School of Biomedical Engineering, McMaster University, 1280 Main Street West, Hamilton, Ontario, L8S 4L7, Canada.
School of Engineering Practice and Technology, McMaster University, 1280 Main Street West, Hamilton, Ontario, L8S 4L7, Canada.
Talanta. 2024 Jul 1;274:125998. doi: 10.1016/j.talanta.2024.125998. Epub 2024 Apr 3.
Artificial nanozymes (enzyme-mimics), specifically metallic nanomaterials, have garnered significant attention recently due to their reduced preparation cost and enhanced stability in a wide range of environments. The present investigation highlights, for the first time, a straightforward green synthesis of biogenic platinum nanoparticles (PtNPs) from a natural resource, namely Prunella vulgaris (Pr). To demonstrate the effectiveness of the phytochemical extract as an effective reducing agent, the PtNPs were characterized by various techniques such as UV-vis spectroscopy, High-resolution Transmission electron microscopy (HR-TEM), zeta-potential analysis, Fourier-transform infrared spectroscopy (FTIR), and Energy dispersive spectroscopy (EDS). The formation of PtNPs with narrow size distribution was verified. Surface decoration of PtNPs was demonstrated with multitudinous functional groups springing from the herbal extract. To demonstrate their use as viable nanozymes, the peroxidase-like activity of Pr/PtNPs was evaluated through a colorimetric assay. Highly sensitive visual detection of HO with discrete linear ranges and a low detection limit of 3.43 μM was demonstrated. Additionally, peroxidase-like catalytic activity was leveraged to develop a colorimetric platform to quantify glutamate biomarker levels with a high degree of selectivity, the limit of detection (LOD) being 7.00 μM. The 2,2-Diphenyl-1-picrylhydrazyl (DPPH) test was used to explore the scavenging nature of the PtNPs via the degradation of DPPH. Overall, the colorimetric assay developed using the Pr/PtNP nanozymes in this work could be used in a broad spectrum of applications, ranging from biomedicine and food science to environmental monitoring.
人工纳米酶(酶模拟物),特别是金属纳米材料,由于其制备成本降低和在广泛的环境中增强的稳定性,最近引起了极大的关注。本研究首次从天然资源夏枯草(Pr)中提出了一种简单的绿色合成生物源铂纳米粒子(PtNPs)的方法。为了证明植物化学提取物作为有效还原剂的有效性,采用紫外可见光谱、高分辨率透射电子显微镜(HR-TEM)、Zeta 电位分析、傅里叶变换红外光谱(FTIR)和能谱(EDS)等多种技术对 PtNPs 进行了表征。验证了 PtNPs 具有较窄的粒径分布。PtNPs 的表面装饰是由草药提取物中大量的功能基团证明的。为了证明它们作为可行的纳米酶的用途,通过比色法评估了 Pr/PtNPs 的过氧化物酶样活性。通过离散线性范围和低检测限 3.43 μM 证明了对 HO 的高度敏感的可视化检测。此外,利用过氧化物酶样催化活性,开发了一种比色平台来定量谷氨酸生物标志物,其选择性高,检测限(LOD)为 7.00 μM。使用 2,2-二苯基-1-苦基肼(DPPH)测试通过 DPPH 的降解来探索 PtNPs 的清除性质。总体而言,本工作中使用 Pr/PtNP 纳米酶开发的比色法可广泛应用于从生物医学和食品科学到环境监测的各种应用。