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    • 5. 发明授权
    • Stimulating vascular growth by administration of DNA sequences encoding VEGF
    • 通过施用编码VEGF的DNA序列刺激血管生长
    • US06228844B1
    • 2001-05-08
    • US08979686
    • 1997-11-26
    • Jon A. WolffDavid J. DukePhilip L. Felgner
    • Jon A. WolffDavid J. DukePhilip L. Felgner
    • A61K3800
    • A61K48/00C12N15/87
    • The present invention provides a method for delivering a pharmaceutical polypeptide to the interior of a cardiac cell of a vertebrate in vivo, comprising the step of introducing a preparation comprising a pharmaceutically acceptable injectable carrier and naked polynucleotide operatively coding for the polypeptide into the interstitial space of the heart, whereby the naked polynucleotide is taken up into the interior of the cell and has a pharmacological effect on the vertebrate such as inducing vascular growth. In a preferred embodiment wherein the polynucleotide encodes polypeptide immunologically foreign to the vertebrate, the delivery method preferably comprises delivering an immunosuppressive agent to the vertebrate to limit immune responses directed to the polypeptide.
    • 本发明提供了一种用于在体内将药物多肽递送至脊椎动物心脏细胞内部的方法,其包括将包含药学上可接受的可注射载体的制剂和可操作地编码多肽的裸核苷酸引入到 心脏,由此裸露的多核苷酸被吸收到细胞的内部并且对脊椎动物具有药理作用,例如诱导血管生长。 在其中多核苷酸编码对脊椎动物免疫外源的多肽的优选实施方案中,递送方法优选包括将免疫抑制剂递送至脊椎动物以限制针对多肽的免疫应答。
    • 6. 发明授权
    • Expression of exogenous polynucleotide sequences in a vertebrate
    • 外源多核苷酸序列在脊椎动物中的表达
    • US06706694B1
    • 2004-03-16
    • US09588655
    • 2000-06-06
    • Jon A. WolffDavid J. DukePhilip L. Felgner
    • Jon A. WolffDavid J. DukePhilip L. Felgner
    • A61K4800
    • B82Y5/00A61K48/00C12N15/87
    • The present invention provides a method for delivering a pharmaceutical polypeptide to the interior of a cardiac cell of a vertebrate in vivo, comprising the step of introducing a preparation comprising a pharmaceutically acceptable injectable carrier and naked polynucleotide operatively coding for the polypeptide into the interstitial space of the heart, whereby the naked polynucleotide is taken up into the interior of the cell and has a pharmacological effect on the vertebrate. In a preferred embodiment wherein the polynucleotide encodes polypeptide immunologically foreign to the vertebrate, the delivery method preferably comprises delivering an immunosuppressive agent to the vertebrate to limit immune responses directed to the polypeptide.
    • 本发明提供了一种用于在体内将药物多肽递送至脊椎动物心脏细胞内部的方法,其包括将包含药学上可接受的可注射载体的制剂和可操作地编码多肽的裸核苷酸引入到 心脏,其中裸多核苷酸被吸收到细胞内部并且对脊椎动物具有药理作用。 在其中多核苷酸编码对脊椎动物免疫外源的多肽的优选实施方案中,递送方法优选包括将免疫抑制剂递送至脊椎动物以限制针对多肽的免疫应答。