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首页> 外文期刊>ACS nano >Intracellular release of endocytosed nanoparticles upon a change of ligand-receptor interaction
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Intracellular release of endocytosed nanoparticles upon a change of ligand-receptor interaction

机译:配体-受体相互作用改变后胞内释放的纳米颗粒在细胞内释放

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摘要

During passive endocytosis, nanosized particles are initially encapsulated by a membrane separating it from the cytosol. Yet, in many applications the nanoparticles need to be in direct contact with the cytosol in order to be active. We report a simulation study that elucidates the physical mechanisms by which such nanoparticles can shed their bilayer coating. We find that nanoparticle release can be readily achieved by a pH-induced lowering of the attraction between nanoparticle and membrane only if the nanoparticle is either very small or nonspherical. Interestingly, we find that in the case of large spherical nanoparticles, the reduction of attraction needs to be accompanied by exerting an additional tension on the membrane (e.g., via nanoparticle expansion) to achieve release. We expect these findings will contribute to the rational design of drug delivery strategies via nanoparticles.
机译:在被动内吞过程中,纳米颗粒最初是由将其与细胞溶胶分开的膜包裹的。然而,在许多应用中,纳米颗粒需要与细胞溶胶直接接触以使其具有活性。我们报告了一项模拟研究,阐明了此类纳米粒子可以脱落其双层涂层的物理机制。我们发现,仅当纳米颗粒非常小或非球形时,才可以通过pH诱导的纳米颗粒与膜之间的吸引力降低来轻松实现纳米颗粒的释放。有趣的是,我们发现,在大的球形纳米颗粒的情况下,吸引力的降低需要伴随着对膜施加额外的张力(例如,通过纳米颗粒膨胀)以实现释放。我们希望这些发现将有助于通过纳米颗粒合理设计药物递送策略。

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