Institute of Medicinal Plant Development (IMPLAD), Chinese Academy of Medical Sciences & Peking Union Medical College, Haidian District, Beijing, 100193, P. R. China.
Laboratory of Nano- and Translational Medicine, Lineberger Comprehensive Cancer Center, Carolina Center for Cancer Nanotechnology Excellence, Carolina Institute of Nanomedicine, University of North Carolina at Chapel Hill, Chapel Hill, NC, 27599, USA.
Small. 2020 Feb;16(7):e1906360. doi: 10.1002/smll.201906360. Epub 2020 Jan 23.
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.
肝毒性是纳米疗法临床转化的一个关键问题,因为临床前研究一致表明,纳米疗法会在肝脏中大量积累。然而,临床阶段的纳米疗法并未显示出肝毒性增加。除了纳米颗粒(NPs)的固有肝毒性之外,导致纳米疗法肝毒性的因素还了解甚少。由于这一知识空白,临床转化工作避免了具有肝毒性的分子。通过检查已知肝毒性化合物的纳米制剂的肝毒性,证明纳米疗法的肝毒性低于其小分子对应物。还发现,肝毒性的降低与纳米疗法被肝脏中的巨噬细胞摄取有关。这些发现可以促进纳米疗法的进一步开发和临床转化。