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Buccal absorption drug transport mechanism

Penetration enhancers are low molecular weight compounds that can increase the absorption of poorly absorbed hydrophilic drugs such as peptides and proteins from the nasal, buccal, oral, rectal, and vaginal routes of administration [186], Chelators, bile salts, surfactants, and fatty acids are some examples of penetration enhancers that have been widely tested [186], The precise mechanisms by which these enhancers increase drug penetration are largely unknown. Bile salts, for instance, have been shown to increase the transport of lipophilic cholesterol [187] as well as the pore size of the epithelium [188], indicating enhancement in both transcellular and paracellular transport. Bile salts are known to break down mucus [189], form micelles [190], extract membrane proteins [191], and chelate ions [192], While breakdown of mucus, formation of micelles, and lipid extraction may have contributed predominantly to the bile salt-induced enhancement of transcellular transport, chelation of ions possibly accounts for their effect on the paracellular pathway. In addition to their lack of specificity in enhancing mem-... [Pg.364]


See other pages where Buccal absorption drug transport mechanism is mentioned: [Pg.94]    [Pg.94]    [Pg.95]    [Pg.212]    [Pg.204]    [Pg.1073]    [Pg.346]    [Pg.2672]    [Pg.2675]    [Pg.130]    [Pg.564]   
See also in sourсe #XX -- [ Pg.197 ]




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