Department of Physical Chemistry and EMaS, Universitat Rovira i Virgili, 43007 Tarragona, Spain.
ICREA, Passeig Lluís Companys 23, 08010 Barcelona, Spain.
Int J Mol Sci. 2020 Mar 24;21(6):2253. doi: 10.3390/ijms21062253.
Cancer heterogeneity increasingly requires ultrasensitive techniques that allow early diagnosis for personalized treatment. In addition, they should preferably be non-invasive tools that do not damage surrounding tissues or contribute to body toxicity. In this context, liquid biopsy of biological samples such as urine, blood, or saliva represents an ideal approximation of what is happening in real time in the affected tissues. Plasmonic nanoparticles are emerging as an alternative or complement to current diagnostic techniques, being able to detect and quantify novel biomarkers such as specific peptides and proteins, microRNA, circulating tumor DNA and cells, and exosomes. Here, we review the latest ideas focusing on the use of plasmonic nanoparticles in coded and label-free surface-enhanced Raman scattering (SERS) spectroscopy. Moreover, surface plasmon resonance (SPR) spectroscopy, colorimetric assays, dynamic light scattering (DLS) spectroscopy, mass spectrometry or total internal reflection fluorescence (TIRF) microscopy among others are briefly examined in order to highlight the potential and versatility of plasmonics.
癌症异质性越来越需要超灵敏的技术,以便早期诊断和个性化治疗。此外,这些技术最好是非侵入性的,不会损伤周围组织或导致身体毒性。在这种情况下,对尿液、血液或唾液等生物样本的液体活检代表了对受影响组织中实时情况的理想近似。等离子体纳米粒子作为当前诊断技术的替代或补充,正在出现,能够检测和定量新型生物标志物,如特定的肽和蛋白质、microRNA、循环肿瘤 DNA 和细胞以及外泌体。在这里,我们综述了最新的研究思路,重点介绍了等离子体纳米粒子在编码和无标记表面增强拉曼散射 (SERS) 光谱学中的应用。此外,简要考察了表面等离子体共振 (SPR) 光谱学、比色分析、动态光散射 (DLS) 光谱学、质谱或全内反射荧光 (TIRF) 显微镜等方法,以突出等离子体的潜力和多功能性。