MOE Key Laboratory of Macromolecular Synthesis and Functionalization, Department of Polymer Science and Engineering, Zhejiang University , Hangzhou, China.
Langmuir. 2013 Nov 19;29(46):14101-7. doi: 10.1021/la4033332. Epub 2013 Nov 7.
The design of positively charged ultrathin films for surface modification is of crucial importance for biomedical applications. Herein, we report the layer-by-layer assembly of pure positively charged ultrathin films based on the host-guest interaction of cucurbit[8]uril (CB[8]). Two positively charged poly(ethylenimine)s (PEI) functionalized with guest moieties methyl viologen (MV) and indole (ID) were alternately assembled with the formation of CB[8] ternary complex under basic conditions. The growth of the (PEI-MV@CB[8]/PEI-ID) films was monitored by spectroscopic ellipsometry and quartz crystal microbalance. The morphology and structure of the films were characterized by scanning electron microscopy and UV-vis spectroscopy, respectively. These positively charged (PEI-MV@CB[8]/PEI-ID) films were very stable in the pH range from 4 to 9 but disassembled immediately when subjected to a competitive guest adamantylamine. Finally, the films were successfully employed as nanocontainers for DNA loading and subsequent directing the transfection of the adhered cells.
用于表面修饰的带正电荷的超薄膜的设计对于生物医学应用至关重要。在此,我们报告了基于葫芦[8]脲(CB[8])主客体相互作用的纯带正电荷的超薄膜的层层组装。两种带正电荷的聚(乙二胺)(PEI)用客体部分甲紫(MV)和吲哚(ID)官能化,在碱性条件下形成 CB[8]三元配合物,从而进行交替组装。通过光谱椭圆测量法和石英晶体微量天平监测(PEI-MV@CB[8]/PEI-ID)膜的生长。通过扫描电子显微镜和紫外可见光谱分别对薄膜的形貌和结构进行了表征。这些带正电荷的(PEI-MV@CB[8]/PEI-ID)薄膜在 pH 值为 4 到 9 的范围内非常稳定,但当受到竞争性客体金刚烷胺时,它们会立即解体。最后,这些薄膜成功地用作 DNA 负载的纳米容器,并随后指导附着细胞的转染。