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金纳米颗粒作为一种临床纳米材料,应该了解蛋白质冠。

Gold nanoparticle should understand protein corona for being a clinical nanomaterial.

机构信息

Pharmaceutical Research Center, Pharmaceutical Technology Institute, Mashhad University of Medical Sciences, Mashhad, Iran.

Department of Pharmaceutical Chemistry, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran.

出版信息

J Control Release. 2018 Feb 28;272:39-53. doi: 10.1016/j.jconrel.2018.01.002. Epub 2018 Jan 4.

Abstract

Gold nanoparticles (AuNPs) have attracted great attention in biomedical fields due to their unique properties. However, there are few reports on clinical trial of these nanoparticles. In vivo, AuNPs face complex biological fluids containing abundant proteins, which challenge the prediction of their fate that is known as "bio-identity". These proteins attach onto the AuNPs surface forming protein corona that makes the first step of nano-bio interface and dictates the subsequent AuNPs fate. Protein corona formation even stealth active targeting effect of AuNPs. Manipulating the protein corona identity based on the researcher goal is the way to employ corona to achieve maximum effect in therapy or other applications. In this review, we provide details on the biological identity of AuNPs under various environmental- and/or physiological conditions. We also highlight how the particular corona can direct the biodistribution of AuNPs. We further discuss the strategies available for controlling or reducing corona formation on AuNPs surface and achieving desired effects using AuNPs in vivo by engineering protein corona on their surface.

摘要

金纳米粒子(AuNPs)由于其独特的性质,在生物医学领域引起了极大的关注。然而,关于这些纳米粒子的临床试验报告却很少。在体内,AuNPs 面临着含有丰富蛋白质的复杂生物流体,这对它们的命运预测构成了挑战,这种预测被称为“生物识别”。这些蛋白质附着在 AuNPs 表面形成蛋白质冠,这是纳米生物界面的第一步,并决定了随后 AuNPs 的命运。蛋白质冠的形成甚至使 AuNPs 的主动靶向效果“隐身”。根据研究人员的目标来操纵蛋白质冠的特性是利用这种冠来实现治疗或其他应用中最大效果的一种方式。在这篇综述中,我们详细介绍了在各种环境和/或生理条件下 AuNPs 的生物学特性。我们还强调了特定的蛋白质冠如何指导 AuNPs 的生物分布。我们进一步讨论了控制或减少 AuNPs 表面蛋白质冠形成的策略,以及通过在其表面工程化蛋白质冠来实现使用 AuNPs 在体内获得所需效果的策略。

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