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Employing a plasmonic decoupling mechanism, we report the design of a colorimetric pressure sensor that can respond to applied pressure with instant color changes. The sensor consists of a thin film of stacked uniform resorcinol-formaldehyde nanoshells with their inner surfaces functionalized with silver nanoparticles. Upon compression, the flexible polymer nanoshells expand laterally, inducing plasmonic decoupling between neighboring silver nanoparticles and a subsequent blue-shift. The initial color of the sensor is determined by the extent of plasmonic coupling, which can be controlled by tuning the interparticle distance through a seeded growth process. The sensing range can be conveniently customized by controlling the polymer shell thickness or incorporating hybrid nanoshells into various polymer matrices. The new colorimetric pressure sensors are easy to fabricate and highly versatile, allow for convenient tuning of the sensing range, and feature significant color shifts, holding great promise for a wide range of practical applications.
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Colloidal self-assembly refers to a solution-processed assembly of nanometer-/micrometer-sized, well-dispersed particles into secondary structures, whose collective properties are controlled by not only nanoparticle property but also the superstructure symmetry, orientation, phase, and dimension. This combination of characteristics makes colloidal superstructures highly susceptible to remote stimuli or local environmental changes, representing a prominent platform for developing stimuli-responsive materials and smart devices. Chemists are achieving even more delicate control over their active responses to various practical stimuli, setting the stage ready for fully exploiting the potential of this unique set of materials. This review addresses the assembly of colloids into stimuli-responsive or smart nanostructured materials. We first delineate the colloidal self-assembly driven by forces of different length scales. A set of concepts and equations are outlined for controlling the colloidal crystal growth, appreciating the importance of particle connectivity in creating responsive superstructures. We then present working mechanisms and practical strategies for engineering smart colloidal assemblies. The concepts underpinning separation and connectivity control are systematically introduced, allowing active tuning and precise prediction of the colloidal crystal properties in response to external stimuli. Various exciting applications of these unique materials are summarized with a specific focus on the structure-property correlation in smart materials and functional devices. We conclude this review with a summary of existing challenges in colloidal self-assembly of smart materials and provide a perspective on their further advances to the next generation.
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Nanopartículas , Nanoestruturas , Coloides/química , Cristalização , Nanopartículas/química , Nanoestruturas/químicaRESUMO
Integrating plasmonic resonance into photonic bandgap nanostructures promises additional control over their optical properties. Here, one-dimensional (1D) plasmonic photonic crystals with angular-dependent structural colors are fabricated by assembling magnetoplasmonic colloidal nanoparticles under an external magnetic field. Unlike conventional 1D photonic crystals, the assembled 1D periodic structures show angular-dependent colors based on the selective activation of optical diffraction and plasmonic scattering. They can be further fixed in an elastic polymer matrix to produce a photonic film with angular-dependent and mechanically tunable optical properties. The magnetic assembly enables precise control over the orientation of the 1D assemblies within the polymer matrix, producing photonic films with designed patterns displaying versatile colors from the dominant backward optical diffraction and forward plasmonic scattering. The combination of optical diffraction and plasmonic properties within a single system holds the potential for developing programmable optical functionalities for applications in various optical devices, color displays, and information encryption systems.
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We demonstrate the effective establishment of long-range electrostatic interactions among colloidal silica nanospheres through acid treatment, enabling their assembly into colloidal crystals at remarkably low concentrations. This novel method overcomes the conventional limitation in colloidal silica assembly by removing entrapped NH4+ ions and enhancing the electrical double layer (EDL) thickness, offering a time-efficient alternative to increase electrostatic interactions compared with methods like dialysis. The increased EDL thickness facilitates the assembly of SiO2 nanospheres into a body-centered-cubic lattice structure at low particle concentrations, allowing for broad spectrum tunability and high tolerance to particle size polydispersity. Further, we uncover a disorder-order transition during colloidal crystallization at low particle concentrations, with the optimal concentration for crystal formation governed by both thermodynamic and kinetic factors. This work not only provides insights into assembly mechanisms but also paves the way for the design and functionalization of colloidal silica-based photonic crystals in diverse applications.
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We report the unconventional space-free confined growth of Au nanoshells with well-defined plasmonic properties and active tuning of their plasmon coupling by the nanoscale magnetic assembly. The seeded growth of Au exclusively occurred at the hard-soft interfaces between the Fe3O4 core and phenolic resin without the need of creating a limiting space, which represents a general and elegant approach to various core-shell nanostructures. The deformability of permeable phenolic layers plays an essential role in regulating the interfacial growth of Au nanoshells. While the polymer elasticity suppresses the radial deposition of Au atoms, their high deformability can afford enough spaces for the formation of conformal metallic shells. The coupled magnetic-plasmonic properties allow active tuning of the plasmon coupling and the resonant scattering of Au nanoshells by the magnetic assembly of the hybrid nanoparticles into plasmonic chains, whose potentials in applications have been demonstrated in designing transparent displays and anticounterfeiting devices.
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Deoxynivalenol (DON) is a toxic secondary metabolite produced by Fusarium graminearum. It is one of the most common feed contaminants that poses a serious threat to the health and performance of dairy cows. This study investigated the in vitro cytotoxicity of DON on bovine mammary epithelial cells (MAC-T). DON at different concentrations (0.25, 0.3, 0.5, 0.8, 1 or 2 µg/ml) inhibited the growth of MAC-T cells after 24 hr of exposure (p < .001). DON at 0.25 µg/ml increased lactate dehydrogenase (LDH) leakage (p < .05); decreased glutathione (GSH) levels (p < .001), total superoxide dismutase (T-SOD) activity and total antioxidant capacity (T-AOC; p < .01); and increased malondialdehyde (MDA) concentration (p < .01) in MAC-T cells after 24 hr of exposure. We also observed that DON increased reactive oxygen species (ROS) levels in cells incubated for 9, 15 and 24 hr (p < .001). DON at 0.25 µg/ml triggered oxidative damage in MAC-T cells. Furthermore, it induced an inflammatory response in the cells incubated for 9, 15 and 24 hr (p < .05) by increasing the mRNA expression levels of nuclear factor kappa B, myeloid differentiation factor 88 (MyD88), tumour necrosis factor-α (TNF-α), interleukin-1ß (IL-1ß), IL-6, cyclooxygenase-2 and IL-8. We further examined the effect of DON on apoptosis. DON prevented normal proliferation of MAC-T cells by blocked cell cycle progression in 24 hr (p < .001). In addition, the apoptosis rate measured using annexin V-FITC significantly increased (p < .05) with increase in the mRNA expression level of Bax (p < .01) and increase in the Bax/Bcl-2 ratio (p < .01) in cells incubated for 24 hr. In summary, DON exerts toxic effects in MAC-T cells by causing oxidative stress, inducing an inflammatory response, affecting cell cycle and leading to apoptosis.
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Apoptose/efeitos dos fármacos , Bovinos , Células Epiteliais/efeitos dos fármacos , Inflamação/veterinária , Estresse Oxidativo/efeitos dos fármacos , Tricotecenos/farmacologia , Transportadores de Cassetes de Ligação de ATP/metabolismo , Animais , Anexina A5/metabolismo , Antioxidantes/metabolismo , Ciclo Celular/efeitos dos fármacos , Linhagem Celular , Sobrevivência Celular , Células Epiteliais/fisiologia , Feminino , Fluoresceína-5-Isotiocianato/análogos & derivados , Fluoresceína-5-Isotiocianato/metabolismo , Regulação da Expressão Gênica/efeitos dos fármacos , Inflamação/induzido quimicamente , Malondialdeído/metabolismo , Glândulas Mamárias Animais , Proteínas Periplásmicas de Ligação/metabolismo , RNA Mensageiro/genética , RNA Mensageiro/metabolismo , Espécies Reativas de Oxigênio/metabolismo , Superóxido Dismutase/metabolismoRESUMO
Plasmonic nanostructures exhibiting dynamically tunable chiroptical responses hold great promise for broad applications such as sensing, catalysis, and enantioselective analysis. Despite the successful fabrication of chiral structures through diverse templates, creating dynamic chiroptical materials with fast and reversible responses to external stimuli is still challenging. This work showcases reversible magnetic assembly and active tuning of plasmonic chiral superstructures by introducing a chiral magnetic field from a cubic permanent magnet. Manipulating the strength and direction of the magnetic field controls both the chiral arrangement and plasmonic coupling of the nanoparticle assembly, enabling fast and reversible tunability in not only the handedness of the superstructures but also the spectral characteristics of their chiroptical properties. The dynamic tunability further enables the fabrication of color-changing optical devices based on the optical rotatory dispersion effect, showcasing their potential for application in anti-counterfeiting and stress sensors.
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Colloidal assembly has emerged as an effective avenue for achieving polarized light emission. Here, we showcase the efficacy and versatility of the magnetic colloidal assembly in enabling both linearly and circularly polarized luminescence. Colloidal europium-doped NaYF4 nanorods with surface-bound Fe3O4 nanoparticles are magnetically assembled into linear or chiral superstructures using corresponding fields created in permanent magnets. In a uniform magnetic field generated by opposing poles, the assemblies exhibit photoluminescence with intensity tunable in response to the magnetic field direction, which is higher when the nanorods are perpendicular to light propagation than when they are parallel. The obtained superstructures display strong linearly polarized luminescence when the nanorods are aligned vertically, exhibiting a high degree of polarization up to 0.61. In a quadrupole chiral field generated by permanent magnets, the assemblies emit left-handed or right-handed polarized light depending on the position of the sample placement, attaining a g-factor of 0.04. Furthermore, the superstructures immobilized in a hydrogel film are found to retain their chirality, exhibiting opposite chiroptical responses depending on the sample orientation. The magnetic colloidal assembly approach facilitates the convenient and efficient generation of polarized light emissions from nonmagnetic luminescent materials, thus creating opportunities for tailoring light behavior in developing innovative optoelectronic devices.
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As an important fishery resource and endangered species, studying the habitat of Coilia nasus (C. nasus) is highly significant. This study used fishery survey data from southern Zhejiang coastal waters from 2016 to 2020, employing a maximum entropy model (MaxEnt) to map the habitat distribution of C. nasus. Model performance was evaluated using two metrics: the area under the curve (AUC) of the receiver operating characteristic curve for the training and test sets and true skill statistics (TSS). This study aimed to predict the habitat distribution of C. nasus and explore how environmental variables influence habitat suitability. The results indicated that the models for each season had strong predictive performance, with AUC values above 0.8 and TSS values exceeding 0.6, indicating that they could accurately predict the presence of C. nasus. In the study area, C. nasus was primarily found in brackish or marine waters near bays and coastal islands. Among all environmental factors, salinity (S) and bottom temperature (BOT) had the highest correlations with habitat distribution, although these correlations varied across seasons. The findings of this study provide empirical evidence and a reference for the conservation and management of C. nasus and for the designation of its protected areas.
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The wide accessibility to nanostructures with high uniformity and controllable sizes and morphologies provides great opportunities for creating complex superstructures with unique functionalities. Employing anisotropic nanostructures as the building blocks significantly enriches the superstructural phases, while their orientational control for obtaining long-range orders has remained a significant challenge. One solution is to introduce magnetic components into the anisotropic nanostructures to enable precise control of their orientations and positions in the superstructures by manipulating magnetic interactions. Recognizing the importance of magnetic anisotropy in colloidal assembly, we provide here an overview of magnetic field-guided self-assembly of magnetic nanoparticles with typical anisotropic shapes, including rods, cubes, plates, and peanuts. The Review starts with discussing the magnetic energy of nanoparticles, appreciating the vital roles of magneto-crystalline and shape anisotropies in determining the easy magnetization direction of the anisotropic nanostructures. It then introduces superstructures assembled from various magnetic building blocks and summarizes their unique properties and intriguing applications. It concludes with a discussion of remaining challenges and an outlook of future research opportunities that the magnetic assembly strategy may offer for colloidal assembly.
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Colloidal assembly into chiral superstructures is usually accomplished with templating or lithographic patterning methods that are only applicable to materials with specific compositions and morphologies over narrow size ranges. Here, chiral superstructures can be rapidly formed by magnetically assembling materials of any chemical compositions at all scales, from molecules to nano- and microstructures. We show that a quadrupole field chirality is generated by permanent magnets caused by consistent field rotation in space. Applying the chiral field to magnetic nanoparticles produces long-range chiral superstructures controlled by field strength at the samples and orientation of the magnets. Transferring the chirality to any achiral molecules is enabled by incorporating guest molecules such as metals, polymers, oxides, semiconductors, dyes, and fluorophores into the magnetic nanostructures.
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White blood cell (WBC) detection in microscopic images is indispensable in medical diagnostics; however, this work, based on manual checking, is time-consuming, labor-intensive, and easily results in errors. Using object detectors for WBCs with deep convolutional neural networks can be regarded as a feasible solution. In this paper, to improve the examination precision and efficiency, a one-stage and lightweight CNN detector with an attention mechanism for detecting microscopic WBC images, and a white blood cell detection vision system are proposed. The method integrates different optimizing strategies to strengthen the feature extraction capability through the combination of an improved residual convolution module, hybrid spatial pyramid pooling module, improved coordinate attention mechanism, efficient intersection over union (EIOU) loss and Mish activation function. Extensive ablation and contrast experiments on the latest public Raabin-WBC dataset verify the effectiveness and robustness of the proposed detector for achieving a better overall detection performance. It is also more efficient than other existing studies for blood cell detection on two additional classic public BCCD and LISC datasets. The novel detection approach is significant and flexible for medical technicians to use for blood cell microscopic examination in clinical practice.
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Trabalho de Parto , Leucócitos , Gravidez , Feminino , Humanos , Microscopia , Redes Neurais de ComputaçãoRESUMO
Incorporating stimuli-responsive mechanisms into chiral assemblies of nanostructures offers numerous opportunities to create optical materials capable of dynamically modulating their chiroptical properties. In this study, we demonstrate the formation of chiral superstructures by assembling Fe3O4@polyaniline hybrid nanorods by using a gradient magnetic field. The resulting superstructures exhibit a dual response to changes in both the magnetic field and solution pH, enabling dynamic regulation of the position, intensity, and sign of its circular dichroism peaks. Such responsiveness allows for convenient control over the optical rotatory dispersion properties of the assemblies, which are further integrated into the design of a chiroptical switch that can display various colors and patterns when illuminated with light of different wavelengths and polarization states. Finally, an optical information encryption system is constructed through the controlled assembly of the hybrid nanorods to showcase the potential opportunities for practical applications brought by the resulting responsive chiral superstructures.
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BACKGROUND AND OBJECTIVE: At present, the COVID-19 epidemic is still spreading worldwide and wearing a mask in public areas is an effective way to prevent the spread of the respiratory virus. Although there are many deep learning methods used for detecting the face masks, there are few lightweight detectors having a good effect on small or medium-size face masks detection in the complicated environments. METHODS: In this work we propose an efficient and lightweight detection method based on YOLOv4-tiny, and a face mask detection and monitoring system for mask wearing status. Two feasible improvement strategies, network structure optimization and K-means++ clustering algorithm, are utilized for improving the detection accuracy on the premise of ensuring the real-time face masks recognition. Particularly, the improved residual module and cross fusion module are designed to aim at extracting the features of small or medium-size targets effectively. Moreover, the enhanced dual attention mechanism and the improved spatial pyramid pooling module are employed for merging sufficiently the deep and shallow semantic information and expanding the receptive field. Afterwards, the detection accuracy is compensated through the combination of activation functions. Finally, the depthwise separable convolution module is used to reduce the quantity of parameters and improve the detection efficiency. Our proposed detector is evaluated on a public face mask dataset, and an ablation experiment is also provided to verify the effectiveness of our proposed model, which is compared with the state-of-the-art (SOTA) models as well. RESULTS: Our proposed detector increases the AP (average precision) values in each category of the public face mask dataset compared with the original YOLOv4-tiny. The mAP (mean average precision) is improved by 4.56% and the speed reaches 92.81 FPS. Meanwhile, the quantity of parameters and the FLOPs (floating-point operations) are reduced by 1/3, 16.48%, respectively. CONCLUSIONS: The proposed detector achieves better overall detection performance compared with other SOTA detectors for real-time mask detection, demonstrated the superiority with both theoretical value and practical significance. The developed system also brings greater flexibility to the application of face mask detection in hospitals, campuses, communities, etc.
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COVID-19 , Algoritmos , Humanos , Máscaras , Pandemias/prevenção & controleRESUMO
Metal-organic frameworks (MOFs) have many attractive features, including tunable composition, rigid structure, controllable pore size, and large specific surface area, and thus are highly applicable in molecular analysis. Depending on the MOF structure, a high number of unsaturated metal sites can be exposed to catalyze chemical reactions. In the present work, we report that using both Co(II) and Fe(III) to prepare the MIL-88(NH2) MOF, we can produce the bimetallic MOF that can catalyze the conversion of 3,3',5,5â³-tetramethylbenzidine (TMB) to a color product through a reaction with H2O2 at a higher reaction rate than the monometallic Fe-MIL-88(NH2). The Michaelis constants (Km) of the catalytic reaction for TMB and H2O2 are 3-5 times smaller, and the catalytic constants (kcat) are 5-10 times higher than those of the horseradish peroxidase (HRP), supporting ultrahigh peroxidase-like activity. These values are also much more superior to those of the HRP-mimicking MOFs reported previously. Interestingly, the bimetallic MOF can be coupled with glucose oxidase (GOx) to trigger the cascade enzymatic reaction for highly sensitive detection of extracellular vesicles (EVs), a family of important biomarkers. Through conjugation to the aptamer that recognizes the marker protein on EV surface, the MOF can help isolate the EVs from biological matrices, which are subsequently labeled by GOx via antibody recognition. The cascade enzymatic reaction between MOF and GOx enables the detection of EVs at a concentration as low as 7.8 × 104 particles/mL. The assay can be applied to monitor EV secretion by cultured cells and also can successfully detect the different EV quantities in the sera samples collected from cancer patients and healthy controls. Overall, we prove that the bimetallic Fe/Co-MIL-88(NH2) MOF, with its high peroxidase activity and high biocompatibility, is a valuable tool deployable in clinical assays to facilitate disease diagnosis and prognosis.
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Vesículas Extracelulares , Estruturas Metalorgânicas , Benzidinas , Colorimetria , Corantes/química , Vesículas Extracelulares/química , Compostos Férricos , Glucose Oxidase/metabolismo , Peroxidase do Rábano Silvestre , Peróxido de Hidrogênio/química , Estruturas Metalorgânicas/química , Peroxidase/química , Peroxidases/químicaRESUMO
The variations of life history traits have been observed for many fish species, which gains much concerns in the study of aquatic biology and ecology. In this study, the biological characteristics were explored for yellow croaker (Larimichthys polyactis) in the offshore waters of southern Zhejiang, based on 4920 individuals collected from 13 fishery-independent seasonal surveys from autumn 2015 to autumn 2018. Linear mixed effects models were used to estimate the growth, maturity characteristics, and their heterogeneity. The body length of yellow croaker samples ranged from 13 to 215 mm with the dominant body of 110 to 154 mm. The body weight ranged from 0.5 to 182.2 g, with the dominant body weight from 20 to 55 g. The results showed that the linear mixed effects models with random effects from season, gender, and year performed best for length-weight relationship, with the lowest AIC and RMSE values. The effects of season were much larger than those of genders and years. When the length exceeded 160 mm, the weight gain rate of yellow croaker was faster in spring and summer, lower in autumn and winter, while the male individuals gained more weight than the females with the same body length. Among 4841 individuals of specimens with gonadal data, the individuals at maturity â ¡ stage occupied 50.4%, and the individuals at maturity stage contributed to 19.6%. The results from the best linear mixed effects model showed that season had the most significant influence on the maturity of yellow croaker. The 50% maturity length (L50%) was much lower in winter (124.6 mm) with no much difference between other seasons, indicating that yellow croaker matures earlier in winter. Our results indicated that linear mixed effect model could reflect the biological heterogeneity of yellow croaker conveniently and that the growth and maturity of yellow croaker had significantly sexual and temporal variations, which should be considered in the stock assessment and fishery management for yellow croaker.
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Perciformes , Animais , China , Feminino , Pesqueiros , Peixes , Humanos , Modelos Lineares , MasculinoRESUMO
Responsive chromic materials are highly desirable in the fields of displays, anti-counterfeiting, and camouflage, but their advanced applications are usually limited by the unrealized delicate and independent tunability of their three intrinsic attributes of color. This work achieves the separate, continuous, and reversible modulation of structural color brightness and hue with an aqueous suspension of dual-responsive Fe3O4@polyvinylpyrrolidone (PVP)@poly(N-isopropyl acrylamide) (PNIPAM) flexible photonic nanochains. The underlying modulation mechanism of color brightness was experimentally and numerically deciphered by analyzing the morphological responses to stimuli. When an increasing magnetic field was applied, the random worm-like flexible photonic nanochains gradually orientated along the field direction, due to the dominant magnetic dipole interaction over the thermal motion, lengthening the orientation segment length up to the whole of the nanochains. Consequently, the suspension displays increased color brightness (characterized by diffraction intensity). Meanwhile, the color hue (characterized by diffraction frequency) could be controlled by temperature, due to the volume changes of the interparticle PNIPAM. The achieved diverse color modulation advances the next-generation responsive chromic materials and enriches the basic understanding of the color tuning mechanisms. With versatile and facile color tunability and shape patterning, the developed responsive chromic liquid promises to have attractive potential in full-color displays and in adaptive camouflages.
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Photothermal actuators have attracted increasing attention due to their ability to convert light energy into mechanical deformation and locomotion. This work reports a freestanding, multidirectional photothermal robot that can walk along a predesigned pathway by modulating laser polarization and on-off switching. Magnetic-plasmonic hybrid Fe3 O4 /Ag nanorods are synthesized using an unconventional templating approach. The coupled magnetic and plasmonic anisotropy allows control of the rod orientation, plasmonic excitation, and photothermal conversion by simply applying a magnetic field. Once the rods are fixed with desirable orientations in a bimorph actuator by magnetic-field-assisted lithography, the bending of the actuator can be controlled by switching the laser polarization. A bipedal robot is created by coupling the rod orientation with the alternating actuation of its two legs. Irradiating the robot by a laser with alternating or fixed polarization synergistically results in basic movement (backward and forward) and turning (including left-, right-, and U-turn), respectively. A complex walk along predesigned pathways can be potentially programmed by combining the movement and turning modes of the robots. This strategy provides an alternative driving mechanism for preparing functional soft robots, thus breaking through the limitations in the existing systems in terms of light sources and actuation manners.
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Titania nanocrystals have been investigated for fast color switching through photocatalytic reduction of dyes and hexacyanometalate pigments. Here we reveal that direct binding of sacrificial electron donors (SEDs) to the surface of titania nanocrystals can significantly promote the charge transfer rate by more efficiently scavenging photogenerated holes and releasing more photogenerated electrons for reduction reactions. Using diethylene glycol (DEG) as an example, we show that its binding to the nanoparticle surface, which can be achieved either during or after the nanoparticle formation, greatly enhances the photocatalytic reduction in comparison with the case where free DEG molecules are simply added as external SEDs.
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Adipose tissue is the body largest free cholesterol reservoir and abundantly expresses ATP binding cassette transporter A1 (ABCA1), which maintains plasma high-density lipoprotein (HDL) levels. HDLs have a protective role in atherosclerosis by mediating reverse cholesterol transport (RCT). Soluble epoxide hydrolase (sEH) is a cytosolic enzyme whose inhibition has various beneficial effects on cardiovascular disease. The sEH is highly expressed in adipocytes, and it converts epoxyeicosatrienoic acids (EETs) into less bioactive dihydroxyeicosatrienoic acids. We previously showed that increasing EETs levels with a sEH inhibitor (sEHI) (t-AUCB) resulted in elevated ABCA1 expression and promoted ABCA1-mediated cholesterol efflux from 3T3-L1 adipocytes. The present study investigates the impacts of t-AUCB in mice deficient for the low density lipoprotein (LDL) receptor (Ldlr(-/-) mice) with established atherosclerotic plaques. The sEH inhibitor delivered in vivo for 4 weeks decreased the activity of sEH in adipose tissue, enhanced ABCA1 expression and cholesterol efflux from adipose depots, and consequently increased HDL levels. Furthermore, t-AUCB enhanced RCT to the plasma, liver, bile and feces. It also showed the reduction of plasma LDL-C levels. Consistently, t-AUCB-treated mice showed reductions in the size of atherosclerotic plaques. These studies establish that raising adipose ABCA1 expression, cholesterol efflux, and plasma HDL levels with t-AUCB treatment promotes RCT, decreasing LDL-C and atherosclerosis regression, suggesting that sEH inhibition may be a promising strategy to treat atherosclerotic vascular disease.