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Hepatic-targeting microcapsules construction by self-assembly of bioactive galactose-branched polyelectrolyte for controlled drug release system.

Hepatic-targeting microcapsules construction by self-assembly of bioactive galactose-branched polyelectrolyte for controlled drug release system. Research Abstract Details 

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  • Hepatic-targeting microcapsules construction by self-assembly of bioactive galactose-branched polyelectrolyte for controlled drug release system. Abstract Text:

    fu zhangFu Zhang,qi wuQi Wu,zhi-chun chenZhi-Chun Chen,ming zhangMing Zhang,xian-fu linXian-Fu Lin,fu zhangFu Zhang,qi wuQi Wu,zhi-chun chenZhi-Chun Chen,ming zhangMing Zhang,xian-fu linXian-Fu Lin,fu zhangFu Zhang,qi wuQi Wu,zhi-chun chenZhi-Chun Chen,ming zhangMing Zhang,xian-fu linXian-Fu Lin,

    We describe the construction of hepatic-targeting microcapsules by self-assembly of chemo-enzymatic synthesized poly(vinyl galactose ester-co-methacryloxyethyl trimethylammonium chloride) (PGEDMC) containing galactose branches, which can be specifically recognized by membrane bound galactose receptors (ASGPR), for acyclovir (ACV) controlled release system. Alternate deposition of PGEDMC and poly(sodium 4-styrenesulfonate) (PSS) was carried out on ACV microcrystals. It was revealed that the drug release rate decreases with the increase of coated layer number and a microcapsule-drying treatment would enhance the sustained release effect probably because of a multilayer shrink and tightness during the process. The complete release of ACV yielded a hollow PGEDMC/PSS multilayered network with favorable integrity and nano-thickness by TEM and SEM. The potential targetability of the system was proved in vitro by PNA lectin recognition. Lectin hardly adsorbed on the film where the outmost layer was a polyanion or a polycation without galactose component. Whilst the galactose-containing layer (PGEDMC) was the outmost layer, a significant lectin combination was observed. This technique could provide a promising way to encapsulate and deliver various target substances in biological and pharmaceutical applications.

    Hepatic-targeting microcapsules construction by self-assembly of bioactive galactose-branched polyelectrolyte for controlled drug release system. Publishing Authors By Initials

    f zhangF Zhang,q wuQ Wu,zc chenZC Chen,m zhangM Zhang,xf linXF Lin,f zhangF Zhang,q wuQ Wu,zc chenZC Chen,m zhangM Zhang,xf linXF Lin,f zhangF Zhang,q wuQ Wu,zc chenZC Chen,m zhangM Zhang,xf linXF Lin,

    For similar abstracts research abstracts see: abstracts research

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    Hepatic-targeting microcapsules construction by self-assembly of bioactive galactose-branched polyelectrolyte for controlled drug release system. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: Journal of colloid and interface science

    VOLUME: 317

    Page Numbers: 477-84

    Journal Abbreviation:

    ISSN: 0021-9797

    DAY: 29

    MONTH: 09

    YEAR: 2007

    Hepatic-targeting microcapsules construction by self-assembly of bioactive galactose-branched polyelectrolyte for controlled drug release system. Information

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    LANGUAGE: eng

    NlmUniqueID: 43125

    Hepatic-targeting microcapsules construction by self-assembly of bioactive galactose-branched polyelectrolyte for controlled drug release system. Keywords Mesh Terms:

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    Grant and Affiliation Information for Hepatic-targeting microcapsules construction by self-assembly of bioactive galactose-branched polyelectrolyte for controlled drug release system.

    AFFILIATION: Department of Chemistry, Zhejiang University, Hangzhou 310027, People's Republic of China.

    Country: United States

    United States Research PublicationUnited States Research Publication

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    MEDLINETA: J Colloid Interface Sci

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