Number Of Microparticles Research Articles

A simple platform for the electro-catalytic detection of the dimetridazole using an electrochemical sensor fabricated by electro-deposition of Ag on carbon graphite: application: orange juice, tomato juice and tap water

The objective of this paper is to evaluate and optimize the experimental parameters of the electro-deposition of silver atom nuclei on a graphite carbon paste to elaborate an electrochemical sensor. The electro-deposition process was performed using the cyclic voltammetry. The electrochemical studies show that the deposited silver micro-particle array offers an excellent electro-catalytic activity towards the NO2 attractor group of the dimetridazole side chain. SEM morphological analysis of the silver deposits indicates the presence of a large number of Ag micro-particles on the graphite carbon with good nucleation. The size of the Ag micro-particles is of the order of 19,7621 μm and their distribution is normal over the entire range of the pulp. DRX analysis of the deposit also indicates that the microcrystalline structure of the silver microcrystals in the deposit is face-centered cubic. The electrochemical behavior of dimetridazole is totally irreversible, the transfer process is controlled by diffusion phenomena on the surface of the electrode covered by a silver deposit realized μAg@CPE. The analytical performance of the constructed electrode shows a good selectivity. Calibration curves for the detection of dimetridazole have been drawn in the concentration range of 3,5 × 10−4 mol/L to 10−6 mol/L using cyclic voltammetry method, with a detection and quantification limits of 6.565 × 10−7 mol/L and 2.216 × 10−6 mol/L respectively. The applicability of the constructed electrode has been tested in real samples including orange juice, tomato juice, tap water. The results obtained show a recovery rate above 94%, which is very satisfactory.

Comparative Evaluation of CD34+/CD33+/CD3+/CD19+ Microparticles in Peripheral Blood of Patients during Allogeneic Stem Cell Transplantation

Introduction Allogeneic hematopoietic cell transplantation (allo-HCT) has been widely used as a potential curative strategy of hematological malignancies. In principle, the conditioning and the immunological response of the graft are basic mediators of the procedure. Cell-derived microparticles (MPs) are small membrane vesicles considered as markers of cell activation and apoptosis. Recently it was shown that they participate in important biological functions at pathological conditions associated mainly with endothelial injury, thrombosis and inflammation. The potential role of MPs from hematopoietic cells during HCT has not been addressed yet. In our previous work we have shown that CD34+ cells from cord blood transplants release MPs that carry microRNAs. The aim of this study was to quantify the MPs of CD34+/CD33+/CD19+/CD3+ cells in the peripheral blood of patients undergoing allo-HCT, compare them with the MPs of the graft that they have received and investigate their relationship with various parameters.Methods Samples were collected from the graft and from the peripheral blood of 7 patients who underwent allo-HCT in our department. Four patients were diagnosed with acute myeloid leukemia (AML) and 3 with acute lymphoblastic leukemia (ALL). Informed consent was obtained from all patients. Patients received mobilized blood stem cell transplant from sibling donors. All patients were at complete remission before allo-HCT. Regarding the conditioning 5 patients received myeloablative regimen and 2 reduced intensity conditioning (RIC). All patients achieved successful and prompt engraftment. The MPs were isolated after centrifugation of the plasma and immunophenotyped by four-color fluorescence using antibodies against CD34, CD33, CD19 and CD3 as well as Annexin V (AnnV+). The number of MPs has been estimated in the graft as well as in the peripheral blood of the patients at days 0, 4 and 14 (day0, +4d, +14d) from the transplantation. Statistical analysis was performed using t-test, Pearson's and Spearman's depending on the normality of the distribution of variables. Alterations in the number of MPs after day0 might be the result of the conditioning's effect and regarding the CD34+ MPs might be a correlation with the engraftment.Results Myeloid-derived MPs(CD33+MPs) were decreased significantly from day0 to +14d (p<0,019,Spearman's rho =0,836) as well at +4d to +14d (p<0,049,Spearman's rho =0,757). Interestingly, stem cell derived-MPs (CD34+MPs) were significantly associated with B-lymphocyte-derived MPs (CD19+MPs) at +4d and +14d respectively (p<0,007,Spearman's rho =0,890; p<0,001,Spearman's rho =0,944). CD3+cells correlated significantly with CD3+MPs at +14d(p<0,034, Spearman's rho=0,791). The number of all measured AnnV+/CD34+/CD33+/CD19+/CD3+ MPs at +d14 was decreased compared to the number of AnnV+/CD34+/CD33+/CD19+/CD3+ MPs at day0 and +4d.Conclusions In this study we have identified and monitored hematopoietic stem cell and MPs in the peripheral blood of patients undergoing allo-HCT. We have to mention that the number of MPs at day 0 represents the profile of the patient immediately after conditioning and before receiving the graft. The possible role of MPs in the engraftment could serve as a valuable parameter. DisclosuresNo relevant conflicts of interest to declare.

Engineering the Surface Pattern of Microparticles: From Raspberry-like to Golf Ball-like.

Control of the shape and uniformity of colloid particles is essential for realizing their functionality in various applications. Herein, we report a facile approach for the synthesis of narrowly dispersed anisotropic microparticles with well-defined raspberry-like and golf ball-like surface patterns. First, we demonstrate that hybrid raspberry-like particles can be achieved through a one-pot polymerization method using glycidyl polyhedral oligomeric silsesquioxane (GPOSS) and pentaerythritol tetra(3-mercaptopropionate) (PETMP) as monomers. Varying the polymerization parameters such as catalyst loading, monomer concentration, and the molar ratio of monomers, we are able to regulate the sizes and surface protrusion numbers of these raspberry-like microparticles. The formation mechanism is attributed to a competition balance between thiol-epoxy reaction and thiol-thiol coupling reaction. The former promotes rapid formation of large core particles between PETMP and GPOSS droplets (which can serve as core particles), while the latter allows for generation of surface protrusions by PETMP self-polymerization, leading to the formation of raspberry-like surface patterns. Based on the different POSS contents in the surface protrusions and cores of the raspberry-like microparticles, we demonstrate that they can be used as precursors to produce microporous silica (sub)microparticles with golf ball-like morphology via pyrolysis subsequently. Overall, this work provides a facile yet controllable approach to synthesize narrowly dispersed anisotropic microparticles with diverse surface patterns.

Extracellular vesicles from thalassemia patients carry iron-containing ferritin and hemichrome that promote cardiac cell proliferation.

Extracellular vesicles (EVs) are bioactive, submicron-sized membrane vesicles released from all cell types upon activation or apoptosis. EVs including microparticles (MPs) and exosomes have emerged as important mediators of cell-to-cell communication in both normal and pathological states including thalassemia (thal). However, the role of EVs derived from β-thal patients with iron overload (+ IO) and without iron overload (-IO) on cardiac cells is unclear. We hypothesized plasma EVs in thal patients containing ferritin (iron storage protein) and a denaturated hemoglobin-hemichrome that induce cardiac cell proliferation. The origins and numbers of EVs isolated from plasma of normal, thal (+ IO), and (- IO) patients were compared and determined for their iron and iron-containing proteins along with their effects on cardiac and endothelial cells. Data shows that MPs were originated from many cell sources with marked numbers of platelet origin. Only the number of RBC-derived MPs in thal (+ IO) patients was significantly high when compared to normal controls. Although MPs derived from both normal and thal patients promoted cardiac cell proliferation in a dose-dependent manner, only exosomes from thal patients promoted cardiac cell proliferation compared to the untreated. Moreover, the exosomes from thal (+ IO) potentially induce higher cardiac cell proliferation and angiogenesis in terms of tube number than thal (- IO) and normal controls. Interestingly, ferritin content in the exosomes isolated from thal (+ IO) was higher than that found in the MPs isolated from the same patient. The exosomes of thal patients with higher serum ferritin level also contained greater level of ferritin inside the exosomes. Apart from ferritin, there were trends of increasing hemichrome and iron presented in the plasma EVs and EV-treated H9C2 cells. Findings from this study support the hypothesis that EVs from β-thal patients carry iron-load proteins that leads to the induction of cardiac cell proliferation.

Long-term evolution of the three-dimensional structure of string-fluid complex plasmas in the PK-4 experiment.

Microparticle suspensions in a polarity-switched discharge plasma of the Plasmakristall-4 facility on board the International Space Station exhibit string-like order. As pointed out in [Phys. Rev. Research 2, 033314 (2020)2643-156410.1103/PhysRevResearch.2.033314], the string-order is subject to evolution on the timescale of minutes at constant gas pressure and constant parameters of polarity switching. We perform a detailed analysis of this evolution using the pair correlations and length spectrum of the string-like clusters (SLCs). Average exponential decay rate of the SLC length spectrum is used as a measure of string order. The analysis shows that the improvement of the string-like order is accompanied by the decrease of the thickness of the microparticle suspension, microparticle number density, and total amount of microparticles in the field of view. This suggests that the observed long-term evolution of the string-like order is caused by the redistribution of the microparticles, which significantly modifies the plasma conditions.

Microparticles and microplastics released from daily use of plastic feeding and water bottles and plastic injectors: potential risks to infants and children in China.

Daily use of plastic feeding and water bottles occur widely in China, and they could be sources for release of microplastics (MPs), which threaten the health of Chinese infants and children during daily usage. In this work, we investigated the use of polycarbonate (PC) and polypropylene (PP) for making water bottles (WBs) and polyphenylene sulfone resins (PPSU) for making feeding bottles (FBs), and we found that feeding bottles and water bottles released microparticles in amounts ranging from 53 to 393 particles/mL during 100 opening/closing cycles. The good linear regressions for plots of microparticles released vs. abrasion distance (r2 = 0.811) indicated that thick-necked bottles release more microparticles than thin-necked bottles. The brands and types of bottles (plastic vs. glass) influence microparticle release, and this indicates that high-quality plastic and glass bottles release fewer microparticles and are good for the health of infants and children. In addition to calcium stearate and silicone additives, the identified MPs account for 7.5 to 42.1% of released microparticles with different polymer types, sizes (from 20 to 500 μm) and shapes (cubic, spherical and irregular shapes). Additionally, an average of 1.74 MPs were released from an injection with a single-use plastic injector. Nevertheless, a number of microparticles and nanosized plastics were observed with all samples, suggesting that the health risks of micro- and nanosized particles to humans, especially babies and children, and the environment should be considered seriously.Supplementary InformationThe online version contains supplementary material available at 10.1007/s11356-021-14939-7.

The Vasculopathy of Juvenile Dermatomyositis: Endothelial Injury, Hypercoagulability, and Increased Arterial Stiffness.

Vasculopathy is considered central to the pathogenesis of juvenile dermatomyositis (DM) and is associated with severe extramuscular manifestations. We undertook this study to investigate the hypothesis that the vasculopathy of juvenile DM can be noninvasively tracked by examining biomarkers of endothelial injury, subclinical inflammation, hypercoagulability, and vascular arterial stiffness. The study population was a UK cohort of children with juvenile DM. Circulating endothelial cells (CECs) and microparticles (MPs) were identified using immunomagnetic bead extraction and flow cytometry, respectively. Plasma thrombin generation was determined using a fluorogenic assay. Cytokine and chemokine levels were measured by electrochemiluminescence. Arterial stiffness was assessed using pulse wave velocity (PWV). Results were expressed as the median and interquartile range (IQR), and statistical significance was assessed using nonparametric analyses. Ninety patients with juvenile DM and 79 healthy control subjects were included. The median age of the patients was 10.21 years (IQR 6.68-13.40), and the median disease duration was 1.63 years (IQR 0.28-4.66). CEC counts were higher in all patients with juvenile DM compared to controls (median 96 cells/ml [IQR (40-192] and 12 cells/ml [IQR 8-24], respectively; P < 0.0001). Circulating MP numbers were also significantly higher in patients with active juvenile DM compared to controls (median 204.7 × 103 /ml [IQR 87.9-412.6] and 44.3 × 103 /ml [IQR 15.0-249.1], respectively; P < 0.0001). MPs were predominantly of platelet and endothelial origin. Enhanced plasma thrombin generation was demonstrated in patients with active juvenile DM compared to those with inactive disease (P = 0.0003) and controls (P < 0.0001). Carotid-radial PWV adjusted for age was increased in patients with juvenile DM compared to controls (P = 0.003). We observed increased endothelial injury and increased levels of proinflammatory cytokines in patients with active juvenile DM. MP profiles reflected distinct disease activity status in juvenile DM and are markers of vascular pathology, platelet activation, and thrombotic propensity. Ongoing long-term vascular injury may result in increased arterial stiffness in patients with juvenile DM.

Abstract P031: Endothelial Microparticles In Pediatric Obesity

Introduction: Endothelial activation represents one of the earliest signs of the atherosclerotic process. Microparticles (MPs) in plasma, particularly endothelial MPs (EMPs) are reproducible biomarkers of endothelial dysfunction with a simple blood draw. The goal of this study was to examine the association of obesity with MPs, EMPs (CD31+/CD41– and/or CD 144+/CD31–), and activated EMPs (CD106+). Hypothesis: We hypothesized that higher body mass index (BMI), body fat percent (BF%), and visceral adipose tissue (VAT) would be associated with higher levels of MPs, EMPs, and activated EMPs. Methods: This was a cross-sectional study of 280 children and adolescents ages 8-18 years old. Whole venous blood was collected and processed for platelet free-plasma (PFP) collection less than 3 hours after being drawn. PFP samples were prepared using serial centrifugations and then frozen as 100 μl aliquots at -80 ° C. MPs were measured using flow cytometry with size ranging from 0.3 to 1.0 μm. EMPs were defined as MP with CD31+/CD41– and/or CD 144+/CD31–. Active EMP was identified as EMP with CD 106+. BF% and VAT were measured using dual X-ray absorptiometry. Linear (total MPs and EMPs) and logistic (activated EMPs) regression models were used to examine the associations with adiposity group, BF%, and VAT, adjusting for Tanner stage, sex, and race. Results: The mean age of the cohort was 12.7 years, consisting of 147 females and BMI distribution: 112 normal-weight, 77 overweight/obesity, 91 severe obesity. Youth with overweight/obesity and severe obesity had higher numbers of total MPs (28,690 per μL PFP/g [-2,315, 59,695], p=0.07 and 52,744 per μL PFP/g [22,163, 83,324], p&lt;0.001, respectively) and total EMPs (350 per μL PFP/g [81, 618], p=0.011 and 278 per μL PFP/g [13, 543], p=0.040, respectively) compared to peers with normal weight. In the entire cohort, higher BF% was associated with higher MPs (1,646 per μL PFP per percent [509, 2,783], p=0.005) and EMPs (11 per μL PFP per percent [2, 21], p=0.023), and higher VAT was associated with higher MPs (34 per μL PFP/g [11, 57], p=0.004) but not EMPs. Logistic regression analysis showed higher odds of active EMPs (odds ratio, 1.72 [1.0, 2.97], p=0.0502) in those with a BMI &gt;85 th percentile compared to youth with a BMI &lt;85 th percentile. In the entire cohort, BF% (odds ratio, 1.02 [1.00, 1.04], p=0.108) and VAT (odds ratio, 1.00 [1.00, 1.00], p=0.472) were not significantly associated with active EMPs. Conclusions: Higher levels of endothelial cell damage and activation were associated with obesity and excess adiposity in youth. The potential role of MPs and EMPs as useful biomarkers of cardiovascular disease risk merits further study.

Effect of Dexamethasone on Thermoresponsive Behavior of Poly(2-Oxazoline) Diblock Copolymers.

Thermoresponsive polymers play an important role in designing drug delivery systems for biomedical applications. In this contribution, the effect of encapsulated hydrophobic drug dexamethasone on thermoresponsive behavior of diblock copolymers was studied. A small series of diblock copoly(2-oxazoline)s was prepared by combining thermoresponsive 2-n-propyl-2-oxazoline (nPrOx) and hydrophilic 2-methyl-2-oxazoline (MeOx) in two ratios and two polymer chain lengths. The addition of dexamethasone affected the thermoresponsive behavior of one of the copolymers, nPrOx20-MeOx180, in the aqueous medium by shifting the cloud point temperature to lower values. In addition, the formation of microparticles containing dexamethasone was observed during the heating of the samples. The morphology and number of microparticles were affected by the structure and concentration of copolymer, the drug concentration, and the temperature. The crystalline nature of formed microparticles was confirmed by polarized light microscopy, confocal Raman microscopy, and wide-angle X-ray scattering. The results demonstrate the importance of studying drug/polymer interactions for the future development of thermoresponsive drug carriers.

Determination Method and Characteristics of Particle Size Multiplier of PM2.5 in Road Dust

The particle size multiplier is a valuable parameter for depicting the particle size distribution characteristics of road dust and calculating road dust emissions. In order to realize the localization of the particle size multiplier, the AP-42 and TRAKER methods were used for sampling on typical and different types of roads in Baoding in March 2019. Then, the particle size multiplier of road dust PM2.5 (K2.5) was calculated using the correction formula, and the characteristics were analyzed. The results indicated:① The K2.5 obtained separately by AP-42 and TRAKER were 0.21 g·VKT-1 and 0.23 g·VKT-1 on average, which correlated well, with a high correlation coefficient of 0.6. The PM2.5 emission factors calculated using the K2.5 of the different methods were almost at the same value, indicating that TRAKER method based on a laser sensor could measure and calculate the K2.5 and could be directly used to obtain the particle size multiplier or be converted using the fitting equation. ② The characteristics of the K2.5 in Baoding were ranked as:Expressway<Secondary roads<Branch roads<Major Roads. ③ Further study results of K2.5 characteristics demonstrated that the average K2.5 was higher than 0.15 g·VKT-1 (the value recommended by US EPA) in Baoding City, which would cause an underestimate of road dust emissions and increase the uncertainty of the emissions inventory if the recommended value from the EPA were adopted. The K2.5 in Baoding City is relatively high, indicating that the road dust contains a significant number of micro particles, increasing the contribution of road dust to urban atmospheric PM2.5.

Direct single-molecule imaging for diagnostic and blood screening assays

Every year, over 100 million units of donated blood undergo mandatory screening for HIV, hepatitis B, hepatitis C, and syphilis worldwide. Often, donated blood is also screened for human T cell leukemia-lymphoma virus, Chagas, dengue, Babesia, cytomegalovirus, malaria, and other infections. Several billion diagnostic tests are performed annually around the world to measure more than 400 biomarkers for cardiac, cancer, infectious, and other diseases. Considering such volumes, every improvement in assay performance and/or throughput has a major impact. Here, we show that medically relevant assay sensitivities and specificities can be fundamentally improved by direct single-molecule imaging using regular epifluorescence microscopes. In current microparticle-based assays, an ensemble of bound signal-generating molecules is measured as a whole. By contrast, we acquire intensity profiles to identify and then count individual fluorescent complexes bound to targets on antibody-coated microparticles. This increases the signal-to-noise ratio and provides better discrimination over nonspecific effects. It brings the detection sensitivity down to the attomolar (10-18 M) for model assay systems and to the low femtomolar (10-16 M) for measuring analyte in human plasma. Transitioning from counting single-molecule peaks to averaging pixel intensities at higher analyte concentrations enables a continuous linear response from 10-18 to 10-5 M. Additionally, our assays are insensitive to microparticle number and volume variations during the binding reaction, eliminating the main source of uncertainties in standard assays. Altogether, these features allow for increased assay sensitivity, wide linear detection ranges, shorter incubation times, simpler assay protocols, and minimal reagent consumption.

Enteral nutrition modulation with n-3 PUFAs directs microbiome and lipid metabolism in mice

Nutritional support using exclusive enteral nutrition (EEN) has been studied as primary therapy for the management of liver diseases, Crohn’s disease, and cancers. EEN can also increase the number of beneficial microbiotas in the gut, improve bile acid and lipid metabolism, and decrease the number of harmful dietary micro-particles, possibly by influencing disease occurrence and increasing immunity. This study investigated the effects of EEN-n-3 polyunsaturated fatty acids (3PUFAs) (EEN-3PUFAs) on the gut microbiome, intestinal barrier, and lipid or bile acid metabolism in mice. Metagenomic sequencing technology was used to analyze the effects of EEN-3PUFAs on the composition of gut microbiome signatures. The contents of short-chain fatty acids (SCFAs) and bile acids in the feces and liver of the mice were assayed by gas chromatography and ultra-high-pressure liquid chromatography/high-resolution tandem mass spectrometry, respectively. The levels of lipopolysaccharide (LPS) and D-lactic acid in the blood were used to assess intestinal permeability. The results indicated that EEN-3PUFAs could improve the composition of gut microbiome signatures and increase the abundance of Barnesiella and Lactobacillus (genus), Porphyromonadaceae, and Bacteroidia (species), and Bacteroidetes (phylum) after EEN-3PUFAs initiation. In addition, EEN-3PUFAs induced the formation of SCFAs (mainly including acetic acid, propionic acid, and butyric acid) and increased the intestinal wall compared to the control group. In conclusion, EEN-3PUFAs modulate the alterations in gut microbiome signatures, enhanced intestinal barrier, and regulated the fatty acid composition and lipid metabolism shifts and the putative mechanisms underlying these effects.

Cryopreserved buffy-coat-derived platelets reconstituted in platelet additive solution: A safe and available product with sufficient haemostatic effectiveness

BackgroundPlatelets (PLTs) stored at 20–24 °C have a short shelf life of only 5 days, which can result in their restricted availability. PLT cryopreservation extends the shelf life to 2 years. MethodsWe implemented a method of PLT freezing at −80 °C in 5–6% dimethyl sulfoxide. Buffy-coat-derived leucodepleted fresh PLTs blood group O (FP) were used for cryopreservation. Cryopreserved pooled leucodepleted PLTs (CPP) were thawed at 37 °C, reconstituted in PLT additive solution SSP + and compared to FP regarding PLT content, PLT concentration, pH, volume, PLT loss, anti-A/B antibody titre, total protein, plasma content, and PLT swirling. Clot properties were evaluated via rotational thromboelastometry. PLT microparticle number and surface receptor phenotype were assessed via flow cytometry. ResultsCPP met the required quality parameters. The mean freeze-thaw PLT loss was 22.24 %. Anti-A/B antibody titre and plasma content were significantly lower in CPP. CPP were characterised by faster clot initiation and form stable PLT clots. The number of PLT microparticles increased 25 times in CPP and there were more particles positive for the activation marker CD62 P compared to FP. ConclusionThawing and reconstitution are easy and fast processes if platelet additive solution is used. Low anti-A/B antibody titre and plasma content make possible the use of CPP of blood group O reconstituted in SSP + as universal ABO products, including clinical situations where washed PLTs are required. Clot properties evaluated via rotational thromboelastometry demonstrated that CPP retain a significant part of their activity compare to FP and are haemostatically effective.

Microplastics in Seafood: How Much Are People Eating?

Microplastics in Seafood: How Much Are People Eating?

Qualitative and quantitative analysis of microplastics and microfiber contamination in effluents of the City of Saskatoon wastewater treatment plant.

In recent years, contamination of the environment with microplastics has received increasing scientific and public attention. Wastewater treatment plants (WWTPs) are considered important emitters of microparticles into aquatic systems. Among these microparticles are microplastics from, e.g., cosmetic products, and microfibers that are released during laundry of textiles made from synthetic fibers. The purpose of this study was to qualitatively and quantitatively characterize microplastic and microfiber contamination in effluents of the City of Saskatoon WWTP, Saskatchewan, Canada. The WWTP discharges directly into the South Saskatchewan River, which is an important water resource of central economic and environmental importance to the Canadian Prairies. To achieve this goal, a reference dataset was developed by determining Raman and Fourier-transform infrared (FTIR) spectra of neat plastic standards. Subsequently, samples were obtained from the final effluent of the Saskatoon WWTP during winter, spring, and summer 2019 by use of fine-meshed plankton nets. Microplastics and microfibers were extracted using Fenton oxidation and filtration, counted, and their identity determined by comparing Raman and FTIR spectra of individual microplastics and microfibers with the previously developed reference dataset. The number concentrations of both microplastics and microfibers were relatively stable across seasons, and fibers accounted for 82% of the total number of synthetic microparticles. Although the average total number concentration of microplastics and microfibers was only 1.76 per liter of effluent, at an average daily discharge of 80 million liters, this would amount to the emission of 141 million particles into the river per day. While the environmental relevance of these findings remains to be demonstrated, these results are an important first step toward understanding the magnitude of microplastic contamination in the Canadian Prairies.

Green Thermoplastic Vulcanizates Based on Silicone Rubber and Poly(butylene succinate) via In Situ Interfacial Compatibilization.

Presenting a combination of sustainability and environmental friendliness, a new class of green and non-petroleum-based thermoplastic vulcanizates (TPVs) was successfully developed from silica-filled silicone rubber (FSR) and poly(butylene succinate) (PBS) via dynamic vulcanization. The phase morphology, interfacial compatibilization, and microstructural properties of FSR/PBS TPVs were investigated. Notably, a large number of FSR microparticles were observed and were dispersed in the continuous PBS phase, indicating complete phase inversion during the dynamic vulcanization. The fine phase morphology of FSR/PBS TPVs was achieved by a fine phase morphology of the SR/PBS premix, the good interfacial compatibility between the PBS phase and the cross-linked FSR phase, and complete phase inversion. The as-prepared TPVs possessed high tensile strength, good elastic behavior, easy processability, and reprocessability. These novel non-petroleum-based TPVs have potential applications in packagings, biomedical devices, and three-dimensional (3D) printing materials.

Relationship between heavy metal consolidation and H2S removal by biochar from microwave pyrolysis of municipal sludge: effect and mechanism.

The synergistic effects of pyrolysis byproduct, biochar (BC) on heavy metal consolidation, and H2S removal during and after from microwave pyrolysis of municipal sludge were studied in this paper. The results showed that above 80% of heavy metals (Zn and Pb) were enriched in the biochar and the leaching toxicity of both heavy metals was lower than the national emission standards. The chemical specification analysis found the sum of acid-soluble/exchangeable fraction (F1) and reducible fraction (F2) for Pb and Zn metals decreased by 26 and 40%; however, the residual fraction (F4) increased 33 and 46%, which contributed to the good stabilization of heavy metals in biochar. Besides, biochar achieved high H2S removal efficiency of 78.4% compared with the commercial activated carbon (AC). Furthermore, the biochar prepared by microwave pyrolysis had excellent adsorption performance, which was attributed to its larger specific surface area of 476.87m2/g under nitrogen atmosphere at 650oC compared with traditional pyrolysis. The mechanism analysis showed that microwave pyrolysis resulted in the high alkaline condition and formation of a large number of microparticles containing large metal elements on the biochar surface, which mainly contributed to the stabilization of heavy metals. The metal oxides adsorbed on the surface of biochar can catalyze the oxidation of H2S absorption, which will change the pH atmosphere of biochar reducing the leaching behavior of heavy metals. This study provided the good application potential of solid waste (biochar) for simultaneous heavy metal stabilization and H2S capture.

Prediction of the Therapeutic Effects of Pembrolizumab and Nivolumab in Advanced Non-Small Cell Lung Cancer by Platelet-Derived Microparticles in Circulating Blood.

Background:There are limited methods to predict the therapeutic effect of immune checkpoint inhibitors (ICIs). The purpose of this study was to explore the value of circulating microparticles (MPs) in predicting thetherapeutic effects of immunotherapy.Methods:A prospective study was conducted at the cancer center of PLA general hospital, including all patients with advanced non-small cell lung cancer (NSCLC) who were treated with pembrolizumab or nivolumab from December 2018 to December 2019. The patients were divided into an immune-related objective response (iOR) group and an immune-related disease progression (iPD) group.The numbers of total MPs, platelet-derived microparticles (PMPs) and T-lymphocyte-derived microparticles (T-LyMPs) at baseline and after immunotherapy were detected using a flow cytometer. Univariate analysis and multivariate logistic regression analysis were used to determine the independent influencing factors.Results:We identified 32 patients in the iOR group and 18 patients in the iPD group. No significant difference were found intotal MPs, PMPs and T-LyMPs at the baseline between the 2 groups. While total MPs, PMPs and T-LyMPs in the iPD group were significantly higher than those in the iOR group after immunotherapy(P < 0.05). In the multivariate logistic regression analysis, PMPs ≥80 events/µL after immunotherapy(OR, 7.270; 95% CI, 1.092-48.404, P = 0.04) were associated with disease progression in advanced NSCLC and could independently predict the therapeutic effect of immunotherapy.Conclusions:PMPs after immunotherapy independently predicted the therapeutic effects of ICIs, making it possible to monitor the therapeutic effect in real time and rapidly adjust treatment regimens. In addition, this study found for the first time that elevated circulating T-LyMPs were associated with disease progression in advanced NSCLC.

Affinity of Anti-Spike Antibodies in SARS-CoV-2 Patient Plasma and Its Effect on COVID-19 Antibody Assays

Background: Measuring anti-spike protein antibodies in human plasma or serum is commonly used to determine prior exposure to SARS-CoV-2 infection and to assess the anti-viral protection capacity. According to the mass-action law, a lesser concentration of tightly binding antibody can produce the same quantity of antibody-antigen complexes as higher concentrations of lower affinity antibody. Thus, measurements of antibody levels reflect both affinity and concentration. These two fundamental parameters cannot be disentangled in clinical immunoassays, and so produce a bias which depends on the assay format. Methods: To determine the apparent affinity of anti-spike protein antibodies, a small number of antigen-coated magnetic microparticles were imaged by fluorescence microscopy after probing antigen-antibody equilibria directly in patient plasma. Direct and indirect anti-SARS-CoV-2 immunoassays were used to measure antibody levels in the blood of infected and immunized individuals. Findings: We observed affinity maturation of antibodies in convalescent and vaccinated individuals, showing that higher affinities are achieved much faster by vaccination. We demonstrate that direct and indirect immunoassays for measuring anti-spike protein antibodies depend differently on antibody affinity which, in turn, affects accurate interpretation of the results. Interpretation: Direct immunoassays show substantial antibody affinity dependence. This makes them useful for identifying past SARS-CoV-2 exposure. Indirect immunoassays provide more accurate quantifications of anti-viral antibody levels. Funding: No external funding sources were used in this study.Declaration of Interest: All authors are employed by Abbott LabsEthical Approval: Patient plasma/serum samples used for this study were purchased from New York Biologics (Southampton, NY), Access Biologicals, LLC (Vista, CA) and New York Blood Center (New York, NY). The samples purchased from Access Biologicals LLC were collected under an IRB protocol approved by Ballad Health System IRB. The samples purchased from New York Biologics were collected under an IRB approved by Ethical and Independent Review Services (E&I). The patient plasma samples purchased from New York Blood Center (New York, NY), were collected from volunteer blood donors who consented to the use of their samples for research purposes at the time of collection.

Microplastics and other anthropogenic particles are prevalent in mussels from San Francisco Bay, and show no correlation with PAHs.

Microplastics are an emerging contaminant of high environmental concern due to their widespread distribution and availability to aquatic organisms. Filter-feeding organisms like bivalves have been identified as particularly susceptible to microplastics, and because of this, it has been suggested bivalves could be useful bioindicators of microplastic pollution in ecosystems. We sampled resident mussels and clams from five sites within San Francisco Bay for microplastics and other anthropogenic microparticles. Cages of depurated mussels (denoted transplants) were also deployed at four sites in the Bay for 90 days to investigate temporal uptake of microplastics and microparticles. Because microplastics can sorb PAHs, and thus may act as a source of these chemicals upon ingestion, transplant mussels and resident clams were also analyzed for PAHs. We found anthropogenic microparticles in all samples at all sites, some of which were identified as microplastics. There was no statistical difference between the mean number of microparticles found in resident and transplant species. There were significant site-specific differences among microparticle abundances in the Bay, with the highest abundances observed in the South Bay. No correlation was found between the number of microparticles and the sum concentrations of PAHs, priority PAHs, or any individual PAH, suggesting the chemical concentrations observed reflect broader chemical trends in the Bay rather than direct exposure through microplastic ingestion. The pattern of spatial distribution of microparticles in transplanted mussels matched that of sediment samples from the Bay, suggesting bivalves could be a useful bioindicator of microplastic abundances in sediment, but not surface water.