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

被引:32
|
作者
Fiering, J. [1 ]
Mescher, M. J. [1 ]
Swan, E. E. Leary [1 ,2 ]
Holmboe, M. E. [1 ]
Murphy, B. A. [3 ]
Chen, Z. [3 ,4 ,5 ]
Peppi, M. [3 ,4 ,5 ]
Sewell, W. F. [3 ,4 ,5 ,6 ]
McKenna, M. J. [4 ,5 ]
Kujawa, S. G. [3 ,4 ,5 ,7 ,8 ]
Borenstein, J. T. [1 ]
机构
[1] Charles Stark Draper Lab, Cambridge, MA USA
[2] MIT, Dept Mech Engn, Cambridge, MA 02139 USA
[3] Massachusetts Eye & Ear Infirm, Eaton Peabody Lab, Boston, MA 02114 USA
[4] Harvard Univ, Sch Med, Dept Otol & Laryngol, Boston, MA 02115 USA
[5] Massachusetts Eye & Ear Infirm, Dept Otolaryngol, Boston, MA 02114 USA
[6] Harvard Univ, Sch Med, Program Neurosci, Boston, MA 02115 USA
[7] Massachusetts Eye & Ear Infirm, Dept Audiol, Boston, MA 02114 USA
[8] Harvard MIT, Program Speech & Hearing Biosci, Boston, MA USA
基金
美国国家卫生研究院;
关键词
Drug delivery; Microsystems; Microfluidics; Controlled release; Hearing; Cochlea; IN-VIVO; MICRONEEDLES;
D O I
10.1007/s10544-008-9265-5
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
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 pulses delivered 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.
引用
收藏
页码:571 / 578
页数:8
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