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Volumn 9, Issue 1, 2002, Pages 18-22

Refinement of lower acceptance value of the similarity factor f2 incomparison of dissolution profiles

Author keywords

[No Author keywords available]

Indexed keywords

DISSOLUTION; DRUG INDUSTRY; MARKETING;

EID: 84962091049     PISSN: 1521298X     EISSN: None     Source Type: Journal    
DOI: 10.14227/DT090102P18     Document Type: Article
Times cited : (14)

References (17)
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  • 2
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    • Guidance for industry, Center for Drug Evaluation and Research, November 1995
    • Guidance for industry: Immediate release solid oral dosage forms:Scale-up and post-approval changes (SUPAC-IR): Chemistry, Manufacturing and Controls, In vitro dissolution testing,and in vivo bioequiva-lence documentation.US Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research, November 1995.
    • Vitro Dissolution Testing,And in Vivo Bioequiva-Lence Documentation.Us Department of Health and Human Services, Food and Drug Administration
  • 4
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    • Leeson, L.J.1
  • 5
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    • "Pharmaceutical Dissolution Testing
    • Swarbrick J. (Ed.), Marcel Dekker, New York
    • U.V. Banakar, "Pharmaceutical Dissolution Testing, In: Drug and the Pharmaceutical Sciences," Swarbrick J. (Ed.),Volume 49, Marcel Dekker, New York,p-407,1992
    • (1992) Drug and the Pharmaceutical Sciences," , vol.49 , pp. 407
    • Banakar, U.V.1
  • 6
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    • "Mathematical comparison of dissolution profiles
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    • (1996) Pharmaceutical Technology , vol.20 , Issue.6 , pp. 64-74
    • Moore, J.W.1    Flanner, H.H.2
  • 9
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    • Human Medicines Evaluation Unit, Oral dosage forms; B.Transdermal dosage forms;Section I (Quality)
    • Human Medicines Evaluation Unit, EMEA, Notes for guidance on quality of modified release products:A. Oral dosage forms; B.Transdermal dosage forms;Section I (Quality),1999.
    • (1999) EMEA, Notes for Guidance on Quality of Modified Release Products:A
  • 10
    • 0031779119 scopus 로고    scopus 로고
    • In-vitro dissolution profile comparison-Statistics and analysis of the similarity factor f2
    • V.P. Shah et al., "In-vitro dissolution profile comparison-Statistics and analysis of the similarity factor f2," Pharmaceutical Research 15(6):889-896 (1998)
    • (1998) Pharmaceutical Research , vol.15 , Issue.6 , pp. 889-896
    • Shah, V.P.1
  • 13
    • 0034061372 scopus 로고    scopus 로고
    • Comparison of in vitro dissolution profiles using a novel, model-independent approach
    • M.C. Gohel, and M.K. Panchal, "Comparison of in vitro dissolution profiles using a novel, model-independent approach" Pharmaceutical Technology 24 (3):92-102 (2000)
    • (2000) Pharmaceutical Technology , vol.24 , Issue.3 , pp. 92-102
    • Gohel, M.C.1    Panchal, M.K.2
  • 14
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    • M.C. Gohel, and M.K. Panchal, "Novel use of similarity factors f2 and Sd for the development of diltiazem HCl modified release tablets using a 32 factorial design", Drug Development and Industrial Pharmacy 28(1):77-87 (2001)
    • (2001) Drug Development and Industrial Pharmacy , vol.28 , Issue.1 , pp. 77-87
    • Gohel, M.C.1    Panchal, M.K.2
  • 15
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    • Novel mathematical method for quantitative expression of deviation from the Higuchi model
    • article 31
    • M.C. Gohel et al., "Novel mathematical method for quantitative expression of deviation from the Higuchi model" AAPS Pharm Sci Tech 1 (4):article 31 (2000)
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  • 16
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.