Yang Huanghao, Liu Haipeng, Kang Huaizhi, Tan Weihong
Center for Research at the Bio/Nano Interface, Department of Chemistry and Shands Cancer Center, UF Genetics Institute and McKnight Brian Institute, University of Florida, Gainesville, Florida 32611-7200, USA.
J Am Chem Soc. 2008 May 21;130(20):6320-1. doi: 10.1021/ja801339w. Epub 2008 Apr 29.
In this communication, we report a simple, but highly adaptable, method of constructing selective target-responsive hydrogels using DNA aptamers. The simplicity of the design is accomplished by using linear polymer chains as the hydrogel backbone and a DNA aptamer as the cross-linker. In this design, competitive binding of target to the aptamer causes the decrease of cross-linking density and, hence, dissolution of the hydrogel. The adaptability of this strategy for therapeutic applications was demonstrated using two different types of targets, small molecules and proteins. Our results indicated that this molecular engineering provides a highly selective and controllable release system whereby efficient release of therapeutic agents can occur at specific environments in which the target biomarker is found.
在本通讯中,我们报道了一种使用DNA适配体构建选择性靶标响应水凝胶的简单但高度可适应的方法。该设计的简单性通过使用线性聚合物链作为水凝胶主链和DNA适配体作为交联剂来实现。在这种设计中,靶标与适配体的竞争性结合导致交联密度降低,从而使水凝胶溶解。使用小分子和蛋白质这两种不同类型的靶标证明了该策略在治疗应用中的适应性。我们的结果表明,这种分子工程提供了一种高度选择性和可控的释放系统,由此治疗剂可以在发现靶标生物标志物的特定环境中有效释放。