Wu Yanheng, Gu Wenyi, Chen Chen, Do Son Trong, Xu Zhi Ping
Australian Institute for Bioengineering and Nanotechnology and School of Biomedical Sciences, The University of Queensland, St Lucia, Queensland 4072, Australia.
The Princess Alexandra Hospital, 199 Ipswich Rd, Woolloongabba, Queensland 4102, Australia.
ACS Omega. 2018 May 31;3(5):4871-4877. doi: 10.1021/acsomega.8b00397. Epub 2018 May 2.
Layered double hydroxide (LDH) nanoparticles (NPs) are safe and effective vectors for small interfering RNA (siRNA) delivery. However, it is unclear whether there are optimal parameters for the efficient delivery of functional siRNA using LDH NPs. In this research, we comprehensively examined the effect of parameters, such as the mixing method and LDH/siRNA mass ratio on siRNA silencing capability. We first noted that the best way for loading gene segments (25 bp dsDNA and siRNA) is to add gene molecules to 100 nm LDH and then diluting in Dulbecco's modified Eagle's medium. Very interestingly, the optimal LDH/gene mass ratio is around 20:1 in terms of cellular uptake amount of gene segments, whereas this ratio is shifted to around 5:1 in terms of target gene silencing efficacy, which has been reasonably explained. The optimization for LDH NP-based gene delivery system may provide the guidance for more efficient in vitro and in vivo siRNA delivery using the optimal parameters.
层状双氢氧化物(LDH)纳米颗粒(NPs)是用于小干扰RNA(siRNA)递送的安全有效载体。然而,目前尚不清楚使用LDH NPs高效递送功能性siRNA是否存在最佳参数。在本研究中,我们全面研究了诸如混合方法和LDH/siRNA质量比等参数对siRNA沉默能力的影响。我们首先注意到,加载基因片段(25 bp双链DNA和siRNA)的最佳方法是将基因分子添加到100 nm的LDH中,然后在杜尔贝科改良伊格尔培养基中稀释。非常有趣的是,就基因片段的细胞摄取量而言,最佳的LDH/基因质量比约为20:1,而就靶基因沉默效率而言,该比例则变为约5:1,这已得到合理的解释。基于LDH NP的基因递送系统的优化可为使用最佳参数更有效地进行体外和体内siRNA递送提供指导。