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揭示聚合物药物纳米载体蛋白冠的陷阱。

Unveiling the pitfalls of the protein corona of polymeric drug nanocarriers.

机构信息

Center for Research in Molecular Medicine and Chronic Diseases, 15782, Santiago de Compostela, Spain.

Instituto de Investigación Sanitaria de Santiago de Compostela (IDIS), IDIS Research Institute, 15706, Santiago de Compostela, Spain.

出版信息

Drug Deliv Transl Res. 2020 Jun;10(3):730-750. doi: 10.1007/s13346-020-00745-0.

Abstract

The protein corona is a natural protein layer spontaneously formed around nanomaterials when exposed to biological media. This layer can alter the nanosystems' biological performance, particularly their tissue accumulation, cellular uptake, clearance by the immune system, toxicity, and even the release profile of their payloads. Hence, the characterization of this protein layer has become a critical step when developing a new nanomedicine. The modification of the nanosystem fate by the protein corona, systematically ignored in the vast majority of the nanotechnology-based research, may have contributed to the low in vitro/in vivo correlation. Actually, the protein corona of polymeric nanosystems has been scarcely studied in the literature, and most studies have been focused instead on metallic nanoparticles and liposomes. In this review, we analyzed the influence of the physicochemical properties and composition of the polymeric nanosystems on the protein layer deposited around them. In addition, we present some recommendations on how to perform the protein corona studies of polymeric nanoparticles, which, hopefully, will contribute to obtain more reliable and reproducible data in the future. Graphical abstract.

摘要

蛋白质冠是纳米材料暴露于生物介质时自然形成的一层天然蛋白质。这一层可以改变纳米系统的生物学性能,特别是它们在组织中的积累、细胞摄取、免疫系统清除、毒性,甚至它们有效载荷的释放情况。因此,当开发一种新的纳米药物时,对这种蛋白质层进行特征描述已成为一个关键步骤。在绝大多数基于纳米技术的研究中,系统地忽略了蛋白质冠对纳米系统命运的修饰,这可能导致了体外/体内相关性低。实际上,聚合物纳米系统的蛋白质冠在文献中研究甚少,而大多数研究集中在金属纳米粒子和脂质体上。在这篇综述中,我们分析了聚合物纳米系统的物理化学性质和组成对沉积在其周围的蛋白质层的影响。此外,我们还就如何进行聚合物纳米粒子的蛋白质冠研究提出了一些建议,希望这些建议能有助于未来获得更可靠和可重复的数据。

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