A new substrate,aligned Ag nanowires decorated with silver nanoparticle composite structure(AgNWs@AgNPs),was fabricated to investigate metalenhanced fluorescence(MEF) and its mechanism.The new composite structure was ...A new substrate,aligned Ag nanowires decorated with silver nanoparticle composite structure(AgNWs@AgNPs),was fabricated to investigate metalenhanced fluorescence(MEF) and its mechanism.The new composite structure was fabricated via a three-phase interface assembly method followed by SnCl2 sensitization and AgNO3 reduction process.The size and distribution of the nanoparticles on silver nanowires increased with the sensitization and reduction cycles.The formation of AgNPs on the surfaces of AgNWs was confirmed by multiple characterization methods including scanning electron microscopy(SEM),transmission electron microscope(TEM),atomic force microscopy(AFM) and X-ray diffraction(XRD).The results show that the fluorescence intensity of the poly(3-hexylthiophene)(P3HT) on the composite structure was greatly enhanced compared with that on bare glass substrate,and the intensity increased with the increase in particle sizes and density.The mechanism was basedo n the increase in excitation rate and the radiation decay rate.The new type of substrate could serve as a good and efficient MEF substrate for high-performance fluorescence-based devices.展开更多
A new water-stable europium MOF,(Me_(2)NH_(2))[Eu(abtc)(phen)]·2H_(2)O (1),has been synthesized from Eu(NO_(3))_(3)·6H_(2)O with 1,10-phenanthroline (phen) and 3,3′,5,5′-azobenzenetetracarboxylic acid (H_4...A new water-stable europium MOF,(Me_(2)NH_(2))[Eu(abtc)(phen)]·2H_(2)O (1),has been synthesized from Eu(NO_(3))_(3)·6H_(2)O with 1,10-phenanthroline (phen) and 3,3′,5,5′-azobenzenetetracarboxylic acid (H_4abtc) ligands under solvothermal conditions and structurally characterized by single-crystal X-ray diffraction analysis,IR,TGA and PXRD.It crystallizes in monoclinic system,C2/c space group,with a=16.278(3),b=14.261(3),c=27.936(5)?,b=103.464(3)°,V=6307(2)A^(3),Z=8,C_(30)H_(26)Eu N_5O_(10),M_(r)=768.5,D_(c)=1.543 g/cm^(3),F(000)=2912,m(Mo Ka)=2.044 mm^(-1),R=0.0315 and w R=0.0663.In the structure of 1,the Eu O_7N_(2) polyhedra are assembled into a 2D layer with rhombic windows and these layers are further condensed to form a 3D framework.It can be used as selective and sensitive fluorescence sensors capable of detecting diethyl ether vapor.展开更多
Fluorescence enhancement of red and blue concurrently emitting Ba3MgSi2O8:Eu2+,Mn2+ phosphors for plant cultivation has been investigated by Dy3+ addition.The Ba3MgSi2O8:Eu2+,Mn2+,Dy3+(BMS-EMD) phosphors have two-colo...Fluorescence enhancement of red and blue concurrently emitting Ba3MgSi2O8:Eu2+,Mn2+ phosphors for plant cultivation has been investigated by Dy3+ addition.The Ba3MgSi2O8:Eu2+,Mn2+,Dy3+(BMS-EMD) phosphors have two-color emissions at the wavelength peak values of 437 nm and 620 nm at the excitation of 350 nm.The two emission bands are coincident with the absorption spectrum for photosynthesis of plants.An obvious enhancement effect has been observed upon addition of Dy3+ with amount of 0.03 mol%,in which the intensities of both blue and red bands reach a maximum.The origin of red and blue emission bands is analysed.The photochromic parameters of the samples at the nearly UV excitation are tested.This fluoresence enhancement is of great significance for special solid state lighting equipment used in plant cultivation.展开更多
The effect of cucurbit[7]uril(CB[7]) on fluorescence properties and biocompatibility of the bis-viologen biphenyl molecule(BPV22+) was investigated by using 1 H NMR spectroscopy,fluorescence emission titration,and in ...The effect of cucurbit[7]uril(CB[7]) on fluorescence properties and biocompatibility of the bis-viologen biphenyl molecule(BPV22+) was investigated by using 1 H NMR spectroscopy,fluorescence emission titration,and in vitro cytotoxicity experiments.CB[7] can be combined with BPV22+ in a stoichiometric ratio of 1:1 and 2:1.After the formation of host-guest complex,the fluorescence emission intensity of BPV22+ increased significantly,and the emission spectrum blue shifted.Meanwhile,the host-guest complexes showed better biocompatibility than BPV22+ in cell cytotoxicity studies.Results of this paper lay a foundation for the development of host-guest type of fluo rescent probes,biological imaging and so forth.展开更多
The surface enhanced fluorescence effect of acridine orange fluorophore in the proximity of Au nanoparticles has been investigated experimentally in the system of aqueous solution.Significant enhancement of the fluore...The surface enhanced fluorescence effect of acridine orange fluorophore in the proximity of Au nanoparticles has been investigated experimentally in the system of aqueous solution.Significant enhancement of the fluorescence intensity was observed when the system was excited with 532 nm or 442 nm CW lasers.The influence of the distances between neighboring Au particles as well as that between the fluorophore molecules and the Au surface were explored experimentally.The results demonstrated that a compact distribution of metallic particles was able to produce stronger fluorescence enhancement.Proper separation between the fluorophore molecules and the metal surface was favorable for a better enhancement.展开更多
The regulator of expression of virion(Rev)protein binds specifically to the Rev-responsive element(RRE)RNA in order to regulate the expression of the human immunodeficiency virus(HIV)-1 genes.Fluorescence indicator di...The regulator of expression of virion(Rev)protein binds specifically to the Rev-responsive element(RRE)RNA in order to regulate the expression of the human immunodeficiency virus(HIV)-1 genes.Fluorescence indicator displacement assays have been used to identify ligands that can inhibit the ReveRRE interaction;however,the small fluorescence indicators cannot fully replace the Rev peptide or protein.As a result,a single rhodamine B labeled Rev(RB-Rev)model peptide was utilized in this study to develop a direct and efficient ReveRRE inhibitor screening model.Due to photon-induced electron transfer quenching of the tryptophan residue on the RB fluorophore,the fluorescence of RB in Rev was weakened and could be dramatically reactivated by interaction with RRE RNA in ammonium acetate buffer(approximately six times).The interaction could reduce the electron transfer between tryptophan and RB,and RRE could also increase RB fluorescence.The inhibitor screening model was evaluated using three known positive ReveRRE inhibitors,namely,proflavin,6-chloro-9-[3-(2-chloroethylamino)propylamino]-2-methoxyacridine(ICR 191),and neomycin,as well as a negative drug,arginine.With the addition of the positive drugs,the fluorescence of the ReveRRE decreased,indicating the displacement of RB-Rev.This was confirmed using atomic force microscopy(AFM)and the fluorescence was essentially unaffected by the addition of arginine.The results demonstrated that RB-Rev can be used as a fluorescent probe for recognizing small ligands that target RRE RNA.The ReveRRE inhibitor screening model offers a novel approach to evaluating and identifying long-acting Rev inhibitors.展开更多
A facile and rapid approach for detecting low concentration of iron ion(Fe3+) with improved sensitivity was developed on the basis of plasmon enhanced fluorescence and subsequently amplified fluorescence quenching.Au1...A facile and rapid approach for detecting low concentration of iron ion(Fe3+) with improved sensitivity was developed on the basis of plasmon enhanced fluorescence and subsequently amplified fluorescence quenching.Au1Ag4@Si O2 nanoparticles were synthesized and dispersed into fluorescein isothiocyanate(FITC) solution. The fluorescence of the FITC solution was improved due to plasmon enhanced fluorescence. However, efficient fluorescence quenching of the FITC/Au1Ag4@Si O2 solution was subsequently achieved when Fe3+, with a concentration ranging from17 n M to 3.4 l M, was added into the FITC/Au1Ag4@Si O2 solution, whereas almost no fluorescence quenching was observed for pure FITC solution under the same condition. FITC/Au1Ag4@Si O2 solution shows a better sensitivity for detecting low concentration of Fe3+compared to pure FITC solution. The quantized limit of detection toward Fe3+was improved from 4.6 l M for pure FITC solution to 20 n M for FITC/Au1Ag4@Si O2 solution.展开更多
Ti_(2)C quantum dots(QDs)with rich surface functional groups have been synthesized using a hydrothermal method,and used to detect tetracycline(Tc)based on enhanced fluorescence.The interaction between the surface func...Ti_(2)C quantum dots(QDs)with rich surface functional groups have been synthesized using a hydrothermal method,and used to detect tetracycline(Tc)based on enhanced fluorescence.The interaction between the surface functional groups of Ti_(2)C QDs and Tc enhanced the fluorescence of Tc at 514 nm,which is used to detect Tc quickly and accurately.Under optimal conditions,the fluorescence intensity was linear to the concentration of Tc in the range of 50.0–30.0μM,with a detection limit of 21.6 nM.Furthermore,the Tc-Ti_(2)C QDs detection system was evaluated for detection of Tc in milk and artificial urine.This study demonstrates a new and simple strategy for Tc detection,which is important for food safety and human health.展开更多
Al nanoparticles(NPs)exhibit excellent localized surface plasmon resonance(LSPR)properties and have been considered a promising alternative to plasmonic Au or Ag NPs.However,it remains difficult to fabricate Al NPs wi...Al nanoparticles(NPs)exhibit excellent localized surface plasmon resonance(LSPR)properties and have been considered a promising alternative to plasmonic Au or Ag NPs.However,it remains difficult to fabricate Al NPs with uniform size and controllable morphology over a large area on substrates,which seriously hinders the in-depth exploration of their properties and applications.Herein,we have developed a self-assembly nanoparticle template method to realize the controllable preparation of bowl-shaped Al NPs(Al nanobowls(Al NBs))with tunable sizes from 36 to 131 nm on the substrate surface,accompanied by tunable LSPR spectral responses from 272 to 480 nm.Among them,131 nm Al NBs exhibit superior fluorescence enhancement ability(1932.2-fold)and a low detection limit(78.6 pM)towards 5-carboxyfluorescein,exceeding comparable Ag NBs and Au nanospheres(NSs).This can be attributed to the strong electromagnetic enhancement induced by the LSPR effect and the effective inhibition of fluorescence quenching caused by the self-passivated oxide layer.Therefore,the successful fabrication of Al NBs on substrates is of vital significance for their promising applications,including surface-enhanced spectroscopy,sensitive fluorescence detection,light-harvesting devices,biosensing,and ultraviolet(UV)plasmonics.展开更多
Some studies indicate that adipose derived stem cells(ADSCs)can differentiate into adipogenic,chondrogenic,myogenic,and osteogenic cells in vitro.However,whether ADSCs can be induced to differentiate into neural cells...Some studies indicate that adipose derived stem cells(ADSCs)can differentiate into adipogenic,chondrogenic,myogenic,and osteogenic cells in vitro.However,whether ADSCs can be induced to differentiate into neural cells in vitro has not been clearly demonstrated.In this study,the ADSCs isolated from the murine adipose tissue were cultured and transfected with the EGFP gene,and then the cells were induced for neural differentiation.The morphology of those ADSCs began to change within two days which developed into characteristics of round cell bodies with several branching extensions,concomitantly expressing EGFP fluorescence.Approximately 60% of the total cell populations were bipolar or multipolar in shape.Some of them appeared to make contact with their neighboring cells.RT-PCR,Western blot and Immunocytochemistry revealed that the expression levels of the markers of neurons and oligodendrocytes such as MAP2,NF-70,Neu N and RIP upon neural induction were increased,but the expression of the special marker of astrocytes,GFAP,was undetectable until 96h after induction when a small signal was observed.It was concluded that the ADSCs transfected with EGFP possessed the ability to undergo morphologic and phenotypic changes consistent with neural differentiation in vitro.It suggests that these cells might provide an ideal source for further stem cell research with possible therapeutic application for spinal cord injury.展开更多
Objective To develop retrovirus-mediated transfer of the fusion gene encoding EGFP-BMP2 in mesenchymal stem cells.Methods Mesenchymal stem cells from New Zealand white rabbits were transduced with retroviral pLEGFP-BM...Objective To develop retrovirus-mediated transfer of the fusion gene encoding EGFP-BMP2 in mesenchymal stem cells.Methods Mesenchymal stem cells from New Zealand white rabbits were transduced with retroviral pLEGFP-BMP2 vector by the optimized retroviral transduction protocol.Fluorescent microscopy’s examination was to evaluate the results of the transduction,flow cytometer’s analysis was to evaluate the transduction efficiency and the Fluorescence-activated cell sorting method was to sort the transduced cells.Bioactivity test from C2C12K4 cells was to show the expression and bio-activity of the fusion gene.Results Fluorescent microscopy showed the success of the transduction.By flow cytometer’s analysis,the mean efficiency of the transduction with EGFP was（42.8±6.1）% SD.Transduced cells were sorted efficiently by the fluorescence-activated cell sorting method and after sorting,almost of those showed the expression of BMP2.Fluorescently and strongly bioactivity test for C2C12K4 cells demonstrated that fluorescent materials were located the surface of cells and the activity of luciferase increased compared with the control.Analysis of long-term expression showed there was no difference between 2 week-time point and 3 month-time point of culture post-sorting.Conclusion Mesenchymal stem cells can be transduced efficiently by retrovirus-mediated transfer of the fusion gene encoding EGFP-BMP2,the highly pure transduced cells are obtained by the fluorescence-activated cell sorting technique,the expressed chimeric protein embraced the double bioactivity of EGFP and BMP2,and moreover,the expression had not attenuated over time.展开更多
We previously demonstrated that gene-modified umbilical cord blood mononuclear cells overexpressing a combination of recombinant neurotrophic factors are a promising therapeutic approach for cell-mediated gene therapy...We previously demonstrated that gene-modified umbilical cord blood mononuclear cells overexpressing a combination of recombinant neurotrophic factors are a promising therapeutic approach for cell-mediated gene therapy for neurodegenerative diseases,neurotrauma,and stroke.In this study,using a mini pig model of spinal cord injury,we proposed for the first time the use of gene-modified leucoconcentrate prepared from peripheral blood in the plastic blood bag for personalized ex vivo gene therapy.Leucoconcentrate obtained from mini pig peripheral blood was transduced with a chimeric adenoviral vector(Ad5/35 F)that carried an enhanced green fluorescent protein(EGFP)reporter gene in the plastic blood bag.The day after blood donation,the mini pigs were subjected to moderate SCI and four hours post-surgery they were intravenously autoinfused with gene-modified leucoconcentrate.A week after gene-modified leucoconcentrate therapy,fluorescent microscopy revealed EGFP-expressing leucocytes in spinal cord at the site of contusion injury.In the spleen the groups of EGFP-positive cells located in the lymphoid follicles were observed.In vitro flow cytometry and fluorescent microscopy studies of the gene-modified leucoconcentrate samples also confirmed the production of EGFP by leucocytes.Thus,the efficacy of leucocytes transduction in the plastic blood bag and their migratory potential suggest their use for temporary production of recombinant biologically active molecules to correct certain pathological conditions.This paper presents a proof-of-concept of simple,safe and effective approach for personalized ex vivo gene therapy based on gene-modified leucoconcentrate autoinfusion.The animal protocols were approved by the Kazan State Medical University Animal Care and Use Committee(approval No.5)on May 27,2014.展开更多
The spectral attenuation of a 400-nm probe laser propagating through a femtosecond plasma in air is studied.Defocusing effect of the low-density plasma is an obvious effect by examining the far-field patterns of the 4...The spectral attenuation of a 400-nm probe laser propagating through a femtosecond plasma in air is studied.Defocusing effect of the low-density plasma is an obvious effect by examining the far-field patterns of the 400-nm pulse.Besides,the energy of 400-nm pulse drops after interaction with the plasma,which is found to be another effect leading to the attenuation.To reveal the physical origin behind the energy loss,we measure fluorescence emissions of the interaction area.The fluorescence is hardly detected with the weak 400-nm laser pulse,and the line spectra from the plasma filament induced by the 800-nm pump pulse are clearly shown.However,when the 400-nm pulse propagates through the plasma filament,the fluorescence at 391 nm from the first negative band system of N2+is enhanced,while that from the second positive band of neutral N2 at 337 nm remains constant.Efficient near-resonant absorption of the 400-nm pulse by the first negative band system occurs inside the plasma,which results in the enhanced fluorescence.Furthermore,the spectral attenuation of the 400-nm probe laser is measured as a function of the pump–probe time delay as well as the pump-pulse energy.展开更多
We present a technique for fabricating a fluorescence enhancement device composed of metal nanoparticles(NPs) and porous silicon(PSi) diffraction grating.The fluorescence emission enhancement properties of the PSi and...We present a technique for fabricating a fluorescence enhancement device composed of metal nanoparticles(NPs) and porous silicon(PSi) diffraction grating.The fluorescence emission enhancement properties of the PSi and the fluorescence enhancement of the probe molecules are studied on PSi gratings.The fluorescence enhancement of the probe molecules on a fluorescence enhancement device is further improved through the deposition of metal NPs onto the PSi grating.In comparison to metal NP/PSi devices,metal NP periodic distributions can produce a stronger fluorescence enhancement that couples with the PSi grating fluorescence enhancement to achieve an overall three-fold enhancement of the fluorescence intensity.展开更多
Type-A spermatogonia first appear at between 3-7 d postnatally in mice and are the only immortalized diploid cells that reproduce in adulthood in these animals. In our current study, we explored the feasibility of pro...Type-A spermatogonia first appear at between 3-7 d postnatally in mice and are the only immortalized diploid cells that reproduce in adulthood in these animals. In our current study, we explored the feasibility of producing stable transgenic mice using these cells. Enhanced pEGFP-N1 plasmids were suspended in ExGen500 transfection reagent and injected at different angles into the testes of 7-d-old male ICR mice. The resulting type-A spermatogonia-mediated gene transfer (TASMGT) mice were then mated with normal females at different stages of sexual maturity (6, 12, and 24 wk). The integration and expression of the introduced EGFP gene was evaluated in the F1 transgenic offspring by PCR and Southern blotting analysis. The foreign gene integration rates for a low-dose group (15 μL gene suspension injected into each testis) and a high-dose group (30 μL suspensions injected) at the three stages of female sexual maturity tested were 11.76% (2/17), 14.29% (3/21), and 11.11% (2/18), and 5% (1/20), 5.56% (1/18), and 0 (0/17), respectively. The average integration rates for these two dose groups were 12.5% (7/56) and 3.64% (2/55), respectively, which was a significant difference (P<0.05). Semi-quantitative RT-PCR analysis further showed that the introduced GFP gene was expressed in 3/9 integration mice. In addition, GFP expression was observed in the sperm cells from the TASMGT mice, and also in the embryos and F2 pups from the F1 generation transgenic mice. Hence, although the foreign gene integration rate for TASMGT is not high and the transgenic offspring show as yet unexplained defects, our results indicate that this method is a potentially feasible and reproducible new approach to creating transgenic mice.展开更多
By the electrochemical anodization method,we achieve the single-layer macroporous silicon on the N-type silicon,and prepare gold nanoparticles with sodium citrate reduction method. Through injecting the gold nanoparti...By the electrochemical anodization method,we achieve the single-layer macroporous silicon on the N-type silicon,and prepare gold nanoparticles with sodium citrate reduction method. Through injecting the gold nanoparticles into the porous silicon by immersion,the fluorescence quenching mechanism of porous silicon influenced by gold nanoparticles is analyzed. Then the macroporous silicon deposited with gold nanoparticles is utilized to enhance the fluorescence of rhodamine 6G(R6G). It is found that when the macroporous silicon is deposited with gold nanoparticles for 6 h,the maximum fluorescence enhancement of R6G(about ten times) can be realized. The N-type porous silicon deposited with gold nanoparticles can be an excellent substrate for fluorescence detection.展开更多
Plasmonic enhanced fluorescence(PEF)technology is a powerful strategy to improve the sensitivity of immunofluorescence microarrays(IFMA),however,current approaches to constructing PEF platforms are either expensive/ti...Plasmonic enhanced fluorescence(PEF)technology is a powerful strategy to improve the sensitivity of immunofluorescence microarrays(IFMA),however,current approaches to constructing PEF platforms are either expensive/time-consuming or reliant on specialized instruments.Here,we develop a completely alternative approach relying on a two-step protocol that includes the self-assembly of gold nanoparticles(GNPs)at the water–oil interface and subsequent annealing-assisted regulation of gold nanogap.Our optimized thermal-annealing GNPs(TA-GNP)platform generates adequate hot spots,and thus produces high-density electromagnetic coupling,eventually enabling 240-fold fluorescence enhancement of probed dyes in the near-infrared region.For clinical detection of human samples,TA-GNP provides super-high sensitivity and low detection limits for both hepatitis B surface antigen and SARS-CoV-2 binding antibody,coupled with a much-improved detection dynamic range up to six orders of magnitude.With fast detection,high sensitivity,and low detection limit,TA-GNP could not only substantially improve the outcomes of IFMA-based precision medicine but also find applications in fields of proteomic research and clinical pathology.展开更多
Ru complexes([Ru(dpp)3]Cl2)were spin coated on poly(methyl methacrylate)(PMMA)opal photonic crystals(PhCs),and a,320-fold luminescence enhancement was observed compared to that on glass,which is the largest luminescen...Ru complexes([Ru(dpp)3]Cl2)were spin coated on poly(methyl methacrylate)(PMMA)opal photonic crystals(PhCs),and a,320-fold luminescence enhancement was observed compared to that on glass,which is the largest luminescence enhancement of dye molecules by the modulation of three-dimensional(3D)PhCs reported until now.The enhancement mechanism was carefully examined and it was shown that the luminescence of[Ru(dpp)3]Cl2 depended on the molecule concentration and temperature.It can be concluded that the suppressed non-radiative relaxation among the molecules and the field enhancement both contribute significantly to the luminescence enhancement.The PMMA PhC/Ru complex composites were then tested for their intracellular oxygen sensing and cell imaging properties;these composites effectively improved the limit of detection(LOD)and the brightness of the cell images.展开更多
Carbon dots(CDs)have been attracted much attention and widely studied due to their excellent fluorescence(FL)properties,better biocompatibility and outstanding photo/chemical stability.However,the disadvantage of lowe...Carbon dots(CDs)have been attracted much attention and widely studied due to their excellent fluorescence(FL)properties,better biocompatibility and outstanding photo/chemical stability.However,the disadvantage of lower quantum yield(QY)still limits its wide application.Herein,we reported a novel and convenient strategy to prepare photo-induced Ag/CDs(p-Ag/CDs)by irradiating the mixed Ag+and hydrophobic CDs(h-CDs)acetone solution with ultraviolet(UV)light.The obtained p-Ag/CDs exhibit a greatly enhanced FL emission together with a blue shift(460 nm)than h-CDs(520 nm).The QY of p-Ag/CDs is measured to be 51.1%,which is 10.4 times higher than that of h-CDs(4.9%),indicating that photo-induced Ag modulation can effectively improve the optical properties of CDs.The mechanisms for the FL enhancement and blue shift of h-CDs are studied in detail.The results prove that the greatly enhanced FL emission is from the generated Ag nanoparticles(AgNPs)by UV light irradiation based on metal-enhanced fluorescence(MEF),and the increased oxygen-contained groups in this process lead to the blue shift in CDs fluorescence.Interestingly,the p-Ag/CDs exhibit higher sensitivity and selectivity for sulfide ions(S2-)detection than that of h-CDs,which have a lower response to S2-.This work not only offers a novel strategy to improve the FL properties of materials but also endows them with new functions and broadens their application fields.展开更多
基金financially supported by the National Natural Science Foundation of China (No.51273048)Science and Technology Planning Project of Guangdong Province (No.2017B090915004)the Open Operation of Guangdong Provincial Key Laboratory of Advanced Coatings Research and Development (No.2017B030314105)
文摘A new substrate,aligned Ag nanowires decorated with silver nanoparticle composite structure(AgNWs@AgNPs),was fabricated to investigate metalenhanced fluorescence(MEF) and its mechanism.The new composite structure was fabricated via a three-phase interface assembly method followed by SnCl2 sensitization and AgNO3 reduction process.The size and distribution of the nanoparticles on silver nanowires increased with the sensitization and reduction cycles.The formation of AgNPs on the surfaces of AgNWs was confirmed by multiple characterization methods including scanning electron microscopy(SEM),transmission electron microscope(TEM),atomic force microscopy(AFM) and X-ray diffraction(XRD).The results show that the fluorescence intensity of the poly(3-hexylthiophene)(P3HT) on the composite structure was greatly enhanced compared with that on bare glass substrate,and the intensity increased with the increase in particle sizes and density.The mechanism was basedo n the increase in excitation rate and the radiation decay rate.The new type of substrate could serve as a good and efficient MEF substrate for high-performance fluorescence-based devices.
基金supported by the National Natural Science Foundation of China(21972060)。
文摘A new water-stable europium MOF,(Me_(2)NH_(2))[Eu(abtc)(phen)]·2H_(2)O (1),has been synthesized from Eu(NO_(3))_(3)·6H_(2)O with 1,10-phenanthroline (phen) and 3,3′,5,5′-azobenzenetetracarboxylic acid (H_4abtc) ligands under solvothermal conditions and structurally characterized by single-crystal X-ray diffraction analysis,IR,TGA and PXRD.It crystallizes in monoclinic system,C2/c space group,with a=16.278(3),b=14.261(3),c=27.936(5)?,b=103.464(3)°,V=6307(2)A^(3),Z=8,C_(30)H_(26)Eu N_5O_(10),M_(r)=768.5,D_(c)=1.543 g/cm^(3),F(000)=2912,m(Mo Ka)=2.044 mm^(-1),R=0.0315 and w R=0.0663.In the structure of 1,the Eu O_7N_(2) polyhedra are assembled into a 2D layer with rhombic windows and these layers are further condensed to form a 3D framework.It can be used as selective and sensitive fluorescence sensors capable of detecting diethyl ether vapor.
基金supported by National Natural Science Foundation of China (Grant No 50872091)the Natural Science Foundation of Tianjin,China(06YFJMJC02300,06TXTJJC14602)
文摘Fluorescence enhancement of red and blue concurrently emitting Ba3MgSi2O8:Eu2+,Mn2+ phosphors for plant cultivation has been investigated by Dy3+ addition.The Ba3MgSi2O8:Eu2+,Mn2+,Dy3+(BMS-EMD) phosphors have two-color emissions at the wavelength peak values of 437 nm and 620 nm at the excitation of 350 nm.The two emission bands are coincident with the absorption spectrum for photosynthesis of plants.An obvious enhancement effect has been observed upon addition of Dy3+ with amount of 0.03 mol%,in which the intensities of both blue and red bands reach a maximum.The origin of red and blue emission bands is analysed.The photochromic parameters of the samples at the nearly UV excitation are tested.This fluoresence enhancement is of great significance for special solid state lighting equipment used in plant cultivation.
基金supported by the National Natural Science Foundation of China (No.21374055)the Fundamental Research Funds of Shandong University (No.11190078614092)。
文摘The effect of cucurbit[7]uril(CB[7]) on fluorescence properties and biocompatibility of the bis-viologen biphenyl molecule(BPV22+) was investigated by using 1 H NMR spectroscopy,fluorescence emission titration,and in vitro cytotoxicity experiments.CB[7] can be combined with BPV22+ in a stoichiometric ratio of 1:1 and 2:1.After the formation of host-guest complex,the fluorescence emission intensity of BPV22+ increased significantly,and the emission spectrum blue shifted.Meanwhile,the host-guest complexes showed better biocompatibility than BPV22+ in cell cytotoxicity studies.Results of this paper lay a foundation for the development of host-guest type of fluo rescent probes,biological imaging and so forth.
基金supported by the Foundation for the Key Project of the Chinese Ministry of Education (Grant No. 108118)the Fundamental Research Funds for the Central Universities (Grant No. GK200901022)
文摘The surface enhanced fluorescence effect of acridine orange fluorophore in the proximity of Au nanoparticles has been investigated experimentally in the system of aqueous solution.Significant enhancement of the fluorescence intensity was observed when the system was excited with 532 nm or 442 nm CW lasers.The influence of the distances between neighboring Au particles as well as that between the fluorophore molecules and the Au surface were explored experimentally.The results demonstrated that a compact distribution of metallic particles was able to produce stronger fluorescence enhancement.Proper separation between the fluorophore molecules and the metal surface was favorable for a better enhancement.
基金supported by the Natural Science Foundation of Shaanxi Province of China(Grant No.:202012119)the Start-up Funding of Shaanxi University of Science and Technology(Grant No.:2019BJ-48)the Innovation Capability Support Program of Shaanxi Province of China(Grant No.:2021PT-044).
文摘The regulator of expression of virion(Rev)protein binds specifically to the Rev-responsive element(RRE)RNA in order to regulate the expression of the human immunodeficiency virus(HIV)-1 genes.Fluorescence indicator displacement assays have been used to identify ligands that can inhibit the ReveRRE interaction;however,the small fluorescence indicators cannot fully replace the Rev peptide or protein.As a result,a single rhodamine B labeled Rev(RB-Rev)model peptide was utilized in this study to develop a direct and efficient ReveRRE inhibitor screening model.Due to photon-induced electron transfer quenching of the tryptophan residue on the RB fluorophore,the fluorescence of RB in Rev was weakened and could be dramatically reactivated by interaction with RRE RNA in ammonium acetate buffer(approximately six times).The interaction could reduce the electron transfer between tryptophan and RB,and RRE could also increase RB fluorescence.The inhibitor screening model was evaluated using three known positive ReveRRE inhibitors,namely,proflavin,6-chloro-9-[3-(2-chloroethylamino)propylamino]-2-methoxyacridine(ICR 191),and neomycin,as well as a negative drug,arginine.With the addition of the positive drugs,the fluorescence of the ReveRRE decreased,indicating the displacement of RB-Rev.This was confirmed using atomic force microscopy(AFM)and the fluorescence was essentially unaffected by the addition of arginine.The results demonstrated that RB-Rev can be used as a fluorescent probe for recognizing small ligands that target RRE RNA.The ReveRRE inhibitor screening model offers a novel approach to evaluating and identifying long-acting Rev inhibitors.
基金supported by the National Natural Science Foundation of China (51003069)Natural Science Foundation of Jiangsu Higher Education Institutions of China (10KJB430014)A Project Funded by the Priority Academic Program Development of Jiangsu Higher Education Institutions
文摘A facile and rapid approach for detecting low concentration of iron ion(Fe3+) with improved sensitivity was developed on the basis of plasmon enhanced fluorescence and subsequently amplified fluorescence quenching.Au1Ag4@Si O2 nanoparticles were synthesized and dispersed into fluorescein isothiocyanate(FITC) solution. The fluorescence of the FITC solution was improved due to plasmon enhanced fluorescence. However, efficient fluorescence quenching of the FITC/Au1Ag4@Si O2 solution was subsequently achieved when Fe3+, with a concentration ranging from17 n M to 3.4 l M, was added into the FITC/Au1Ag4@Si O2 solution, whereas almost no fluorescence quenching was observed for pure FITC solution under the same condition. FITC/Au1Ag4@Si O2 solution shows a better sensitivity for detecting low concentration of Fe3+compared to pure FITC solution. The quantized limit of detection toward Fe3+was improved from 4.6 l M for pure FITC solution to 20 n M for FITC/Au1Ag4@Si O2 solution.
基金supported by the National Natural Science Foundation of China(Nos.22175019 and 52002007)the Fundamental Research Funds for the Central Universitiesthe Youth Teacher International Exchange&Growth Program(No.QNXM20220019).
文摘Ti_(2)C quantum dots(QDs)with rich surface functional groups have been synthesized using a hydrothermal method,and used to detect tetracycline(Tc)based on enhanced fluorescence.The interaction between the surface functional groups of Ti_(2)C QDs and Tc enhanced the fluorescence of Tc at 514 nm,which is used to detect Tc quickly and accurately.Under optimal conditions,the fluorescence intensity was linear to the concentration of Tc in the range of 50.0–30.0μM,with a detection limit of 21.6 nM.Furthermore,the Tc-Ti_(2)C QDs detection system was evaluated for detection of Tc in milk and artificial urine.This study demonstrates a new and simple strategy for Tc detection,which is important for food safety and human health.
基金This work was supported by the National Natural Science Foundation of China(Nos.22072104 and 21822202)Suzhou Key Laboratory of Surface and Interface Intelligent Matter(No.SZS2022011)This is also a project funded by Suzhou Key Laboratory of Functional Nano&Soft Materials,Collaborative Innovation Center of Suzhou Nano Science&Technology,the 111 Project,Joint International Research Laboratory of Carbon-Based Functional Materials and Devices.
文摘Al nanoparticles(NPs)exhibit excellent localized surface plasmon resonance(LSPR)properties and have been considered a promising alternative to plasmonic Au or Ag NPs.However,it remains difficult to fabricate Al NPs with uniform size and controllable morphology over a large area on substrates,which seriously hinders the in-depth exploration of their properties and applications.Herein,we have developed a self-assembly nanoparticle template method to realize the controllable preparation of bowl-shaped Al NPs(Al nanobowls(Al NBs))with tunable sizes from 36 to 131 nm on the substrate surface,accompanied by tunable LSPR spectral responses from 272 to 480 nm.Among them,131 nm Al NBs exhibit superior fluorescence enhancement ability(1932.2-fold)and a low detection limit(78.6 pM)towards 5-carboxyfluorescein,exceeding comparable Ag NBs and Au nanospheres(NSs).This can be attributed to the strong electromagnetic enhancement induced by the LSPR effect and the effective inhibition of fluorescence quenching caused by the self-passivated oxide layer.Therefore,the successful fabrication of Al NBs on substrates is of vital significance for their promising applications,including surface-enhanced spectroscopy,sensitive fluorescence detection,light-harvesting devices,biosensing,and ultraviolet(UV)plasmonics.
基金supported by the "Eleventh Five-Year" plan to support the National Science and Technology key project(No.2007BAI04B07)a grant from National Natural Sciences Foundation of China(No.30772206)
文摘Some studies indicate that adipose derived stem cells(ADSCs)can differentiate into adipogenic,chondrogenic,myogenic,and osteogenic cells in vitro.However,whether ADSCs can be induced to differentiate into neural cells in vitro has not been clearly demonstrated.In this study,the ADSCs isolated from the murine adipose tissue were cultured and transfected with the EGFP gene,and then the cells were induced for neural differentiation.The morphology of those ADSCs began to change within two days which developed into characteristics of round cell bodies with several branching extensions,concomitantly expressing EGFP fluorescence.Approximately 60% of the total cell populations were bipolar or multipolar in shape.Some of them appeared to make contact with their neighboring cells.RT-PCR,Western blot and Immunocytochemistry revealed that the expression levels of the markers of neurons and oligodendrocytes such as MAP2,NF-70,Neu N and RIP upon neural induction were increased,but the expression of the special marker of astrocytes,GFAP,was undetectable until 96h after induction when a small signal was observed.It was concluded that the ADSCs transfected with EGFP possessed the ability to undergo morphologic and phenotypic changes consistent with neural differentiation in vitro.It suggests that these cells might provide an ideal source for further stem cell research with possible therapeutic application for spinal cord injury.
基金This work was supported by the National Natural Science Foundation of China(No.30400163).
文摘Objective To develop retrovirus-mediated transfer of the fusion gene encoding EGFP-BMP2 in mesenchymal stem cells.Methods Mesenchymal stem cells from New Zealand white rabbits were transduced with retroviral pLEGFP-BMP2 vector by the optimized retroviral transduction protocol.Fluorescent microscopy’s examination was to evaluate the results of the transduction,flow cytometer’s analysis was to evaluate the transduction efficiency and the Fluorescence-activated cell sorting method was to sort the transduced cells.Bioactivity test from C2C12K4 cells was to show the expression and bio-activity of the fusion gene.Results Fluorescent microscopy showed the success of the transduction.By flow cytometer’s analysis,the mean efficiency of the transduction with EGFP was（42.8±6.1）% SD.Transduced cells were sorted efficiently by the fluorescence-activated cell sorting method and after sorting,almost of those showed the expression of BMP2.Fluorescently and strongly bioactivity test for C2C12K4 cells demonstrated that fluorescent materials were located the surface of cells and the activity of luciferase increased compared with the control.Analysis of long-term expression showed there was no difference between 2 week-time point and 3 month-time point of culture post-sorting.Conclusion Mesenchymal stem cells can be transduced efficiently by retrovirus-mediated transfer of the fusion gene encoding EGFP-BMP2,the highly pure transduced cells are obtained by the fluorescence-activated cell sorting technique,the expressed chimeric protein embraced the double bioactivity of EGFP and BMP2,and moreover,the expression had not attenuated over time.
基金the Russian Science Foundation(No.16-15-00010to RRI)the Russian Government Program of Competitive Growth of Kazan Federal University。
文摘We previously demonstrated that gene-modified umbilical cord blood mononuclear cells overexpressing a combination of recombinant neurotrophic factors are a promising therapeutic approach for cell-mediated gene therapy for neurodegenerative diseases,neurotrauma,and stroke.In this study,using a mini pig model of spinal cord injury,we proposed for the first time the use of gene-modified leucoconcentrate prepared from peripheral blood in the plastic blood bag for personalized ex vivo gene therapy.Leucoconcentrate obtained from mini pig peripheral blood was transduced with a chimeric adenoviral vector(Ad5/35 F)that carried an enhanced green fluorescent protein(EGFP)reporter gene in the plastic blood bag.The day after blood donation,the mini pigs were subjected to moderate SCI and four hours post-surgery they were intravenously autoinfused with gene-modified leucoconcentrate.A week after gene-modified leucoconcentrate therapy,fluorescent microscopy revealed EGFP-expressing leucocytes in spinal cord at the site of contusion injury.In the spleen the groups of EGFP-positive cells located in the lymphoid follicles were observed.In vitro flow cytometry and fluorescent microscopy studies of the gene-modified leucoconcentrate samples also confirmed the production of EGFP by leucocytes.Thus,the efficacy of leucocytes transduction in the plastic blood bag and their migratory potential suggest their use for temporary production of recombinant biologically active molecules to correct certain pathological conditions.This paper presents a proof-of-concept of simple,safe and effective approach for personalized ex vivo gene therapy based on gene-modified leucoconcentrate autoinfusion.The animal protocols were approved by the Kazan State Medical University Animal Care and Use Committee(approval No.5)on May 27,2014.
基金Project supported by the National Natural Science Foundation of China(Grant Nos.U1932133,51733004,51525303,and 21702085)the Fundamental Research Funds for the Central Universities,China(Grant Nos.lzujbky-2016-35 and lzujbky-2018-it36)
文摘The spectral attenuation of a 400-nm probe laser propagating through a femtosecond plasma in air is studied.Defocusing effect of the low-density plasma is an obvious effect by examining the far-field patterns of the 400-nm pulse.Besides,the energy of 400-nm pulse drops after interaction with the plasma,which is found to be another effect leading to the attenuation.To reveal the physical origin behind the energy loss,we measure fluorescence emissions of the interaction area.The fluorescence is hardly detected with the weak 400-nm laser pulse,and the line spectra from the plasma filament induced by the 800-nm pump pulse are clearly shown.However,when the 400-nm pulse propagates through the plasma filament,the fluorescence at 391 nm from the first negative band system of N2+is enhanced,while that from the second positive band of neutral N2 at 337 nm remains constant.Efficient near-resonant absorption of the 400-nm pulse by the first negative band system occurs inside the plasma,which results in the enhanced fluorescence.Furthermore,the spectral attenuation of the 400-nm probe laser is measured as a function of the pump–probe time delay as well as the pump-pulse energy.
基金supported by the National Natural Science Foundation of China under Grant Nos.61575168 and 61665012
文摘We present a technique for fabricating a fluorescence enhancement device composed of metal nanoparticles(NPs) and porous silicon(PSi) diffraction grating.The fluorescence emission enhancement properties of the PSi and the fluorescence enhancement of the probe molecules are studied on PSi gratings.The fluorescence enhancement of the probe molecules on a fluorescence enhancement device is further improved through the deposition of metal NPs onto the PSi grating.In comparison to metal NP/PSi devices,metal NP periodic distributions can produce a stronger fluorescence enhancement that couples with the PSi grating fluorescence enhancement to achieve an overall three-fold enhancement of the fluorescence intensity.
基金supported by the National Transgenic Breeding Project (2008ZX08010-004)the National Natural Science Foundation of China (30830080)+1 种基金the National 973 Program of China (G2006CB102105,2009CB941604)the National 863 Program of China (20060110Z1039, 2008AA10Z143)
文摘Type-A spermatogonia first appear at between 3-7 d postnatally in mice and are the only immortalized diploid cells that reproduce in adulthood in these animals. In our current study, we explored the feasibility of producing stable transgenic mice using these cells. Enhanced pEGFP-N1 plasmids were suspended in ExGen500 transfection reagent and injected at different angles into the testes of 7-d-old male ICR mice. The resulting type-A spermatogonia-mediated gene transfer (TASMGT) mice were then mated with normal females at different stages of sexual maturity (6, 12, and 24 wk). The integration and expression of the introduced EGFP gene was evaluated in the F1 transgenic offspring by PCR and Southern blotting analysis. The foreign gene integration rates for a low-dose group (15 μL gene suspension injected into each testis) and a high-dose group (30 μL suspensions injected) at the three stages of female sexual maturity tested were 11.76% (2/17), 14.29% (3/21), and 11.11% (2/18), and 5% (1/20), 5.56% (1/18), and 0 (0/17), respectively. The average integration rates for these two dose groups were 12.5% (7/56) and 3.64% (2/55), respectively, which was a significant difference (P<0.05). Semi-quantitative RT-PCR analysis further showed that the introduced GFP gene was expressed in 3/9 integration mice. In addition, GFP expression was observed in the sperm cells from the TASMGT mice, and also in the embryos and F2 pups from the F1 generation transgenic mice. Hence, although the foreign gene integration rate for TASMGT is not high and the transgenic offspring show as yet unexplained defects, our results indicate that this method is a potentially feasible and reproducible new approach to creating transgenic mice.
基金supported by the National Natural Science Foundation of China(Nos.61308120,61575168 and 11264038)the Doctor Startup Project of Xinjiang University(No.BS120122)+1 种基金the Young Talents Project in Xinjiang Uygur Autonomous Region(No.2013731003)the Xinjiang Science and Technology Project(Nos.2015211C262 and 2014211B003)
文摘By the electrochemical anodization method,we achieve the single-layer macroporous silicon on the N-type silicon,and prepare gold nanoparticles with sodium citrate reduction method. Through injecting the gold nanoparticles into the porous silicon by immersion,the fluorescence quenching mechanism of porous silicon influenced by gold nanoparticles is analyzed. Then the macroporous silicon deposited with gold nanoparticles is utilized to enhance the fluorescence of rhodamine 6G(R6G). It is found that when the macroporous silicon is deposited with gold nanoparticles for 6 h,the maximum fluorescence enhancement of R6G(about ten times) can be realized. The N-type porous silicon deposited with gold nanoparticles can be an excellent substrate for fluorescence detection.
基金supported by the National Natural Science Foundation of China(Nos.21975098 and 22275071)the program for JLU Science and Technology Innovative Research Team(No.2017TD-06)the opening funds of State Key Laboratory of Applied Optics,Changchun Institute of Optics,Fine Mechanics and Physics,Chinese Academy of Science,and the China Postdoctoral Science Foundation(Nos.2020TQ0119 and 2020M681046).
文摘Plasmonic enhanced fluorescence(PEF)technology is a powerful strategy to improve the sensitivity of immunofluorescence microarrays(IFMA),however,current approaches to constructing PEF platforms are either expensive/time-consuming or reliant on specialized instruments.Here,we develop a completely alternative approach relying on a two-step protocol that includes the self-assembly of gold nanoparticles(GNPs)at the water–oil interface and subsequent annealing-assisted regulation of gold nanogap.Our optimized thermal-annealing GNPs(TA-GNP)platform generates adequate hot spots,and thus produces high-density electromagnetic coupling,eventually enabling 240-fold fluorescence enhancement of probed dyes in the near-infrared region.For clinical detection of human samples,TA-GNP provides super-high sensitivity and low detection limits for both hepatitis B surface antigen and SARS-CoV-2 binding antibody,coupled with a much-improved detection dynamic range up to six orders of magnitude.With fast detection,high sensitivity,and low detection limit,TA-GNP could not only substantially improve the outcomes of IFMA-based precision medicine but also find applications in fields of proteomic research and clinical pathology.
基金This work was supported by the Major State Basic Research Development Program of China(No.2014CB643506)the National Natural Science Foundation of China(Grant Nos.11374127,11304118,61204015,81201738,61177042 and 11174111)the Program for Chang Jiang Scholars and Innovative Research Teams in the University(No.IRT13018).
文摘Ru complexes([Ru(dpp)3]Cl2)were spin coated on poly(methyl methacrylate)(PMMA)opal photonic crystals(PhCs),and a,320-fold luminescence enhancement was observed compared to that on glass,which is the largest luminescence enhancement of dye molecules by the modulation of three-dimensional(3D)PhCs reported until now.The enhancement mechanism was carefully examined and it was shown that the luminescence of[Ru(dpp)3]Cl2 depended on the molecule concentration and temperature.It can be concluded that the suppressed non-radiative relaxation among the molecules and the field enhancement both contribute significantly to the luminescence enhancement.The PMMA PhC/Ru complex composites were then tested for their intracellular oxygen sensing and cell imaging properties;these composites effectively improved the limit of detection(LOD)and the brightness of the cell images.
基金the National Natural Science Foundation of China(Nos.U1833202 and 21876117)the Open Research Fund of the School of Chemistry and Chemical Engineering,Henan Normal University(No.2021YB05).
文摘Carbon dots(CDs)have been attracted much attention and widely studied due to their excellent fluorescence(FL)properties,better biocompatibility and outstanding photo/chemical stability.However,the disadvantage of lower quantum yield(QY)still limits its wide application.Herein,we reported a novel and convenient strategy to prepare photo-induced Ag/CDs(p-Ag/CDs)by irradiating the mixed Ag+and hydrophobic CDs(h-CDs)acetone solution with ultraviolet(UV)light.The obtained p-Ag/CDs exhibit a greatly enhanced FL emission together with a blue shift(460 nm)than h-CDs(520 nm).The QY of p-Ag/CDs is measured to be 51.1%,which is 10.4 times higher than that of h-CDs(4.9%),indicating that photo-induced Ag modulation can effectively improve the optical properties of CDs.The mechanisms for the FL enhancement and blue shift of h-CDs are studied in detail.The results prove that the greatly enhanced FL emission is from the generated Ag nanoparticles(AgNPs)by UV light irradiation based on metal-enhanced fluorescence(MEF),and the increased oxygen-contained groups in this process lead to the blue shift in CDs fluorescence.Interestingly,the p-Ag/CDs exhibit higher sensitivity and selectivity for sulfide ions(S2-)detection than that of h-CDs,which have a lower response to S2-.This work not only offers a novel strategy to improve the FL properties of materials but also endows them with new functions and broadens their application fields.
