Mohammadifar Ehsan, Ahmadi Vahid, Gholami Mohammad Fardin, Oehrl Alexander, Kolyvushko Oleksandr, Nie Chuanxiong, Donskyi Ievgen S, Herziger Svenja, Radnik Jörg, Ludwig Kai, Böttcher Christoph, Rabe Jürgen P, Osterrieder Klaus, Azab Walid, Haag Rainer, Adeli Mohsen
Institut für Chemie und Biochemie Freie Universität Berlin Takustrasse 3 14195 Berlin Germany.
Department of Physics and Integrative Research Institute for the Sciences IRIS Adlershof Humboldt-Universität zu Berlin Newtonstrasse 15 and Zum Großen Windkanal 2 12489 Berlin Germany.
Adv Funct Mater. 2021 May 26;31(22):2009003. doi: 10.1002/adfm.202009003. Epub 2021 Mar 26.
2D nanomaterials have garnered widespread attention in biomedicine and bioengineering due to their unique physicochemical properties. However, poor functionality, low solubility, intrinsic toxicity, and nonspecific interactions at biointerfaces have hampered their application in vivo. Here, biocompatible polyglycerol units are crosslinked in two dimensions using a graphene-assisted strategy leading to highly functional and water-soluble polyglycerols nanosheets with 263 ± 53 nm and 2.7 ± 0.2 nm average lateral size and thickness, respectively. A single-layer hyperbranched polyglycerol containing azide functional groups is covalently conjugated to the surface of a functional graphene template through pH-sensitive linkers. Then, lateral crosslinking of polyglycerol units is carried out by loading tripropargylamine on the surface of graphene followed by lifting off this reagent for an on-face click reaction. Subsequently, the polyglycerol nanosheets are detached from the surface of graphene by slight acidification and centrifugation and is sulfated to mimic heparin sulfate proteoglycans. To highlight the impact of the two-dimensionality of the synthesized polyglycerol sulfate nanosheets at nanobiointerfaces, their efficiency with respect to herpes simplex virus type 1 and severe acute respiratory syndrome corona virus 2 inhibition is compared to their 3D nanogel analogs. Four times stronger in virus inhibition suggests that 2D polyglycerols are superior to their current 3D counterparts.
二维纳米材料因其独特的物理化学性质在生物医学和生物工程领域受到广泛关注。然而,其功能欠佳、溶解度低、固有毒性以及在生物界面的非特异性相互作用阻碍了它们在体内的应用。在此,采用石墨烯辅助策略在二维空间交联生物相容性聚甘油单元,从而得到功能高度化且水溶性的聚甘油纳米片,其平均横向尺寸和厚度分别为263±53纳米和2.7±0.2纳米。含有叠氮官能团的单层超支化聚甘油通过pH敏感连接子与功能性石墨烯模板表面共价共轭。然后,通过在石墨烯表面负载三炔丙基胺,随后去除该试剂以进行表面点击反应,实现聚甘油单元的横向交联。随后,通过轻微酸化和离心将聚甘油纳米片从石墨烯表面分离,并进行硫酸化以模拟硫酸乙酰肝素蛋白聚糖。为突出合成的硫酸化聚甘油纳米片在纳米生物界面二维性的影响,将其对1型单纯疱疹病毒和严重急性呼吸综合征冠状病毒2的抑制效率与其三维纳米凝胶类似物进行比较。病毒抑制能力强四倍表明二维聚甘油优于其目前的三维对应物。