Proceedings of the National Academy of Sciences of the United States of America · 2019
Battery-free, lightweight, injectable microsystem for in vivo wireless pharmacology and optogenetics.
Оценочное исследованиеСтатьяПоддержка NIH: внешняя программаПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод пока не подготовлен
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Zhang Yi, Castro Daniel C, Han Yuan, Wu Yixin, Guo Hexia, Weng Zhengyan, Xue Yeguang, Ausra Jokubas, Wang Xueju, Li Rui, Wu Guangfu, Vázquez-Guardado Abraham, Xie Yiwen, Xie Zhaoqian, Ostojich Diana, Peng Dongsheng, Sun Rujie, Wang Binbin, Yu Yongjoon, Leshock John P, Qu Subing, Su Chun-Ju, Shen Wen, Hang Tao, Banks Anthony, Huang Yonggang, Radulovic Jelena, Gutruf Philipp, Bruchas Michael R, Rogers John A
Аннотация
Pharmacology and optogenetics are widely used in neuroscience research to study the central and peripheral nervous systems. While both approaches allow for sophisticated studies of neural circuitry, continued advances are, in part, hampered by technology limitations associated with requirements for physical tethers that connect external equipment to rigid probes inserted into delicate regions of the brain. The results can lead to tissue damage and alterations in behavioral tasks and natural movements, with additional difficulties in use for studies that involve social interactions and/or motions in complex 3-dimensional environments. These disadvantages are particularly pronounced in research that demands combined optogenetic and pharmacological functions in a single experiment. Here, we present a lightweight, wireless, battery-free injectable microsystem that combines soft microfluidic and microscale inorganic light-emitting diode probes for programmable pharmacology and optogenetics, designed to offer the features of drug refillability and adjustable flow rates, together with programmable control over the temporal profiles. The technology has potential for large-scale manufacturing and broad distribution to the neuroscience community, with capabilities in targeting specific neuronal populations in freely moving animals. In addition, the same platform can easily be adapted for a wide range of other types of passive or active electronic functions, including electrical stimulation.