Advances in nanotechnology for the diagnosis and management of metabolic dysfunction-associated steatotic liver disease

被引:0
作者
Li, Fenfen [1 ]
Yuan, Ruyan [1 ]
Zhang, Jiamin [1 ]
Su, Bing [1 ]
Qi, Xiaolong [2 ,3 ,4 ]
机构
[1] Zhengzhou Univ, Sch Pharmaceut Sci, Zhengzhou 450001, Peoples R China
[2] Southeast Univ, Zhongda Hosp, Nurturing Ctr Jiangsu Prov, Med Sch,Dept Radiol,Liver Dis Ctr Integrated Tradi, Nanjing 210009, Peoples R China
[3] Southeast Univ, Zhongda Hosp, Minist Educ, Basic Med Res & Innovat Ctr, Nanjing 210009, Peoples R China
[4] State Key Lab Digital Med Engn, Nanjing 210009, Peoples R China
基金
中国国家自然科学基金;
关键词
MASLD; Liver fibrosis; Theranostics; Nanoprobes; Multifunctional nanocarriers; EFFECTIVE DRUG-DELIVERY; HEPATIC STELLATE CELLS; MAGNETIC-RESONANCE; INSULIN-RESISTANCE; PORTAL-HYPERTENSION; FATTY; NANOPARTICLES; FIBROSIS; SIRNA; EFFICACY;
D O I
10.1016/j.ajps.2025.101025
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Metabolic dysfunction-associated steatotic liver disease (MASLD) has a high global incidence and associated with increased lipid accumulation in hepatocytes, elevated hepatic enzyme levels, liver fibrosis, and hepatic carcinoma. Despite decades of research and significant advancements, the treatment of MASLD still faces formidable challenges. Nanoprobes for diagnostics and nanomedicine for targeted drug delivery to the liver present promising options for MASLD diagnosis and treatment, enhancing both imaging contrast and bioavailability. Here, we review recent advances in nanotechnology applied to MASLD diagnosis and treatment, specifically focusing on drug delivery systems targeting hepatocytes, hepatic stellate cells, Kupffer cells, and liver sinusoidal endothelial cells. This review aims to provide an overview of nanomedicine's potential in early MASLD diagnosis and therapeutic interventions, addressing related complications. (c) 2025 Shenyang Pharmaceutical University. Published by Elsevier B.V. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/)
引用
收藏
页数:20
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