Hybrid Nanoplasmonic Porous Biomaterial Scaffold for Liquid Biopsy Diagnostics Using Extracellular Vesicles

被引:53
|
作者
Rojalin, Tatu [1 ]
Koster, Hanna J. [1 ]
Liu, Juanjuan [2 ]
Mizenko, Rachel R. [1 ]
Tran, Di [1 ]
Wachsmann-Hogiu, Sebastian [2 ]
Carney, Randy P. [1 ]
机构
[1] Univ Calif Davis, Dept Biomed Engn, Davis, CA 95616 USA
[2] McGill Univ, Dept Bioengn, Montreal, PQ H3A 0G4, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
cancer; exosomes; nanomaterials; liquid biopsy; biopbotonies; Raman spectroscopy; SERS; SURFACE-ENHANCED RAMAN; EXOSOMES; SERS; CELLS; IDENTIFICATION; MONOLAYERS; GLASSES; SILVER;
D O I
10.1021/acssensors.0c00953
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
For more effective early-stage cancer diagnostics, there is a need to develop sensitive and specific, non- or minimally invasive, and cost-effective methods for identifying circulating nanoscale extracellular vesicles (EVs). Here, we report the utilization of a simple plasmonic scaffold composed of a microscale biosilicate substrate embedded with silver nanoparticles for surface-enhanced Raman scattering (SERS) analysis of ovarian and endometrial cancer EVs. These substrates are rapidly and inexpensively produced without any complex equipment or lithography. We extensively characterize the substrates with electron microscopy and outline a reproducible methodology for their use in analyzing EVs from in vitro and in vivo biofluids. We report effective chemical treatments for (i) decoration of metal surfaces with cysteamine to nonspecifically pull down EVs to SERS hotspots and (ii) enzymatic cleavage of extraluminal moieties at the surface of EVs that prevent localization of complementary chemical features (lipids/proteins) to the vicinity of the metal-enhanced fields. We observe a major loss of sensitivity for ovarian and endometrial cancer following enzymatic cleavage of EVs extraluminal domain, suggesting its critical significance for diagnostic platforms. We demonstrate that the SERS technique represents an ideal tool to assess and measure the high heterogeneity of EVs isolated from clinical samples in an inexpensive, rapid, and label-free assay.
引用
收藏
页码:2820 / 2833
页数:14
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