Encapsulation of water-soluble drugs by a modified solvent evaporation Method. I. Effect of process and formulation variables on drug entrapment

Journal of Microencapsulation

Volumn 7, Issue 3, 1990, Pages 347-355

  Alex, Rainer ^a   Bodmeier, Roland ^a  

^a UNIVERSITY OF TEXAS AT AUSTIN   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

METHACRYLIC ACID METHYL ESTER; PSEUDOEPHEDRINE;

ARTICLE; HUMAN; MICROCAPSULE; SUSTAINED RELEASE PREPARATION;

DELAYED-ACTION PREPARATIONS; DRUG COMPOUNDING; EPHEDRINE; METHYLMETHACRYLATES; MICROSPHERES; SOLUBILITY; SUPPORT, NON-U.S. GOV'T;

EID: 0025110089     PISSN: 02652048     EISSN: None     Source Type: Journal    
DOI: 10.3109/02652049009021845     Document Type: Article

References (12)

1. A new long-acting injectable microcapsule system for the administration of progesterone
2. Polylactic acid microspheres containing quinidine base and quinidine sulphate prepared by the solvent evaporation technique. I. Methods and morphology
3. The preparation and evaluation of drug-containing poly(dl-lactide) microspheres formed by the solvent evaporation method
4. Solvent selection in the preparation of poly(dl-lactide) microspheres prepared by the solvent evaporation method
5. The formulation and stability of multiple emulsions
6. Preparation of microspheres of water-soluble pharmaceuticals
7. Preparation and characterization of poly(styrene) microcapsules containing corrosion inhibitors
8. A new technique to efficiently entrap leuprolide acetate into microcapsules of polylactic acid or copoly(lactic/glycolic) acid
9. Reactivity and stability of microencapsulated placental alkaline phosphatase