Hede McCormick (firedviola56)

In this work, a multicolor visual immunoassay platform was developed. The photoelectric effects of Ag2S NPs@ZnO NTs made the color changes of PANI/PB, which enabled visual inspection of CEA. Under the visible light excitation, Ag2S NPs@ZnO NTs generates electron-holes. Where, photoelectrons will pass electrical circuit to PB and photoinduced holes will oxidize PANI, which making the PANI/PB composite changes from emerald green-blue-purple-black colors. When CEA was incubated, the migration rate of photogenerated carriers is slowed down owing to the steric hindrance, resulting in different color changes of PANI/PB. In addition, the average green channel of PANI/PB read by photoshop has a certain correlated linear relationship with the concentration of CEA. Meanwhile, we can observe the color transformation of PANI/PB with our own eyes. By integrating advantages of photoelectrochemistry and colorimetry, the linear range of CEA detection was 0.1-20 ng/mL, and the detection limit was 0.05 ng/mL (S/N = 3). More importantly, this multicolor sensing method is very convenient, simple and low-cost. The photocarriers-modulated colorimetric strategy also provides a novel idea for visual portable platform design in clinical diagnosis. It is still a high challenge to develop a simple, sensitive and portable approach for bioassay in strong scattering medium. Herein, a photoacoustic (PA) device is developed for the detection of alkaline phosphatase (ALP) in serum with silver nanoparticles (AgNPs) as signal probe, without any requirements for expensive equipment, professional operation and pre-processing of real samples. ALP as an important disease marker could catalyze the breakdown of sodium L-ascorbyl-2-phosphate (AAP) into ascorbic acid (AA), thereby reducing Ag+ to AgNPs. AgNPs could generate strong PA signal under the irradiation of modulated 638-nm laser due to their localized plasmon resonance, and detected by the self-made portable PA device. Under the optimized experimental conditions, the present PA device exhibits excellent photostability and reproducibility with the relative standard deviation (RSD) of 2.2% at the concentration of 25 U L-1 ALP. Linear calibration graph is obtained within 5-70 U L-1 for ALP, along with a detection limit of 1.1 U L-1. This portable PA device is applied to detect ALP in serum samples, providing satisfactory spiking recoveries and competitive analytical performances with the current techniques. NSC16168 cost The PA-based analytical strategy obviously opens up a new avenue to the detection of disease-correlated biomarker in practice. Two novel fluorescent probes were designed to detect the biothiol in foods using the highly efficient Michael addition reaction between maleimide-derived probes and the biothiol. First, maleimide functionalized GQDs (M-GQDs) were synthesized and used for biothiol identification according to the Michael addition principle. The biothiol can be detected in the range of 5 × 10-9 to 4 × 10-7 mol/L and the detection limit was 1.69 × 10-9 mol/L. Then, a fluorescence resonance energy transfer (FRET) system between M-GQDs and tetrakis (4-aminophenyl) porphyrin (TAPP) for biothiol detection was developed. However, the process of FRET was switched off in the presence of biothiols due to the switch of M-GQDs fluorescence emission to the"ON" mode following the Michael addition mechanism. The system could quickly and accurately detect the biothiol with a detection range of 6.7 × 10-10 to 2 × 10-7 mol/L and a detection limit of 2.34 × 10-10 mol/L. Compared to the single detection system, the FRET system had a wider detection range and lower detection limit, and the related biomolecules did not interfere with the quantitative identification of the biothiol. The proposed method was successfully applied for the determination of the biothiol in foods and human blood samples. V.T