Department of Nanomedicine, The Methodist Hospital Research Institute, 6670 Bertner Ave, Houston, TX 77030, USA.
Lab Chip. 2011 Aug 7;11(15):2526-34. doi: 10.1039/c1lc00001b. Epub 2011 Jun 15.
Recent work has elucidated the potential of important new therapeutic paradigms, including metronomic delivery and chronotherapy, in which the precise timing and location of therapeutic administration has a significant impact on efficacy and toxicity. New drug delivery architectures are needed to not only release drug continuously at precise rates, but also synchronize their release with circadian cycles. We present an actively controlled nanofluidic membrane that exploits electrophoresis to control the magnitude, duration, and timing of drug release. The membrane, produced using high precision silicon fabrication techniques, has platinum electrodes integrated at the inlet and outlet that allow both amplification and reversal of analyte delivery with low applied voltage (at or below 2 VDC). Device operation was demonstrated with solutions of both fluorescein isothiocyanate conjugated bovine serum albumin and lysozyme using fluorescence spectroscopy, fluorescence microscopy, and a lysozyme specific bio-assay and has been characterized for long-term molecular release and release reversibility. Through a combination of theoretical and experimental analysis, the relative contributions of electrophoresis and electroosmosis have been investigated. The membrane's clinically relevant electrophoretic release rate at 2 VDC exceeds the passive release by nearly one order of magnitude, demonstrating the potential to realize the therapeutic paradigm goal.
最近的研究阐明了重要的新治疗范例的潜力,包括节拍疗法和时间疗法,其中治疗的精确时间和位置对疗效和毒性有重大影响。需要新的药物输送架构,不仅要以精确的速率持续释放药物,还要使药物释放与生理节律同步。我们提出了一种主动控制的纳米流体膜,该膜利用电泳来控制药物释放的幅度、持续时间和时间。该膜使用高精度硅制造技术生产,在入口和出口处集成了铂电极,允许在低施加电压(2 VDC 或以下)下放大和反转分析物的输送。使用荧光光谱法、荧光显微镜法以及溶菌酶特异性生物测定法,对荧光素异硫氰酸酯结合牛血清白蛋白和溶菌酶的溶液进行了设备操作演示,并且已经对长期分子释放和释放可逆性进行了表征。通过理论和实验分析的结合,研究了电泳和电渗流的相对贡献。该膜在 2 VDC 时的临床相关电泳释放速率超过了被动释放近一个数量级,表明有可能实现治疗范例的目标。