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Simultaneous expression and transportation of insulin by supramolecular polysaccharide nanocluster.


ABSTRACT: Drug/gene transportation systems with stimuli-responsive release behaviors are becoming research hotspots in biochemical and biomedical fields. In this work, a glucose-responsive supramolecular nanocluster was successfully constructed by the intermolecular complexation of phenylboronic acid modified ?-cyclodextrin with adamantane modified polyethylenimine, which could be used as a biocompatible carrier for insulin and pCMV3-C-GFPSpark-Ins DNA which could express insulin co-delivery. Benefiting from the response capability of phenylboronic acid moiety toward glucose, the encapsulated insulin could be specifically released and the corresponding targeted DNA could efficiently express insulin in HepG2 cell, accompanied by the high-level insulin release in vitro. Our results demonstrate that the simultaneous insulin drug delivery and insulin gene transfection in a controlled mode may have great potential in the clinical diabetes treatments.

SUBMITTER: Zhang YH 

PROVIDER: S-EPMC4780080 | biostudies-other | 2016 Mar

REPOSITORIES: biostudies-other

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Simultaneous expression and transportation of insulin by supramolecular polysaccharide nanocluster.

Zhang Yu-Hui YH   Zhang Ying-Ming YM   Zhao Qi-Hui QH   Liu Yu Y  

Scientific reports 20160307


Drug/gene transportation systems with stimuli-responsive release behaviors are becoming research hotspots in biochemical and biomedical fields. In this work, a glucose-responsive supramolecular nanocluster was successfully constructed by the intermolecular complexation of phenylboronic acid modified β-cyclodextrin with adamantane modified polyethylenimine, which could be used as a biocompatible carrier for insulin and pCMV3-C-GFPSpark-Ins DNA which could express insulin co-delivery. Benefiting f  ...[more]

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