Abstract:Surface-enhanced
Raman spectroscopy (SERS) is a promising analytical
tool, but simultaneous detection of multiple targets using SERS remains
a challenge. Herein, a cauliflower-inspired 3D SERS substrate with
intense hot spots was prepared through sputtering Au nanoparticles
(Au NPs) on the surface of polydimethylsiloxane coated anodic aluminum
oxide (PDMS@AAO) complex substrate. As a result, the cauliflower-inspired
3D SERS substrate achieved the highest SERS activities at a sputtering
time of 8 min. Under the… Show more
“…After the cooperation of a surface plasmon polarization (SPP) mechanism with a hotspot effect existing between the metallic nanogaps [3], SERS can increase the sensitivity up to 10 8 -fold in the best case, enabling the detection of even a single molecule [3,4]. It could be also applicable to the analysis of foods [4][5][6][7][8], environmental pollutants [4], and various biological samples 10 8 -fold in the best case, enabling the detection of even a single molecule [3,4]. It could be also applicable to the analysis of foods [4][5][6][7][8], environmental pollutants [4], and various biological samples in life sciences [2,3,9].…”
Section: Introductionmentioning
confidence: 99%
“…After the cooperation of a surface plasmon polarization (SPP) mechanism with a hotspot effect existing between the metallic nanogaps [ 3 ], SERS can increase the sensitivity up to 10 8 -fold in the best case, enabling the detection of even a single molecule [ 3 , 4 ]. It could be also applicable to the analysis of foods [ 4 , 5 , 6 , 7 , 8 ], environmental pollutants [ 4 ], and various biological samples in life sciences [ 2 , 3 , 9 ]. However, in these practical applications, SERS easily encounters the issues of unrepeatable and/or irreproducible measurements.…”
Surface-enhanced Raman scattering (SERS) greatly increases the detection sensitivity of Raman scattering. However, its real applications are often degraded due to the unrepeatable preparation of SERS substrates. Herein presented is a very facile and cost-effective method to reproducibly produce a novel type of SERS substrate, a monolayer photonic crystal (PC). With a building block of laboratory-prepared monodisperse SiO2 particles deposited with space-tunable silver nanobulges (SiO2@nAg), a PC substrate was first assembled at the air–water interface through needle tip flowing, then transferred onto a silicon slide by a pulling technique. The transferred monolayer PCs were characterized by SEM and AFM to have a hexagonal close-packed lattice. They could increase Raman scattering intensity by up to 2.2 × 107-fold, as tested with p-aminothiophenol. The relative standard deviations were all below 5% among different substrates or among different locations on the same substrate. The excellent reproducibility was ascribed to the highly ordered structure of PCs, while the very high sensitivity was attributed to the strong hotspot effect caused by the appropriately high density of nanobulges deposited on SiO2 particles and by a closed lattice. The PC substrates were validated to be applicable to the SERS assay of trace thiol pesticides. Thiram pesticide is an example determined in apple juice samples at a concentration 102-fold lower than the food safety standard of China. This method is extendable to the analysis of other Raman-active thiol chemicals in different samples, and the substrate preparation approach can be modified for the fabrication of more PC substrates from other metallic nanobulge-deposited particles rather than silica only.
“…After the cooperation of a surface plasmon polarization (SPP) mechanism with a hotspot effect existing between the metallic nanogaps [3], SERS can increase the sensitivity up to 10 8 -fold in the best case, enabling the detection of even a single molecule [3,4]. It could be also applicable to the analysis of foods [4][5][6][7][8], environmental pollutants [4], and various biological samples 10 8 -fold in the best case, enabling the detection of even a single molecule [3,4]. It could be also applicable to the analysis of foods [4][5][6][7][8], environmental pollutants [4], and various biological samples in life sciences [2,3,9].…”
Section: Introductionmentioning
confidence: 99%
“…After the cooperation of a surface plasmon polarization (SPP) mechanism with a hotspot effect existing between the metallic nanogaps [ 3 ], SERS can increase the sensitivity up to 10 8 -fold in the best case, enabling the detection of even a single molecule [ 3 , 4 ]. It could be also applicable to the analysis of foods [ 4 , 5 , 6 , 7 , 8 ], environmental pollutants [ 4 ], and various biological samples in life sciences [ 2 , 3 , 9 ]. However, in these practical applications, SERS easily encounters the issues of unrepeatable and/or irreproducible measurements.…”
Surface-enhanced Raman scattering (SERS) greatly increases the detection sensitivity of Raman scattering. However, its real applications are often degraded due to the unrepeatable preparation of SERS substrates. Herein presented is a very facile and cost-effective method to reproducibly produce a novel type of SERS substrate, a monolayer photonic crystal (PC). With a building block of laboratory-prepared monodisperse SiO2 particles deposited with space-tunable silver nanobulges (SiO2@nAg), a PC substrate was first assembled at the air–water interface through needle tip flowing, then transferred onto a silicon slide by a pulling technique. The transferred monolayer PCs were characterized by SEM and AFM to have a hexagonal close-packed lattice. They could increase Raman scattering intensity by up to 2.2 × 107-fold, as tested with p-aminothiophenol. The relative standard deviations were all below 5% among different substrates or among different locations on the same substrate. The excellent reproducibility was ascribed to the highly ordered structure of PCs, while the very high sensitivity was attributed to the strong hotspot effect caused by the appropriately high density of nanobulges deposited on SiO2 particles and by a closed lattice. The PC substrates were validated to be applicable to the SERS assay of trace thiol pesticides. Thiram pesticide is an example determined in apple juice samples at a concentration 102-fold lower than the food safety standard of China. This method is extendable to the analysis of other Raman-active thiol chemicals in different samples, and the substrate preparation approach can be modified for the fabrication of more PC substrates from other metallic nanobulge-deposited particles rather than silica only.
“…In much of the multiplex sensing literature focused on other targets, the collected data have required post-measurement chemometric analyses to distinguish between each target. 34 In this work the toxins' spectral signals do not require additional separation or filtering as seen with many other immunosensors. [35][36][37] This sensing scheme aims to provide molecule-specific information regarding the target and the capture agent.…”
Section: Introductionmentioning
confidence: 99%
“…Additionally, previous literature reports of multiplex detection required multiple affinity agents, such as aptamers and antibodies, to enable such detection. 34,38 Each affinity agent is incredibly specific to the target and must often be paired with SERS tags or labels to achieve low limits of detection. [39][40][41] Thus, the use of a single non-traditional affinity agent, such as the polymer reported herein which relies on non-specific interactions, could remediate the need for multiple affinity agents.…”
A linear, methacrylamide polymer affinity agent was explored to capture two mycotoxins, deoxynivalenol (DON) and ochratoxin A (OTA), for multiplex surface-enhanced Raman scattering (SERS) detection. These mycotoxins are naturally occurring...
“…Simultaneous detection technology has been becoming a hot topic in analytical chemistry. Many methods have been reported for simultaneous detection of multi small molecular contaminants such as mycotoxins (Li et al, 2013(Li et al, , 2019Zhang et al, 2016;Wang et al, 2017a), pesticide residues (Bagheri et al, 2016;Wang et al, 2017b), and veterinary drugs (Taranova et al, 2015;Dasenaki et al, 2016;Zhu et al, 2016). Also, a lot of methods were described for simultaneous detection of multi microorganisms such as pathogenic bacteria (Li et al, 2015;Yoo et al, 2015;Vaisocherova-Lisalova et al, 2016), fungal pathogens (Playford et al, 2006;Priyanka et al, 2015;Rahn et al, 2016), and even varied pathogens that belong to different kingdoms (Leber et al, 2016).…”
Simultaneous detection technology has become a hot topic in analytical chemistry; however, very few reports on how to simultaneously detect small molecular contaminants and microorganisms have been in place. Aflatoxins are a group of highly toxic and carcinogenic compounds, which are produced mainly by Aspergillus flavus and Aspergillus parasiticus from section Flavi responsible for aflatoxin accumulation in stored cereals. Both aflatoxins and Aspergillus section Flavi were used to demonstrate the duplex real-time RCR method of simultaneously detecting small molecular contaminants and microorganisms. The detection of aflatoxins and Aspergillus section Flavi was carried out depending on the anti-idiotypic nanobody-phage V 2−5 and aflatoxin-synthesis related gene nor-1 (=aflD), respectively. The quantitative standard curves for simultaneous detection of aflatoxins and Aspergillus section Flavi were constructed, with detection limits of 0.02 ng/ml and 8 × 10 2 spores/g, respectively. Naturally contaminated maize samples (n = 25) were analyzed for a further validation. The results were in good agreement between the new developed method and the referential methods (high-performance liquid chromatography and the conventional plating counts).
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