dissolution boundaries based on regulatory requirements for once-daily administration. Arzneimittelforschung/Drug Res. 38 1203-1209 (1988).
    • (1988) Arzneimittelforschung/Drug Res , vol.38 , pp. 1203-1209
    • Steinijans, V.E.1    Dietrich, R.2    Trautmann, H.3    Sauter, R.4    Benedikt, G.5
  • 11
    • 0343734878 scopus 로고
    • Description and evaluation of the flow cell dissolution apparatus as an alternative test method for drug release
    • M. Nicklasson and F. Langenbucher. Description and evaluation of the flow cell dissolution apparatus as an alternative test method for drug release. Pharmacopeial Forum 16 (3) 532-540 (1990)
    • (1990) Pharmacopeial Forum , vol.16 , Issue.3 , pp. 532-540
    • Nicklasson, M.1    Langenbucher, F.2
  • 15
    • 84962094706 scopus 로고
    • In vitro in vivo evaluation of dosage forms
    • <1088>
    • <1088> ‘In vitro in vivo evaluation of dosage forms’, USP 23 (1995)
    • (1995) USP , vol.23
  • 17
    • 84923690893 scopus 로고    scopus 로고
    • Guidance for Industry SUPAC-MR: Modified-Release Solid Oral Dosage Forms Scale-Up and Post Approval Changes: Chemistry, Manufacturing, and Controls
    • Guidance for Industry SUPAC-MR: Modified-Release Solid Oral Dosage Forms Scale-Up and Post Approval Changes: Chemistry, Manufacturing, and Controls; In Vitro Dissolution Testing and In Vivo Bioequivalence Documentation (1997).
    • (1997) Vitro Dissolution Testing and in Vivo Bioequivalence Documentation
  • 19
    • 84962082612 scopus 로고    scopus 로고
    • European Pharmacopeia
    • European Pharmacopeia
  • 20
    • 84962050477 scopus 로고
    • USP 23 (1995)
    • (1995) USP , vol.23
  • 21
    • 0022892810 scopus 로고
    • Influence of a high fat breakfast on the bioavailability of theophylline controlled release formulations: An in vitro demonstration of an in vivo observation
    • P. U. Maturu, V. K. Prasad, W. N. Worsely, G. U. Shiu and J. P. Skelly. Influence of a high fat breakfast on the bioavailability of theophylline controlled release formulations: An in vitro demonstration of an in vivo observation. J. Pharm. Sci. 75 1205-1206 (1986).
    • (1986) J. Pharm. Sci , vol.75 , pp. 1205-1206
    • Maturu, P.U.1    Prasad, V.K.2    Worsely, W.N.3    Shiu, G.U.4    Skelly, J.P.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.