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首页> 外文期刊>Pharmaceutical Research >Targeting, Endocytosis, and Lysosomal Delivery of Active Enzymes to Model Human Neurons by ICAM-1-Targeted Nanocarriers
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Targeting, Endocytosis, and Lysosomal Delivery of Active Enzymes to Model Human Neurons by ICAM-1-Targeted Nanocarriers

机译:通过ICAM-1靶向纳米载体靶向,内吞作用和活性酶溶酶体递送以模拟人类神经元

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Purpose Delivery of therapeutics to neurons is paramount to treat neurological conditions, including many lysosomal storage disorders. However, key aspects of drug-carrier behavior in neurons are relatively unknown: the occurrence of non-canonical endocytic pathways (present in other cells); whether carriers that traverse the blood–brain barrier are, contrarily, retained within neurons; if neuron-surface receptors are accessible to bulky carriers compared to small ligands; or if there are differences regarding neuronal compartments (neuron body vs. neurites) pertaining said parameters. We have explored these questions using model polymer nanocarriers targeting intercellular adhesion molecule-1 (ICAM-1).
机译:目的向神经元提供治疗药物对于治疗神经系统疾病(包括许多溶酶体贮积症)至关重要。然而,神经元中药物携带者行为的关键方面还相对未知:非典型的内吞途径的发生(存在于其他细胞中);相反,穿过血脑屏障的携带者是否被保留在神经元内;与小配体相比,大型载体是否可接近神经元表面受体;或有关所述参数的神经元区室(神经元体与神经突)之间存在差异。我们已经使用针对细胞间粘附分子-1(ICAM-1)的模型聚合物纳米载体探索了这些问题。

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  • 来源
    《Pharmaceutical Research》 |2015年第4期|1264-1278|共15页
  • 作者单位

    Fischell Department of Bioengineering University of Maryland">(1);

    Program in Rare and Genetic Diseases IBV/CSIC Associated Unit Centro de Investigación Príncipe Felipe">(2);

    Centro de Investigación Biomédica en Red de Salud Mental (CIBERSAM) ISCIII">(3);

    Fischell Department of Bioengineering University of Maryland">(1);

    Institute for Bioscience and Biotechnology Research University of Maryland">(4);

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