Bhosale Sheshanath V, Bhosale Sidhanath V
School of Applied Sciences, RMIT University, GPO Box 2476, Melbourne, VIC-3001, Australia.
Sci Rep. 2013;3:1982. doi: 10.1038/srep01982.
The development of nanosized drug delivery systems to transport drugs to target cells, are promising tools to improve the drug therapeutic index. Transport systems should have a simple design to control the release of loaded drug to the target areas, thereby increasing concentration and prolonging retention. Herein, we demonstrate the use of yoctoliter wells (1 yL = 10(-24) L) as simple model systems for the encapsulation and release of biologically active molecules, by manipulating pH. The drug molecule employed here is doxorubicin, which diffuses into the bottom of yoctowells from a bulk solution at pH 7. Capping of the yoctowells is achieved by addition of an anionic-porphyrin by electrostatic interaction. Furthermore, controlled release of the Doxorubcin and capping agent from the yoctowells is achieved by pH control. The effectiveness of the sustain release of the bioactive molecule from yoctowells, provides potential for development of a new generation of drug-delivery system for practical application.
开发纳米级药物递送系统以将药物输送到靶细胞,是提高药物治疗指数的有前景的工具。运输系统应具有简单的设计,以控制负载药物向靶区域的释放,从而提高浓度并延长保留时间。在此,我们展示了通过调节pH值,使用飞升孔(1飞升 = 10⁻²⁴升)作为封装和释放生物活性分子的简单模型系统。这里使用的药物分子是阿霉素,它在pH值为7时从本体溶液扩散到飞升孔底部。通过静电相互作用添加阴离子卟啉实现飞升孔的封端。此外,通过pH控制实现阿霉素和封端剂从飞升孔的可控释放。从飞升孔中持续释放生物活性分子的有效性,为开发新一代实际应用的药物递送系统提供了潜力。