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Targeted delivery of photosensitizers: efficacy and selectivity issues revealed by multifunctional ORMOSIL nanovectors in cellular systems

机译:光敏剂的靶向递送:细胞系统中多功能ORMOSIL纳米载体揭示的功效和选择性问题

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摘要

PEGylated and non-PEGylated ORMOSIL nanoparticles prepd. 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, org. modification substantially changes the microstructure and the surface properties. This in turn leads to a modulation of both the photophys. properties of embedded photosensitizers and the interaction of the nanoparticles with biol. entities such as serum proteins. The flexibility of the synthetic procedure allows the rapid prepn. 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 tumor cells may be limited even in the case of efficient targeting because of intrinsic transport limitations of active cellular uptake mechanisms or suboptimum localization.
机译:制备PEG化和非PEG化的ORMOSIL纳米颗粒。通过微乳液缩合反应,对乙烯基三乙氧基硅烷(VTES)的微观结构和传递光敏剂的能力进行了详细研究。关于纯二氧化硅纳米粒子,org。改性实质上改变了微观结构和表面性质。这进而导致两个照相的调制。嵌入的光敏剂的性质以及纳米粒子与生物分子的相互作用。实体,例如血清蛋白。合成过程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。使用叶酸,整联蛋白特异性RGD肽和抗EGFR抗体测试了对模型癌细胞的选择性靶向。数据表明,隐身赋予层(PEG)会干扰小的靶向剂,而不会干扰大的抗体。此外,我们表明,即使在有效靶向的情况下,由于主动细胞摄取机制的内在运输限制或亚最佳定位,对肿瘤细胞的选择性光杀伤也可能受到限制。

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