It is important to understand the evolution of the matter on the polymer membrane surface.The in situ and real-time monitoring of the membrane surface will not only favor the investigation of selective layer formation...It is important to understand the evolution of the matter on the polymer membrane surface.The in situ and real-time monitoring of the membrane surface will not only favor the investigation of selective layer formation but can also track the fouling process during operation.Herein,an aggregation-induced emission(AIE)-active polymer membrane was prepared by the interfacial polymerization of a cyclodextrin-based glycocluster(CD@Glucose)and a tetraphenylethylene derivative modified with boronic acid groups(TPEDB)on the surface of a polyacrylonitrile(PAN)ultrafiltration membrane.This interfacial polymerization method can be stacked layer-by-layer to regulate the hydrophilicity and pore structure of the membrane.With the increase in the number of polymer layers,the separation and antifouling properties of the membrane gradually improved.Owing to the AIE property of the crosslinking agent TPEDB,the occurrence of interfacial polymerization and the degree of fouling during membrane operation can be monitored by the fluorescence distribution and intensity.With the aggravation of membrane fouling,the fluorescence decreased gradually,but recovered after cleaning.Therefore,this AIE effect can be used for real-time monitoring of interfacial polymerization as well as membrane fouling.展开更多
Reversible boronate-catechol linkage was widely used to construct two-dimensional coatings and threedimensional nanostructures or hydrogels.The construction of these functional materials usually requires the pre-synth...Reversible boronate-catechol linkage was widely used to construct two-dimensional coatings and threedimensional nanostructures or hydrogels.The construction of these functional materials usually requires the pre-synthesis of macro molecular building blocks,and direct gelation between natural polyphenols and small molecule boranic acids is yet to be investigated.In this study,we fabricated a family of allsmall-molecule dynamic covalent gels consisting of tannic acid and boronic acids.Transparent and thixotropic gels were formed by boronate affinity towards catechol groups abundant on natural polyphenols.The gels showed multi-responsiveness,such as acid-,base-,reduction-and oxidantsensitive depending on the used boronic acid building blocks.The chemistry for gel formation and stimuli-responsiveness was characterized by11B NMR spectroscopy.The multi-stimuli responsiveness,green processing and facile modular design make the boronic acid-tannic acid gels promising candidates for the development of smart soft materials.展开更多
As an acidic glycoprotein,carcinoembryonic antigen(CEA)is of great value as a broad-spectrum tumor marker in the differential diagnosis and surveillance of malignant tumors.In this work,we report an electrochemical ap...As an acidic glycoprotein,carcinoembryonic antigen(CEA)is of great value as a broad-spectrum tumor marker in the differential diagnosis and surveillance of malignant tumors.In this work,we report an electrochemical aptasensor for the ultrasensitive and highly selective detection of CEA,taking advantage of the dual amplification by the boronate affinity-assisted electrochemically controlled atom transfer radical polymerization(BA-eATRP).Specifically,the BAeATRP-based electrochemical aptasensing of CEA involves the capture of target antigens by nucleic acid aptamers,the covalent crosslinking of ATRP initiators to CEA antigens via the selective interactions between the phenylboronic acid(PBA)group and the cis-diol group of the monosaccharide residues,and the collection of the ferrocene(Fc)reporters via the eATRP of ferrocenylmethyl methacrylate(FcMMA).As CEA is decorated with hundreds of cis-diol groups,the BA-based crosslinking can result in the labeling of each CEA with hundreds of ATRP initiators;furthermore,the eATRP of FcMMA results in the surface-initiated growth of long-chain ferrocenyl polymers,leading to the tethering of each ATRP initiator-conjugated site with hundreds to thousands of Fc reporters.Such that,the BAeATRP can result in the efficient labeling of each CEA with a plenty of Fc reporters.Under the optimized conditions,the BA-eATRP-based strategy enables the highly selective aptasensing of CEA at a concentration as low as 0.34 pg·mL^(-1),with a linear range of 1.01000 pg·mL^(-1).Besides,this aptasensor has been successfully applied to the quantitative analysis of CEA in human serum.The BA-eATRP-based electrochemical aptasensor is cost-effective and simple in operation,holding broad application prospect in the ultrasensitive and highly selective detection of CEA.展开更多
Restricted-access materials （RAMs） have found their broad application in sample pretreatment of bioanalysis. Boronate affinity （BA） adsorption is a very efficient and facile method for isolation and enrichment of ...Restricted-access materials （RAMs） have found their broad application in sample pretreatment of bioanalysis. Boronate affinity （BA） adsorption is a very efficient and facile method for isolation and enrichment of cis-diol containing biomolecules which are a large important group compounds in biosystems. However, preparation of BA-RAMs are rarely reported to date. In this study, a novel BA-RAM with external surface comprised of hydrophilic bottlebrush polymers was prepared exploiting the excellent capability of the bottlebrush polymers for protein exclusion. A diblock copolymer poly（3- acrylamidophenylboronic acid）-block-poly（2-hydroxyethyl methacrylate） （PAAPBA-b-PHEMA） was first grafted from the silica surface via surface-initiated reversible addition-fragmentation chain transfer polymerization （SI-RAFT）, and poly（N-isopropylacrylamide） （PNIPAAm） was then grafted from the PHEMA via surface-initiated atom transfer radical polymerization （SI-ATRP） to yield the BA-RAM. The BA- RAM exhibits high selectivity to cis-diol containing small molecules and has good capability to exclude proteins. Its practical application in bioanalysis was tested by pretreatment of serum sample for analysis of catecholamines with high recoveries and good precision. The preparation strategy for the BA-RAM is very versatile and is easy to be expanded to other modes of RAMs.展开更多
Dipeptidyl boronic acids are suitable candidates for the design of "pro-soft" drugs because recent studies have proven that these acids undergo a p H-dependent cyclization equilibrium, generating an inactive...Dipeptidyl boronic acids are suitable candidates for the design of "pro-soft" drugs because recent studies have proven that these acids undergo a p H-dependent cyclization equilibrium, generating an inactive cyclic form under physiological conditions. Dipeptidyl boronic acids possess a wide range of potential targets, and the 26 S proteasome appears to be one of the main targets.This multicatalytic complex is involved in intracellular protein turnover and is overexpressed in certain pathological conditions, such as malignancies, autoimmune diseases and neurodegenerative diseases. Bortezomib is the first-in-class derivative approved by the Food and Drug Administration for the treatment of hematological malignancies(i.e., relapsed and refractory multiple myeloma and mantle cell lymphoma) but is inactive against solid tumors due to an insufficient tissue distribution. The present study suggests a possible strategy for enhancing the in vivo performance of dipeptidyl boronic acids endowed with promising proteasomeinhibiting properties and their applicability as anticancer agents. In particular, dipeptidyl boronic acids might have a fruitful application as pro-soft drugs when an appropriate recognition motif serves as a substrate for a tumor-specific protease, generating the active form of the drug in situ and preventing systemic side effects after diffusion through cells and tissues.展开更多
Palladium-catalyzed cross-coupling reaction between dichlorotriazines and phenylboronate esters produced the mono-awlated triazines selectively and thus, the corresponding phenyltriazine derivatives could be assembled...Palladium-catalyzed cross-coupling reaction between dichlorotriazines and phenylboronate esters produced the mono-awlated triazines selectively and thus, the corresponding phenyltriazine derivatives could be assembled efficiently in moderate to good overall yields （50-80%）.展开更多
Polysaccharides are of great significance in food production,but their isolation highly relies on multi-staged liquid-liquid extraction.In this study,a boronate affinity-mediated magnetic solid phase extraction(BA-MSP...Polysaccharides are of great significance in food production,but their isolation highly relies on multi-staged liquid-liquid extraction.In this study,a boronate affinity-mediated magnetic solid phase extraction(BA-MSPE)method was initiated for the effortless and efficient extraction of polysaccharides using boronic acid-grafted magnetic nanospheres(MNPs@B(OH)_(2))as extractants.MNPs@B(OH)_(2)showed fine class selectivity toward cis-diol containing compounds at weak alkaline condition(pH 7.5~8.5)and higher binding capacity than that of MNPs without boronic acid functionalization.Fast binding dynamics with a binding equilibrium within 10 min,stronger affinity toward polysaccharides(Kd as low as 10^(−3)~10^(−6)M level)than that of small molecular cis-diol compounds(Kd in the range of 10^(−1)~10^(−4)M level),and good recyclability(the binding capacity decreased less than 13%after ten times consecutive extraction)could also be observed for MNPs@B(OH)2.Finally,the BA-MSPE of polysaccharides was performed with three beverage plants as real samples,including tea leaves,soybeans,and Lycium barbarum.Antioxidant activity of polysaccharide extractives was verified by DPPH radical scavenging assays,giving a radical scavenging rate of 31.4%and 18.8%for crude extractives of TPS(tea polysaccharide)and LBPS(Lycium barbarum polysaccharide),respectively.Microscopic imaging combining with MTT and trypan blue staining trials uncovered that the extractives were of dosage-dependent antitumor bioactivities,giving the cell mortality rates over 91.8%and 77.2%for MCF-7 and A549 cells in the presence of 5.0 mg/mL TPS,and 56.6%and 40.0%with the equal dosage of LBPS,respectively.As the BA-MSPE strategy is simple and eco-friendly,there will be more potential for the application of cis-diol compound purification.展开更多
20-Hydroxyecdysone(20E)derived from plants has a wide range of physiological and pharmacological ef ects on animals and humans,and rapid and sensitive methods for screening of the endogenous 20E in plants are thus req...20-Hydroxyecdysone(20E)derived from plants has a wide range of physiological and pharmacological ef ects on animals and humans,and rapid and sensitive methods for screening of the endogenous 20E in plants are thus required.Herein,a matrixassisted laser desorption/ionization time-of-f ight tandem mass spectrometry(MALDI-TOF/TOF MS)method is described for rapid and sensitive determination of endogenous 20E in plants.It is based on the use of the(3-(acridin-9-ylamino)phenyl)boronic acid(AYPBA)as the mass tag to assist the MS and tandem MS(MS^(n))analysis of 20E on MALDI-TOF/TOF MS.Good linearity was obtained with a determination coef cient(R^(2))larger than 0.99 in the range of 0.025–2.5μΜ.The limit of detection(LOD)was 2.4 fmol.Acceptable precision and accuracy were gained by intra-and inter-day analysis with relative standard deviations less than 19.5%and relative recoveries ranging from 85.7 to 105.2%.In addition,the AYPBA labeled 20E produced abundant characteristic fragment ions under the high energy collision-induced dissociation,which facilitated the identif cation of 20E by MS^(2)analysis on MALDI-TOF/TOF MS.Using the method,we enabled the identif cation and quantif cation of endogenous 20E in four herbs including Cyanotis arachoidea,Achyranthes bidentata,Spinacia oleracea and Chenopodium quinoa willd.,demonstrating the feasibility of the proposed method for screening of the endogenous 20E in plants.展开更多
The treatment of malignant bone tumors by chemotherapeutics often receives poor therapeutic response due to the specific physiological bone environment,and thus calls for the development of new therapeutic options.Her...The treatment of malignant bone tumors by chemotherapeutics often receives poor therapeutic response due to the specific physiological bone environment,and thus calls for the development of new therapeutic options.Here,we reported a bone-targeted protein nanomedicine for this purpose.Saporin,a toxin protein,was co-assembled with a boronated polymer for intracellular protein delivery,and the formed nanoparticles were further coated with an anionic polymer poly(aspartic acid)to shield the positive charges on nanoparticles and provide the bone targeting function.The prepared ternary complex nanoparticles showed high bone accumulation both in vitro and in vivo,and could reverse the surface charge property from negative to positive after locating at tumor site triggered by tumor extracellular acidity.The boronated polymer in the de-shielded nanoparticles further promote intracellular delivery of saporin into tumor cells,exerting the anticancer activity of saporin by inactivation of ribosomes.As a result,the bone-targeted and saporin-loaded nanomedicine could kill cancer cells at a low saporin dose,and efficiently prevented the progression of osteosarcoma xenograft tumors and bone metastatic breast cancer in vivo.This study provides a facile and promising strategy to develop protein-based nanomedicines for the treatment of malignant bone tumors.展开更多
This study investigates the performance boundaries of ramjet and scramjet engines fueled by boronbased propellant through full-scale engine modeling and three-dimensional computational fluid dynamics simulations.Resul...This study investigates the performance boundaries of ramjet and scramjet engines fueled by boronbased propellant through full-scale engine modeling and three-dimensional computational fluid dynamics simulations.Results show that the performance boundary between ramjets and scramjets occurs near Mach 7.Specifically,at Mach 6,the ramjet exhibits a 1290 m/s higher specific impulse than the scramjet;however,at Mach 7,their performance becomes comparable.The ramjet's higher static temperature promotes boron particle vaporization and B_(2)O_(2) dissociation,limiting the total temperature increase,unlike in scramjets.The boron vapor mass fraction significantly impacts this temperature difference,with ramjets exhibiting values 8.5 and 3.9 times higher than scramjets at Mach 6 and Mach 7,respectively.Despite lower total temperatures,ramjets achieve more efficient boron combustion due to the combined effects of higher pressures and longer particle residence times.These findings offer valuable insights for engine designers in selecting ramjet or scramjet configurations for boron-fueled propulsion systems.展开更多
Boron has attracted increasing attention in the field of high-energy explosives and propellants due to its high volume calorific value and mass calorific value.However,the complicated combustion process and low combus...Boron has attracted increasing attention in the field of high-energy explosives and propellants due to its high volume calorific value and mass calorific value.However,the complicated combustion process and low combustion efficiency hinder its wide application.To tackle this challenge,bioinspired polydopamine(PDA)interface reinforced boron-Viton composites,with high structure stability and excellent energy releasing efficiency,are designed and prepared,combining the interface regulation of PDA biomimetic materials and combustion promotion of fluoropolymers.Firstly,the stronger adsorption energy of PDA with boron compared to Viton is demonstrated by molecular dynamics simulations.Next,B@PDA@Viton is prepared by the combination of in-situ dopamine polymerization and solvent/nonsolvent method,and the double-layer core-shell structure is confirmed by XPS,FTIR,and TEM characterizations.TG-DSC analysis shows that B@PDA@Viton possesses superior thermal properties,with a 55.48%increase in oxidation heat compared to raw B.Furthermore,ignition and combustion performance tests indicate that B@PDA@Viton reduces ignition delay by 57.56%and increases heat of combustion by 68.63%relative to raw B.These findings elucidate the ignition and combustion mechanisms of B@PDA@Viton.This work not only developed high-performance boron-based composite fuels but also provided insights into the development of boron-based fuels.展开更多
Peroxymonosulfate(PMS)-based advanced oxidation processes(AOPs)are an effective way to remove emerging contaminants(ECs)from water.The catalytic process involving PMS is hindered by the suboptimal electron trans-fer e...Peroxymonosulfate(PMS)-based advanced oxidation processes(AOPs)are an effective way to remove emerging contaminants(ECs)from water.The catalytic process involving PMS is hindered by the suboptimal electron trans-fer efficiency of current catalysts,the further application of AOPs technology is limited.Here,it is proposed that the interfacial electric field can be controlled by bor(B)-doped FeNC catalysts,which shows significant advantages in the efficient generation,release and participation of reactive oxygen species(ROS)in the reaction.The super exchange interaction between Fe sites and N and B sites is realized through the directional transfer of electrons in the interfacial electric field,which ensures the high efficiency and stability of the PMS catalytic process.B doping increases the d orbitals distribution at Fermi level,which facilitates enhanced electron transition activity,thereby promoting the effective generation of (1)^O_(2).At the same time,orbital hybridization causes the center of the d band to move to a lower energy level,which not only contributes to the desorption process of (1)^O_(2),but also accelerates its release.In addition,B-doping also improved the adsorption capacity of organic pollutants and shortened the migration distance of ROS,thereby significantly improving the degradation efficiency of ECs.The B-doping strategy outlined offers a novel approach to the development of FeNC catalysts,it lays a theoretical foundation and offers technical insights for the integration of PMS/AOPs technology in the ECs management.展开更多
The electronic states of the smallest boron cluster B_(3)with excitation energies up to 5 e V are systematically investigated.Geometries and spectroscopic constants for the low-lying electronic states were calculated ...The electronic states of the smallest boron cluster B_(3)with excitation energies up to 5 e V are systematically investigated.Geometries and spectroscopic constants for the low-lying electronic states were calculated using the multireference configuration interaction method with Davidson correction(MRCI+Q).The nondegenerate 1^(2)B_(2)and 2^(2)A_(1)states are arising from the degenerate~2E~′state in D_(3h)symmetry,this is also the case for 2^(2)B_(2)and 3~2A_(1).Furthermore,vertical excitation energies,oscillator strengths,main configurations,and transitions of the excited state of B_(3)were determined.Notably,the theoretically predicted wavelengths for the X^(2)A_(1)→2^(2)A_(1)and X^(2)A_(1)→2^(2)B_(2)electronic transitions(728 nm and 457 nm,respectively)exhibit excellent agreements with experimental absorption bands observed at 736 nm and 458 nm.These theoretical findings provide critical insights into the electronic structure and geometric configuration of the B_(3)cluster.展开更多
The presence of a surface oxide film(B_(2)O_(3))on boron(B)particles significantly compromises their combustion efficiency and kinetic performance in fuel-rich solid propellants.This study proposes an innovative conti...The presence of a surface oxide film(B_(2)O_(3))on boron(B)particles significantly compromises their combustion efficiency and kinetic performance in fuel-rich solid propellants.This study proposes an innovative continuous modification strategy combining non-thermal plasma(NTP)etching with fluorocarbon passivation.Characterization and kinetic analysis revealed that reactive plasma species—including atomic hydrogen(H),electronically excited molecular hydrogen(H_(2)^(*)),vibrationally excited molecular hydrogen(H_(2)v),and hydrogen ions(H^(+))—dominate the reduction of B_(2)O_(3)through lowering the transition energy barrier and shifting the reaction spontaneity.Subsequent argon plasma fragmentation of C_(8)F_(18)generates fluorocarbon radicals that form conformal passivation coatings(thickness:7 nm)on purified boron surfaces.The modified boron particles exhibit 37.5℃lower exothermic peak temperature and 27.2%higher heat release(14.8 kJ/g vs.11.6 kJ/g)compared to untreated counterparts.Combustion diagnostics reveal 194%increase in maximum flame height(135.10 mm vs.46.03 mm)and 134%enhancement in flame propagation rate(4.44 cm/s vs.1.90 cm/s).This NTP-based surface engineering approach establishes a scalable pathway for developing highperformance boron-based energetic composites.展开更多
A method for the effective in-situ formation of boron-containing Mg-Al layered double hydroxides(LDHs)was developed for boron removal and stabilization.The influence of the B/Al molar ratio and pH on the formation of ...A method for the effective in-situ formation of boron-containing Mg-Al layered double hydroxides(LDHs)was developed for boron removal and stabilization.The influence of the B/Al molar ratio and pH on the formation of Mg-Al-B–LDHs was investigated.Compared with the adsorption method,under a high B/Al ratio,the coprecipitation method increased the boron sorption density from 0.256 to 0.472 of Al.The Toxicity Characteristic Leaching Procedure showed that the boron-coprecipitated LDHs exhibited higher stability than the boron-adsorption LDHs.The synthesized LDH samples were characterized by X-ray diffraction,X-ray photoelectron spectroscopy,and solid-state 11B-NMR.The results showed that boron was effectively incorporated into the LDH structure for the coprecipitation method.Combined with the experimental results,a potential in-situ formation pathway for Mg-Al-B–LDHs was elucidated through density functional theory calculations.The boron tended to directly incorporate into the LDH structure in the coprecipitation method,whereas it was predominantly adsorbed on the LDH surface in the adsorption method.The adsorption energy demonstrated that boron preferentially bonded to Mg^(2+)sites on the surface.The mechanism of boron incorporation in the LDHs for the coprecipitation method involved precipitation of amorphous aluminum hydroxide,layered boehmite transformation,nucleation,and layer stacking.During these processes,boron formed complexes to enhance its stability.Residual boron underwent further reactions with the LDHs,including surface adsorption and ion exchange.These findings provide theoretical insight into the effective removal and long-term immobilization of boron in landfill leachate self-remediation processes.展开更多
Graphite and hexagonal boron nitride(h-BN),despite their structural similarity,exhibit opposing electronic properties,namely,metallic conductivity and wide-bandgap insulation,respectively.In recent years,graphene-h-BN...Graphite and hexagonal boron nitride(h-BN),despite their structural similarity,exhibit opposing electronic properties,namely,metallic conductivity and wide-bandgap insulation,respectively.In recent years,graphene-h-BN heterostructures have attracted significant research interest,with the resulting hybrid B-C-N atomic-layer systems exhibiting distinctive electronic properties.Notably,interface effects play a decisive role in governing the performance of these heterostructures.Nevertheless,owing to the lack of high-quality composites,the interfacial structure in B-C-N materials and the correlation with critical properties such as charge transport and band structure modulation are not fully clear.Here,we report the direct synthesis of a millimeter-sized hexagonal B-C-N composite via a solvent method under high-pressure and high-temperature conditions.Structural characterization reveals that the synthesized B-C-N composite contains isolated graphite and h-BN.Compared with pure h-BN,the B-C-N composite has a narrower bandgap and shows a pronounced photoelectric response in the visible light region.More interestingly,we find a graphite-like B-C compound with a thickness of about 30 nm at the graphite-h-BN interface,which forms Schottky junctions with graphite,thus realizing rectification properties.Our findings provide a method for synthesizing highquality B-C-N composites and offer new insights into the structure of the graphite-h-BN interface.展开更多
The enantioenriched tertiary alcohols are among the most privileged skeletons in pharmaceuticals,natural products and agrochemicals.Therefore,tremendous effects have been devoted to constructing this chiral moiety,whi...The enantioenriched tertiary alcohols are among the most privileged skeletons in pharmaceuticals,natural products and agrochemicals.Therefore,tremendous effects have been devoted to constructing this chiral moiety,which constitutes the cornerstones in modern organic synthesis.Generally,the enantioselective nucleophilic addition of ketones functionality with the organometallics reagents represents one of the most reliable strategies to forge the tertiary carbon-oxygen bond.展开更多
Herein,an efficient strategy to achieve aryl-heteroaryl formation via Rh^(III)-catalyzed ortho-C(sp^(2))–H heteroarylation of(hetero)arenes with heterocyclic boronates using a readily removable N-2,6-difluoro-phenyl ...Herein,an efficient strategy to achieve aryl-heteroaryl formation via Rh^(III)-catalyzed ortho-C(sp^(2))–H heteroarylation of(hetero)arenes with heterocyclic boronates using a readily removable N-2,6-difluoro-phenyl arylamide directing group has been disclosed.A variety of heteroaromatic boronates as the coupling partners were shown to be able to participate in this protocol,providing the desired hetero-arylated products with high reactivity and good tolerance of functional groups.展开更多
Cross C–C bond formation of two vinyl electrophiles is a long-standing challenge in synthetic chemistry.Herein,we report a nickel-catalyzed reductive vinyl–vinyl coupling between vinyl triflates and boron-substitute...Cross C–C bond formation of two vinyl electrophiles is a long-standing challenge in synthetic chemistry.Herein,we report a nickel-catalyzed reductive vinyl–vinyl coupling between vinyl triflates and boron-substituted vinyl bromides.This new protocol offers facile access to dienylboronates with high structural complexity and molecular diversity.The reaction proceeds with a broad substrate scope under very mild conditions.The synthetic utility of the method is highlighted by its gram-scale reaction,modification of complex molecules,and diverse transformation of the products.展开更多
The adsorption and separation of antibody drugs are of great significance,but the promising hydrophobic charge induction chromatography(HCIC)and boronate affinity chromatography(BAC)suffer from low specific due to the...The adsorption and separation of antibody drugs are of great significance,but the promising hydrophobic charge induction chromatography(HCIC)and boronate affinity chromatography(BAC)suffer from low specific due to the limitations of single-site adsorption mechanism as well as low adsorption capacity of adsorbents,resulting in a lower purity and recovery of antibodies.To address this issue,this work proposes a two-site synergistic binding strategy integrating HCIC and BAC mechanism on a polymer brushes-grafted adsorbent.Five adsorbents were easily created by polymerizing the mixed monomers of 5-acryloylaminobenzimidazole,3-acryloylamide phenylboronic acid and acrylamide on surface of agarose gel via activators regenerated by electron transfer for atom transfer radical polymerization(ARGET ATRP).The molecular docking implies that the two-site synergistic binding towards immunoglobulin G(IgG)originates from the closely adjacent boronic and benzimidazole side groups in the polymer chains with monomer ratio of 1:1:0.The inference was verified by the effect of three monomer ratios and adsorption conditions on the adsorption performance of IgG.The adsorbent with two-site synergy possesses an excellent specific,enhanced affinity(K_(d)=3.9×10^(-6)mol/L)and adsorption capacity(Q_(m)=253 mg/g)towards IgG.Benefiting from the advantages,IgG from serum and monoclonal antibody(m Ab)from cell culture achieve purities of 95.8%and 98.3%,and recoveries of 95.7%and 97.5%,respectively.The results are comparable to those with protein A adsorbent considered to have the best specific so far,indicating the potential of the two-site synergistic binding strategy in the purification of antibody drugs.展开更多
基金supported by the Fundamental Research Funds for Central Universities(No.30922010811).
文摘It is important to understand the evolution of the matter on the polymer membrane surface.The in situ and real-time monitoring of the membrane surface will not only favor the investigation of selective layer formation but can also track the fouling process during operation.Herein,an aggregation-induced emission(AIE)-active polymer membrane was prepared by the interfacial polymerization of a cyclodextrin-based glycocluster(CD@Glucose)and a tetraphenylethylene derivative modified with boronic acid groups(TPEDB)on the surface of a polyacrylonitrile(PAN)ultrafiltration membrane.This interfacial polymerization method can be stacked layer-by-layer to regulate the hydrophilicity and pore structure of the membrane.With the increase in the number of polymer layers,the separation and antifouling properties of the membrane gradually improved.Owing to the AIE property of the crosslinking agent TPEDB,the occurrence of interfacial polymerization and the degree of fouling during membrane operation can be monitored by the fluorescence distribution and intensity.With the aggravation of membrane fouling,the fluorescence decreased gradually,but recovered after cleaning.Therefore,this AIE effect can be used for real-time monitoring of interfacial polymerization as well as membrane fouling.
基金supported by the National Natural Science Foundation of China(No.21725402)the Shanghai Municipal Science and Technology Commission(No.17XD1401600)。
文摘Reversible boronate-catechol linkage was widely used to construct two-dimensional coatings and threedimensional nanostructures or hydrogels.The construction of these functional materials usually requires the pre-synthesis of macro molecular building blocks,and direct gelation between natural polyphenols and small molecule boranic acids is yet to be investigated.In this study,we fabricated a family of allsmall-molecule dynamic covalent gels consisting of tannic acid and boronic acids.Transparent and thixotropic gels were formed by boronate affinity towards catechol groups abundant on natural polyphenols.The gels showed multi-responsiveness,such as acid-,base-,reduction-and oxidantsensitive depending on the used boronic acid building blocks.The chemistry for gel formation and stimuli-responsiveness was characterized by11B NMR spectroscopy.The multi-stimuli responsiveness,green processing and facile modular design make the boronic acid-tannic acid gels promising candidates for the development of smart soft materials.
基金This work was co-supported by the Guangdong Basic and Applied Basic Research Foundation(No.2022A1515010618)the Young Talent Support Project of Guangzhou Association for Science and Technology(No.QT-2023-009)+2 种基金the National Natural Science Foundation of China(No.21904026,21974031)the Guangzhou Science and Technology Project(No.202201010600,202201020170,202201000002)the Innovation Training Program for College Students of Guangzhou University(No.202211078113,S202111078031).
文摘As an acidic glycoprotein,carcinoembryonic antigen(CEA)is of great value as a broad-spectrum tumor marker in the differential diagnosis and surveillance of malignant tumors.In this work,we report an electrochemical aptasensor for the ultrasensitive and highly selective detection of CEA,taking advantage of the dual amplification by the boronate affinity-assisted electrochemically controlled atom transfer radical polymerization(BA-eATRP).Specifically,the BAeATRP-based electrochemical aptasensing of CEA involves the capture of target antigens by nucleic acid aptamers,the covalent crosslinking of ATRP initiators to CEA antigens via the selective interactions between the phenylboronic acid(PBA)group and the cis-diol group of the monosaccharide residues,and the collection of the ferrocene(Fc)reporters via the eATRP of ferrocenylmethyl methacrylate(FcMMA).As CEA is decorated with hundreds of cis-diol groups,the BA-based crosslinking can result in the labeling of each CEA with hundreds of ATRP initiators;furthermore,the eATRP of FcMMA results in the surface-initiated growth of long-chain ferrocenyl polymers,leading to the tethering of each ATRP initiator-conjugated site with hundreds to thousands of Fc reporters.Such that,the BAeATRP can result in the efficient labeling of each CEA with a plenty of Fc reporters.Under the optimized conditions,the BA-eATRP-based strategy enables the highly selective aptasensing of CEA at a concentration as low as 0.34 pg·mL^(-1),with a linear range of 1.01000 pg·mL^(-1).Besides,this aptasensor has been successfully applied to the quantitative analysis of CEA in human serum.The BA-eATRP-based electrochemical aptasensor is cost-effective and simple in operation,holding broad application prospect in the ultrasensitive and highly selective detection of CEA.
基金supported by the National Natural Science Foundation of China(Nos. 21575114 and 21475104)the Scientific Research Program Funded by Shaanxi Provincial Education Department(No. 16JS114)
文摘Restricted-access materials （RAMs） have found their broad application in sample pretreatment of bioanalysis. Boronate affinity （BA） adsorption is a very efficient and facile method for isolation and enrichment of cis-diol containing biomolecules which are a large important group compounds in biosystems. However, preparation of BA-RAMs are rarely reported to date. In this study, a novel BA-RAM with external surface comprised of hydrophilic bottlebrush polymers was prepared exploiting the excellent capability of the bottlebrush polymers for protein exclusion. A diblock copolymer poly（3- acrylamidophenylboronic acid）-block-poly（2-hydroxyethyl methacrylate） （PAAPBA-b-PHEMA） was first grafted from the silica surface via surface-initiated reversible addition-fragmentation chain transfer polymerization （SI-RAFT）, and poly（N-isopropylacrylamide） （PNIPAAm） was then grafted from the PHEMA via surface-initiated atom transfer radical polymerization （SI-ATRP） to yield the BA-RAM. The BA- RAM exhibits high selectivity to cis-diol containing small molecules and has good capability to exclude proteins. Its practical application in bioanalysis was tested by pretreatment of serum sample for analysis of catecholamines with high recoveries and good precision. The preparation strategy for the BA-RAM is very versatile and is easy to be expanded to other modes of RAMs.
文摘Dipeptidyl boronic acids are suitable candidates for the design of "pro-soft" drugs because recent studies have proven that these acids undergo a p H-dependent cyclization equilibrium, generating an inactive cyclic form under physiological conditions. Dipeptidyl boronic acids possess a wide range of potential targets, and the 26 S proteasome appears to be one of the main targets.This multicatalytic complex is involved in intracellular protein turnover and is overexpressed in certain pathological conditions, such as malignancies, autoimmune diseases and neurodegenerative diseases. Bortezomib is the first-in-class derivative approved by the Food and Drug Administration for the treatment of hematological malignancies(i.e., relapsed and refractory multiple myeloma and mantle cell lymphoma) but is inactive against solid tumors due to an insufficient tissue distribution. The present study suggests a possible strategy for enhancing the in vivo performance of dipeptidyl boronic acids endowed with promising proteasomeinhibiting properties and their applicability as anticancer agents. In particular, dipeptidyl boronic acids might have a fruitful application as pro-soft drugs when an appropriate recognition motif serves as a substrate for a tumor-specific protease, generating the active form of the drug in situ and preventing systemic side effects after diffusion through cells and tissues.
基金the National Natural Science Foundation of China(Nos.30873137,30772645 and 81172927) for their financial support
文摘Palladium-catalyzed cross-coupling reaction between dichlorotriazines and phenylboronate esters produced the mono-awlated triazines selectively and thus, the corresponding phenyltriazine derivatives could be assembled efficiently in moderate to good overall yields （50-80%）.
基金funded by the National Natural Science Foundation of China(Grant No.21904003)the University Scientific Research Project of Anhui Province(2022AH050296)+2 种基金the Natural Science Foundation of Anhui Province(Grant No.2108085QB85)the Open Project of Anhui Engineering Technology Research Center of Biochemical Pharmaceutical(Bengbu Medical College)(Grant No.2022SYKFZ02)the Student Research Training Program of Anhui University of Technology(Grant No.202210360031,202210360038).
文摘Polysaccharides are of great significance in food production,but their isolation highly relies on multi-staged liquid-liquid extraction.In this study,a boronate affinity-mediated magnetic solid phase extraction(BA-MSPE)method was initiated for the effortless and efficient extraction of polysaccharides using boronic acid-grafted magnetic nanospheres(MNPs@B(OH)_(2))as extractants.MNPs@B(OH)_(2)showed fine class selectivity toward cis-diol containing compounds at weak alkaline condition(pH 7.5~8.5)and higher binding capacity than that of MNPs without boronic acid functionalization.Fast binding dynamics with a binding equilibrium within 10 min,stronger affinity toward polysaccharides(Kd as low as 10^(−3)~10^(−6)M level)than that of small molecular cis-diol compounds(Kd in the range of 10^(−1)~10^(−4)M level),and good recyclability(the binding capacity decreased less than 13%after ten times consecutive extraction)could also be observed for MNPs@B(OH)2.Finally,the BA-MSPE of polysaccharides was performed with three beverage plants as real samples,including tea leaves,soybeans,and Lycium barbarum.Antioxidant activity of polysaccharide extractives was verified by DPPH radical scavenging assays,giving a radical scavenging rate of 31.4%and 18.8%for crude extractives of TPS(tea polysaccharide)and LBPS(Lycium barbarum polysaccharide),respectively.Microscopic imaging combining with MTT and trypan blue staining trials uncovered that the extractives were of dosage-dependent antitumor bioactivities,giving the cell mortality rates over 91.8%and 77.2%for MCF-7 and A549 cells in the presence of 5.0 mg/mL TPS,and 56.6%and 40.0%with the equal dosage of LBPS,respectively.As the BA-MSPE strategy is simple and eco-friendly,there will be more potential for the application of cis-diol compound purification.
基金supported by the National Key R&D Program of China(2017YFC0906800)the National Natural Science Foundation of China(21635006,31670373 and 21721005)
文摘20-Hydroxyecdysone(20E)derived from plants has a wide range of physiological and pharmacological ef ects on animals and humans,and rapid and sensitive methods for screening of the endogenous 20E in plants are thus required.Herein,a matrixassisted laser desorption/ionization time-of-f ight tandem mass spectrometry(MALDI-TOF/TOF MS)method is described for rapid and sensitive determination of endogenous 20E in plants.It is based on the use of the(3-(acridin-9-ylamino)phenyl)boronic acid(AYPBA)as the mass tag to assist the MS and tandem MS(MS^(n))analysis of 20E on MALDI-TOF/TOF MS.Good linearity was obtained with a determination coef cient(R^(2))larger than 0.99 in the range of 0.025–2.5μΜ.The limit of detection(LOD)was 2.4 fmol.Acceptable precision and accuracy were gained by intra-and inter-day analysis with relative standard deviations less than 19.5%and relative recoveries ranging from 85.7 to 105.2%.In addition,the AYPBA labeled 20E produced abundant characteristic fragment ions under the high energy collision-induced dissociation,which facilitated the identif cation of 20E by MS^(2)analysis on MALDI-TOF/TOF MS.Using the method,we enabled the identif cation and quantif cation of endogenous 20E in four herbs including Cyanotis arachoidea,Achyranthes bidentata,Spinacia oleracea and Chenopodium quinoa willd.,demonstrating the feasibility of the proposed method for screening of the endogenous 20E in plants.
基金This study was supported by the Interdisciplinary Program of Shanghai Jiao Tong University(ZH2018ZDA18)We are grateful for the support of ECNU Multifunctional Platform for Innovation(011),and the Flow Cytometry Core Facility at ECNU.
文摘The treatment of malignant bone tumors by chemotherapeutics often receives poor therapeutic response due to the specific physiological bone environment,and thus calls for the development of new therapeutic options.Here,we reported a bone-targeted protein nanomedicine for this purpose.Saporin,a toxin protein,was co-assembled with a boronated polymer for intracellular protein delivery,and the formed nanoparticles were further coated with an anionic polymer poly(aspartic acid)to shield the positive charges on nanoparticles and provide the bone targeting function.The prepared ternary complex nanoparticles showed high bone accumulation both in vitro and in vivo,and could reverse the surface charge property from negative to positive after locating at tumor site triggered by tumor extracellular acidity.The boronated polymer in the de-shielded nanoparticles further promote intracellular delivery of saporin into tumor cells,exerting the anticancer activity of saporin by inactivation of ribosomes.As a result,the bone-targeted and saporin-loaded nanomedicine could kill cancer cells at a low saporin dose,and efficiently prevented the progression of osteosarcoma xenograft tumors and bone metastatic breast cancer in vivo.This study provides a facile and promising strategy to develop protein-based nanomedicines for the treatment of malignant bone tumors.
基金funded by the National Natural Science Foundation of China(Grant No.U21B2086)。
文摘This study investigates the performance boundaries of ramjet and scramjet engines fueled by boronbased propellant through full-scale engine modeling and three-dimensional computational fluid dynamics simulations.Results show that the performance boundary between ramjets and scramjets occurs near Mach 7.Specifically,at Mach 6,the ramjet exhibits a 1290 m/s higher specific impulse than the scramjet;however,at Mach 7,their performance becomes comparable.The ramjet's higher static temperature promotes boron particle vaporization and B_(2)O_(2) dissociation,limiting the total temperature increase,unlike in scramjets.The boron vapor mass fraction significantly impacts this temperature difference,with ramjets exhibiting values 8.5 and 3.9 times higher than scramjets at Mach 6 and Mach 7,respectively.Despite lower total temperatures,ramjets achieve more efficient boron combustion due to the combined effects of higher pressures and longer particle residence times.These findings offer valuable insights for engine designers in selecting ramjet or scramjet configurations for boron-fueled propulsion systems.
基金funded by the National Natural Science Foundation of China,Grant No.22405208。
文摘Boron has attracted increasing attention in the field of high-energy explosives and propellants due to its high volume calorific value and mass calorific value.However,the complicated combustion process and low combustion efficiency hinder its wide application.To tackle this challenge,bioinspired polydopamine(PDA)interface reinforced boron-Viton composites,with high structure stability and excellent energy releasing efficiency,are designed and prepared,combining the interface regulation of PDA biomimetic materials and combustion promotion of fluoropolymers.Firstly,the stronger adsorption energy of PDA with boron compared to Viton is demonstrated by molecular dynamics simulations.Next,B@PDA@Viton is prepared by the combination of in-situ dopamine polymerization and solvent/nonsolvent method,and the double-layer core-shell structure is confirmed by XPS,FTIR,and TEM characterizations.TG-DSC analysis shows that B@PDA@Viton possesses superior thermal properties,with a 55.48%increase in oxidation heat compared to raw B.Furthermore,ignition and combustion performance tests indicate that B@PDA@Viton reduces ignition delay by 57.56%and increases heat of combustion by 68.63%relative to raw B.These findings elucidate the ignition and combustion mechanisms of B@PDA@Viton.This work not only developed high-performance boron-based composite fuels but also provided insights into the development of boron-based fuels.
基金supported by the National Natural Science Foundation of China(No.22278156)the Guangdong Special Support Program Project(No.2021JC060580)+1 种基金the Young Elite Scientists Sponsorship Program by CAST-Doctoral Student Special Plan,the China Scholarship Council Program(No.202406150148)the Natural Science Foundation of Guangdong Province(No.2023A1515011186).
文摘Peroxymonosulfate(PMS)-based advanced oxidation processes(AOPs)are an effective way to remove emerging contaminants(ECs)from water.The catalytic process involving PMS is hindered by the suboptimal electron trans-fer efficiency of current catalysts,the further application of AOPs technology is limited.Here,it is proposed that the interfacial electric field can be controlled by bor(B)-doped FeNC catalysts,which shows significant advantages in the efficient generation,release and participation of reactive oxygen species(ROS)in the reaction.The super exchange interaction between Fe sites and N and B sites is realized through the directional transfer of electrons in the interfacial electric field,which ensures the high efficiency and stability of the PMS catalytic process.B doping increases the d orbitals distribution at Fermi level,which facilitates enhanced electron transition activity,thereby promoting the effective generation of (1)^O_(2).At the same time,orbital hybridization causes the center of the d band to move to a lower energy level,which not only contributes to the desorption process of (1)^O_(2),but also accelerates its release.In addition,B-doping also improved the adsorption capacity of organic pollutants and shortened the migration distance of ROS,thereby significantly improving the degradation efficiency of ECs.The B-doping strategy outlined offers a novel approach to the development of FeNC catalysts,it lays a theoretical foundation and offers technical insights for the integration of PMS/AOPs technology in the ECs management.
基金Project supported by the National Natural Science Foundation of China(Grant No.12274178)。
文摘The electronic states of the smallest boron cluster B_(3)with excitation energies up to 5 e V are systematically investigated.Geometries and spectroscopic constants for the low-lying electronic states were calculated using the multireference configuration interaction method with Davidson correction(MRCI+Q).The nondegenerate 1^(2)B_(2)and 2^(2)A_(1)states are arising from the degenerate~2E~′state in D_(3h)symmetry,this is also the case for 2^(2)B_(2)and 3~2A_(1).Furthermore,vertical excitation energies,oscillator strengths,main configurations,and transitions of the excited state of B_(3)were determined.Notably,the theoretically predicted wavelengths for the X^(2)A_(1)→2^(2)A_(1)and X^(2)A_(1)→2^(2)B_(2)electronic transitions(728 nm and 457 nm,respectively)exhibit excellent agreements with experimental absorption bands observed at 736 nm and 458 nm.These theoretical findings provide critical insights into the electronic structure and geometric configuration of the B_(3)cluster.
基金supported by the National Natural Science Foundation of China(Nos.U2341249,12005076,22205112)the Fundamental Research Funds for the Central Universities(No.2025201012)。
文摘The presence of a surface oxide film(B_(2)O_(3))on boron(B)particles significantly compromises their combustion efficiency and kinetic performance in fuel-rich solid propellants.This study proposes an innovative continuous modification strategy combining non-thermal plasma(NTP)etching with fluorocarbon passivation.Characterization and kinetic analysis revealed that reactive plasma species—including atomic hydrogen(H),electronically excited molecular hydrogen(H_(2)^(*)),vibrationally excited molecular hydrogen(H_(2)v),and hydrogen ions(H^(+))—dominate the reduction of B_(2)O_(3)through lowering the transition energy barrier and shifting the reaction spontaneity.Subsequent argon plasma fragmentation of C_(8)F_(18)generates fluorocarbon radicals that form conformal passivation coatings(thickness:7 nm)on purified boron surfaces.The modified boron particles exhibit 37.5℃lower exothermic peak temperature and 27.2%higher heat release(14.8 kJ/g vs.11.6 kJ/g)compared to untreated counterparts.Combustion diagnostics reveal 194%increase in maximum flame height(135.10 mm vs.46.03 mm)and 134%enhancement in flame propagation rate(4.44 cm/s vs.1.90 cm/s).This NTP-based surface engineering approach establishes a scalable pathway for developing highperformance boron-based energetic composites.
基金supported by the research equipment (Nos. G1006,G1010 and G1018) shared in MEXT Project for promoting public utilization of advanced research infrastructure (Program for supporting construction of core facilities)(No. JPMXS0440500023)financial support of the China Scholarship Council.
文摘A method for the effective in-situ formation of boron-containing Mg-Al layered double hydroxides(LDHs)was developed for boron removal and stabilization.The influence of the B/Al molar ratio and pH on the formation of Mg-Al-B–LDHs was investigated.Compared with the adsorption method,under a high B/Al ratio,the coprecipitation method increased the boron sorption density from 0.256 to 0.472 of Al.The Toxicity Characteristic Leaching Procedure showed that the boron-coprecipitated LDHs exhibited higher stability than the boron-adsorption LDHs.The synthesized LDH samples were characterized by X-ray diffraction,X-ray photoelectron spectroscopy,and solid-state 11B-NMR.The results showed that boron was effectively incorporated into the LDH structure for the coprecipitation method.Combined with the experimental results,a potential in-situ formation pathway for Mg-Al-B–LDHs was elucidated through density functional theory calculations.The boron tended to directly incorporate into the LDH structure in the coprecipitation method,whereas it was predominantly adsorbed on the LDH surface in the adsorption method.The adsorption energy demonstrated that boron preferentially bonded to Mg^(2+)sites on the surface.The mechanism of boron incorporation in the LDHs for the coprecipitation method involved precipitation of amorphous aluminum hydroxide,layered boehmite transformation,nucleation,and layer stacking.During these processes,boron formed complexes to enhance its stability.Residual boron underwent further reactions with the LDHs,including surface adsorption and ion exchange.These findings provide theoretical insight into the effective removal and long-term immobilization of boron in landfill leachate self-remediation processes.
基金supported by the National Key R&D Program of China(Grant No.2023YFA1406200)the National Science Foundation of China(Grant No.U2032215)+1 种基金Jilin Province Major Science and Technology Program,China(Grant No.20240211002GX)the Science and Technology Development Project of Jilin Province(Grant No.SKL202402004).
文摘Graphite and hexagonal boron nitride(h-BN),despite their structural similarity,exhibit opposing electronic properties,namely,metallic conductivity and wide-bandgap insulation,respectively.In recent years,graphene-h-BN heterostructures have attracted significant research interest,with the resulting hybrid B-C-N atomic-layer systems exhibiting distinctive electronic properties.Notably,interface effects play a decisive role in governing the performance of these heterostructures.Nevertheless,owing to the lack of high-quality composites,the interfacial structure in B-C-N materials and the correlation with critical properties such as charge transport and band structure modulation are not fully clear.Here,we report the direct synthesis of a millimeter-sized hexagonal B-C-N composite via a solvent method under high-pressure and high-temperature conditions.Structural characterization reveals that the synthesized B-C-N composite contains isolated graphite and h-BN.Compared with pure h-BN,the B-C-N composite has a narrower bandgap and shows a pronounced photoelectric response in the visible light region.More interestingly,we find a graphite-like B-C compound with a thickness of about 30 nm at the graphite-h-BN interface,which forms Schottky junctions with graphite,thus realizing rectification properties.Our findings provide a method for synthesizing highquality B-C-N composites and offer new insights into the structure of the graphite-h-BN interface.
文摘The enantioenriched tertiary alcohols are among the most privileged skeletons in pharmaceuticals,natural products and agrochemicals.Therefore,tremendous effects have been devoted to constructing this chiral moiety,which constitutes the cornerstones in modern organic synthesis.Generally,the enantioselective nucleophilic addition of ketones functionality with the organometallics reagents represents one of the most reliable strategies to forge the tertiary carbon-oxygen bond.
基金We gratefully thank the National Natural Science Foundation of China(21801108)Natural Science Foundation of Shandong Province(ZR2019PB001)Research Fund for the Doctoral Program of Liaocheng University(318051726)for financial support.
文摘Herein,an efficient strategy to achieve aryl-heteroaryl formation via Rh^(III)-catalyzed ortho-C(sp^(2))–H heteroarylation of(hetero)arenes with heterocyclic boronates using a readily removable N-2,6-difluoro-phenyl arylamide directing group has been disclosed.A variety of heteroaromatic boronates as the coupling partners were shown to be able to participate in this protocol,providing the desired hetero-arylated products with high reactivity and good tolerance of functional groups.
基金The authors thank the National Natural Science Foundation of China for financial support(nos.21772072 and 22071084)。
文摘Cross C–C bond formation of two vinyl electrophiles is a long-standing challenge in synthetic chemistry.Herein,we report a nickel-catalyzed reductive vinyl–vinyl coupling between vinyl triflates and boron-substituted vinyl bromides.This new protocol offers facile access to dienylboronates with high structural complexity and molecular diversity.The reaction proceeds with a broad substrate scope under very mild conditions.The synthetic utility of the method is highlighted by its gram-scale reaction,modification of complex molecules,and diverse transformation of the products.
基金supported by the National Natural Science Foundation of China(Nos.22274129,21974106 and 22074117)。
文摘The adsorption and separation of antibody drugs are of great significance,but the promising hydrophobic charge induction chromatography(HCIC)and boronate affinity chromatography(BAC)suffer from low specific due to the limitations of single-site adsorption mechanism as well as low adsorption capacity of adsorbents,resulting in a lower purity and recovery of antibodies.To address this issue,this work proposes a two-site synergistic binding strategy integrating HCIC and BAC mechanism on a polymer brushes-grafted adsorbent.Five adsorbents were easily created by polymerizing the mixed monomers of 5-acryloylaminobenzimidazole,3-acryloylamide phenylboronic acid and acrylamide on surface of agarose gel via activators regenerated by electron transfer for atom transfer radical polymerization(ARGET ATRP).The molecular docking implies that the two-site synergistic binding towards immunoglobulin G(IgG)originates from the closely adjacent boronic and benzimidazole side groups in the polymer chains with monomer ratio of 1:1:0.The inference was verified by the effect of three monomer ratios and adsorption conditions on the adsorption performance of IgG.The adsorbent with two-site synergy possesses an excellent specific,enhanced affinity(K_(d)=3.9×10^(-6)mol/L)and adsorption capacity(Q_(m)=253 mg/g)towards IgG.Benefiting from the advantages,IgG from serum and monoclonal antibody(m Ab)from cell culture achieve purities of 95.8%and 98.3%,and recoveries of 95.7%and 97.5%,respectively.The results are comparable to those with protein A adsorbent considered to have the best specific so far,indicating the potential of the two-site synergistic binding strategy in the purification of antibody drugs.
