| Literature DB >> 26005135 |
Hiroyuki Kono1, Taichi Nakamura2, Hisaho Hashimoto2, Yuuichi Shimizu2.
Abstract
A series of water-insoluble cyclodextrin polymers (CDP) was prepared by crosslinking β-cyclodextrin (CD) with polyethylene glycol diglycidyl ether (PEGDE). Similarly, a reference CDP was prepared using ethylene glycol diglycidyl ether (EGDE). Increasing the feed ratio of PEGDE to CD in the reaction mixture led to high degrees of crosslinking. Relaxation measurements revealed structural homogeneity among the CDPs, which exhibited mobilities that strongly depended on the chain lengths of the crosslinking agents. In addition, all the CDPs displayed high encapsulation abilities toward bisphenol A (BPA) in aqueous media. In particular, the CDP sample with a low degree of crosslinking by PEGDE showed the highest encapsulation ability toward BPA. In contrast, the CDP crosslinked by EGDE exhibited low encapsulation ability because its highly dense structure, which results from the short chain lengths of the crosslinking agents, hinders the penetration of BPA molecules.Entities:
Keywords: Adsorption isotherm; Cyclodextrin polymer; Encapsulation ability; Epoxy-functionalized PEG; Molecular dynamics
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Year: 2015 PMID: 26005135 DOI: 10.1016/j.carbpol.2015.04.009
Source DB: PubMed Journal: Carbohydr Polym ISSN: 0144-8617 Impact factor: 9.381