Effect of poly(lactide-co-glycolide) molecular weight on the release of dexamethasone sodium phosphate from microparticles

Journal of Microencapsulation

Volumn 24, Issue 2, 2007, Pages 117-128

  Jaraswekin, Saowanee ^a,b   Prakongpan, Sompol ^a   Bodmeier, Roland ^b  

^a MAHIDOL UNIVERSITY   (Thailand)

^b FREIE UNIVERSITÄT BERLIN   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

DEXAMETHASONE SODIUM PHOSPHATE; POLYGLACTIN; SODIUM CHLORIDE;

AQUEOUS SOLUTION; ARTICLE; BIODEGRADABILITY; CONTROLLED STUDY; CORRELATION ANALYSIS; DISPERSION; DRUG DELIVERY SYSTEM; DRUG SOLUBILITY; EVAPORATION; INFLAMMATION; INTERMETHOD COMPARISON; MICROENCAPSULATION; MOLECULAR WEIGHT; PARTICLE SIZE; POROSITY; RHEUMATOID ARTHRITIS; SUSTAINED RELEASE FORMULATION;

DELAYED-ACTION PREPARATIONS; DEXAMETHASONE; DRUG COMPOUNDING; EMULSIONS; MICROSCOPY, ELECTRON, SCANNING; MOLECULAR WEIGHT; PARTICLE SIZE; POLYGLACTIN 910; SOLUBILITY; SOLUTIONS; SOLVENTS;

EID: 33947622085     PISSN: 02652048     EISSN: 14645246     Source Type: Journal    
DOI: 10.1080/02652040701233655     Document Type: Article

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