The Potential of ICP-MS as a Complementary Tool in Nanoparticle-Protein Corona Analysis

被引:9
|
作者
Fuentes-Cervantes, Ana [1 ]
Allica, Julia Ruiz [1 ]
Celis, Francisco Calderon [1 ]
Costa-Fernandez, Jose M. [1 ]
Encinar, Jorge Ruiz [1 ]
机构
[1] Univ Oviedo, Dept Phys & Analyt Chem, Avda Julian Claveria 8, Oviedo 33006, Spain
关键词
protein corona; ICP-MS; nanomaterials; proteins; nanoparticles; PLASMA-MASS SPECTROMETRY; GOLD NANOPARTICLES; QUANTUM-DOTS; SIZE; QUANTIFICATION; NANOMATERIALS; POPULATIONS; NUMBER;
D O I
10.3390/nano13061132
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The prolific applicability of nanomaterials has made them a common citizen in biological systems, where they interact with proteins forming a biological corona complex. These complexes drive the interaction of nanomaterials with and within the cells, bringing forward numerous potential applications in nanobiomedicine, but also arising toxicological issues and concerns. Proper characterization of the protein corona complex is a great challenge typically handled with the combination of several techniques. Surprisingly, despite inductively coupled plasma mass spectrometry (ICP-MS) being a powerful quantitative technique whose application in nanomaterials characterization and quantification has been consolidated in the last decade, its application to nanoparticle-protein corona studies is scarce. Furthermore, in the last decades, ICP-MS has experienced a turning point in its capabilities for protein quantification through sulfur detection, hence becoming a generic quantitative detector. In this regard, we would like to introduce the potential of ICP-MS in the nanoparticle protein corona complex characterization and quantification complementary to current methods and protocols.
引用
收藏
页数:16
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