Mathematics and Physics "E. De Giorgi" Department, University of Salento, Via Arnesano, 73100, Lecce, Italy.
Department of Neuroscience and Brain Technologies (NBT), Istituto Italiano di Tecnologia (IIT), Via Morego, 16163, Genova, Italy.
Sci Rep. 2020 Dec 3;10(1):21142. doi: 10.1038/s41598-020-77957-4.
Ubiquitous in nature, polyamines (PAs) are a class of low-molecular aliphatic amines critically involved in cell growth, survival and differentiation. The polycation behavior is validated as a successful strategy in delivery systems to enhance oligonucleotide loading and cellular uptake. In this study, the chemical features and the functional roles of the PA spermidine are synergistically exploited in the synthesis and bioactive functionalization of SiO-based structures. Inspired by biosilicification, the role of spermidine is assessed both as catalyst and template in a biomimetic one-pot synthesis of dense silica-based particles (SPs) and as a competitive agent in an interfacial reassembly strategy, to empty out SPs and generate spermidine-decorated hollow silica nanoporous pods (spd-SNPs). Spermidine bioactivity is then employed for targeting tumor cell over-expressed polyamine transport system (PTS) and for effective delivery of functional miRNA into melanoma cells. Spermidine decoration promotes spd-SNP cell internalization mediated by PTS and along with hollow structure enhances oligonucleotide loading. Accordingly, the functional delivery of the tumor suppressor miR-34a 3p resulted in intracellular accumulation of histone-complexed DNA fragments associated with apoptosis. Overall, the results highlight the potential of spd-SNP as a multi-agent anticancer therapy.
多胺(PAs)是一类低分子量脂肪族胺,广泛存在于自然界中,在细胞生长、存活和分化中起着至关重要的作用。聚阳离子行为已被验证为一种成功的策略,可用于提高寡核苷酸的负载和细胞摄取。在这项研究中,多胺精胺的化学特性和功能作用被协同利用于基于 SiO2 的结构的合成和生物活性功能化。受生物矿化的启发,评估了精胺在致密二氧化硅基颗粒(SPs)的仿生一锅法合成中的作用,既作为催化剂,又作为模板,以及在界面再组装策略中的竞争性试剂,以排空 SPs 并生成精胺修饰的中空二氧化硅纳米多孔荚(spd-SNPs)。然后,利用精胺的生物活性靶向肿瘤细胞过度表达的多胺转运系统(PTS),并将功能性 miRNA 有效递送至黑色素瘤细胞。精胺修饰促进了 PTS 介导的 spd-SNP 细胞内化,并且中空结构增强了寡核苷酸的负载。因此,肿瘤抑制因子 miR-34a 3p 的功能性递送导致与细胞凋亡相关的组蛋白复合 DNA 片段在细胞内积累。总之,这些结果突出了 spd-SNP 作为多效抗癌治疗的潜力。