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Multilayered films fabricated from combinations of degradable polyamines: Tunable erosion and release of anionic polyelectrolytes

机译:由可降解多胺组合制成的多层膜:阴离子聚电解质的可调节侵蚀和释放

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摘要

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 similar to 60 nm thick using sodium poly(styrenesulfonate) (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.
机译:这项研究试图开发一种方法,该方法可以对多层聚电解质组件的腐蚀和生理相关介质中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)的不同组合制备的类似于60 nm厚的多层膜的制备和表征。我们研究了两种不同的膜制造方法:(1)使用由两种不同多胺定义的混合物组成的溶液进行制造,以及(2)由两种不同多胺的不同层组成的膜的制造。通常,使用由两种不同多胺的确定混合物组成的多胺溶液制备的薄膜具有几乎完全由用于制造薄膜的最具疏水性的多胺决定的侵蚀和释放曲线。相反,具有不同数量的不同多胺层的膜的制造允许对膜腐蚀和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)结构的薄膜所释放的SPS的轮廓与仅由聚合物1或聚合物2制成的薄膜的轮廓是中间的。此外,我们证明了通过改变掺入薄膜中的(1 / SPS)或(2 / SPS)的相对层数,可以对SPS的释放进行系统的控制。本文报道的方法提供了可控制的阴离子聚合物从涂有超薄多层膜的表面释放的速率的控制。随着进一步的发展,这项工作可能有助于超薄膜的设计,该薄膜允许对治疗相关大分子(例如蛋白质或DNA)从表面的释放和传递进行可调节的控制。

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