Andreozzi Patrizia, Tamberi Lorenza, Tasca Elisamaria, Giacomazzo Gina Elena, Martinez Marta, Severi Mirko, Marradi Marco, Cicchi Stefano, Moya Sergio, Biagiotti Giacomo, Richichi Barbara
Department of Chemistry 'Ugo Schiff', University of Florence, Via della Lastruccia 3/13, 50019 Sesto Fiorentino, FI, Italy.
Soft Matter Nanotechnology Group, CIC biomaGUNE, Paseo Miramón 182 C, 20014 San Sebastián, Guipúzcoa, Spain.
Beilstein J Org Chem. 2020 Sep 11;16:2272-2281. doi: 10.3762/bjoc.16.188. eCollection 2020.
Mechanochemistry is an emerging and reliable alternative to conventional solution (batch) synthesis of complex molecules under green and solvent-free conditions. In this regard, we report here on the conjugation of a dextran polysaccharide with a fluorescent probe, a phenylboronic acid (PBA)-functionalized boron dipyrromethene (BODIPY) applying the ball milling approach. The ball milling formation of boron esters between PBA BODIPY and dextran proved to be more efficient in terms of reaction time, amount of reactants, and labelling degree compared to the corresponding solution-based synthetic route. PBA-BODIPY dextran assembles into nanoparticles of around 200 nm by hydrophobic interactions. The resulting PBA-BODIPY dextran nanoparticles retain an apolar interior as proved by pyrene fluorescence, suitable for the encapsulation of hydrophobic drugs with high biocompatibility while remaining fluorescent.
机械化学是在绿色无溶剂条件下合成复杂分子的传统溶液(间歇)合成方法的一种新兴且可靠的替代方法。在这方面,我们在此报告了采用球磨法将葡聚糖多糖与荧光探针、苯基硼酸(PBA)功能化的硼二吡咯亚甲基(BODIPY)进行共轭。与相应的基于溶液的合成路线相比,PBA BODIPY与葡聚糖之间硼酯的球磨形成在反应时间、反应物用量和标记程度方面被证明更有效。PBA-BODIPY葡聚糖通过疏水相互作用组装成约200 nm的纳米颗粒。芘荧光证明,所得的PBA-BODIPY葡聚糖纳米颗粒保留了非极性内部,适合封装具有高生物相容性的疏水性药物,同时保持荧光性。