Influence of pH and agitation intensity on drug dissolution from tablets evaluated by means of factorial design

Pharmazeutische Industrie

Volumn 63, Issue 7, 2001, Pages 774-779

  Parojcic J ^a   Duric Z ^a   Jovanovic M ^a   Ibric S ^a   Nikolic L ^a  

^a Faculty of Pharmacy   (Serbia)

Author keywords

Acetylsalicylic acid; CAS 103 90 2; CAS 50 78 2; Dissolution testing, experimental design, factorial design; Paracetamol; Tablets

Indexed keywords

ACETYLSALICYLIC ACID; PARACETAMOL;

ARTICLE; DRUG SOLUBILITY; DRUG STABILITY; METHODOLOGY; PH; REGRESSION ANALYSIS; TABLET;

EID: 0034891108     PISSN: 0031711X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (10)

1. Influence of higher rates of agitation on release patterns of immediate-release drug products
2. In vitro dissolution of sparingly water-soluble drug dosage forms
3. Novel approach for determination of correlation between in vivo and in vitro dissolution using the optimization technique
4. Development of a dissolution medium for glibenclamide
5. The use of statistical moment analysis to elucidate the mechanism of release of a model drug from pellets produced by extrusion and spheronisation
6. In vitro/in vivo correlation of dissolution using moments of dissolution and transit times
7. Comparative bioavailability of three commercial acetaminophen tablets
8. An attempt on establishing in vitro-in vivo correlation: Case of paracetamol immediate release tablets
9. Bioavailability studies on a buffered acetylsalicylic acid preparation