Flexible nanoplasmonic sensor for multiplexed and rapid quantitative food safety analysis with a thousand-times sensitivity improvement.

The accumulation of trace amounts of certain small molecules in food poses considerable human health challenges, including the potential for carcinogenesis and mutagenesis. Here, an ultrasensitive gold-platinum nanoflower-coupled metasurface plasmon resonance (MetaSPR) (APNMSPR) biosensor, based on a competitive immunoassay, was developed for the multiplexed and rapid quantitative analysis of trace small molecules in eggs, offering timely monitoring of food safety. This one-step biosensor can be integrated into either a newly designed detachable high-throughput MetaSPR chip-strip plate device or a standard 96-well plate for multiplexed small-molecule detection within a single egg. The limits of detection were 0.81, 1.12, and 1.74 ppt for florfenicol, fipronil, and enrofloxacin, respectively, demonstrating up to 1000-fold increased sensitivity and a 15-fold reduction in analysis time compared with those of traditional methods. The results obtained using the APNMSPR biosensor showed a strong correlation with those obtained using liquid chromatography-tandem mass spectrometry. The APNMSPR biosensor holds immense promise for the multiplexed, highly sensitive, and rapid quantitative analysis of small molecules for applications in food safety control, early diagnosis, and environmental monitoring.

A Metasurface Plasmonic Analysis Platform Combined with Gold Nanoparticles for Ultrasensitive Quantitative Detection of Small Molecules.

Food safety related to drug residues in food has become a widespread public concern. Small-molecule drug residue analysis often relies on mass spectrometry, thin-layer chromatography, or enzyme-linked immunosorbent assays (ELISA). Some of these techniques have limited sensitivity and accuracy, while others are time-consuming, costly, and rely on specialized equipment that requires skilled operation. Therefore, the development of a sensitive, fast, and easy-to-operate biosensor could provide an accessible alternative to conventional small-molecule analysis. Here, we developed a nanocup array-enhanced metasurface plasmon resonance (MetaSPR) chip coupled with gold nanoparticles (AuNPs) (MSPRAN) to detect small molecules. As sulfamethazine drug residues in poultry eggs may cause health issues, we selected this as a model to evaluate the feasibility of using MSPRAN for small-molecule detection. The MSPRAN biosensor employed competitive immunoassay technology for sulfamethazine detection. The limit of detection was calculated as 73 pg/mL, with sensitivity approximately twice that of previously reported detection methods. Additionally, the recovery rate of the biosensor, tested in egg samples, was similar to that measured using ELISA. Overall, this newly developed MSPRAN biosensor platform for small-molecule detection provides fast and reliable results, facile operation, and is relatively cost-effective for application in food safety testing, environmental monitoring, or clinical diagnostics.

A self-powered aptasensor using the capacitor-amplified signal of a photofuel cell and a portable digital multimeter readout.

A self-powered aptasensor for streptomycin detection was constructed with a photofuel cell combined with a capacitor and a digital multimeter. The sensitivity of the proposed sensor was 8.7 times of that without using a capacitor amplifier circuit.

An antibody-aptamer sandwich cathodic photoelectrochemical biosensor for the detection of progesterone.

The progesterone (P4) level in body fluids can act as an indicator for early pregnancy diagnosis and offers insight into mammalian somatic function. In this work, we designed an antibody-aptamer based sandwich assay as a cathodic photoelectrochemical (PEC) biosensor for P4 detection. The composites of carbon dots and graphene oxide (CDs-GO) with favorable cathodic photocurrent response were used as photoactive materials on which the antibody (Ab) of P4 was immobilized. Meanwhile, high affinity truncated P4 aptamer was immobilized on Au-CuO-Cu2O to act as a bioconjugate. When P4 was present, the aptamer-Au-CuO-Cu2O bioconjugate could amplify the cathodic photocurrent of CDs-GO modified electrode through Ab-P4-aptamer interactions. Under optimum conditions, the cathodic photocurrent of the constructed PEC biosensor was found to increase linearly with P4 in a wide concentration range from 0.5 nM to 180 nM, with a low detection limit (3S/N) of 0.17 nΜ. The proposed cathodic PEC sensing platform demonstrated high selectivity, satisfying reproducibility, good stability. The sensor was successfully applied in the determination of P4 in human serum samples.

Synthesis of a CdS-decorated Eu-MOF nanocomposite for the construction of a self-powered photoelectrochemical aptasensor.

A composite of CdS nanoparticles and a europium metal organic framework (Eu-MOF) (CdS/Eu-MOF) was synthesized. The unique properties of MOFs help to improve the photoelectrochemical (PEC) properties of CdS by reducing charge carrier recombination and utilizing a broader spectrum for light harvesting. Under visible light illumination, the photocurrent of the CdS/Eu-MOF composite modified electrode was about 2.5-fold higher than that of the CdS modified electrode. When an ampicillin (AMP)-binding aptamer was immobilized on the CdS/Eu-MOF modified electrode as a recognition element, a self-powered PEC aptasensor exhibiting a specific photocurrent response to AMP was constructed. Several experimental conditions such as the ratio of CdS to MOF, the coating amount of the CdS/Eu-MOF suspension and the concentration of the aptamer were studied. Under optimum conditions, the photocurrent of the developed sensor was linearly related to the logarithm AMP concentration in the range of 1 × 10-10 to 2 × 10-7 M, with a detection limit (3S/N) of 9.3 × 10-11 M. Moreover, this sensor exhibited excellent selectivity, good repeatability and desirable stability. It was successfully applied to the detection of AMP in lake water and milk samples.

Photofuel cell coupling with redox cycling as a highly sensitive and selective self-powered sensing platform for the detection of tyrosinase activity.

A visible light-induced self-powered sensor for the detection of tyrosinase activity was proposed. A tyrosinase-responsive photoelectrochemical-chemical redox cycling strategy was integrated with a photofuel cell for signal amplification.

Visible Light-Driven Membraneless Photocatalytic Fuel Cell toward Self-Powered Aptasensing of PCB77.

Artificial photocatalytic systems have been extensively established to mimic the natural solar-energy conversion process for developing useful photoelectric devices. In this work, a membraneless, hydrogen peroxide (H2O2)-based photocatalytic fuel cell (PFC) operated under visible light was proposed and applied in self-powered sensing of 3,3',4,4'-tetrachlorobiphenyl (PCB77). The PFC was comprised of a photoanode fabricated with gold nanoparticles-decorated graphitic C3N4 nanosheet and a cathode modified with hemin-graphene nanocomposites. The combination of both photocatalytic oxidation and electrochemical reduction of H2O2 processes led to electron transfer in the external circuit, which could generate a certain electric power output. Taking the advantage of the inhibited output performance of PFC by PCB77 which interacted with aptamer immobilize on the photoanode, a self-powered aptasensor driven by visible light was achieved, without applying an external electric source. Thus, a highly sensitive and selective self-powered aptasensor for PCB77 was successfully demonstrated.