Dipartimento di Scienze Chimiche, Università di Padova, via Marzolo 1, Padova I-35131, Italy.
Nanoscale. 2013 Jul 7;5(13):6106-16. doi: 10.1039/c3nr00402c. Epub 2013 May 31.
PEGylated and non-PEGylated ORMOSIL nanoparticles prepared by microemulsion condensation of vinyltriethoxy-silane (VTES) were investigated in detail for their micro-structure and ability to deliver photoactive agents. With respect to pure silica nanoparticles, organic modification substantially changes the microstructure and the surface properties. This in turn leads to a modulation of both the photophysical properties of embedded photosensitizers and the interaction of the nanoparticles with biological entities such as serum proteins. The flexibility of the synthetic procedure allows the rapid preparation and screening of multifunctional nanosystems for photodynamic therapy (PDT). Selective targeting of model cancer cells was tested by using folate, an integrin specific RGD peptide and anti-EGFR antibodies. Data suggest the interference of the stealth-conferring layer (PEG) with small targeting agents, but not with bulky antibodies. Moreover, we showed that selective photokilling of tumour cells may be limited even in the case of efficient targeting because of intrinsic transport limitations of active cellular uptake mechanisms or suboptimum localization.
通过乙烯基三乙氧基硅烷 (VTES) 的微乳液缩合制备了聚乙二醇化和非聚乙二醇化的 ORMOSIL 纳米粒子,并详细研究了它们的微观结构和传递光活性剂的能力。与纯二氧化硅纳米粒子相比,有机修饰会极大地改变微结构和表面性质。这反过来又会调节嵌入的光敏剂的光物理性质以及纳米粒子与血清蛋白等生物实体的相互作用。合成程序的灵活性允许快速制备和筛选用于光动力疗法 (PDT) 的多功能纳米系统。通过使用叶酸、整联蛋白特异性 RGD 肽和抗 EGFR 抗体测试了模型癌细胞的选择性靶向。数据表明,赋予隐身性的层(PEG)会干扰小分子靶向剂,但不会干扰大体积的抗体。此外,我们还表明,即使在有效靶向的情况下,由于主动细胞摄取机制的固有运输限制或最佳定位不足,肿瘤细胞的选择性光杀伤也可能受到限制。