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Tuning Hydrophobe Density and Length in an Anionic Polymer for Enhanced Intracellular Delivery of a CPP-based MAPKAP Kinase Ⅱ Inhibitor

机译:调节疏水聚合物的密度和长度的阴离子聚合物,以增强基于CPP的MAPKAP激酶Ⅱ抑制剂的细胞内传递。

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We demonstrate that tuning the ratio of polymer anionic to hydrophobic groups can optimize pH-responsive membrane destabilization and enhance intracellularization of a polycationic peptide drug. These results contribute critical knowledge of cell-material interactions that could have broad applicability towards expanding polymer-drug formulations for peptide and protein-based therapeutics.
机译:我们证明调整聚合物阴离子与疏水基团的比例可以优化pH响应膜去稳定化,并增强聚阳离子肽药物的胞内化。这些结果为细胞-材料相互作用的关键知识提供了知识,这些知识可能对扩展用于基于肽和蛋白质的治疗剂的聚合物-药物制剂具有广泛的适用性。

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