Human mesenchymal stem cells(hMSCs)were labeled with Dotarem or(Gd-DOTA)2-EM7(EM7Gd2)via electroporation(EP).Cellular transmission electron microscopy(TEM)reveals free distribution of Gd agents and formation of EM7Gd2...Human mesenchymal stem cells(hMSCs)were labeled with Dotarem or(Gd-DOTA)2-EM7(EM7Gd2)via electroporation(EP).Cellular transmission electron microscopy(TEM)reveals free distribution of Gd agents and formation of EM7Gd2 clusters in the cytosol.Cellular magnetic resonance imaging(MRI)reveals that the free Gd agents induce MRI signal enhancement effect due to its fast exocytosis and subsequent interaction with intercellular water molecules.The EM7Gd2 clusters exhibits a longer intracellular retention time and induce a persistent MRI signal reduction effect.The cellular MRI results are interpreted by taking into account both T1 and T2 relaxation rates and their correlation with cellular binding structures of Dotarem and EM7Gd2.展开更多
Aflatoxin B1(AFB1)is one of the most common mycotoxins that threatens human health.As singlestranded oligonucleotides with high affinity and specificity,aptamers have incomparable effect on the targeted detection of A...Aflatoxin B1(AFB1)is one of the most common mycotoxins that threatens human health.As singlestranded oligonucleotides with high affinity and specificity,aptamers have incomparable effect on the targeted detection of AFB1.Herein,after 11 rounds of selection and analysis using a modified affinity chromatography-based SELEX strategy,the truncated 37 nt aptamer AF11-2 was successfully obtained.The aptamer shows good detection performance for AFB1,and can sensitively detect AFB1 in the range of 100-1000 nmol/L,with a detection limit of 42 nmol/L.In the detection of pretreated edible peanut oil samples,AF11-2 aptamer also showed a high recovery rate and good stability for AFB1,and achieved satisfactory results.In addition,AF11-2 aptamer can significantly enhance the fluorescence ability of AFB1,which is not available in traditional Afla17-2-3 aptamer.After molecular docking analysis,it was found that AF11-2 and Afla17-2-3 had different nucleotide binding sites for AFB1.Afla17-2-3 binds to the carbonyl O of AFB1,while AF11-2 binds to the pyrrolic O of AFB1,which may be the main reason that AF11-2 can enhance the fluorescence of AFB1.展开更多
Mesenchymal stem cells(MSCs)have emerged as promising candidates for idiopathic pulmonary fibrosis(IPF)therapy.Increasing the MSC survival rate and deepening the understanding of the behavior of transplanted MSCs are ...Mesenchymal stem cells(MSCs)have emerged as promising candidates for idiopathic pulmonary fibrosis(IPF)therapy.Increasing the MSC survival rate and deepening the understanding of the behavior of transplanted MSCs are of great significance for improving the efficacy of MSC-based IPF treatment.Therefore,dual-functional Au-based nanoparticles(Au@PEG@PEI@TAT NPs,AuPPT)were fabricated by sequential modification of cationic polymer polyetherimide(PEI),polyethylene glycol(PEG),and transactivator of transcription(TAT)penetration peptide on AuNPs,to co-deliver retinoic acid(RA)and microRNA(miRNA)for simultaneously enhancing MSC survive and real-time imaging tracking of MSCs during IPF treatment.AuPPT NPs,with good drug loading and cellular uptake abilities,could efficiently deliver miRNA and RA to protect MSCs from reactive oxygen species and reduce their expression of apoptosis executive protein Caspase 3,thus prolonging the survival time of MSC after transplantation.In themeantime,the intracellular accumulation of AuPPT NPs enhanced the computed tomography imaging contrast of transplantedMSCs,allowing them to be visually tracked in vivo.This study establishes an Au-based dual-functional platform for drug delivery and cell imaging tracking,which provides a new strategy for MSC-related IPF therapy.展开更多
Biosynthesis of gold nanostructures has drawn increasing concerns because of its green and sustainable synthetic process. However, biosynthesis of gold nanoplates is still a challenge because of the expensive source a...Biosynthesis of gold nanostructures has drawn increasing concerns because of its green and sustainable synthetic process. However, biosynthesis of gold nanoplates is still a challenge because of the expensive source and difficulties of controllable formation of morphology and size. Herein, one-pot biosynthesis of gold nanoplates is proposed, in which cheap yeast was extracted as a green precursor. The morphologies and sizes of the gold nanostructures can be controlled via varying the pH value of the biomedium. In acid condition, gold nanoplates with side length from 1300 ± 200 to 300 ± 100 nm and height from 18 to 15 nm were obtained by increasing the pH value. Whereas, in neutral or basic condition, only gold nanoflowers and nanoparticles were obtained. It was determined that organic molecules, such as succinic acid, lactic acid, malic acid, and glutathione, which are generated in metabolism process, played important role in the reduction of gold ions. Besides, it was found that the gold nanoplates exhibited plasmonic property with prominent dipole infrared resonance in near-infrared region, indicating their potential in surface plasmon-enhanced applications, such as bioimaging and photothermal therapy.展开更多
Electrochemical CO_(2)reduction(ECR)is one of the most effective methods to obtain carbonaceous chemicals and reduce greenhouse gases passingly under the ambient condition.However,efficient electrocatalysts featured w...Electrochemical CO_(2)reduction(ECR)is one of the most effective methods to obtain carbonaceous chemicals and reduce greenhouse gases passingly under the ambient condition.However,efficient electrocatalysts featured with high selectivity and stability are still lacking.A novel molecule-mediated Ag electrocatalyst with capped thiols is rationally designed for high-performance ECR.The thiol-capped and carbon-supported Ag nanostructures(Ag-TC)are formed by in situ electrochemical reduction from three-dimentional(3D)Ag-thiol metal-organic compound with cysteine as the anchor agent and carbon source.Ag-TC exhibits high selectivity and stability for CO_(2)conversion to CO(86.7%),which is more catalytically active than that of common Ag nanoparticles.The function of thiols for ECR is proved by replacing cysteine with alanine without thiol group.Meanwhile,alternatively replacing and removing the surface molecules on the Ag foil further demonstrate the effct of thiols.This work enlightens the promise of in situ construction method for molecule capped metal electrocatalyst towards selective and stable ECR.展开更多
Erratum to Nano Research 2022,15(4):3283−3289 https://doi.org/10.1007/s12274-021-3978-7 One funding number in the Acknowledgements section was unfortunately mistakenly used.This error did not affect any of the conclus...Erratum to Nano Research 2022,15(4):3283−3289 https://doi.org/10.1007/s12274-021-3978-7 One funding number in the Acknowledgements section was unfortunately mistakenly used.This error did not affect any of the conclusions from the published paper.展开更多
The second near-infrared(NIR-II,1000-1700 nm)circularly polarized light holds significant untapped potential in areas such as optical anti-counterfeiting and information encryption due to its deeply covert nature.Howe...The second near-infrared(NIR-II,1000-1700 nm)circularly polarized light holds significant untapped potential in areas such as optical anti-counterfeiting and information encryption due to its deeply covert nature.However,the typically low luminescence dissymmetry factor(glum)of circularly polarized luminescence(CPL)materials,particularly in NIR CPL materials,limits their practical application.Addressing this challenge,it is crucial to develop NIR CPL materials with enhanced glum.In this study,we present a series of chiral photonic micro-particles(CPMPs)with tunable chiral photonic bandgaps in the NIR-II range,capable of modulating NIR-II luminescent quantum dots to produce NIR CPL.These CPMPs not only impart chirality to the quantum dots,but also act as carriers,minimizing luminescence quenching from external environments.The tunable chiral photonic bandgap in CPMPs enables the generation of NIR CPL with a high|glum|value of up to 0.81,facilitating the advanced application in covert optical anti-counterfeiting.This work offers a straightforward and viable strategy for the development of NIR CPL materials,broadening their use in invisible information encryption and optical anti-counterfeiting technologies.展开更多
In this article, we report a facile precursor pyrolysis method to prepare porous spinel-type cobalt manganese oxides （CoxMng-xO4） with controllable morphologies and crystalline structures. The capping agent in the r...In this article, we report a facile precursor pyrolysis method to prepare porous spinel-type cobalt manganese oxides （CoxMng-xO4） with controllable morphologies and crystalline structures. The capping agent in the reaction was found to be crucial on the formation of the porous spinel cobalt manganese oxides from cubic Co2MnO4 nanorods to tetragonal CoMn2O4 microspheres and tetragonal CoMn204 cubes, respectively. All of the prepared spinel materials exhibit brilliant oxygen reduction reaction （ORR） electrocatalysis along with high stability. In particular, the cubic Co2MnO4 nanorods show the best performance with an onset potential of 0.9 V and a half-wave potential of 0.72 V which are very close to the commercial Pt/C. Meanwhile, the cubic Co2MnO4 nanorods present superior stability with negligible degradation of their electrocatalytic activity after a continuous operation time of 10,000 seconds, which is much better than the commercial Pt/C electrocatalvst.展开更多
Real-time and objective feedback of therapeutic efficacies would be of great value for tumor treatment. Here, we report a smart Ag2S QD-based theranostic nanoplatform （DOX@PEG-Ag2S） obtained by loading the anti-canc...Real-time and objective feedback of therapeutic efficacies would be of great value for tumor treatment. Here, we report a smart Ag2S QD-based theranostic nanoplatform （DOX@PEG-Ag2S） obtained by loading the anti-cancer drug doxorubicin （DOX） into polyethylene glycol-coated silver sulfide quantum dots （PEG-Ag2S QDs） through hydrophobic-hydrophobic interactions, which exhibited high drug loading capability （93 wt.% of DOX to Ag2S QDs）, long circulation in blood （t1/2 = 10.3 h）, and high passive tumor-targeting efficiency （8.9% ID/gram） in living mice where % ID/gram reflects the probe concentration in terms of the percentage of the injected dose （ID） per gram of tissue. After targeting the tumor tissue, DOX from PEG-AgRS cargoes was selectively and rapidly released into cancer cells, giving rise to a significant tumor inhibition. Owing to the deep tissue penetration and high spatio-temporal resolution of Ag2S QDs fluorescence in the second near-infrared window （NIR-II）, the DOX@PEG-Ag2S enabled real-time in vivo reading of the drug targeting process and therapeutic efficacy. We expect that such a novel theranostic nanoplatform, DOX@PEG-Ag2S, with integrated drug delivery, therapy and assessment functionalities, will be highly useful for personalized treatments of tumors.展开更多
A facile colloidal route to synthesize MoSe2 porous microspheres with diameters of 400-600 nm made up of MoSe2 monolayer flakes （-0.7 nm in thickness） is reported. The solvents trioctylamine （TOA） and oleylamine ...A facile colloidal route to synthesize MoSe2 porous microspheres with diameters of 400-600 nm made up of MoSe2 monolayer flakes （-0.7 nm in thickness） is reported. The solvents trioctylamine （TOA） and oleylamine （OAM） are found to play important roles in the formation of MoSe2 microspheres, whereby TOA determines the three-dimensional （3D） microspherical morphology and OAM directs the formation of MoSes monolayer flakes. The robust 3D MoSe2 microspheres exhibit remarkable activity and durability for the electrocatalytic hydrogen evolution reaction （HER） in acid, maintaining a small onset overpotential of -77 mV and keeping a small overpotential of 100 mV for a current density of 5 mA/cm2 after 1,000 cycles. In addition, similar 3D WSe2 microspheres can also be prepared by using this method. We expect this facile colloidal route could further be expanded to synthesize other porous structures which will find applications in fields such as in energy storage, catalysis, and sensing.展开更多
Nanocomposites combining magnetic and plasmonic components have received widespread attention in recent years due to their potential applications in biomedical research. Herein, we describe a facile method for growing...Nanocomposites combining magnetic and plasmonic components have received widespread attention in recent years due to their potential applications in biomedical research. Herein, we describe a facile method for growing small iron oxide nanoparticles on various plasmonic core materials with different shapes and surfaces by utilizing a polypyrrole interlayer. By focusing on Au nanorod@polypyrrole@iron oxide （Au NR@PPy@FexO） nanocomposites, we show that these systems exhibit a low r2/rl ratio of 4.8, making them efficient T1 positive contrast-enhancing agents for magnetic resonance imaging （MRI）. Moreover, we show that the nanocomposites are excellent photothermal agents in the second near infrared region, with high photothermal conversion efficiency, reaching up to 46%. In addition, the Au NR@PPy@FexO nanocomposites show very low cytotoxicity. In summary, the present results highlight the great potential of the synthetic method and the nanocomposites developed in this study for T~ MRI and/or infrared thermal imaging-guided photothermal cancer therapeutic applications.展开更多
Cost-effective electrocatalysts for the hydrogen evolution reaction （HER） play a key role in the field of renewable energy. Although tremendous efforts have been devoted to the search of alternative materials, Pt/C ...Cost-effective electrocatalysts for the hydrogen evolution reaction （HER） play a key role in the field of renewable energy. Although tremendous efforts have been devoted to the search of alternative materials, Pt/C is still the most efficient electrocatalyst for the HER. Nevertheless, decreasing the loading of Pt in the designed eletrocatalysts is of significance. However, with low Pt loading, it is challenging to maintain excellent catalytic performance. Herein, a new catalyst （Pt/NPC） was prepared by dispersing Pt nanoparticles （PtNPs） with an average diameter of 1.8 nm over a three-dimensional （3D） carbon network co-doped with N and P. Because of the high electronegativity of the N and P dopants, PtNPs were uniformly dispersed on the carbon network via high electronic affinity between Pt and carbon, affording a Pt/NPC catalyst; Pt/NPC exhibited superior HER activity, attributed to the down-shift of the Pt d-band caused by the donation of charge from N and P to Pt. The results show that Pt/NPC with an ultralow Pt loading of 1.82 wt.% exhibits excellent HER performance, which corresponds to a HER mass activity 20.6-fold greater than that observed for commercial 20% Pt/C at an overpotential of 20 mV vs. RHE.展开更多
Water pollution is a serious problem around the world. It causes the lack of clean drinking water and brings risks to human health.Membrane technology has become a competitive candidate to treat the contaminated waste...Water pollution is a serious problem around the world. It causes the lack of clean drinking water and brings risks to human health.Membrane technology has become a competitive candidate to treat the contaminated wastewater due to its high separation efficiency and low energy consumption. In this review, we introduce the recent development of several kinds of bioinspired separation membranes, involving the membrane design and applications. We emphasize the multi-phase liquid separation membranes inspired from nature with special wettability applied for oil/water separation, organic liquids mixture separation, and emulsion separation. After separating multi-phase liquids using these membranes, small molecule pollutants still exist in singlephase liquid. Therefore, we also expand the scope to small molecule-scale separation membranes, such as the nacre-like graphene oxide separation membrane and other nanofiltration membranes. Summary and outlook concerning the future development of separation membranes are also introduced briefly.展开更多
Clean energy technologies such as water splitting and fuel cells have been intensively pursued in the last decade for their free pollution. However, there is plenty of fossil energy consumed in the preparation of the ...Clean energy technologies such as water splitting and fuel cells have been intensively pursued in the last decade for their free pollution. However, there is plenty of fossil energy consumed in the preparation of the catalysts,which results in a heavy pollution. Therefore, it is much desired but challenging to fabricate high-efficiency catalysts without extra energy input. Herein, we used a facile one-pot room-temperature method to synthesize a highly efficient electrocatalyst of nickel iron layered double hydroxide grown on Ni foam(NiFe LDH/NF) for oxygen evolution reaction(OER). The formation of the NiFe LDH follows a dissolutionprecipitation process, in which the acid conditions by hydrolysis of Fe^3+ combined with NO3^- could etch the NF to form Ni^2+. Then, the obtained Ni^2+ was co-precipitated with the hydrolysed Fe^3+ to in situ generate NiFe LDH on the NF. The NiFe LDH/NF exhibits excellent OER performance with a low potential of about 1.411 V vs. reversible hydrogen electrode(RHE) at a current density of 10 m A cm^-2, a small Tafel slope of 42.3 mV dec^-1 and a significantly low potential of ~1.452 V vs. RHE at 100 mA cm^-2 in 1 mol L^-1 KOH. Moreover, the material also keeps its original morphology and structure over 20 h. This energy-efficient strategy to synthesize NiFe LDH is highly promising for widespread application in OER catalyst industry.展开更多
The synthesis of atomic-scale metal catalysts is a promising but very challenging project. In this work, we successfully fabricated a hybrid catalyst of PL/Ni（OH）2 with atomic-scale Pt clusters uniformly decorated o...The synthesis of atomic-scale metal catalysts is a promising but very challenging project. In this work, we successfully fabricated a hybrid catalyst of PL/Ni（OH）2 with atomic-scale Pt clusters uniformly decorated on porous Ni（OH）2 nanowires （NWs） via a facile room-temperature synthesis strategy. The as-obtained Ptc/Ni（OH）2 catalyst exhibits highly efficient hydrogen evolution reaction （HER） performance under basic conditions. In 0.1moll-1 KOH, the Ptc/Ni（OH）2 has an onset overpotential of -0 mV vs. RHE, and a significantly low overpotential of 32 mV at a current density of 10mAcm-2, lower than that of the com- mercial 20% Pt/C （58 mV）. The mass current density data illustrated that the PL/Ni（OH）2 reached a high current den- sity of 6.34Amg^-1i at an overpotential of 50 mV, which was approximately 28 times higher than that of the commercial Pt/C （0.223Amg^-1i） at the same overpotential, proving the high-efficiency electrocatalytic activity of the as-obtained Ptc/Ni（OH）2 for HER under alkaline conditions.展开更多
Cation exchange(CE)has been emerged as a promising post-synthesis strategy of colloidal nanocrystals.However,it is unclear how the cation precursor affects the CE process and the final colloidal nanocrystals.Herein,we...Cation exchange(CE)has been emerged as a promising post-synthesis strategy of colloidal nanocrystals.However,it is unclear how the cation precursor affects the CE process and the final colloidal nanocrystals.Herein,we utilized two Zn-B Lewis acidbase adduct complexes(B=oleylamine(OAM)and methanol(MeOH))as Zn precursors for CE with Ag_(2)S quantum dots(QDs).Our study revealed that the steric hindrance and complexing capabilities of Zn precursor significantly affect the CE kinetics.As a result,the Zn-doped Ag_(2)S(Zn:Ag_(2)S)and Ag_(2)S@ZnS core–shell QDs were successfully obtained with enormous enhancement of their photoluminescence(PL)intensities.Theoretical simulation showed that the Zn-OAM with higher desolvation energy and spatial hindrance tended to form doped Zn:Ag_(2)S QDs due to the inefficient cation exchange.Whereas the Zn-MeOH with lower exchange barrier promoted the conversion of Ag-S to Zn-S,thus forming Ag_(2)S@ZnS core–shell QDs.We anticipate that this finding will enrich the regulatory approaches of post-synthesis of colloidal nanocrystals with desirable properties.展开更多
Significant chiroptical responses could be generated by chiral coupling of achiral plasmonic nanoparticles,or originated from intrinsically chiral plasmonic nanoparticles.Here we create dimeric plasmonic metamolecules...Significant chiroptical responses could be generated by chiral coupling of achiral plasmonic nanoparticles,or originated from intrinsically chiral plasmonic nanoparticles.Here we create dimeric plasmonic metamolecules possessing both chiral coupling between nanoparticles and intrinsic chiroptical responses derived from nanoparticles themselves.These plasmonic metamolecules are prepared by assembling helical plasmonic nanorods(HPNRs)with intrinsic chirality in chiral manners on DNA origami template.Two HPNRs with the same or opposite chirality,or one HPNR and one achiral gold nanorod,are coupled chirally into dimeric metamolecules with intriguing plasmonic circular dichroism(PCD).We found that both of the intrinsic chirality of constituent HPNRs and the chiral coupling contribute to the overall PCD while their weights are different in different metamolecules and vary in different wavelength range for a certain metamolecule.Comparing to conventional chiral plasmonic metamolecules from achiral nanoparticles,or discrete chiral nanoparticles,these metamolecules bring more dimensions for tailoring chiroptical responses and make it more flexible to design plasmonic nanodevices with custom PCD.展开更多
Surface ligands of colloidal quantum dots(QDs)have a profound influence on their surface states,which has been verified in the studies of the effect of ligand head groups on the photoluminescence(PL)properties of QDs....Surface ligands of colloidal quantum dots(QDs)have a profound influence on their surface states,which has been verified in the studies of the effect of ligand head groups on the photoluminescence(PL)properties of QDs.However,the investigation of the ligand chain length is limited.Here,we systematically explored the effect of chain length on the Ag_(2)Se QDs by selecting three ligands,1-octanethiol(OTT),1-dodecanethiol(DDT),and 1-hexadecanethiol(HDT),with diverse chain lengths.We found that the PL intensity of Ag_(2)Se QDs increased with the decrease of the ligand chain length due to the enhanced passivation of surface defects emerging from the robust QD-ligand interface binding affinity and the weaker hydrophobic chain–chain interaction.Subsequently,AgAuSe QDs terminated with OTT were obtained by alloying parent OTT-Ag_(2)Se QDs with Au precursor with a record absolute PL quantum yield(PLQY)of 87.2%at 970 nm,facilitating ultrasensitive in vivo angiography imaging in a nude mouse model.We expect that our finding of the important role of the ligand chain length on the optical properties of QDs will be suggestive to the design and synthesis of high-quality QDs,and also look forward to the clinical applications of the ultra-bright AgAuSe QDs.展开更多
Real-time tracking drug release behavior is fundamentally important for avoiding adverse effects or unsuccessful treatment in personalizemedical treatment.However,the development of a non-invasive drug reporting platf...Real-time tracking drug release behavior is fundamentally important for avoiding adverse effects or unsuccessful treatment in personalizemedical treatment.However,the development of a non-invasive drug reporting platform still remains challenging.Herein the design of a novelsyn thetic magnetic resonance imaging(MRI)agent for drug release tracking(SMART)is reported,which integrates photothermal core andparamagnetic ion/drug loading shell with a thermal valve in a hybrid structure.Through near-infrared(NIR)-II photothermal effect originatingfrom inner Au-Cu9S5 nanohybrid core,burst release of drugs loaded in the mesoporous silica shell is achieved.The concomitant use of aphase change material not only prevents premature drug release,but also regulates heating effect,keeping local temperature below 45℃,enabling synergistic chemotherapy and mild hyperthermia in vitro and in vivo.Furthermore,the drug release from SMART facilitates protonaccessibility to the paramagnetic ions anchored inside mesopores channels,enhancing Iongitudinal T1 relaxation rate and displaying positivesignal correlation to the amount of released drug,thus allowing norvinvasive real-time monitoring of drug release event.The current studyhighlights the potential of designed MRI nanophores such as SMART for real-time and in-situ monitoring of drug delivery for precisionthera nostic applications.展开更多
The plasma membrane of cells is a crucial biological membrane that involved in a variety of cellular processes including cell signaling transduction through membrane electrical activity.Recently,monitoring membrane el...The plasma membrane of cells is a crucial biological membrane that involved in a variety of cellular processes including cell signaling transduction through membrane electrical activity.Recently,monitoring membrane electrical activity using fluorescence imaging has attracted numerous attentions for its potential applications in evaluating how the nervous system works.However,the development of ideal fluorescent voltage-sensitive probes with both high membrane labeling efficiency and voltage sensitivity is still retain a big challenge.Herein,glutathionecapped CdSe@ZnS quantum dots (CdSe@ZnS-GSH QDs) with a size of 2.5 nm and an emission peak at 520 nm are synthesized using a facile ligand exchange method for plasma membrane labeling and membrane potential imaging.The as-synthesized CdSe@ZnS-GSH QDs can effectively label cell membrane at neutral pH within 30 min and exhibit excellent optical stability in continuous imaging for up to 60 min.With the test concentration up to 200 nM,CdSe@ZnS-GSH QDs show high biocompatibility to cells and do not affect cell proliferation,disturb cell membrane integrity or cause apoptosis and necrosis of cells.Then,a two-component voltage sensor strategy based on fluorescence resonance energy transfer (FRET) between CdSe@ZnS-GSH QDs and the dipicrylamine (DPA) is successfully developed to monitor the membrane potential by the fluorescence of CdSe@ZnS-GSH QDs.This study offers a facile strategy for labeling plasma membrane and monitoring the membrane potential of cells and will hold great potential in the research of signaling within intact neuronal circuits.展开更多
基金the Natural Science Foundation of China(21673281,31870982)a National Key R&D Program from MOST of China(2017YFA0104301).
文摘Human mesenchymal stem cells(hMSCs)were labeled with Dotarem or(Gd-DOTA)2-EM7(EM7Gd2)via electroporation(EP).Cellular transmission electron microscopy(TEM)reveals free distribution of Gd agents and formation of EM7Gd2 clusters in the cytosol.Cellular magnetic resonance imaging(MRI)reveals that the free Gd agents induce MRI signal enhancement effect due to its fast exocytosis and subsequent interaction with intercellular water molecules.The EM7Gd2 clusters exhibits a longer intracellular retention time and induce a persistent MRI signal reduction effect.The cellular MRI results are interpreted by taking into account both T1 and T2 relaxation rates and their correlation with cellular binding structures of Dotarem and EM7Gd2.
基金supported by the National Natural Science Foundation of China(Nos.32071392,21775160 and 31900999)the Natural Science Foundation of Jiangsu Province(No.BE2020766)the Science Foundation of Jiangxi Province(No.20192ACB21033)。
文摘Aflatoxin B1(AFB1)is one of the most common mycotoxins that threatens human health.As singlestranded oligonucleotides with high affinity and specificity,aptamers have incomparable effect on the targeted detection of AFB1.Herein,after 11 rounds of selection and analysis using a modified affinity chromatography-based SELEX strategy,the truncated 37 nt aptamer AF11-2 was successfully obtained.The aptamer shows good detection performance for AFB1,and can sensitively detect AFB1 in the range of 100-1000 nmol/L,with a detection limit of 42 nmol/L.In the detection of pretreated edible peanut oil samples,AF11-2 aptamer also showed a high recovery rate and good stability for AFB1,and achieved satisfactory results.In addition,AF11-2 aptamer can significantly enhance the fluorescence ability of AFB1,which is not available in traditional Afla17-2-3 aptamer.After molecular docking analysis,it was found that AF11-2 and Afla17-2-3 had different nucleotide binding sites for AFB1.Afla17-2-3 binds to the carbonyl O of AFB1,while AF11-2 binds to the pyrrolic O of AFB1,which may be the main reason that AF11-2 can enhance the fluorescence of AFB1.
基金supported by the National Natural Science Foundation of China(Grant No.32171367)Natural Science Foundation of Jiangsu Province(Grant No.BK20230236)+1 种基金Science and Technology Project of Suzhou(Grant No.SS202135)CAS-VPST Silk Road Science Fund 2021(Grant No.121E32KYSB20200021).
文摘Mesenchymal stem cells(MSCs)have emerged as promising candidates for idiopathic pulmonary fibrosis(IPF)therapy.Increasing the MSC survival rate and deepening the understanding of the behavior of transplanted MSCs are of great significance for improving the efficacy of MSC-based IPF treatment.Therefore,dual-functional Au-based nanoparticles(Au@PEG@PEI@TAT NPs,AuPPT)were fabricated by sequential modification of cationic polymer polyetherimide(PEI),polyethylene glycol(PEG),and transactivator of transcription(TAT)penetration peptide on AuNPs,to co-deliver retinoic acid(RA)and microRNA(miRNA)for simultaneously enhancing MSC survive and real-time imaging tracking of MSCs during IPF treatment.AuPPT NPs,with good drug loading and cellular uptake abilities,could efficiently deliver miRNA and RA to protect MSCs from reactive oxygen species and reduce their expression of apoptosis executive protein Caspase 3,thus prolonging the survival time of MSC after transplantation.In themeantime,the intracellular accumulation of AuPPT NPs enhanced the computed tomography imaging contrast of transplantedMSCs,allowing them to be visually tracked in vivo.This study establishes an Au-based dual-functional platform for drug delivery and cell imaging tracking,which provides a new strategy for MSC-related IPF therapy.
基金supported by the National Key Research and Development Program of China(2016YFC0102700)National Natural Science Foundation of China(21171117,21271181,21473240,and 81270209)+1 种基金Medical-Engineering Crossover Fund of Shanghai Jiao Tong University(YG2015MS51 and YG2014MS66)the Program for Professor of Special Appointment(Eastern Scholar)at Shanghai Institutions of Higher Learning
文摘Biosynthesis of gold nanostructures has drawn increasing concerns because of its green and sustainable synthetic process. However, biosynthesis of gold nanoplates is still a challenge because of the expensive source and difficulties of controllable formation of morphology and size. Herein, one-pot biosynthesis of gold nanoplates is proposed, in which cheap yeast was extracted as a green precursor. The morphologies and sizes of the gold nanostructures can be controlled via varying the pH value of the biomedium. In acid condition, gold nanoplates with side length from 1300 ± 200 to 300 ± 100 nm and height from 18 to 15 nm were obtained by increasing the pH value. Whereas, in neutral or basic condition, only gold nanoflowers and nanoparticles were obtained. It was determined that organic molecules, such as succinic acid, lactic acid, malic acid, and glutathione, which are generated in metabolism process, played important role in the reduction of gold ions. Besides, it was found that the gold nanoplates exhibited plasmonic property with prominent dipole infrared resonance in near-infrared region, indicating their potential in surface plasmon-enhanced applications, such as bioimaging and photothermal therapy.
基金This work was supported by the National Natural Science Foundation of China(No.2210011636)the Natural Science Foundation of Jiangsu Province(No.BK20210311)+3 种基金China Postdoctoral Science Foundation(Nos.2021M691561 and 2021T140319)Jiangsu Planned Projects for Postdoctoral Research Funds(No.2021K547C)CAS Key Laboratory of Nano-Bio Interface(No.21NBI02)the Fundamental Research Funds for the Central Universities(No.NS2021037).
文摘Electrochemical CO_(2)reduction(ECR)is one of the most effective methods to obtain carbonaceous chemicals and reduce greenhouse gases passingly under the ambient condition.However,efficient electrocatalysts featured with high selectivity and stability are still lacking.A novel molecule-mediated Ag electrocatalyst with capped thiols is rationally designed for high-performance ECR.The thiol-capped and carbon-supported Ag nanostructures(Ag-TC)are formed by in situ electrochemical reduction from three-dimentional(3D)Ag-thiol metal-organic compound with cysteine as the anchor agent and carbon source.Ag-TC exhibits high selectivity and stability for CO_(2)conversion to CO(86.7%),which is more catalytically active than that of common Ag nanoparticles.The function of thiols for ECR is proved by replacing cysteine with alanine without thiol group.Meanwhile,alternatively replacing and removing the surface molecules on the Ag foil further demonstrate the effct of thiols.This work enlightens the promise of in situ construction method for molecule capped metal electrocatalyst towards selective and stable ECR.
基金the National Natural Science Foundation of China(No.2210011636)the Natural Science Foundation of Jiangsu Province(No.BK20210311)+3 种基金China Postdoctoral Science Foundation(Nos.2021M691561 and 2021T140319)Jiangsu Planned Projects for Postdoctoral Research Funds(No.2021K547C)CAS Key Laboratory of Nano-Bio Interface(No.21NBI02)the Fundamental Research Funds for the Central Universities(No.NS2021037).
文摘Erratum to Nano Research 2022,15(4):3283−3289 https://doi.org/10.1007/s12274-021-3978-7 One funding number in the Acknowledgements section was unfortunately mistakenly used.This error did not affect any of the conclusions from the published paper.
基金supported by Beijing Natural Science Foundation(No.JQ21003)the National Key Basic R&D Research Program of Ministry of Science and Technology of the People’s Republic of China(No.2021YFA1200303)the National Natural Science Foundation of China(Nos.22302046,22172041,52173159,92256304,and 22271308).
文摘The second near-infrared(NIR-II,1000-1700 nm)circularly polarized light holds significant untapped potential in areas such as optical anti-counterfeiting and information encryption due to its deeply covert nature.However,the typically low luminescence dissymmetry factor(glum)of circularly polarized luminescence(CPL)materials,particularly in NIR CPL materials,limits their practical application.Addressing this challenge,it is crucial to develop NIR CPL materials with enhanced glum.In this study,we present a series of chiral photonic micro-particles(CPMPs)with tunable chiral photonic bandgaps in the NIR-II range,capable of modulating NIR-II luminescent quantum dots to produce NIR CPL.These CPMPs not only impart chirality to the quantum dots,but also act as carriers,minimizing luminescence quenching from external environments.The tunable chiral photonic bandgap in CPMPs enables the generation of NIR CPL with a high|glum|value of up to 0.81,facilitating the advanced application in covert optical anti-counterfeiting.This work offers a straightforward and viable strategy for the development of NIR CPL materials,broadening their use in invisible information encryption and optical anti-counterfeiting technologies.
基金We acknowledge the funding by the National Natural Science Foundation of China （Nos. 21303249, 81401464, 21425103, and 21501192）, and the Natural Science Foundation of Jiangsu Province （No. SBK201341397）.
文摘In this article, we report a facile precursor pyrolysis method to prepare porous spinel-type cobalt manganese oxides （CoxMng-xO4） with controllable morphologies and crystalline structures. The capping agent in the reaction was found to be crucial on the formation of the porous spinel cobalt manganese oxides from cubic Co2MnO4 nanorods to tetragonal CoMn2O4 microspheres and tetragonal CoMn204 cubes, respectively. All of the prepared spinel materials exhibit brilliant oxygen reduction reaction （ORR） electrocatalysis along with high stability. In particular, the cubic Co2MnO4 nanorods show the best performance with an onset potential of 0.9 V and a half-wave potential of 0.72 V which are very close to the commercial Pt/C. Meanwhile, the cubic Co2MnO4 nanorods present superior stability with negligible degradation of their electrocatalytic activity after a continuous operation time of 10,000 seconds, which is much better than the commercial Pt/C electrocatalvst.
基金This work was financially supported by the Chinese Academy of Sciences ＂Strategic Priority Research Program＂ （No. XDA01030200）, the Ministry of Science and Technology of China （No. 2011CB965004）, the National Natural Science Foundation of China （Nos. 21303249, 21301187, and 81401464）, and the Natural Science Foundation of Jiangsu Province （Nos. BK2012007 and BK20130366）.
文摘Real-time and objective feedback of therapeutic efficacies would be of great value for tumor treatment. Here, we report a smart Ag2S QD-based theranostic nanoplatform （DOX@PEG-Ag2S） obtained by loading the anti-cancer drug doxorubicin （DOX） into polyethylene glycol-coated silver sulfide quantum dots （PEG-Ag2S QDs） through hydrophobic-hydrophobic interactions, which exhibited high drug loading capability （93 wt.% of DOX to Ag2S QDs）, long circulation in blood （t1/2 = 10.3 h）, and high passive tumor-targeting efficiency （8.9% ID/gram） in living mice where % ID/gram reflects the probe concentration in terms of the percentage of the injected dose （ID） per gram of tissue. After targeting the tumor tissue, DOX from PEG-AgRS cargoes was selectively and rapidly released into cancer cells, giving rise to a significant tumor inhibition. Owing to the deep tissue penetration and high spatio-temporal resolution of Ag2S QDs fluorescence in the second near-infrared window （NIR-II）, the DOX@PEG-Ag2S enabled real-time in vivo reading of the drug targeting process and therapeutic efficacy. We expect that such a novel theranostic nanoplatform, DOX@PEG-Ag2S, with integrated drug delivery, therapy and assessment functionalities, will be highly useful for personalized treatments of tumors.
文摘A facile colloidal route to synthesize MoSe2 porous microspheres with diameters of 400-600 nm made up of MoSe2 monolayer flakes （-0.7 nm in thickness） is reported. The solvents trioctylamine （TOA） and oleylamine （OAM） are found to play important roles in the formation of MoSe2 microspheres, whereby TOA determines the three-dimensional （3D） microspherical morphology and OAM directs the formation of MoSes monolayer flakes. The robust 3D MoSe2 microspheres exhibit remarkable activity and durability for the electrocatalytic hydrogen evolution reaction （HER） in acid, maintaining a small onset overpotential of -77 mV and keeping a small overpotential of 100 mV for a current density of 5 mA/cm2 after 1,000 cycles. In addition, similar 3D WSe2 microspheres can also be prepared by using this method. We expect this facile colloidal route could further be expanded to synthesize other porous structures which will find applications in fields such as in energy storage, catalysis, and sensing.
基金This work is funded by the ＂Hundred Talents＂ program of Chinese Academy of Sciences, and National Natural Science Foundation of China （Nos. 21175148 and 21473243）.
文摘Nanocomposites combining magnetic and plasmonic components have received widespread attention in recent years due to their potential applications in biomedical research. Herein, we describe a facile method for growing small iron oxide nanoparticles on various plasmonic core materials with different shapes and surfaces by utilizing a polypyrrole interlayer. By focusing on Au nanorod@polypyrrole@iron oxide （Au NR@PPy@FexO） nanocomposites, we show that these systems exhibit a low r2/rl ratio of 4.8, making them efficient T1 positive contrast-enhancing agents for magnetic resonance imaging （MRI）. Moreover, we show that the nanocomposites are excellent photothermal agents in the second near infrared region, with high photothermal conversion efficiency, reaching up to 46%. In addition, the Au NR@PPy@FexO nanocomposites show very low cytotoxicity. In summary, the present results highlight the great potential of the synthetic method and the nanocomposites developed in this study for T~ MRI and/or infrared thermal imaging-guided photothermal cancer therapeutic applications.
基金Acknowledgements This work was financially supported by National Natural Science Foundation of China （No. 21425103） and Natural Science Foundation of Jiangsu Province （No. SBK201341397）.
文摘Cost-effective electrocatalysts for the hydrogen evolution reaction （HER） play a key role in the field of renewable energy. Although tremendous efforts have been devoted to the search of alternative materials, Pt/C is still the most efficient electrocatalyst for the HER. Nevertheless, decreasing the loading of Pt in the designed eletrocatalysts is of significance. However, with low Pt loading, it is challenging to maintain excellent catalytic performance. Herein, a new catalyst （Pt/NPC） was prepared by dispersing Pt nanoparticles （PtNPs） with an average diameter of 1.8 nm over a three-dimensional （3D） carbon network co-doped with N and P. Because of the high electronegativity of the N and P dopants, PtNPs were uniformly dispersed on the carbon network via high electronic affinity between Pt and carbon, affording a Pt/NPC catalyst; Pt/NPC exhibited superior HER activity, attributed to the down-shift of the Pt d-band caused by the donation of charge from N and P to Pt. The results show that Pt/NPC with an ultralow Pt loading of 1.82 wt.% exhibits excellent HER performance, which corresponds to a HER mass activity 20.6-fold greater than that observed for commercial 20% Pt/C at an overpotential of 20 mV vs. RHE.
基金supported by the National Natural Science Foundation of China(21433012,21774005,21374001,21503005,51772010)the National Instrumentation Program(2013YQ120355)+3 种基金the Program for New Century Excellent Talents in University of Chinathe Fundamental Research Funds for the Central Universitiesthe National Program for Support of Top-notch Young Professionalsthe Program of Introducing Talents of Discipline to Universities of China(B14009)
文摘Water pollution is a serious problem around the world. It causes the lack of clean drinking water and brings risks to human health.Membrane technology has become a competitive candidate to treat the contaminated wastewater due to its high separation efficiency and low energy consumption. In this review, we introduce the recent development of several kinds of bioinspired separation membranes, involving the membrane design and applications. We emphasize the multi-phase liquid separation membranes inspired from nature with special wettability applied for oil/water separation, organic liquids mixture separation, and emulsion separation. After separating multi-phase liquids using these membranes, small molecule pollutants still exist in singlephase liquid. Therefore, we also expand the scope to small molecule-scale separation membranes, such as the nacre-like graphene oxide separation membrane and other nanofiltration membranes. Summary and outlook concerning the future development of separation membranes are also introduced briefly.
基金financially supported by the National Natural Science Foundation of China (21425103 and 21501192)
文摘Clean energy technologies such as water splitting and fuel cells have been intensively pursued in the last decade for their free pollution. However, there is plenty of fossil energy consumed in the preparation of the catalysts,which results in a heavy pollution. Therefore, it is much desired but challenging to fabricate high-efficiency catalysts without extra energy input. Herein, we used a facile one-pot room-temperature method to synthesize a highly efficient electrocatalyst of nickel iron layered double hydroxide grown on Ni foam(NiFe LDH/NF) for oxygen evolution reaction(OER). The formation of the NiFe LDH follows a dissolutionprecipitation process, in which the acid conditions by hydrolysis of Fe^3+ combined with NO3^- could etch the NF to form Ni^2+. Then, the obtained Ni^2+ was co-precipitated with the hydrolysed Fe^3+ to in situ generate NiFe LDH on the NF. The NiFe LDH/NF exhibits excellent OER performance with a low potential of about 1.411 V vs. reversible hydrogen electrode(RHE) at a current density of 10 m A cm^-2, a small Tafel slope of 42.3 mV dec^-1 and a significantly low potential of ~1.452 V vs. RHE at 100 mA cm^-2 in 1 mol L^-1 KOH. Moreover, the material also keeps its original morphology and structure over 20 h. This energy-efficient strategy to synthesize NiFe LDH is highly promising for widespread application in OER catalyst industry.
基金financial support from the National Natural Science Foundation of China(21425103,21673280 and 11374039)
文摘The synthesis of atomic-scale metal catalysts is a promising but very challenging project. In this work, we successfully fabricated a hybrid catalyst of PL/Ni（OH）2 with atomic-scale Pt clusters uniformly decorated on porous Ni（OH）2 nanowires （NWs） via a facile room-temperature synthesis strategy. The as-obtained Ptc/Ni（OH）2 catalyst exhibits highly efficient hydrogen evolution reaction （HER） performance under basic conditions. In 0.1moll-1 KOH, the Ptc/Ni（OH）2 has an onset overpotential of -0 mV vs. RHE, and a significantly low overpotential of 32 mV at a current density of 10mAcm-2, lower than that of the com- mercial 20% Pt/C （58 mV）. The mass current density data illustrated that the PL/Ni（OH）2 reached a high current den- sity of 6.34Amg^-1i at an overpotential of 50 mV, which was approximately 28 times higher than that of the commercial Pt/C （0.223Amg^-1i） at the same overpotential, proving the high-efficiency electrocatalytic activity of the as-obtained Ptc/Ni（OH）2 for HER under alkaline conditions.
基金the National Key Research and Development Program of China(No.2021YFF0701804)the financial support from the National Natural Science Foundation of China(Nos.21934007,22001262,22177128,and 22271308)+1 种基金the Science and Technology Project of Suzhou(No.SZS201904)the Natural Science Foundation of Jiangsu Province(Nos.BK20222016,BK20200254,and BK20221262).
文摘Cation exchange(CE)has been emerged as a promising post-synthesis strategy of colloidal nanocrystals.However,it is unclear how the cation precursor affects the CE process and the final colloidal nanocrystals.Herein,we utilized two Zn-B Lewis acidbase adduct complexes(B=oleylamine(OAM)and methanol(MeOH))as Zn precursors for CE with Ag_(2)S quantum dots(QDs).Our study revealed that the steric hindrance and complexing capabilities of Zn precursor significantly affect the CE kinetics.As a result,the Zn-doped Ag_(2)S(Zn:Ag_(2)S)and Ag_(2)S@ZnS core–shell QDs were successfully obtained with enormous enhancement of their photoluminescence(PL)intensities.Theoretical simulation showed that the Zn-OAM with higher desolvation energy and spatial hindrance tended to form doped Zn:Ag_(2)S QDs due to the inefficient cation exchange.Whereas the Zn-MeOH with lower exchange barrier promoted the conversion of Ag-S to Zn-S,thus forming Ag_(2)S@ZnS core–shell QDs.We anticipate that this finding will enrich the regulatory approaches of post-synthesis of colloidal nanocrystals with desirable properties.
基金supported by the National Natural Science Foundation of China(Nos.21977112,and 21934007)the Natural Science Foundation of Jiangsu Province(No.BK20190227)+1 种基金the Strategic Priority Research Program of Chinese Academy of Sciences(No.XDB36000000)the Science and Technology Project of Suzhou(No.SZS201904).
文摘Significant chiroptical responses could be generated by chiral coupling of achiral plasmonic nanoparticles,or originated from intrinsically chiral plasmonic nanoparticles.Here we create dimeric plasmonic metamolecules possessing both chiral coupling between nanoparticles and intrinsic chiroptical responses derived from nanoparticles themselves.These plasmonic metamolecules are prepared by assembling helical plasmonic nanorods(HPNRs)with intrinsic chirality in chiral manners on DNA origami template.Two HPNRs with the same or opposite chirality,or one HPNR and one achiral gold nanorod,are coupled chirally into dimeric metamolecules with intriguing plasmonic circular dichroism(PCD).We found that both of the intrinsic chirality of constituent HPNRs and the chiral coupling contribute to the overall PCD while their weights are different in different metamolecules and vary in different wavelength range for a certain metamolecule.Comparing to conventional chiral plasmonic metamolecules from achiral nanoparticles,or discrete chiral nanoparticles,these metamolecules bring more dimensions for tailoring chiroptical responses and make it more flexible to design plasmonic nanodevices with custom PCD.
基金the National Natural Science Foundation of China(Nos.21934007 and 22001262)the Strategic Priority Research Program of Chinese Academy of Sciences(No.XDB36000000)+1 种基金the Natural Science Foundation of Jiangsu Province(No.BK20200254)China Postdoctoral Science Foundation(No.2019M661966).
文摘Surface ligands of colloidal quantum dots(QDs)have a profound influence on their surface states,which has been verified in the studies of the effect of ligand head groups on the photoluminescence(PL)properties of QDs.However,the investigation of the ligand chain length is limited.Here,we systematically explored the effect of chain length on the Ag_(2)Se QDs by selecting three ligands,1-octanethiol(OTT),1-dodecanethiol(DDT),and 1-hexadecanethiol(HDT),with diverse chain lengths.We found that the PL intensity of Ag_(2)Se QDs increased with the decrease of the ligand chain length due to the enhanced passivation of surface defects emerging from the robust QD-ligand interface binding affinity and the weaker hydrophobic chain–chain interaction.Subsequently,AgAuSe QDs terminated with OTT were obtained by alloying parent OTT-Ag_(2)Se QDs with Au precursor with a record absolute PL quantum yield(PLQY)of 87.2%at 970 nm,facilitating ultrasensitive in vivo angiography imaging in a nude mouse model.We expect that our finding of the important role of the ligand chain length on the optical properties of QDs will be suggestive to the design and synthesis of high-quality QDs,and also look forward to the clinical applications of the ultra-bright AgAuSe QDs.
基金This work was funded by the National Natural Science Foundation of China(No.21473243)Six Talent Peaks Project in Jiangsu Province(No.SWYY-243).
文摘Real-time tracking drug release behavior is fundamentally important for avoiding adverse effects or unsuccessful treatment in personalizemedical treatment.However,the development of a non-invasive drug reporting platform still remains challenging.Herein the design of a novelsyn thetic magnetic resonance imaging(MRI)agent for drug release tracking(SMART)is reported,which integrates photothermal core andparamagnetic ion/drug loading shell with a thermal valve in a hybrid structure.Through near-infrared(NIR)-II photothermal effect originatingfrom inner Au-Cu9S5 nanohybrid core,burst release of drugs loaded in the mesoporous silica shell is achieved.The concomitant use of aphase change material not only prevents premature drug release,but also regulates heating effect,keeping local temperature below 45℃,enabling synergistic chemotherapy and mild hyperthermia in vitro and in vivo.Furthermore,the drug release from SMART facilitates protonaccessibility to the paramagnetic ions anchored inside mesopores channels,enhancing Iongitudinal T1 relaxation rate and displaying positivesignal correlation to the amount of released drug,thus allowing norvinvasive real-time monitoring of drug release event.The current studyhighlights the potential of designed MRI nanophores such as SMART for real-time and in-situ monitoring of drug delivery for precisionthera nostic applications.
基金the Strategic Priority Research Program (No.XDB32030200)Youth Innovation Promotion Association Program from Chinese Academy of Sciences+2 种基金the National Key Research and Development Program (Nos.2016YFA0101503 and 2017YFA0205503)the National Natural Science Foundation of China (Nos.21778070,2167119& 21425103,and 21501192)the National Natural Science Foundation of Jiangsu Province (Nos.BK20170066 and BE2016682).
文摘The plasma membrane of cells is a crucial biological membrane that involved in a variety of cellular processes including cell signaling transduction through membrane electrical activity.Recently,monitoring membrane electrical activity using fluorescence imaging has attracted numerous attentions for its potential applications in evaluating how the nervous system works.However,the development of ideal fluorescent voltage-sensitive probes with both high membrane labeling efficiency and voltage sensitivity is still retain a big challenge.Herein,glutathionecapped CdSe@ZnS quantum dots (CdSe@ZnS-GSH QDs) with a size of 2.5 nm and an emission peak at 520 nm are synthesized using a facile ligand exchange method for plasma membrane labeling and membrane potential imaging.The as-synthesized CdSe@ZnS-GSH QDs can effectively label cell membrane at neutral pH within 30 min and exhibit excellent optical stability in continuous imaging for up to 60 min.With the test concentration up to 200 nM,CdSe@ZnS-GSH QDs show high biocompatibility to cells and do not affect cell proliferation,disturb cell membrane integrity or cause apoptosis and necrosis of cells.Then,a two-component voltage sensor strategy based on fluorescence resonance energy transfer (FRET) between CdSe@ZnS-GSH QDs and the dipicrylamine (DPA) is successfully developed to monitor the membrane potential by the fluorescence of CdSe@ZnS-GSH QDs.This study offers a facile strategy for labeling plasma membrane and monitoring the membrane potential of cells and will hold great potential in the research of signaling within intact neuronal circuits.
