A Wirelessly Controlled Scalable 3D-Printed Microsystem for Drug Delivery

被引:6
|
作者
Forouzandeh, Farzad [1 ]
Ahamed, Nuzhet N. [1 ]
Zhu, Xiaoxia [2 ]
Bazard, Parveen [2 ]
Goyal, Krittika [1 ]
Walton, Joseph P. [2 ,3 ,4 ]
Frisina, Robert D. [2 ,3 ,4 ]
Borkholder, David A. [1 ]
机构
[1] Rochester Inst Technol, Dept Microsyst Engn, Rochester, NY 14623 USA
[2] Univ S Florida, Dept Med Engn, Global Ctr Hearing & Speech Res, Tampa, FL 33620 USA
[3] Univ S Florida, Dept Chem Biol & Mat Engn, Tampa, FL 33620 USA
[4] Univ S Florida, Dept Commun Sci & Disorders, Global Ctr Hearing & Speech Res, Tampa, FL 33620 USA
基金
美国国家卫生研究院;
关键词
drug delivery; micropump; microreservoir; 3D printing; implantable; transdermal; VENOUS ACCESS; MICROPUMP; SYSTEMS; DEVICE; PORT;
D O I
10.3390/ph14060538
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Here we present a 3D-printed, wirelessly controlled microsystem for drug delivery, comprising a refillable microreservoir and a phase-change peristaltic micropump. The micropump structure was inkjet-printed on the back of a printed circuit board around a catheter microtubing. The enclosure of the microsystem was fabricated using stereolithography 3D printing, with an embedded microreservoir structure and integrated micropump. In one configuration, the microsystem was optimized for murine inner ear drug delivery with an overall size of 19 x 13 x 3 mm(3). Benchtop results confirmed the performance of the device for reliable drug delivery. The suitability of the device for long-term subcutaneous implantation was confirmed with favorable results of implantation of a microsystem in a mouse for six months. The drug delivery was evaluated in vivo by implanting four different microsystems in four mice, while the outlet microtubing was implanted into the round window membrane niche for infusion of a known ototoxic compound (sodium salicylate) at 50 nL/min for 20 min. Real-time shifts in distortion product otoacoustic emission thresholds and amplitudes were measured during the infusion, demonstrating similar results with syringe pump infusion. Although demonstrated for one application, this low-cost design and fabrication methodology is scalable for use in larger animals and humans for different clinical applications/delivery sites.
引用
收藏
页数:16
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