[1]
Viventi, J.; Kim, D. H.; Vigeland, L.; Frechette, E. S.; Blanco, J. A.; Kim, Y. S.; Avrin, A. E.; Tiruvadi, V. R.; Hwang, S. W.; Vanleer, A. C. et al. Flexible, foldable, actively multiplexed, high-density electrode array for mapping brain activity in vivo. Nat. Neurosci. 2011, 14, 1599-1605.
[2]
Uhlhaas, P. J.; Singer, W. Neural synchrony in brain disorders: Relevance for cognitive dysfunctions and pathophysiology. Neuron 2006, 52, 155-168.
[3]
Lozano, R.; Naghavi, M.; Foreman, K.; Lim, S.; Shibuya, K.; Aboyans, V.; Abraham, J.; Adair, T.; Aggarwal, R.; Ahn, S. Y. et al. Global and regional mortality from 235 causes of death for 20 age groups in 1990 and 2010: A systematic analysis for the Global Burden of Disease Study 2010. Lancet 2012, 380, 2095-2128.
[4]
Schwarzbold, M.; Diaz, A.; Martins, E. T.; Rufino, A.; Amante, L. N.; Thais, M. E.; Quevedo, J.; Hohl, A.; Linhares, M. N.; Walz, R. Psychiatric disorders and traumatic brain injury. Neuropsychiatr. Dis. Treat. 2008, 4, 797-816.
[5]
Roberts, I.; Sydenham, E. Barbiturates for acute traumatic brain injury. Cochrane Database Syst. Rev. 2012, 12, CD000033.
[6]
Chesnut, R. M.; Temkin, N.; Carney, N.; Dikmen, S.; Rondina, C.; Videtta, W.; Petroni, G.; Lujan, S.; Pridgeon, J.; Barber, J. et al. A trial of intracranial-pressure monitoring in traumatic brain injury. N. Engl. J. Med. 2012, 367, 2471-2481.
[7]
Shin, J.; Liu, Z. H.; Bai, W. B.; Liu, Y. H.; Yan, Y.; Xue, Y. G.; Kandela, I.; Pezhouh, M.; MacEwan, M. R.; Huang, Y. G. et al. Bioresorbable optical sensor systems for monitoring of intracranial pressure and temperature. Sci. Adv. 2019, 5, eaaw1899.
[8]
Werner, C.; Engelhard, K. Pathophysiology of traumatic brain injury. BJA Br. J. Anaesth. 2007, 99, 4-9.
[9]
Bai, W. B.; Shin, J.; Fu, R. X.; Kandela, I.; Lu, D.; Ni, X. Y.; Park, Y.; Liu, Z. H.; Hang, T.; Wu, D. et al. Bioresorbable photonic devices for the spectroscopic characterization of physiological status and neural activity. Nat. Biomed. Eng. 2019, 3, 644-654.
[10]
Shalf, J. The future of computing beyond Moore’s Law. Philos. Trans. A Math. Phys. Eng. Sci. 2020, 378, 20190061.
[11]
Wang, C. J.; Sim, K.; Chen, J.; Kim, H.; Rao, Z. L.; Li, Y. H.; Chen, W. Q.; Song, J. Z.; Verduzco, R.; Yu, C. J. Soft ultrathin electronics innervated adaptive fully soft robots. Adv. Mater. 2018, 30, 1706695.
[12]
Um, D. S.; Lim, S.; Lee, Y.; Lee, H.; Kim, H. J.; Yen, W. C.; Chueh, Y. L.; Ko, H. Vacuum-induced wrinkle arrays of InGaAs semiconductor nanomembranes on polydimethylsiloxane microwell arrays. ACS Nano 2014, 8, 3080-3087.
[13]
Wang, J. X.; Cai, G. F.; Li, S. H.; Gao, D. C.; Xiong, J. Q.; Lee, P. S. Printable superelastic conductors with extreme stretchability and robust cycling endurance enabled by liquid-metal particles. Adv. Mater. 2018, 30, 1706157.
[14]
Park, J.; Kim, J.; Kim, S. Y.; Cheong, W. H.; Jang, J.; Park, Y. G.; Na, K.; Kim, Y. T.; Heo, J. H.; Lee, C. Y. et al. Soft, smart contact lenses with integrations of wireless circuits, glucose sensors, and displays. Sci. Adv. 2018, 4, eaap9841.
[15]
Yang, Q. S.; Lee, S.; Xue, Y. G.; Yan, Y.; Liu, T. L.; Kang, S. K.; Lee, Y. J.; Lee, S. H.; Seo, M. H.; Lu, D. et al. Materials, mechanics designs, and bioresorbable multisensor platforms for pressure monitoring in the intracranial space. Adv. Funct. Mater. 2020, 30, 1910718.
[16]
Park, J.; Ahn, D. B.; Kim, J.; Cha, E.; Bae, B. S.; Lee, S. Y.; Park, J. U. Printing of wirelessly rechargeable solid-state supercapacitors for soft, smart contact lenses with continuous operations. Sci. Adv. 2019, 5, eaay0764.
[17]
Kim, J.; Cha, E.; Park, J. U. Recent advances in smart contact lenses. Adv. Mater. Technol. 2020, 5, 1900728.
[18]
Park, Y. G.; Cha, E.; An, H. S.; Lee, K. P.; Song, M. H.; Kim, H. K.; Park, J. U. Wireless phototherapeutic contact lenses and glasses with red light-emitting diodes. Nano Res. 2020, 13, 1347-1353.
[19]
Ku, M.; Kim, J.; Won, J. E.; Kang, W.; Park, Y. G.; Park, J.; Lee, J. H.; Cheon, J.; Lee, H. H.; Park, J. U. Smart, soft contact lens for wireless immunosensing of cortisol. Sci. Adv. 2020, 6, eabb2891.
[20]
Im, C.; Seo, J. M. A review of electrodes for the electrical brain signal recording. Biomed. Eng. Lett. 2016, 6, 104-112.
[21]
Fattahi, P.; Yang, G.; Kim, G.; Abidian, M. R. A review of organic and inorganic biomaterials for neural interfaces. Adv. Mater. 2014, 26, 1846-1885.
[22]
Hong, G. S.; Lieber, C. M. Novel electrode technologies for neural recordings. Nat. Rev. Neurosci. 2019, 20, 330-345.
[23]
Buzsáki, G.; Anastassiou, C. A.; Koch, C. The origin of extracellular fields and currents—EEG, ECoG, LFP and spikes. Nat. Rev. Neurosci. 2012, 13, 407-420.
[24]
Tallgren, P.; Vanhatalo, S.; Kaila, K.; Voipio, J. Evaluation of commercially available electrodes and gels for recording of slow EEG potentials. Clin. Neurophysiol. 2005, 116, 799-806.
[25]
Ferree, T. C.; Luu, P.; Russell, G. S.; Tucker, D. M. Scalp electrode impedance, infection risk, and EEG data quality. Clin. Neurophysiol. 2001, 112, 536-544.
[26]
Leleux, P.; Badier, J. M.; Rivnay, J.; Bénar, C.; Hervé, T.; Chauvel, P.; Malliaras, G. G. Conducting polymer electrodes for electroencephalography. Adv. Healthc. Mater. 2014, 3, 490-493.
[27]
Lin, S.; Liu, J. C.; Li, W. Z.; Wang, D.; Huang, Y.; Jia, C.; Li, Z. W.; Murtaza, M.; Wang, H. Y.; Song, J. N. et al. A flexible, robust, and gel-free electroencephalogram electrode for noninvasive brain-computer interfaces. Nano Lett. 2019, 19, 6853-6861.
[28]
Velcescu, A.; Lindley, A.; Cursio, C.; Krachunov, S.; Beach, C.; Brown, C. A.; Jones, A. K. P.; Casson, A. J. Flexible 3D-printed EEG electrodes. Sensors 2019, 19, 1650.
[29]
Tian, L. M.; Zimmerman, B.; Akhtar, A.; Yu, K. J.; Moore, M.; Wu, J.; Larsen, R. J.; Lee, J. W.; Li, J. H.; Liu, Y. H. et al. Large-area MRI-compatible epidermal electronic interfaces for prosthetic control and cognitive monitoring. Nat. Biomed. Eng. 2019, 3, 194-205.
[30]
Norton, J. J. S.; Lee, D. S.; Lee, J. W.; Lee, W.; Kwon, O.; Won, P.; Jung, S. Y.; Cheng, H. Y.; Jeong, J. W.; Akce, A. et al. Soft, curved electrode systems capable of integration on the auricle as a persistent brain-computer interface. Proc. Natl. Acad. Sci. USA 2015, 112, 3920-3925.
[31]
Lacour, S. P.; Benmerah, S.; Tarte, E.; FitzGerald, J.; Serra, J.; McMahon, S.; Fawcett, J.; Graudejus, O.; Yu, Z.; Morrison III, B. Flexible and stretchable micro-electrodes for in vitro and in vivo neural interfaces. Med. Biol. Eng. Comput. 2010, 48, 945-954.
[32]
Márton, G.; Tóth, E. Z.; Wittner, L.; Fiáth, R.; Pinke, D.; Orbán, G.; Meszéna, D.; Pál, I.; Győri, E. L.; Bereczki, Z. et al. The neural tissue around SU-8 implants: A quantitative in vivo biocompatibility study. Mater. Sci. Eng. C 2020, 112, 110870.
[33]
Chen, H.; Yuan, L.; Song, W.; Wu, Z. K.; Li, D. Biocompatible polymer materials: Role of protein-surface interactions. Prog. Polym. Sci. 2008, 33, 1059-1087.
[34]
Nicolelis, M. A. L.; Dimitrov, D.; Carmena, J. M.; Crist, R.; Lehew, G.; Kralik, J. D.; Wise, S. P. Chronic, multisite, multielectrode recordings in macaque monkeys. Proc. Natl. Acad. Sci. USA 2003, 100, 11041-11046.
[35]
Wise, K. D.; Najafi, K. Microfabrication techniques for integrated sensors and microsystems. Science 1991, 254, 1335-1342.
[36]
Yeager, J. D.; Phillips, D. J.; Rector, D. M.; Bahr, D. F. Characterization of flexible ECoG electrode arrays for chronic recording in awake rats. J. Neurosci. Methods 2008, 173, 279-285.
[37]
Kim, D. H.; Viventi, J.; Amsden, J. J.; Xiao, J. L.; Vigeland, L.; Kim, Y. S.; Blanco, J. A.; Panilaitis, B.; Frechette, E. S.; Contreras, D. et al. Dissolvable films of silk fibroin for ultrathin conformal bio-integrated electronics. Nat. Mater. 2010, 9, 511-517.
[38]
Khodagholy, D.; Gelinas, J. N.; Thesen, T.; Doyle, W.; Devinsky, O.; Malliaras, G. G.; Buzsáki, G. NeuroGrid: Recording action potentials from the surface of the brain. Nat. Neurosci. 2015, 18, 310-315.
[39]
Li, J. H.; Song, E. M.; Chiang, C. H.; Yu, K. J.; Koo, J.; Du, H. N.; Zhong, Y. S.; Hill, M.; Wang, C.; Zhang, J. Z. et al. Conductively coupled flexible silicon electronic systems for chronic neural electrophysiology. Proc. Natl. Acad. Sci. USA 2018, 115, E9542-E9549.
[40]
Chiang, C. H.; Won, S. M.; Orsborn, A. L.; Yu, K. J.; Trumpis, M.; Bent, B.; Wang, C.; Xue, Y. G.; Min, S.; Woods, V. et al. Development of a neural interface for high-definition, long-term recording in rodents and nonhuman primates. Sci. Transl. Med. 2020, 12, eaay4682.
[41]
Jang, J.; Kim, H.; Ji, S.; Kim, H. J.; Kang, M. S.; Kim, T. S.; Won, J. E.; Lee, J. H.; Cheon, J.; Kang, K. et al. Mechanoluminescent, air-dielectric MoS2 transistors as active-matrix pressure sensors for wide detection ranges from footsteps to cellular motions. Nano Lett. 2020, 20, 66-74.
[42]
Jang, J.; Oh, B.; Jo, S.; Park, S.; An, H. S.; Lee, S.; Cheong, W. H.; Yoo, S.; Park, J. U. Human-interactive, active-matrix displays for visualization of tactile pressures. Adv. Mater. Technol. 2019, 4, 1900082.
[43]
Wark, H. A. C.; Sharma, R.; Mathews, K. S.; Fernandez, E.; Yoo, J.; Christensen, B.; Tresco, P.; Rieth, L.; Solzbacher, F.; Normann, R. A. et al. A new high-density (25 electrodes/mm2) penetrating microelectrode array for recording and stimulating sub-millimeter neuroanatomical structures. J. Neural Eng. 2013, 10, 045003.
[44]
Won, S. M.; Song, E. M.; Zhao, J. N.; Li, J. H.; Rivnay, J.; Rogers, J. A. Recent advances in materials, devices, and systems for neural interfaces. Adv. Mater. 2018, 30, 1800534.
[45]
Jun, J. J.; Steinmetz, N. A.; Siegle, J. H.; Denman, D. J.; Bauza, M.; Barbarits, B.; Lee, A. K.; Anastassiou, C. A.; Andrei, A.; Aydın, Ç. et al. Fully integrated silicon probes for high-density recording of neural activity. Nature 2017, 551, 232-236.
[46]
Liu, J.; Fu, T. M.; Cheng, Z. G.; Hong, G. S.; Zhou, T.; Jin, L. H.; Duvvuri, M.; Jiang, Z.; Kruskal, P.; Xie, C. et al. Syringe-injectable electronics. Nat. Nanotechnol. 2015, 10, 629-636.
[47]
Fu, T. M.; Hong, G. S.; Zhou, T.; Schuhmann, T. G.; Viveros, R. D.; Lieber, C. M. Stable long-term chronic brain mapping at the single-neuron level. Nat. Methods 2016, 13, 875-882.
[48]
Yang, Q. R.; Wu, B. C.; Eles, J. R.; Vazquez, A. L.; Kozai, T. D. Y.; Cui, X. T. Zwitterionic polymer coating suppresses microglial encapsulation to neural implants in vitro and in vivo. Adv. Biosyst. 2020, 4, 1900287.
[49]
Zhang, W. G.; Zhou, X. H.; He, Y. X.; Xu, L. Y.; Xie, J. Implanting mechanics of PEG/DEX coated flexible neural probe: Impacts of fabricating methods. Biomed. Microdevices 2021, 23, 17.
[50]
Grienberger, C.; Konnerth, A. Imaging calcium in neurons. Neuron 2012, 73, 862-885.
[51]
Berridge, M. J.; Lipp, P.; Bootman, M. D. The versatility and universality of calcium signalling. Nat. Rev. Mol. Cell Biol. 2000, 1, 11-21.
[52]
Oh, J.; Lee, C.; Kaang, B. K. Imaging and analysis of genetically encoded calcium indicators linking neural circuits and behaviors. Korean J. Physiol. Pharmacol. 2019, 23, 237-249.
[53]
Chemla, S.; Chavane, F. Voltage-sensitive dye imaging: Technique review and models. J. Physiol. Paris 2010, 104, 40-50.
[54]
Kim, C. K.; Yang, S. J.; Pichamoorthy, N.; Young, N. P.; Kauvar, I.; Jennings, J. H.; Lerner, T. N.; Berndt, A.; Lee, S. Y.; Ramakrishnan, C. et al. Simultaneous fast measurement of circuit dynamics at multiple sites across the mammalian brain. Nat. Methods 2016, 13, 325-328.
[55]
Pozzan, T.; Arslan, P.; Tsien, R. Y.; Rink, T. J. Anti-immunoglobulin, cytoplasmic free calcium, and capping in B lymphocytes. J. Cell Biol. 1982, 94, 335-340.
[56]
Baker, B. J.; Kosmidis, E. K.; Vucinic, D.; Falk, C. X.; Cohen, L. B.; Djurisic, M.; Zecevic, D. Imaging brain activity with voltage- and calcium-sensitive dyes. Cell. Mol. Neurobiol. 2005, 25, 245-282.
[57]
Denk, W.; Strickler, J. H.; Webb, W. W. Two-photon laser scanning fluorescence microscopy. Science 1990, 248, 73-76.
[58]
Burton, A.; Obaid, S. N.; Vázquez-Guardado, A.; Schmit, M. B.; Stuart, T.; Cai, L.; Chen, Z. Y.; Kandela, I.; Haney, C. R.; Waters, E. A. et al. Wireless, battery-free subdermally implantable photometry systems for chronic recording of neural dynamics. Proc. Natl. Acad. Sci. USA 2020, 117, 2835-2845.
[59]
Lu, L. Y.; Gutruf, P.; Xia, L.; Bhatti, D. L.; Wang, X. Y.; Vazquez-Guardado, A.; Ning, X.; Shen, X. R.; Sang, T.; Ma, R. X. et al. Wireless optoelectronic photometers for monitoring neuronal dynamics in the deep brain. Proc. Natl. Acad. Sci. USA 2018, 115, E1374-E1383.
[60]
Adelsberger, H.; Garaschuk, O.; Konnerth, A. Cortical calcium waves in resting newborn mice. Nat. Neurosci. 2005, 8, 988-990.
[61]
Lütcke, H.; Murayama, M.; Hahn, T.; Margolis, D. J.; Astori, S.; Borgloh, S. M. Z. A.; Göbel, W.; Yang, Y.; Tang, W. N.; Kügler, S. et al. Optical recording of neuronal activity with a genetically-encoded calcium indicator in anesthetized and freely moving mice. Front. Neural Circuits 2010, 4, 9.
[62]
Sych, Y.; Chernysheva, M.; Sumanovski, L. T.; Helmchen, F. High-density multi-fiber photometry for studying large-scale brain circuit dynamics. Nat. Methods 2019, 16, 553-560.
[63]
Deuschl, G.; Schade-Brittinger, C.; Krack, P.; Volkmann, J.; Schäfer, H.; Bötzel, K.; Daniels, C.; Deutschländer, A.; Dillmann, U.; Eisner, W. et al. Randomized trial of deep-brain stimulation for Parkinson’s disease. N. Engl. J. Med. 2006, 355, 896-908.
[64]
Limousin, P.; Foltynie, T. Long-term outcomes of deep brain stimulation in Parkinson disease. Nat. Rev. Neurol. 2019, 15, 234-242.
[65]
Mayberg, H. S.; Lozano, A. M.; Voon, V.; McNeely, H. E.; Seminowicz, D.; Hamani, C.; Schwalb, J. M.; Kennedy, S. H. Deep brain stimulation for treatment-resistant depression. Neuron 2005, 45, 651-660.
[66]
Perlmutter, J. S.; Mink, J. W. Deep brain stimulation. Annu. Rev. Neurosci. 2006, 29, 229-257.
[67]
Yuk, H.; Lu, B. Y.; Zhao, X. H. Hydrogel bioelectronics. Chem. Soc. Rev. 2019, 48, 1642-1667.
[68]
Cogan, S. F. Neural stimulation and recording electrodes. Annu. Rev. Biomed. Eng. 2008, 10, 275-309.
[69]
Merrill, D. R.; Bikson, M.; Jefferys, J. G. R. Electrical stimulation of excitable tissue: Design of efficacious and safe protocols. J. Neurosci. Methods 2005, 141, 171-198.
[70]
Rousche, P. J.; Normann, R. A. Chronic recording capability of the Utah Intracortical Electrode Array in cat sensory cortex. J. Neurosci. Methods 1998, 82, 1-15.
[71]
Wise, K. D.; Anderson, D. J.; Hetke, J. F.; Kipke, D. R.; Najafi, K. Wireless implantable microsystems: High-density electronic interfaces to the nervous system. Proc. IEEE 2004, 92, 76-97.
[72]
Johnson, M. D.; Lim, H. H.; Netoff, T. I.; Connolly, A. T.; Johnson, N.; Roy, A.; Holt, A.; Lim, K. O.; Carey, J. R.; Vitek, J. L. et al. Neuromodulation for brain disorders: Challenges and opportunities. IEEE Trans. Biomed. Eng. 2013, 60, 610-624.
[73]
Salatino, J. W.; Ludwig, K. A.; Kozai, T. D. Y.; Purcell, E. K. Glial responses to implanted electrodes in the brain. Nat. Biomed. Eng. 2017, 1, 862-877.
[74]
Minev, I. R.; Musienko, P.; Hirsch, A.; Barraud, Q.; Wenger, N.; Moraud, E. M.; Gandar, J.; Capogrosso, M.; Milekovic, T.; Asboth, L. et al. Electronic dura mater for long-term multimodal neural interfaces. Science 2015, 347, 159-163.
[75]
Vachicouras, N.; Tarabichi, O.; Kanumuri, V. V.; Tringides, C. M.; Macron, J.; Fallegger, F.; Thenaisie, Y.; Epprecht, L.; McInturff, S.; Qureshi, A. A. et al. Microstructured thin-film electrode technology enables proof of concept of scalable, soft auditory brainstem implants. Sci. Transl. Med. 2019, 11, eaax9487.
[76]
Yeo, W. H.; Kim, Y. S.; Lee, J.; Ameen, A.; Shi, L. K.; Li, M.; Wang, S. D.; Ma, R.; Jin, S. H.; Kang, Z. et al. Multifunctional epidermal electronics printed directly onto the skin. Adv. Mater. 2013, 25, 2773-2778.
[77]
Boehler, C.; Vieira, D. M.; Egert, U.; Asplund, M. NanoPt—A nanostructured electrode coating for neural recording and microstimulation. ACS Appl. Mater. Interfaces 2020, 12, 14855-14865.
[78]
Abbott, J.; Ye, T. Y.; Krenek, K.; Gertner, R. S.; Ban, S.; Kim, Y.; Qin, L.; Wu, W. X.; Park, H.; Ham, D. A nanoelectrode array for obtaining intracellular recordings from thousands of connected neurons. Nat. Biomed. Eng. 2020, 4, 232-241.
[79]
Chen, C.; Ruan, S. C.; Bai, X.; Lin, C. M.; Xie, C. G.; Lee, I. S. Patterned iridium oxide film as neural electrode interface: Biocompatibility and improved neurite outgrowth with electrical stimulation. Mater. Sci. Eng. C 2019, 103, 109865.
[80]
Chen, N.; Tian, L. L.; Patil, A. C.; Peng, S. J.; Yang, I. H.; Thakor, N. V.; Ramakrishna, S. Neural interfaces engineered via micro- and nanostructured coatings. Nano Today 2017, 14, 59-83.
[81]
Lu, L. L.; Fu, X. F.; Liew, Y.; Zhang, Y. Y.; Zhao, S. Y.; Xu, Z.; Zhao, J. N.; Li, D.; Li, Q. W.; Stanley, G. B. et al. Soft and MRI compatible neural electrodes from carbon nanotube fibers. Nano Lett. 2019, 19, 1577-1586.
[82]
Wang, K. Z.; Frewin, C. L.; Esrafilzadeh, D.; Yu, C. C.; Wang, C. Y.; Pancrazio, J. J.; Romero-Ortega, M.; Jalili, R.; Wallace, G. High-performance graphene-fiber-based neural recording microelectrodes. Adv. Mater. 2019, 31, 1805867.
[83]
Gutruf, P.; Yin, R. T.; Lee, K. B.; Ausra, J.; Brennan, J. A.; Qiao, Y.; Xie, Z. Q.; Peralta, R.; Talarico, O.; Murillo, A. et al. Wireless, battery-free, fully implantable multimodal and multisite pacemakers for applications in small animal models. Nat. Commun. 2019, 10, 5742.
[84]
Boyden, E. S.; Zhang, F.; Bamberg, E.; Nagel, G.; Deisseroth, K. Millisecond-timescale, genetically targeted optical control of neural activity. Nat. Neurosci. 2005, 8, 1263-1268.
[85]
Won, S. M.; Song, E. M.; Reeder, J. T.; Rogers, J. A. Emerging modalities and implantable technologies for neuromodulation. Cell 2020, 181, 115-135.
[86]
Pashaie, R.; Anikeeva, P.; Lee, J. H.; Prakash, R.; Yizhar, O.; Prigge, M.; Chander, D.; Richner, T. J.; Williams, J. Optogenetic brain interfaces. IEEE Rev. Biomed. Eng. 2014, 7, 3-30.
[87]
Gradinaru, V.; Thompson, K. R.; Zhang, F.; Mogri, M.; Kay, K.; Schneider, M. B.; Deisseroth, K. Targeting and readout strategies for fast optical neural control in vitro and in vivo. J. Neurosci. 2007, 27, 14231-14238.
[88]
Williams, J. C.; Denison, T. From optogenetic technologies to neuromodulation therapies. Sci. Transl. Med. 2013, 5, 177ps6.
[89]
Wang, L. L.; Zhong, C.; Ke, D. N.; Ye, F. M.; Tu, J.; Wang, L. P.; Lu, Y. Ultrasoft and highly stretchable hydrogel optical fibers for in vivo optogenetic modulations. Adv. Opt. Mater. 2018, 6, 1800427.
[90]
Kim, D.; Yokota, T.; Suzuki, T.; Lee, S.; Woo, T.; Yukita, W.; Koizumi, M.; Tachibana, Y.; Yawo, H.; Onodera, H. et al. Ultraflexible organic light-emitting diodes for optogenetic nerve stimulation. Proc. Natl. Acad. Sci. USA 2020, 117, 21138-21146.
[91]
Wu, F.; Stark, E.; Ku, P. C.; Wise, K. D.; Buzsáki, G.; Yoon, E. Monolithically integrated μLEDs on silicon neural probes for high-resolution optogenetic studies in behaving animals. Neuron 2015, 88, 1136-1148.
[92]
Kim, T. I.; McCall, J. G.; Jung, Y. H.; Huang, X.; Siuda, E. R.; Li, Y. H.; Song, J. Z.; Song, Y. M.; Pao, H. A.; Kim, P. H. et al. Injectable, cellular-scale optoelectronics with applications for wireless optogenetics. Science 2013, 340, 211-216.
[93]
Qazi, R.; Gomez, A. M.; Castro, D. C.; Zou, Z. N.; Sim, J. Y.; Xiong, Y. Y.; Abdo, J.; Kim, C. Y.; Anderson, A.; Lohner, F. et al. Wireless optofluidic brain probes for chronic neuropharmacology and photostimulation. Nat. Biomed. Eng. 2019, 3, 655-669.
[94]
Zhang, Y.; Castro, D. C.; Han, Y.; Wu, Y. X.; Guo, H. X.; Weng, Z. Y.; Xue, Y. G.; Ausra, J.; Wang, X. J.; Li, R. et al. Battery-free, lightweight, injectable microsystem for in vivo wireless pharmacology and optogenetics. Proc. Natl. Acad. Sci. USA 2019, 116, 21427-21437.
[95]
Jeong, J. W.; McCall, J. G.; Shin, G.; Zhang, Y. H.; Al-Hasani, R.; Kim, M.; Li, S.; Sim, J. Y.; Jang, K. I.; Shi, Y. et al. Wireless optofluidic systems for programmable in vivo pharmacology and optogenetics. Cell 2015, 162, 662-674.
[96]
Gutruf, P.; Krishnamurthi, V.; Vázquez-Guardado, A.; Xie, Z. Q.; Banks, A.; Su, C. J.; Xu, Y. S.; Haney, C. R.; Waters, E. A.; Kandela, I. et al. Fully implantable optoelectronic systems for battery-free, multimodal operation in neuroscience research. Nat. Electron. 2018, 1, 652-660.
[97]
Zhang, X.; Medow, J. E.; Iskandar, B. J.; Wang, F.; Shokoueinejad, M.; Koueik, J.; Webster, J. G. Invasive and noninvasive means of measuring intracranial pressure: A review. Physiol. Meas. 2017, 38, R143-R182.
[98]
Kim, M. O.; Eide, P. K.; O’Rourke, M. F.; Adji, A.; Avolio, A. P. Intracranial pressure waveforms are more closely related to central aortic than radial pressure waveforms: Implications for pathophysiology and therapy. In Intracranial Pressure and Brain Monitoring XV; Ang, B. T., Ed.; Springer: Cham, 2016; pp 61-64.
[99]
Evensen, K. B.; O’Rourke, M.; Prieur, F.; Holm, S.; Eide, P. K. Non-invasive estimation of the intracranial pressure waveform from the central arterial blood pressure waveform in idiopathic normal pressure hydrocephalus patients. Sci. Rep. 2018, 8, 4714.
[100]
Gosling, R. G.; King, D. H. The role of measurement in peripheral vascular surgery: Arterial assessment by Doppler-shift ultrasound. Proc. R. Soc. Med. 1974, 67, 447-449.
[101]
Behrens, A.; Lenfeldt, N.; Ambarki, K.; Malm, J.; Eklund, A.; Koskinen, L. O. Transcranial Doppler pulsatility index: Not an accurate method to assess intracranial pressure. Neurosurgery 2010, 66, 1050-1057.
[102]
Evensen, K. B.; Eide, P. K. Measuring intracranial pressure by invasive, less invasive or non-invasive means: Limitations and avenues for improvement. Fluids Barriers CNS 2020, 17, 34.
[103]
Marchbanks, R. J.; Reid, A.; Martin, A. M.; Brightwell, A. P.; Bateman, D. The effect of raised intracranial pressure on intracochlear fluid pressure: Three case studies. Br. J. Audiol. 1987, 21, 127-130.
[104]
Evensen, K. B.; Paulat, K.; Prieur, F.; Holm, S.; Eide, P. K. Utility of the tympanic membrane pressure waveform for non-invasive estimation of the intracranial pressure waveform. Sci. Rep. 2018, 8, 15776.
[105]
Maissan, I. M.; Dirven, P. J. A. C.; Haitsma, I. K.; Hoeks, S. E.; Gommers, D.; Stolker, R. J. Ultrasonographic measured optic nerve sheath diameter as an accurate and quick monitor for changes in intracranial pressure. J. Neurosurg. 2015, 123, 743-747.
[106]
Kerscher, S. R.; Schöni, D.; Neunhoeffer, F.; Wolff, M.; Haas-Lude, K.; Bevot, A.; Schuhmann, M. U. The relation of optic nerve sheath diameter (ONSD) and intracranial pressure (ICP) in pediatric neurosurgery practice—Part II: Influence of wakefulness, method of ICP measurement, intra-individual ONSD-ICP correlation and changes after therapy. Child's Nerv. Syst. 2020, 36, 107-115.
[107]
Zoerle, T.; Caccioppola, A.; D’Angelo, E.; Carbonara, M.; Conte, G.; Avignone, S.; Zanier, E. R.; Birg, T.; Ortolano, F.; Triulzi, F. et al. Optic nerve sheath diameter is not related to intracranial pressure in subarachnoid hemorrhage patients. Neurocrit. Care 2020, 33, 491-498.
[108]
Naldi, A.; Provero, P.; Vercelli, A.; Bergui, M.; Mazzeo, A. T.; Cantello, R.; Tondo, G.; Lochner, P. Optic nerve sheath diameter asymmetry in healthy subjects and patients with intracranial hypertension. Neurol. Sci. 2020, 41, 329-333.
[109]
Heldt, T.; Zoerle, T.; Teichmann, D.; Stocchetti, N. Intracranial pressure and intracranial elastance monitoring in neurocritical care. Annu. Rev. Biomed. Eng. 2019, 21, 523-549.
[110]
Pappu, S.; Lerma, J.; Khraishi, T. Brain CT to assess intracranial pressure in patients with traumatic brain injury. J. Neuroimaging 2016, 26, 37-40.
[111]
Jaeger, M.; Khoo, A. K.; Conforti, D. A.; Cuganesan, R. Relationship between intracranial pressure and phase contrast cine MRI derived measures of intracranial pulsations in idiopathic normal pressure hydrocephalus. J. Clin. Neurosci. 2016, 33, 169-172.
[112]
Brain Trauma Foundation; American Association of Neurological Surgeons; Congress of Neurological Surgeons; Joint Section on Neurotrauma and Critical Care, AANS/CNS; Bratton, S. L.; Chestnut, R. M.; Ghajar, J.; McConnell Hammond, F. F.; Harris, O. A.; Hartl, R. et al. Guidelines for the management of severe traumatic brain injury. VII. Intracranial pressure monitoring technology. J. Neurotrauma 2007, 24 Suppl 1, S45-S54.
[113]
Yau, Y. H.; Piper, I. R.; Clutton, R. E.; Whittle, I. R. Experimental evaluation of the Spiegelberg intracranial pressure and intracranial compliance monitor. Technical note. J. Neurosurg. 2000, 93, 1072-1077.
[114]
Raboel, P. H.; Bartek, J.; Andresen, M.; Bellander, B. M.; Romner, B. Intracranial pressure monitoring: Invasive versus non-invasive methods—A review. Crit. Care Res. Pract. 2012, 2012, 950393.
[115]
Stendel, R.; Heidenreich, J.; Schilling, A.; Akhavan-Sigari, R.; Kurth, R.; Picht, T.; Pietilä, T.; Suess, O.; Kern, C.; Meisel, J. et al. Clinical evaluation of a new intracranial pressure monitoring device. Acta Neurochir. (Wien) 2003, 145, 185-193.
[116]
Ji, S. Y.; Jang, J.; Hwang, J. C.; Lee, Y.; Lee, J. H.; Park, J. U. Amorphous oxide semiconductor transistors with air dielectrics for transparent and wearable pressure sensor arrays. Adv. Mater. Technol. 2020, 5, 1900928.
[117]
Jang, J.; Jun, Y. S.; Seo, H.; Kim, M.; Park, J. U. Motion detection using tactile sensors based on pressure-sensitive transistor arrays. Sensors 2020, 20, 3624.
[118]
Park, Y. G.; Lee, S.; Park, J. U. Recent progress in wireless sensors for wearable electronics. Sensors 2019, 19, 4353.
[119]
Jang, J.; Kim, H.; Song, Y. M.; Park, J. U. Implantation of electronic visual prosthesis for blindness restoration. Opt. Mater. Express 2019, 9, 3878-3894.
[120]
Coyle, P. Middle cerebral artery occlusion in the young rat. Stroke 1982, 13, 855-859.
[121]
Kang, S. K.; Murphy, R. K. J.; Hwang, S. W.; Lee, S. M.; Harburg, D. V.; Krueger, N. A.; Shin, J.; Gamble, P.; Cheng, H. Y.; Yu, S. et al. Bioresorbable silicon electronic sensors for the brain. Nature 2016, 530, 71-76.
[122]
Shin, J.; Yan, Y.; Bai, W. B.; Xue, Y. G.; Gamble, P.; Tian, L. M.; Kandela, I.; Haney, C. R.; Spees, W.; Lee, Y. et al. Bioresorbable pressure sensors protected with thermally grown silicon dioxide for the monitoring of chronic diseases and healing processes. Nat. Biomed. Eng. 2019, 3, 37-46.
[123]
Yu, L.; Kim, B. J.; Meng, E. Chronically implanted pressure sensors: Challenges and state of the field. Sensors 2014, 14, 20620-20644.
[124]
Fang, H.; Zhao, J. N.; Yu, K. J.; Song, E. M.; Farimani, A. B.; Chiang, C. H.; Jin, X.; Xue, Y. G.; Xu, D.; Du, W. B. et al. Ultrathin, transferred layers of thermally grown silicon dioxide as biofluid barriers for biointegrated flexible electronic systems. Proc. Natl. Acad. Sci. USA 2016, 113, 11682-11687.
[125]
Xu, K. D.; Li, S. J.; Dong, S. R.; Zhang, S. M.; Pan, G.; Wang, G. M.; Shi, L.; Guo, W.; Yu, C. N.; Luo, J. K. Bioresorbable electrode array for electrophysiological and pressure signal recording in the brain. Adv. Healthc. Mater. 2019, 8, 1801649.
[126]
Omidbeigi, M.; Mousavi, M. S.; Meknatkhah, S.; Edalatfar, M.; Bari, A.; Sharif-Alhoseini, M. Telemetric intracranial pressure monitoring: A systematic review. Neurocrit. Care 2021, 34, 291-300.
[127]
Chen, L. Y.; Tee, B. C. K.; Chortos, A. L.; Schwartz, G.; Tse, V.; Lipomi, D. J.; Wong, H. S. P.; McConnell, M. V.; Bao, Z. N. Continuous wireless pressure monitoring and mapping with ultra-small passive sensors for health monitoring and critical care. Nat. Commun. 2014, 5, 5028.
[128]
Lu, D.; Yan, Y.; Deng, Y. J.; Yang, Q. S.; Zhao, J.; Seo, M. H.; Bai, W. B.; MacEwan, M. R.; Huang, Y. G.; Ray, W. Z. et al. Bioresorbable wireless sensors as temporary implants for in vivo measurements of pressure. Adv. Funct. Mater. 2020, 30, 2003754.
[129]
Eftekhari, S.; Westgate, C. S. J.; Johansen, K. P.; Bruun, S. R.; Jensen, R. H. Long-term monitoring of intracranial pressure in freely-moving rats; impact of different physiological states. Fluids Barriers CNS 2020, 17, 39.
[130]
Dong, X. W. Current strategies for brain drug delivery. Theranostics 2018, 8, 1481-1493.
[131]
Haumann, R.; Videira, J. C.; Kaspers, G. J. L.; van Vuurden, D. G.; Hulleman, E. Overview of current drug delivery methods across the blood-brain barrier for the treatment of primary brain tumors. CNS Drugs 2020, 34, 1121-1131.
[132]
Chen, Y.; Dalwadi, G.; Benson, H. A. E. Drug delivery across the blood-brain barrier. Curr. Drug Deliv. 2004, 1, 361-376.
[133]
Patel, M. M.; Patel, B. M. Crossing the blood-brain barrier: Recent advances in drug delivery to the brain. CNS Drugs 2017, 31, 109-133.
[134]
Iadecola, C. Neurovascular regulation in the normal brain and in Alzheimer’s disease. Nat. Rev. Neurosci. 2004, 5, 347-360.
[135]
Abbott, N. J.; Rönnbäck, L.; Hansson, E. Astrocyte-endothelial interactions at the blood-brain barrier. Nat. Rev. Neurosci. 2006, 7, 41-53.
[136]
Lu, C. T.; Zhao, Y. Z.; Wong, H. L.; Cai, J.; Peng, L.; Tian, X. Q. Current approaches to enhance CNS delivery of drugs across the brain barriers. Int. J. Nanomedicine 2014, 9, 2241-2257.
[137]
Bobo, R. H.; Laske, D. W.; Akbasak, A.; Morrison, P. F.; Dedrick, R. L.; Oldfield, E. H. Convection-enhanced delivery of macromolecules in the brain. Proc. Natl. Acad. Sci. USA 1994, 91, 2076-2080.
[138]
Lonser, R. R.; Sarntinoranont, M.; Morrison, P. F.; Oldfield, E. H. Convection-enhanced delivery to the central nervous system. J. Neurosurg. 2015, 122, 697-706.
[139]
Greig, N. H. Optimizing drug delivery to brain tumors. Cancer Treat. Rev. 1987, 14, 1-28.
[140]
Harbaugh, R. E.; Saunders, R. L.; Reeder, R. F. Use of implantable pumps for central nervous system drug infusions to treat neurological disease. Neurosurgery 1988, 23, 693-698.
[141]
DiMeco, F.; Li, K. W.; Tyler, B. M.; Wolf, A. S.; Brem, H.; Olivi, A. Local delivery of mitoxantrone for the treatment of malignant brain tumors in rats. J. Neurosurg. 2002, 97, 1173-1178.
[142]
Neuwelt, E. A. Mechanisms of disease: The blood-brain barrier. Neurosurgery 2004, 54, 131-142.
[143]
Sim, J. Y.; Haney, M. P.; Park, S. I.; McCall, J. G.; Jeong, J.W. Microfluidic neural probes: In vivo tools for advancing neuroscience. Lab Chip 2017, 17, 1406-1435.
[144]
Canales, A.; Jia, X. T.; Froriep, U. P.; Koppes, R. A.; Tringides, C. M.; Selvidge, J.; Lu, C.; Hou, C.; Wei, L.; Fink, Y. et al. Multifunctional fibers for simultaneous optical, electrical and chemical interrogation of neural circuits in vivo. Nat. Biotechnol. 2015, 33, 277-284.
[145]
Jeong, J. W.; McCall, J. G.; Zhang, Y.; Huang, Y.; Bruchas, M. R.; Rogers, J. A. Soft microfluidic neural probes for wireless drug delivery in freely behaving mice. In Proceedings of the 2015 Transducers - 2015 18th International Conference on Solid-State Sensors, Actuators and Microsystems (TRANSDUCERS), Anchorage, AK, USA, 2015, pp 2264-2267.
[146]
Ramadi, K. B.; Bashyam, A.; Frangieh, C. J.; Rousseau, E. B.; Cotler, M. J.; Langer, R.; Graybiel, A. M.; Cima, M. J. Computationally guided intracerebral drug delivery via chronically implanted microdevices. Cell Rep. 2020, 31, 107734.
[147]
Altuna, A.; Bellistri, E.; Cid, E.; Aivar, P.; Gal, B.; Berganzo, J.; Gabriel, G.; Guimerà, A.; Villa, R.; Fernández, L. J. et al. SU-8 based microprobes for simultaneous neural depth recording and drug delivery in the brain. Lab Chip 2013, 13, 1422-1430.
[148]
Cotler, M. J.; Rousseau, E. B.; Ramadi, K. B.; Fang, J.; Graybiel, A. M.; Langer, R.; Cima, M. J. Steerable microinvasive probes for localized drug delivery to deep tissue. Small 2019, 15, 1901459.
[149]
McCall, J. G.; Qazi, R.; Shin, G.; Li, S.; Ikram, M. H.; Jang, K. I.; Liu, Y. H.; Al-Hasani, R.; Bruchas, M. R.; Jeong, J. W. et al. Preparation and implementation of optofluidic neural probes for in vivo wireless pharmacology and optogenetics. Nat. Protoc. 2017, 12, 219-237.
[150]
Shin, H.; Lee, H. J.; Chae, U.; Kim, H.; Kim, J.; Choi, N.; Woo, J.; Cho, Y.; Justin Lee, C.; Yoon, E. S. et al. Neural probes with multi-drug delivery capability. Lab Chip 2015, 15, 3730-3737.
[151]
Shin, H.; Son, Y.; Chae, U.; Kim, J.; Choi, N.; Lee, H. J.; Woo, J.; Cho, Y.; Yang, S. H.; Lee, C. J. et al. Multifunctional multi-shank neural probe for investigating and modulating long-range neural circuits in vivo. Nat. Commun. 2019, 10, 3777.
[152]
Cai, D. J.; Aharoni, D.; Shuman, T.; Shobe, J.; Biane, J.; Song, W. L.; Wei, B.; Veshkini, M.; La-Vu, M.; Lou, J. et al. A shared neural ensemble links distinct contextual memories encoded close in time. Nature 2016, 534, 115-118.
[153]
Lee, H. J.; Son, Y.; Kim, D.; Kim, Y. K.; Choi, N.; Yoon, E. S.; Cho, I. J. A new thin silicon microneedle with an embedded microchannel for deep brain drug infusion. Sens. Actuators B Chem. 2015, 209, 413-422.
[154]
Parada, M. A.; Puig de Parada, M.; Hoebel, B. G. A new triple-channel swivel for fluid delivery in the range of intracranial (10 nL) and intravenous (100 μL) self-administration volumes and also suitable for microdialysis. J. Neurosci. Methods 1994, 54, 1-8.
[155]
Spieth, S.; Schumacher, A.; Kallenbach, C.; Messner, S.; Zengerle, R. The NeuroMedicator—A micropump integrated with silicon microprobes for drug delivery in neural research. J. Micromech. Microeng. 2012, 22, 065020.
[156]
Dagdeviren, C.; Ramadi, K. B.; Joe, P.; Spencer, K.; Schwerdt, H. N.; Shimazu, H.; Delcasso, S.; Amemori, K. I.; Nunez-Lopez, C.; Graybiel, A. M. et al. Miniaturized neural system for chronic, local intracerebral drug delivery. Sci. Transl. Med. 2018, 10, eaan2742.
[157]
Noh, K. N.; Park, S. I.; Qazi, R.; Zou, Z. N.; Mickle, A. D.; Grajales-Reyes, J. G.; Jang, K. I.; Gereau IV, R. W.; Xiao, J. L.; Rogers, J. A. et al. Miniaturized, battery-free optofluidic systems with potential for wireless pharmacology and optogenetics. Small 2018, 14, 1702479.
[158]
Roh, D.; Park, S. Brain multimodality monitoring: Updated perspectives. Curr. Neurol. Neurosci. Rep. 2016, 16, 56.
[159]
Tisdall, M. M.; Smith, M. Multimodal monitoring in traumatic brain injury: Current status and future directions. BJA Br. J. Anaesth. 2007, 99, 61-67.
[160]
González, R. G. Imaging-guided acute ischemic stroke therapy: From “time is brain” to “physiology is brain”. AJNR Am. J. Neuroradiol. 2006, 27, 728-735.
[161]
Saver, J. L.; Smith, E. E.; Fonarow, G. C.; Reeves, M. J.; Zhao, X.; Olson, D. M.; Schwamm, L. H. The “golden hour” and acute brain ischemia. Stroke 2010, 41, 1431-1439.
[162]
Zhao, Z. T.; Luan, L.; Wei, X. L.; Zhu, H. L.; Li, X.; Lin, S. Q.; Siegel, J. J.; Chitwood, R. A.; Xie, C. Nanoelectronic coating enabled versatile multifunctional neural probes. Nano Lett. 2017, 17, 4588-4595.
[163]
Park, S.; Guo, Y. Y.; Jia, X. T.; Choe, H. K.; Grena, B.; Kang, J.; Park, J.; Lu, C.; Canales, A.; Chen, R. et al. One-step optogenetics with multifunctional flexible polymer fibers. Nat. Neurosci. 2017, 20, 612-619.
[164]
Mickle, A. D.; Won, S. M.; Noh, K. N.; Yoon, J.; Meacham, K. W.; Xue, Y. G.; McIlvried, L. A.; Copits, B. A.; Samineni, V. K.; Crawford, K. E. et al. A wireless closed-loop system for optogenetic peripheral neuromodulation. Nature 2019, 565, 361-365.
[165]
An, H. S.; Park, Y. G.; Kim, K.; Nam, Y. S.; Song, M. H.; Park, J. U. High-resolution 3D printing of freeform, transparent displays in ambient air. Adv. Sci. 2019, 6, 1901603.
[166]
Cheong, W. H.; Oh, B.; Kim, S. H.; Jang, J.; Ji, S.; Lee, S.; Cheon, J.; Yoo, S.; Lee, S. Y.; Park, J. U. Platform for wireless pressure sensing with built-in battery and instant visualization. Nano Energy 2019, 62, 230-238.
[167]
Jo, Y.; Young Kim, J.; Kim, S. Y.; Seo, Y. H.; Jang, K. S.; Yeon Lee, S.; Jung, S.; Ryu, B. H.; Kim, H. S.; Park, J. U. et al. 3D-printable, highly conductive hybrid composites employing chemically-reinforced, complex dimensional fillers and thermoplastic triblock copolymers. Nanoscale 2017, 9, 5072-5084.
[168]
Yu, K. J.; Kuzum, D.; Hwang, S. W.; Kim, B. H.; Juul, H.; Kim, N. H.; Won, S. M.; Chiang, K.; Trumpis, M.; Richardson, A. G. et al. Bioresorbable silicon electronics for transient spatiotemporal mapping of electrical activity from the cerebral cortex. Nat. Mater. 2016, 15, 782-791.
[169]
Tao, H.; Hwang, S. W.; Marelli, B.; An, B.; Moreau, J. E.; Yang, M.; Brenckle, M. A.; Kim, S.; Kaplan, D. L.; Rogers, J. A. et al. Silk-based resorbable electronic devices for remotely controlled therapy and in vivo infection abatement. Proc. Natl. Acad. Sci. USA 2014, 111, 17385-17389.
[170]
Bettinger, C. J.; Bao, Z. N. Organic thin-film transistors fabricated on resorbable biomaterial substrates. Adv. Mater. 2010, 22, 651-655.
[171]
Irimia-Vladu, M.; Głowacki, E. D.; Troshin, P. A.; Schwabegger, G.; Leonat, L.; Susarova, D. K.; Krystal, O.; Ullah, M.; Kanbur, Y.; Bodea, M. A. et al. Indigo—A natural pigment for high performance Ambipolar organic field effect transistors and circuits. Adv. Mater. 2012, 24, 375-380.
[172]
Lei, T.; Guan, M.; Liu, J.; Lin, H. C.; Pfattner, R.; Shaw, L.; McGuire, A. F.; Huang, T. C.; Shao, L. L.; Cheng, K. T. et al. Biocompatible and totally disintegrable semiconducting polymer for ultrathin and ultralightweight transient electronics. Proc. Natl. Acad. Sci. USA 2017, 114, 5107-5112.
[173]
Omenetto, F. G.; Kaplan, D. L. A new route for silk. Nat. Photonics 2008, 2, 641-643.
[174]
Jin, H. J.; Park, J.; Karageorgiou, V.; Kim, U. J.; Valluzzi, R.; Cebe, P.; Kaplan, D. L. Water-stable silk films with reduced β-sheet content. Adv. Funct. Mater. 2005, 15, 1241-1247.
[175]
Lu, Q.; Hu, X.; Wang, X. Q.; Kluge, J. A.; Lu, S. Z.; Cebe, P.; Kaplan, D. L. Water-insoluble silk films with silk I structure. Acta Biomater. 2010, 6, 1380-1387.
[176]
Jiang, C.; Wang, X.; Gunawidjaja, R.; Lin, Y. H.; Gupta, M. K.; Kaplan, D. L.; Naik, R. R.; Tsukruk, V. V. Mechanical properties of robust ultrathin silk fibroin films. Adv. Funct. Mater. 2007, 17, 2229-2237.
[177]
Perry, H.; Gopinath, A.; Kaplan, D. L.; Dal Negro, L.; Omenetto, F. G. Nano- and micropatterning of optically transparent, mechanically robust, biocompatible silk fibroin films. Adv. Mater. 2008, 20, 3070-3072.
[178]
Zhou, Y. H.; Khan, T. M.; Liu, J. C.; Fuentes-Hernandez, C.; Shim, J. W.; Najafabadi, E.; Youngblood, J. P.; Moon, R. J.; Kippelen, B. Efficient recyclable organic solar cells on cellulose nanocrystal substrates with a conducting polymer top electrode deposited by film-transfer lamination. Org. Electron. 2014, 15, 661-666.
[179]
Jung, Y. H.; Chang, T. H.; Zhang, H. L.; Yao, C. H.; Zheng, Q. F.; Yang, V. W.; Mi, H. Y.; Kim, M.; Cho, S. J.; Park, D. W. et al. High-performance green flexible electronics based on biodegradable cellulose nanofibril paper. Nat. Commun. 2015, 6, 7170.
[180]
Huang, X.; Liu, Y. H.; Hwang, S. W.; Kang, S. K.; Patnaik, D.; Cortes, J. F.; Rogers, J. A. Biodegradable materials for multilayer transient printed circuit boards. Adv. Mater. 2014, 26, 7371-7377.
[181]
Chang, J. K.; Fang, H.; Bower, C. A.; Song, E. M.; Yu, X. G.; Rogers, J. A. Materials and processing approaches for foundry-compatible transient electronics. Proc. Natl. Acad. Sci. USA 2017, 114, E5522-E5529.
[182]
Hwang, S. W.; Song, J. K.; Huang, X.; Cheng, H. Y.; Kang, S. K.; Kim, B. H.; Kim, J. H.; Yu, S.; Huang, Y. G.; Rogers, J. A. High-performance biodegradable/transient electronics on biodegradable polymers. Adv. Mater. 2014, 26, 3905-3911.
[183]
Kang, S. K.; Hwang, S. W.; Yu, S.; Seo, J. H.; Corbin, E. A.; Shin, J.; Wie, D. S.; Bashir, R.; Ma, Z. Q.; Rogers, J. A. Biodegradable thin metal foils and spin-on glass materials for transient electronics. Adv. Funct. Mater. 2015, 25, 1789-1797.
[184]
Yin, L.; Cheng, H. Y.; Mao, S. M.; Haasch, R.; Liu, Y. H.; Xie, X.; Hwang, S. W.; Jain, H.; Kang, S. K.; Su, Y. W. et al. Dissolvable metals for transient electronics. Adv. Funct. Mater. 2014, 24, 645-658.
[185]
Kang, S. K.; Park, G.; Kim, K.; Hwang, S. W.; Cheng, H. Y.; Shin, J.; Chung, S.; Kim, M.; Yin, L.; Lee, J. C. et al. Dissolution chemistry and biocompatibility of silicon- and germanium-based semiconductors for transient electronics. ACS Appl. Mater. Interfaces 2015, 7, 9297-9305.
[186]
Badawy, W. A.; Al-Kharafi, F. M. Corrosion and passivation behaviors of molybdenum in aqueous solutions of different pH. Electrochim. Acta 1998, 44, 693-702.
[187]
Luo, M. D.; Martinez, A. W.; Song, C.; Herrault, F.; Allen, M. G. A microfabricated wireless RF pressure sensor made completely of biodegradable materials. J. Microelectromechan. Syst. 2014, 23, 4-13.
[188]
Yao, Q. Q.; Liu, Y. X.; Selvaratnam, B.; Koodali, R. T.; Sun, H. L. Mesoporous silicate nanoparticles/3D nanofibrous scaffold-mediated dual-drug delivery for bone tissue engineering. J. Control. Release 2018, 279, 69-78.
[189]
Macdonald, M. L.; Samuel, R. E.; Shah, N. J.; Padera, R. F.; Beben, Y. M.; Hammond, P. T. Tissue integration of growth factor-eluting layer-by-layer polyelectrolyte multilayer coated implants. Biomaterials 2011, 32, 1446-1453.
[190]
Makadia, H. K.; Siegel, S. J. Poly lactic-co-glycolic acid (PLGA) as biodegradable controlled drug delivery carrier. Polymers 2011, 3, 1377-1397.
[191]
Koo, J.; Kim, S. B.; Choi, Y. S.; Xie, Z. Q.; Bandodkar, A. J.; Khalifeh, J.; Yan, Y.; Kim, H.; Pezhouh, M. K.; Doty, K. et al. Wirelessly controlled, bioresorbable drug delivery device with active valves that exploit electrochemically triggered crevice corrosion. Sci. Adv. 2020, 6, eabb1093.
[192]
Choi, Y. S.; Koo, J.; Lee, Y. J.; Lee, G.; Avila, R.; Ying, H. Z.; Reeder, J.; Hambitzer, L.; Im, K.; Kim, J. et al. Biodegradable polyanhydrides as encapsulation layers for transient electronics. Adv. Funct. Mater. 2020, 30, 2000941.
[193]
Goriely, A.; Geers, M. G. D.; Holzapfel, G. A.; Jayamohan, J.; Jérusalem, A.; Sivaloganathan, S.; Squier, W.; van Dommelen, J. A. W.; Waters, S.; Kuhl, E. Mechanics of the brain: Perspectives, challenges, and opportunities. Biomech. Model. Mechanobiol. 2015, 14, 931-965.
[194]
Kim, K.; Park, Y. G.; Hyun, B. G.; Choi, M.; Park, J. U. Recent advances in transparent electronics with stretchable forms. Adv. Mater. 2019, 31, 1804690.
[195]
Park, J. Y.; Hyun, B. G.; An, B. W.; Im, H. G.; Park, Y. G.; Jang, J.; Park, J. U.; Bae, B. S. Flexible transparent conductive films with high performance and reliability using hybrid structures of continuous metal nanofiber networks for flexible optoelectronics. ACS Appl. Mater. Interfaces 2017, 9, 20299-20305.
[196]
Oh, S. J.; Kim, T. G.; Kim, S. Y.; Jo, Y.; Lee, S. S.; Kim, K.; Ryu, B. H.; Park, J. U.; Choi, Y.; Jeong, S. Newly designed Cu/Cu10Sn3 core/shell nanoparticles for liquid phase-photonic sintered copper electrodes: Large-area, low-cost transparent flexible electronics. Chem. Mater. 2016, 28, 4714-4723.
[197]
Lee, S.; Kim, S. W.; Ghidelli, M.; An, H. S.; Jang, J.; Bassi, A. L.; Lee, S. Y.; Park, J. U. Integration of transparent supercapacitors and electrodes using nanostructured metallic glass films for wirelessly rechargeable, skin heat patches. Nano Lett. 2020, 20, 4872-4881.
[198]
Jang, J.; Hyun, B. G.; Ji, S.; Cho, E.; An, B. W.; Cheong, W. H.; Park, J. U. Rapid production of large-area, transparent and stretchable electrodes using metal nanofibers as wirelessly operated wearable heaters. NPG Asia Mater. 2017, 9, e432.
[199]
Zhang, Z. X.; Wang, L.; Yu, H. T.; Zhang, F.; Tang, L.; Feng, Y. Y.; Feng, W. Highly transparent, self-healable, and adhesive organogels for bio-inspired intelligent ionic skins. ACS Appl. Mater. Interfaces 2020, 12, 15657-15666.
[200]
Son, D.; Kang, J.; Vardoulis, O.; Kim, Y.; Matsuhisa, N.; Oh, J. Y.; To, J. W.; Mun, J.; Katsumata, T.; Liu, Y. X. et al. An integrated self-healable electronic skin system fabricated via dynamic reconstruction of a nanostructured conducting network. Nat. Nanotechnol. 2018, 13, 1057-1065.
[201]
Yoon, J. H.; Kim, S. M.; Park, H. J.; Kim, Y. K.; Oh, D. X.; Cho, H. W.; Lee, K. G.; Hwang, S. Y.; Park, J.; Choi, B. G. Highly self-healable and flexible cable-type pH sensors for real-time monitoring of human fluids. Biosens. Bioelectron. 2020, 150, 111946.
[202]
Park, Y. G.; Kim, H.; Park, S. Y.; Kim, J. Y.; Park, J. U. Instantaneous and repeatable self-healing of fully metallic electrodes at ambient conditions. ACS Appl. Mater. Interfaces 2019, 11, 41497-41505.
[203]
Ding, Y. R.; Zeng, M. Q.; Fu, L. Surface chemistry of gallium-based liquid metals. Matter 2020, 3, 1477-1506.
[204]
Park, Y. G.; Min, H.; Kim, H.; Zhexembekova, A.; Lee, C. Y.; Park, J. U. Three-dimensional, high-resolution printing of carbon nanotube/liquid metal composites with mechanical and electrical reinforcement. Nano Lett. 2019, 19, 4866-4872.
[205]
Park, Y. G.; An, H. S.; Kim, J. Y.; Park, J. U. High-resolution, reconfigurable printing of liquid metals with three-dimensional structures. Sci. Adv. 2019, 5, eaaw2844.