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Volumn 3, Issue 3, 2011, Pages 560-567

The "gI dissolution" method: A low volume, in vitro apparatus for assessing the dissolution/precipitation behaviour of an active pharmaceutical ingredient under biorelevant conditions

Author keywords

[No Author keywords available]

Indexed keywords

ACTIVE PHARMACEUTICAL INGREDIENTS; DRUG COMPOUNDS; EXPERIMENTAL CONDITIONS; GASTROINTESTINAL TRACT; IN-VITRO; PH CONTROL; PHYSIOLOGICAL CONDITION; PRECIPITATION BEHAVIOUR;

EID: 79952941668     PISSN: 17599660     EISSN: 17599679     Source Type: Journal    
DOI: 10.1039/c0ay00434k     Document Type: Article
Times cited : (29)

References (28)
  • 2
    • 79952969093 scopus 로고    scopus 로고
    • Dissolution testing of solid oral dosage forms
    • The Stationery Office, London, pp. A419-A421
    • Dissolution Testing of Solid Oral Dosage Forms, British Pharmacopoeia, The Stationery Office, London, 2002, pp. A419-A421
    • (2002) British Pharmacopoeia
  • 4
    • 79952944062 scopus 로고
    • Dissolution
    • Rockville, MD, United States Pharmacopeial Convention, pp. 1791-1793
    • Dissolution, United States Pharmacopeia 23, Rockville, MD, United States Pharmacopeial Convention, 1995a, pp. 1791-1793
    • (1995) United States Pharmacopeia 23
  • 5
    • 79952982896 scopus 로고
    • In Vitro and in Vivo Evaluation of Dosage Forms
    • United States Pharmacopeial Convention, Rockville, MD, pp. 1924-1929
    • In Vitro and In Vivo Evaluation of Dosage Forms, United States Pharmacopeia 23, United States Pharmacopeial Convention, Rockville, MD, 1995b, pp. 1924-1929
    • (1995) United States Pharmacopeia 23
  • 12
    • 28444487852 scopus 로고    scopus 로고
    • Extended Release Oral Dosage Forms; Development, Evaluation and Application of in Vitro/In Vivo Correlations
    • Food and Drug Administration, Rockville, MD
    • Extended Release Oral Dosage Forms; Development, Evaluation and Application of In Vitro/In Vivo Correlations, Guidance for Industry, Food and Drug Administration, Rockville, MD, 1997
    • (1997) Guidance for Industry
  • 14
    • 0004234237 scopus 로고    scopus 로고
    • Immediate Release Solid Oral Dosage Forms. Scale-up and Postapproval Changes: Chemistry, Manufacturing, and Controls; In Vitro Dissolution Testing and in Vivo Bioequivalence Documentation
    • Food and Drug Administration, Rockville, MD
    • Immediate Release Solid Oral Dosage Forms. Scale-up and Postapproval Changes: Chemistry, Manufacturing, and Controls; In Vitro Dissolution Testing and In Vivo Bioequivalence Documentation, Guidance for industry, Food and Drug Administration, Rockville, MD, 1995
    • (1995) Guidance for Industry
  • 15
    • 0004234237 scopus 로고    scopus 로고
    • Modified Release Solid Oral Dosage Forms. Scale-up and Postapproval Changes: Chemistry, Manufacturing, and Controls; In Vitro Dissolution Testing and in Vivo Bioequivalence Documentation
    • Food and Drug Administration, Rockville, MD
    • Modified Release Solid Oral Dosage Forms. Scale-up and Postapproval Changes: Chemistry, Manufacturing, and Controls; In Vitro Dissolution Testing and In Vivo Bioequivalence Documentation, Guidance for Industry, Food and Drug Administration, Rockville, MD, 1997
    • (1997) Guidance for Industry


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.