Center for Education and Research on Macromolecules (CERM), University of Liege, B6a Sart-Tilman, B-4000, Liege, Belgium.
CNRS, University of Bordeaux, ICMCB, UPR 9048, F-33600, Pessac, France.
Small. 2015 May 20;11(19):2323-32. doi: 10.1002/smll.201402145. Epub 2015 Jan 12.
In this study, we report the synthesis of a nanoscaled drug delivery system, which is composed of a gold nanorod-like core and a mesoporous silica shell (GNR@MSNP) and partially uploaded with phase-changing molecules (1-tetradecanol, TD, T(m) 39 °C) as gatekeepers, as well as its ability to regulate the release of doxorubicin (DOX). Indeed, a nearly zero premature release is evidenced at physiological temperature (37 °C), whereas the DOX release is efficiently achieved at higher temperature not only upon external heating, but also via internal heating generated by the GNR core under near infrared irradiation. When tagged with folate moieties, GNR@MSNPs target specifically to KB cells, which are known to overexpress the folate receptors. Such a precise control over drug release, combining with the photothermal effect of GNR cores, provides promising opportunity for localized synergistic photothermal ablation and chemotherapy. Moreover, the performance in killing the targeted cancer cells is more efficient compared with the single phototherapeutic modality of GNR@MSNPs. This versatile combination of local heating, phototherapeutics, chemotherapeutics and gating components opens up the possibilities for designing multifunctional drug delivery systems.
在这项研究中,我们报告了一种纳米级药物输送系统的合成,该系统由金纳米棒状核和介孔硅壳(GNR@MSNP)组成,部分上传有相变分子(1-十四醇,TD,T(m)39°C)作为门控分子,以及其调节阿霉素(DOX)释放的能力。事实上,在生理温度(37°C)下,几乎没有出现过早释放,而在更高温度下,不仅通过外部加热,而且通过 GNR 核在近红外辐射下产生的内部加热,有效地实现了 DOX 的释放。当与叶酸部分标记时,GNR@MSNPs 特异性地靶向 KB 细胞,众所周知,KB 细胞过度表达叶酸受体。这种对药物释放的精确控制,结合 GNR 核的光热效应,为局部协同光热消融和化学疗法提供了有前途的机会。此外,与 GNR@MSNPs 的单一光治疗模式相比,靶向杀伤癌细胞的效果更为高效。这种局部加热、光疗、化疗和门控组件的多功能组合为设计多功能药物输送系统开辟了可能性。