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生物分子冠赋予纳米材料生物身份。

Biomolecular coronas provide the biological identity of nanosized materials.

机构信息

Centre for BioNano Interactions, School of Chemistry and Chemical Biology, Belfield, Dublin 4, Ireland.

出版信息

Nat Nanotechnol. 2012 Dec;7(12):779-86. doi: 10.1038/nnano.2012.207.

DOI:10.1038/nnano.2012.207
PMID:23212421
Abstract

The search for understanding the interactions of nanosized materials with living organisms is leading to the rapid development of key applications, including improved drug delivery by targeting nanoparticles, and resolution of the potential threat of nanotechnological devices to organisms and the environment. Unless they are specifically designed to avoid it, nanoparticles in contact with biological fluids are rapidly covered by a selected group of biomolecules to form a corona that interacts with biological systems. Here we review the basic concept of the nanoparticle corona and its structure and composition, and highlight how the properties of the corona may be linked to its biological impacts. We conclude with a critical assessment of the key problems that need to be resolved in the near future.

摘要

对纳米材料与生物体相互作用的研究正在推动关键应用的快速发展,包括通过靶向纳米粒子来改善药物输送,以及解决纳米技术设备对生物体和环境的潜在威胁。除非专门设计来避免,否则与生物流体接触的纳米粒子会迅速被一组选定的生物分子覆盖,形成与生物系统相互作用的冠。在这里,我们回顾了纳米粒子冠的基本概念及其结构和组成,并强调了冠的特性如何与其生物影响相关联。最后,我们对未来需要解决的关键问题进行了批判性评估。

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Nat Nanotechnol. 2013 Feb;8(2):137-43. doi: 10.1038/nnano.2012.237. Epub 2013 Jan 20.
2
Effects of the presence or absence of a protein corona on silica nanoparticle uptake and impact on cells.有无蛋白质冠对硅纳米颗粒摄取及其对细胞影响的作用。
ACS Nano. 2012 Jul 24;6(7):5845-57. doi: 10.1021/nn300223w. Epub 2012 Jun 29.
3
Transformations of nanomaterials in the environment.
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Pharmaceutics. 2025 Aug 10;17(8):1037. doi: 10.3390/pharmaceutics17081037.
4
Machine Learning and Artificial Intelligence in Nanomedicine.纳米医学中的机器学习与人工智能
Wiley Interdiscip Rev Nanomed Nanobiotechnol. 2025 Jul-Aug;17(4):e70027. doi: 10.1002/wnan.70027.
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In vivo genome editing of human haematopoietic stem cells for treatment of blood disorders using mRNA delivery.利用信使核糖核酸递送对人类造血干细胞进行体内基因组编辑以治疗血液疾病
Nat Biomed Eng. 2025 Aug 12. doi: 10.1038/s41551-025-01480-y.
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Predicting the protein corona on nanoparticles using random forest models with nanoparticle, protein, and experimental features.使用具有纳米颗粒、蛋白质和实验特征的随机森林模型预测纳米颗粒上的蛋白质冠层。
Nanoscale Adv. 2025 Jul 29. doi: 10.1039/d5na00425j.
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Nat Protoc. 2025 Aug 5. doi: 10.1038/s41596-025-01229-6.
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