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Excipient aqueous-based solubilized

In recent years there has been an increased interest in the utility of lipid-based delivery systems to enhance oral bioavailability (4). It is generally known that membrane permeability is directly correlated to a drug s water-lipid partition coefficient however, the systemic availability of highly lipophilic drugs is impeded by their low aqueous solubility. In an effort to improve this solubility-limited bio-availabiliy,formulators have turned to the use of lipid excipients to solubilize the compounds before oral administration. Several formulations are currently on the market, for example, Sandimmun/Neoral (cyclosporin microemulsion), Norvir (ritonavir), and Fortovase (saquinavir)... [Pg.252]


See other pages where Excipient aqueous-based solubilized is mentioned: [Pg.158]    [Pg.259]    [Pg.158]    [Pg.81]    [Pg.120]    [Pg.203]    [Pg.148]    [Pg.241]    [Pg.233]    [Pg.240]    [Pg.243]    [Pg.203]    [Pg.609]    [Pg.386]   
See also in sourсe #XX -- [ Pg.3351 , Pg.3352 , Pg.3353 ]




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Aqueous base

Excipient

Excipients

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