Department of Pharmaceutical Sciences, Bouvé College of Health Sciences, Boston, Massachusetts, USA.
Dicerna Pharmaceuticals, Inc., Lexington, Massachusetts, 02421, USA.
AAPS J. 2020 Jun 3;22(4):83. doi: 10.1208/s12248-020-00464-x.
Upon systemic administration, nanoparticles encounter serum proteins in the biological system resulting in the formation of "protein corona" on the surface. Increased understanding of the relationship between nanoparticles' "chemical identity" and "biological identity" can contribute to improved clinical translation. Recent studies of protein corona composition on nanoparticles, including from our group, suggest that a strategic choice of materials can influence the types of protein adsorbed from plasma and lead to improved delivery efficiency. This mini-review reflects on the fundamental knowledge of nanoparticle protein corona and highlights the recent applications of protein corona on nanoparticles' systemic circulation, cell, and tissue-specific delivery. Important considerations on the safety and efficacy aspects pertaining to the exploration of nanoparticle protein corona's targeting effect are also summarized. Finally, the future perspectives of protein corona research are discussed.
系统给药后,纳米颗粒会在生物系统中遇到血清蛋白,从而在表面形成“蛋白冠”。增加对纳米颗粒“化学特性”和“生物特性”之间关系的了解有助于改善临床转化。最近对纳米颗粒上蛋白冠组成的研究,包括我们小组的研究,表明材料的战略性选择可以影响从血浆中吸附的蛋白质类型,并提高输送效率。这篇微型综述反映了纳米颗粒蛋白冠的基本知识,并强调了蛋白冠在纳米颗粒系统循环、细胞和组织特异性输送中的最新应用。还总结了与探索纳米颗粒蛋白冠靶向作用的安全性和有效性方面有关的重要考虑因素。最后,讨论了蛋白冠研究的未来展望。
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