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In vitro determination of disintegration time of quick-dissolve tablets using a new method

Author
DOR, Philippe J. M1 ; FIX, Joseph A1
[1] Yamanouchi Pharma Technologies, Inc., Stanford Research Center, 1050 Arastradero Road, Palo Alto, California 94304, United States
Source

Pharmaceutical development and technology. 2000, Vol 5, Num 4, pp 575-577 ; ref : 10 ref

ISSN
1083-7450
Scientific domain
Pharmacology drugs
Publisher
Informa Healthcare, New York, NY
Publication country
United States
Document type
Article
Language
English
Keyword (fr)
Analyse texture Appareillage Compression directe Comprimé poudre Dureté Délitement Excipient Forme pharmaceutique Homme In vitro In vivo Individu sain Liant Lubrifiant Maltose Mannitol Méthode étude Technologie pharmaceutique Voie orale
Keyword (en)
Texture analysis Instrumentation Direct compression Powder compact Hardness Disintegration Vehicle(excipient) Dosage form Human In vitro In vivo Healthy subject Binders Lubricant Maltose Mannitol Investigation method Pharmaceutical technology Oral administration
Keyword (es)
Análisis textura Instrumentación Compresión directa Compacto polvo Dureza Deslecho Excipiente(vehiculo) Forma farmacéutica Hombre In vitro In vivo Individuo sano Ligante Lubricante Maltosa Manitol Método estudio Tecnología farmacéutica Vía oral
Classification
Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B02 Pharmacology. Drug treatments / 002B02A General pharmacology / 002B02A03 Pharmaceutical technology. Pharmaceutical industry

Discipline
General pharmacology
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
798583

Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS

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