Key Lab of Analytical Chemistry for Living Bio-systems, Institute of Chemistry, Chinese Academy of Sciences, No. 2 Zhongguancun Beiyijie, Beijing 100190, P.R. China.
College of Chemistry & Environmental Science, Hebei University, Baoding 071002, P. R. China.
Analyst. 2022 Mar 28;147(7):1509-1514. doi: 10.1039/d2an00158f.
More recently, gold nanoparticle (AuNP)-based nanozymes have become one of the burgeoning research hot topics. However, few studies have focused on these AuNP-nanozymes with polymers as ligands. A significant challenge is to reveal their catalytic mechanism and to improve their catalytic activity by changing the structures of the polymers. In this study, polyacrylamide (PAM) with different chain lengths was synthesized and used as the ligand to prepare PAM@AuNPs. The resultant nanozymes exhibited good peroxidase-like activity for catalyzing the oxidation of 3,3',5,5'-tetramethylbenzidine (TMB) in the presence of hydrogen peroxide (HO). In particular, due to the electrostatic interaction between the negatively charged PAM@AuNPs and the positively charged drug, the addition of ciprofloxacin in the oxidation system induced the aggregation of PAM@AuNPs and produced more amount of reactive oxygen species, which greatly promoted the catalytic activity of PAM@AuNPs. Inspired by the attractive property, a highly selective and sensitive colorimetric assay for the monitoring of ciprofloxacin was created. A good linear relationship between the UV-Vis absorption intensity of PAM@AuNPs-TMB-HO at 650 nm wavelength and the ciprofloxacin concentration was observed ranging from 1.0 μM to 12.0 μM ( = 0.998), providing the detection limit of 0.5 μM. The ciprofloxacin metabolism was further studied in rats. It reveals great potential of polymer protected AuNP-nanozymes in practical drug analysis.
最近,基于金纳米粒子(AuNP)的纳米酶已成为新兴研究热点之一。然而,很少有研究关注具有聚合物配体的这些 AuNP-纳米酶。一个重大的挑战是揭示它们的催化机制,并通过改变聚合物的结构来提高它们的催化活性。在本研究中,合成了不同链长的聚丙烯酰胺(PAM)并用作配体制备 PAM@AuNPs。所得纳米酶在过氧化氢(HO)存在下对 3,3',5,5'-四甲基联苯胺(TMB)的氧化具有良好的过氧化物酶样活性。特别是,由于带负电荷的 PAM@AuNPs 和带正电荷的药物之间的静电相互作用,在氧化体系中加入环丙沙星会诱导 PAM@AuNPs 的聚集并产生更多的活性氧物种,这极大地促进了 PAM@AuNPs 的催化活性。受这种吸引力的启发,创建了一种用于监测环丙沙星的高选择性和灵敏的比色测定法。在 650nm 波长处 PAM@AuNPs-TMB-HO 的紫外-可见吸收强度与环丙沙星浓度之间观察到良好的线性关系,检测限为 0.5μM( = 0.998),检测范围为 1.0μM 至 12.0μM。进一步在大鼠中研究了环丙沙星的代谢。它揭示了聚合物保护的 AuNP-纳米酶在实际药物分析中的巨大潜力。