EARLY CATARACT DETECTION BY DYNAMIC LIGHT SCATTERING WITH SPARSE BAYESIAN LEARNING

Dynamic light scattering(DLS)is a promising technique for early cataract detection and for studying cataractogenesis.A novel probabilistic analysis tool,the sparse Bayesian learning(SBL)algorithm,is described for reconstructing the most-probable size distribution ofα-crystallin and their aggregates in an ocular lens from the DLS data.The performance of the algorithm is evaluated by analyzing simulated correlation data from known distributions and DLS data from the ocular lenses of a fetal calf,a Rhesus monkey,and a man,so as to establish the required efficiency of the SBL algorithm for clinical studies.

Polarized imaging dynamic light scattering for simultaneous measurement of nanoparticle size and morphology

The performance of nanoparticles is often affected by particle size and morphology.Currently,electron microscopy or atomic force microscopy is typically utilized to determine the size and morphology of nanoparticles.However,there are issues such as difficult sample preparation,long processing times,and challenges in quantitative characterization.Therefore,it is of great significance to develop a fast,accu-rate,and statistical method to measure the size and morphology of nanoparticles.In this study,a new method,called polarized imaging dynamic light scattering(PIDLS),is proposed.The nanoparticles are irradiated with a vertical linearly polarized laser beam,and a polarization camera collected the dynamic light scattering images of particles at four different polarization directions(0°,45°,90°,and 135°)at a scattering angle of 90°.The average particle size and distribution are obtained using the imaging dy-namic light scattering method at 0°polarization direction,and the morphology of the particles is ob-tained based on the depolarization patterns of the scattered light.The optical sphericityΦis defined based on the degree of linear polarization(DoLP).It is also implemented for the quantitative evaluation of the sphericity of the nanoparticles,including spherical,octahedral,nanoplate,nanorod,and linear ones.Together with the Poincarésphere parameterψ,the morphology of the nanoparticles can be roughly identified.In addition,PIDLS enables the measurement of particle size and morphology distributions simultaneously for evaluating the uniformity of particles.The effectiveness of PIDLS is verified by the measurement of five kinds of industrial titanium dioxide as well.

Applying dynamic light scattering to investigate the self-assembly process of DNA nanostructures

Understanding the dynamic assembly process of DNA nanostructures is important for developing novel strategy to design and construct functional devices.In this work,temperature-controlled dynamic light scattering(DLS)strategy has been applied to study the global assembly process of DNA origami and DNA bricks.Through the temperature dependent size and intensity profiles,the self-assembly process of various DNA nanostructures with different morphologies have been well-studied and the temperature transition ranges could be observed.Taking advantage of the DLS information,rapid preparation of the DNA origami and the brick assembly has been realized through a constant temperature annealing.Our results demonstrate that the DLS-based strategy provides a convenient and robust tool to study the dynamic process of forming hieratical DNA structures,which will benefit understanding the mechanism of self-assembly of DNA nanostructures.

Spectroscopic and dynamic light scattering studies of the interaction between pterodontic acid and bovine serum albumin

Pterodontic acid(PA)has been isolated from Laggera pterodonta,a Chinese herbal medicine,and shown to possess antibacterial activity in vitro.To facilitate its preclinical development,the interaction between PA and bovine serum albumin(BSA)was studied using a fluorescence quenching technique,ultraviolet–visible spectrophotometry and dynamic light scattering(DLS).At temperatures of 297 K and 310 K and an excitation wavelength of 282 nm,the fluorescence intensity of BSA decreased significantly with increasing concentration of PA attributed to the formation of a PA–BSA complex.The apparent binding constant,number of binding sites and corresponding thermodynamic parameters were calculated and the main intermolecular attraction shown to result from hydrogen bonding and van der Waals forces.Synchronous fluorescence spectrometry revealed that the binding site in the complex approached the microenvironment of Trp and three-dimensional fluorescence spectroscopy showed the binding induced conformational changes in BSA.Using DLS,increasing PA concentration was shown to cause a gradual increase in hydrodynamic diameter and significant aggregation of the complex.

Dissolution and enzymatic hydrolysis of casein micelles studied by dynamic light scattering

The effects of temperature,ionic strength,and enzymatic hydrolysis on the average hydrodynamic radius(Rh)of casein micelles in phosphate buffer were studied by using dynamic light scattering.The results showed that the average Rh value of casein micelles decreased irreversibly during the heating,decreased with the increase of ionic strength in lower ionic strength solution(less than 0.05 mol/L),but opposite in higher ionic strength solution(above 0.1 mol/L).The Rh value of casein increased rapidly during the process of enzymatic hydrolysis,and the structural model of casein micelles in the enzymatic hydrolysis process was also proposed,i.e.the casein micelle changed from compact sphere into unfolded and regularly flocky peptides.

Spectroscopic Evaluation of Effects of Heat Treatments on the Structures and Emulsifying Properties of Caseins

The effects of heat treatment(heating temperature and pH) on the structures and emulsifying properties of caseins were systematically studied by spectroscopy.Heat treatment from 60to 100℃resulted in an increase in their fluorescence intensity,hydrodynamic diameter,turbidity and emulsifying activity index,but decreased the size polydispersity of caseins.In the pH range of 5.5to 7.0,the fluorescence intensity,hydrodynamic diameter,turbidity and emulsifying properties decreased with increased heating pH,but the size polydispersity of caseins increased with increased pH.The relationship between the surface fluorescence intensity and emulsifying activity was also investigated,revealing a correlation coefficient of 0.90.These results suggested that heat treatment could be used to modify the structures and emulsifying properties of caseins by appropriately selecting heating conditions.

THE OBSERVATION OF INTERNAL MOTION OF LINEAR POLYSTYRENE CHAINS IN CYCLOHEXANE AROUND 0 TEMPERATURE

A high molecular weight (M_w=1.85×10~7) polystyrene (PS) with narrow distribution was prepared by high vacuum anionic polymerization in tetrahydrofuran.By use of dynamic light scattering,the dynamics of PS chains in cyclohexane was studied around theθtemperature.For the first time,we have observed the internal motion of polymer chains in solutions below theθtemperature by using dynamic light scattering at smaller angles (even qR_g<1).

Whether the Microemulsion is a Nano-pesticide: Exploration from the Perspective of Particle Size and Morphology

[Objectives] The paper was to explore whether the microemulsion is a nano-pesticide. [Methods] Several microemulsions commonly available on the market were studied from the perspective of particle size and morphological characteristics. With ZIF nano-pesticide prepared earlier as the control, the changes in particle size of microemulsions diluted at different concentrations and the microscopic morphology of dispersed particles were tested and compared by dynamic light scattering laser particle size analyzer combined with scanning electron microscope. [Results] Conventional microemulsions were in dynamic equilibrium, and the particle size changed irregularly after dilution at different concentrations. Especially under scanning electron microscope, the particle distribution of pesticide-bearing droplets were uneven after drying, with aggregation and precipitation of large particles, while the particle size of nano-pesticide changed little after dilution at different concentrations, ranging from 1 to 300 nm. Moreover, the microscopic morphology of nano-pesticide observed under scanning electron microscope was in monodisperse nano state, without aggregation. [Conclusions] The particle size measured by dynamic light scattering alone can not judge whether the microemulsion is a nanometer pesticide, and it is necessary to observe the microscopic disperse state and particle size distribution with the help of electron microscopy.

Study of asphaltene reaggregation in toluene/heptane mixture by dynamic and static light scattering

This paper presents the study of the effect of multiple ultrasonic impacts on submicron asphaltene aggregates in a toluene/heptane solution,conducted with dynamic light scattering technique.The objects of the study were four samples of asphaltenes obtained from four different oils.For all samples,the change in the average size of the asphaltene submicron aggregates with time was measured after the addition of a precipitant(heptane)to a solution of asphaltenes in toluene at an amount above the threshold concentration.Asphaltene aggregates formed in solution after the addition of the precipitant and were subjected to ultrasonic treatment,which led to the destruction of the asphaltene aggregates.Aggregation of destroyed asphaltenes was observed.The kinetics of this aggregation were similar to the kinetics of aggregation of asphaltenes after the addition of a precipitant.Multiple iterations of asphaltene aggregate destruction in the sample led to a significant change in the kinetics of aggregation:the growth of aggregates slowed and stabilized at a size of approximately 200 nm and 30 nm for the different studied samples.

Specific ion effect of H^(+) on variably charged soil colloid aggregation

Specific ion effects(Hofmeister effects)have recently attracted the attention of soil scientists,and it has been found that ionic non-classic polarization plays an important role in the specific ion effect in soil.However,this explanation cannot be applied to H+.The aim of this work was to characterize the specific ion effect of H+on variably charged soil(yellow soil)colloid aggregation.The total average aggregation(TAA)rate,critical coagulation concentration(CCC),activation energy,and zeta potential were used to characterize and compare the specific ion effects of H+,K+,and Na+.Results showed that strong specific ion effects of H+,K+,and Na+existed in variably charged soil colloid aggregation.The TAA rate,CCC,and activation energy were sensitive to H+,and the addition of a small amount of H+changed the TAA rate,CCC,and activation energy markedly.The zeta potential results indicated that the specific ion effects of H+,K+,and Na+on soil colloid aggregation were caused by the specific ion effects of H+,K+,and Na+on the soil electric field strength.In addition,the origin of the specific ion effect for H+was its chemical adsorption onto surfaces,while those for alkali cations were non-classic polarization.This study indicated that H+,which occurs naturally in variably charged soils,will dominate variably charged soil colloid aggregation.

Molecular diffusion in ternary poly(vinyl alcohol)solutions

The diffusion kinetics of a molecular probe-rhodamine B-in ternary aqueous solutions containing poly(vinyl alcohol),glycerol,and surfactants was investigated using fluorescence correlation spectroscopy and dynamic light scattering.We show that the diffusion characteristics of rhodamine B in such complex systems is determined by a synergistic effect of molecular crowding and intermolecular interactions between chemical species.The presence of glycerol has no noticeable impact on rhodamine B diffusion at low concentration,but significantly slows down the diffiision of rhodamine B above 3.9%(w/v)due to a dominating steric inhibition effect.Furthermore,introducing surfactants(cationic/nonionic/anionic)to the system results in a decreased diffusion coefficient of the molecular probe.In solutions containing nonionic surfactant,this can be explained by an increased crowding effect.For ternary poly(vinyl alcohol)solutions containing cationic or anionic surfactant,surfactant-polymer and surfactant-rhodamine B interactions alongside the crowding effect of the molecules slow down the overall diffiisivity of rhodamine B.The results advance our insight of molecular migration in a broad range of industrial complex formulations that incorporate multiple compounds,and highlight the importance of selecting the appropriate additives and surfactants in formulated products.

Water Soluble Polyphenylenepyridyl Dendrimers.Interpolyele ctrolyte Complexes Formed by DNA and Dendrimers

1 Results Recently[1] we synthesized rigid polypyridylphenylene dendrimers (PPD) of different generations. The rigidity endows the dendrimers with shape persistence and well ordered 3D structure that allows one to control the arrangement of functional (pyridine) groups in the molecule. The arrangement can be freely varied from practically uniform distribution through the molecule to a pronounced localization either on the periphery or in the interior of the dendrimer. The desirable distribution can be r...