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Local drug delivery with a self-contained, programmable, microfluidic system

机译:带有独立的可编程微流体系统的局部药物递送

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摘要

The development and optimization of many new drug therapies requires long-term local delivery with controlled, but variable dosage. Current methods for chronic drug delivery have limited utility because they either cannot deliver drugs locally to a specific organ or tissue, do not permit changes in delivery rate in situ, or cannot be used in clinical trials in an untethered, wearable configuration. Here, we describe a small, self-contained system for liquid-phase drug delivery. This system enables studies lasting several months and infusion rates can be programmed and modified remotely. A commercial miniature pump is integrated with microfabricated components to generate ultralow flow rates and stroke volumes. Solutions are delivered in pulses as small as 370 nL, with pulsesrndelivered at any interval of 1 min or longer. A unique feature of the system is the ability to infuse and immediately withdraw liquid, resulting in zero net volume transfer while compounds are exchanged by mixing and diffusion with endogenous fluid. We present in vitro results demonstrating repeatability of the delivered pulse volume for nearly 3 months. Furthermore, we present in vivo results in an otology application, infusing into the cochlea of a guinea pig a glutamate receptor antagonist, which causes localized and reversible changes in auditory sensitivity.
机译:许多新药疗法的开发和优化要求以可控但剂量可变的长期局部给药。当前的用于慢性药物递送的方法用途有限,因为它们要么不能将药物局部递送到特定的器官或组织,不允许就地改变递送速率,要么不能以不受束缚的,可穿戴的配置用于临床试验。在这里,我们描述了一个小型的,独立的液相药物输送系统。该系统可以进行持续数月的研究,并且可以远程编程和修改输液速度。商业微型泵与微制造的部件集成在一起,以产生超低流速和冲程量。溶液以小至370 nL的脉冲传送,脉冲以1分钟或更长时间的任意间隔传送。该系统的独特功能是能够注入并立即抽出液体,从而使净体积转移为零,同时通过与内源性流体混合和扩散来交换化合物。我们目前的体外结果表明近3个月内所传递的脉冲量具有可重复性。此外,我们目前在体内的结果在耳科应用,向豚鼠的耳蜗注入谷氨酸受体拮抗剂,这会导致听觉敏感性的局部和可逆变化。

著录项

  • 来源
    《Biomedical Microdevices》 |2009年第3期|571-578|共8页
  • 作者单位

    Charles Stark Draper Laboratory, Cambridge, MA, USA;

    Charles Stark Draper Laboratory, Cambridge, MA, USA;

    Charles Stark Draper Laboratory, Cambridge, MA, USA Department of Mechanical Engineering, Massachusetts Institute of Technology, Cambridge, MA, USA;

    Charles Stark Draper Laboratory, Cambridge, MA, USA;

    Eaton Peabody Laboratory, Massachusetts Eye and Ear Infirmary, Boston, MA, USA;

    Eaton Peabody Laboratory, Massachusetts Eye and Ear Infirmary, Boston, MA, USA Department of Otology and Laryngology, Harvard Medical School, Boston, MA, USA Department of Otolaryngology, Massachusetts Eye and Ear Infirmary, Boston, MA, USA;

    Department of Otology and Laryngology, Harvard Medical School, Boston, MA, USA Department of Otolaryngology, Massachusetts Eye and Ear Infirmary, Boston, MA, USA;

    Eaton Peabody Laboratory, Massachusetts Eye and Ear Infirmary, Boston, MA, USA Department of Otology and Laryngology, Harvard Medical School, Boston, MA, USA Department of Otolaryngology, Massachusetts Eye and Ear Infirmary, Boston, MA, USA Program in Neuroscience, Harvard Medical School, Boston, MA, USA;

    Department of Otology and Laryngology, Harvard Medical School, Boston, MA, USA Department of Otolaryngology, Massachusetts Eye and Ear Infirmary, Boston, MA, USA;

    Eaton Peabody Laboratory, Massachusetts Eye and Ear Infirmary, Boston, MA, USA Department of Otology and Laryngology, Harvard Medical School, Boston, MA, USA Department of Otolaryngology, Massachusetts Eye and Ear Infirmary, Boston, MA, USA Department of Audiology, Massachusetts Eye and Ear Infirmary, Boston, MA, USA Harvard-MIT Program in Speech and Hearing Bioscience and Technology, Boston, MA, USA;

    Charles Stark Draper Laboratory, Cambridge, MA, USA;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    drug delivery; microsystems; microfluidics; controlled release; hearing; cochlea;

    机译:药物输送;微系统微流体控释;听力;耳蜗;

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