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1.
    
Quantum dots (QDs) are significant fluorescent materials for energy transfer studies with phthalocyanines (Pcs) and phthalocyanine (Pc)-like biomolecules (such as chlorophylls). Carbon-based QDs, especially, have been used in numerous studies concerning energy transfer with chlorophylls, but the numbers of studies concerning energy transfer between phthalocyanines and carbon-based QDs are limited. In this study, peripherally, hydroxythioethyl terminal group substituted metal-free phthalocyanine (H2Pc) and zinc phthalocyanine (ZnPc) were noncovalently (electrostatic and/or π–π interaction) attached to carbon QDs containing boron and nitrogen to form QD-Pc nanoconjugates. The QD-Pc conjugates were characterized using different spectroscopic techniques (Fourier transform infrared spectroscopy and transmission electron microscopy). The absorption and fluorescence properties of QD-Pc structures in solution were studied. It was found that the quantum yields of the QDs slightly decreased from 30% to 25% upon doping the QDs with heteroatoms B and N. Förster resonance energy transfer efficiency was calculated as 33% for BCN-QD/ZnPc. For the other conjugates, almost no energy transfer from QDs to Pc cores was observed. It was shown that the energy transfer between QDs to Pc cores was completely different from the energy transfer between QDs and photosynthetic pigments, and therefore we concluded that heteroatom doping in the QD structure and the existence of zinc metal in the phthalocyanine structure is obligatory for an efficient energy transfer.  相似文献   

2.
    
We compared the effects of several ligands frequently used in aqueous synthesis, including L‐cysteine, L‐cysteine hydrochloride, N‐acetyl‐L‐cysteine (NAC), glutathione and 3‐mercaptopropionic acid, for microwave synthesis of CdTe quantum dots (QDs) in a sealed vessel with varied temperatures and times, and then developed a rapid microwave‐assisted protocol for preparing highly luminescent, photostable and biocompatible CdTe/CdS/ZnS core–multishell QDs. The effects of molecular structures of these ligands on QD synthesis under high temperatures were explored. Among these ligands, NAC was found to be the optimal ligand in terms of the optical properties of resultant QDs and reaction conditions. The emission wavelength of NAC‐capped CdTe QDs could reach 700 nm in 5 min by controlling the reaction temperature, and the resultant CdTe/CdS/ZnS core–multishell QDs could achieve the highest quantum yields up to 74% with robust photostability. In addition, the effects of temperature, growth time and shell–precursor ratio on shell growth were examined. Finally, cell culturing indicated the low cytotoxicity of CdTe/CdS/ZnS core–multishell QDs as compared to CdTe and CdTe/CdS QDs, suggesting their high potential for applications in biomedical imaging and diagnostics. Copyright © 2014 John Wiley & Sons, Ltd.  相似文献   

3.
    
Two quantum dots (QDs), a green emitter, CdSe and a red emitter, CdSe with ZnS shell are encapsulated into novel liposomes in two different formulations including cationic liposomes. Quantum dots have proven themselves as powerful inorganic fluorescent probes, especially for long‐term, multiplexed imaging and detection. Upon delivery into a cell, in endocytic vesicles such as endosomes, their fluorescence is quenched. We have investigated the potential toxic effects, photophysical properties and cell internalization of QDs in new formulation of liposomes as an in vitro vesicle model. Entrapment of QDs into liposomes is brought about with a decrease in their intrinsic fluorescence and toxicities and an increase in their photostability and lifetime. The biomimetic lipid bilayer of liposomes provides high biocompatibility, thereby enhancing the effectiveness of fluorescent nanoparticles for biological recognition in vitro and in vivo. The prepared lipodots could effectively prevent QDs from photo‐oxidation during storage and when exposed to ultraviolet (UV) light. Moreover, the flow cytometry of HEK 293 T cells showed that the cell internalization of encapsulated QDs in (DSPC/CHO/DOPE/DOAB) liposome is enhanced 10 times compared with non‐encapsulated QD (bare QDs).  相似文献   

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In this paper, we described a strategy for synthesis of thiol‐coated CdTe/CdS/ZnS (core–shell–shell) quantum dots (QDs) via aqueous synthesis approach. The synthesis conditions were systematically optimized, which included the size of CdTe core, the refluxing time and the number of monolayers and the ligands, and then the chemical and optical properties of the as‐prepared products were investigated. We found that the mercaptopropionic acid (MPA)‐coated CdTe/CdS/ZnS QDs presented highly photoluminescent quantum yields (PL QYs), good photostability and chemical stability, good salt tolerance and pH tolerance and favorable biocompatibility. The characterization of high‐resolution transmission electron microscopy (HRTEM), X‐ray powder diffraction (XRD) and fluorescence correlation spectroscopy (FCS) showed that the CdTe/CdS/ZnS QDs had good monodispersity and crystal structure. The fluorescence life time spectra demonstrated that CdTe/CdS/ZnS QDs had a longer lifetime in contrast to fluorescent dyes and CdTe QDs. Furthermore, the MPA‐stabilized CdTe/CdS/ZnS QDs were applied for the imaging of cells. Compared with current synthesis methods, our synthesis approach was reproducible and simple, and the reaction conditions were mild. More importantly, our method was cost‐effective, and was very suitable for large‐scale synthesis of CdTe/CdS/ZnS QDs for future applications. Copyright © 2010 John Wiley & Sons, Ltd.  相似文献   

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7.
Intracellular trafficking of endocytic vesicles in eukaryotes varies with the nature of the cargo molecules and the targeted organelle, and proceeds through an intricate network of internal endosomal compartments. However, the path for fluid-phase endocytosis (FPE), the internalization of external solutes from the apoplast via plasmalemma generated vesicles, remains unresolved despite some indication of a direct transport route to the vacuole. To test this hypothesis, we made use of the membrane-impermeable Na-dependent fluorescent marker Coro-Na in combination with the fluorescent membrane marker FM 4-64 and confocal laser scanning microscopy. When protoplasts from sweet lime juice cells were incubated in Na-free solution, FM 4-64, Coro-Na, and 200 mM sucrose, two distinct types of labeled vesicles were evident. A set of vesicles (1 μm in diameter) was intensely labeled with Coro-Na and to a lesser extent with FM 4-64, whereas the second type of 1–7 μm structures appeared exclusively labeled with FM 4-64. These data demonstrate the parallel functioning of two endocytic pathways in plant cells. In one system, a set of small endocytic vesicles merge with the endosome, whereas a separate set of vesicles fuse to form larger vesicles independent from the endosome. Although it is likely that both vesicle systems eventually contribute to solutes reaching the vacuole, given their size (1–7 μm), and based on previous observations of endocytic vesicle formation protruding from the plasmalemma and merging with the vacuole, we conclude that these latter vesicles constitute the primary FPE vesicle system.  相似文献   

8.
    
The use of nanoparticles in stem cell research is relatively recent, although very significant in the last 5 years with the publication of about 400 papers. The recent advances in the preparation of some nanomaterials, growing awareness of material science and tissue engineering researchers regarding the potential of stem cells for regenerative medicine, and advances in stem cell biology have contributed towards the boost of this research field in the last few years. Most of the research has been focused in the development of new nanoparticles for stem cell imaging; however, these nanoparticles have several potential applications such as intracellular drug carriers to control stem cell differentiation and biosensors to monitor in real time the intracellular levels of relevant biomolecules/enzymes. This review examines recent advances in the use of nanoparticles for stem cell tracking, differentiation and biosensing. We further discuss their utility and the potential concerns regarding their cytotoxicity. J. Cell. Biochem. 108: 746–752, 2009. © 2009 Wiley‐Liss, Inc.  相似文献   

9.
    
The dissociation of O2 and HO2 are important reactions that occur at the cathode of fuel cells and require catalysts to proceed. There is a need to replace the presently used platinum catalyst with less expensive materials. Modelling has been used to identify potential two-dimensional catalysts such as boron- and nitrogen-doped graphene. Here, the possibility of boron nitride nano-ribbons and nano-tubes which do not require doping are considered. Density functional calculations are used to show that O2 and HO2 can bond to zig–zag and armchair boron nitride nano-ribbons and nano-tubes. The bond dissociation energies (BDEs) to remove an O and an OH from O2 and HO2 bonded to the boron nitride ribbons and tubes are calculated and are a measure of the catalytic effectiveness of the boron nitride structures. The results show that both the zig–zag and armchair boron nitride ribbons could be a catalyst for HO2 dissociation but not O2 dissociation. However, zig–zag boron nitride nano-tubes are shown not to be effective catalysts for the dissociation of O2 or HO2. An armchair boron nitride nano-tube is shown to have a very low BDEs to remove OH from HO2 bonded to it and could be an affective catalyst.  相似文献   

10.
    
A series of glutathione (GSH)-capped aqueous CdS quantum dots (QDs) with strong photoluminescence (PL) were prepared by changing the reaction temperatures and times on the basis of optimization of the mole ratio of S to Cd. The reaction time was shortened to about 1/10 compared with that reported previously by increasing the reaction temperature. The absorption and fluorescence spectra indicated good optical properties with PL full width of half-maximum (FWHM) of about 100 nm. The excitation spectrum was broad and continuous in the range 200-480 nm. The PL quantum efficiency (QE) of the prepared QDs was about 36% compared with rhodamine 6G (95%). The shape and size of the CdS QDs were characterized using high-resolution transmission electron microscopy (HRTEM). The prepared QDs were conjugated with bovine serum albumin (BSA) and onion inner pellicle cells and used as fluorescence probes for the first time. The results demonstrated that the fluorescence of CdS can be enhanced by BSA and the enhanced fluorescence intensity is proportional to the concentration of BSA in the range 1.0-10 mg/L. The aggregation of CdS in onion inner pellicle cells and its fluorescence images indicated that the QDs can aggregate around cells soaked for 8 h in CdS solution but enter the interior of cells and become aggregated to the nucleus when they are soaked in CdS solution for longer, e.g. 98 h.  相似文献   

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半导体量子点具有长时间、多目标和灵敏度高等独特的光化学性质,这些特性使量子点成为细胞标记和生物应用中得到了广泛的应用。利用量子点目标定位癌细胞,对于寻找癌变部位具有指导的作用。近年来,利用量子点作为光动力学治疗癌症的能量供体也得到了一定的研究。简单地介绍了量子点独特的光学性质,并从量子点标记癌细胞、可视化癌细胞表面功能和在光动力学治疗癌症等方面综述了量子点在癌症诊断和治疗中的应用。  相似文献   

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14.
Bellaloui  Nacer  Brown  Patrick H. 《Plant and Soil》1998,198(2):153-158
Species and cultivar differences in boron (B) uptake at low B availability and tolerance to high external B are known for many species but mechanisms explaining such differences remain obscure. Here we contrast B uptake and distribution between two cultivars of tomato and celery that differ significantly in their susceptibility to B deficiency. The celery cultivar S48-54-1 and tomato cultivar Brittle are known to be more susceptible to B deficiency (inefficient) than the closely related cultivars Emerson Pascal and Rutgers (efficient), respectively. B uptake and distribution was also compared in two wheat lines differing in tolerance to B excess (Chinese Spring, sensitive and Lophopyrum Amphiploid, tolerant). Results showed that there is no significant difference in either the specific uptake rate (IM) of 10B or the relative growth rate (RGR) between the efficient cultivar (Emerson Pascal) and less efficient cultivar (S48-54-1) of celery. However, the distribution of 10B among plant organs (leaves, stems and roots) of Emerson Pascal was different from S48-54-1. In Emerson Pascal more than 63% of accumulated B was present in the shoots while in S48-54-1 only 45% of accumulated B was present in shoots. In tomato plants, in addition to differences in B distribution among plant organs between the efficient (Rutgers) and less efficient (Brittle) cultivars, the specific uptake rate of 10B was significantly higher in the efficient cultivar. In wheat, the tolerant line (Amphiploid) took up less B than the less tolerant cultivar (Chinese Spring), and the pattern of B distribution among plant organs was different with a greater percentage of B found in roots of Chinese Spring compared to Amphiploid. Differences in sensitivity to B deficiency and excess amongst cultivars and species were a consequence of either reduced B uptake as in wheat (Amphiploid), a restriction in B translocation from roots to shoot as in celery (S48-54-1) or a combination of both process as in tomato (Brittle).  相似文献   

15.
    
Herein, a one‐step solvothermal strategy to synthesize amphiphilic, highly fluorescent graphene quantum dots (GQDs) as nucleus‐targeted fluorescence probes is reported. The edge‐functionalization of GQDs with N and Cl ligands renders them amphiphilic and positive charged for boosting membrane crossing and histone binding in the nuclei. The fluorescent properties of the GQDs can be markedly enhanced by Cl doping, and thus their fluorescence quantum yield is raised to 30% under optimized Cl doping. The self‐targeted GQDs exhibit multicolor cell imaging capability for visualization of fine architectures of the nucleus such as the nuclear envelope and nucleoli, which can be associated with their distinct surface features like amphiphilicity and high positive charge. These findings serve as a simple nuclear targeting strategy for cancer diagnosis and therapy.  相似文献   

16.
    
In this study, we report for the first time a one‐pot approach for the synthesis of new CdSeTeS quaternary‐alloyed quantum dots (QDs) in aqueous phase by microwave irradiation. CdCl2 was used as a Cd precursor during synthesis, NaHTe and NaHSe were used as Te and Se precursors and mercaptopropionic acid (MPA) was used as a stabilizer and source of sulfur. A series of quaternary‐alloyed QDs of different sizes were prepared. CdSeTeS QDs exhibited a wide emission range from 549 to 709 nm and high quantum yield (QY) up to 57.7 %. Most importantly, the quaternary‐alloyed QDs possessed significantly long fluorescence lifetimes > 100 ns as well as excellent photostability. Results of high‐resolution transmission electron microscopy (HRTEM), energy dispersive X‐ray spectroscopy (EDX) and powder X‐ray diffraction (XRD) spectroscopy showed that the nanocrystals possessed a quaternary alloy structure with good crystallinity. Fluorescence correlation spectroscopy (FCS) showed that QDs possessed good water solubility and monodispersity in aqueous solution. Furthermore, CdSeTeS QDs were modified with alpha‐thio‐omega‐carboxy poly(ethylene glycol) (HS‐PEG‐COOH) and the modified QDs were linked to anti‐epidermal growth factor receptor (EGFR) antibodies. QDs with the EGFR antibodies as labeling probes were successfully applied to targeted imaging for EGFR on the surface of SiHa cervical cancer cells. We believe that CdSeTeS QDs can become useful probes for in vivo targeted imaging and clinical diagnosis. Copyright © 2012 John Wiley & Sons, Ltd.  相似文献   

17.
This contribution investigates structural and electronic properties as well as stability phase diagrams of surfaces of the cubic boron nitride (c-BN). Our calculated parameters for bulk c-BN agree reasonably well with both experimental and computed values available in the literature. Based on the energies of the three experimentally recognised phases of bulk boron, i.e. α-B36, β-B105 and γ-B28, we estimate enthalpy of formation of c-BN to be ?2.8 eV. The c-BN(1?0?0) surface offers separate B and N terminations (denoted as c-BN(1?0?0)_B and c-BN(1?0?0)_N), whereas c-BN(1?1?1) and c-BN(1?1?0) are truncated with combinations of boron and nitrogen atoms (denoted as c-BN(1?1?1)_BN and c-BN(1?1?0)_BN). Optimised geometries of surfaces display interlayer displacements up to the three topmost layers. Downward displacement of surface boron atoms signifies a common geometric feature of all surfaces. Bulk c-BN and its most stable surface c-BN(1?0?0)_N possess no metallic character, with band gaps of 5.46 and 2.7 eV, respectively. We find that, only c-BN(1?0?0)_B configuration exhibits a metallic character. c-BN(1?1?0)_BN and c-BN(1?1?1)_BN surfaces display corresponding band gaps of 2.5 and 3.9 eV and, hence, afford no metallic property.  相似文献   

18.
量子点在生物学中的应用   总被引:1,自引:0,他引:1  
量子点是一种无机荧光材料,它具有独特的光物理特性,如其激发光谱宽且连续分布,而发射光谱呈对称分布且宽度窄,而且可通过改变量子点内核的尺寸对其发射光波长进行精细调节等。量子点的这些特性正引起人们日益广泛的关注,并在很多领域得到了应用。本文介绍了量子点的组成以及它的光学特性,同时介绍并讨论了近年来量子点在生物学领域应用的进展以及存在的问题。  相似文献   

19.
目的:探讨链亲和素修饰的CdSe/ZnS核壳结构量子点(CdSe/ZnS-SA)对稳定转染pcDNA3.1/APP595/596质粒的人胚肾(HEK293)细胞的短期毒性作用.方法:将CdSe/ZnS-SA量子点与稳定转染pcD-NA3.1/APP595/596质粒的HEK293细胞共培育,在倒置荧光显微镜下观察细胞形态学变化;MTT法测定细胞活性;流式细胞术检测细胞凋亡率.结果:终浓度为2.5 nmol/L-20 nmol/L的CdSe/ZnS-SA量子点与HEK293细胞分别共育8h、16h、24 h后,细胞的形态无明显改变;终浓度为2.5 nmol/L-25 nmol/L的CdSe/ZnS-SA量子点与HEK293细胞分别共育8h、16 h、24 h,各处理组与对照组间,各处理组间的吸光度值、细胞凋亡率差异均无统计学意义(P>0.05).结论:一定浓度范围的CdSe/ZnS-SA量子点在短期内对稳定转染pcDNA3.1/APP595/596质粒的HEK293细胞无明显的毒性作用,具有较好的生物相容性.  相似文献   

20.
    
Water‐soluble ZnS:Mn quantum dots (QDs) were synthesized using a hydrothermal method with 3‐mercaptopropionic acid as stabilizer. The optical properties of ZnS:Mn QDs were thoroughly investigated by tuning the doping concentration of Mn2+ and the Zn/S precursor ratio, to obtain an optimal parameter for QDs with excellent fluorescence characteristics. ZnS:Mn QDs excited at only one wavelength, however, which seriously limited their further application. Here, a trace Cd ion was doped into a ZnS host, resulting in QD excitation covering a wide adjustable waveband. Furthermore, when a ZnS shell was coated onto the surface of the ZnCdS:Mn QDs, photoluminescence intensity and stability were further enhanced. After coupling with an anti‐CK 19 antibody, the ZnCdS:Mn/ZnS core/shell QDs were able to function by labeling cancer cells, indicating that they could be considered as a suitable bio‐probe for cells and tissue imaging.  相似文献   

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