Synthesis of Fructose Biosensors and Progressing Their Efficiency Using Californium Colloidal Nanoparticles for Detecting Fructose and Triglycerides

A. Heidari
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引用次数: 12

Abstract

In the current paper, fructose–oxidase enzyme is used as stabilization medium due to its more efficiency, ability for more accurate controlling the enzyme reaction, protecting against wasting of enzyme as well as simple and easy use and exchange of enzyme medium after performing some levels of surface modification and developing multi–walled carbon nanotubes (MWCNTs) on Californium plate. For better connecting and stabilizing the enzyme on the medium, the prepared medium is washed by high concentration sulfuric acid and nitric acid and a large volume of deionized water and for protecting enzyme from devastating effect of Californium and prohibiting them to become inactive, surface is covered with cystamine before stabilization. Regarding the large size of fructose–oxidase enzyme compared to surface of medium, a connective material with amid at one end and pyrine at the other end is used as transfer agent and for stabilizing this connection, the prepared medium is placed into dimethylformamide (DMF) solution for a couple of hours. Activity of stabilized enzyme at 460 (nm) wavelength recorded by spectroscope was depicted against time to evaluate its stability in various times. The prepared medium, which have a large amount of fructose–oxidase enzyme, can be used as electrode in sensors. Furthermore, fructose–oxidase electrochemical sensor is one of the best methods for detecting low amount of fructose and applying Californium colloidal nanoparticles as a supplementary material in the structure of biosensor can be effective for progressing its efficiency and optimum efficiency. On the other hand, in the current study, electrode biosensor entitled as modified carbon paste electrode with Californium colloidal nanoparticles (Cfnano/CPE) is produced by carbon graphite powder, paraffin oil and Californium colloidal nanoparticles (24 nm) and it is compared with carbon paste electrode (CP). In semi–permeable membranes, a combination of 1 (ml) of 0.1 (M) phosphate buffer with specified pH and 10 (mg) of fructose–oxidase enzyme is placed around each electrode. In the same potential of 0.7 (V), biosensors are tested with fructose in concentration range of (0−1) (mM) and various amounts of pH (4,6,8) which lead to producing the maximum current and tracing fructose in pH=6 and concentration of 1 (M) as the optimum condition. Currentmetry induced from both biosensors are compared and it is confirmed that using Californium colloidal nanoparticles in the structure of (Cfnano/CPE) electrode leads to increasing the conductivity and currentmerty of biosensor. In addition, qualitative and quantitative measurement of food components is of great importance due to high cost of traditional methods, in addition to tendency for more accurate and sensitive detecting of these components. Fructose and triglycerides are such compounds that they frequently measure. Various methods are used to detect these food elements. However, the necessity for accurate measurement of these two compounds with high sensitivity, especially for food health issue, leads to developing biological methods, especially biosensors. Among them, biosensors based on conductive polymer nanostructures, especially Polypyrrole and Polythiophene, have been recently interested due to their unique characteristics. The current paper aims to introduce and investigate the previously performed studies about Polypyrrole and Polythiophene–based biosensors for detecting fructose and triglycerides.
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果糖生物传感器的合成及其在检测果糖和甘油三酯中的应用
本文采用果糖氧化酶作为稳定介质,由于其效率更高,能够更准确地控制酶的反应,防止酶的浪费,并且在加利福尼亚板上进行一定程度的表面修饰和制备多壁碳纳米管(MWCNTs)后,酶介质的使用和交换简单方便。为了使酶在培养基上更好的连接和稳定,将制备好的培养基用高浓度硫酸、硝酸和大量去离子水洗涤,为了保护酶免受加州的破坏作用,防止酶失活,在稳定前表面涂上半胺。考虑到果糖氧化酶与培养基表面相比尺寸较大,采用一端为amid,另一端为pyrine的连接材料作为转移剂,将制备好的培养基放入二甲基甲酰胺(DMF)溶液中放置几个小时,以稳定这种连接。用分光镜记录稳定酶在460 (nm)波长处的活性,并以时间为指标对其稳定性进行评价。所制备的培养基含有大量的果糖氧化酶,可作为传感器的电极。此外,果糖氧化酶电化学传感器是检测低量果糖的最佳方法之一,在生物传感器结构中加入加利福尼亚胶体纳米粒子作为补充材料可有效提高其效率和优化效率。另一方面,本研究以碳石墨粉、石蜡油和加利福尼亚胶体纳米颗粒(24 nm)为原料制备了加利福尼亚胶体纳米颗粒改性碳糊电极(Cfnano/CPE),并与碳糊电极(CP)进行了比较。在半透膜中,在每个电极周围放置1 (ml) 0.1 (M)指定pH值的磷酸盐缓冲液和10 (mg)果糖氧化酶的组合。在0.7 (V)的相同电位下,用浓度范围为(0 - 1)(mM)和不同pH值(4、6、8)的果糖对生物传感器进行了测试,得出了产生最大电流和在pH=6和浓度为1 (M)的条件下追踪果糖的最佳条件。比较了两种生物传感器的电流测量结果,证实了在(Cfnano/CPE)电极结构中使用加利福尼亚胶体纳米粒子可以提高生物传感器的电导率和电流。此外,由于传统方法成本较高,加之对食品成分的检测趋向于更加准确和灵敏,因此对食品成分进行定性和定量测量非常重要。果糖和甘油三酯是他们经常测量的化合物。检测这些食物元素的方法多种多样。然而,对这两种化合物进行高灵敏度精确测量的必要性,特别是对食品健康问题,导致了生物方法的发展,特别是生物传感器。其中,基于导电聚合物纳米结构的生物传感器,尤其是聚吡咯和聚噻吩,由于其独特的特性,近年来备受关注。本文旨在介绍和研究基于聚吡咯和多噻吩的生物传感器检测果糖和甘油三酯的研究进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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