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用于测定食品和生物样品中氧化酶底物的比色纳米生物传感器设计

Colorimetric Nanobiosensor Design for Determining Oxidase Enzyme Substrates in Food and Biological Samples.

作者信息

Avan Aslı Neslihan, Demirci-Çekiç Sema, Apak Reşat

机构信息

Department of Chemistry, Faculty of Engineering, Istanbul University-Cerrahpasa, Avcilar, 34320Istanbul, Turkiye.

Department of Chemistry, Institute of Graduate Studies, Istanbul University-Cerrahpasa, 34320Istanbul, Turkiye.

出版信息

ACS Omega. 2022 Nov 23;7(48):44372-44382. doi: 10.1021/acsomega.2c06053. eCollection 2022 Dec 6.

Abstract

Biological enzymes have high catalytic activity and unique substrate selectivity; their immobilization may provide cost reduction and reusability. Using magnetic nanoparticles (MNPs) as support materials for enzymes ensures easy separation from reaction media by an external magnetic field. Thus, MNPs were prepared by the coprecipitation method, coated with silanol groups, then -NH-functionalized, and finally activated with glutaraldehyde. Finally, three different oxidase enzymes, i.e., uricase, glucose oxidase, and choline oxidase, were separately immobilized on their surfaces by covalent attachment. Hence, colorimetric nanobiosensors for the determination of three biologically important substrates, i.e., uric acid (UA), glucose (Glu), and choline (Ch), were developed. Hydrogen peroxide liberated from enzyme-substrate reactions was determined by the cupric ion reducing antioxidant capacity (CUPRAC) reagent, bis-neocuproine copper(II) chelate. In addition, UA-free total antioxidant capacity could also be measured via the developed system. Kinetic investigations were carried out for these nanobiosensors to enable the calculation of their Michaelis constants ( ), revealing no affinity loss for the substrate as a result of immobilization. Enzyme-immobilized MNPs could be reused at least five times. The linear concentration ranges were 5.43-65.22 μM for UA, 11.1-111.1 μM for Glu, and 2.78-44.4 μM for Ch, and the limit of detection (LOD) values with the same order were 0.34, 0.59, and 0.20 μM, respectively. Besides phenolic and thiol-type antioxidants, UA could be determined with an error range of 0.18-4.87%. The method is based on a clear redox reaction with a definite stoichiometry for the enzymatically generated HO (which minimizes chemical deviations from Beer's law of optical absorbances), and it was successfully applied to the determination of Glu and UA in fetal bovine serum and Ch in infant formula as real samples.

摘要

生物酶具有高催化活性和独特的底物选择性;将其固定化可降低成本并实现可重复使用。使用磁性纳米颗粒(MNPs)作为酶的载体材料可确保通过外部磁场轻松从反应介质中分离。因此,通过共沉淀法制备MNPs,用硅醇基团包覆,然后进行-NH功能化,最后用戊二醛活化。最后,通过共价连接将三种不同的氧化酶,即尿酸酶、葡萄糖氧化酶和胆碱氧化酶分别固定在其表面。因此,开发了用于测定三种生物重要底物,即尿酸(UA)、葡萄糖(Glu)和胆碱(Ch)的比色纳米生物传感器。通过铜离子还原抗氧化能力(CUPRAC)试剂双(新亚铜灵)铜(II)螯合物测定酶-底物反应释放的过氧化氢。此外,还可通过所开发的系统测量不含UA的总抗氧化能力。对这些纳米生物传感器进行了动力学研究,以便计算其米氏常数( ),结果表明固定化后对底物无亲和力损失。固定化酶的MNPs可重复使用至少五次。UA的线性浓度范围为5.43 - 65.22 μM,Glu为11.1 - 111.1 μM,Ch为2.78 - 44.4 μM,相同量级的检测限(LOD)值分别为0.34、0.59和0.20 μM。除了酚类和硫醇类抗氧化剂外,UA的测定误差范围为0.18 - 4.87%。该方法基于具有明确化学计量的清晰氧化还原反应,用于酶促生成的HO(这使光学吸光度与比尔定律的化学偏差最小化),并成功应用于实际样品胎牛血清中Glu和UA以及婴儿配方奶粉中Ch的测定。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3ff/9730783/c02ce37c573a/ao2c06053_0002.jpg

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