Department of Pharmaceutical Analysis, Faculty of Pharmacy, Fujian Medical University, Fuzhou, 350122, China; Nano Medical Technology Research Institute, Fujian Medical University, Fuzhou, 350122, China; Fujian Key Laboratory of Drug Target Discovery and Structural and Functional Research, Fujian Medical University, Fuzhou, 350122, China; Higher Educational Key Laboratory for Nano Biomedical Technology of Fujian Province, Fujian Medical University, Fuzhou, 350122, China.
Department of Pharmaceutical Analysis, Faculty of Pharmacy, Fujian Medical University, Fuzhou, 350122, China; Nano Medical Technology Research Institute, Fujian Medical University, Fuzhou, 350122, China.
Anal Chim Acta. 2020 Apr 8;1105:162-168. doi: 10.1016/j.aca.2020.01.035. Epub 2020 Jan 18.
Nanozymes, or nanomaterials that mimic the behaviors of enzymes, are highly promising materials for biomedical applications because of their excellent chemical stability under harsh conditions, simple preparation method and lower costs compared with natural enzymes. We herein report the intrinsic oxidase-mimicking activity of molybdenum oxide nanoparticles (MoO NPs). MoO NPs catalyzed the oxidation of colorless 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) to green product. The catalytic mechanism of the oxidase-mimicking activity of the MoO NPs was investigated in detail using electron spin resonance and a radical inhibition method. The oxidation of ABTS stems from O generated from the interaction between MoO NPs and dissolved oxygen in the solution. Acid phosphatase (ACP) catalyzes the hydrolysis of the ascorbic acid 2-phosphate (AAP) substrate to produce ascorbic acid (AA). AA was found to fade the coloration process of the MoO NP-mediated ABTS oxidation. By combining the oxidase-mimicking property of the MoO NPs and the ACP-catalyzed hydrolysis of AAP, a novel and simple colorimetric method for detecting ACP was established. The linear range for ACP determination is 0.09-7.3 U/L with a detection limit of 0.011 U/L. This new colorimetric method was successfully applied to the detection of ACP in diluted human serum samples and screening of ACP inhibitors. The present study proposes MoO NPs as a new oxidase mimic for establishing various biosensing method.
纳米酶,或模拟酶行为的纳米材料,由于其在恶劣条件下具有优异的化学稳定性、与天然酶相比更简单的制备方法和更低的成本,是极具应用前景的生物医学材料。我们在此报告了氧化钼纳米粒子(MoO NPs)的固有氧化酶模拟活性。MoO NPs 催化无色 2,2'-联氮双(3-乙基苯并噻唑啉-6-磺酸)(ABTS)氧化为绿色产物。详细研究了 MoO NPs 氧化酶模拟活性的催化机制,使用电子自旋共振和自由基抑制方法。ABTS 的氧化源于 MoO NPs 与溶液中溶解氧相互作用产生的 O。酸性磷酸酶(ACP)催化抗坏血酸 2-磷酸(AAP)底物的水解,产生抗坏血酸(AA)。发现 AA 使 MoO NP 介导的 ABTS 氧化的显色过程褪色。通过结合 MoO NPs 的氧化酶模拟特性和 ACP 催化的 AAP 水解,建立了一种新颖且简单的检测 ACP 的比色法。ACP 测定的线性范围为 0.09-7.3 U/L,检测限为 0.011 U/L。该新比色法成功应用于稀释人血清样品中 ACP 的检测和 ACP 抑制剂的筛选。本研究提出 MoO NPs 作为建立各种生物传感方法的新型氧化酶模拟物。