药品
翻译(生物学)
药物输送
纳米技术
化学
纳米医学
小分子
药理学
肝损伤
纳米颗粒
医学
材料科学
生物化学
基因
信使核糖核酸
作者
Feifei Yang,Yusra B. Medik,Liantao Li,Xi Tian,Dong Fu,Kim L. R. Brouwer,Kyle Wagner,Bo Sun,Hossein Sendi,Yu Mi,Andrew Z. Wang
出处
期刊:Small
[Wiley]
日期:2020-01-23
卷期号:16 (7)
被引量:19
标识
DOI:10.1002/smll.201906360
摘要
Abstract Hepatotoxicity is a key concern in the clinical translation of nanotherapeutics because preclinical studies have consistently shown that nanotherapeutics accumulates extensively in the liver. However, clinical‐stage nanotherapeutics have not shown increased hepatotoxicity. Factors that can contribute to the hepatotoxicity of nanotherapeutics beyond the intrinsic hepatotoxicity of nanoparticles (NPs) are poorly understood. Because of this knowledge gap, clinical translation efforts have avoided hepatotoxic molecules. By examining the hepatotoxicity of nanoformulations of known hepatotoxic compounds, it is demonstrated that nanotherapeutics are associated with lower hepatotoxicity than their small‐molecule counterparts. It is also found that the reduced hepatotoxicity is related to the uptake of nanotherapeutics by macrophages in the liver. These findings can facilitate further development and clinical translation of nanotherapeutics.
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