Surface-enhanced Raman Scattering Intensity Research Articles

Nanozyme and bifunctional nanobody-based colorimetric-SERS dual-mode Immunosensor for microcystin-LR detection

Microcystin-LR (MC-LR), a potent cyanotoxin in freshwater, poses a risk of severe liver damage and other health issues, making its detection vital. However, the detection capabilities of conventional antibodies are constrained, which limited their use in immunoassays. In this work, we designed a new bifunctional nanobody, named A2.3-SBP (comprised of nanobody and streptavidin binding peptide), capable of binding with MC-LR and streptavidin. Based on A2.3-SBP and Fe3O4@Au-Pt nanozyme, we introduced an enzyme-free immunosensor that operated in microplate with colorimetric and surface-enhanced Raman scattering (SERS) detection modes. The dual-mode assay showed color changes and SERS intensity directly correlating to MC-LR concentrations with a range from 1.0 to 500 ng/mL and a limit of detection of 0.26 and 0.032 ng/mL, respectively. This strategy eliminated the need for complex enzymatic reactions and realized dual-signal detection of MC-LR in 96 water samples (0.03 μg/kg) within 30 min, suggesting its potential in drinking water detection.

Lithium-doped ZrO2 nanoparticles for SERS-based norfloxacin drug detection

Surface-enhanced Raman scattering (SERS) spectroscopy is a highly specific and ultrasensitive analytical technique; thus, it is an ideal candidate for therapeutic drug monitoring. However, SERS measurements of drugs in a sample are inevitably affected by the environment. In this study, we synthesized ZrO2 nanoparticles (NPs) doped with the first group of elements (Li, Na, and K) in the main block and evaluated their SERS performance. The results showed that Li-ion doping could significantly enhance the SERS effect, and the degree of enhancement depended on the type and concentration of the doped ions. Compared with the highly stable ZrO2, Li ion-doped ZrO2 (Li-ZrO2) exhibited a significant increase in SERS activity. In particular, 1 % Li-ZrO2 NPs exhibited excellent SERS enhancement with an enhancement factor (EF) of 2.60 × 104, which was attributed to the decreased band gap and improved the charge transfer (CT) process after Li ion doping. The adsorption capacity of the Li-ZrO2 NPs for norfloxacin (NOR) molecules was gradually saturated with time. In addition, both acidic and alkaline conditions were unfavorable for NOR detection by the substrate. The SERS intensity exhibited a linear relationship within the NOR concentration range of 10−3–10–6 mol/L, and approximately 97.51 % of the active ingredients were detected, with a competitive detection limit of 10−6 mol/L. Furthermore, NOR detection is cost-effective and time-efficient, and the results of our study can aid in the research process and support practical applications. The proposed study provides a guidance for improving the SERS activity of semiconductors for sensing.

Application of stealth nanobeacon for traceability assurance in pharmaceutical tablets via surface-enhanced Raman scattering during the tablet coating process

Microtaggant technologies for on-dose authentication have garnered significant interest for use in the anti-counterfeit activities and traceability of pharmaceutical dosage forms. Previously, we proposed a stealth nanobeacon (NB) comprising self-assembled colloidal gold nanoparticles with reporter molecules that demonstrated characteristic surface-enhanced Raman scattering (SERS) activity. However, the integration of such microtaggants into standard production lines remains underexplored. In this study, we demonstrate the incorporation of NB into tablet coatings using a simple mixing method with conventional coating solutions. Rapid and discernible SERS responses from the NB-coated tablets were observed in response to laser excitation at 785 nm for 0.1s, implying that it is an advanced and efficient method for counterfeit detection. In addition, the SERS intensity of NB increased with coating time, suggesting that NB can be used as a tracer for the real-time monitoring of coating thickness. Furthermore, NB-coated tablets were indistinguishable from NB-free tablets, even during colorimetric analysis. These results suggest that the NB possesses stealth properties and can be easily incorporated into counterfeit detection products.

Ag@ZIF-8 core-shell nanocomposites as sensitive and stable SERS substrates: Synthesis, optimization, and application in pollutant detection

Although surface-enhanced Raman scattering (SERS) is a powerful spectral analysis technique, its practical application is restricted due to the poor chemical stability of some noble metal nanoparticles. In this work, Ag@ZIF-8 nanocomposites with different ZIF-8 core-shell thicknesses were prepared by coating AgNP surfaces with polyvinylpyrrolidone and adjusting the dosage of zinc nitrate and 2-methylimidazole. Several characterizations have confirmed that the Ag@ZIF-8 nanocomposites was successfully prepared. Based on transmission electron microscopy images and SERS spectral intensity, it was determined that Ag@ZIF-8 nanocomposites with a ZIF-8 shell thickness of 30 nm exhibited optimal SERS performance. As a result of evaluating the uniformity and stability of the composite with 4-ATP as the probe molecule, it showed a relative standard deviation of 6.91 % and a decrease in SERS intensity of 4.5 % after 28 days. Based on the results obtained with Ag@ZIF-8 nanocomposites as the SERS substrate, the detection limits of 4-mercaptopyridine and thiram were as low as 5.87×10−9 M and 6.61×10−8 M, respectively. Furthermore, the finite-difference time-domain simulation reveals an enhancement factor of 2.6×106, which is in good agreement with the experimental value of 1.8×106, confirming its effectiveness as a SERS substrate.

Signal-amplified surface-enhanced Raman scattering using core/shell satellite nanoparticles for norovirus detection.

The development of an innovative approachis exploredto amplify the signal of a surface-enhanced Raman scattering (SERS)-based detection system using a novel nanotag: Au@Ag NPs covered by satellite AuNPs and conjugated by 4-mercaptbenzoic acid (4-MBA) as a Raman tag (Au@Ag-MBA-AuNPs). The Au@Ag-MBA-AuNPs nanotags showed strong SERS activities with an enhancement factor in the 108 order of magnitude. This indicates the formation of many hot spots due to the combination of core-shell nanoparticles and satellite AuNPs on the surface of Au@Ag-MBA NPs. The newly fabricated nanotags were employed in a small-sized Palmtop Raman spectrometer. A concentration-dependent increase in SERS intensity was observed in the norovirus-like particle (NoV-LP) concentration range 10fg/mL to 100pg/mL with a detection limit of 0.76fg/mL. Even in the severe interfering matrices, this detection method's coefficient of variation was less than 10%. This detection system was approximately 107 times more sensitive than commercially available ELISA kits. Norovirus in clinical samples was detected over a wide concentration range of 1.0 × 101 - 1.0 × 106 RNA copy number/mL with a detection limit of 7.8 RNA copy number/mL, indicating sensitivity comparable to real-time PCR. These results suggest that this detection system is stable in a complex matrix and has the potential for detectingnorovirus inclinical samples with a small Palmtop Raman spectrometer.

Phenylboronic Acid-Functionalized Ratiometric Surface-Enhanced Raman Scattering Nanoprobe for Selective Tracking of Hg2+ and CH3Hg+ in Aqueous Media and Living Cells.

The development of appropriate molecular tools to monitor different mercury speciation, especially CH3Hg+, in living organisms is attractive because its persistent accumulation and toxicity are very harmful to human health. Herein, we develop a novel activity-based ratiometric SERS nanoprobe to selectively monitor Hg2+ and CH3Hg+ in aqueous media and in vivo. In this nanoprobe, a new bifunctional Raman probe bis-s-s'-[(s)-(4-(ethylcarbamoyl)phenyl)boronic acid] (b-(s)-EPBA) was synthesized and immobilized on the surface of gold nanoparticles via a Au-S bond, in which the phenylboronic acid group was employed as the recognition unit for Hg2+ and CH3Hg+ based on the Hg-promoted transmetalation reaction. In the presence of Hg2+ and CH3Hg+, a new surface-enhanced Raman scattering (SERS) peak aroused from of C-Hg appeared at 1080 cm-1, and the SERS intensity at 1002 cm-1 belonged to the B-O symmetric stretching decreased simultaneously. The quantitative tracking of Hg2+ and CH3Hg+ was realized based on the SERS intensity ratio (I1080/I1303) with rapid response (∼4 min) and high sensitivity, with detection limits of 10.05 and 25.13 nM, respectively. Moreover, the SERS sensor was used for the quantitative detection of Hg2+ and CH3Hg+ in four actual water samples with a high accuracy and excellent recovery. More importantly, cell imaging experiments showed that AuNPs@b-(s)-EPBA could quantitatively detect intracellular CH3Hg+ and had a good concentration dependence in ratiometric SERS imaging. Meanwhile, we demonstrated that AuNPs@b-(s)-EPBA could detect and image CH3Hg+ in zebrafish. We anticipate that AuNPs@b-(s)-EPBA could potentially be used to study the physiological functions related to CH3Hg+ in the future.

Application of Gap Mode Ultrasensitive P-GERTs in SERS-Based Rapid Detection

In surface-enhanced Raman scattering (SERS) detection research, the shape, structure, surface modification, and material selection of nanoparticles can significantly impact the SERS intensity. Petal-like gap-enhanced Raman tags (P-GERTs) possess numerous sharp tips and edges, which generate localized electric field enhancements, further amplifying the electric field enhancement effect on neighboring molecules and enhancing the SERS signal. Additionally, the surface of P-GERTs can be modified with functional molecules, enabling their application in the detection of disease biomarkers. Using COVID-19 as an example, the performance of P-GERTs in disease biomarker detection was validated, demonstrating that the signal intensity of this probe can reach 55 times that of regular gold nanoparticles and 36.7 times that of smooth shell gap-enhanced Raman tags (S-GERTs). Furthermore, in combination with magnetically retrievable magnetic bead substrates, the N-protein antigen was specifically detected in a one-step process. N-protein was detected within 15 min using a portable Raman spectrometer. The limit of detection (LOD) for the standard sample was 4.28 pg/mL, and the LOD for the actual throat swab sample system was 25.4 pg/mL. This workflow can be extended to the detection of other biomarkers, making it widely applicable.

Grating-Integrated Gold Nanograsses Encapsulated with ZIF-8: A Quantitative and Ultrasensitive Surface-Enhanced Raman Scattering Substrate.

We proposed and demonstrated highly sensitive hybrid surface-enhanced Raman scattering (SERS) substrates, which are grating-integrated gold nanograsses (GIGN) that are tip-selectively encapsulated by ZIF-8 nanospheres (GIGN/tip-ZIF). This unique structure is realized through the tip-selective modification of GIGN by polyvinylpyrrolidone (PVP), and then, the tips of the GIGN were encapsulated by ZIF-8 nanospheres. The ZIF-8 nanospheres can adsorb analyte molecules, resulting in the spatial overlap between the analyte molecules and the "hotspots" on the tips of GIGN. Such a unique GIGN/tip-ZIF hybrid SERS substrate exhibits high sensitivity and quantitative detection ability. The detection limits can reach as low as 10-11 M, and the relative standard deviation is 5.59% for 4-aminothiophenol (4-ATP). In a wide range of concentrations from 10-5 to 10-11 M, the SERS intensity and concentration relationship can be fitted as a sigmoidal curve with R2 = 0.988. These indicate that the GIGN/tip-ZIF hybrid SERS substrates have broad applications in detecting toxic and harmful substances in food safety, disease diagnosis, and environmental monitoring.

Enantioselective Surface-Enhanced Raman Scattering by Chiral Au Nanocrystals with Finely Modulated Chiral Fields and Internal Standards.

The chiral discrimination of enantiomers is crucial for drug screening and agricultural production. Surface-enhanced Raman scattering (SERS) is proposed for discriminating enantiomers benefiting from chiral plasmonic materials. However, the mechanism of enantioselective SERS is unclear, and fluctuating SERS intensities may result in errors. Herein, this work demonstrates a reliable SERS substrate using chiral Au nanocrystals with finely modulated chiral fields and internal standards. Chiral electromagnetic fields are enhanced after modulation, which is conducive to increasing the difference in the enantiomeric SERS intensity, as evidenced by the experimental and simulation results. Furthermore, the SERS stability is improved by the corrective effect of the internal standards, and the relative standard deviation is significantly reduced. Using finely modulated chiral fields and internal standards, L- and D-phenylalanine exhibit a stable six times difference in SERS ratio. Theoretical simulations reveal that linearly polarized light can also excite the chiral fields of chiral Au nanocrystals, indicating non-chiral far-field light is converted into chiral near-field sources by chiral Au nanocrystals. Thus, the mechanism of enantioselective SERS can be elucidated by the scattering difference of chiral molecules in chiral near fields. This study will pave the way for the development of enantioselective SERS and related chiroptical technologies.

Comparison of Gap-Enhanced Raman Tags and Nanoparticle Aggregates with Polarization Dependent Super-Resolution Spectral SERS Imaging.

Strongly confined electric fields resulting from nanogaps within nanoparticle aggregates give rise to significant enhancement of surface-enhanced Raman scattering (SERS). Nanometer differences in gap sizes lead to drastically different confined field strengths; so much attention has been focused on the development and understanding of nanostructures with controlled gap sizes. In this work, we report a novel petal gap-enhanced Raman tag (GERT) consisting of a bipyramid core and a nitrothiophenol (NTP) spacer to support the growth of hundreds of small petals and compare its SERS emission and localization to a traditional bipyramid aggregate. To do this, we use super resolution spectral SERS imaging that simultaneously captures the SERS images and spectra while varying the incident laser polarization. Intensity fluctuations inherent of SERS enabled super resolution algorithms to be applied, which revealed subdiffraction limited differences in the localization with respect to polarization direction for both particles. Interestingly, however, only the traditional bipyramid aggregates experienced a strong polarization dependence in their SERS intensity and in the plasmon-induced conversion of NTP to dimercaptoazobenzene (DMAB), which was localized with nanometer precision to regions of intense electromagnetic fields. The lack of polarization dependence (validated through electromagnetic simulations) and surface reactions from the bipyramid-GERTs suggests that the emissions arising from the bipyramid-GERTs are less influenced by confined fields.

Detecting antimony(III) on-site using novel gel-based techniques: Colorimetric diffusive equilibrium in thin films for two-dimensional imaging and surface-enhanced Raman scattering for sensitive quantification

Antimony (Sb) pollution has raised increasing public concerns and its rapid on-site screening is central for the risk assessment. Herein, we proposed two gel-based methods based on colorimetric diffusive equilibrium in thin films (DET) and surface-enhanced Raman scattering (SERS), for two-dimensional imaging and sensitive detection of Sb(III) by revisiting the phenylfluorone (PhF) complexation reaction. PhF was well dispersed in the polyvinyl alcohol (PVA) hydrogel and reacted with Sb(III) in the DET gel to form a strong PhF-Sb(III) complex. The distribution of Sb(III) was easily visualized at a submillimeter resolution using computer imaging densitometry, with a detection limit (LOD) of ∼100 nmol L−1. Field application in the Sb mine area reveals limited dissolved Sb(III) penetrating the redox barrier below the sediment-water interface by 20 mm in rivers and tailing pond sediments. To improve the detection sensitivity and apply the principle to trace Sb quantification, a SERS platform was established by anchoring PhF on the hydrogel-stabilized Ag nanoparticles via C–O–Ag bonding to specifically detect Raman-inactive Sb(III). Benefiting from the high SERS activity of PhF and enrichment ability of hydrogel, Sb(III) was quantified with a LOD of 1.2–10.7 nmol L−1 depending on the sample volume. The coexisting ions at a 100-fold higher concentration than Sb(III) resulted in only 3.3–10.4 % variation in SERS intensity, indicating a negligible interference on the SERS platform. The platform exhibited a RSD of 6.6–13.1 % and acceptable recoveries for various environmental matrices, highlighting its promise in on-site application.

Construction of selectively enhanced MOF-SERS sensor and highly sensitive detection of hCE1 in HepG2 cells

In this paper, a surface-enhanced Raman scattering (SERS) magnetic immunosensor for human carboxylesterase 1 (hCE1) assay was developed using a sandwich structure consisting of a magnetic support substrate, a SERS tag, and a target. The objective was to investigate the correlation between changes in hCE1 levels and liver injury. The utilization of Co-MOF-74@Au@methylene blue (MB) magnetic support substrate facilitated the expedient separation of biological samples while uniformly distributing the AuNPs, thereby enhancing the SERS intensity and improving the reproducibility. The introduction of Co-MOF-74 metal–organic frameworks (MOFs), endowed with its own selective SERS-enhancing properties, into the Co-MOF-74@Au@MB SERS tag further enhances the SERS sensing capability. The proposed SERS sensor exhibited good linearity over the concentration range of hCE1 from 10−2 to 102 μg·mL−1, with a correlation coefficient (R2) of 0.990 and a limit of detection (LOD) of 8.3 ng·mL−1. This demonstrates the potential of this strategy for the detection of trace proteins or enzymes in complex biological samples. In the meantime, the selective SERS enhancement mechanism of MOFs on Raman reporter molecules was preliminarily explored. This provides a new idea for the development of SERS substrates and SERS assays.

Bilateral efforts to improve SERS detection efficiency of exosomes by Au/Na7PMo11O39 Combined with Phospholipid Epitope Imprinting

Detection of cancer-related exosomes in body fluids has become a revolutionary strategy for early cancer diagnosis and prognosis prediction. We have developed a two-step targeting detection method, termed PS-MIPs-NELISA SERS, for rapid and highly sensitive exosomes detection. In the first step, a phospholipid polar site imprinting strategy was employed using magnetic PS-MIPs (phospholipids-molecularly imprinted polymers) to selectively isolate and enrich all exosomes from urine samples. In the second step, a nanozyme-linked immunosorbent assay (NELISA) technique was utilized. We constructed Au/Na7PMo11O39 nanoparticles (NPs) with both surface-enhanced Raman scattering (SERS) property and peroxidase catalytic activity, followed by the immobilization of CD9 antibodies on the surface of Au/Na7PMo11O39 NPs. The Au/Na7PMo11O39-CD9 antibody complexes were then used to recognize CD9 proteins on the surface of exosomes enriched by magnetic PS-MIPs. Lastly, the high sensitivity detection of exosomes was achieved indirectly via the SERS activity and peroxidase-like activity of Au/Na7PMo11O39 NPs. The quantity of exosomes in urine samples from pancreatic cancer patients obtained by the PS-MIPs-NELISA SERS technique showed a linear relationship with the SERS intensity in the range of 6.21 × 107–2.81 × 108 particles/mL, with a limit of detection (LOD) of 5.82 × 107 particles/mL. The SERS signal intensity of exosomes in urine samples from pancreatic cancer patients was higher than that of healthy volunteers. This bidirectional MIPs-NELISA-SERS approach enables noninvasive, highly sensitive, and rapid detection of cancer, facilitating the monitoring of disease progression during treatment and opening up a new avenue for rapid early cancer screening.

Two-dimensional tellurium nanosheet: A novel sensitive and stable surface-enhanced Raman scattering substrate

Two-dimensional (2D) materials with merits such as low cost, high chemical inertness and tunable electronic structure have become favorable candidates for next generation of surface-enhanced Raman scattering (SERS) platforms. However, the SERS sensitivity of 2D materials still needs to be improved and the large-scale synthesis methods should be developed to meet the requirements of practical applications. In this work, we explored performances of a brand-new SERS substrate made of 2D Te nanosheets (NSs), which exhibited thickness-dependent SERS properties, with thinner nanosheets yielding stronger SERS intensity. Under optimized conditions, the limits of detection (LODs) reached the order of 10−9 M combining with SERS enhancement factors (EFs) as high as 105 for copper phthalocyanine (CuPc) and methylene blue (MB). This impressive SERS performance could be attributed to the strong interaction and photoinduced charge transfer (PICT) processes between 2D Te NSs and molecules. Benefiting from the appropriate positions of valence band (VB) and conduction band (CB), the 2D Te NSs showed significant Raman enhancement for various molecules. Furthermore, the 2D Te NSs exhibited good air-stability for up to ∼2 months. These outstanding performances establish 2D Te NSs as a favorable SERS detection material with enormous potential in practical applications.

Honeycomb-Inspired Surface-Enhanced Raman Scattering Microarray for Large-Area Automated Testing of Urease in Saliva Samples.

Surface-enhanced Raman scattering (SERS) technology, as an important analytical tool, has been widely applied in the field of chemical and biomedical sensing. Automated testing is often combined with biochemical analysis technologies to shorten the detection time and minimize human error. The present SERS substrates for sample detection are time-consuming and subject to high human error, which are not conducive to the combination of SERS and automated testing. Here, a novel honeycomb-inspired SERS microarray is designed for large-area automated testing of urease in saliva samples to shorten the detection time and minimize human error. The honeycomb-inspired SERS microarray is decorated with hexagonal microwells and a homogeneous distribution of silver nanostars. Compared with the other four common SERS substrates, the optimal honeycomb-inspired SERS microarray exhibits the best SERS performance. The RSD of 100 SERS spectra continuously collected from saliva samples is 6.56%, and the time of one detection is reduced from 5 min to 10 s. There is a noteworthy linear relationship with a R2 of 0.982 between SERS intensity and urease concentration, indicating the quantitative detection capability of the urease activity in saliva samples. The honeycomb-inspired SERS microarray, combined with automated testing, provides a new way in which SERS technology can be widely used in biomedical applications.

Hollow gold nanoparticles coated with ZnS with distance-dependent plasma coupling and surface enhanced Raman spectroscopy for applications

Metal@semiconductor core-shell heterostructure with strong exciton-plasmon coupling can integrate multiple functions of each component and exhibit extraordinary benefits in the optical, catalytic, electrical, and magnetic properties due to its excellent synergistic properties at the heterointerfaces. In our work, hollow gold nanoparticles (HGNs)- 4-mercaptobenzoic acid (MBA) @ZnS core-shell heterostructure with the adjustable shell thickness (tshell) of ZnS varied from 1 to 19 nm were successfully prepared for the first time by low temperature and simple two-step method. Here, we report our findings that the surface enhanced Raman scattering (SERS) spectral intensity of HGNs-MBA@ZnS under the 633 nm excitation correlates with the tshell of ZnS, and the experimental results are consistent with theoretical studies. Furthermore, we also investigated the excitation wavelength-dependent SERS enhancement mechanism of HGNs-MBA@ZnS (tshell = 2 nm) and the result showed that the near-field enhancement and plasmon-induced interfacial charge transfer transition (PICTT) synergistically increase the SERS intensity under the excitation line at 633 nm. Our work not only provides guidance for the design and synthesis of other important metal@semiconductor core-shell heterostructure, but presents significant insights into their SERS enhancement mechanism.

Unique gap-related SERS behaviors of p-aminothiophenol molecules absorbed on TiO2 surface in periodic TiO2/Ni nanopillar arrays

We observed a unique interpillar gap-related surface-enhanced Raman scattering (SERS) behavior of p-aminothiophenol (PATP) molecules from periodic TiO2 nanopillar arrays with three gap sizes of 191, 297 and 401 nm, which is completely different from that on Ag and Ni nanopillar arrays. Especially, the gap-size-dependent charge-transfer (CT) resonance enhancement from TiO2/Ni has been indicated through comparisons of variation trend of SERS intensities with inter-pillar gap size between TiO2/Ni and Ag/TiO2/Ni as well as Ni nanoarrays, and been confirmed by spectra of ultraviolet–visible absorption and photoluminescence. Results demonstrate that the CT resonance enhancement is more susceptible to the change of the gap size compared with the surface plasmon resonance (SPR) enhancement in TiO2/Ni nanoarrays. Hence, SPR and CT enhancement showing different variation trend and rate with the gap size that leads to a different relative contribution of CT resonance to the overall SERS enhancement as gap size changes, and consequently results in a unique gap-related SERS behavior for TiO2/Ni nanoarrays. The present study is not only helpful for investigating SERS mechanism for semiconductors but also providing a method to design and optimize periodic metal/semiconductor SERS substrates in a controllable way.

Purines recognition and quantitative analysis by surface-enhanced Raman spectroscopy

The common quantification methods of purines, including high-performance liquid chromatography, micellar electrokinetic chromatography, reverse phase ion pair chromatography, and capillary zone electrophoresis, have been used for the analysis of purines. These conventional techniques are limited by long operation times, large sample volumes, requirements for pretreatment and separation processes, or sophisticated, bulky and expensive equipment. Here, we have developed a simple method to prepare a probe for the quantitative analysis of purines using the surface-enhanced Raman scattering (SERS) method. The SERS probe is a rough Ag wire obtained with simple electrochemical treatment, which is optimized to reach the maximum SERS signal enhancement. The Raman enhancement factor (EF) of Ag wire after roughening can reach ∼106. Under optimized conditions, the rough Ag wire is capable of recognizing four purine bases (namely, guanine, adenine, hypoxanthine, and xanthine) in the range of 10−5 to 10−1 mg/mL with a linear relationship between SERS intensity of signature peak and purine concentration. The recovery rate of each purine base is higher than 80% in the mixture of four purines. The overall method was successfully applied to the monitoring of the level of purines in marketplace beer beverages. The novel wire-based SERS sensor used with portable Raman spectroscopy is prospective in diet safety and personalized point-of-care medical detection.

Flexible Surface-Enhanced Raman Scattering Tape Based on Ag Nanostructured Substrate for On-Site Analyte Detection.

Surface-enhanced Raman scattering (SERS) has emerged as a powerful surface analytical technique that amplifies Raman scattering signals of molecules adsorbed onto metal nanostructured surfaces. The droplet reaction method has recently been employed to fabricate large-scale microring patterns of silver (Ag) nanostructures on rigid substrates, which enables sensitive detection within the ring area. However, these rigid substrates present limitations for direct on-site detection of analyte residues on irregular sample surfaces. There is a need to develop soft and flexible SERS substrates that can intimately conform to arbitrary surfaces. In this study, we presented a SERS substrate using flexible and adhesive tape as the supporting material. This SERS tape was fabricated by repeatedly transferring presynthesized Ag nanostructures from a rigid substrate to the tape. For a model compound adenine, our SERS tape exhibited a good linear response from 5 × 10-4 M to 5 × 10-5 M with a low limit of detection (LOD) of 5 × 10-7 M and displayed a SERS enhancement factor (EF) of 3.2 × 105. The relative standard deviation (RSD) of SERS intensity achieved was as low as 1.93%, indicating its outstanding uniformity. The as-prepared SERS tape was used for in situ detection of pesticide residue on an apple surface and dye residue on human hair. Leveraging the large surface area of Ag nanostructure patterns from the droplet reaction, the developed SERS tape demonstrates excellent performance in terms of sensitivity and uniformity. The successful detection of analyte residues on arbitrary surfaces of apple and human hair highlights the potential of this flexible SERS tape for real-world applications across various industries for enhanced diagnostic accuracy.

Au@Ag core-shell nanorods enhance surface-enhanced Raman scattering aptasensor for ultrasensitive detection of Salmonella Typhimurium

Salmonella Typhimurium is the prevalent pathogenic bacterium that causes foodborne-related diseases. Here, we developed a surface-enhanced Raman scattering (SERS) biosensor for S. Typhimurium detection. The biosensor was based on Au@Ag core-shell nanorods (Au@Ag NRs) to enhance Raman signal and aptamer-specific identification. 4-mercaptobenzoic acid (4-MBA) and aptamer-modified Au@Ag NRs were used as Raman signal probes. The aptamer adsorbed on the Au@Ag NRs surface when the reaction system was free of bacteria. Once S. Typhimurium was added, the aptamer then specifically identified and captured the cells. The decrease of free aptamers in solution restoring the SERS “hot spot” between the Au@Ag NRs and enhancing the 4-mercaptobenzoic acid (4-MBA) Raman signal. Quantitative analysis of S. Typhimurium was performed using Raman-enhanced spectroscopy. Under optimised conditions, the 4-MBA SERS intensity at 1072 cm−1 was used to determine S. Typhimurium in the range of 102–107 CFU mL−1 (y = 1660.84x+2340.7, R2 = 0.9912). The limit of detection was 64 CFU mL−1. This method also has high specificity and is not interfered by the other five control bacteria to complete the detection of S. Typhimurium. The developed method is simple, rapid, sensitive and specificity, which can be used to detect actual samples. It can be potentially used for detecting bacteria.