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Active modulation of drug release by ionic field effect transistor for an ultra-low power implantable nanofluidic system

机译:离子场效应晶体管对超低功率可植入纳米流体系统的药物释放进行主动调节

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摘要

We report an electro-nanofluidic membrane for tunable, ultra-low power drug delivery employing an ionic field effect transistor. Therapeutic release from a drug reservoir was successfully modulated, with high energy efficiency, by actively adjusting the surface charge of slit-nanochannels 50, 110, and 160 nm in size, by the polarization of a buried gate electrode and the consequent variation of the electrical double layer in the nanochannel. We demonstrated control over the transport of ionic species, including two relevant hypertension drugs, atenolol and perindopril, that could benefit from such modulation. By leveraging concentration-driven diffusion, we achieve a 2 to 3 order of magnitude reduction in power consumption as compared to other electrokinetic phenomena. The application of a small gate potential (±5 V) in close proximity (150 nm) of 50 nm nanochannels generated a sufficiently strong electric field, which doubled or blocked ionic flux depending on the polarity of the voltage applied. These compelling findings can lead to next generation, more reliable, smaller, and longer lasting drug delivery implants with ultra-low power consumption.
机译:我们报告了使用离子场效应晶体管的可调,超低功率药物输送的电纳米流体膜。通过掩埋栅电极的极化和随之而来的电学变化,通过主动调节尺寸为50、110和160 nm的狭缝纳米通道的表面电荷,成功地调节了药物储库的治疗释放纳米通道中的双层。我们证明了对离子物质运输的控制,其中包括两种相关的高血压药物阿替洛尔和培哚普利,它们可以从这种调节中受益。通过利用浓度驱动的扩散,与其他电动现象相比,我们将功耗降低了2到3个数量级。在50 nm纳米通道的紧密接近(150 nm)处施加较小的栅极电势(±5 V)会产生足够强的电场,根据所施加电压的极性,该电场会使离子通量加倍或受阻。这些令人信服的发现可以带来具有超低功耗的下一代,更可靠,更小巧且使用寿命更长的药物植入物。

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