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
相关论文
共 121 条
[1]   A novel tetraester construct that reduces cationic lipid-associated cytotoxicity. Implications for the onset of cytotoxicity [J].
Aberle, AM ;
Tablin, F ;
Zhu, J ;
Walker, NJ ;
Gruenert, DC ;
Nantz, MH .
BIOCHEMISTRY, 1998, 37 (18) :6533-6540
[2]  
Ai Jafar, 2011, Int J Nanomedicine, V6, P1117, DOI 10.2147/IJN.S16603
[3]   Toxicogenomics of non-viral drug delivery systems for RNAi: Potential impact on siRNA-mediated gene silencing activity and specificity [J].
Akhtar, Saghir ;
Benter, Ibrahim .
ADVANCED DRUG DELIVERY REVIEWS, 2007, 59 (2-3) :164-182
[5]   Cellular Uptake and Cytotoxicity of Gold Nanorods: Molecular Origin of Cytotoxicity and Surface Effects [J].
Alkilany, Alaaldin M. ;
Nagaria, Pratik K. ;
Hexel, Cole R. ;
Shaw, Timothy J. ;
Murphy, Catherine J. ;
Wyatt, Michael D. .
SMALL, 2009, 5 (06) :701-708
[6]   Delivery of siRNA from lyophilized polymeric surfaces [J].
Andersen, Morten O. ;
Howard, Kenneth A. ;
Paludan, Soren R. ;
Besenbacher, Flemming ;
Kjems, Jorgen .
BIOMATERIALS, 2008, 29 (04) :506-512
[7]  
[Anonymous], 2010, The Nobel Prize in Physiology or Medicine 1998
[8]   Nanotoxicology and in vitro studies: The need of the hour [J].
Arora, Sumit ;
Rajwade, Jyutika M. ;
Paknikar, Kishore M. .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2012, 258 (02) :151-165
[9]   Polycation-based nanoparticle delivery of RNAi therapeutics: Adverse effects and solutions [J].
Ballarin-Gonzalez, Borja ;
Howard, Kenneth Alan .
ADVANCED DRUG DELIVERY REVIEWS, 2012, 64 (15) :1717-1729
[10]   Inflammatory responses to pulmonary application of PEI-based siRNA nanocarriers in mice [J].
Beyerle, Andrea ;
Braun, Andrea ;
Banerjee, Atrayee ;
Ercal, Nuran ;
Eickelberg, Oliver ;
Kissel, Thomas H. ;
Stoeger, Tobias .
BIOMATERIALS, 2011, 32 (33) :8694-8701