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    • 1. 发明公开
    • DEGRADABLE MICROCAPSULES
    • ABBAUBARE MIKROKAPSELN
    • EP2303245A2
    • 2011-04-06
    • EP09780410.8
    • 2009-07-10
    • ETH ZurichSwissgenetics
    • KEMMER, ChristianFLURI, DavidWITSCHI, UlrichWEBER, WilfriedFUSSENEGGER, Martin
    • A61K9/50
    • A61K35/52A61K9/5042A61K9/5068
    • The invention relates to microcapsules consisting of a polymer degradable by a polypeptide comprising a drug or other compound of interest and a genetically engineered cell expressing said polypeptide in response to a triggering compound, and to methods of directed release of the compound of interest. The preferred polymer is optionally modified cellulose sulfate/poly-diallyl-dimethyl-ammonium chloride. Such microcapsules are non-toxic, do not elicit an immunological response and have an extended half-life time in mammals. The expression system for cellulase is, for example, based on TET and doxycycline, or E.REX and erythromycin. In another example, expression of cellulase is triggered by luteinizing hormone, which can be used for artificial insemination with microcapsules carrying sperm.
    • 本发明涉及由可由可包含药物或目的的其它化合物的多肽降解的聚合物和响应于引发化合物表达所述多肽的遗传工程改造的细胞组成的微胶囊以及目的化合物的定向释放方法。 优选的聚合物是任选改性的硫酸纤维素/聚二烯丙基二甲基氯化铵。 这样的微胶囊是无毒的,不引起免疫应答并且在哺乳动物中具有延长的半衰期。 纤维素酶的表达系统例如是基于TET和多西环素,或E.REX和红霉素。 在另一个实例中,纤维素酶的表达是由黄体生成激素引发的,其可用于携带精子的微胶囊的人工授精。