Abstract:
:A series of branched cationic beta-cyclodextrin polymers (CPbetaCDs) with designed chemical structures were synthesized from beta-cyclodextrin (beta-CD), epichlorohydrin (EP) and choline chloride (CC). Indomethacin (IDM), an anionic drug, was chosen as a model drug to evaluate the drug loading capacities of CPbetaCDs. The formation of IDM-CPbetaCD complex was confirmed by (1)H NMR and DSC. Phase solubility studies and Job plots indicated that CPbetaCDs can solubilize IDM up to 100 times of its intrinsic solubility in a 1:1 complexation form. Mechanism studies with the help of adamantane revealed that the effective complexation is a combination of inclusion complexation, charge interaction and hydrophobic interaction. In addition, IDM-CPbetaCDs loaded alginate hydrogels were prepared and obtained controllable release profile in dissolution tests. The tunable structures of CPbetaCDs make them promising drug carriers with superior drug loading capacities and controllable drug release abilities.
journal_name
Int J Pharmjournal_title
International journal of pharmaceuticsauthors
Xin J,Guo Z,Chen X,Jiang W,Li J,Li Mdoi
10.1016/j.ijpharm.2009.11.024subject
Has Abstractpub_date
2010-02-15 00:00:00pages
221-8issue
1-2eissn
0378-5173issn
1873-3476pii
S0378-5173(09)00845-Xjournal_volume
386pub_type
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