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Drug release liquid

Sustained Drug Release from Solid, Semisolid, and Liquid Formulations... [Pg.143]

Sustained release from disperse systems such as emulsions and suspensions can be achieved by the adsorption of appropriate mesogenic molecules at the interface. The drug substance, which forms the inner phase or is included in the dispersed phase, cannot pass the liquid ciystals at the interface easily and thus diffuses slowly into the continuous phase and from there into the organism via the site of application. This sustained drug release is especially pronounced in the case of multilamellar liquid crystals at the interface. [Pg.143]

Schneeweis, A., Papantoniou, I., and Mueller-Goymann, C.C., Diclofenac sodium plasma concentrations in dogs after peroral application of soft gelatine capsules enabling application induced transformation (AIT) into a semisolid system of liquid crystals (SSLC) compared to in vitro drug release, Pharm. Pharmacol Lett., 7 42-44 (1997). [Pg.146]

Baert L, Remon JP. Influence of amount of granulation liquid on the drug release rate from pellets made by extrusion spheronization. Int J Pharm 1993 95 135-141. [Pg.368]

Dordunoo, S.K., Sustained release liquid lled hard gelatin capsules in drug discovery and development a small pharmaceutical company s perspectiB, . Techn. Gattefos e29, 29-39,... [Pg.633]

See other pages where Drug release liquid is mentioned: [Pg.249]    [Pg.220]    [Pg.264]    [Pg.267]    [Pg.113]    [Pg.115]    [Pg.380]    [Pg.142]    [Pg.143]    [Pg.144]    [Pg.249]    [Pg.99]    [Pg.419]    [Pg.228]    [Pg.211]    [Pg.484]    [Pg.121]    [Pg.514]    [Pg.621]    [Pg.625]    [Pg.127]    [Pg.140]    [Pg.162]    [Pg.225]    [Pg.920]    [Pg.140]    [Pg.329]    [Pg.329]    [Pg.69]    [Pg.475]    [Pg.300]    [Pg.392]    [Pg.83]    [Pg.105]    [Pg.292]    [Pg.341]    [Pg.375]    [Pg.652]    [Pg.665]    [Pg.1198]    [Pg.1201]    [Pg.1269]    [Pg.1328]   
See also in sourсe #XX -- [ Pg.1129 ]



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Drug release

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Sustained drug release, liquid crystals

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