首页> 外文期刊>Langmuir: The ACS Journal of Surfaces and Colloids >Membrane Wrapping Pathway of Injectable Hydrogels: From Vertical Capillary Adhesion to Lateral Compressed Wrapping
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Membrane Wrapping Pathway of Injectable Hydrogels: From Vertical Capillary Adhesion to Lateral Compressed Wrapping

机译:注射水凝胶的膜包裹途径:从垂直毛细管粘附到侧向压缩包装

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摘要

Membrane wrapping pathway of injectable hydrogels (IHs) plays a vital role in the nanocarrier effectiveness and biomedical safety. Although considerable progress in understanding this complicated process has been made, the mechanism behind this process has remained elusive. Herein, with the help of large-scale dissipative particle dynamics simulations, we explore the molecular mechanism of membrane wrapping by systematically examining the IH architectures and hydrogel-lipid binding strengths. To the best of our knowledge, this is the first report on the membrane wrapping pathway on which IHs transform from vertical capillary adhesion to lateral compressed wrapping. This transformation results from the elastocapillary deformation of networked gels and nanoscale confinement of the bilayer membrane, and it takes long time for the IHs to be fully wrapped owing to the high energy barriers and wrapping- induced shape deformation. Collapsed morphologies and small compressed angles are identified in the IH capsules with a thick shell or strong binding strength to lipids. In addition, the IHs binding intensively to the membrane exhibit special nanoscale mixing and favorable deformability during the wrapping process. Our study provides a detailed mechanistic understanding of the influence of architecture and binding strength on the IH membrane wrapping efficiency. This work may serve as rational guidance for the design and fabrication of IH-based drug carriers and tissue engineering.
机译:可注射水凝胶(IHS)的膜包裹途径在纳米载体效力和生物医学安全中起着至关重要的作用。虽然已经取得了相当大的进展,但已经取得了相当大的进展,但该过程背后的机制仍然难以捉摸。在此,在大规模耗散粒子动力学模拟的帮助下,我们通过系统地检查IH架构和水凝胶 - 脂质结合强度来探讨膜包装的分子机制。据我们所知,这是关于膜包裹途径的第一个报告,其中IHS从垂直毛细管粘附到横向压缩包装的膜包裹途径。这种转化产生了网络化凝胶的弹性变形和双层膜的纳米尺度限制,因此由于高能量屏障和包装诱导的形状变形而完全包裹的IHS需要很长时间。在IH胶囊中鉴定坍塌的形态和小压缩角,具有厚厚的壳体或对脂质的强粘合强度。另外,在包装过程中,IHS与膜强烈结合到膜上表现出特殊的纳米级混合和有利的变形性。我们的研究提供了对结构和结合强度对IH膜包装效率的影响的详细机制理解。这项工作可作为IH基药载体和组织工程的设计和制造的合理指导。

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