Controlled-release naproxen using micronized ethyl cellulose by wet-granulation and solid-dispersion method

Drug Development and Industrial Pharmacy

Volumn 28, Issue 2, 2002, Pages 129-134

  Iqbal, Zabed ^a   Babar, Almas ^b   Ashraf, Muhammad ^a  

^a PFIZER INC   (United States)

^b LONG ISLAND UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ETHYL CELLULOSE; LACTOSE; MAGNESIUM STEARATE; NAPROXEN; POLYMER;

ANALYTIC METHOD; ARTICLE; CONTROLLED DRUG RELEASE; DISPERSION; DRUG FORMULATION; INTERMETHOD COMPARISON; SOLID; TABLET;

ANTI-INFLAMMATORY AGENTS, NON-STEROIDAL; CELLULOSE; CHEMISTRY, PHARMACEUTICAL; DELAYED-ACTION PREPARATIONS; NAPROXEN; POLYMERS; SCLEROSING SOLUTIONS; TABLETS;

EID: 0036122552     PISSN: 03639045     EISSN: None     Source Type: Journal    
DOI: 10.1081/DDC-120002445     Document Type: Article

References (6)

1. Bioavailability and bioequivalence of extended release oral dosage forms
2. Sustained release drug delivery systems. Part II. Preformulation consideration
3. Sustained release drug delivery systems. Part I. An overview
4. Comparative evaluation of controlled release solid oral dosage forms prepared with solid dispersion and coprecipitates