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ROS 生成聚多巴胺对药物诱导的骨组织再生的协同作用。

Synergistic effect of ROS-generating polydopamine on drug-induced bone tissue regeneration.

机构信息

Department of Chemistry, Kyungpook National University, Daegu 41566, South Korea.

KNU Institute of Basic Sciences and KNU G-LAMP Project Group, Kyungpook National University, Daegu 41566, South Korea.

出版信息

Nanoscale. 2024 Nov 7;16(43):20118-20130. doi: 10.1039/d4nr02887b.

Abstract

A PHD (prolyl hydroxylase) inhibitor, 1,4-dihydrophenonthrolin-4-one-3-carboxylic acid (1,4-DPCA), is a drug that can artificially promote tissue regeneration by enhancing metabolic activity through the upregulation of hypoxia inducible factor 1 subunit alpha (Hif-1α) under normoxic conditions. This study presents a novel design methodology for a drug delivery system to maximize the regenerative effect of 1,4-DPCA. Specifically, by encapsulating 1,4-DPCA in polydopamine (PDA) that generates reactive oxygen species (ROS), the combined effects of Hif-1α upregulation and the induction of cellular antioxidant defense mechanisms by localized ROS can significantly enhance tissue regeneration. The study confirmed that each material (PDA and 1,4-DPCA) triggers a positive synergistic effect on the regenerative mechanisms. As a result, the use of a PDA drug delivery system loaded with 1,4-DPCA showed approximately six times greater bone regeneration compared to the control (no treatment) in a mouse calvarial defect model.

摘要

一种脯氨酰羟化酶(PHD)抑制剂,1,4-二氢苯并恶嗪-4-酮-3-羧酸(1,4-DPCA),是一种药物,可通过在常氧条件下上调缺氧诱导因子 1 亚基α(Hif-1α)来增强代谢活性,从而人为地促进组织再生。本研究提出了一种新的药物传递系统设计方法,以最大限度地提高 1,4-DPCA 的再生效果。具体来说,通过将 1,4-DPCA 封装在产生活性氧(ROS)的聚多巴胺(PDA)中,Hif-1α 的上调和局部 ROS 诱导细胞抗氧化防御机制的联合作用可以显著增强组织再生。研究证实,每种材料(PDA 和 1,4-DPCA)都对再生机制产生积极的协同作用。结果,与对照(无治疗)相比,在小鼠颅骨缺损模型中,负载 1,4-DPCA 的 PDA 药物传递系统的使用使骨再生增加了约六倍。

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