Prussian Blue-Derived Nanoplatform for In Situ Amplified Photothermal/Chemodynamic/Starvation Therapy

IF 8.2 2区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY
Jingyi Liang, Yaning Sun, Kaili Wang, Yawen Zhang, Linqing Guo, Zhihong Bao, Dun Wang, Haiyan Xu, Jiani Zheng and Yue Yuan*, 
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引用次数: 1

Abstract

Chemodynamic therapy (CDT) is an emerging tumor treatment; however, it is hindered by insufficient endogenous hydrogen peroxide (H2O2) and high glutathione (GSH) concentrations in the tumor microenvironment (TME). Furthermore, CDT has limited therapeutic efficacy as a monotherapy. To overcome these limitations, in this study, a nanoplatform is designed and constructed from Cu-doped mesoporous Prussian blue (CMPB)-encapsulated glucose oxidase (GOx) with a coating of hyaluronic acid (HA) modified with a nitric oxide donor (HN). In the proposed GOx@CMPB-HN nanoparticles, the dopant Cu2+ ions are crucial to combining and mutually promoting multiple therapeutic approaches, namely, CDT, photothermal therapy (PTT), and starvation therapy. The dopant Cu2+ ions in CMPB protect against reactive oxygen species to deplete the intracellular GSH in the TME. Additionally, the byproduct Cu+ ions act as a substrate for a Fenton-like reaction that activates CDT. Moreover, H2O2, which is another important substrate, is produced in large quantities through intracellular glucose depletion caused by the nanoparticle-loaded GOx, and the gluconic acid produced in this reaction further enhances the TME acidity and creates a better catalytic environment for CDT. In addition, Cu2+ doping greatly improves the mesoporous Prussian blue (MPB) photothermal conversion performance, and the resultant increase in temperature accelerates CDT catalysis. Finally, the HN coating enables the nanoparticles to actively target CD44 receptors in cancer cells and also enhances vascular permeability. Therefore, this coating has multiple effects, such as facilitating enhanced permeability and retention and deep laser penetration. In vitro and in vivo experiments demonstrate that the proposed GOx@CMPB-HN nanoplatform significantly inhibits tumor growth with the help of in situ enhanced synergistic therapies based on the properties of the TME. The developed nanoplatform has the potential to be applied to cancer treatment and introduces new avenues for tumor treatment research.

Abstract Image

用于原位放大光热/化学动力学/饥饿治疗的普鲁士蓝衍生纳米平台
化学动力疗法是一种新兴的肿瘤治疗方法;然而,肿瘤微环境(TME)中内源性过氧化氢(H2O2)不足和谷胱甘肽(GSH)浓度过高阻碍了肿瘤的发展。此外,CDT作为单一疗法的治疗效果有限。为了克服这些限制,在本研究中,设计并构建了一个纳米平台,该平台由cu掺杂的介孔普鲁士蓝(CMPB)包裹葡萄糖氧化酶(GOx),并在透明质酸(HA)涂层上修饰了一氧化氮供体(HN)。在提出的GOx@CMPB-HN纳米颗粒中,掺杂Cu2+离子对于多种治疗方法(CDT、光热治疗(PTT)和饥饿治疗)的结合和相互促进至关重要。CMPB中的掺杂Cu2+离子可防止活性氧消耗TME中的胞内谷胱甘肽。此外,副产物Cu+离子作为激活CDT的芬顿样反应的底物。此外,纳米颗粒负载的GOx引起细胞内葡萄糖消耗,从而大量产生H2O2作为另一种重要的底物,该反应产生的葡萄糖酸进一步增强了TME的酸度,为CDT创造了更好的催化环境。此外,Cu2+的掺杂大大提高了介孔普鲁士蓝(MPB)的光热转化性能,温度的升高加速了CDT的催化作用。最后,HN涂层使纳米颗粒能够主动靶向癌细胞中的CD44受体,并增强血管通透性。因此,该涂层具有多种效果,如促进增强透气性和保留性以及深度激光穿透。体外和体内实验表明,所提出的GOx@CMPB-HN纳米平台在基于TME特性的原位增强协同治疗的帮助下显著抑制肿瘤生长。所开发的纳米平台具有应用于癌症治疗的潜力,并为肿瘤治疗研究引入了新的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ACS Applied Materials & Interfaces
ACS Applied Materials & Interfaces 工程技术-材料科学:综合
CiteScore
16.00
自引率
6.30%
发文量
4978
审稿时长
1.8 months
期刊介绍: ACS Applied Materials & Interfaces is a leading interdisciplinary journal that brings together chemists, engineers, physicists, and biologists to explore the development and utilization of newly-discovered materials and interfacial processes for specific applications. Our journal has experienced remarkable growth since its establishment in 2009, both in terms of the number of articles published and the impact of the research showcased. We are proud to foster a truly global community, with the majority of published articles originating from outside the United States, reflecting the rapid growth of applied research worldwide.
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