Label-free and liquid state SERS detection of multi-scaled bioanalytes via light-induced pinpoint colloidal assembly

Surface-enhanced Raman scattering (SERS) has been extensively applied to detect complex analytes due to its ability to enhance the fingerprint signals of molecules around nanostructured metallic surfaces. Thus, it is essential to design SERS-active nanostructures with abundant electromagnetic hotspo...

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Veröffentlicht in:Biosensors & bioelectronics 2024-11, Vol.264, p.116663, Article 116663
Hauptverfasser: Han, Seungyeon, Park, Junhee, Moon, Sunghyun, Eom, Seonghyeon, Jin, Chang Min, Kim, Seungmin, Ryu, Yong-Sang, Choi, Yeonho, Lee, Jong Bum, Choi, Inhee
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container_title Biosensors & bioelectronics
container_volume 264
creator Han, Seungyeon
Park, Junhee
Moon, Sunghyun
Eom, Seonghyeon
Jin, Chang Min
Kim, Seungmin
Ryu, Yong-Sang
Choi, Yeonho
Lee, Jong Bum
Choi, Inhee
description Surface-enhanced Raman scattering (SERS) has been extensively applied to detect complex analytes due to its ability to enhance the fingerprint signals of molecules around nanostructured metallic surfaces. Thus, it is essential to design SERS-active nanostructures with abundant electromagnetic hotspots in a probed volume according to the dimensions of the analytes, as the analytes must be located in their hotspots for maximum signal enhancement. Herein, we demonstrate a simple method for detecting robust SERS signals from multi-scaled bioanalytes, regardless of their dimensions in the liquid state, through a photothermally driven co-assembly with colloidal plasmonic nanoparticles as signal enhancers. Under resonant light illumination, plasmonic nanoparticles and analytes in the solution quickly assemble at the focused surface area by convective movements induced by the photothermal heating of the plasmonic nanoparticles without any surface modification. Such collective assemblies of plasmonic nanoparticles and analytes were optimized by varying the optical density and surface charge of the nanoparticles, the viscosity of the solvent, and the light illumination time to maximize the SERS signals. Using these light-induced co-assemblies, the intrinsic SERS signals of small biomolecules can be detected down to nanomolar concentrations based on their fingerprint spectra. Furthermore, large-sized biomarkers, such as viruses and exosomes, were successfully detected without labels, and the complexity of the collected spectra was statistically analyzed using t-distributed stochastic neighbor embedding combined with support vector machine (t-SNE + SVM). The proposed method is expected to provide a robust and convenient method to sensitively detect biologically and environmentally relevant analytes at multiple scales in liquid samples. A method utilizing photothermally driven assembly of colloidal plasmonic nanoparticles and multi-scaled bioanalytes is presented for enhancing SERS signals. This approach enables label-free detection of various biomolecules, including small biomolecules and larger biomarkers like viruses and exosomes, offering a robust and sensitive means to detect analytes in liquid samples. [Display omitted]
doi_str_mv 10.1016/j.bios.2024.116663
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Such collective assemblies of plasmonic nanoparticles and analytes were optimized by varying the optical density and surface charge of the nanoparticles, the viscosity of the solvent, and the light illumination time to maximize the SERS signals. Using these light-induced co-assemblies, the intrinsic SERS signals of small biomolecules can be detected down to nanomolar concentrations based on their fingerprint spectra. Furthermore, large-sized biomarkers, such as viruses and exosomes, were successfully detected without labels, and the complexity of the collected spectra was statistically analyzed using t-distributed stochastic neighbor embedding combined with support vector machine (t-SNE + SVM). The proposed method is expected to provide a robust and convenient method to sensitively detect biologically and environmentally relevant analytes at multiple scales in liquid samples. 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A method utilizing photothermally driven assembly of colloidal plasmonic nanoparticles and multi-scaled bioanalytes is presented for enhancing SERS signals. This approach enables label-free detection of various biomolecules, including small biomolecules and larger biomarkers like viruses and exosomes, offering a robust and sensitive means to detect analytes in liquid samples. 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source MEDLINE; Elsevier ScienceDirect Journals
subjects Biomarkers
Biosensing Techniques - methods
Colloids - chemistry
Exosomes
Exosomes - chemistry
Gold - chemistry
Humans
Light
Metal Nanoparticles - chemistry
Photothermal convection
Plasmonic nanoparticles
Silver - chemistry
Spectrum Analysis, Raman - methods
Surface-enhanced Raman spectroscopy
Viruses
title Label-free and liquid state SERS detection of multi-scaled bioanalytes via light-induced pinpoint colloidal assembly
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