The effects of formulation factors on the moist granulation technique for controlled-release tablets

Drug Development and Industrial Pharmacy

Volumn 27, Issue 9, 2001, Pages 893-898

  Railkar, Aniruddha M ^a   Schwartz, Joseph B ^b  

^a JOHNSON AND JOHNSON PHARMACEUTICAL RESEARCH AND DEVELOPMENT   (United States)

^b UNIVERSITY OF THE SCIENCES   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AEROSIL; HYDROXYPROPYLCELLULOSE; KLUCEL HXF; MAGNESIUM STEARATE; MICROCRYSTALLINE CELLULOSE; PARACETAMOL; POVIDONE;

ANALYTIC METHOD; ARTICLE; CALCULATION; COMPRESSION; CONTROLLED DRUG RELEASE; DRUG BINDING; DRUG FORMULATION; DRUG GRANULATION; DRUG SOLUBILITY; MOISTURE; PARTICLE SIZE; TECHNIQUE;

ACETAMINOPHEN; ALGORITHMS; ANALGESICS, NON-NARCOTIC; DELAYED-ACTION PREPARATIONS; DRUG COMPOUNDING; EXCIPIENTS; KINETICS; PARTICLE SIZE; POLYMERS; POVIDONE; POWDERS; SOLUBILITY; SURFACE PROPERTIES; TABLETS;

EID: 0035190921     PISSN: 03639045     EISSN: None     Source Type: Journal    
DOI: 10.1081/DDC-100107669     Document Type: Article

References (7)

1. Moisture activated dry granulation: A general process
2. Evaluation and comparison of a moist granulation technique (MGT) to conventional methods
3. Log normal distribution of tablet pore diameters
4. A simple equation for description of solute release I: Fickian and non-Fickian release from non-swellable devices in the form of slabs, spheres, cylinders or discs
5. Rate of release of medicaments from ointment bases containing drug suspensions
6. The influence of drugs on the properties of gels and swelling characteristics of matrices containing methylcellulose or hydroxypropylmethylcellulose