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Photoelectric imaging systems typically employ a focal plane detector structure, rendering them vulnerable to laser damage. Laser damage can severely impair or even completely deprive the information acquisition capability of photoelectric imaging systems. A laser damage protection method based on a microlens array light field imaging system is proposed to prevent photoelectric imaging systems from laser damage. The technique utilizes the light field modulation effect of the microlens array to homogenize the spot energy, thereby reducing the maximum single-pixel receiving power at the image sensor. The method's effectiveness has been verified through numerical simulations and experimental validation. First, the laser transmission theoretical model of light field imaging is proposed. Then an experimental setup is established, and measurements are conducted to capture the spot profiles and intensity distributions on the imaging plane across various defocus distances. Finally, the impact of the propagation distance on the maximum single-pixel receiving power and suppression ratio of the light field imaging system is experimentally measured. The simulation and experimental results indicate that, with the proposed method, the energy suppression ratio can easily reach two orders of magnitude, significantly reducing the probability of laser damage in photoelectric imaging systems.
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In recent years, there has been growing concern among consumers about pesticide contamination in fruits. Therefore, rapid, reliable, and consistent detection methods for OPPs, especially dimethoate, are crucially needed. The existing quantitative methods for detecting dimethoate are not suitable for rapid measuring system such as the dimethoate samples from two channels. Hence this paper examines the utilization of a dual-channel system for utilize the absorption variations of the Localized Surface Plasmon Resonance (LSPR) bands of gold nanoparticles (AuNPs) were investigate for detection of dimethoate. Under optimized conditions, the relationship between concentrations of dimethoate and absorbance ratios (A(520)/A(640)) was linearly found in the concentration range of 10-100 nM. Result from the experiment shows that both channels exhibit a linear correlation coefficient as high as 0.97 and a limit of detection (LOD) as low as 5.5 nM. This LSPR detection system was characterized by testing the dimethoate in apple samples and the recovery rates were found to be in the range of 85.90% to 107.37%. The proposed dual-channel LSPR system for detecting dimethoate creating a new approach for detecting organophosphate insecticide in agricultural fields. It could lay the foundation for designing a high-throughput analysis of the insecticides using a wavelength division multiplexing switch (WDMS).
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Productos Agrícolas/normas , Dimetoato/análisis , Análisis de los Alimentos/métodos , Contaminación de Alimentos/análisis , Frutas/normas , Insecticidas/análisis , Resonancia por Plasmón de Superficie/métodos , Productos Agrícolas/química , Análisis de los Alimentos/normas , Frutas/química , Sensibilidad y Especificidad , Resonancia por Plasmón de Superficie/normasRESUMEN
This publisher's note corrects information in the author affiliations in Appl. Opt.58, 7205 (2019).APOPAI0003-693510.1364/AO.58.007205.
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Since some previous methods sacrifice too much imaging quality to achieve the valid retroreflection reduction, a novel image plane tilted system combined with the wavefront coding is proposed in this paper, which could improve the privacy and security of the imaging equipment by eliminating the retroreflection without suffering significant degradation in imaging quality. First, the theoretical model of the tilted wavefront coding system is established based on the wave-optics theory. According to the derived point spread function and the modulation transfer function, the maximum tilt angle of the image plane is obtained. Second, the target system is designed and optimized by Zemax, and the later simulation analyzes the effects of the tilting on both the retroreflection and the imaging property. Finally, the experiments verify the simulation results. It shows that when the tilt angle equals 5°, there is no longer significant retroreflection on the observation plane with the total receiving power decreasing to nearly 4 orders of magnitude compared with the state without tilting. Moreover, within the maximum tilt angle, the final decoded images of the wavefront coding system still maintain superior clarity and uniformity for both the artificial and the natural objects. Consequently, the BRISQUE index is reduced by 15.92% and 28.19%, respectively, compared with the conventional imaging system, which indicates that the image quality is significantly improved by the proposed system. In conclusion, the technique of wavefront coding could effectively compensate for the high-order aberrations induced by the tilting and preserve a large field of view for precise imaging with no retroreflection, which shows us a broad prospect.
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Poly( N-vinylcaprolactam) (PVCL) is a thermo-responsive polymer, which exhibits a lower critical solution temperature (LCST) in an aqueous solution. The LCST of this hydrophilic-to-hydrophobic transition is found to be strongly dependent on the salt-type and salt-concentration as well as on the molecular weight and concentration of the polymer. Here, atomistic molecular dynamics simulations have been successfully conducted for the first time to investigate the LCST transition of a 100 degree of polymerization PVCL chain in water, 1 M NaCl, 3.5 M NaCl, and 0.5 M CaCl2 solutions. Our results show that steric hindrance resulting from the bulky 7-member ring on the PVCL chain plays a critical role in the conformational transition. Moreover, the degrees of hydration and dehydration below or above the transition temperature are highly dependent on the specific solution condition and temperature. Water molecules are found to be trapped inside the collapsed polymer chains leading to the varying degrees of hydration and dehydration of the polymer chain in different solutions. Calculated water diffusion coefficients for both trapped and free water molecules agree very well with experimental measurements.
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Although aptamer-functionalized AuNPs technology exhibits great potential in analytical and biological chemistry, direct analysis of molecules at a low concentration using colorimetric assay remains challenging. The development of intuitive methods has attracted interest for promising detection of melamine in milk samples due to a demand for stable and understandable process. In this study, we propose a rapid and facile colorimetric measurement method of melamine combined aptamer-functionalized AuNPs in contaminated milk samples. To realize the high stability and the lower limit of detection, the aptamer-functionalized surface of AuNPs via a coordinated bond was used in combination with ultra-sonication. The kinetics of this colorimetric assay based on aptamer-functionalized AuNPs was analyzed to illustrate that the higher the concentration of melamine, the faster the aggregation of AuNPs induced. The sensitivity, selectivity, limit of detection and recovery rate were sufficiently validated to understand the measurement principle of melamine using aptamer-functionalized AuNPs. The calibration curve established by the absorption peak ratio (A640 /A520) was linear in the concentration range of 0~1µM of melamine in aqueous solutions with the correlation coefficient (R2) of 0.986 and the limit of detection (LOD) of 22 nM, whereas, the correlation coefficient (R2) of 0.998 and the LOD of 14.9 nM were achieved at the concentration of melamine below 0.5 µM in milk samples. The optimized performance of this colorimetric assay of melamine using aptamer-functionalized AuNPs in milk samples was obtained with 100 µL of 13 nm AuNPs solution, 40 µL of 1 µM (100 dilutions) aptamers and the pre-reaction time of 30 min. This simple colorimetric measurement of melamine using aptamer-functionalized AuNPs provides a promising target for various applications of the sample source with complex sample matrices.
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Aptámeros de Nucleótidos/química , Nanopartículas del Metal/química , Leche/química , Triazinas/análisis , Animales , Colorimetría , Oro/química , Cinética , Límite de Detección , Cloruro de Sodio/química , Triazinas/químicaRESUMEN
Corn stalk lodging is caused by different factors, including severe wind storms, stalk cannibalization, and stalk rots, and it leads to yield loss. Determining how to rapidly evaluate corn lodging resistance will assist scientists in the field of crop breeding to understand the contributing factors in managing the moisture, chemical fertilizer, and weather conditions for corn growing. This study proposes a non-destructive and direction-insensitive method, using a strain sensor and two single axis angle sensors to measure the corn stalk lodging resistance in the field. An equivalent force whose direction is perpendicular to the stalk is utilized to evaluate the corn lodging properties when a pull force is applied on the corn stalk. A novel measurement device is designed to obtain the equivalent force with the coefficient of variation (CV) of 4.85%. Five corn varieties with two different planting densities are arranged to conduct the experiment using the novel measurement device. The experimental results show that the maximum equivalent force could reach up to 44 N. A strong relationship with the square of the correlation coefficient of 0.88 was obtained between the maximum equivalent forces and the corn field’s stalk lodging rates. Moreover, the stalk lodging angles corresponding to the different pull forces over a measurement time of 20 s shift monotonically along the equivalent forces. Thus, the non-destructive and direction-insensitive method is an excellent tool for rapid analysis of stalk lodging resistance in corn, providing critical information on in-situ lodging dynamics.
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Purification of biologically-derived therapeutics is a major cost contributor to the production of this rapidly growing class of pharmaceuticals. Monoclonal antibodies comprise a large percentage of these products, therefore new antibody purification tools are needed. Small peptides, as opposed to traditional antibody affinity ligands such as Protein A, may have advantages in stability and production costs. Multiple heptapeptides that demonstrate Fc binding behavior that have been identified from a combinatorial peptide library using M13 phage display are presented herein. Seven unique peptide sequences of diverse hydrophobicity and charge were identified. All seven peptides showed strong binding to the four major human IgG isotypes, human IgM, as well as binding to canine, rat, and mouse IgG. These seven peptides were also shown to bind human IgG4 from DMEM cell culture media with 5% FCS and 5 g/L ovalbumin present. These peptides may be useful as surface ligands for antibody detection and purification purposes. Molecular docking and classical molecular dynamics (MD) simulations were conducted to elucidate the mechanisms and energetics for the binding of these peptides to the Fc region. The binding site was found to be located between the two glycan chains inside the Fc fragment. Both hydrogen bonding and hydrophobic interactions were found to be crucial for the binding interactions. Excellent agreement for the binding strength was obtained between experimental results and simulations.
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Magnetite nanoparticles of Fe3O4 were found to assemble into monodisperse hollow Fe3O4 microspheres with tunable diameters ranging from 200 to 400 nm and open pores on the shells in ethylene glycol in the presence of dodecylamine (DDA). The oriented assembly of nanoparticles conferred the individual hollow Fe3O4 microspheres a remarkable feature of single crystals. The morphologies of the products could be easily manipulated by varying the synthesis parameters. Increasing the concentration of DDA led to an obvious shape evolution of the products from rhombic nanoparticles to hollow microspheres, solid microspheres, and finally irregular nanoparticles, which were mainly attributed to the special self-assembly phenomenon of Fe3O4 nanoparticles in the solvothermal process.