Purifying chylous plasma by precluding triglyceride via carboxylated polyethersulfone microfiltration membrane

Precluding the excessive lipoproteins from plasma rapidly and effectively is highly needed for biomedical detection and reducing plasma product scrap in blood donation stations.The current centrifugation procedure is high-cost and time-consuming.Herein,we fabricated an anionic microfiltration polyethersulfone(PES)membrane modified by interface swelling and implanting of acrylic acid(AA)for screening out large particle lipoprotein chylomicron(CM)and adsorbing cationic very low-density lipoproteins(VLDL).To improve the separation efficiency,a two-stage filtration through carboxylated polyethersulfone microfiltration membranes with the mean pore size of 0.45 and 0.22μm respectively were conducted.Attenuated total reflection Fourier transform infrared technique(ATR-FTIR),water contact angle(WCA),Zeta potential and scanning electron microscope(SEM)were employed to characterize the modified membrane.To test the effectiveness of this membrane,plasma flux and concentration variation of plasma components were examined to study the purification effectiveness.Furthermore,the hemocompatibility of modified membranes was tested to confirm its practicability on bloodcontacting materials.The carboxylated polyethersulfone microfiltration membrane shows its promising potential application to purify chylous plasma.

Dispersive Ability of Carboxylated Cellulose Nanofibrils for Aqueous Monolayer Montmorillonite Dispersion:Influence of Na^(+) and Ca^(2+) Concentrations

Carboxylated cellulose nanofibrils(CNFs)have emerged as effective green dispersants for monolayer montmorillonite(MMT)dispersions.However,their dispersion capability is sensitive to the metal ion concentration in aqueous solutions.Hence,this study investigated the effects of Na^(+) and Ca^(2+) concentrations on the dispersive ability of carboxylated CNFs for monolayer MMTs in water.Quartz crystal microbalance with dissipation monitoring(QCM-D)and atomic force microscopy(AFM)were utilized to explore the interfacial interactions between the carboxylated CNFs and monolayer MMTs under different Na^(+) and Ca^(2+) concentrations.When the concentration of Na^(+) reached 0.1 mmol/L,the adhesion mass of carboxylated CNFs on MMT-coated wafer peaked at 24.47 mg/m^(2),higher than control sample(carboxylated CNF-dispersed monolayer MMT dispersion without metal ions,16.03 mg/m^(2)).Moreover,the electrostatic shielding effect promoted a better dispersion of monolayer MMTs by carboxylated CNF dispersant.With a further increase in the Na^(+) concentration,the surface charge of CNFs and MMTs would be reversed resulting from the improved electrostatic shielding effect,which weaken the dispersive ability of carboxylated CNFs.The addition of Ca^(2+) reduced the dispersive ability of carboxylated CNFs for monolayer MMTs,because Ca^(2+) required a lower concentration for the onset of charge reversal compared to Na^(+).This study provides interfacial scale insights into the influence of metal ion concentration on carboxylated CNF-dispersed monolayer MMT dispersions.It also provides a strategy to enhance the dispersive ability of carboxylated CNFs for monolayer MMTs.

Simultaneous Extraction of Carboxylated Celulose Nanocrystals and Nanofibrils via Citric Acid Hydrolysis--A Sustainable Route

In this study, cellulose nanocrystals(CNC) with surface carboxylic groups were prepared from bleached softwood pulp by hydrolysis with concentrated citric acid at concentrations of 60 wt%~80 wt%. The solid residues from acid hydrolysis were collected for producing cellulose nanofibrils(CNF) via post high-pressure homogenization. Citric acid could be easily recovered after hydrolysis reactions through crystallization due to its low water solubility or through precipitation as a calcium salt followed by acidification. Several important properties of CNC and CNF, such as dimension, crystallinity, surface chemistry, thermal stability, were evaluated. Results showed that the obtained CNC and CNF surfaces contained carboxylic acid groups that facilitated functionalization and dispersion in aqueous processing. The recyclability of citric acid and the carboxylated CNC/CNF give the renewable cellulose nanomaterial huge potential for a wide range of industrial applications. Furthermore, the resultant CNC and CNF were used as reinforcing agents to make sodium carboxymethyl cellulose(CMC) films. Both CNC and CNF showed reinforcing effects in CMC composite films. The tensile strength of CMC films increased by 54.3% and 85.7% with 10 wt% inclusion of CNC and CNF, respectively. This study provides detailed information on carboxylated nanocellulose prepared by critic acid hydrolysis; a sustainable approach for the preparation of CNC/CNF is of significant importance for their various uses.

Molecularly imprinted sensor based on carboxylated carbon nanotubes/Keggin-type polyoxometalates nanocomposite for the detection of furazolidone

Due to its properties of mutagenic,teratogenic,and carcinogenic,the detection of furazolidone(FZD)in aquaculture is of great importance for food safety and human health.In this study,molecularly imprinted fi lms modifi ed with carboxylated multi-walled carbon nanotube-phosphomolybdic acid composite were used to fabricate an electrochemical sensor for the determination of FZD.The nanocomposites were characterized using infrared spectroscopy,scanning electron microscopy,energy-dispersive X-ray spectroscopy,and X-ray diff raction.The electrochemical characteristics of the modifi ed electrodes were examined using electrochemical impedance spectroscopy,cyclic voltammetry,and diff erential pulse voltammetry.The sensor exhibited exceptional catalytic performance.The calibration curves were acquired in the concentration range of 6 nmol·L^(−1)to 0.6μmol·L^(−1),with a limit of detection of 3.38 nmol·L^(−1).Additionally,the sensor proved successful in recognizing FZD in shrimp samples with satisfactory recoveries and precision.The method provides a strategy to construct a molecularly imprinted electrochemical sensing platform using nanomaterials,which has great promise in the field of food safety.

Using Electrodeposition of Carboxylated Chitosan for Green Preparation of Copper Nanoclusters and Nanocomposite Films

On the basis of coordinated electrodeposition of carboxylated chitosan(CCS),we presented a green method to prepare Cu NCs and Cu NCs/CCS nanocomposite films.The method shows a range of benefits,such as the convenient and eco-friendly process,mild conditions,and simple post-treatment.The experimental results reveal that a homogeneous deposited film(Cu NCs/CCS nanocomposite film)is generated on the Cu plate(the anode)after electrodeposition,which exhibits an obvious red florescence.The results from TEM observation suggest there are nanoparticles(with the average particle size of 2.3 nm)in the deposited film.Spectral analysis results both demonstrate the existence of Cu NCs in the deposited film.Moreover,the Cu NCs/CCS film modified electrode is directly created through electrodeposition of CCS,which enables promising application in the electrochemical sensing.By means of fluorescence properties of Cu NCs,the Cu NCs/CCS film also owns the potential in fluorescence detection.Therefore,this work builds a novel method for the green synthesis of Cu NCs,meanwhile it offers a convenient and new electrodeposition strategy to prepare polysaccharide-based Cu NCs nanocomposites for uses in functional nanocomposites and bioelectronic devices.

Enabling heterogeneous catalysis to achieve carbon neutrality: Directional catalytic conversion of CO_(2) into carboxylic acids

The increase in anthropogenic carbon dioxide(CO_(2))emissions has exacerbated the deterioration of the global environment,which should be controlled to achieve carbon neutrality.Central to the core goal of achieving carbon neutrality is the utilization of CO_(2) under economic and sustainable conditions.Recently,the strong need for carbon neutrality has led to a proliferation of studies on the direct conversion of CO_(2) into carboxylic acids,which can effectively alleviate CO_(2) emissions and create high-value chemicals.The purpose of this review is to present the application prospects of carboxylic acids and the basic principles of CO_(2) conversion into carboxylic acids through photo-,electric-,and thermal catalysis.Special attention is focused on the regulation strategy of the activity of abundant catalysts at the molecular level,inspiring the preparation of high-performance catalysts.In addition,theoretical calculations,advanced technologies,and numerous typical examples are introduced to elaborate on the corresponding process and influencing factors of catalytic activity.Finally,challenges and prospects are provided for the future development of this field.It is hoped that this review will contribute to a deeper understanding of the conversion of CO_(2) into carboxylic acids and inspire more innovative breakthroughs.

Effective and selective adsorption of uranyl ions by porous polyethylenimine-functionalized carboxylated chitosan/oxidized activated charcoal composite

Composite materials have elicited much interest because of their superior performance in the removal of toxic and radioactive uranyl ions from aqueous solutions.With polyethyleneimine as a functional group,carboxylated chitosan as a matrix,and oxidizing activated carbon as a nanofiller,this study synthesized a novel environment-friendly polyethylenimine-functionalized carboxylated chitosan/oxidized activated charcoal(PCO)biocomposite with a unique three-dimensional porous structure.PCO was synthesized through an easy chemical cross-linking method.Detailed characterization certified the formation of the unique three-dimensional porous structure.The obtained PCO was used to remove uranyl ions from an aqueous solution,demonstrating the maximum adsorption capacity of 450 mg·g^(−1).The adsorption capacity of PCO decreased by less than 7.51%after five adsorption-desorption cycles.PCO exhibited good adsorption selectivity(K_(d)=3.45×10^(4) mL·g^(−1))for uranyl ions.The adsorption mechanism of PCO was also discussed.The material showed good potential for application in the treatment of wastewater containing uranyl ions.

Immobilization of nano-zero-valent irons by carboxylated cellulose nanocrystals for wastewater remediation

Nano-zero-valent irons(nZVI)have shown great potential to function as universal a nd low-cost magnetic adsorbents.Yet,the rapid agglomeration and easy surface corrosion of nZVI in solution greatly hinders their overall applicability.Here,carboxylated cellulose nanocrystals(CCNC),widely available from renewable biomass resources,wer e prepared and applied for the immobilization of nZVI.In doing so,carboxylated cellulose nanocrystals supporting nano-zero-valent irons(CCNC-nZVI)were obtained via an in-situ growth method.The CCNC-nZVI were characterized and then evaluated for their performances in wastewater treatment.The results obtained show that nZVI nanoparticles could attach to the carboxyl and hydroxyl groups of CCNC,and well disperse on the CCNC surface with a size of〜10nm.With the CCNC acting as corrosion inhibitors improving the reaction activity of nZVI,CCNC-nZVI exhibited an improved dispersion stability and electron utilization efficacy.The Pb(II)adsorption capacity of CCNC-nZVI reached 509.3 mg·g^-1(298.15 K,pH=4.0),significantly higher than that of CCNC.The adsorption was a spontaneous exothermic process and could be perfectly fitted by the pseudo-second-order kinetics model.This study may provide a novel and green method for immobilizing magnetic nanomaterials by using biomassbased resources to develop effective bio-adsorbents for wastewater decontamination.

Carboxyl Ester Lipase Protects Against Metabolic Dysfunction-Associated Steatohepatitis by Binding to Fatty Acid Synthase

Carboxyl ester lipase(CEL),a pivotal enzyme involved in lipid metabolism,is recurrently mutated in obese mice.Here,we aimed to elucidate the functional significance,molecular mechanism,and therapeutic potential of CEL in metabolic dysfunction-associated steatohepatitis(MASH).Hepatocyte-specific carboxyl ester lipase gene(Cel)knockout(Cel^(DHEP))and wildtype(WT)littermates were fed with cholinedeficient high-fat diet(CD-HFD)for 16 weeks,or methionine-and choline-deficient diet(MCD)for three weeks to induce MASH.Liquid chromatography–mass spectrometry and co-immunoprecipitation were employed to identify the downstream targets of CEL.CD-HFD/MCD-fed WT mice received intravenous injections of CEL-adeno-associated viral,serotype 8(AAV8)to induce specific overexpression of CEL in the liver.We observed a decrease in CEL protein levels in MASH induced by CD-HFD or MCD in mice.Cel^(DHEP) mice fed with CD-HFD or MCD exhibited pronounced hepatic steatosis,inflammation,lipid peroxidation,and liver injury compared to WT littermates,accompanied by increased hepatic nuclear factor kappa-light-chain-enhancer of activated B cell(NF-jB)activation.Consistently,Cel knockdown in mouse primary hepatocytes and AML12 cells aggravated lipid accumulation and inflammation,whereas CEL overexpression exerted the opposite effect.Mechanistically,CEL directly bound to fatty acid synthase(FASN),resulting in reduced FASN SUMOylation,which in turn promoted FASN degradation through the proteasome pathway.Furthermore,inhibition of FASN ameliorated hepatocyte lipid accumulation and inflammation induced by Cel knockdown in vivo and in vitro.Hepatocyte-specific CEL overexpression using AAV8-Cel significantly mitigated steatohepatitis in mice fed with CD-HFD or MCD.CEL protects against steatohepatitis development by directly interacting with FASN and suppressing its expression for de novo lipogenesis.CEL overexpression confers a therapeutic benefit in steatohepatitis.

Tale of mitochondria and mitochondria-associated ER membrane in patient-derived neuronal models of Wolfram syndrome

Mitochondria and mitochondria-associated endoplasmic reticulum membrane in neurodegenerative diseases:Mitochondria generate most of the chemical energy needed to power the biochemical reactions of cells,and thus are often referred to as the"powerhouse"of the cell.Nevertheless,this organelle is also involved in a pleth,ora of different cellular functions such as calcium(Ca^(2+))homeostasis,apoptosis,oxidative stress,and several metabolic pathways including oxidative phosphorylation,tricarboxylic acid cycle,andβ-oxidation of fatty acids.

AAV mediated carboxyl terminus of Hsp70 interacting protein overexpression mitigates the cognitive and pathological phenotypes of APP/PS1 mice

The E3 ubiquitin ligase,carboxyl terminus of heat shock protein 70(Hsp70)interacting protein(CHIP),also functions as a co-chaperone and plays a crucial role in the protein quality control system.In this study,we aimed to investigate the neuroprotective effect of overexpressed CHIP on Alzheimer’s disease.We used an adeno-associated virus vector that can cross the blood-brain barrier to mediate CHIP overexpression in APP/PS1 mouse brain.CHIP overexpression significantly ameliorated the performance of APP/PS1 mice in the Morris water maze and nest building tests,reduced amyloid-βplaques,and decreased the expression of both amyloid-βand phosphorylated tau.CHIP also alleviated the concentration of microglia and astrocytes around plaques.In APP/PS1 mice of a younger age,CHIP overexpression promoted an increase in ADAM10 expression and inhibitedβ-site APP cleaving enzyme 1,insulin degrading enzyme,and neprilysin expression.Levels of HSP70 and HSP40,which have functional relevance to CHIP,were also increased.Single nuclei transcriptome sequencing in the hippocampus of CHIP overexpressed mice showed that the lysosomal pathway and oligodendrocyte-related biological processes were up-regulated,which may also reflect a potential mechanism for the neuroprotective effect of CHIP.Our research shows that CHIP effectively reduces the behavior and pathological manifestations of APP/PS1 mice.Indeed,overexpression of CHIP could be a beneficial approach for the treatment of Alzheimer’s disease.

Uncinatic acids A-C,three new carboxylated flavonoids from Selaginella uncinata

Three new carboxylated flavonoids, uncinatic acids A-C（1–3）, were isolated from the whole herb of Selaginella uncinata. Their structures were established on the basis of extensive NMR analysis including1 D, 2D NMR experiments and HR-ESIMS techniques. All of them share the carboxylation structural characteristic. Compounds 1 and 2 belong to novel naturally occuring furanoflavonoids which is firstly reported in genus Selaginella. Such furanoflavonoids with dicarboxylic acid structrure have never been discovered before. In addition, the isolates were tested for their cytotoxicity against A549 and BGC-823 cell lines in vitro.

Amine-functionalized metal organic framework@graphene oxide as filler in PAEK-containing carboxyl group membrane for ultrafiltration with ultra-high permeability and strong fouling resistance

Achieving high fouling resistance and permeability using membrane separation technology in water treatment processes remains a challenge.In this work,a novel mixed-matrix membrane(MMM)(poly(arylene ether ketone)[PAEK]-containing carboxyl groups[PAEK-COOH]/UiO-66-NH_(2)@graphene oxide[GO])with superb fouling resistance and high permeability was prepared by the nonsolvent-induced phase separation method,by in-situ growth of UiO-66-NH_(2) on the GO layer,and by preparing hydrophilic PAEK-COOH.On the basis of the structure and performance analysis of the MMM,the maximum water flux reached 591.25 L·m^(-2)·h^(-1) for PAEK-COOH/UiO-66-NH_(2)@GO,whereas the retention rate for bovine serum albumin increased from 85.40%to 94.87%.As the loading gradually increased,the hydrophilicity of the MMMs increased,significantly enhancing their fouling resistance.The strongest anti-fouling ability observed was 94.74%,which was 2.02 times greater than that of the pure membrane.At the same time,the MMMs contained internal amide and hydrogen bonds during the preparation process,forming a cross-linked structure,which further enhanced the mechanical strength and chemical stability.In summary,the MMMs with high retention rate,strong permeability,and anti-fouling ability were successfully prepared.

Carboxylic bacterial cellulose fiber-based hydrogel electrolyte with imidazole-type ionic liquid for dendrite-free zinc metal batteries

Aqueous zinc metal batteries are regarded as the most promising energy storage system due to their advantages of high safety,low cost,and high theoretical capacity.However,the growth of dendrites and the occurrence of side reactions hinder the development of zinc metal batteries.Despite previous attempts to design advanced hydrogel electrolytes,achieving high mechanical performance and ionic conductivity of hydrogel electrolytes has remained challenging.In this work,a hydrogel electrolyte with an ionic crosslinked network is prepared by carboxylic bacterial cellulose fiber and imidazole-type ionic liquid,following by a covalent network of polyacrylamide.The hydrogel electrolyte possesses a superior ionic conductivity of 43.76 mS cm^(−1),leading to a Zn^(2+)migration number of 0.45,and high mechanical performance with an elastic modulus of 3.48 GPa and an elongation at breaking of 38.36%.More importantly,under the anion-coordination effect of the carboxyl group in bacterial cellulose and[BF4]−in imidazole-type ionic liquid,the solvation sheath of hydrated Zn^(2+)ions and the nucleation overpotential of Zn plating are regulated.The results of cycled testing show that the growth of zinc dendrites is effectively inhibited and the generation of irreversible by-products is reduced.With the carboxylic bacterial cellulose-based hydrogel electrolyte,the Zn||Zn symmetric batteries offer good cyclability as well as Zn||Ti batteries.

Electrochemistry of carboxylated nanodiamond films

The electrochemical behavior of nanodiamond （ND） film functionalized with carboxylic acid groups was studied systemati- cally on a glassy carbon （GC） electrode. One stable redox couple corresponding to the carboxylic acid group was observed. At the scan rate of 0.1 V/s, the cathodic and anodic peak potentials were -0.093 V and 0.088 V （vs. Ag/AgCI）, respectively. The carboxylic acid groups on the ND surface were reduced to CH2OH via a four electron redox process. The ND film modified electrode showed favorable electrocatalytic behavior toward the oxidation as well as the reduction of biomolecules, such as tryptophan and nicotinamide adenine dinucleotide.

Electrochemical Reaction Mechanism of Phenacetin at a Carboxylated Multiwall Carbon Nanotube Modified Electrode and Its Analytical Applications

A novel type of carboxylated multiwalled carbon nanotube modified electrode（c-MWCNTs/GCE） was constructed and the electrochemical properties of phenacetin（PHE） at it were studied. In a buffer solution of 0.1 mol/L HAc-NaAc（pH=5.3）, PHE exhibited a couple of quasi-reversible redox peaks and an anodic peak in the poten- tial range of 0.2--1.2 V at c-MWCNTs/GCE. The peak current was proportional to the concentration of PHE in the range of 4.0× 10^-6_ 1.0 × 10^-4 mol/L with a detection limit of 1.0× 10^-6 mol/L（S/N=3）. The c-MWCNTs/GCE showed excellent repeatability and stability and the electrochemical reaction mechanism of PHE was proposed. This method was used to determine the content of PHE in medical tablets and the recovery was determined to be 96.5%--104.2% by means of a standard addition method.

Fabrication of nanocomposite electrochemical sensors with poly(3,4-ethylenedioxythiophene)conductive polymer and Au nanoparticles adsorbed on carboxylated nanocrystalline cellulose

Au nanoparticles(AuNPs)were prepared by reducing HAuCl4 with NaBH4,and then adsorbed uniformly on the surface of carboxylated nanocrystalline cellulose(CNCC).The obtained AuNPs/CNCC particles were doped into a conductive polymer of poly(3,4-ethylenedioxythiophene)(PEDOT)to yield a highly conductive nanocomposite,which was deposited onto a glassy carbon electrode(GCE)by an electrochemical method.The PEDOT/AuNPs/CNCC nanocomposite showed low electrochemical impedance and good electrocatalytic activity toward ascorbic acid.Based on this novel nanocomposite material,an amperometric sensor was developed for the detection of ascorbic acid with a detection limit as low as 0.29μM.When operated at-0.15 V,the sensor detected ascorbic acid in the range of 0.88μM to 15000μM.

A simple structure copolymer donor based on carboxylated benzodithiophene for polymer solar cells

The design and development of low-cost and efficient photovoltaic materials remain a major challenge for the research and application of polymer solar cells(PSCs).Therefore,developing efficient photovoltaic polymers with simple structure and easy preparation has become an important research topic.Here we report a facilely synthesized electron-donating polymer X1 with a simple chemical structure,which is composed of carboxylated benzo[1,2-b:4,5-b′]dithiophene(BDT)and thiophene unit.The carboxylate substituents on the BDT unit endowed the polymer with appropriate solubility,low-lying highest occupied molecular orbital(HOMO)energy level,and superior absorption.The PSCs based on X1 as the donor showed a high power conversion efficiency of 16.6%,with a remarkable short-circuit current density of 27.07 m A cm^(-2).These results demonstrated that X1 is a highly promising candidate for low-cost and efficient PSCs.Furthermore,this study revealed the potential of carboxylated BDT as an effective building block in the research and development of high-performance photovoltaic materials.

Carboxylated carbon nanotubes with high electrocatalytic activity for oxygen evolution in acidic conditions

Since most electrocatalysts for oxygen evolution reaction(OER),except for precious metal oxides RuO_(2) and IrO_(2),are unstable in harsh acidic solutions,it is highly desirable to develop high-performance OER electrocatalysts for acidic media,though it is still a big challenge.Herein,we report a simple strategy to produce carboxyl-enriched multiwalled carbon nanotubes(COOH-MWNTs)that exhibit stable and high electrocatalytic activities for OER in acidic solutions,showing an overpotential at a current density of 10 mA cm^(–2) and a Tafel slope as low as of 265 mV and 82 mV dec^(–1),respectively.As far as we are aware,these results represent the best OER performance for metal-free electrocatalysts,even comparable to those of RuO_(2) and IrO_(2).We have further revealed the catalytic mechanism,which involves one electron lose from the COOH-MWNTs catalyst at the beginning of the OER process to trigger H_(2)O molecule oxidation by forming peralcohol,followed by the recapture of one electron from water molecule to oxidize water and to recover the initial state for the COOH-MWNTs catalyst.The unravel of this new OER mechanism is important as it provides new insights into the crucial role of organic functional groups in electrocatalytic processes.Also,the mechanistic understanding can be used to guide the design and development of novel metalfree catalysts for acidic OER electrocatalysis and beyond.

基于Auto Dock Vina软件的药物化学虚拟仿真实验构建与应用

目前药物化学实验偏有机合成技能的培养,忽视了药物化学课程的主要内容。因此我们尝试在药物化学实验课程中构建Oseltamivir carboxylate与神经氨酸酶的分子对接虚拟仿真实验,帮助学生理解药物与靶蛋白的作用方式,提高学习兴趣。本研究通过提前发布学习视频、靶蛋白的下载与预处理、靶分子的结构获取与预处理、AutoDock vina参数设置与对接、Py MOL软件分析结果与图片制作以及学生PPT汇报结果等实验内容。该实验的实施将帮助学生掌握分子对接的基本技能,深入理解立体化学结构对药物与靶蛋白相互作用的影响,提高学生学习药物化学的兴趣,为AutoDock vina软件在药物化学教学中的应用提供参考。