Nanotoxicity: a key obstacle to clinical translation of siRNA-based nanomedicine

被引:202
作者
Xue, Hui Yi [1 ]
Liu, Shimeng [1 ]
Wong, Ho Lun [1 ]
机构
[1] Temple Univ, Sch Pharm, Philadelphia, PA 19140 USA
关键词
cationic lipid; clinical trial; delivery; nanocarrier; nanoparticle; nanotoxicity; polymer; RNAi; siRNA; toxicological evaluation; SMALL-INTERFERING RNA; IRON-OXIDE NANOPARTICLES; CALCIUM-PHOSPHATE NANOPARTICLES; DRUG-DELIVERY SYSTEMS; GENE DELIVERY; IN-VIVO; GOLD NANOPARTICLES; CARBON NANOTUBES; HIGHLY EFFICIENT; LINEAR POLYETHYLENIMINE;
D O I
10.2217/nnm.13.204
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
siRNAs have immense therapeutic potential for the treatment of various gene-related diseases ranging from cancer, viral infections and neuropathy to autoimmune diseases. However, their bench-to-bedside translation in recent years has faced several challenges, with inefficient siRNA delivery being one of the most frequently encountered issues. In order to improve the siRNA delivery especially for systemic treatment, nanocarriers made of polymers, lipids or inorganic materials have become almost essential. The negative' aspects of these carriers such as their nanotoxicity and immunogenicity thus can no longer be overlooked. In this article, we will extensively review the nanotoxicity of siRNA carriers. The strategies for mitigating the risks of nanotoxicity and the methodology for evaluating these strategies will also be discussed. By addressing this often overlooked but important issue, it will help clear the way for siRNAs to fulfill their promise as a versatile class of therapeutic agents.
引用
收藏
页码:295 / 312
页数:18
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