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Mechanism and cellular kinetic studies of the enhancement of antioxidant activity by using surface-functionalized gold nanoparticles

机译:表面功能化金纳米粒子增强抗氧化活性的机理和细胞动力学研究

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The enhanced antioxidant activity of surface-functionalized gold nanoparticles (AuNPs) synthesized by self-assembly has attracted great attention, but little is known about the mechanism behind the enhanced activity. To address this challenge, the antioxidant activity of Au@PEG3SA (i.e., surface-functionalization of spherical AuNPs with the antioxidant salvianic acid A) was used as an example to illustrate the mechanism of the enhanced activity. Evaluation of the antioxidant activity was performed in a radical-scavenging reaction between Au@PEG3SA and 2,2-diphenyl-1-picrylhydrazyl (DPPH) radical. As expected, the rate constant for the reaction of Au@PEG3SA with DPPH was about nine times greater than that for the salvianic acid A monomer. A comparative analysis of the spectral characteristics of Au@PEG3SA and the salvianic acid A monomer further imply that the enhancement of the antioxidative reaction kinetics may be ascribed to the variation in the transition state for the DPPH-radical scavenging reaction through π-π stacking interactions between and among adjacent groups on the surface of Au@PEG3SA. On the other hand, the kinetic enhancement of Au@PEG3SA on reactive-oxygen-species (ROS) scavenging can be observed in living cells and in vivo, which possibly provides new insight for the bioapplication of self-assembly of surface-functionalized AuNPs.
机译:通过自组装合成的表面官能化金纳米粒子(AuNPs)增强的抗氧化活性引起了极大的关注,但对增强活性背后的机制知之甚少。为了解决这一挑战,以Au @ PEG3SA的抗氧化活性(即用抗氧化丹酚酸A对球形AuNPs进行表面官能化)为例来说明增强活性的机理。在Au @ PEG3SA和2,2-二苯基-1-吡啶并肼基(DPPH)自由基之间的自由基清除反应中评估抗氧化剂的活性。如预期的那样,Au @ PEG3SA与DPPH反应的速率常数约为丹参酸A单体的速率常数的九倍。对Au @ PEG3SA和丹酚酸A单体光谱特征的比较分析进一步暗示,抗氧化反应动力学的增强可能归因于通过π-π堆积相互作用进行DPPH自由基清除反应的过渡态变化。在Au @ PEG3SA表面上相邻基团之间和之间。另一方面,可以在活细胞和体内观察到Au @ PEG3SA对活性氧(ROS)清除的动力学增强,这可能为表面功能化AuNPs自组装的生物应用提供新的见解。

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