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扩展介孔硅包裹的超小 Pt 纳米团簇作为人工酶,用于跟踪活细胞中过氧化氢的分泌。

Expanded mesoporous silica-encapsulated ultrasmall Pt nanoclusters as artificial enzymes for tracking hydrogen peroxide secretion from live cells.

机构信息

College of Pharmaceutical Sciences, Hebei Medical University, Shijiazhuang, 050017, China.

College of Pharmaceutical Sciences, Hebei Medical University, Shijiazhuang, 050017, China.

出版信息

Anal Chim Acta. 2020 Apr 1;1104:180-187. doi: 10.1016/j.aca.2020.01.015. Epub 2020 Jan 9.

Abstract

Design of synthetic structures that possess the similar functions to natural enzymes held great promise in environmental detection and biomedical application. Herein, a new concept for the fabrication of solid-supported catalysts as peroxidase mimic have been proposed to realize high-catalytic activity and stability by utilizing expanded mesoporous silica (EMSN)-encapsulated Pt nanoclusters. Compared with PtNCs, the introduction of amino group modified EMSN would enrich HO on the surface of PtNCs and increase the catalytic sites for HO decomposition, which gave rise to the higher catalytic activity of EMSN-PtNCs over a broad pH range, especially in weakly acidic and neural solutions. This would facilitate their applications for real-time monitoring the secretion of HO from living cancer cells stimulated by various anticancer drugs. Our findings not only pave the way to use porous matrix as the structural component for the design of the biomimetic catalysts, but also provide a simple and reliable platform to monitor HO released from living cells in real time, which holds great potential for elucidating the biological roles of HO and underlying molecular mechanisms of drug cytotoxicity as well as drug therapeutic effects.

摘要

设计具有与天然酶相似功能的合成结构在环境检测和生物医学应用中具有很大的前景。在此,提出了一种新的概念,用于制备固体载体催化剂作为过氧化物酶模拟物,通过利用膨胀介孔硅(EMSN)封装的 Pt 纳米团簇来实现高催化活性和稳定性。与 PtNCs 相比,氨基修饰的 EMSN 的引入会在 PtNCs 表面富集 HO,并增加 HO 分解的催化位点,从而导致 EMSN-PtNCs 在较宽的 pH 范围内具有更高的催化活性,尤其是在弱酸性和中性溶液中。这将有助于它们实时监测各种抗癌药物刺激的活癌细胞中 HO 的分泌。我们的研究结果不仅为使用多孔基质作为仿生催化剂设计的结构组件铺平了道路,而且还为实时监测活细胞中释放的 HO 提供了一个简单可靠的平台,这对于阐明 HO 的生物学作用以及药物细胞毒性的潜在分子机制和药物治疗效果具有很大的潜力。

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