Kasza Karolina, Elsherbeny Amr, Moloney Cara, Hardie Kim R, Cámara Miguel, Alexander Cameron, Gurnani Pratik
Division of Molecular Therapeutics and Formulation School of Pharmacy University of Nottingham Nottingham NG7 2RD UK.
National Biofilms Innovation Centre School of Life Sciences, Biodiscovery Institute University Park, University of Nottingham Nottingham NG7 2RD UK.
Macromol Chem Phys. 2023 Dec;224(24):2300262. doi: 10.1002/macp.202300262. Epub 2023 Nov 7.
The biocompatibility, biodegradability, and responsiveness of poly(-amino esters) (PBAEs) has led to their widespread use as biomaterials for drug and gene delivery. Nonetheless, the step-growth polymerization mechanism that yields PBAEs limits the scope for their structural optimization toward specific applications because of limited monomer choice and end-group modifications. Moreover, to date the post-synthetic functionalization of PBAEs has relied on grafting-to approaches, challenged by the need for efficient polymer-polymer coupling and potentially difficult post-conjugation purification. Here a novel grafting-from approach to grow reversible addition-fragmentation chain transfer (RAFT) polymers from a PBAE scaffold is described. This is achieved through PBAE conversion into a macromolecular chain transfer agent through a multistep capping procedure, followed by RAFT polymerization with a range of monomers to produce PBAE-RAFT hybrid triblock copolymers. Following successful synthesis, the potential biological applications of these ABA triblock copolymers are illustrated through assembly into polymeric micelles and encapsulation of a model hydrophobic drug, followed by successful nanoparticle (NP) uptake in breast cancer cells. The findings demonstrate this novel synthetic methodology can expand the scope of PBAEs as biomaterials.
聚(氨基酯)(PBAEs)的生物相容性、生物降解性和响应性使其作为药物和基因递送的生物材料得到了广泛应用。尽管如此,由于单体选择和端基修饰有限,生成PBAEs的逐步增长聚合机制限制了其针对特定应用进行结构优化的范围。此外,迄今为止,PBAEs的合成后功能化依赖于接枝法,但这种方法面临着高效聚合物-聚合物偶联的需求以及潜在的共轭后纯化困难的挑战。本文描述了一种从PBAE支架生长可逆加成-断裂链转移(RAFT)聚合物的新型接枝法。这是通过多步封端程序将PBAE转化为大分子链转移剂,然后与一系列单体进行RAFT聚合以制备PBAE-RAFT杂化三嵌段共聚物来实现的。成功合成后,通过组装成聚合物胶束和包封一种模型疏水药物,随后在乳腺癌细胞中成功摄取纳米颗粒(NP),展示了这些ABA三嵌段共聚物潜在的生物学应用。研究结果表明,这种新型合成方法可以扩大PBAEs作为生物材料的应用范围。