PH-RESPONSIVE NANOPARTICLE USING MUSSEL ADHESIVE PROTEIN FOR DRUG DELIVERY AND METHOD FOR PREPARING THE SAME
    2.
    发明申请
    PH-RESPONSIVE NANOPARTICLE USING MUSSEL ADHESIVE PROTEIN FOR DRUG DELIVERY AND METHOD FOR PREPARING THE SAME 有权
    使用马斯胶粘蛋白进行药物输送的PH反应性纳米颗粒及其制备方法

    公开(公告)号:US20160263136A1

    公开(公告)日:2016-09-15

    申请号:US15000551

    申请日:2016-01-19

    Abstract: The present invention relates to a pH-responsive metal-catechol derivative nanoparticle for drug delivery based on a mussel adhesive protein, particularly Fe(III)-DOPA nanoparticle, and a method for preparing the same. A nanoparticle for drug delivery according to the present invention is prepared using a pH responsive substance, catechol derivative-metal complex, particularly Fe(III)-DOPA complex, based on a mussel adhesive protein. Thereby, the present invention has excellent biocompatibility, is capable of easily and quickly penetrating into a target cell, and releases a loaded drug under acidic conditions, which enables to selectively deliver a drug to a specific disease having an acidic environment.

    Abstract translation: 本发明涉及一种基于贻贝粘合蛋白,特别是Fe(III)-DOPA纳米颗粒的用于药物递送的pH响应性金属 - 儿茶酚衍生物纳米颗粒及其制备方法。 根据本发明的用于药物递送的纳米颗粒是使用基于贻贝粘合蛋白的pH响应物质,儿茶酚衍生物 - 金属络合物,特别是Fe(III)-DOPA复合物制备的。 因此,本发明具有优异的生物相容性,能够容易且快速地渗透到靶细胞中,并在酸性条件下释放负载药物,能够选择性地将药物递送至具有酸性环境的特定疾病。

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