细胞外基质
材料科学
纤维化
胶原酶
平衡
基质(化学分析)
细胞外
肝纤维化
细胞生物学
纳米颗粒
黑色素
生物物理学
纳米技术
生物化学
生物
医学
酶
内科学
复合材料
作者
Tingting Li,Weihua Fu,Xueqi Li,Yong Huo,Huifang Ji,Taigang Liang,Ruiping Zhang
标识
DOI:10.1021/acsami.4c15494
摘要
Liver fibrosis is a chronic disease that lacks effective drug treatment. Chronic damage and inflammation lead to the formation of collagen and fibrous scars. However, the excessive accumulation of collagen I significantly hinders the delivery of drugs into liver tissue. Therefore, this study developed a quercetin-loaded melanin nanoparticle codecorated collagenase (MNP-QUE-COL) for the treatment of liver fibrosis. These results showed that MNP-QUE-COL degraded excessive collagen I, thereby efficiently delivering melanin and quercetin into the liver tissue. MNP-QUE-COL exhibited optimal PA/MRI dual-mode imaging ability. In addition, the synergistic anti-inflammatory and reactive oxygen species scavenging function of quercetin and melanin was achieved by regulation of M1-M2 macrophage polarization and inhibition of pro-inflammatory cytokine release, reshaping the imbalanced extracellular interstitial inflammatory environment. The results of this research suggest that MNP-QUE-COL is a safe and efficient therapeutic nanoplatform for liver fibrosis, showing promise as a potential therapeutic strategy for liver fibrosis and associated diseases.
科研通智能强力驱动
Strongly Powered by AbleSci AI