Ultrasensitive Fluorescent Microsensors Based on Aptamers Modified with SYBR Green I for Visual Quantitative Detection of Organophosphate Pesticides.

Organophosphate pesticides (OPs) are widely utilized in agricultural production, and the residues threaten public health and environmental safety due to their toxicity. Herein, a novel and simple DNA aptamer-based sensor has been fabricated for the rapid, visual, and quantitative detection of profenofos and isocarbophos. The proposed DNA aptamers with a G-quadruplex spatial structure could be recognized by SYBR Green I (SG-I), resulting in strong green fluorescence emitted by SG-I. The DNA aptamers exhibit a higher specific binding ability to target OP molecules through aromatic ring stacking, disrupting the interaction between SG-I and DNA aptamers to induce green fluorescence quenching. Meanwhile, the fluorescence wavelength of G-quadruplex fluorescence emission peaks changes, accompanied by an obvious fluorescence variation from green to blue. SG-I-modified aptasensor without any additive reference fluorescence units for use in multicolor fluorescence assay for selective monitoring of OPs was first developed. The developed aptasensor provides a favorable linear range from 0 to 200 nM, with a low detection limit of 2.48 and 3.01 nM for profenofos and isocarbophos, respectively. Moreover, it offers high selectivity and stability in real sample detection with high recoveries. Then, a self-designed portable smartphone sensing platform was successfully used for quantitative result outputs, demonstrating experience in designing a neotype sensing strategy for point-of-care pesticide monitoring.

Photoinduced Electron Transfer-Triggered g-C3N4\Rhodamine B Sensing System for the Ratiometric Fluorescence Quantitation of Carbendazim.

Assays for carbendazim (Car) with high sensitivity and on-site screening have been urgently required to protect the ecosystem and prevent disease. In this work, a simple, sensitive, and reliable sensing system based on photoinduced electron transfer was established to detect carbendazim utilizing ultrathin graphitic carbon nitride (g-C3N4) nanosheets and rhodamine B (RB). Carbendazim reacts with g-C3N4 by electrostatic interactions to form π-π stacking, and the quenching of the blue fluorescence is caused by electron transfer. While RB works as a reference fluorescence sensor without any fluorescence change, leading to obvious ratiometric fluorescence variation from blue to purple. Under optimal conditions, a favorable linear range from 20 to 180 nM was obtained, with a low detection limit of 5.89 nM. In addition, a portable smartphone sensing platform was successfully used for carbendazim detection in real samples with excellent anti-interference capability, demonstrating the potential applications of carbendazim monitoring.

Enzyme-free and rapid visual quantitative detection for pesticide residues utilizing portable smartphone integrated paper sensor.

Serious toxicity for organisms from pesticide glyphosate (Gly) residues to the ecosystem and human health has become a consensus. Rapid and selective detection of glyphosate, especially using a simple and portable instrument, is highly desired. In this work, we develop a novel enzyme-free rapid and visual ratiometric fluorescence sensor for selectively quantitative detecting glyphosate by integrating the designed blue carbon nanodots (CDs) and gold nanoclusters (Au NCs). The fluorescence of CDs can be quickly quenched via aggregation-caused quenching (ACQ) within 2 s after introducing glyphosate, resulting from the formation of CDs-Gly-CDs complex aggregation. While the Au NCs serve as the reference signal without any change, therefore leading to obvious and instant ratiometric fluorescence variation from blue to pink to orange. The broad linear range was obtained from 0 to 180 nM with a satisfactory detection limit of 4.19 nM. Furthermore, this approach was successfully applied to detect glyphosate in real samples and a portable smartphone platform integrated paper sensor was developed for in-site visual quantitative glyphosate detection, offering a promising strategy for the construction of enzyme-free trace hazard detection system.

Colorimetric fluorescent paper strip with smartphone platform for quantitative detection of cadmium ions in real samples.

Instrument-free, portable and direct read-out mini-devices have wider application prospects in various fields, especially for real-time/on-site detection in environmental science. Herein, a colorimetric fluorescent sensor for detecting cadmium ions (Cd2+) based on aggregation-induced emission (AIE) was established, fluorescent paper strips integrated with smartphone platform was further designed for the visualization, on-site and quantitative detection of Cd2+. The colorimetric fluorescent sensor was prepared by mixing orange emission glutathione-stabilized gold nanoclusters (AuNCs) with blue emission ethylenediamine functionalized graphene oxide (EDA-GO), and introducing copper ions (Cu2+) to quench the orange emission of AuNCs while the blue emission served as a background reference without color change. The Cd2+ can induce Cu2+-GSH-AuNCs to aggregation and emit orange fluorescence, causing the fluorescent color of the sensor changed from blue to red with the limit of detection (LOD) as low as 33.3 nM in solution. Moreover, fluorescent paper strips integrated with smartphone platform has a sensitive detection of Cd2+ with the LOD of 0.1 µM in rice samples. The method reported here might have great application prospects in real-time monitoring of foods safety and environmental protection.