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Journal of Microencapsulation
Micro and Nano Carriers
Volume 16, 1999 - Issue 5
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Research Article

Modification of the initial release of a highly water-soluble drug from ethyl cellulose microspheres

W.-J. LIN, T.-L. WU School of Pharmacy, College of Medicine, National Taiwan University, Taipei 100, Taiwan
Pages 639-646 | Published online: 29 Sep 2008

References

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  • JAM, G. K., and GOHEL, M. C., 1997, Effects of selected formulation parameters on the entrapment of diclofenac sodium in ethyl cellulose microspheres. Journal of Controlled Release, 43, 245–250.
  • JEERY, H., DAMS, S. S., and O'HAGAN, D. T., 1993, The preparation and characterization of poly(lactide-co-glycolide) microspheres lithe entrapment of a model protein using a (water in oil) in water emulsion solvent evaporation technique. Pharmaceutical Research, 10, 362–368.
  • JONES, D. S., and PEARCE, K. J., 1996, Contribution of process variables to the entrapment efficiency of propranolol hydrochloride within ethylcellulose microspheres prepared by the solvent evaporation method as evaluated using a factorial design. International Journal of Pharmacy, 131, 25–31.
  • WADA, R., H YON, S. H., and IKADA, Y., 1990, Lactic acid oligomer microspheres containing hydrophilic drugs. Journal of Pharmaceutical Science, 79, 919–924.
  • WANG, H. T., S CHMITT, E., F LANAGAN, D. R., and LINHARDT, R. J., 1991, Influence of formulation methods on the in vitro controlled release of protein from poly(ester) microspheres. Journal of Controlled Release, 17, 23–32.
  • UKSEL, N., and BAYKARA, T., 1997, Preparation of polymeric microspheres by the solvent evaporation method using sucrose stearate as a droplet stabilizer. Journal of Microencapsulation, 14, 725–733.

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