Kitiri Elina N, Shegani Antonio, Kopanos Ioannis, Pirmettis Nektarios, Triantis Charalampos, Rikkou-Kalourkoti Maria
Department of Pharmacy, Frederick University, Nicosia 1036, Cyprus.
Institute of Nuclear & Radiological Sciences & Technology, Energy & Safety, National Centre for Scientific Research "Demokritos", 15310 Athens, Greece.
Polymers (Basel). 2025 Jun 9;17(12):1608. doi: 10.3390/polym17121608.
Amphiphilic diblock copolymers comprising polyethylene glycol (PEG) and 1-vinyl imidazole (VIM) were synthesized using reversible addition-fragmentation chain transfer (RAFT) polymerization. The study focused on the synthesis of well-defined nanostructures with tunable composition and their functional modification for biomedical applications. The successful polymerization of PEG--PVIM diblock copolymers was confirmed via H NMR spectroscopy, and their molecular weights were analyzed using gel permeation chromatography (GPC). The copolymers exhibited pH-responsive behavior, with effective pK values of approximately 4.2. To facilitate radiolabeling and in vivo tracking, a post-polymerization modification enabled the conjugation of a 1,4,7-Triazacyclononane-1,4,7-triacetic acid (NOTA) chelator via aminolysis. The final conjugates were purified and characterized, confirming successful functionalization. These findings highlight the potential of PEG--PVIM diblock copolymers for biomedical applications.
采用可逆加成-断裂链转移(RAFT)聚合法合成了由聚乙二醇(PEG)和1-乙烯基咪唑(VIM)组成的两亲性二嵌段共聚物。该研究聚焦于合成具有可调组成的明确纳米结构及其在生物医学应用中的功能修饰。通过核磁共振氢谱(H NMR)光谱证实了PEG-PVIM二嵌段共聚物的成功聚合,并使用凝胶渗透色谱法(GPC)分析了它们的分子量。这些共聚物表现出pH响应行为,有效pK值约为4.2。为便于放射性标记和体内追踪,聚合后修饰通过氨解实现了1,4,7-三氮杂环壬烷-1,4,7-三乙酸(NOTA)螯合剂的共轭。对最终的共轭物进行了纯化和表征,证实了功能化的成功。这些发现突出了PEG-PVIM二嵌段共聚物在生物医学应用中的潜力。