Jewell Christopher M, Zhang Jingtao, Fredin Nathaniel J, Wolff Matthew R, Hacker Timothy A, Lynn David M
Department of Chemical and Biological Engineering, Division of Cardiovascular Medicine, University of Wisconsin-Madison, 1415 Engineering Drive, Madison, Wisconsin 53706, USA.
Biomacromolecules. 2006 Sep;7(9):2483-91. doi: 10.1021/bm0604808.
Materials that permit control over the release of DNA from the surfaces of topologically complex implantable devices, such as intravascular stents, could contribute to the development of new approaches to the localized delivery of DNA. We report the fabrication of ultrathin, multilayered polyelectrolyte films that permit both the immobilization and controlled release of plasmid DNA from the surfaces of stainless steel intravascular stents. Our approach makes use of an aqueous-based, layer-by-layer method for the assembly of nanostructured thin films consisting of alternating layers of plasmid DNA and a hydrolytically degradable polyamine. Characterization of coated stents using scanning electron microscopy (SEM) demonstrated that stents were coated uniformly with an ultrathin film ca. 120 nm thick that adhered conformally to the surfaces of stent struts. These ultrathin films did not crack, peel, or delaminate substantially from the surface after exposure to a range of mechanical challenges representative of those encountered during stent deployment (e.g., balloon expansion). Stents coated with eight bilayers of degradable polyamine and a plasmid encoding enhanced green fluorescent protein (EGFP) sustained the release of DNA into solution for up to four days when incubated in phosphate buffered saline at 37 degrees C, and coated stents were capable of mediating the expression of EGFP in a mammalian cell line without the aid of additional transfection agents. The approach reported here could, with further development, contribute to the development of localized gene-based approaches to the treatment of cardiovascular diseases or related conditions.
能够控制拓扑结构复杂的可植入设备(如血管内支架)表面DNA释放的材料,可能有助于开发DNA局部递送的新方法。我们报道了超薄多层聚电解质膜的制备,该膜可使质粒DNA固定在不锈钢血管内支架表面并实现可控释放。我们的方法采用基于水相的逐层组装法来制备纳米结构薄膜,该薄膜由质粒DNA和可水解降解的多胺交替层组成。使用扫描电子显微镜(SEM)对包被支架进行表征,结果表明支架被一层约120纳米厚的超薄膜均匀包被,该超薄膜与支架支柱表面紧密贴合。在经历一系列代表支架展开过程中所遇到的机械挑战(如球囊扩张)后,这些超薄膜并未出现明显的开裂、剥落或分层现象。当在37℃的磷酸盐缓冲盐水中孵育时,涂有八层可降解多胺和编码增强型绿色荧光蛋白(EGFP)质粒的支架能够将DNA持续释放到溶液中长达四天,并且包被支架能够在不借助额外转染剂的情况下介导哺乳动物细胞系中EGFP的表达。本文报道的方法经过进一步开发,可能有助于开发基于局部基因的心血管疾病或相关病症治疗方法。