Ultrasonic-driven chemical reduction synthesis of alizarin complexone-modified gold nanoparticles for dual-signal colorimetric and fluorometric sensing of histamine in seafood products.

Alizarin complexone-modified gold nanoparticles (Au0-NPsALz) were synthesized using a proposed ultrasonic irradiation-assisted chemical reduction method. Ultrasonic irradiation powers, reaction time and alizarin complexone concentration had been proven to be the main parameters for controlling the nucleation and growth of Au0-NPsALz. In the synthesized ultrasonic irradiation-assisted chemical reduction conditions, Au0-NPsALz had a spherical oriented morphology with a uniform size of 17.84 ± 1.37 nm and are shiny red with a surface plasmon resonance (SPR) of 535 nm. A rapid colorimetric and fluorometric dual-mode detection strategy for selective detection of histamine in seafood was developed based on the self-assembly of Au0-NPsALz-Ni (II) complexes. Ni (II) can capture the histamine molecules close to Au0-NPsALz surfaces, making changes in the colorimetric and fluorometric responses of the solution. The quantitative analysis of histamine was realized through the variation of dual-signal colorimetric and fluorometric responses. Such Au0-NPsALz sensor offered good detection sensitivity for histamine with a detection limit (LOD) of 59.32 µmol L-1 and 116.20 µmol L-1 and wide linear response within the range of 10-10000 µmol L-1 (R2 = 0.9952) and 100-5000 µmol L-1 (R2 = 0.9947) for colorimetric and fluorometric measurement, respectively. Recoveries ranging from 94.99 to 103.29 % and 97.67-106.88 % for colorimetric and fluorometric assay were obtained, showing low levels of matrix effects. Particularly, the results of the dual-mode sensor were also validated by comparing with the HPLC method for improving the assay accuracy and dependability. Ultimately, the developed Au0-NPsALz colorimetric and fluorometric probe performs excellently in practical applications, with promising results for detecting histamine in seafood products.

Facile construction of magnetic solid-phase extraction of polyaniline blend poly(amidoamine) dendrimers modified graphene oxide quantum dots for efficient adsorption of polycyclic aromatic hydrocarbons in environmental water.

An efficient magneto-adsorbent composed of polyaniline blend poly(amidoamine) dendrimers modified graphene oxide quantum dots and magnetic Fe3O4 particles (Fe3O4@PANI-PSS/PAMAM-QGO) for magnetic solid-phase extraction (MSPE) of polycyclic aromatic hydrocarbons (PAHs) in environmental water was synthesized. Fe3O4@PANI-PSS/PAMAM-QGO exhibited exceptional adsorption property for most PAHs analytes. The nanocomposite sorbent demonstrated a ferromagnetic behavior of 17.457 emu g-1, which is adequate for subsequent use in MSPE. Key parameters affecting the processes of adsorption and desorption, including the sorbent amount, vortex adsorption time, vortex extraction time, sample volume, a solvent for desorption and the solvent volume were all examined and optimized. The performance of MSPE using Fe3O4@PANI-PSS/PAMAM-QGO as adsorbent for four PAHs, including fluoranthene, acenaphthene, phenanthrene and pyrene were studied through high performance liquid chromatography equipped with spectrofluorometer. Under the optimal conditions, Fe3O4@PANI-PSS/PAMAM-QGO showed a wide linearity of 10-1,000 ng mL-1, low detection limit (LOD) ranging from 1.92 to 4.25 ng mL -1 and high accuracy (recoveries of 93.6-96.5 %). Enrichment factors up to 185 were achieved. Furthermore, Fe3O4@PANI-PSS/PAMAM-QGO exhibited good recyclability (10 times, RSDs ≤ 5.35%), while maintaining its high efficiency in the extraction of PAHs. The proposed method was successfully applied for environmental samples. Recoveries ranging from 81.2 to 106.2 % were obtained, indicating a low matrix effect and the robustness of the optimized MSPE method. Based on these features and under the optimal extraction conditions, Fe3O4@PANI-PSS/PAMAM-QGO was demonstrated to be a successful tool for the rapid and sensitive extraction of PAHs in the samples.

A Ratiometric Fluorescence Amplification Using Copper Nanoclusters with o-Phenylenediamine Sensor for Determination of Mercury (II) in Natural Water.

A simple and rapid method for determining mercury (II) has been developed using L-cysteine-capped copper nanocluster (CuNCs) with o-phenylenediamine (OPD) as the sensor. The characteristic fluorescence peak of the synthesized CuNCs was observed at 460 nm. The fluorescence properties of CuNCs were strongly influenced by the addition of mercury (II). Upon addition, CuNCs were oxidized to form Cu2+. Then, the OPD were rapidly oxidized by Cu2+ to form o-phenylenediamine oxide (oxOPD), as evidenced by the strong fluorescence peak at 547 nm, resulting in a decrease in the fluorescence intensity at 460 nm and an increase in the fluorescence intensity at 547 nm. Under optimal conditions, a calibration curve between the fluorescence ratio (I547/I460) and mercury (II) concentration was constructed with a linearity of 0-1000 µg L-1. The limit of detection (LOD) and limit of quantification (LOQ) were found at 18.0 µg L-1 and 62.0 µg L-1, respectively. The recovery percentage was in the range of 96.8-106.4%. The developed method was also compared with the standard ICP-OES method. The results were found to be not significantly different at a 95% confidence level (tstat = 0.365 < tcrit = 2.262). This demonstrated that the developed method could be applied for detecting mercury (II) in natural water samples.

New Chitosan-Grafted Thymol Coated on Gold Nanoparticles for Control of Cariogenic Bacteria in the Oral Cavity.

Chitosan-grafted thymol (CST) coated on gold nanoparticles has been synthesized and characterized for the design of antimicrobial materials. CST was synthesized via adapting the Mannich reaction, and it acted as the capping agent for the synthesis of gold nanoparticles (AuNPs). The grafting of thymol onto the side chain of chitosan has provided a degree of substitution value (%DSNMR) of 10.0%, calculated by nuclear magnetic resonance spectroscopy. UV-visible spectrometry and elemental analysis were used to confirm the successful synthesis of CST through adapting the Mannich reaction. The appropriate concentration of CST for AuNP synthesis was found to be 0.020%w/v. A red-wine colloidal AuNP solution of 2.41-3.30 nM particle size exhibits a strong surface plasmon resonance at 502 nm, which shows negative charges at pH = 9 of -36.37 mV. This result evidenced that the AuNPs showed electrostatic repulsion and CST played a role as a capping agent to provide a good dispersion and stability state. CST coated on the AuNP surface was successfully utilized for the control of cariogenic bacteria in the oral cavity. The results obtained from this study show that the tuning of the capping agent used in the synthesis step strongly influences the latter antimicrobial activity of the nanoparticles against Streptococcus mutans ATCC 25175 and Streptococcus sobrinus ATCC 33402 activity, with an inhibition zone of 15.90 and 14.25 mm, respectively. The average minimum inhibitory concentration values against S. mutans ATCC 25175 and S. sobrinus ATCC 33402 were found to be 25 and 100 mg/L, respectively, whereas the minimum bactericidal concentration values were 100 and 200 mg/L, respectively.

Highly Sensitive and Selective Colorimetric Sensor of Mercury (II) based on Layer-by-Layer Deposition of Gold/Silver Bimetallic Nanoparticles.

A new colorimetric sensor based on gold/silver bimetallic nanoparticles (Au-Ag BNPs) for the sensitive and selective detection of mercury (II) was developed. Gold nanoparticles (AuNPs) were synthesized by Turkevich method. The surface modification of AuNPs was modified by the layer-by-layer technique using poly(diallyl dimethylammonium chloride) which provided positively charged of AuNPs. Negatively charged silver nanoparticles (AgNPs) were synthesized by chemical reduction using poly(4-styrenesulfonic acid-co-maleic acid) as the stabilizing agent. The layer-by-layer assembly deposition technique was used to prepare Au-Ag BNPs of positively and negatively charged of AuNPs and AgNPs, respectively. The synthesized Au-Ag BNPs were characterized by a UV-visible spectrophotometer, zeta potential analyzer, FT-IR, TEM, XRD, and EDX. The Au-Ag BNPs sensor was able to detect mercury (II) in aqueous solution, visibly changing from brownish-orange to purple. The linear relationships of the UV-visible spectrometry demonstrate that the Au-Ag BNPs-based colorimetric sensor can be used for the quantitative analysis of mercury (II) in the range of 0.5-80 mg L-1, with the correlation coefficient, r2 = 0.9818. The limit of detection (LOD) of mercury (II) was found to be 0.526 + 0.001 mg L-1. The BNPs is also verified to have a good practical applicability for mercury (II) detection in the real samples.