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具有按需释放 Celastrol 能力的酶/ROS 双重敏感纳米平台,通过清除 ROS、微生物群重平衡、缓解炎症来增强溃疡性结肠炎的治疗效果。

Enzyme/ROS dual-sensitive nanoplatform with on-demand Celastrol release capacity for enhanced ulcerative colitis therapy by ROS scavenging, microbiota rebalancing, inflammation alleviating.

机构信息

College of Pharmacy, Chengdu Medical College, No.783 Xindu Avenue, Xindu District, Chengdu, 610500, China.

State Key Laboratory of Quality Research in Chinese Medicine, Institute of Chinese Medical Sciences, University of Macau, Taipa, Macau SAR, 999078, China.

出版信息

J Nanobiotechnology. 2024 Jul 26;22(1):437. doi: 10.1186/s12951-024-02725-9.

Abstract

BACKGROUND

The oral administration of drugs for treating ulcerative colitis (UC) is hindered by several factors, including inadequate gastrointestinal stability, insufficient accumulation in colonic lesions, and uncontrolled drug release.

METHODS

A multiple sensitive nano-delivery system comprising β-cyclodextrin (CD) and 4-(hydroxymethyl)phenylboronic acid (PAPE) with enzyme/reactive oxygen species (ROS) sensitivity was developed to load celastrol (Cel) as a comprehensive treatment for UC.

RESULTS

Owing to the positive charge in the site of inflamed colonic mucosa, the negatively charged nanomedicine (Cel/NPs) could efficiently accumulate. Expectedly, Cel/NPs showed excellent localization ability to colon in vitro and in vivo tests. The elevated concentration of ROS and intestinal enzymes in the colon microenvironment quickly break the CD, resulting in Cel release partially to rebalance microbiota and recover the intestinal barrier. The accompanying cellular internalization of residual Cel/NPs, along with the high concentration of cellular ROS to trigger Cel burst release, could decrease the expression of inflammatory cytokines, inhibit colonic cell apoptosis, promote the macrophage polarization, scavenge ROS, and regulate the TLR4/NF-κB signaling pathway, which certified that Cel/NPs possessed a notably anti-UC therapy outcome.

CONCLUSIONS

We provide a promising strategy for addressing UC symptoms via an enzyme/ROS-sensitive oral platform capable of releasing drugs on demand.

摘要

背景

口服药物治疗溃疡性结肠炎(UC)受到多种因素的阻碍,包括胃肠道稳定性不足、在结肠病变部位积累不足和药物释放失控。

方法

开发了一种包含β-环糊精(CD)和 4-(羟甲基)苯硼酸(PAPE)的多重敏感纳米递药系统,具有酶/活性氧(ROS)敏感性,用于负载雷公藤红素(Cel)作为 UC 的综合治疗方法。

结果

由于炎症性结肠黏膜部位带正电荷,带负电荷的纳米药物(Cel/NPs)可以有效地积累。预计 Cel/NPs 在体外和体内试验中具有出色的定位于结肠的能力。结肠微环境中 ROS 和肠道酶的浓度升高会迅速破坏 CD,导致 Cel 部分释放,以重新平衡微生物群并恢复肠道屏障。残留的 Cel/NPs 的细胞内吞作用,以及高浓度的细胞 ROS 引发 Cel 爆发释放,可以降低炎症细胞因子的表达,抑制结肠细胞凋亡,促进巨噬细胞极化,清除 ROS,并调节 TLR4/NF-κB 信号通路,这证明了 Cel/NPs 具有显著的抗 UC 治疗效果。

结论

我们提供了一种有前途的策略,通过能够按需释放药物的酶/ROS 敏感口服平台来解决 UC 症状。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/078e/11282782/7c1c8748cf0e/12951_2024_2725_Fig1_HTML.jpg

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