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Surface enhanced fluorescence of anti-tumoral drug emodin adsorbed on silver nanoparticles and loaded on porous silicon

机译:表面增强的抗肿瘤药物大黄素的荧光吸附在银纳米粒子上并负载在多孔硅上

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摘要

Fluorescence spectra of anti-tumoral drug emodin loaded on nanostructured porous silicon have been recorded. The use of colloidal nanoparticles allowed embedding of the drug without previous porous silicon functionalization and leads to the observation of an enhancement of fluorescence of the drug. Mean pore size of porous silicon matrices was 60 nm, while silver nanoparticles mean diameter was 50 nm. Atmospheric and vacuum conditions at room temperature were used to infiltrate emodin-silver nanoparticles complexes into porous silicon matrices. The drug was loaded after adsorption on metal surface, alone, and bound to bovine serum albumin. Methanol and water were used as solvents. Spectra with 1 μm spatial resolution of cross-section of porous silicon layers were recorded to observe the penetration of the drug. A maximum fluorescence enhancement factor of 24 was obtained when protein was loaded bound to albumin, and atmospheric conditions of inclusion were used. A better penetration was obtained using methanol as solvent when comparing with water. Complexes of emodin remain loaded for 30 days after preparation without an apparent degradation of the drug, although a decrease in the enhancement factor is observed. The study reported here constitutes the basis for designing a new drug delivery system with future applications in medicine and pharmacy
机译:已经记录了负载在纳米结构多孔硅上的抗肿瘤大黄素的荧光光谱。胶体纳米颗粒的使用允许药物的包埋而没有先前的多孔硅官能化,并且导致观察到药物的荧光增强。多孔硅基质的平均孔径为60 nm,而银纳米颗粒的平均直径为50 nm。使用室温的大气压和真空条件将大黄素-银纳米颗粒复合物渗透到多孔硅基质中。吸附后,将药物单独加载到金属表面,并与牛血清白蛋白结合。甲醇和水用作溶剂。记录具有1μm的多孔硅层的横截面空间分辨率的光谱以观察药物的渗透。当蛋白质被装载到白蛋白上时,获得最大的荧光增强因子为24,并使用了大气条件。与水相比,使用甲醇作为溶剂可获得更好的渗透性。大黄素的复合物在制备后保持负载30天,而药物没有明显降解,尽管观察到增强因子降低。此处报道的研究报告是设计一种新的药物输送系统的基础,该系统将在医学和药学领域得到进一步应用

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