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Improving Targeting of Metal-Phenolic Capsules by the Presence of Protein Coronas

机译:蛋白质电晕的存在改善金属酚类胶囊的靶向。

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Particles adsorb proteins when they enter a physiological environment; this results in a surface coating termed a "protein corona". A protein corona can affect both the properties and functionalities of engineered particles. Here, we prepared hyaluronic acid (HA)-based capsules through the assembly of metal phenolic networks (MPNs) and engineered their targeting ability in the absence and presence of protein coronas by varying the HA molecular weight. The targeting ability of the capsules was HA molecular weight dependent, and a high HA molecular weight (>50 kDa) was required for efficient targeting. The specific interactions between high molecular weight HA capsules and receptor-expressing cancer cells were negligibly affected by the presence of protein coronas, whereas nonspecific capsule cell interactions were significantly reduced in the presence of a protein corona derived from human serum. Consequently, the targeting specificity of HA-based MPN capsules was enhanced due to the formation of a protein corona. This study highlights the significant and complex roles of a protein corona in biointeractions and demonstrates how protein coronas can be used to improve the targeting specificity of engineered particles.
机译:粒子进入生理环境时会吸收蛋白质。这导致表面涂层被称为“蛋白质电晕”。蛋白质电晕可以影响工程颗粒的性质和功能。在这里,我们通过组装金属酚醛网络(MPNs)制备了基于透明质酸(HA)的胶囊,并通过改变HA分子量设计了在不存在和存在蛋白质电晕的情况下的靶向能力。胶囊的靶向能力取决于HA分子量,有效的靶向需要高HA分子量(> 50 kDa)。高分子量HA胶囊与表达受体的癌细胞之间的特异性相互作用受蛋白质电晕的影响可忽略不计,而存在源自人血清的蛋白质电晕则非特异性胶囊细胞的相互作用显着降低。因此,由于形成蛋白质电晕,增强了基于HA的MPN胶囊的靶向特异性。这项研究突出了蛋白质电晕在生物相互作用中的重要和复杂的作用,并展示了蛋白质电晕如何用于改善工程颗粒的靶向特异性。

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