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1.
A vortex-assisted dispersive micro-solid-phase extraction procedure using a new and green sorbent was developed as a simple, fast, and efficient sample preparation method for the extracting five pesticides in several fruit juice samples. In this study, for the first time, riboflavin was used as an efficient sorbent. A few milligrams of riboflavin was directly added into the aqueous solution containing the analytes to adsorb them. After adsorption the analytes, they were desorbed and more concentrated by a dispersive liquid–liquid microextraction procedure. The influence of several effective parameters such as amount of riboflavin, pH, vortex time, eluent nature and volume, and extraction solvent type and volume on the extraction efficiency was investigated. In optimal conditions, linear ranges of the calibration curves were broad. The limits of detection and quantification were attained in the ranges of 0.56–1.5  and 1.9–0.52 ng mL−1, respectively. The proposed method demonstrated to be suitable for concurrent extraction of the studied pesticides in various fruit juice samples with high enrichment factors (320–360) and precision (relative standard deviation ≤7.8% for intra- [n = 6] and interday [n = 4] precisions at a concentration of 25 ng mL−1 of each pesticide).  相似文献   
2.
《Analytical letters》2012,45(17):3138-3146
Abstract

A new, simple, and sensitive method for the determination of riboflavin based on the single-sweep polarographic reduction wave of the photolysis products of riboflavin has been developed. Under the irradiation of an iodine-tungsten lamp, the photolysis reaction of riboflavin in pH 9.3 NH3-NH4Cl buffer solution can be complete in about 20 min. The reaction products yield a single adsorptive reduction wave at ?0.63 V (vs. SCE) negative to the reduction wave of riboflavin by 0.18 V. The derivative wave height is linearly proportional to the concentration of riboflavin in the range of 0.01–17.5 µg/mL (correlation coefficient 0.996). The detection limit is 0.00 5µg/mL. The proposed method has been applied to the determination of multivitamin tablets with satisfactory results. In comparison with the methods directly using the reduction wave of riboflavin for the determination, this method eliminates the effect of the degradation of riboflavin on the determination accuracy and is much more sensitive. The new method could be useful in many fields.  相似文献   
3.
We report a hybrid singlet oxygen production system, where strong resonance coupling between plasmonic nanoparticles and photosensitizing molecules results in exceptionally high singlet oxygen production under both visible light and near‐infrared light excitation, even for the photosensitizing molecules without near‐infrared absorption. The light‐harvesting property of the plasmon‐photosensitizer hybrids leads to an enhanced, broad‐spectrum photodynamic inactivation of bacteria under a wide range of excitations, including that with near‐infrared light.  相似文献   
4.
亚硫酸氢钠(Na HSO3)和过氧化氢(H2O2)反应可产生微弱的化学发光。核黄素对亚硫酸氢钠和过氧化氢的化学发光有极大的增强作用,且化学发光强度在0.02~2.0μg/m L范围内与核黄素浓度呈良好的线性关系。据此,建立了核黄素的高灵敏化学发光分析方法,方法检出限为0.007μg/m L,相对标准偏差(n=11)不大于1.6%。利用荧光光谱、化学发光谱对核黄素增强Na HSO3-H2O2体系化学发光的机理进行探讨,为该体系的应用研究提供了新思路。  相似文献   
5.
Using time-resolved techniques of 337 and 248 nm laser flash photolysis, the photo physical and photochemical processes of riboflavin (RF, vitamin B2) were studied in detail in aqueous solution. The excited triplet state of riboflavin (3RF*) was produced with 337 nm laser, while under 248 nm irradiation, both3RF* and hydrated electron (eaq) formed from photoionization could be detected. Photobiological implications have been inferred on the basis of reactivity of3RF* including energy transfer, electron transfer and hydrogen abstraction. The RF·+ was generated by oxidation of SO4 ·-radical with the aim of confirming the results of photolysis.  相似文献   
6.
Using time-resolved techniques of 337 and 248 nm laser flash photolysis, the photo-physical and photochemical processes of riboflavin (RF, vitamin B2) were studied in detail in aqueous solution. The excited triplet state of riboflavin (3RF*) was produced with 337 nm laser, while under 248 nm irradiation, both 3RF* and hydrated electron (eaq) formed from photoionizationcould be detected. Photobiological implications have been inferred on the basis of reactivity of 3RF* including energy transfer, electron transfer and hydrogen abstraction. The RF.+ was generated by oxidation of SO4.- radical with the aim of confirming the results of photolysis.  相似文献   
7.
核黄素光敏氧化噻吩脱硫研究   总被引:9,自引:5,他引:4  
以噻吩的正辛烷溶液模拟FCC汽油,以水为萃取剂,以空气中的O2为氧化剂,以核黄素为光敏剂,研究了噻吩在500W高压汞灯照射下的光化学氧化。实验结果表明,在通气量为150mL/min、水油比为1∶1、核黄素加入量为30μmol/L的条件下,反应3h后噻吩的脱硫率能够达到85.4%。核黄素的敏化作用是通过激发基态氧为单线态氧实现的,噻吩氧化脱硫为一级动力学反应,加入光敏剂时反应速率常数k=9.10×10-5s-1,半衰期t1/2=2.12h。  相似文献   
8.
The photooxidation damage of lysozyme under 315-375 nm irradiation in the presence of riboflavin was studied by using sodium dodecyl sulfate-polyacrylamide gel electrophoresis(SDS-PAGE).Indica- tions showed that the mechanisms and products of oxidative damage were relative to the concentra- tion of riboflavin,the time of irradiation and the ambience.The type I process was examined in a nitrogen saturated solution,whereas both type I and type II were observed in an aerobic atmosphere and type II was the dominant process.The study also suggested that antioxidants,such as melatonin, can reduce the damage of lysozyme effectively.  相似文献   
9.
The square-wave voltammetric (SWV) behaviour of riboflavin and folic acid was studied at a static mercury drop electrode by square wave voltammetry. In 0.05M KCl (pH 5.89) a cathodic scan gave peaks at — 0.56 and — 0.87 V vs. Ag/AgCl for riboflavin and folic acid, respectively. The reduction peak currents are linearly dependent on the concentration of vitamins. Both vitamins can be simultaneously determined from the same voltammogram. The method proposed for the determination of riboflavin and folic acid in multivitamin tablets is very simple, rapid and does not involve time-consuming separation steps. The average contents of riboflavin and folic acid were found to be 14.8 ± 1.26% and 1.46 ± 2.66%, for tablet A and 9.86 ±1.40% and 1.47 ± 2.0% for tablet B, respectively.  相似文献   
10.
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