Controlled release of diclofenac sodium through acrylamide grafted hydroxyethyl cellulose and sodium alginate

Carbohydrate Polymers

Volumn 104, Issue 1, 2014, Pages 151-157

  Al Kahtani, Ahmed A ^a   Sherigara, B S ^b  

^a Department of Chemistry   (Yemen)

^b KUVEMPU UNIVERSITY   (India)

Author keywords

In vitro release; IPN; Microspheres; Sodium alginate; Synthesis

Indexed keywords

ANTI-INFLAMMATORY DRUGS; CROSS LINKING AGENTS; ENCAPSULATION EFFICIENCY; HYDROXYETHYL CELLULOSE; IN-VITRO; INTERPENETRATING NETWORK (IPN); IPN; PHARMACEUTICAL APPLICATIONS;

AMIDES; DIFFUSION IN LIQUIDS; DRUG DELIVERY; EMULSIFICATION; ENCAPSULATION; FOURIER TRANSFORM INFRARED SPECTROSCOPY; FREE RADICAL POLYMERIZATION; GRAFTING (CHEMICAL); MICROSPHERES; SODIUM; SODIUM ALGINATE; SYNTHESIS (CHEMICAL); TRANSPORT PROPERTIES;

HYDROGELS;

ACRYLAMIDE; ALGINIC ACID; CELLULOSE; DICLOFENAC; DRUG CARRIER; GLUCURONIC ACID; HEXURONIC ACID; HYDROXYETHYLCELLULOSE; NONSTEROID ANTIINFLAMMATORY AGENT;

ANALOGS AND DERIVATIVES; CHEMISTRY; POLYMERIZATION;

ACRYLAMIDE; ALGINATES; ANTI-INFLAMMATORY AGENTS, NON-STEROIDAL; CELLULOSE; DICLOFENAC; DRUG CARRIERS; GLUCURONIC ACID; HEXURONIC ACIDS; POLYMERIZATION;

EID: 84893305924     PISSN: 01448617     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.carbpol.2014.01.018     Document Type: Article

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