Highly fluorescent CdTe/ZnSe quantum dot-based "turn-off" sensor for the on-site rapid detection of Lead ions in aqueous medium.

Lead (Pb) is a heavy metal known for its adverse effects on both human health and the environment. In recent years, the industrial utilization of Pb2+ has surged, underscoring the imperative need for efficient measurement methods. In this study, a rapid and simple photochemical method was used to synthesize thioglycolic acid (TGA)-stabilized CdTe/ZnSe core-shell quantum dots (QDs). These CdTe/ZnSe QDs emit vibrant green fluorescence and exhibit remarkable quenching in the presence of Pb2+ ions. This property enables the development of an on-site on/off sensor without the necessity of additional modifications. The proposed sensor possesses an outstanding sensitivity to Pb2+, with a detection limit and linear range of 31.8 nM and 50 nM-10 µM, respectively. Importantly, the selectivity of this fluorescence-based sensor was validated by analyzing various positively and negatively charged ions. Furthermore, the developed sensor showed reliable performance against real river, agricultural, and tap water, as confirmed by Inductively Coupled Plasma (ICP) analysis. Additionally, CdTe/ZnSe QDs immobilized on glass slides were successfully employed for on-site water sample analysis, providing a versatile solution for environmental monitoring.

Interfacial rheology of lanthanide binding peptide surfactants at the air-water interface.

Peptide surfactants (PEPS) are studied to capture and retain rare earth elements (REEs) at air-water interfaces to enable REE separations. Peptide sequences, designed to selectively bind REEs, depend crucially on the position of ligands within their binding loop domain. These ligands form a coordination sphere that wraps and retains the cation. We study variants of lanthanide binding tags (LBTs) designed to complex strongly with Tb3+. The peptide LBT5- (with net charge -5) is known to bind Tb3+ and adsorb with more REE cations than peptide molecules, suggesting that undesired non-specific coulombic interactions occur. Rheological characterization of interfaces of LBT5- and Tb3+ solutions reveal the formation of an interfacial gel. To probe whether this gelation reflects chelation among intact adsorbed LBT5-:Tb3+ complexes or destruction of the binding loop, we study a variant, LBT3-, designed to form net neutral LBT3-:Tb3+ complexes. Solutions of LBT3- and Tb3+ form purely viscous layers in the presence of excess Tb3+, indicating that each peptide binds a single REE in an intact coordination sphere. We introduce the variant RR-LBT3- with net charge -3 and anionic ligands outside of the coordination sphere. We find that such exposed ligands promote interfacial gelation. Thus, a nuanced requirement for interfacial selectivity of PEPS is proposed: that anionic ligands outside of the coordination sphere must be avoided to prevent the non-selective recruitment of REE cations. This view is supported by simulation, including interfacial molecular dynamics simulations, and interfacial metadynamics simulations of the free energy landscape of the binding loop conformational space.

Efficient Mercury Ion Detection in Water: CdTe/CdS/ZnS Quantum Dots as a Simple, Sensitive, and Rapid Fluorescence Sensor.

Mercury (Hg), a notorious heavy metal with detrimental impacts on human health and the environment, necessitates the development of precise measurement methods. This study introduces an expeditious and straightforward photochemical approach to synthesize thioglycolic acid (TGA)-stabilized CdTe/CdS/ZnS core/multi-shell quantum dots (QDs). The synthesized CdTe/CdS/ZnS QDs were comprehensively characterized using fluorescence spectroscopy, transmission electron microscopy (TEM), energy-dispersive X-ray spectroscopy (EDS), Field Emission Scanning Electron Microscopy (FESEM), and X-Ray diffraction (XRD). XRD and EDS results confirmed the successful formation of CdTe/CdS/ZnS structure. Also, FESEM and TEM results showed that CdTe/CdS/ZnS QDs were spherical. Results showed that synthesized Exhibiting vibrant green fluorescence and notable quenching in the presence of Hg2+ ions, these QDs emerge as promising candidates for fabricating a fluorescent sensor. The proposed sensor demonstrates notable sensitivity to Hg2+, featuring a detection limit of 16.32 nM and a linear range from 20 nM to 70 nM. The sensor's selectivity was confirmed by analyzing various anions and cations. Moreover, when tested with tap water, river water, and agricultural samples, the sensor exhibited reliable performance, validated by Inductively Coupled Plasma (ICP) analysis. Additionally, CdTe/CdS/ZnS QDs immobilized on micro pads proved effective for on-site water sample analysis, presenting a versatile solution for environmental monitoring.

Swimmers at interfaces enhance interfacial transport.

The behavior of fluid interfaces far from equilibrium plays central roles in nature and in industry. Active swimmers trapped at interfaces can alter transport at fluid boundaries with far reaching implications. Swimmers can become trapped at interfaces in diverse configurations and swim persistently in these surface adhered states. The self-propelled motion of bacteria makes them ideal model swimmers to understand such effects. We have recently characterized the swimming of interfacially trapped Pseudomonas aeruginosa PA01 moving in pusher mode. The swimmers adsorb at the interface with pinned contact lines, which fix the angle of the cell body at the interface and constrain their motion. Thus, swimmers become trapped at interfaces in diverse configurations and swim persistently in these surface adhered states. We observe that most interfacially trapped bacteria swim along circular paths. Fluid interfaces also typically form incompressible two-dimensional layers. These effects influence the flow generated by the swimmers. In our previous work, we have visualized the interfacial flow around a pusher bacterium and described the flow field using two dipolar hydrodynamic modes; one stresslet mode whose symmetries differ from those in bulk, and another bulk mode unique to incompressible fluid interfaces. Based on this understanding, swimmer-induced tracer displacements and swimmer-swimmer pair interactions are explored using analysis and experiment. The settings in which multiple interfacial swimmers with circular motion can significantly enhance interfacial transport of tracers or promote mixing of other swimmers on the interface are identified through simulations and compared to experiment. This study shows the importance of biomixing by swimmers at fluid interfaces and identifies important factors in the design of biomimetic active colloids to enhance interfacial transport.

Preparation of rGO/MoSe2 nanocomposites for enhanced microwave absorption of whole X and Ku bands.

rGO-MoSe2 nanocomposites were prepared via a one-pot hydrothermal method in which MoSe2 microspheres (MS) were decorated on rGO sheets. Three nanocomposites named F1, F2, and F3 were prepared using different weight ratios of MoSe2 MS to rGO: (3 : 1), (4 : 1), and (5 : 1), respectively. FESEM images showed a flower-like porous morphology of the MoSe2 microspheres. All the rGO-MoSe2 nanocomposites exhibited remarkable microwave absorption properties as demonstrated by strong reflection loss (-58 dB to -99 dB) and an ultrabroad effective absorption bandwidth (equivalent to 90% attenuation), which covers whole X and Ku frequency bands at matching thicknesses of 2.8-3.2 mm. The minimum reflection loss reached -98, -99, and -75 dB for F1, F2 and F3, respectively. The excellent absorption properties of the rGO-MoSe2 nanocomposites is related to the unique morphology and micro size of MoSe2 in which incident waves are attenuated by multiple reflections and scattering.

Motor crosslinking augments elasticity in active nematics.

In active materials, uncoordinated internal stresses lead to emergent long-range flows. An understanding of how the behavior of active materials depends on mesoscopic (hydrodynamic) parameters is developing, but there remains a gap in knowledge concerning how hydrodynamic parameters depend on the properties of microscopic elements. In this work, we combine experiments and multiscale modeling to relate the structure and dynamics of active nematics composed of biopolymer filaments and molecular motors to their microscopic properties, in particular motor processivity, speed, and valency. We show that crosslinking of filaments by both motors and passive crosslinkers not only augments the contributions to nematic elasticity from excluded volume effects but dominates them. By altering motor kinetics we show that a competition between motor speed and crosslinking results in a nonmonotonic dependence of nematic flow on motor speed. By modulating passive filament crosslinking we show that energy transfer into nematic flow is in large part dictated by crosslinking. Thus motor proteins both generate activity and contribute to nematic elasticity. Our results provide new insights for rationally engineering active materials.

Effect of dry and wet finishing and polishing on color change and opacity of nanofill and nanohybrid composites.

BACKGROUND: As superior esthetic is one of the main reasons for using composite resins, it is very important to be familiar with factors and techniques affecting their optical properties and appearance. AIM: The aim of this study was comparing the effect of finishing and polishing with and without water coolant, on the color change and opacity of composite resin materials. METHODS: Composites used for preparing samples were Z250 (microhybrid), Z350XT (nanofilled), and Z550 (nanohybrid). Then divided into 4 groups of 5 depending on finishing and polishing technique (dry or wet) and time (immediate and after twenty-four hours). After polishing, samples were assessed using a spectrophotometer. Color change and opacity were determined. Data was analyzed using Kolmogorov-Smirnov, ANOVA and Tukey HSD tests. RESULTS: Type of material at both time had a significant effect on ΔE and opacity. Our results in dry and wet technique immediately(T0) showed that the highest and lowest ΔE and opacity belong to Z350XT (p < 0.001). After Twenty-four hours (T24), opacity of Z250 in wet condition was higher than dry condition (p < 0.001). CONCLUSIONS: Wet or dry technique was only effective on color in immediate polishing. Regarding opacity, technique was only effective in case of delayed polishing.

Efficient Gamma Ray Detection Using CdTe/CdS Core/Shell Quantum Dots: A Simple and Rapid Fluorescence Approach.

Gamma rays, as hazardous nuclear radiation, necessitate effective and rapid detection methods. This paper introduces a low-cost, fast, and simple fluorescence method based on CdTe/CdS core/shell quantum dots for gamma-ray detection. CdTe/CdS quantum dots, subjected to gamma irradiation from a 60Co source under various conditions, were investigated to assess their fluorescence sensor capabilities. The obtained results showed that an increase in CdTe/CdS nanoparticle size was associated with decreased sensitivity, while a reduction in CdTe/CdS concentration correlated with increased sensitivity. To further validate the practicality of CdTe/CdS core/shell quantum dots in gamma-ray detection, the structural properties of the quantum dots were meticulously studied. Raman spectroscopy, X-ray diffraction (XRD), and Fourier-transform infrared (FT-IR) analysis were conducted before and after gamma-ray radiation. The results demonstrated the crystalline stability of CdTe/CdS core/shell quantum dots under gamma irradiation, highlighting their robust structural integrity. In conclusion, the experimental findings underscore the exceptional potential of CdTe/CdS quantum dots as an off-fluorescence probe for simple, low-cost, fast, and on-site detection of gamma rays. This research contributes to the advancement of efficient and practical methods for gamma-ray sensing in various applications.

Limiting pool and actin architecture controls myosin cluster sizes in adherent cells.

The actomyosin cytoskeleton generates mechanical forces that power important cellular processes, such as cell migration, cell division, and mechanosensing. Actomyosin self-assembles into contractile networks and bundles that underlie force generation and transmission in cells. A central step is the assembly of the myosin II filament from myosin monomers, regulation of which has been extensively studied. However, myosin filaments are almost always found as clusters within the cell cortex. While recent studies characterized cluster nucleation dynamics at the cell periphery, how myosin clusters grow on stress fibers remains poorly characterized. Here, we utilize a U2OS osteosarcoma cell line with endogenously tagged myosin II to measure the myosin cluster size distribution in the lamella of adherent cells. We find that myosin clusters can grow with Rho-kinase (ROCK) activity alone in the absence of myosin motor activity. Time-lapse imaging reveals that myosin clusters grow via increased myosin association to existing clusters, which is potentiated by ROCK-dependent myosin filament assembly. Enabling myosin motor activity allows further myosin cluster growth through myosin association that is dependent on F-actin architecture. Using a toy model, we show that myosin self-affinity is sufficient to recapitulate the experimentally observed myosin cluster size distribution, and that myosin cluster sizes are determined by the pool of myosin available for cluster growth. Together, our findings provide new insights into the regulation of myosin cluster sizes within the lamellar actomyosin cytoskeleton.

Measuring response functions of active materials from data.

From flocks of birds to biomolecular assemblies, systems in which many individual components independently consume energy to perform mechanical work exhibit a wide array of striking behaviors. Methods to quantify the dynamics of these so-called active systems generally aim to extract important length or time scales from experimental fields. Because such methods focus on extracting scalar values, they do not wring maximal information from experimental data. We introduce a method to overcome these limitations. We extend the framework of correlation functions by taking into account the internal headings of displacement fields. The functions we construct represent the material response to specific types of active perturbation within the system. Utilizing these response functions we query the material response of disparate active systems composed of actin filaments and myosin motors, from model fluids to living cells. We show we can extract critical length scales from the turbulent flows of an active nematic, anticipate contractility in an active gel, distinguish viscous from viscoelastic dissipation, and even differentiate modes of contractility in living cells. These examples underscore the vast utility of this method which measures response functions from experimental observations of complex active systems.

New realm of precision multiplexing enabled by massively-parallel single molecule UltraPCR.

PCR has been a reliable and inexpensive method for nucleic acid detection in the past several decades. In particular, multiplex PCR is a powerful tool to analyze many biomarkers in the same reaction, thus maximizing detection sensitivity and reducing sample usage. However, balancing the amplification kinetics between amplicons and distinguishing them can be challenging, diminishing the broad adoption of high order multiplex PCR panels. Here, we present a new paradigm in PCR amplification and multiplexed detection using UltraPCR. UltraPCR utilizes a simple centrifugation workflow to split a PCR reaction into ∼34 million partitions, forming an optically clear pellet of spatially separated reaction compartments in a PCR tube. After in situ thermocycling, light sheet scanning is used to produce a 3D reconstruction of the fluorescent positive compartments within the pellet. At typical sample DNA concentrations, the magnitude of partitions offered by UltraPCR dictate that the vast majority of target molecules occupy a compartment uniquely. This single molecule realm allows for isolated amplification events, thereby eliminating competition between different targets and generating unambiguous optical signals for detection. Using a 4-color optical setup, we demonstrate that we can incorporate 10 different fluorescent dyes in the same UltraPCR reaction. We further push multiplexing to an unprecedented level by combinatorial labeling with fluorescent dyes - referred to as "comboplex" technology. Using the same 4-color optical setup, we developed a 22-target comboplex panel that can detect all targets simultaneously at high precision. Collectively, UltraPCR has the potential to push PCR applications beyond what is currently available, enabling a new class of precision genomics assays.

Motor crosslinking augments elasticity in active nematics.

In active materials, uncoordinated internal stresses lead to emergent long-range flows. An understanding of how the behavior of active materials depends on mesoscopic (hydrodynamic) parameters is developing, but there remains a gap in knowledge concerning how hydrodynamic parameters depend on the properties of microscopic elements. In this work, we combine experiments and multiscale modeling to relate the structure and dynamics of active nematics composed of biopolymer filaments and molecular motors to their microscopic properties, in particular motor processivity, speed, and valency. We show that crosslinking of filaments by both motors and passive crosslinkers not only augments the contributions to nematic elasticity from excluded volume effects but dominates them. By altering motor kinetics we show that a competition between motor speed and crosslinking results in a nonmonotonic dependence of nematic flow on motor speed. By modulating passive filament crosslinking we show that energy transfer into nematic flow is in large part dictated by crosslinking. Thus motor proteins both generate activity and contribute to nematic elasticity. Our results provide new insights for rationally engineering active materials.

Experimental observations of fractal landscape dynamics in a dense emulsion.

Many soft and biological materials display so-called 'soft glassy' dynamics; their constituents undergo anomalous random motions and complex cooperative rearrangements. A recent simulation model of one soft glassy material, a coarsening foam, suggested that the random motions of its bubbles are due to the system configuration moving over a fractal energy landscape in high-dimensional space. Here we show that the salient geometrical features of such high-dimensional fractal landscapes can be explored and reliably quantified, using empirical trajectory data from many degrees of freedom, in a model-free manner. For a mayonnaise-like dense emulsion, analysis of the observed trajectories of oil droplets quantitatively reproduces the high-dimensional fractal geometry of the configuration path and its associated local energy minima generated using a computational model. That geometry in turn drives the droplets' complex random motion observed in real space. Our results indicate that experimental studies can elucidate whether the similar dynamics in different soft and biological materials may also be due to fractal landscape dynamics.

Limiting Pool and Actin Architecture Controls Myosin Cluster Sizes in Adherent Cells.

The actomyosin cytoskeleton generates mechanical forces that power important cellular processes, such as cell migration, cell division, and mechanosensing. Actomyosin self-assembles into contractile networks and bundles that underlie force generation and transmission in cells. A central step is the assembly of the myosin II filament from myosin monomers, regulation of which has been extensively studied. However, myosin filaments are almost always found as clusters within the cell cortex. While recent studies characterized cluster nucleation dynamics at the cell periphery, how myosin clusters grow on stress fibers remains poorly characterized. Here, we utilize a U2OS osteosarcoma cell line with endogenously tagged myosin II to measure the myosin cluster size distribution in the lamella of adherent cells. We find that myosin clusters can grow with Rho-kinase (ROCK) activity alone in the absence of myosin motor activity. Time-lapse imaging reveals that myosin clusters grow via increased myosin association to existing clusters, which is potentiated by ROCK-dependent myosin filament assembly. Enabling myosin motor activity allows further myosin cluster growth through myosin association that is dependent on F-actin architecture. Using a toy model, we show that myosin self-affinity is sufficient to recapitulate the experimentally observed myosin cluster size distribution, and that myosin cluster sizes are determined by the pool of myosin available for cluster growth. Together, our findings provide new insights into the regulation of myosin cluster sizes within the lamellar actomyosin cytoskeleton.

Application of CdTe/ZnS Core/Shell Quantum Dots as on Fluorescence Sensor for Detection of Gamma Rays.

Gamma rays are a type of ionizing radiation that are extremely hazardous and dangerous for humans and the environment. The fluorescence method is a simple, useful, and fast method for the detection of gamma rays. In this research, CdTe/ZnS core/shell quantum dots were used as on fluorescence sensor for the detection of gamma rays. CdTe/ZnS core/shell QDs were prepared via a simple and rapid photochemical method. The shell thickness and concentration of CdTe/ZnS core/shell quantum dots were studied as two important factors in the optical behavior of CdTe/ZnS quantum dots. The obtained results showed that the PL intensity of CdTe/ZnS QDs after gamma irradiation was increased and also a slight redshift in the PL spectrum was observed. X-ray diffractions (XRD) and Raman analyses were used to study the effect of gamma irradiation on the structural properties of CdTe/ZnS QDs. The obtained results showed that gamma irradiation couldn't damage the crystalline structure of CdTe/ZnS core/shell QDs.

Effect of Wet and Dry Finishing and Polishing Technique on Microhardness and Flexural Strength of Nanocomposite Resins.

Objectives: This in vitro study was aimed to assess the effect of wet and dry finishing and polishing techniques on the flexural strength and microhardness of different commercial nanoparticle contained composite resins. Methods and Materials: The samples were made of Z250 (microhybrid), Z350 XT (nanofilled), and Z550 (nanohybrid) resin composites. Each group was subdivided into 2 subgroups according to polishing protocols. Subgroup 1 for each composite underwent wet polishing, and subgroup 2 was subject to dry polishing technique. Flexural strength and microhardness of the samples were measured at two different times of polishing (T 0 and T 24). The flexural strength test and microhardness test were measured by a 3-point bending test using a universal testing machine, and a Vickers machine, respectively. Data were analyzed by Kolmogorov-Smirnov, two-way ANOVA, and Tukey HSD tests. Results: ANOVA showed that the type of composite has a significant effect on flexural strength. Two-way ANOVA showed that, at T 0, flexural strength of all composites in the dry technique was higher than in the wet technique (p = 0.019). At T 24, Z350 XT had the lowest, and Z250 had the highest flexural strength in both techniques. The time and technique of polishing were also significantly effective on hardness. At T 0, hardness was higher in the wet compared to the dry method (p = 0.008). Tukey test showed that, at T 24, the hardness of Z350 XT was significantly higher than the other materials in both techniques. Conclusion: Immediate wet finishing and polishing presented lower flexural strength. Delayed dry/wet finishing and polishing significantly enhanced the hardness of the samples.

CdS Semiconductor Quantum Dots; Facile Synthesis, Application as Off Fluorescent Sensor for Detection of Lead (Pb2+) Ions and Catalyst for Degradation of Dyes from Water.

The CdS quantum dots (QDs) were prepared by rapid, one-pot, and novel photochemical method, which used Thioglycolic acid (TGA) molecules as both stabilizer and sulfur source. The structure and morphology of the prepared CdS QDs were characterized by different analyses such as XRD, FT-IR, Raman, EDS, TEM, PL, and absorption. In this work, was used of CdS QDs as off fluorescence sensor for rapid and simple detection of lead (Pb2+) ions in water. The PL intensity of CdS QDs in the presence of lead ions decreased gradually and in the presence of 100 µM lead ions, photo emission completely quenched. The photocatalyst performance of CdS QDs was investigated by methylene blue (MB), methylene orange (MO), and rhodamine b (RB) pollutant dyes under both UV and sun lights. The obtained results showed that CdS QDs had excellent photocatalyst activity with dyes under UV light and 94.9% of MO dye, 94.4% of RB dye, and 81.2% of MB was degraded after 60 min UV irradiation. For understanding about which parameter have a key role in the photodegradation process of MO by CdS QDs under UV illumination, several radical scavengers were used, and results showed that holes have a key role in the degradation process.

Mercury (Hg2+) Detection in Aqueous Media, Photocatalyst, and Antibacterial Applications of CdTe/ZnS Quantum Dots.

In the present work, CdTe/ZnS high luminescence quantum dots (QDs) were synthesized by a facile, fast, one-pot, and room temperature photochemical method. Synthesized QDs were characterized by different structural and optical analyses such as X-ray diffraction (XRD), energy dispersive X-ray spectroscopy (EDS), field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), Fourier transform-infrared spectroscopy (FT-IR), Raman, photoluminescence (PL) and UV-visible (UV-vis) spectroscopies. The results confirmed the successful growth of the ZnS shell and formation of CdTe/ZnS core/shell structure. CdTe/ZnS prepared QDs indicated a PL quantum yield of about 51%. These high luminescence QDs were used for detection of Hg2+ ions in aqueous media, as catalyst for photodegradation of different organic dyes, and as antibacterial material for the inhibition of bacterial growth. PL intensity of the CdTe/ZnS QDs was completely quenched after addition of 1 m molar Hg2+in to the media. Photocatalyst activity of CdTe/ZnS QDs was studied by rhodamine b, methylene blue, and methylene orange as organic dyes under both the sun and UV illuminations, and results showed that CdTe/ZnS QDs had the best photocatalyst activity for methylene blue degradation under UV irradiation and radical scavenger results indicated that electrons have a main role in photodegradation of methylene blue dye by CdTe/ZnS QDs under UV illumination. Antibacterial effects of CdTe/ZnS QDs evaluated by Minimum Inhibitory Concentration (MIC), and Minimum Bactericidal Concentration (MBC) methods against two strains of bacteria. The results of the antibacterial test showed that CdTe/ZnS could inhibit bacterial growth in Bacillus cereus (Gram-positive) and Escherichia coli (Gram-negative G) bacteria.

Probing lipid membrane bending mechanics using gold nanorod tracking.

Lipid bilayer membranes undergo rapid bending undulations with wavelengths from tens of nanometers to tens of microns due to thermal fluctuations. Here, we probe such undulations and the membranes' mechanics by measuring the time-varying orientation of single gold nanorods (GNRs) adhered to the membrane, using high-speed dark field microscopy. In a lipid vesicle, such measurements allow the determination of the membrane's viscosity, bending rigidity, and tension as well as the friction coefficient for sliding of the monolayers over one another. The in-plane rotation of the GNR is hindered by undulations in a tension dependent manner, consistent with simulations. The motion of single GNRs adhered to the plasma membrane of living cultured cells similarly reveals the membrane's complex physics and coupling to the cell's actomyosin cortex.