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磷修饰的碳点的过氧化物酶样活性用于比色法检测酸性磷酸酶。

Phosphorus Modulated Peroxidase-Like Activity of Carbon Dots for Colorimetric Detection of Acid Phosphatase.

机构信息

Guangzhou Key Laboratory of Analytical Chemistry for Biomedicine, School of Chemistry, South China Normal University, Guangzhou, Guangdong, China.

出版信息

Appl Spectrosc. 2024 Jun;78(6):633-643. doi: 10.1177/00037028241238246. Epub 2024 Mar 26.

Abstract

The precise regulation of nanoenzyme activity is of great significance for application to biosensing analysis. Herein, the peroxidase-like activity of carbon dots was effectively modulated by doping phosphorus, which was successfully employed for sensitive, selective detection of acid phosphatase (ACP). Phosphorus-doped carbon dots (P-CDs) with excellent peroxidase-like activity were synthesized by a one-pot hydrothermal method, and the catalytic activity could be easily modulated by controlling the additional amount of precursor phytic acid. P-CDs could effectively catalyze the oxidation of colorless 3,3',5,5'-tetramethylbenzidine (TMB) to blue TMB oxidation products in the presence of hydrogen peroxide. While ACP was able to catalyze the hydrolysis of L-ascorbyl-2-phosphate trisodium salt (AAP) to produce ascorbic acid (AA), which inhibited the peroxidase-like activity of P-CDs, by combining P-CDs nanoenzymes and ACP-catalyzed hydrolysis the colorimetric method was established for ACP detection. The absorbance variation showed a good linear relationship with ACP concentration in the range of 0.4-4.0 mU/mL with a limit of detection at 0.12 mU/mL. In addition, the method was successfully applied to detect ACP in human serum samples with recoveries in the range of 98.7-101.6%. The work provides an effective strategy for regulating nanoenzymes activity and a low-cost detection technique for ACP.

摘要

纳米酶活性的精确调控对于应用于生物传感分析具有重要意义。在此,通过掺杂磷有效地调节了碳点的过氧化物酶样活性,并成功地应用于酸性磷酸酶(ACP)的灵敏、选择性检测。通过一锅水热法合成了具有优异过氧化物酶样活性的磷掺杂碳点(P-CDs),并且可以通过控制前体植酸的添加量来轻松调节催化活性。在存在过氧化氢的情况下,P-CDs 可以有效地催化无色 3,3',5,5'-四甲基联苯胺(TMB)的氧化,生成蓝色 TMB 氧化产物。而 ACP 能够催化 L-抗坏血酸-2-磷酸三钠盐(AAP)的水解,生成抗坏血酸(AA),从而抑制 P-CDs 的过氧化物酶样活性,通过结合 P-CDs 纳米酶和 ACP 催化的水解反应,建立了用于 ACP 检测的比色法。吸光度变化与 0.4-4.0 mU/mL 范围内的 ACP 浓度呈良好的线性关系,检测限为 0.12 mU/mL。此外,该方法成功地应用于人血清样品中 ACP 的检测,回收率在 98.7-101.6%范围内。该工作为调节纳米酶活性提供了一种有效策略,并为 ACP 的低成本检测技术提供了新的思路。

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