CdSe/ZnS量子点的合成及表征

本文于水溶液中采用3-巯基丙酸作为稳定剂,成功合成了CdSe/ZnS核壳型量子点。透射电子显微镜观察表明,所合成的量子点尺寸均一,形貌近似球形,粒子大小在5 nm以下。紫外吸收光谱和荧光光谱分析表明,所合成的CdSe/ZnS核壳型量子点较之CdSe量子点更具良好光学特性。     

Determination of lysozyme at the nanogram level in chicken egg white using Resonance Rayleigh-scattering method with Cd-doped ZnSe quantum dots as probe

A new method for the determination of lysozyme with high sensitivity based on Resonance Rayleigh scattering (RRS) by using Cd doped ZnSe quantum dots (QDs) as a probe was proposed in this experiment. Cd doped ZnSe QDs capped with glutathione were prepared in the water phase. Further, the RRS spectrum, transmission electron microscope, and absorption spectrum of the QDs-lysozyme system have been characterized. In addition, the effects of several factors on scattering intensities were investigated, including pH value of solution, amount of QDs, mixing sequence of each reagent and the coexisting substances. Moreover, the possible mechanism for the RRS enhancement of Cd doped ZnSe QDs-lysozyme system was preliminary discussed. The RRS method for the determination of lysozyme has good sensitivity with the detection limits 6.5 × 10⁻¹⁰ g mL⁻¹. The contents of lysozyme were determined with recoveries of 97.1-101.6% and relativity standard deviation of 2.5-3.1%, respectively. It proved that the method established in our study is very sensitive, rapid, convenient and tolerant for the determination of lysozyme in synthetically and chicken egg white.     

近红外荧光磁性复合载药脂质体的制备及应用

拟建立以近红外荧光磁性复合脂质体(NFMSLs)为模型药物载体、盐酸多柔比星(DOX)为包封药物的药物输送系统,研究了近红外荧光磁性载药复合脂质体(DOX-NFMSLs)的制备、性质及初步应用.采用共沉淀法制备FeO4磁流体,CdTe掺杂Se制备近红外量子点CdSeTe,薄膜分散法制备DOX-NFMSLs.用DOX荧光分光光度法测定DOX-NFMSLs的包封率和体外药物释放率;用DOX-NFMSLs与HepG2肝癌细胞共孵育来进行细胞成像和细胞毒性实验.结果表明,近红外CdSeTe量子点粒径约为5nm,闪锌矿结构,发射波长824 nm.磷脂与胆固醇质量比为8∶1,药脂比为1∶20的DOX-NFMSLs平均粒径为252.9 nm,Zeta电位为-48.6 mV,理想释放药物温度为41℃,平均包封率为(74.84±0.89)％.DOX-NFMSLs对HepG2肝癌细胞有一定的抗癌效果.得到了具有良好磁响应、释药温度T=41℃、可近红外成像的载药脂质体.     

近红外荧光磁性复合载药脂质体的制备及应用

拟建立以近红外荧光磁性复合脂质体(NFMSLs)为模型药物载体、盐酸多柔比星(DOX)为包封药物的药物输送系统,研究了近红外荧光磁性载药复合脂质体(DOX-NFMSLs)的制备、性质及初步应用。采用共沉淀法制备Fe3O4磁流体,CdTe掺杂Se制备近红外量子点CdSeTe,薄膜分散法制备DOX-NFMSLs。用DOX荧光分光光度法测定DOX-NFMSLs的包封率和体外药物释放率;用DOX-NFMSLs与HepG2肝癌细胞共孵育来进行细胞成像和细胞毒性实验。结果表明,近红外CdSeTe量子点粒径约为5nm,闪锌矿结构,发射波长824nm。磷脂与胆固醇质量比为8∶1,药脂比为1∶20的DOX-NFMSLs平均粒径为252.9nm,Zeta电位为-48.6mV,理想释放药物温度为41℃,平均包封率为(74.84±0.89)%。DOX-NFMSLs对HepG2肝癌细胞有一定的抗癌效果。得到了具有良好磁响应、释药温度T=41℃、可近红外成像的载药脂质体。     

Study of thiol capped CdSe quantum dots using SeO2 precursor for selenium source

CdSe quantum dots in aqueous medium using thioglycollic acid as capping agent have been synthesized. The reaction was carried out in an open atmosphere at pH of 12 and refluxed at 100 °C for 8 h. Selenium dioxide which is less expensive and less toxic has been used as a precursor for selenium source by replacing Se powder and sodium selenite. For characterization QD solutions was taken at different time intervals ranging from 15 min to 6 h. UV–Vis spectroscopy shows that there is a strong blue shift in the prepared quantum dots due to quantum confinement effect. Band gap calculated at different time intervals lies between 2.34 and 2.73 eV which is more than the bulk band gap 1.74 eV and with the increase in size of the QDs, bandgap also decreases. Photoluminescence study was carried out at excitation wavelength of 350 nm and results shows that with increase in time the peak position shift toward higher wavelength. FTIR spectroscopy shows peaks of thioglycollic acid. SEM micrographs of the prepared quantum dots show zero dimensional spherical particles in nm range. For electrical conductivity dc conductivity measurement has been done which shows that with increase of temperature conductivity increases, it confirms the semiconducting nature of the quantum dot. Conduction mechanism found to be mainly due to localized states.     

Improving optical properties of CdTe quantum dots by a new multidentae biopolymer based on salep

In this work, we have successfully modified aqueous CdTe quantum dots (QDs) by a biopolymer based on poly (2-hydroxyethyl methacrylate) grafted onto salep via a facile method at room temperature. The obtained QDs were characterized using Fourier transform infrared spectroscopy (FT-IR), thermo-gravimetric analysis (TG), X-ray diffraction (XRD), and transmission electron microscopy (TEM). The size of the prepared QDs was estimated around 1.5 nm by TEM and XRD. Optical properties of modified QDs were monitored by absorption and fluorescence spectrophotometers. It was found that the fluorescence intensity of CdTe QDs was enhanced after coating by biopolymer. Finally, the fluorescence intensity of CdTe QDs was investigated at different temperatures and times.     

Quantum‐dots‐based detection of hepatitis C virus (HCV) NS3 using RNA aptamer on chip

BACKGROUND: Over 170 million people, more than 3% of the world's population, suffer from the hepatitis C virus (HCV) infection and the rate of death from liver‐related mortality to HCV has increased. In respect of this, the development of assays for biological imaging should be urgently considered as an essential factor in diagnosis. RESULTS: A novel HCV‐detecting technique using a nanoparticle‐supported aptamer probe was demonstrated. With the aid of nanoparticle quantum dots (QDs) with carboxyl group as an imaging probe, and 5′‐end‐amine‐modified RNA oligonucleotide as a capturing probe, target HCV NS3 was visually detected on chip. The QDs‐based RNA aptamer for HCV NS3 showed high selectivity and specificity against other protein such as BSA. The detection limit of HCV NS3 protein was 5 ng mL^?1 level. CONCLUSION: With a novel strategy for protein–aptamer interaction, the feasibility of applying QDs‐based fluorescent detection technique to HCV viral protein assay for the development of a protein biochip was demonstrated. This scheme of QDs‐mediated imaging with a target‐oriented specific RNA aptamer for the detection of infectious HCV diseases provides an efficient strategy and a promising new platform for monitoring applications. Copyright © 2010 Society of Chemical Industry     

自组织InAs/GaAs量子点的表面氮化研究

用低温光荧光(PL)和透射电子显微镜(TEM)研究了表面氮化自组织InAs/GaAs量子点的光学性能和微观结构。结果表明氮化后形成薄层的InAsN薄膜作为应变缓和层覆盖在量子点的表面,使得随着氮化时间的增加,InAs量子点的位错密度提高、尺寸变大、纵横比提高、发光波长变长、强度变低。     

CdSe量子点的制备及荧光性能改善

主要讨论了CdSe量子点的制备及荧光性能的改善.采用水相合成方法制备了CdSe量子点,并用X射线粉末衍射仪对所合成的量子点进行表征,用荧光分光光度计研究了量子点的荧光性质.结果表明,采用样品处理温度的调节和ZnS壳层的包覆能在一定程度上改善CdSe量子点的荧光性能.     

CdS量子点的优化合成及其在离子检测中的应用

实验探讨了采用胶体法合成荧光CdS QDs的一些因素.对样品进行了TEM、XRD、UV-vis等表征.将合成的QDs应用于Cu2 检测,并探讨了作用机理.