Nanotheranostics for the Management of Hepatic Ischemia-Reperfusion Injury

被引:84
作者
Guan, Yu [1 ]
Yao, Weifeng [1 ]
Yi, Ke [1 ]
Zheng, Chunxiong [1 ,2 ]
Lv, Shixian [3 ]
Tao, Yu [1 ,2 ]
Hei, Ziqing [1 ]
Li, Mingqiang [1 ,2 ]
机构
[1] Sun Yat Sen Univ, Affiliated Hosp 3, Lab Biomat & Translat Med, Ctr Nanomed,Dept Anesthesiol, Guangzhou 510630, Peoples R China
[2] Guangdong Prov Key Lab Liver Dis Res, Guangzhou 510630, Peoples R China
[3] Univ Washington, Dept Bioengn, Seattle, WA 98195 USA
基金
中国国家自然科学基金;
关键词
anti‐ inflammatory nanoparticles; hepatic ischemia‐ reperfusion injury; nanoscale probes; nanosized antioxidants; LIVER ISCHEMIA/REPERFUSION INJURY; CERIUM OXIDE NANOPARTICLES; MEMBRANE-COATED NANOPARTICLES; FOCAL CEREBRAL-ISCHEMIA; BOX; RELEASE; NF-KAPPA-B; REACTIVE OXYGEN; OXIDATIVE STRESS; IN-VIVO; SUPEROXIDE-DISMUTASE;
D O I
10.1002/smll.202007727
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Hepatic ischemia-reperfusion injury (IRI), in which an insufficient oxygen supply followed by reperfusion leads to an inflammatory network and oxidative stress in disease tissue to cause cell death, always occurs after liver transplantations and sections. Although pharmacological treatments favorably prevent or protect the liver against experimental IRI, there have been few successes in clinical applications for patient benefits because of the incomprehension of complicated IRI-induced signaling events as well as short blood circulation time, poor solubility, and severe side reactions of most antioxidants and anti-inflammatory drugs. Nanomaterials can achieve targeted delivery and controllable release of contrast agents and therapeutic drugs in desired hepatic IRI regions for enhanced imaging sensitivity and improved therapeutic effects, emerging as novel alternative approaches for hepatic IRI diagnosis and therapy. In this review, the application of nanotechnology is summarized in the management of hepatic IRI, including nanomaterial-assisted hepatic IRI diagnosis, nanoparticulate systems-mediated remission of reactive oxygen species-induced tissue injury, and nanoparticle-based targeted drug delivery systems for the alleviation of IRI-related inflammation. The current challenges and future perspectives of these nanoenabled strategies for hepatic IRI treatment are also discussed.
引用
收藏
页数:24
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