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Nanoparticle delivery systems, microparticle drug deliver

A large variety of drug delivery systems are described in the literature, such as liposomes (Torchilin, 2006), micro and nanoparticles (Kumar, 2000), polymeric micelles (Torchilin, 2006), nanocrystals (Muller et al., 2011), among others. Microparticles are usually classified as microcapsules or microspheres (Figure 8). Microspheres are matrix spherical microparticles where the drug may be located on the surface or dissolved into the matrix. Microcapsules are characterized as spherical particles more than Ipm containing a core substance (aqueous or lipid), normally lipid, and are used to deliver poor soluble molecules... [Pg.70]

Microparticles and nanoparticles present some advantageous features, namely mucoadhesive properties. They have demonstrated some potential in vaginal drug delivery, particularly in the formulation of delivery systems for vaccines or peptides and proteins [160, 161], Nonetheless, these particles have to be incorporated in adequate carrier systems in order to be delivered. This task has been shown to be complex, it being hard to achieve controlled-release and steady-release profiles. [Pg.834]


See other pages where Nanoparticle delivery systems, microparticle drug deliver is mentioned: [Pg.147]    [Pg.503]    [Pg.1263]    [Pg.288]    [Pg.65]    [Pg.129]    [Pg.402]    [Pg.164]    [Pg.316]    [Pg.569]    [Pg.118]    [Pg.175]    [Pg.58]    [Pg.164]    [Pg.533]    [Pg.160]    [Pg.125]    [Pg.1713]    [Pg.438]   
See also in sourсe #XX -- [ Pg.487 ]




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