Department of Chemistry, University of Wisconsin-Madison, 1415 Engineering Drive, Madison, WI 53706, United States.
Department of Chemistry, University of Wisconsin-Madison, 1415 Engineering Drive, Madison, WI 53706, United States; Department of Chemical and Biological Engineering, University of Wisconsin-Madison, 1415 Engineering Drive, Madison, WI 53706, United States.
J Control Release. 2010 Nov 20;148(1):91-100. doi: 10.1016/j.jconrel.2010.07.112. Epub 2010 Jul 30.
We report an approach to the design of multilayered polyelectrolyte thin films (or 'polyelectrolyte multilayers', PEMs) that can be used to provide tunable control over the release of plasmid DNA (or multiple different DNA constructs) from film-coated surfaces. Our approach is based upon methods for the layer-by-layer assembly of DNA-containing thin films, and exploits the properties of a new class of cationic 'charge-shifting' polymers (amine functionalized polymers that undergo gradual changes in net charge upon side chain ester hydrolysis) to provide control over the rates at which these films erode and release DNA. We synthesized two 'charge-shifting' polymers (polymers 1 and 2) containing different side chain structures by ring-opening reactions of poly(2-alkenyl azlactone)s with two different tertiary amine functionalized alcohols (3-dimethylamino-1-propanol and 2-dimethylaminoethanol, respectively). Subsequent characterization revealed large changes in the rates of side chain ester hydrolysis for these two polymers; whereas the half-life for the hydrolysis of the esters in polymer 1 was ~200 days, the half-life for polymer 2 was ~6 days. We demonstrate that these large differences in side chain hydrolysis make possible the design of PEMs that erode and promote the surface-mediated release of DNA either rapidly (e.g., over ~3 days for films fabricated using polymer 2) or slowly (e.g., over ~1 month for films fabricated using polymer 1). We demonstrate further that it is possible to design films with release profiles that are intermediate to these two extremes by fabricating films using solutions containing different mixtures of these two polymers. This approach can thus expand the usefulness of these two polymers and achieve a broader range of DNA release profiles without the need to synthesize polymers with new structures or properties. Finally, we demonstrate that polymers 1 and 2 can be used to fabricate multilayered films with hierarchical structures that promote the sequential release of two different DNA constructs with separate and distinct release profiles (e.g., the release of a first construct over a period of ~3 days, followed by the sustained release of a second for a period of ~70 days). With further development, this approach could contribute to the design of functional thin films and surface coatings that provide sophisticated control over the timing and the order of the release of two or more DNA constructs (or other agents) of interest in a range of biomedical contexts.
我们报告了一种设计多层聚电解质薄膜(或“聚电解质多层”,PEMs)的方法,该方法可用于从涂膜表面对质粒 DNA(或多种不同的 DNA 构建体)的释放进行可调控制。我们的方法基于含 DNA 薄膜的逐层组装方法,并利用一类新型阳离子“电荷转移”聚合物(伯胺官能化聚合物,其侧链酯水解时净电荷逐渐变化)的特性来控制这些薄膜侵蚀和释放 DNA 的速率。我们通过聚(2-烯基氮杂内酯)与两种不同的叔胺官能化醇(3-二甲氨基-1-丙醇和 2-二甲氨基乙醇)的开环反应合成了两种含有不同侧链结构的“电荷转移”聚合物(聚合物 1 和 2)。随后的表征表明,这两种聚合物的侧链酯水解速率有很大差异;而聚合物 1 中酯的半衰期约为 200 天,聚合物 2 的半衰期约为 6 天。我们证明,这些侧链水解的巨大差异使得设计聚电解质多层膜成为可能,这些膜要么快速侵蚀并促进 DNA 的表面介导释放(例如,使用聚合物 2 制备的膜在3 天内),要么缓慢释放(例如,使用聚合物 1 制备的膜在1 个月内)。我们进一步证明,通过使用这两种聚合物的不同混合物的溶液来制备膜,可以设计出介于这两种极端之间的释放曲线的膜。因此,这种方法可以扩展这两种聚合物的用途,并实现更广泛的 DNA 释放曲线,而无需合成具有新结构或性质的聚合物。最后,我们证明聚合物 1 和 2 可用于制造具有分层结构的多层膜,该结构促进具有单独和不同释放曲线的两种不同 DNA 构建体的顺序释放(例如,在3 天内释放第一构建体,然后在70 天内持续释放第二构建体)。随着进一步的发展,这种方法可以有助于设计功能性薄膜和表面涂层,在一系列生物医学环境中对两种或多种 DNA 构建体(或其他试剂)的释放时间和顺序提供复杂的控制。