以16种中小学生作业本为检测对象,首先以白度颜色测定仪进行荧光白度检测,其次以水为溶剂对其中V B L荧光增白剂进行提取,采用紫外分光光度计进行V B L含量分析。同时,以V B L为标样添加到纸页中,抄造含有不同V B L含量的纸张样品。对...以16种中小学生作业本为检测对象,首先以白度颜色测定仪进行荧光白度检测,其次以水为溶剂对其中V B L荧光增白剂进行提取,采用紫外分光光度计进行V B L含量分析。同时,以V B L为标样添加到纸页中,抄造含有不同V B L含量的纸张样品。对实验所制备的样品经白度颜色测试仪以及紫外分光光度计测试,验证荧光白度与紫外分光光度计的分析吻合程度,也佐证学生作业本中V B L含量的检验结果。结果表明,荧光白度与紫外分光光度分析方法均可测定纸页中VB L的含量。16种试样中全部含有VB L荧光增白剂,VB L含量最高为0.23%,最少为0.05%;荧光白度最大为14.47%,最小为5.32%。展开更多
The interaction between cisplatin and erythrocyte membrane proteins was studied based on the quenching effect of cisplatin on the intrinsic fluorescence of proteins.A concentration-dependent quenching effect was obser...The interaction between cisplatin and erythrocyte membrane proteins was studied based on the quenching effect of cisplatin on the intrinsic fluorescence of proteins.A concentration-dependent quenching effect was observed.The presence of chloride and sulphate weakens the effect significantly.A pH-dependence was also noted with a stronger effect in acidic solution. The nature of the interaction is considered to be platinum-thiol group binding according to the effect of cisplatin on the fluorescence of FMA labeled membrane. The mechanism of the cisplatin-protein interactions was discussed based on the effect of coexisting anion展开更多
Chitosan was modified by conjugating coupling with linolenic acid through the 1-ethyl-3-（3-dimethylami- nopropyyl） carbodiimide （EDC）-mediated reaction. The degree of substitution 1.8% （ i.e. 1.8 linolenic acid g...Chitosan was modified by conjugating coupling with linolenic acid through the 1-ethyl-3-（3-dimethylami- nopropyyl） carbodiimide （EDC）-mediated reaction. The degree of substitution 1.8% （ i.e. 1.8 linolenic acid group per 100 anhydroglucose units） was measured by ^1H NMR. The critical aggregation concentration （CAC） of the self-aggregate of hydrophobically modified chitosan was determined by measuring the fluorescence intensity of the pyrene as a fluorescent probe. The CAC value in phosphate-buffered saline （PBS） solution （pH 7.4） was 5 × 10^-2 mg mL^-1. The average particle size of selfaggregates of hydrophobically modified chitosan in PBS solution （pH7.4） was 210.8 nm with a unimodal size distribution ranging from 100 to 500 nm. Transmission electron microscopy （TEM） study showed that the formation of near spherical shape nanoparticles has enough structural integrity. The loading ability of hydrophibically modified chitosan （LA-chitosan） was investigated by using bovine serum albumin （BSA） as the model. The loading capacity of self-aggregated nanoparticles increases （ 19.85 % ± 0.04 % to 37.57 % ± 0.25 % ） with the concentration of BSA （0.1-0.5 mg mL^-1 ）.展开更多
To improve the sensitivity of protein microarray, a prism surface replaces the surface of the common microscope slide.The protein targets arrayed on the surface are hybridized and labelled by fluorescent probes. Evane...To improve the sensitivity of protein microarray, a prism surface replaces the surface of the common microscope slide.The protein targets arrayed on the surface are hybridized and labelled by fluorescent probes. Evanescent excitation occurs when the convergent laser reaches the surface, and a photomultiplier tube detects the emitted fluorescent signal. A two-dimensional actuator scans the whole surface to achieve planar laser excitation and fluorescence collection. The penetration depth of the evanescent field into the protein targets is only some hundred nanometers and can be controlled by different incident angle of the laser beam, so the undesired background signals are reduced dramatically and the detection sensitivity is improved by a factor of 50 to 100 comparing to confocal excitation. This approach can detect low abundance analytes without signal amplification.展开更多
The BaAl2Si2O8:Eu2+blue emitting phosphor was obtained through the one-step calcination process of precursors prepared bychemical co-precipitation method. The phase structure and luminescence propertied of the phospho...The BaAl2Si2O8:Eu2+blue emitting phosphor was obtained through the one-step calcination process of precursors prepared bychemical co-precipitation method. The phase structure and luminescence propertied of the phosphor were investigated usingX-ray diffraction (XRD) and a fluorescence spectrophotometer. The excitation spectrum exhibited a broad band between 230nm and 400 nm and the emission peaking at about 470 nm was observed, which originated from the allowed f-d transition ofEu2+ions at Ba2+sites. Owing to the different optimal concentrations under different excitation wavelengths (254 nm and 365nm), the energy-transfer mechanism in this phosphor has changed from the dipole-dipole interaction to the exchange interac-tion of Eu2+ions.展开更多
Advanced fluorescence microscopy including single-molecule localization-based super-resolution imaging techniques requires bright and photostable dyes orproteins asfluorophores.The photophysical properties of fluoroph...Advanced fluorescence microscopy including single-molecule localization-based super-resolution imaging techniques requires bright and photostable dyes orproteins asfluorophores.The photophysical properties of fluorophores have been proven to be crucial for super-resolution microscopy's localization precision and imaging resolution.Fluorophores TAMRA and Atto Rho6 G,which can interact with macrocyclic host cucurbit[7]uril(CB7) to form host-guest compounds,were found to improve the fluorescence intensity and lifetimes of these dyes.We enhanced the localization precision of direct stochastic optical reconstruction microscopy(dSTORM) by introducing CB7 into the imaging buffer,and showed that the number of photons as well as localizations of both TAMRA and Atto Rho6 G increase over 2 times.展开更多
文摘以16种中小学生作业本为检测对象,首先以白度颜色测定仪进行荧光白度检测,其次以水为溶剂对其中V B L荧光增白剂进行提取,采用紫外分光光度计进行V B L含量分析。同时,以V B L为标样添加到纸页中,抄造含有不同V B L含量的纸张样品。对实验所制备的样品经白度颜色测试仪以及紫外分光光度计测试,验证荧光白度与紫外分光光度计的分析吻合程度,也佐证学生作业本中V B L含量的检验结果。结果表明,荧光白度与紫外分光光度分析方法均可测定纸页中VB L的含量。16种试样中全部含有VB L荧光增白剂,VB L含量最高为0.23%,最少为0.05%;荧光白度最大为14.47%,最小为5.32%。
文摘The interaction between cisplatin and erythrocyte membrane proteins was studied based on the quenching effect of cisplatin on the intrinsic fluorescence of proteins.A concentration-dependent quenching effect was observed.The presence of chloride and sulphate weakens the effect significantly.A pH-dependence was also noted with a stronger effect in acidic solution. The nature of the interaction is considered to be platinum-thiol group binding according to the effect of cisplatin on the fluorescence of FMA labeled membrane. The mechanism of the cisplatin-protein interactions was discussed based on the effect of coexisting anion
基金National Natural Science Foundation of China(30370344)Korea Science and Engineering Foundation(19992-220-009-4)supported this study
文摘Chitosan was modified by conjugating coupling with linolenic acid through the 1-ethyl-3-（3-dimethylami- nopropyyl） carbodiimide （EDC）-mediated reaction. The degree of substitution 1.8% （ i.e. 1.8 linolenic acid group per 100 anhydroglucose units） was measured by ^1H NMR. The critical aggregation concentration （CAC） of the self-aggregate of hydrophobically modified chitosan was determined by measuring the fluorescence intensity of the pyrene as a fluorescent probe. The CAC value in phosphate-buffered saline （PBS） solution （pH 7.4） was 5 × 10^-2 mg mL^-1. The average particle size of selfaggregates of hydrophobically modified chitosan in PBS solution （pH7.4） was 210.8 nm with a unimodal size distribution ranging from 100 to 500 nm. Transmission electron microscopy （TEM） study showed that the formation of near spherical shape nanoparticles has enough structural integrity. The loading ability of hydrophibically modified chitosan （LA-chitosan） was investigated by using bovine serum albumin （BSA） as the model. The loading capacity of self-aggregated nanoparticles increases （ 19.85 % ± 0.04 % to 37.57 % ± 0.25 % ） with the concentration of BSA （0.1-0.5 mg mL^-1 ）.
文摘To improve the sensitivity of protein microarray, a prism surface replaces the surface of the common microscope slide.The protein targets arrayed on the surface are hybridized and labelled by fluorescent probes. Evanescent excitation occurs when the convergent laser reaches the surface, and a photomultiplier tube detects the emitted fluorescent signal. A two-dimensional actuator scans the whole surface to achieve planar laser excitation and fluorescence collection. The penetration depth of the evanescent field into the protein targets is only some hundred nanometers and can be controlled by different incident angle of the laser beam, so the undesired background signals are reduced dramatically and the detection sensitivity is improved by a factor of 50 to 100 comparing to confocal excitation. This approach can detect low abundance analytes without signal amplification.
基金supported by the Scientific and Technological Project of Chongqing, China (Grant No. CSTC, 2009AB4171)the Innovation Foundation for Technology Based Firms of Ministry of Science and Technology, China (Grant No. 04C26225100807)
文摘The BaAl2Si2O8:Eu2+blue emitting phosphor was obtained through the one-step calcination process of precursors prepared bychemical co-precipitation method. The phase structure and luminescence propertied of the phosphor were investigated usingX-ray diffraction (XRD) and a fluorescence spectrophotometer. The excitation spectrum exhibited a broad band between 230nm and 400 nm and the emission peaking at about 470 nm was observed, which originated from the allowed f-d transition ofEu2+ions at Ba2+sites. Owing to the different optimal concentrations under different excitation wavelengths (254 nm and 365nm), the energy-transfer mechanism in this phosphor has changed from the dipole-dipole interaction to the exchange interac-tion of Eu2+ions.
基金supported by the National Natural Science Foundation of China(31330082,21373200,21525314)the Instrument Developing Project of the Chinese Academy of Sciences(YZ201455)
文摘Advanced fluorescence microscopy including single-molecule localization-based super-resolution imaging techniques requires bright and photostable dyes orproteins asfluorophores.The photophysical properties of fluorophores have been proven to be crucial for super-resolution microscopy's localization precision and imaging resolution.Fluorophores TAMRA and Atto Rho6 G,which can interact with macrocyclic host cucurbit[7]uril(CB7) to form host-guest compounds,were found to improve the fluorescence intensity and lifetimes of these dyes.We enhanced the localization precision of direct stochastic optical reconstruction microscopy(dSTORM) by introducing CB7 into the imaging buffer,and showed that the number of photons as well as localizations of both TAMRA and Atto Rho6 G increase over 2 times.
