| Literature DB >> 26189679 |
Jae-Woong Jeong1, Jordan G McCall2, Gunchul Shin3, Yihui Zhang4, Ream Al-Hasani5, Minku Kim3, Shuo Li3, Joo Yong Sim6, Kyung-In Jang3, Yan Shi7, Daniel Y Hong8, Yuhao Liu3, Gavin P Schmitz8, Li Xia9, Zhubin He10, Paul Gamble11, Wilson Z Ray11, Yonggang Huang12, Michael R Bruchas13, John A Rogers14.
Abstract
In vivo pharmacology and optogenetics hold tremendous promise for dissection of neural circuits, cellular signaling, and manipulating neurophysiological systems in awake, behaving animals. Existing neural interface technologies, such as metal cannulas connected to external drug supplies for pharmacological infusions and tethered fiber optics for optogenetics, are not ideal for minimally invasive, untethered studies on freely behaving animals. Here, we introduce wireless optofluidic neural probes that combine ultrathin, soft microfluidic drug delivery with cellular-scale inorganic light-emitting diode (μ-ILED) arrays. These probes are orders of magnitude smaller than cannulas and allow wireless, programmed spatiotemporal control of fluid delivery and photostimulation. We demonstrate these devices in freely moving animals to modify gene expression, deliver peptide ligands, and provide concurrent photostimulation with antagonist drug delivery to manipulate mesoaccumbens reward-related behavior. The minimally invasive operation of these probes forecasts utility in other organ systems and species, with potential for broad application in biomedical science, engineering, and medicine.Entities:
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Year: 2015 PMID: 26189679 PMCID: PMC4525768 DOI: 10.1016/j.cell.2015.06.058
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582