Xue Hui Yi, Liu Shimeng, Wong Ho Lun
School of Pharmacy, Temple University, 3307 North Broad Street, Philadelphia, PA 19140, USA.
Nanomedicine (Lond). 2014 Feb;9(2):295-312. doi: 10.2217/nnm.13.204.
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.
小干扰RNA(siRNAs)在治疗从癌症、病毒感染、神经病变到自身免疫性疾病等各种基因相关疾病方面具有巨大的治疗潜力。然而,近年来它们从实验室到临床应用面临着几个挑战,其中小干扰RNA递送效率低下是最常遇到的问题之一。为了改善小干扰RNA递送,特别是用于全身治疗,由聚合物、脂质或无机材料制成的纳米载体几乎已成为必需。因此,这些载体的“负面”方面,如它们的纳米毒性和免疫原性,再也不能被忽视。在本文中,我们将广泛综述小干扰RNA载体的纳米毒性。还将讨论减轻纳米毒性风险的策略以及评估这些策略的方法。通过解决这个经常被忽视但很重要的问题,将有助于为小干扰RNA作为一类多功能治疗剂实现其前景扫清道路。