Abstract：
:Cyclodextrins are useful functional excipients that have enjoyed widespread attention and use. The basis for this popularity from a pharmaceutical standpoint, is the ability of these materials to interact with poorly water-soluble drugs and drug candidates resulting in an increase in their apparent water solubility. The mechanism for this solubilization is rooted in the ability of cyclodextrin to form non-covalent dynamic inclusion complexes in solution. Other solubilizing attribute may include the ability to form non-inclusion based complexes, the formation of aggregates and related domains and the ability of cyclodextrins to form and stabilize supersaturated drug solutions. The increase in solubility also can increase dissolution rate and thus improve the oral bioavailability of BCS Class II and IV materials. A number of cyclodextrin-based products have reached the market based on their ability to camouflage undesirable physicochemical properties. This review is intended to give a general background to the use of cyclodextrin as solubilizers as well as highlight kinetic and thermodynamic tools and parameters useful in the study of drug solubilization by cyclodextrins.
journal_name
Adv Drug Deliv Revjournal_title
Advanced drug delivery reviewsauthors
Brewster ME,Loftsson Tdoi
10.1016/j.addr.2007.05.012subject
Has Abstractpub_date
2007-07-30 00:00:00pages
645-66issue
7eissn
0169-409Xissn
1872-8294pii
S0169-409X(07)00084-1journal_volume
59pub_type
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