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Diffusional devices, controlled drug

Controlled Drug Release—Because the degradation products of Type III bioerosion are small, water soluble molecules, the principal application of polymers undergoing such degradation is for the systemic administration of therapeutic agents from subcutaneous, intramuscular or intraperitoneal implantation sites. Application of Type III bioerosion to controlled drug release was first described in 1970 (32) and has since then been extensively investigated. The various types of devices currently under development can be classified into (a) diffusional and (b) monolithic (7). [Pg.381]

Perale, G., Arosio, P., Moscatelli, D., Barri, V., Muller, M., Maccagnan, S. Masi, M. 2009. A new model of resorbable device degradation and drug release Transient 1-dimension diffusional model. Journal of Controlled Release, 136, 196. [Pg.95]

See other pages where Diffusional devices, controlled drug is mentioned: [Pg.381]    [Pg.114]    [Pg.521]    [Pg.106]    [Pg.153]    [Pg.326]    [Pg.2032]    [Pg.177]    [Pg.106]    [Pg.485]    [Pg.216]   


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