Del Castillo Gustav Ferrand-Drake, Kyriakidou Maria, Adali Zeynep, Xiong Kunli, Hailes Rebekah L N, Dahlin Andreas
Department of Chemistry and Chemical Engineering, Chalmers University of Technology, Kemigården 4, 41296, Göteborg, Sweden.
Angew Chem Int Ed Engl. 2022 May 23;61(22):e202115745. doi: 10.1002/anie.202115745. Epub 2022 Mar 30.
Interfaces functionalized with polymers are known for providing excellent resistance towards biomolecular adsorption and for their ability to bind high amounts of protein while preserving their structure. However, making an interface that switches between these two states has proven challenging and concepts to date rely on changes in the physiochemical environment, which is static in biological systems. Here we present the first interface that can be electrically switched between a high-capacity (>1 μg cm ) multilayer protein binding state and a completely non-fouling state (no detectable adsorption). Switching is possible over multiple cycles without any regeneration. Importantly, switching works even when the interface is in direct contact with biological fluids and a buffered environment. The technology offers many applications such as zero fouling on demand, patterning or separation of proteins as well as controlled release of biologics in a physiological environment, showing high potential for future drug delivery in vivo.
用聚合物功能化的界面以对生物分子吸附具有优异抗性以及在保持其结构的同时能够结合大量蛋白质的能力而闻名。然而,制造在这两种状态之间切换的界面已被证明具有挑战性,并且迄今为止的概念依赖于物理化学环境的变化,而这种环境在生物系统中是静态的。在这里,我们展示了第一个可以在高容量(>1 μg cm)多层蛋白质结合状态和完全抗污染状态(无可检测吸附)之间进行电切换的界面。可以在多个循环中进行切换而无需任何再生。重要的是,即使界面与生物流体和缓冲环境直接接触,切换也能起作用。该技术提供了许多应用,例如按需零污染、蛋白质的图案化或分离以及在生理环境中生物制剂的控释,显示出未来体内药物递送的巨大潜力。