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Concentration-dependent protein adsorption at the nano-bio interfaces of polymeric nanoparticles and serum proteins

机译:聚合物纳米颗粒和血清蛋白的纳米生物界面处的浓度依赖性蛋白质吸附

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Aim: A comprehensive understanding of nanoparticle (NP)-protein interaction (protein corona formation) is required. So far, many factors influencing this interaction have been investigated, like size and zeta potential. However, NPs exposure concentration has always been ignored. Herein, we aim to disclose the correlation of NPs exposure concentration with protein adsorption. Materials & methods: Four polymeric NPs systems possessing similar sizes (230 +/- 20 nm) but varied zeta potentials (-30 similar to+ 40 mv) were prepared. Physicochemical properties and protein adsorption upon NP-protein interaction were characterized. Results: Protein adsorption capacity and adsorbed protein types were NPs concentration-dependent. Conclusion: Considering the critical impacts of protein adsorption on NPs delivery, our work could be an urgent warning about the possible risks of dosage adjustment of nanoformulations.
机译:目的:需要综合理解纳米粒子(NP) - 蛋白相互作用(蛋白质电晕形成)。 到目前为止,已经研究了影响这种相互作用的许多因素,如尺寸和Zeta潜力。 然而,NPS曝光浓度一直被忽略。 这里,我们的目的是公开NPS暴露浓度与蛋白质吸附的相关性。 材料和方法:制备具有相似尺寸的四种聚合物NPS系统(230 +/-20nm)但是制备了各种Zeta电位(-30类似于+ 40mV)的变化。 表征了在NP-蛋白质相互作用时的物理化学性质和蛋白质吸附。 结果:蛋白吸附能力和吸附蛋白质类型是NPS浓度依赖性。 结论:考虑到蛋白质吸附对NPS递送的关键影响,我们的工作可能是关于纳米族种类的可能性调节可能风险的紧急警告。

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