Zhang Jingtao, Lynn David M
Department of Chemical and Biological Engineering, University of Wisconsin - Madison, 1415 Engineering Drive, Madison, Wisconsin 53706.
Macromolecules. 2006 Jan 26;39(26):8928-8935. doi: 10.1021/ma061815g.
This investigation sought to develop methods that permit broad and tunable control over the erosion of multilayered polyelectrolyte assemblies and the release of anionic polymers in physiologically relevant media. We report the fabrication and characterization of multilayered films ~60 nm thick using sodium poly(styrene sulfonate) (SPS) and different combinations of three different hydrolytically degradable polyamines (1-3). We investigated two different approaches to film fabrication: 1) fabrication using solutions comprised of defined mixtures of two different polyamines, and 2) fabrication of films composed of different numbers of layers of two different polyamines. In general, films fabricated using polyamine solutions composed of defined mixtures of two different polyamines had erosion and release profiles that were dictated almost entirely by the most hydrophobic polyamine used to fabricate the films. In contrast, the fabrication of films having different numbers of layers of different polyamines permitted broad and tunable control over film erosion and the release of SPS. For example, films having the architecture (1/SPS)(n)(2/SPS)(m) released SPS with profiles that were intermediate to those of films fabricated exclusively from polymer 1 or polymer 2. Further, we demonstrated that it is possible to exert systematic control over the release of SPS by varying the relative numbers of layers of (1/SPS) or (2/SPS) incorporated into the films. The approaches reported here provide tunable control over the rate of the release of anionic polymers from surfaces coated with ultrathin multilayered films. This work could, with further development, contribute to the design of ultrathin films that permit tunable control over the release and delivery of therapeutically relevant macromolecules, such as proteins or DNA, from surfaces.
本研究旨在开发一些方法,以便在生理相关介质中对多层聚电解质组装体的侵蚀以及阴离子聚合物的释放进行广泛且可调节的控制。我们报告了使用聚苯乙烯磺酸钠(SPS)和三种不同的可水解降解多胺(1 - 3)的不同组合制备并表征了厚度约为60 nm的多层膜。我们研究了两种不同的成膜方法:1)使用由两种不同多胺的特定混合物组成的溶液进行制备,以及2)制备由两种不同多胺的不同层数组成的膜。一般来说,使用由两种不同多胺的特定混合物组成的多胺溶液制备的膜,其侵蚀和释放曲线几乎完全由用于制备膜的最疏水的多胺决定。相比之下,制备具有不同层数的不同多胺的膜允许对膜的侵蚀和SPS的释放进行广泛且可调节的控制。例如,具有(1/SPS)(n)(2/SPS)(m)结构的膜释放SPS的曲线介于仅由聚合物1或聚合物2制备的膜的曲线之间。此外,我们证明了通过改变掺入膜中的(1/SPS)或(2/SPS)的相对层数,可以对SPS的释放进行系统控制。这里报道的方法提供了对从涂有超薄多层膜的表面释放阴离子聚合物速率的可调节控制。随着进一步的发展,这项工作可能有助于设计超薄膜,从而允许对治疗相关大分子(如蛋白质或DNA)从表面的释放和递送进行可调节控制。