Departments of Chemistry and Polymer Science & Technology , Istanbul Technical University , Maslak, 34469 Istanbul , Turkey.
ACS Appl Mater Interfaces. 2018 Mar 7;10(9):8296-8306. doi: 10.1021/acsami.8b00168. Epub 2018 Feb 22.
We present mechanically strong and self-healable clay hydrogels containing 2-8 w/v % ds-DNA together with a synthetic biocompatible polymer, poly( N, N-dimethylacrylamide). Clay nanoparticles in the hydrogels act like a chemical cross-linker and promote their elastic behavior, whereas DNA contributes to their viscoelastic energy dissipation. The extent of mechanical hysteresis during cyclic tensile tests reveals that the strength of intermolecular bonds in DNA/clay hydrogels is in the range of the strength of hydrogen bonds. The hydrogels exhibit a high stretchability (up to 1500%) and a tensile strength between 20 and 150 kPa. They have the ability to self-heal, which is induced by heating the damaged gel samples above the melting temperature of ds-DNA. When comparing the mechanical properties of the hydrogels before and after healing, the healing efficiency is greater than 100%. We also demonstrate that ds-DNA molecules entrapped in the gel network undergoes thermal denaturation/renaturation cycles, leading to a further improvement in the mechanical properties of the hydrogels.
我们制备了一种机械强度高且可自修复的黏土水凝胶,其中包含 2-8 w/v % 的 ds-DNA 以及一种合成的生物相容性聚合物聚(N,N-二甲基丙烯酰胺)。水凝胶中的黏土纳米颗粒充当化学交联剂,从而促进其弹性行为,而 DNA 则有助于其黏弹性能量耗散。在循环拉伸测试中的力学滞后程度表明,DNA/黏土水凝胶中分子间键的强度处于氢键强度的范围内。水凝胶具有高拉伸性(可达 1500%)和 20-150kPa 的拉伸强度。它们具有自修复能力,这是通过将受损的凝胶样品加热到 ds-DNA 的熔融温度以上来实现的。当比较修复前后水凝胶的力学性能时,修复效率大于 100%。我们还证明了束缚在凝胶网络中的 ds-DNA 分子经历了热变性/复性循环,从而进一步提高了水凝胶的力学性能。