Digital colloid-enhanced Raman spectroscopy by single-molecule counting.

Quantitative detection of various molecules at very low concentrations in complex mixtures has been the main objective in many fields of science and engineering, from the detection of cancer-causing mutagens and early disease markers to environmental pollutants and bioterror agents1-5. Moreover, technologies that can detect these analytes without external labels or modifications are extremely valuable and often preferred6. In this regard, surface-enhanced Raman spectroscopy can detect molecular species in complex mixtures on the basis only of their intrinsic and unique vibrational signatures7. However, the development of surface-enhanced Raman spectroscopy for this purpose has been challenging so far because of uncontrollable signal heterogeneity and poor reproducibility at low analyte concentrations8. Here, as a proof of concept, we show that, using digital (nano)colloid-enhanced Raman spectroscopy, reproducible quantification of a broad range of target molecules at very low concentrations can be routinely achieved with single-molecule counting, limited only by the Poisson noise of the measurement process. As metallic colloidal nanoparticles that enhance these vibrational signatures, including hydroxylamine-reduced-silver colloids, can be fabricated at large scale under routine conditions, we anticipate that digital (nano)colloid-enhanced Raman spectroscopy will become the technology of choice for the reliable and ultrasensitive detection of various analytes, including those of great importance for human health.

Hydroxyl-rich ferrofluid for efficient liquid phase microextraction of cinnamic acid derivatives in traditional Chinese medicine.

In this study, a hydroxyl-rich ferrofluid was prepared by dispersing silica-coated magnetic nanoparticles into a methyltrioctylammonium chloride-glycerol deep eutectic solvent and then employed in the preconcentration of trace-level of cinnamic acid derivatives (caffeic acid, p-hydroxycinnamic acid, ferulic acid, and cinnamic acid) in traditional Chinese medicine prior to high-performance liquid chromatography analysis. The structures of the synthesized materials were characterized by X-ray diffraction and infrared spectroscopy. The experimental parameters affecting the extraction performance, such as deep eutectic solvent composition, dosage of ferrofluid, pH of aqueous sample solution, salt concentration, extraction time, type, and volume of desorption solvent, were studied and optimized. Under the optimum conditions, the enrichment factors of four cinnamic acid derivatives were in the range of 107-114. Low detection limits (0.2-0.9 ng/mL), good precisions (relative standard deviations 1.2%-9.5%), and satisfactory recoveries (96.0%-104.7%) were achieved. Subsequently, the possible microextraction mechanism of the proposed method was explored and elucidated. It showed that the prepared ferrofluid is easily dispersed in the aqueous sample and achieved recovery after the extraction. The developed approach is a simple, convenient, and efficient method for preconcentration and determination of cinnamic acid derivatives in complex matrices.

Xanthan gum and pectin as beverage stabilizers reduce the digestive enzyme hydrolysis of antioxidant and antihypertensive peptides obtained from a brewery byproduct.

An acidic beverage was formulated with xanthan gum (XG), pectin (P) and brewer spent grain (BSG) peptides with antioxidant and antihypertensive properties. The impact of hydrocolloids levels on peptide bioaccessibility was studied. Peptides were obtained from BSG using Purazyme and Flavourzyme enzymes. BSG peptides were fractionated by ultrafiltration (UF) and four fractions were obtained: F1 (>10 kDa), F2 (10-5 kDa), F3 (1-5 kDa), and F4 (<1 kDa). F3 showed the highest protein purity, ferulic acid content, proportion of amphipathic peptides, and bioactive properties (ABTS+ radical scavenging and ACE-I inhibitory activity). The identified peptides from F3 by tandem mass spectrometry were 138. In silico analysis showed that 26 identified peptides had ABTS+ inhibitory activity, while 59 ones presented good antihypertensive properties. The effect of XG and P levels on bioaccessibility of F3 peptides in the formulated beverages was studied by a central composite experimental design. It was observed that F3 peptides interacted with hydrocolloids by electrostatic forces at pH of formulated beverages. The addition of hydrocolloids to formulation modulated the release of the antioxidant peptides and protected the degradation of ACE-I inhibitory peptides from F3 during simulated gastrointestinal digestion. Finally, the level of hydrocolloids that produced intermediate viscosities in the formulated beverages improved the bioaccessibility of the F3 peptides.

Spectral characteristic of the waters with different sizes of particles: impact of water quality and land-use type.

Natural colloids (NCs) are heterogeneous mixtures of particles in the aquatic environments that are strongly influenced by land use and water quality between terrestrial and aquatic environments. However, the relevant study paid little attention to the difference among the waters with different sizes of particles (e.g., suspended particulate matter (SPM), NCs, and the truly soluble substances). In this study, the spectral properties of these different waters were investigated from different land-use types in the Yuan River basin, China. Results of the UV-visible absorption spectral showed that with the particle size increased, the aromaticity, chromophoric dissolved organic matter, and humification degree of organic matter increased, while the condensation degree decreased. Data analysis from the fluorescence indices indicated that the source and the autochthonous feature of the truly soluble substances differed from that of NCs and SPM, whereas the protein-like component was mainly combined with the relatively larger size of particles (i.e., SPM and NCs), especially the downstream. Although the spectral characteristics of the water samples were strongly influenced by the water quality (> 45%), the land-use type might be the real potential impactor. Furthermore, the influence of land-use type on the spectral properties differed between the large and small scale of the buffer strips and between the mainstream and the tributaries. And this effect was more significant on the fluorescence properties in the mainstream and the spectral properties for NCs than for SPM. The study helps to understand the biogeochemical effects of the waters with different particle sizes.

Effect of hazelnut type, hydrocolloid concentrations and ultrasound applications on physicochemical and sensory characteristics of hazelnut-based milks.

Effect of hazelnut type, hydrocolloid concentrations and ultrasound applications on physicochemical and sensory characteristics of hazelnut-based milks was studied. Hazelnut- based milks were prepared in three different formulas (F1, F2 and F3) by using raw kernels (Group G1) and roasted hazelnut (Group G2) kernels and homogenized after heat treatment by applying ultrasound (US) (20 KHz, 100 W) with two different durations (5 and 10 min). Physicochemical and structural properties of the samples were extremely affected by heat treatments and US applications. Homogenization process after heat treatment improved protein solubility, zeta potential values for the samples belonged both groups. Homogenized hazelnut-based milk samples showed a significant reduction of particle size. Hazelnut type significantly affected the sensory characteristics of the hazelnut-based milks. Using of gellan gum (GG) and Carboxy methyl cellulose (CMC) together in hazelnut- based milk formulas decreased the stability of the samples.

Mobilization of colloids during sediment resuspension and its effect on the release of heavy metals and dissolved organic matter.

Natural colloids are important in mobilizing pollutants in aquatic environments. This study investigated the mobilization and aggregation of natural colloids during the sediment resuspension and re-sedimentation processes using nanoparticle tracking analysis. The metals and organic matter in overlying water were divided and examined in dissolved (<0.45 µm), colloidal (3 kDa - 0.45 µm), and truly dissolved (<3 kDa) forms. Excitation emission matrix-parallel factor analysis (EEM-PARAFAC) was used to characterize the dissolved organic matter (DOM). In overlying water, most natural colloids were < 200 nm before resuspension. An evident mobilization of colloids and an increase in colloid size were observed during resuspension. The formation of particles (>0.45 µm) and decreases of small colloids (<200 nm) indicated that resuspension promoted the aggregation of colloids. Mobilization of colloids was accompanied by increases in concentrations of Fe, Al, and organic carbon in colloidal fractions, which could be related to the formation of mineral-organic complexes under an oxic environment. The release of DOM from sediments mainly contributed to the truly dissolved humic-like fraction, and colloidal organic carbon accounted for, on average, 20 % of the total dissolved organic carbon (DOC). Fe and Al had the highest colloidal proportions as they are major compositions of inorganic colloids. Substantial removal of dissolved Al, Fe, Pb, and Zn occurred when colloids aggregated in the overlying water. Although the adsorption of suspended particles may also decrease the concentrations of dissolved metals, the increased proportions of colloidal metals indicated a possible role of colloids in this process. These findings provide insight into the behavior of colloids during the resuspension process and indicate that the aggregation of colloids could promote the removal of dissolved matter.

Nano-scale analysis of uranium release behavior from river sediment in the Ili basin.

Due to the limitations of the conventional water sample pretreatment methods, some of the colloidal uranium (U) has long been misidentified as "dissolved" phase. In this work, the U species in river water in the Ili Basin was classified into submicron-colloidal (0.1-1 µm), nano-colloidal (0.1 µm-3 kDa) and dissolved phases (< 3 kDa) by using high-speed centrifugation and ultrafiltration. The U concentration in the river water was 5.39-8.75 µg/L, which was dominated by nano-colloidal phase (55-70%). The nano-colloidal particles were mainly composed of particulate organic matter (POM) and had a very high adsorption capacity for U (accounting for 70 ± 23% of colloidal U). Sediment disturbance, low temperature, and high inorganic carbon greatly improved the release of nano-colloidal U, but high levels of Ca2+ inhibited it. The simulated river experiments indicated that the flow regime determined the release of nano-colloidal U, and large amounts of nano-colloidal U might be released during spring floods in the Ili basin. Moreover, global warming increases river flow and inorganic carbon content, which may greatly promote the release and migration of nano-colloidal U.

Plutonium reactive transport in fractured granite: Multi-species experiments and simulations.

Plutonium (Pu) in the subsurface environment can transport in different oxidation states as an aqueous solute or as colloidal particles. The transport behavior of Pu is affected by the relative abundances of these species and can be difficult to predict when they simultaneously exist. This study investigates the concurrent transport of Pu intrinsic colloids, Pu(IV)(aq) and Pu(V-VI)(aq) through a combination of controlled experiments and semi-analytical dual-porosity transport modeling. Pu transport experiments were conducted in a fractured granite at high and low flow rates to elucidate sorption processes and their scaling behavior. In the experiments, Pu(IV)(aq) was the least mobile of the Pu species, Pu(V-VI)(aq) had intermediate mobility, and the colloidal Pu, which consisted mainly of precipitated and/or hydrolyzed Pu(IV), was the most mobile. The semi-analytical modeling revealed that the sorption of each Pu species was rate-limited, as the sorption could not be described by assuming local equilibrium in the experiments. The model was able to describe the sorption of the different Pu species that occurring either on fracture surfaces, in the pores of the rock matrix, or simultaneously in both locations. While equally good fits to the data could be achieved using any of these assumptions, a fracture-dominated process was considered to be the most plausible because it provided the most reasonable estimates of sorption rate constants. Importantly, a key result of this work is that the sorption rate constant of all Pu species tends to decrease with increasing time scales, which implies that Pu will tend to be more mobile at longer time scales than observations at shorter time scales suggest. This result has important implications for predicting the environmental impacts of Pu in the safety assessments of geologic repositories for radioactive waste disposal, and we explore potential mechanistic bases for upscaling the sorption rate constants to time and distance scales that cannot be practically evaluated in experiments.

Aggregation of microplastics and clay particles in the nearshore environment: Characteristics, influencing factors, and implications.

Since nearly half of the world's population lives near the coast, coastal areas have become hotspots for microplastic (MP) pollution due to human activity. The ubiquity of natural colloids in coastal waters plays a critical role in the potential fate of, and risks posed by, MPs. Nevertheless, far less has been known regarding the aggregation of MPs with inorganic natural clay colloids, especially in the complicated nearshore environment. In this study, the aggregation behavior of MPs as well as the interaction between MPs and clay particles were investigated under different nearshore environmental conditions (MP-to-clay ratio, salinity gradient, humic acid concentration, and wave energy). The aggregation behavior was subjected by the repulsive energy barrier between particles and external energy transferred to the system. The low energy associated with mild wave conditions was favorable for the occurrence of aggregation, whereas sustained high energy under intense wave conditions was found to be detrimental to the aggregation behavior, and the aggregates were prone to fragmentation even if particles coalesced into large clusters. The analysis for the environmental fate of MPs demonstrated that the shoreline was likely to be the sink for most MPs ultimately.

Application of temporal moment analysis to interpret colloid and colloid-facilitated solute transport under varying size exclusion and attachment coefficient.

Colloidal particles can attach the contaminants like heavy metals and radionuclides and act as contaminant carriers to provide a faster movement of pollutants through the interconnecting pores of the porous medium. The electrostatic repulsive force between the negatively charged colloids and the solid surface restricts the transport of the mobile colloids to the larger pores of the porous medium and initiates the size exclusion mechanism. The temporal moment analysis is treated as an effective tool to interpret the solute breakthrough curves for analyzing the statistical behavior of the contaminants. In past literature, the temporal moments have not been incorporated with the breakthrough curves of colloids and colloid-facilitated contaminants for statistical interpretation. In this research study, the temporal variations of concentrations of mobile colloids, solute attached to the mobile colloids, and the dissolved solute are obtained numerically in a fully saturated one-dimensional column considering a continuous source for varying size exclusion and colloid attachment coefficient. Utilizing the simulated spatially varying breakthrough curves, the temporal moments are estimated to calculate the mass recovery, average residence time, and the spreading of mobile colloids and dissolved solutes. The temporal moment analysis suggests that the velocity enhancement for higher size exclusion reduces the average residence time of the mobile colloids and the solute adsorbed to the mobile colloids significantly. The mass recovery of mobile colloids and the solute attached to the mobile colloids increases at a specific depth for higher size exclusion. The estimated second central moment attributes that the solute spreading follows the nonlinear trend for low size exclusion. The peaks of the relative concentration of mobile colloids and solute attached to mobile colloids drastically decrease with an increase in attachment coefficient. The peak of the relative concentration of dissolved contaminant enhances with attachment coefficient. The high second temporal moment of the dissolved contaminant at a higher attachment coefficient indicates the slow interaction of dissolved solute and porous medium and that enables a greater spreading of solute through the interconnecting porous medium. The study suggests that the faster movement of mobile colloids and the solute attached to the mobile colloids at higher exclusion imparts a potential risk of groundwater contamination and thorough statistical interpretation is needful to analyze the behavior of colloids and colloid-facilitated contaminants. The research work does not consider the transient flow field and the effect of the presence of air phase in the partially saturated soil column in the groundwater system.

A novel source of food hydrocolloids from Trigonella elliptica seeds: extraction of mucilage and comprehensive characterization.

BACKGROUND: In this study, the effects of seed weight (4, 8, and 12 g), extraction temperature (30, 60, and 90 °C), and pH (4, 7, and 10) on the yield of mucilage extraction from fenugreek seeds and its chemical properties were investigated using response-surface methodology. RESULTS: The optimum condition for mucilage extraction was a seed weight of 8.30 g, a temperature of 86.10 °C, and pH 6.90. The results showed that the dry weight of extracted mucilage increased with increase and decrease of extraction temperature and pH respectively at high seed weight. Increasing temperature and pH increased the extraction yield, and the effect was more considerable at low seed weight. The maximum carbohydrate content of mucilage was achieved at average levels of variables. The protein, flavonoid, and total phenolic contents of extracted mucilage increased with increasing temperature. Both flavonoid and total phenolic contents were maximum at neutral pH, but they were maximum at moderate and low levels of seed weight respectively. Maximum antioxidant activity was obtained at the highest extraction temperature, seed weight of 8 g, and neutral pH. The study of rheological properties indicated that extracted mucilage solution showed mainly elastic and shear-thinning behavior. CONCLUSION: The Fourier transform infrared spectra of extracted mucilage exhibited the existence of polysaccharides and protein chains in fenugreek seeds mucilage. The X-ray diffraction corroborated the presence of crystals in the mucilage structure. The proton nuclear magnetic resonance spectra confirmed the polysaccharides and protein composition of extracted mucilage. The maximum mucilage mass loss was observed at 190-350 °C using thermogravimetric analysis. © 2022 Society of Chemical Industry.

Key factors controlling colloids-bulk soil distribution of polybrominated diphenyl ethers (PBDEs) at an e-waste recycling site: Implications for PBDE mobility in subsurface environment.

Accumulation of polybrominated diphenyl ethers (PBDEs) in surface soils at elevated concentrations is common at e-waste recycling sites. Even though highly insoluble, migration of PBDEs into the vadose zone and groundwater is possible, due to their association with soil colloids. Here, we show that upon equilibration with artificial rainwater surface and subsurface soil samples collected at an e-waste recycling site release significant quantities of colloids, with the total concentrations of 14 PBDE congeners as high as 990 ng/g dw. The concentrations of different congeners vary markedly in the colloids, and that of BDE-209 is the highest in all the samples. Notably, even the colloids released from the soil collected at a depth of 95-105 cm contain high concentrations of PBDEs. Preferential binding of PBDEs to soil colloids is observed, with the colloids-soil distribution coefficients above 10 in certain cases. The extent of preferential binding displays no apparent correlation with the relative hydrophobicity of the PBDEs, nor can it be explained simply by considering the higher specific surface area, pore volume, and clay content of the soil colloids than the respective bulk soil. Principal component analysis shows that multiple soil properties are collectively responsible for the preferential distribution of PBDEs. Specifically, the differences in pore volume, soil organic carbon content, and pore size between colloids and soils are likely the major factors affecting the distribution of high-concentration PBDEs, whereas the differences in clay content, pore volume and specific surface area are the key factors affecting the distribution of low-concentration PBDEs. The findings clearly show that colloids are an important medium with which PBDEs are associated at contaminated sites, and underline the need of understanding colloid-facilitated transport of PBDEs at e-waste sites.

Accountancy for intrinsic colloids on thorium solubility: The fractionation of soluble species and the characterization of solubility limiting phase.

The extensive hydrolysis of tetravalent actinides leads to polynuclear formations through oxygen bridging facilitating the formation of colloids as end products. The pH, ionic strength has phenomenal effects on Thorium colloids formation. The quantitative estimation of colloids facilitates the fraction of soluble fraction into ionic, polymeric and colloidal forms of thorium. The colloids accountability and precipitate characterization explains the discrepancies in estimated solubility limits. The supernatants of long equilibrated (∼3 years) saturated thorium solution under various pH (5- 11) and ionic strengths (0-3 M NaClO4) were analysed by Inductively Coupled Plasma Mass Spectrometer (ICP-MS) and Ion Chromatography (IC) to determine total and ionic thorium respectively. Laser Induced Breakdown Detection (LIBD) was employed to determine the colloid size and concentrations. The precipitates were characterized by calorimetry and XRD to determine the solubility limiting phase. The results of pH, IC, ICP-MS, and LIBD measurements on the aged thorium samples are discussed with regard to the mechanism of the formation of thorium colloids. The results revealed the formation of colloids having particle size (10-40 nm) at concentrations (109-1011 particles/mL). The colloids accountancy resulted in estimated solubility products to 2-4 orders lower than their inclusion as soluble thorium. The soluble thorium was fractionated quantitatively into ionic, polymeric and colloidal forms of thorium. The precipitates formed are found to be semi amorphous.

Large colloidal probes for atomic force microscopy: Fabrication and calibration issues.

Atomic force microscopy (AFM) is a powerful tool to investigate interaction forces at the micro and nanoscale. Cantilever stiffness, dimensions and geometry of the tip can be chosen according to the requirements of the specific application, in terms of spatial resolution and force sensitivity. Colloidal probes (CPs), obtained by attaching a spherical particle to a tipless (TL) cantilever, offer several advantages for accurate force measurements: tunable and well-characterisable radius; higher averaging capabilities (at the expense of spatial resolution) and sensitivity to weak interactions; a well-defined interaction geometry (sphere on flat), which allows accurate and reliable data fitting by means of analytical models. The dynamics of standard AFM probes has been widely investigated, and protocols have been developed for the calibration of the cantilever spring constant. Nevertheless, the dynamics of CPs, and in particular of large CPs, with radius well above 10 µm and mass comparable, or larger, than the cantilever mass, is at present still poorly characterized. Here we describe the fabrication and calibration of (large) CPs. We describe and discuss the peculiar dynamical behaviour of CPs, and present an alternative protocol for the accurate calibration of the spring constant.

Keratin 17-positive Civatte bodies in oral lichen planus-distribution variety, diagnostic significance and histopathogenesis.

Although emergence of keratin 17 (K17) and reciprocal loss of K13 are immunohistochemical hallmarks for oral mucosal malignancy, we report here findings of K17-positive (+) speckles, possibly equivalent to Civatte bodies, in benign oral lichen planus. Sixty-two biopsy samples from oral lichen planus cases were subjected to immunohistochemical examinations to analyze the distribution as well as histopathogenesis of Civatte bodies. K17 was irregularly positive among oral lichen planus-affected epithelial cells, and K17-positive (+) filamentous structures were irregularly distributed within the cytoplasm in confocal images. K17+ speckles were identified as Civatte bodies, and they were mainly distributed in the interface between epithelial cells and lymphocytic infiltrates (type A, 52.8%), followed by distribution within the epithelial layer (type B, 24.7%) or within the lamina propria with lymphocytic infiltration (type C, 22.5%). Apoptotic figures were often engulfed by macrophages and clearly distinguished from Civatte bodies by the presence TUNEL signals. These results indicate that K17 is a sensitive immunohistochemical marker for Civatte bodies and useful for differential diagnosis of oral lichen planus from other oral mucosal lesions. Civatte bodies are generated from denucleation of K17+ epithelial cells during the process of cell death via dyskeratosis, which is possibly related to blood capillary collapse.

Cross-linked polydimethylsiloxane colloid as novel contrast agent for gastrointestinal magnetic resonance imaging: Transient nuclear Overhauser effect within the interface.

With good contrast in T1 and T2 weighted imaging as well as low toxicity in 3- (4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) assay, this work proposes the cross-linked polydimethylsiloxane colloids as a novel non-ionic contrast agent for gastrointestinal magnetic resonance imaging. The experiments of nuclear magnetic resonance spectra and relaxation show that within the interface of the colloids, there are nuclear Overhauser effect and transient nuclear Overhauser effect (cross-relaxation). Regarding the longitudinal relaxation experiments of CH2CH2O segments of Tween 80, a two spins system is found and modeled well by the equation IZ-I0= S0((1-X) e-tD1 -(1+X) e-tT1) which is deduced based on the transient nuclear Overhauser effect proposed by Solomon. The arbitrary constant X is additionally added with the initial conditions (Iz - I0)t=0 = -2XS0 and (Sz - S0)t=0 = -2S0. For the two spins system, D1 and T1 are corresponding to longitudinal relaxation times of the bound water and the CH2CH2O respectively. Concerning the transverse relaxation experiments of the CH2CH2O, they agree with the equation with three exponential decays, defined by three relaxation times, likely corresponding to three mechanisms. These mechanisms possibly are intramolecular and intermolecular dipole-dipole (DD) interactions and scalar coupling. Within the interface, hydrogen bonding causes the positive nuclear Overhauser effect of the CH2CH2O's nuclear magnetic resonance spectra, the transient nuclear Overhauser effect of the CH2CH2O's longitudinal relaxation experiments and the intermolecular dipole-dipole interactions of the CH2CH2O's transverse relaxation experiments.

Geochemical behaviour and risk assessment of trace elements in a tropical river, Northwest Borneo.

By convention, dissolved trace elements in the river water are considered to be the fraction that passes through a 0.45 µm filter. However, several researchers have considered filtration cut-off other than 0.45 µm for the separation of dissolved trace elements from particulate fraction. Recent research indicated that trace elements could exist in particulate form as colloids and natural nanoparticles. Moreover, the trace elements in the continental dust (aerosols) constitute a significant component in their geochemical cycling. Due to their high mobility, the trace elements in the micron and sub-micron scale have biogeochemical significance in the coastal zone. In this context, this study focuses on the highly mobile fraction of trace elements in particulates (<11 µm) and dissolved form in the Lower Baram River. A factor model utilizing trace elements in the dissolved and mobile phase in the particulates (<11 µm) along with water column characteristics and the partition coefficient (Kd) of the trace elements indicated a more significant role for manganese oxyhydroxides in trace element transport. Perhaps, iron oxyhydroxides play a secondary role. The factor model further illustrated the dissolution of aluminium and authigenic clay formation. Except for Fe and Al, the contamination risk of mobile trace elements in particulates (<11 µm) together with dissolved form are within the permissible limits of the Malaysian water quality standards during monsoon (MON) and postmonsoon (POM) seasons.

Viscosity drives texture perception of protein beverages more than hydrocolloid type.

Hydrocolloids are added to alter rheological properties of beverages but have other properties that can contribute to overall taste and texture perception. In this study, tapioca starch and λ-carrageenan were used to determine how hydrocolloid type, viscosity level (4-6 mPa·s, 25-30 mPa·s, and 50-60 mPa·s at 50 s-1 ), and complexity of the system (aqueous, skim milk, or whole milk) influence sensory taste and texture of fluids. All fluids were shear thinning; however, skim milk and whole milk solutions that contained carrageenan had much higher low shear viscosity and lower high shear viscosity than those with starch. There was a significant effect of viscosity level on sensory perception of consistency, creamy/oily, mouthcoating, and residual mouthcoating in aqueous, skim milk, and whole milk beverages, and a weak effect of hydrocolloid type. However, normalizing creamy/oily, paste, and mouthcoating against sensory consistency removed the effect of hydrocolloid type. Flavors (cream, cooked, cardboard, and melon/cardboard) were associated with the type of hydrocolloid and milk protein ingredient. Temporal dominance of sensations showed that samples exhibit similar temporal sensory profiles, although the addition of hydrocolloids enhanced dominance of creaminess even in samples without fat. Hydrocolloid type did not significantly influence mouthcoating or the persistence of astringency. Additionally, increasing viscosity from 3 to 74 mPa·s at 50 s-1 did not suppress perceived sweet or salty taste. The results suggest that in fluid systems with viscosity levels typically found in beverages, textural properties are determined by viscosity and independent of the type of hydrocolloid.

Comparative safety analysis of bactericidal nano-colloids: Assessment of potential functional toxicity and radical scavenging action.

Extensive utilization of silver nanoparticles (AgNP) has raised concerns of their safety profile upon interaction with biological system. In past decade, various nanoparticles (NPs) with excellent antimicrobial potential have been synthesized, a majority of which have struggled with the established toxicity in biological systems. The NPs safety is still a hot debate and various strategies are being adopted to overcome this giant limitation. This paper successfully reports comparative toxicity profiles of previously synthesized antimicrobial NPs in our lab and concludes the effectiveness of biologically synthesized NPs for its safe usage in biological systems. In this study, five of our previously synthesized NPs that showed excellent antimicrobial potential were compared for their in vivo toxicity and corresponding radical scavenging activities. Based on lowest morbidity, mortality, weight loss, toxicity and agglomeration profile, best NPs with highest antimicrobial potentials were screened out and used for further biomedical applications. The previously reported NPs used in this study included Aerva javanica synthesized nanoparticles (AjNPs), Heliotropium crispium synthesized nanoparticles (HcNPs), and violacein capped nanoparticles (VNPs), these showed least toxicity upon in vivo histological analysis. AjNPs among them showed maximum safety and efficacy profile and consistently showed least production of reactive oxygen species, least mortality and morbidity rate as compared to other groups. Present study establishes that all these biologically synthesized NPs and specifically AjNPs can be efficiently employed as antimicrobial agents as they have not exhibited toxic profile and have shown least accumulation into the organs such as liver spleen and kidney.

A systematic evaluation of Flow Field Flow Fractionation and single-particle ICP-MS to obtain the size distribution of organo-mineral iron oxyhydroxide colloids.

Colloidal iron(III) oxyhydroxides (FeOx) are important reactive adsorbents in nature. This study was set up to determine the size of environmentally relevant FeOx colloids with new methods, i.e. Flow Field Flow Fractionation (FlFFF-UV-ICP-MS) and single-particle ICP-MS/MS (sp-ICP-MS) and to compare these with standard approaches, i.e. dynamic light scattering (DLS), nanoparticle tracking analysis (NTA), microscopy (TEM), membrane filtration, centrifugation and dialysis. Seven synthetic nano- and submicron FeOx with different mineralogy and coating were prepared and two soil solutions were included. The FlFFF was optimized for Fe recovery, yielding 70-90%. The FlFFF determines particle size with high resolution in a 1 mM NH4HCO3 (pH 8.3) background and can detect Fe-NOM complexes <5 nm and organo-mineral FeOx particles ranging 5-300 nm. The sp-ICP-MS method had a size detection limit for FeOx of about 32-47 nm. The distribution of hydrodynamic diameters of goethite particles detected with FlFFF, NTA and DLS were similar but the values were twice as large as the Fe cores of particles detected with sp-ICP-MS and TEM. Conventional fractionation by centrifugation and dialysis generally yielded similar fractions as FlFFF but membrane filtration overestimated the large size fractions. Particles formed from Fe(II) oxidation in the presence of NOM showed strikingly smaller organo-mineral Fe-Ox colloids as the NOM/Fe ratio increased. The soil solution obtained with centrifugation of an acid peat was dominated by small (<30 nm) Fe-OM complexes and organo-mineral FeOx colloids whereas that of a mineral pH neutral soil mainly contains larger (30-200 nm) Fe-rich particles. The FlFFF-UV-ICP-MS is recommended for environmental studies of colloidal FeOx since it has a wide size detection range, it fractionates in an environmentally relevant background (1 mM NH4HCO3) and it has acceptable element recoveries.