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Wirelessly controlled, bioresorbable drug delivery device with active valves that exploit electrochemically triggered crevice corrosion

Authors
Koo, JahyunKim, Sung BongChoi, Yeon SikXie, ZhaoqianBandodkar, Amay J.Khalifeh, JawadYan, YingKim, HojunPezhouh, Maryam KheradDoty, KarenLee, GeumbeeChen, Yu-YuLee, Seung MinD'Andrea, DominicJung, KiminLee, KunHyuckLi, KanJo, SeongbinWang, HelingKim, Jae-HwanKim, JeonghyunChoi, Sung-GeunJang, Woo JinOh, Yong SukPark, InkyuKwak, Sung SooPark, Ji-HyeonHong, DoosunFeng, XueLee, Chi-HwanBanks, AnthonyLeal, CeciliaLee, Hyuck MoHuang, YonggangFranz, Colin K.Ray, Wilson Z.MacEwan, MatthewKang, Seung-KyunRogers, John A.
Issue Date
8월-2020
Publisher
AMER ASSOC ADVANCEMENT SCIENCE
Citation
SCIENCE ADVANCES, v.6, no.35
Indexed
SCIE
SCOPUS
Journal Title
SCIENCE ADVANCES
Volume
6
Number
35
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/54294
DOI
10.1126/sciadv.abb1093
ISSN
2375-2548
Abstract
Implantable drug release platforms that offer wirelessly programmable control over pharmacokinetics have potential in advanced treatment protocols for hormone imbalances, malignant cancers, diabetic conditions, and others. We present a system with this type of functionality in which the constituent materials undergo complete bioresorption to eliminate device load from the patient after completing the final stage of the release process. Here, bioresorbable polyanhydride reservoirs store drugs in defined reservoirs without leakage until wirelessly triggered valve structures open to allow release. These valves operate through an electrochemical mechanism of geometrically accelerated corrosion induced by passage of electrical current from a wireless, bioresorbable power-harvesting unit. Evaluations in cell cultures demonstrate the efficacy of this technology for the treatment of cancerous tissues by release of the drug doxorubicin. Complete in vivo studies of platforms with multiple, independently controlled release events in live-animal models illustrate capabilities for control of blood glucose levels by timed delivery of insulin.
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