免疫系统
体内
体内分布
补体系统
体外
化学
抗体
纳米毒理学
先天免疫系统
生物物理学
纳米技术
细胞生物学
纳米颗粒
计算生物学
生物
材料科学
免疫学
生物化学
生物技术
作者
Sonia Panico,Sara Capolla,Sara Bozzer,Giuseppe Toffoli,Michele Dal Bo,Paolo Macor
出处
期刊:Pharmaceutics
[Multidisciplinary Digital Publishing Institute]
日期:2022-11-26
卷期号:14 (12): 2605-2605
被引量:48
标识
DOI:10.3390/pharmaceutics14122605
摘要
Nanoparticles (NPs) are versatile candidates for nanomedical applications due to their unique physicochemical properties. However, their clinical applicability is hindered by their undesirable recognition by the immune system and the consequent immunotoxicity, as well as their rapid clearance in vivo. After injection, NPs are usually covered with layers of proteins, called protein coronas (PCs), which alter their identity, biodistribution, half-life, and efficacy. Therefore, the characterization of the PC is for in predicting the fate of NPs in vivo. The aim of this review was to summarize the state of the art regarding the intrinsic factors closely related to the NP structure, and extrinsic factors that govern PC formation in vitro. In addition, well-known opsonins, including complement, immunoglobulins, fibrinogen, and dysopsonins, such as histidine-rich glycoprotein, apolipoproteins, and albumin, are described in relation to their role in NP detection by immune cells. Particular emphasis is placed on their role in mediating the interaction of NPs with innate and adaptive immune cells. Finally, strategies to reduce PC formation are discussed in detail.
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