TY - JOUR
T1 - Advanced strategies based on nanomedicine for Liver fibrosis treatment
AU - Zhang, Lu
AU - Liu, Tingting
AU - Shen, Huan
AU - Liu, Boheng
AU - Mei, Yun
AU - Liu, Yang
AU - Chen, Shuo
AU - Ma, Xingcong
AU - He, Chenyang
AU - Hu, Tinghua
AU - Li, Bin
AU - Cao, Gang
AU - Yu, Shuo
N1 - Publisher Copyright:
© 2025 Elsevier B.V.
PY - 2026/1/10
Y1 - 2026/1/10
N2 - Liver fibrosis (LF) is a significant pathological manifestation in various types of chronic liver diseases and is associated with substantial global morbidity and mortality. While liver transplantation remains a treatment option, existing clinical pharmacological interventions face limitations, highlighting the urgent need for novel therapeutic approaches. The emergence of nanobiotechnology has introduced nanoparticle-based drug delivery systems as a promising avenue for the treatment of liver-related ailments. This review systematically categorizes and synthesizes the diverse nanomaterials currently employed in the management of LF. It analyzes existing nanoplatforms used for LF treatment, focusing on various mechanisms for targeting and regulating specific cell types, including hepatic stellate cells, liver sinusoidal endothelial cells, and Kupffer cells. Additionally, strategies for regulating the fibrotic microenvironment, such as modulating extracellular matrix (ECM) deposition and degradation and mitigating inflammatory and oxidative stress, are explored. Finally, potential future directions and challenges for nanoparticle-based LF therapies are discussed.
AB - Liver fibrosis (LF) is a significant pathological manifestation in various types of chronic liver diseases and is associated with substantial global morbidity and mortality. While liver transplantation remains a treatment option, existing clinical pharmacological interventions face limitations, highlighting the urgent need for novel therapeutic approaches. The emergence of nanobiotechnology has introduced nanoparticle-based drug delivery systems as a promising avenue for the treatment of liver-related ailments. This review systematically categorizes and synthesizes the diverse nanomaterials currently employed in the management of LF. It analyzes existing nanoplatforms used for LF treatment, focusing on various mechanisms for targeting and regulating specific cell types, including hepatic stellate cells, liver sinusoidal endothelial cells, and Kupffer cells. Additionally, strategies for regulating the fibrotic microenvironment, such as modulating extracellular matrix (ECM) deposition and degradation and mitigating inflammatory and oxidative stress, are explored. Finally, potential future directions and challenges for nanoparticle-based LF therapies are discussed.
KW - Cell-targeted therapy
KW - Liver fibrosis
KW - Microenvironment regulation-based therapy
KW - Nanomaterials
KW - NO-mediated therapy
UR - https://www.scopus.com/pages/publications/105023489840
U2 - 10.1016/j.ijpharm.2025.126437
DO - 10.1016/j.ijpharm.2025.126437
M3 - 文献综述
C2 - 41325829
AN - SCOPUS:105023489840
SN - 0378-5173
VL - 688
JO - International Journal of Pharmaceutics
JF - International Journal of Pharmaceutics
M1 - 126437
ER -