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Pharmaceutical dosage forms nanoparticles

Allemann, E., J. C. Leroux, and R. Gurny. 1998. Biodegradable nanoparticles of poly(lactic acid) and poly(lactic-c-glycolic acid) for parenteral administration. Pharmaceutical Dosage Forms Disperse Systems, H. Lieberman, M. Rieger, G. Banker (Eds.), Vol. 3, New York, Marcel Dekker. pp. 163-193. [Pg.364]

Because of its inherent costs, spray drying is not always considered as a processing option for many conventional formulations. However, when a specialized particle type is required by the active ingredient or dosage form, spray drying can become a feasible alternative to more conventional manufacturing processes. Such particle types include microcapsules, controlled release particles, nanoparticles, and liposomes. The application of spray drying to pharmaceuticals has been extensively discussed in review articles (21,22). [Pg.147]


See other pages where Pharmaceutical dosage forms nanoparticles is mentioned: [Pg.274]    [Pg.4117]    [Pg.560]    [Pg.3]    [Pg.69]    [Pg.371]    [Pg.495]    [Pg.4299]    [Pg.1117]    [Pg.334]    [Pg.344]    [Pg.405]    [Pg.435]    [Pg.405]    [Pg.191]    [Pg.33]    [Pg.276]    [Pg.479]    [Pg.26]   
See also in sourсe #XX -- [ Pg.4117 ]




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Pharmaceutical dosage forms

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