α-Cyclodextrin concentration-controlled thermo-sensitive supramolecular hydrogels

Biocompatibility Nucleobase
DOI: 10.1016/j.msec.2017.08.045 Publication Date: 2017-08-14T12:01:17Z
ABSTRACT
Supramolecular hydrogels (SHGs) built from inclusion complex of macrocyclic compound α-cyclodextrin (α-CD) and poly(ethylene glycol) (PEG) have attracted much interest due to their excellent biocompatibility and great potential for biomedical applications. In this work, the hydrogen bond of nucleic acid was introduced into the above-mentioned SHG by syntheses of nucleobase guanine/cytosine (G/C)-terminated PEG (G-PEG-G/C-PEG-C). The base-pairing interaction between G and C as an additional network junction effectively enhanced storage moduli (G's) of the hydrogels. Moreover, the prepared hydrogels exhibited excellent cytocompatibility and property for controlled drug release, outlining the potential of thermo-sensitive construct for biomedical applications, such as local chemotherapy of cancers.
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