LUNAM Université, Université d'Angers, Angers, France.
Eur J Pharm Biopharm. 2012 Jun;81(2):448-52. doi: 10.1016/j.ejpb.2012.02.010. Epub 2012 Feb 21.
Several siRNA (small interfering RNA) therapeutics are undergoing clinical trials for cancer, respiratory diseases or macular degeneration, but most are administrated locally. In order to overcome the different barriers to attain an efficient siRNA action after systemic administration, nanocarriers able to carry and protect siRNA are awaited. With this aim, we developed a new platform of siRNA lipid nanocapsules (LNCs) using different cationic lipids, combining the properties of LNCs (siRNA protection and targeting) and lipoplexes (efficient siRNA delivery into the cell). The formulation was revealed to contain different compartments. A siRNA quantification method based on UV spectroscopy was developed to locate and quantify siRNA in each compartment. All in all, these novel siRNA LNCs presented sizes of about 55 nm with a neutral surface charge and siRNA encapsulation efficiencies up to 65% representing appropriate characteristics for systemic administration.
几种用于癌症、呼吸道疾病或黄斑变性的小干扰 RNA (siRNA) 疗法正在进行临床试验,但大多数都是局部给药。为了克服系统给药后实现有效 siRNA 作用的不同障碍,需要能够携带和保护 siRNA 的纳米载体。为此,我们使用不同的阳离子脂质开发了一种新型 siRNA 脂质纳米胶囊 (LNC) 平台,结合了 LNC 的特性(siRNA 保护和靶向)和脂质体(有效将 siRNA 递送到细胞内)。该制剂被揭示含有不同的隔室。开发了一种基于紫外光谱的 siRNA 定量方法,以定位和定量每个隔室中的 siRNA。总的来说,这些新型 siRNA LNC 的大小约为 55nm,表面电荷呈中性,siRNA 包封效率高达 65%,这些特性适合系统给药。