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Colloidal systems, parenteral drug delivery

Marty and her colleagues (1978) pointed out that colloidal drug delivery systems were well suited for parenteral administration and may have use as sustained release products. Since gelatin is readily available, has low antigenicity, and has been utilized... [Pg.227]

Parenteral administration (injection), which is the immediate option for orally undeliverable drugs, has advanced greatly in recent years for systemic and local drug delivery. " The novel drug delivery system has metamorphosed from simple polymer and antibody conjugates to sterically stabilized colloidal systems. Liposomes and nanoparticles can improve pharmacokinetic-pharmacody-... [Pg.487]

Westesen and Siekmann [11] used suspensions of colloidal solid lipid particles as well as lyophilizates as delivery systems for the parenteral administration of the drug for its particle morphology determination. [Pg.71]

See other pages where Colloidal systems, parenteral drug delivery is mentioned: [Pg.244]    [Pg.49]    [Pg.196]    [Pg.210]    [Pg.1339]    [Pg.636]    [Pg.1112]    [Pg.661]    [Pg.463]    [Pg.385]    [Pg.468]    [Pg.523]    [Pg.661]    [Pg.146]    [Pg.151]    [Pg.212]    [Pg.91]   
See also in sourсe #XX -- [ Pg.463 ]



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Colloidal systems

Parenteral drug delivery

Parenteral drugs

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