Department of Chemical Engineering, University of Rhode Island , 16 Greenhouse Road, Kingston, Rhode Island 02881, United States.
Department of Mechanical Engineering, University of Utah , 1495 E 100 S, Salt Lake City, Utah 84112, United States.
Biomacromolecules. 2016 Nov 14;17(11):3838-3844. doi: 10.1021/acs.biomac.6b01467. Epub 2016 Oct 17.
Layer-by-layer deposition of polyelectrolytes (PEs) onto self-assembled liposomes represents an alternative to PE deposition on solid particles for the formation of hollow nanoscale capsules. This work examines how competition between PE-liposome and inter-PE interactions drives the structure and colloidal stability of layersomes. Unlike solid particles, liposomes respond to adsorbed material through lipid reorganization and changes in size and shape. This responsive nature could yield new types of layered PE structures. We show that sequential deposition of strong biopolyelectrolytes, dextran sulfate-sodium salt (DxS) and poly-l-arginine (PA), onto cationic liposomes in water yields the expected charge inversion behavior commonly observed for dispersed particles. However, cryogenic transmission electron microscopy results show that the layersomes formed and their PE coatings were heterogeneous. The PE coatings contained PE complexes (PECs) that were formed when an even number of layers (2 or 4) was deposited. PECs remained attached as patches that were spatially distinguishable. This behavior was confirmed through fluorescence anisotropy measurements of liposome bilayer fluidity, where PA counteracted the ordering effects of DxS on the lipid bilayer through charge neutralization and local PEC desorption. With increased charge screening, DxS desorbed from the layersomes, whereas the patchy layersomes terminating in PA retained their PE coatings and colloidal stability at higher salt concentrations. To our knowledge, this is the first time such patchy layersome structures have been observed.
层层沉积聚电解质 (PEs) 到自组装脂质体上代表了一种替代方法,用于在固体颗粒上沉积 PEs 以形成中空纳米胶囊。这项工作研究了 PEs-脂质体和 PEs 之间的相互作用竞争如何驱动层状囊泡的结构和胶体稳定性。与固体颗粒不同,脂质体通过脂质重组和大小形状的变化来响应吸附物质。这种响应特性可能产生新型的层状 PE 结构。我们表明,在水中顺序沉积强生物聚电解质,硫酸葡聚糖钠盐 (DxS) 和聚精氨酸 (PA) 到阳离子脂质体上,会产生通常在分散颗粒中观察到的预期电荷反转行为。然而,低温透射电子显微镜结果表明,形成的层状囊泡及其 PE 涂层是不均匀的。PE 涂层包含当沉积偶数层(2 或 4)时形成的 PE 复合物 (PECs)。PECs 作为空间上可区分的斑块附着。这一行为通过脂质双层流动性的荧光各向异性测量得到了证实,其中 PA 通过电荷中和和局部 PEC 解吸来抵消 DxS 对脂质双层的有序化作用。随着电荷屏蔽的增加,DxS 从层状囊泡中解吸,而终止于 PA 的片状层状囊泡在更高的盐浓度下保留其 PE 涂层和胶体稳定性。据我们所知,这是首次观察到这种片状层状囊泡结构。