Institute for Molecules and Materials, Radboud University, Heyendaalseweg 135, 6525 AJ Nijmegen, The Netherlands.
Biomacromolecules. 2020 May 11;21(5):1853-1864. doi: 10.1021/acs.biomac.9b01734. Epub 2020 Feb 19.
Functionalizing polymersomes remains a challenge due to the limitation in reaction conditions applicable to the chemistry on the surface, hindering their application for selective targeting. In order to overcome this limitation, functionalization can be introduced right before the self-assembly. Here, we have synthesized a library (32 examples) of PEG--PS and PEG--PDLLA with various functional groups derived from the amine-functionalized polymers, leading to functionally active polymersomes. We show that polymersome formation is possible via the general method with all functionalized groups and that these handles are present on the surface and are able to undergo reactions. Additionally, this methodology provides a general synthetic tool to tailor the functional group of the polymersome right before self-assembly, without limitation on the reaction conditions.
由于聚合物囊泡表面化学适用的反应条件有限,功能化聚合物囊泡仍然是一个挑战,这阻碍了它们在选择性靶向方面的应用。为了克服这一限制,可以在自组装之前引入功能化。在这里,我们合成了一个由胺功能化聚合物衍生而来的具有各种官能团的 PEG-PS 和 PEG-PDLLA 的库(32 个实例),得到了功能活性聚合物囊泡。我们证明了通过通用方法可以实现所有官能团的聚合物囊泡形成,并且这些接头存在于表面上,并且能够进行反应。此外,该方法学为在自组装之前定制聚合物囊泡的官能团提供了一种通用的合成工具,而不受反应条件的限制。