Shin Hojeong, Woo Jiwon, Hong Seongin, Yoo Soeun, Cho Hyeonwoo, Hong Byung Hee, Hwang Yun Jeong, Min Dal-Hee
Department of Chemistry, Seoul National University, Seoul, 08826, Republic of Korea.
Department of Chemistry, Seoul National University, Seoul, 08826, Republic of Korea.
Talanta. 2025 Sep 1;292:127946. doi: 10.1016/j.talanta.2025.127946. Epub 2025 Mar 22.
Glutathione (GSH) is a critical antioxidant in biological systems involved in various cellular processes such as cell proliferation and apoptosis, and is considered as one of the cancer biomarkers. However, the conventional methods for detecting GSH levels often involve complex and time-consuming preparation and sophisticated equipment, posing challenges for rapid and straightforward analysis. Herein, we develop a colorimetric nanosensor using porous single-atom nanozymes (SAzymes), particularly those consisting of atomically dispersed metals on nitrogen-doped carbon supports (M-N-C), to monitor GSH quantitatively. The Mn-N-C SAzymes catalyze the oxidation of 3,3',5,5'-tetramethylbenzidine (TMB) by hydrogen peroxide (HO), resulting in a measurable color change. The high porosity of the Mn-N-C SAzymes offers a large surface area accommodating a high density of accessible active sites for efficient catalysis. The addition of GSH in this system leads to a notable reduction in color intensity, offering an effective method for the quantitative measurement of GSH. The Mn-N-C SAzymes demonstrate high efficacy in the rapid colorimetric detection of GSH, with a low detection limit of 0.70 μM and a broad dynamic range of 0-40 μM. This method is further applied for a simple and rapid colorimetric analysis of the cancer biomarker in various biological samples, including tissues and serum. Demonstrating the potential for diagnostic applications, this approach offers a promising tool for clinical diagnostics, enabling reliable and convenient monitoring of GSH levels, which is crucial for assessing disease progression.
谷胱甘肽(GSH)是生物系统中的一种关键抗氧化剂,参与细胞增殖和凋亡等各种细胞过程,被视为癌症生物标志物之一。然而,传统的检测GSH水平的方法通常涉及复杂且耗时的样品制备以及精密的设备,这对快速直接的分析构成了挑战。在此,我们开发了一种比色纳米传感器,使用多孔单原子纳米酶(SAzymes),特别是那些由原子分散在氮掺杂碳载体(M-N-C)上的金属组成的纳米酶,来定量监测GSH。Mn-N-C SAzymes催化过氧化氢(HO)氧化3,3',5,5'-四甲基联苯胺(TMB),导致可测量的颜色变化。Mn-N-C SAzymes的高孔隙率提供了较大的表面积,可容纳高密度的可及活性位点以实现高效催化。在该体系中加入GSH会导致颜色强度显著降低,为GSH的定量测量提供了一种有效方法。Mn-N-C SAzymes在快速比色检测GSH方面表现出高效性,检测限低至0.70 μM,动态范围宽达0 - 40 μM。该方法进一步应用于对包括组织和血清在内的各种生物样品中的癌症生物标志物进行简单快速的比色分析。该方法展示了诊断应用的潜力,为临床诊断提供了一种有前景的工具,能够可靠且方便地监测GSH水平,这对于评估疾病进展至关重要。