基于脂质体模板的响应性藻酸盐纳米凝胶超分子组装
Liposome-templated supramolecular assembly of responsive alginate nanogels.
作者信息
Hong Jennifer S, Vreeland Wyatt N, Lacerda Silvia H DePaoli, Locascio Laurie E, Gaitan Michael, Raghavan Srinivasa R
机构信息
Semiconductor Electronics Division, National Institute of Standards and Technology, Gaithersburg, MD 20899, USA.
出版信息
Langmuir. 2008 Apr 15;24(8):4092-6. doi: 10.1021/la7031219. Epub 2008 Mar 14.
Nanosized gel particles (nanogels) are of interest for a variety of applications, including drug delivery and single-molecule encapsulation. Here, we employ the cores of nanoscale liposomes as reaction vessels to template the assembly of calcium alginate nanogels. For our experiments, a liposome formulation with a high bilayer melting temperature (Tm) is selected, and sodium alginate is encapsulated in the liposomal core. The liposomes are then placed in an aqueous buffer containing calcium chloride, and the temperature is raised up to Tm. This allows permeation of Ca2+ ions through the bilayer and into the core, whereupon these ions gel the encapsulated alginate. Subsequently, the lipid bilayer covering the gelled core is removed by the addition of a detergent. The resulting alginate nanogels have a size distribution consistent with that of the template liposomes (ca. 120-200 nm), as confirmed by transmission electron microscopy and light scattering. Nanogels of different average sizes can be synthesized by varying the template dimensions, and the gel size can be further tuned after synthesis by the addition of monovalent salt to the solution.
纳米凝胶颗粒(纳米凝胶)因其在多种应用中的潜力而备受关注,包括药物递送和单分子封装。在此,我们利用纳米级脂质体的核心作为反应容器,来模板化海藻酸钙纳米凝胶的组装。在我们的实验中,选择了具有高双层熔化温度(Tm)的脂质体制剂,并将海藻酸钠封装在脂质体核心中。然后将脂质体置于含有氯化钙的水性缓冲液中,并将温度升至Tm。这使得Ca2+离子能够透过双层进入核心,随后这些离子使封装的海藻酸凝胶化。随后,通过添加去污剂去除覆盖凝胶化核心的脂质双层。透射电子显微镜和光散射证实,所得的海藻酸纳米凝胶的尺寸分布与模板脂质体一致(约120 - 200 nm)。通过改变模板尺寸可以合成不同平均尺寸的纳米凝胶,并且在合成后通过向溶液中添加单价盐可以进一步调整凝胶尺寸。