Zhou Kejin, Kos Petra, Yan Yunfeng, Xiong Hu, Min Yi-Li, Kinghorn Karina A, Minnig Jonathan T, Miller Jason B, Siegwart Daniel J
The University of Texas Southwestern Medical Center, Simmons Comprehensive Cancer Center, Department of Biochemistry, Dallas, Texas 75390, USA.
Chem Commun (Camb). 2016 Oct 6;52(82):12155-12158. doi: 10.1039/c6cc06024b.
Tremendous effort has been made to improve stability and delivery efficacy of small RNA therapeutics. However, nearly all current nano-encapsulation carriers utilize the critical balance between only two interacting parameters: RNA-binding electrostatic interactions and nanoparticle-stabilizing hydrophobic interactions. We report the development of intercalation-meditated nucleic acid (IMNA) nanoparticles, which utilize intercalation as a third interaction to enhance small RNA delivery. This toolbox expansion of interaction parameters may inspire the use of additional forces in nanoparticle drug carriers to increase potency and stability.
人们已经付出了巨大努力来提高小RNA疗法的稳定性和递送效果。然而,几乎所有当前的纳米封装载体仅利用两个相互作用参数之间的关键平衡:RNA结合静电相互作用和纳米颗粒稳定疏水相互作用。我们报告了嵌入介导核酸(IMNA)纳米颗粒的开发,其利用嵌入作为第三种相互作用来增强小RNA递送。这种相互作用参数的工具箱扩展可能会激发在纳米颗粒药物载体中使用额外的作用力,以提高效力和稳定性。