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具有高效抗炎作用的天然无载体自组装二萜纳米颗粒,通过抑制 NF-κB 通路加速伤口愈合。

Natural carrier-free self-assembled diterpene nanoparticles with its efficient anti-inflammation through the inhibition of NF-κB pathway for accelerated wound healing.

机构信息

Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences & Peking Union Medical College, No. 151, Malianwa North Road, Haidian District, Beijing 100193, China.

College of Pharmaceutical Sciences, Key Laboratory of Pharmaceutical Quality Control of Hebei Province, Hebei University, No. 180, East Wusi Road, Baoding 071002, China.

出版信息

Biomed Pharmacother. 2023 Sep;165:115041. doi: 10.1016/j.biopha.2023.115041. Epub 2023 Jun 23.

Abstract

Nanoscience has set off a wave in biomedicine to improve the performance of drugs in recent years, but additional materials are usually required for supramolecular nanoconstruction, undoubtedly increasing the health risks. Herein, we discovered a novel diterpene supramolecular self-assembly system without additional chemicals, Nepebracteatalic Acid nanoparticles (NA NPs), mediated through hydrogen bond, hydrophobic and electrostatic interaction. NA NPs performed sustained release behavior, lower expression levels for IL-6 and TNF-α than clinical anti-inflammatory drug Indometacin. Furthermore, the effect of NA NPs on the related protein p65 expression levels of nuclear factor-κB (NFκB) signaling pathway is quantified to confirm the enhanced anti-inflammatory property based on the self-assembly strategy. Meanwhile, the prepared nanoparticles have good biocompatibility which ensures outstanding inflammation inhibition, collagen deposition, angiogenesis during wound healing. This work opens up new prospects that carrier-free nanoparticles from NPMs have great potential to exert clinical application value, meanwhile providing reference for developing green nanoscience.

摘要

近年来,纳米科学在生物医药领域掀起了一场提高药物性能的浪潮,但超分子纳米构建通常需要额外的材料,这无疑增加了健康风险。在此,我们发现了一种新型二萜超分子自组装体系,无需额外的化学物质,通过氢键、疏水相互作用和静电相互作用介导的 Nepebracteatalic Acid 纳米粒子(NA NPs)。NA NPs 表现出持续释放行为,与临床抗炎药物吲哚美辛相比,IL-6 和 TNF-α 的表达水平更低。此外,还定量分析了 NA NPs 对核因子-κB(NFκB)信号通路相关蛋白 p65 表达水平的影响,以基于自组装策略证实增强的抗炎特性。同时,所制备的纳米粒子具有良好的生物相容性,可确保出色的炎症抑制、胶原蛋白沉积和血管生成,促进伤口愈合。这项工作开辟了新的前景,即无载体的 NPM 纳米粒子具有很大的潜力发挥临床应用价值,同时为开发绿色纳米科学提供了参考。

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