Department of Physiology and Biomedical Engineering, Mayo Clinic, Rochester, Minnesota 55905, USA.
Biomater Sci. 2018 Feb 27;6(3):623-632. doi: 10.1039/c8bm00004b.
Functionalization of microbubbles (MBs) is a difficult issue due to their unstable nature. Here we report a fast and versatile method using a strain promoted alkyne-azide cycloaddition (SPAAC) click reaction for microbubble functionalization. An azadibenzocyclooctyne (DBCO) group was first introduced onto the MB surface and then an azide group into the desired ligand. Without any initiators or catalysts, essential click ligation occurred within 1 min and a majority of the reaction completed in 5 min at 37 °C. This fast ligation shortens the microbubble reaction time and preserves essential amounts of microbubbles for further in situ imaging and delivery of therapeutics.
由于微泡(MBs)的不稳定性,其功能化是一个难题。在这里,我们报告了一种使用应变促进的叠氮化物-炔烃环加成(SPAAC)点击反应快速且通用的微泡功能化方法。首先将叠氮二苯并环辛炔(DBCO)基团引入 MB 表面,然后将叠氮基团引入所需配体中。无需任何引发剂或催化剂,在 37°C 下,重要的点击连接在 1 分钟内发生,并且大部分反应在 5 分钟内完成。这种快速连接缩短了微泡反应时间,并保留了大量的微泡,用于进一步的原位成像和治疗药物的输送。