Influence of processing parameters and formulation factors on the drug release from tablets powder-coated with Eudragit® L 100-55

European Journal of Pharmaceutics and Biopharmaceutics

Volumn 67, Issue 2, 2007, Pages 464-475

  Sauer, Dorothea ^a   Zheng, Weijia ^b   Coots, Lonique B ^a   McGinity, James W ^a  

^a UNIVERSITY OF TEXAS AT AUSTIN   (United States)

^b NOVARTIS INSTITUTES FOR BIOMEDICAL RESEARCH   (United States)

Author keywords

Chlorpheniramine maleate; Enteric polymers; Eudragit L 100 55; Film formation; Powder coating; Theophylline

Indexed keywords

CHLORPHENIRAMINE MALEATE; CITRIC ACID TRIETHYL ESTER; EUDRAGIT; MACROGOL 3350; PLASTICIZER; POLYACRYLIC ACID; POLYMER; SOLVENT; TALC; THEOPHYLLINE; WATER;

ARTICLE; DRUG COATING; DRUG MANUFACTURE; DRUG PELLET; DRUG RELEASE; DRUG SOLUBILITY; DRUG STABILITY; DRUG STORAGE; DRY POWDER; FILM COATING; PELLET EXTRUSION; SPHERONIZATION; TABLET FORMULATION;

CALORIMETRY, DIFFERENTIAL SCANNING; CHEMISTRY, PHARMACEUTICAL; DELAYED-ACTION PREPARATIONS; DRUG STABILITY; MICROSCOPY, ELECTRON, SCANNING; PHARMACEUTICAL PREPARATIONS; POLYETHYLENE GLYCOLS; POLYMERS; POLYMETHACRYLIC ACIDS; POWDERS; SOLUBILITY; TABLETS; TABLETS, ENTERIC-COATED; TECHNOLOGY, PHARMACEUTICAL; TEMPERATURE; THEOPHYLLINE;

EID: 34547684259     PISSN: 09396411     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ejpb.2007.02.021     Document Type: Article

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