Cargando…

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

[Image: see text] 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 sca...

Descripción completa

Detalles Bibliográficos
Autores principales: Rojalin, Tatu, Koster, Hanna J., Liu, Juanjuan, Mizenko, Rachel R., Tran, Di, Wachsmann-Hogiu, Sebastian, Carney, Randy P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7522966/
https://www.ncbi.nlm.nih.gov/pubmed/32935542
http://dx.doi.org/10.1021/acssensors.0c00953
_version_ 1783588296684732416
author Rojalin, Tatu
Koster, Hanna J.
Liu, Juanjuan
Mizenko, Rachel R.
Tran, Di
Wachsmann-Hogiu, Sebastian
Carney, Randy P.
author_facet Rojalin, Tatu
Koster, Hanna J.
Liu, Juanjuan
Mizenko, Rachel R.
Tran, Di
Wachsmann-Hogiu, Sebastian
Carney, Randy P.
author_sort Rojalin, Tatu
collection PubMed
description [Image: see text] 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.
format Online
Article
Text
id pubmed-7522966
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher American Chemical Society
record_format MEDLINE/PubMed
spelling pubmed-75229662020-09-29 Hybrid Nanoplasmonic Porous Biomaterial Scaffold for Liquid Biopsy Diagnostics Using Extracellular Vesicles Rojalin, Tatu Koster, Hanna J. Liu, Juanjuan Mizenko, Rachel R. Tran, Di Wachsmann-Hogiu, Sebastian Carney, Randy P. ACS Sens [Image: see text] 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. American Chemical Society 2020-09-16 2020-09-25 /pmc/articles/PMC7522966/ /pubmed/32935542 http://dx.doi.org/10.1021/acssensors.0c00953 Text en Copyright © 2020 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Rojalin, Tatu
Koster, Hanna J.
Liu, Juanjuan
Mizenko, Rachel R.
Tran, Di
Wachsmann-Hogiu, Sebastian
Carney, Randy P.
Hybrid Nanoplasmonic Porous Biomaterial Scaffold for Liquid Biopsy Diagnostics Using Extracellular Vesicles
title Hybrid Nanoplasmonic Porous Biomaterial Scaffold for Liquid Biopsy Diagnostics Using Extracellular Vesicles
title_full Hybrid Nanoplasmonic Porous Biomaterial Scaffold for Liquid Biopsy Diagnostics Using Extracellular Vesicles
title_fullStr Hybrid Nanoplasmonic Porous Biomaterial Scaffold for Liquid Biopsy Diagnostics Using Extracellular Vesicles
title_full_unstemmed Hybrid Nanoplasmonic Porous Biomaterial Scaffold for Liquid Biopsy Diagnostics Using Extracellular Vesicles
title_short Hybrid Nanoplasmonic Porous Biomaterial Scaffold for Liquid Biopsy Diagnostics Using Extracellular Vesicles
title_sort hybrid nanoplasmonic porous biomaterial scaffold for liquid biopsy diagnostics using extracellular vesicles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7522966/
https://www.ncbi.nlm.nih.gov/pubmed/32935542
http://dx.doi.org/10.1021/acssensors.0c00953
work_keys_str_mv AT rojalintatu hybridnanoplasmonicporousbiomaterialscaffoldforliquidbiopsydiagnosticsusingextracellularvesicles
AT kosterhannaj hybridnanoplasmonicporousbiomaterialscaffoldforliquidbiopsydiagnosticsusingextracellularvesicles
AT liujuanjuan hybridnanoplasmonicporousbiomaterialscaffoldforliquidbiopsydiagnosticsusingextracellularvesicles
AT mizenkorachelr hybridnanoplasmonicporousbiomaterialscaffoldforliquidbiopsydiagnosticsusingextracellularvesicles
AT trandi hybridnanoplasmonicporousbiomaterialscaffoldforliquidbiopsydiagnosticsusingextracellularvesicles
AT wachsmannhogiusebastian hybridnanoplasmonicporousbiomaterialscaffoldforliquidbiopsydiagnosticsusingextracellularvesicles
AT carneyrandyp hybridnanoplasmonicporousbiomaterialscaffoldforliquidbiopsydiagnosticsusingextracellularvesicles