Leung Alex K K, Hafez Ismail M, Baoukina Svetlana, Belliveau Nathan M, Zhigaltsev Igor V, Afshinmanesh Elham, Tieleman D Peter, Hansen Carl L, Hope Michael J, Cullis Pieter R
J Phys Chem C Nanomater Interfaces. 2012 Aug 30;116(34):18440-18450. doi: 10.1021/jp303267y. Epub 2012 Jul 18.
Lipid nanoparticles (LNP) containing ionizable cationic lipids are the leading systems for enabling therapeutic applications of siRNA; however, the structure of these systems has not been defined. Here we examine the structure of LNP siRNA systems containing DLinKC2-DMA(an ionizable cationic lipid), phospholipid, cholesterol and a polyethylene glycol (PEG) lipid formed using a rapid microfluidic mixing process. Techniques employed include cryo-transmission electron microscopy, (31)P NMR, membrane fusion assays, density measurements, and molecular modeling. The experimental results indicate that these LNP siRNA systems have an interior lipid core containing siRNA duplexes complexed to cationic lipid and that the interior core also contains phospholipid and cholesterol. Consistent with experimental observations, molecular modeling calculations indicate that the interior of LNP siRNA systems exhibits a periodic structure of aqueous compartments, where some compartments contain siRNA. It is concluded that LNP siRNA systems formulated by rapid mixing of an ethanol solution of lipid with an aqueous medium containing siRNA exhibit a nanostructured core. The results give insight into the mechanism whereby LNP siRNA systems are formed, providing an understanding of the high encapsulation efficiencies that can be achieved and information on methods of constructing more sophisticated LNP systems.
含有可电离阳离子脂质的脂质纳米颗粒(LNP)是实现siRNA治疗应用的主要体系;然而,这些体系的结构尚未明确。在此,我们研究了通过快速微流混合工艺形成的、包含DLinKC2-DMA(一种可电离阳离子脂质)、磷脂、胆固醇和聚乙二醇(PEG)脂质的LNP siRNA体系的结构。所采用的技术包括冷冻透射电子显微镜、³¹P NMR、膜融合测定、密度测量和分子建模。实验结果表明,这些LNP siRNA体系具有一个内部脂质核心,其中包含与阳离子脂质复合的siRNA双链体,并且内部核心还含有磷脂和胆固醇。与实验观察结果一致,分子建模计算表明,LNP siRNA体系的内部呈现出水相区室的周期性结构,其中一些区室含有siRNA。得出的结论是,通过将脂质的乙醇溶液与含有siRNA的水性介质快速混合而配制的LNP siRNA体系呈现出纳米结构化核心。这些结果深入了解了LNP siRNA体系的形成机制,有助于理解能够实现的高封装效率,并提供了构建更复杂LNP体系方法的相关信息。