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Self-Assembly Mechanism of a Peptide-Based Drug Delivery Vehicle

机译:肽基药物传递载体的自组装机制

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We report the mechanism of the concentration-dependent self-assembly of a tetrapeptide. Peptide Boc-Trp-Leu-Trp-Leu-OMe self-assembles to form discrete nanospheres at a low concentration. Tryptophan side chains point outwards of the nanospheres while leucine side chains point towards the core of the nanospheres. The nanospheres fuse together to become microspheres with the increase in the peptide concentration. At higher concentrations of the peptide, the microspheres start clustering. This is stabilized by the aromatic interactions between the side chains of the tryptophan residues that cover the outer surface of the peptide microspheres. In addition to behaving like the conventional hollow sphere-based drug delivery vehicles which entraps the drug and performs stimuli-responsive release, this prototype can interact, stabilize, and intercalate hydrophobic dye carboxyfluorescein and anti-cancer drug curcumin even on the surface through aromatic interactions. The dye/drug can be released in acidic pH and in the presence of physiologically relevant ions such as potassium.
机译:我们报告了四肽浓度依赖性自组装的机制。肽Boc-Trp-Leu-Trp-Leu-OMe自组装形成低浓度的离散纳米球。色氨酸侧链指向纳米球的外部,而亮氨酸侧链指向纳米球的核心。随着肽浓度的增加,纳米球融合在一起成为微球。在较高的肽浓度下,微球开始聚集。这通过覆盖肽微​​球外表面的色氨酸残基的侧链之间的芳族相互作用而稳定。除了具有像传统的基于空心球的中空药物递送载体的功能一样,该载体可以截留药物并执行刺激响应性释放,该原型甚至可以通过芳族相互作用在表面上相互作用,稳定和插入疏水性染料羧基荧光素和抗癌姜黄素。染料/药物可以在酸性pH值和生理相关离子(例如钾)的存在下释放。

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