Extralong hot-spots sensor for SERS sensitive detection of phthalate plasticizers in biological tear and serum fluids.

Phthalate plasticizers (PAEs) illegally used in food pose a great threat to human health. A new and efficient sensing platform for the sensitive detection of the PAE residues in biological fluids needs to be designed and developed. Here, we report a simple and reliable surface-enhanced Raman spectroscopy (SERS) active platform with extralong hot spots of Au nanobipyramids@Ag nanorods (Au NBPs@Ag NRs) for the rapid and sensitive detection of PAEs in biological fluids. To achieve high activity, Au NBPs@Ag NRs with different shell lengths were fabricated by controlling the synthesis conditions, and the corresponding SERS properties were investigated by using crystal violet (CryV) and butyl benzyl phthalate (BBP). The experimental results showed that a longer shell length correlated to greater Raman activity, which was confirmed by finite-difference time-domain (FDTD) electromagnetic simulation. More importantly, the extralong hot spots of the Au NBPs@Ag NR SERS-active substrate showed excellent homogeneity and reproducibility for the CryV probe molecules (6.21%), and the detection limit was 10-9 M for both BBP and diethylhexyl phthalate (DEHP). Furthermore, through the standard addition method, an extralong hot spots SERS substrate could achieve highly sensitive detection of BBP and DEHP in serum and tears fluids, and the detection limit was as low as 3.52 × 10-8 M and 2.82 × 10-8 M. Therefore, the Au NBPs@Ag NR substrate with an extraordinarily long surface is efficient and versatile, and can potentially be used for high-efficiency sensing analysis in complex biological fluids.

Mussel-inspired PDA-based MIP-SERS sensor for the detection of trace MG in environmental water.

The abuse of antibiotics such as malachite green (MG) has caused its residues in foods and environmental water, and therefore, it is important to establish a rapid and reliable method for sensitive detection of antibiotics. In this work, a novel molecularly imprinted polymer surface-enhanced Raman spectroscopy (SERS) sensor integrating high sensitivity, selectivity, and reusability is fabricated for the detection of trace MG in environmental water. SiO2@Au, by adjusting the gap between nanoparticles, provides SERS activity, and then the template MG is molecularly imprinted and wrapped by oxidative self-polymerization properties of dopamine (SA-100@MIP). The prepared SA-100@MIP achieved sensitive and selective detection of MG in pond water (0.1 nM) and presented a good linear correlation in the range of 10-6-10-10 M. Moreover, the substrate still has excellent SERS performance after 12 times of repeated use. These properties indicate that this sensor may provide broad prospects for the practical application of SERS in food and environmental monitoring.

Quantitative SERS sensor based on self-assembled Au@Ag heterogeneous nanocuboids monolayer with high enhancement factor for practical quantitative detection.

Accurate and rapid quantitative detection of pesticide and pollutant levels in the actual sample can aid in protecting food security, environmental security, and human health. A high Raman enhancement factor and good repeatability of the surface-enhanced Raman spectroscopy (SERS) substrates are favorable to quantitative analysis. Herein, a quantitative SERS sensor based on constructed self-assembled plasmonic Au@Ag heterogeneous nanocuboids (Au@Ag NCs) monolayer was developed. The sensor was used to quantitatively detect the trace pesticides extracted from pear surfaces and pollutants in fishpond water. Densely packed Au@Ag NCs fabricated into large-scale monolayer films were chemically functionalized using 4-methyl-thiobenzoic acid (4-MBA) at the organic/aqueous interface, in which plentiful nanogaps contribute to increase hotspots. Their sharp corners and edges make the sensor have high SERS performance through providing abundant "hot spots." The obtained optically SERS-based sensor with uniform liquid-state interfacial nanoparticle arrays appeared to have nice SERS performance and uniformity using crystal violet (CV) as a probe molecule. In particular, the proposed SERS sensor was applied for quantitative detection of thiabendazole (TBZ) extracted from pear surfaces and malachite green (MG) in fishpond water down to levels of 0.0105 nM and 0.87 nM for SERS assay respectively. As a result, our proposed SERS quantitative detection strategy is quite preferred to on-site analysis and supervision of contaminant in food samples.

Size-dependent surface enhanced Raman scattering activity of plasmonic AuNS@AgNCs for rapid and sensitive detection of Butyl benzyl phthalate.

Phthalate plasticizers (PAEs) are heavily applied to plastic products and poses severe threat to human health. Herein, it is especially urgent to find a stable and reliable method for detecting PAEs. In this report, a Surface Enhanced Raman Scatting (SERS) strategy coupled with plasmonic core-shell Au nanospheres@Ag nanocubes (AuNS@AgNCs) as substrates were employed for the rapid and sensitive detection of Butyl benzyl phthalate (BBP) in liquor samples, and plasmonic core-shell AuNS@AgNCs tend to perform richer localized surface plasmon resonance (LSPR) than AuNS. In this work, different sizes AuNS@AgNCs comprised of Au nanospheres as core and Ag nanocubes as shells were synthesized. Based on this, we then investigated the SERS activity of BBP and crystal violet (CV) reached a maximum level when the thickness of Ag coating shell arrived in a threshold, and even very low signal of trace BBP dissolved in liquor sample can be detected in existence of the plasmonic AuNS@AgNCs active substrate of 50 nm. The sensitivity and repeatability of the optimized size AuNs@AgNCs have been estimated and limits of detection (LOD) was 10-9 M for BBP. In addition, finite difference time domain (FDTD) electromagnetic simulations also performed in great agreement with our experimental results.