Abstract
The stability of the interface between neural tissue and chronically implanted devices is crucial for interrogation for both the central and peripheral nervous systems. One of the main challenges of chronic implants is the degradation of recording and stimulation performance over time. This is partly due to the inflammatory host tissue responses to the implanted devices, resulting in decreased density and health of neuronal elements at the electrode vicinity and scar encapsulation. In the last decade, a significant effort has been made in the development of devices that have subcellular features and/or made with soft, flexible, and stretchable materials. These strategies can trigger less foreign body response and improve the integration of the implanted device and neural tissue. In this chapter, we will discuss the most recent strategies adopted to tune the structural, functional, and dimensional properties of materials with the aim to match the mechanical, chemical, and electrical properties of the nervous system. We will discuss these strategies applied to different components of an implanted device from insulation substrate and conductive electrode materials to soft tethers and modulus-matching coatings.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Abbreviations
- BBB:
-
Blood-brain barrier
- BNB:
-
Blood nerve barrier
- CNS:
-
Central nervous system
- CNT:
-
Carbon nanotube
- DA:
-
Dopamine
- E:
-
Young’s Modulus
- EEG:
-
Electroenceophalography
- F:
-
Force
- FINE:
-
Flat interface nerve electrode
- G:
-
Conductance G
- GPa:
-
GigaPascals
- I:
-
Moment of inertia
- ITO:
-
Indium tin oxide
- MECH:
-
Micropatterned electrically conductive hydrogel-based elastronics
- MEMS:
-
Microelectromechanical systems
- MS:
-
Microspheres
- NET:
-
Neural integration, ultraflexiblenanoelectronic thread
- PDMS:
-
Polydimethylsiloxane
- PEDOT:
-
Poly(3,4-ethylenedioxythiophene)
- PEG:
-
Poly(ethyleneglycol)
- PLGA:
-
Poly(lactic-co-glycolic) acid
- PNS:
-
Peripheral nervous system
- PPy:
-
Polypyrrole
- PSS:
-
Polystyrene sulfonate
- SCP:
-
Slow cortical potential
- SCS:
-
Spinal cord stimulation
- SMP:
-
Shape-memory polymer
- Tf-LIFE:
-
The thin-film longitudinal intrafascicular electrodes
- Tg:
-
Glass transition temperature
- TIME:
-
Transverse intrafascicular multichannel electrodes
- μECoG:
-
Micro-electrocorticography
- μIPs:
-
Micro-invasive probes
- μ-ILED:
-
Microscale-inorganic LED
- USEA:
-
Utah slanted microelectrode array
References
Jablensky, A., Johnson, R., Bunney, W., Cruz, M., Durkin, M., Familusi, J., Gourie-Devi, M., Jamison, D., Jenkins, R., Kaaya, S.: Neurological, psychiatric, and developmental disorders; meeting the challenge in the developing world. In: Institute of Medicine. The National Academies Press, Washington, DC (2001). https://doi.org/10.17226/10111
Nirmala, B.P., Vranda, M.N.: Burden, coping and functionality of the patients with neurological disability availing treatment at neuro rehabilitation ward. Indian J. Neurosci. 3(3), 88–91 (2017)
Park, S., Loke, G., Fink, Y., Anikeeva, P.: Flexible fiber-based optoelectronics for neural interfaces. Chem. Soc. Rev. 48(6), 1826–1852 (2019)
Moritz, C.T.: Now is the critical time for engineered neuroplasticity. Neurotherapeutics. 15(3), 628–634 (2018)
Chapman, C.A., Goshi, N., Seker, E.: Multifunctional neural interfaces for closed-loop control of neural activity. Adv. Funct. Mater. 28(12), 1703523 (2018). https://doi.org/10.1002/adfm.201703523
Elkin, B.S., Azeloglu, E.U., Costa, K.D., Morrison Iii, B.: Mechanical heterogeneity of the rat hippocampus measured by atomic force microscope indentation. J. Neurotrauma. 24(5), 812–822 (2007). https://doi.org/10.1089/neu.2006.0169
Elkin, B.S., Ilankovan, A., Morrison III, B.: Age-dependent regional mechanical properties of the rat hippocampus and cortex. J. Biomech. Eng. 132(1) (2009). https://doi.org/10.1115/1.4000164
Sharp, A.A., Ortega, A.M., Restrepo, D., Curran-Everett, D., Gall, K.: In vivo penetration mechanics and mechanical properties of mouse brain tissue at micrometer scales. IEEE Trans. Biomed. Eng. 56(1), 45–53 (2009). https://doi.org/10.1109/TBME.2008.2003261
Karimi, A., Shojaei, A., Tehrani, P.: Mechanical properties of the human spinal cord under the compressive loading. J. Chem. Neuroanat. 86, 15–18 (2017). https://doi.org/10.1016/j.jchemneu.2017.07.004
Ju, M.-S., Lin, C.-C.K., Chang, C.-T.: Researches on biomechanical properties and models of peripheral nerves – a review. J. Biomech. Sci. Eng. 12(1), 16-00678 (2017). https://doi.org/10.1299/jbse.16-00678
Borschel, G.H., Kia, K.F., Kuzon Jr., W.M., Dennis, R.G.: Mechanical properties of acellular peripheral nerve. J. Surg. Res. 114(2), 133–139 (2003). https://doi.org/10.1016/s0022-4804(03)00255-5
Ogneva, I.V., Lebedev, D.V., Shenkman, B.S.: Transversal stiffness and Young's modulus of single fibers from rat soleus muscle probed by atomic force microscopy. Biophys. J. 98(3), 418–424 (2010). https://doi.org/10.1016/j.bpj.2009.10.028
Weltman, A., Yoo, J., Meng, E.: Flexible, penetrating brain probes enabled by advances in polymer microfabrication. Micromachines (Basel). 7(10), 180 (2016). https://doi.org/10.3390/mi7100180
Maikos, J.T., Elias, R.A.I., Shreiber, D.I.: Mechanical properties of Dura mater from the rat brain and spinal cord. J. Neurotrauma. 25(1), 38–51 (2008). https://doi.org/10.1089/neu.2007.0348
Choi, H.-Y.: Numerical human head model for traumatic injury assessment. KSME Int. J. 15(7), 995–1001 (2001)
McGarvey, K.A., Lee, J.M., Boughner, D.R.: Mechanical suitability of glycerol-preserved human dura mater for construction of prosthetic cardiac valves. Biomaterials. 5(2), 109–117 (1984). https://doi.org/10.1016/0142-9612(84)90011-5
González-González, M.A., Kanneganti, A., Joshi-Imre, A., Hernandez-Reynoso, A.G., Bendale, G., Modi, R., Ecker, M., Khurram, A., Cogan, S.F., Voit, W.E.: Thin film multi-electrode softening cuffs for selective neuromodulation. Sci. Rep. 8(1), 1–15 (2018)
Szostak, K.M., Grand, L., Constandinou, T.G.: Neural interfaces for intracortical recording: requirements, fabrication methods, and characteristics. Front. Neurosci. 11, 665 (2017)
Zelechowski, M., Valle, G., Raspopovic, S.: A computational model to design neural interfaces for lower-limb sensory neuroprostheses. J. Neuroeng. Rehabil. 17(1), 1–13 (2020)
Greiner, N., Barra, B., Schiavone, G., James, N., Falleger, F., Borgognon, S., Lacour, S., Bloch, J., Courtine, G., Capogrosso, M.: Recruitment of upper-limb motoneurons with epidural electrical stimulation of the primate cervical spinal cord. Nat. Commun. 12(435), 1–19 (2021)
Mondello, S.E., Kasten, M.R., Horner, P.J., Moritz, C.T.: Therapeutic intraspinal stimulation to generate activity and promote long-term recovery. Front. Neurosci. 8, 21 (2014)
Fernández, E., Greger, B., House, P.A., Aranda, I., Botella, C., Albisua, J., Soto-Sánchez, C., Alfaro, A., Normann, R.A.: Acute human brain responses to intracortical microelectrode arrays: challenges and future prospects. Front. Neuroeng. 7, 24 (2014)
Rijnbeek, E.H., Eleveld, N., Olthuis, W.: Update on peripheral nerve electrodes for closed-loop neuroprosthetics. Front. Neurosci. 12, 350 (2018)
Castagnola, E., Ansaldo, A., Maggiolini, E., Ius, T., Skrap, M., Ricci, D., Fadiga, L.: Smaller, softer, lower-impedance electrodes for human neuroprosthesis: a pragmatic approach. Front. Neuroeng. 7, 8 (2014)
Polikov, V.S., Tresco, P.A., Reichert, W.M.: Response of brain tissue to chronically implanted neural electrodes. J. Neurosci. Methods. 148, 1–18 (2005)
Agorelius, J., Tsanakalis, F., Friberg, A., Thorbergsson, P.T., Pettersson, L.M.E., Schouenborg, J.: An array of highly flexible electrodes with a tailored configuration locked by gelatin during implantation – initial evaluation in cortex cerebri of awake rats. Front. Neurosci. 9, 331 (2015)
Luan, L., Wei, X., Zhao, Z., Siegel, J.J., Potnis, O., Tuppen, C.A., Lin, S., Kazmi, S., Fowler, R.A., Holloway, S.: Ultraflexible nanoelectronic probes form reliable, glial scar–free neural integration. Sci. Adv. 3(2), e1601966 (2017)
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. 18(2), 310–315 (2015)
Zhao, Z., Li, X., He, F., Wei, X., Lin, S., Xie, C.: Parallel, minimally-invasive implantation of ultra-flexible neural electrode arrays. J. Neural Eng. 16(3), 035001 (2019)
Beer, F.P.: Vector mechanics for engineering. McGraw-Hill Education, New York City (1972)
Wellman, S.M., Eles, J.R., Ludwig, K.A., Seymour, J.P., Michelson, N.J., McFadden, W.E., Vazquez, A.L., Kozai, T.D.: A materials roadmap to functional neural interface design. Adv. Funct. Mater. 28(12), 1701269 (2018)
Seo, J.H., Zhang, K., Kim, M., Zhao, D., Yang, H., Zhou, W., Ma, Z.: Flexible phototransistors based on single-crystalline silicon nanomembranes. Adv. Opt Mater. 4(1), 120–125 (2016)
Liu, D., Zhou, W., Ma, Z.: Semiconductor nanomembrane-based light-emitting and photodetecting devices. In: Photonics 2016, vol. 2, p. 40. Multidisciplinary Digital Publishing Institute (2016). https://doi.org/10.3390/photonics3020040
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.: Flexible, foldable, actively multiplexed, high-density electrode array for mapping brain activity in vivo. Nat. Neurosci. 14(12), 1599 (2011)
Escabí, M.A., Read, H.L., Viventi, J., Kim, D.-H., Higgins, N.C., Storace, D.A., Liu, A.S., Gifford, A.M., Burke, J.F., Campisi, M.: A high-density, high-channel count, multiplexed μECoG array for auditory-cortex recordings. J. Neurophysiol. 112(6), 1566–1583 (2014)
Sim, K., Rao, Z., Li, Y., Yang, D., Yu, C.: Curvy surface conformal ultra-thin transfer printed Si optoelectronic penetrating microprobe arrays. NPJ Flex. Electron. 2(1), 2 (2018)
Kozai, T.D.Y., Langhals, N.B., Patel, P.R., Deng, X., Zhang, H., Smith, K.L., Lahann, J., Kotov, N.A., Kipke, D.R.: Ultrasmall implantable composite microelectrodes with bioactive surfaces for chronic neural interfaces. Nat. Mater. 11(12), 1065–1073 (2012)
Schwerdt, H.N., Kim, M.J., Amemori, S., Homma, D., Yoshida, T., Shimazu, H., Yerramreddy, H., Karasan, E., Langer, R., Graybiel, A.M.: Subcellular probes for neurochemical recording from multiple brain sites. Lab Chip. 17(6), 1104–1115 (2017). https://doi.org/10.1039/C1106LC01398H
Vitale, F., Summerson, S.R., Aazhang, B., Kemere, C., Pasquali, M.: Neural stimulation and recording with bidirectional, soft carbon nanotube fiber microelectrodes. ACS Nano. 9(4), 4465–4474 (2015)
Li, J., Song, E., Chiang, C.-H., Yu, K.J., Koo, J., Du, H., Zhong, Y., Hill, M., Wang, C., Zhang, J.: Conductively coupled flexible silicon electronic systems for chronic neural electrophysiology. Proc. Natl. Acad. Sci. 115(41), E9542–E9549 (2018)
Fang, H., Zhao, J., Yu, K.J., Song, E., Farimani, A.B., Chiang, C.-H., Jin, X., Xue, Y., Xu, D., Du, W.: Ultrathin, transferred layers of thermally grown silicon dioxide as biofluid barriers for biointegrated flexible electronic systems. Proc. Natl. Acad. Sci. 113(42), 11682–11687 (2016)
Schwerdt, H.N., Zhang, E., Kim, M.J., Yoshida, T., Stanwicks, L., Amemori, S., Dagdeviren, H.E., Langer, R., Cima, M.J., Graybiel, A.M.: Cellular-scale probes enable stable chronic subsecond monitoring of dopamine neurochemicals in a rodent model. Commun. Biol. 1(1), 144 (2018)
Guitchounts, G., Markowitz, J.E., Liberti, W.A., Gardner, T.J.: A carbon-fiber electrode array for long-term neural recording. J. Neural Eng. 10(4), 046016 (2013)
Patel, P.R., Zhang, H., Robbins, M.T., Nofar, J.B., Marshall, S.P., Kobylarek, M.J., Kozai, T.D., Kotov, N.A., Chestek, C.A.: Chronic in vivo stability assessment of carbon fiber microelectrode arrays. J. Neural Eng. 13(6), 066002 (2016). https://doi.org/10.1088/1741-2560/13/6/066002
Schwerdt, H.N., Shimazu, H., Amemori, K.-i., Amemori, S., Tierney, P.L., Gibson, D.J., Hong, S., Yoshida, T., Langer, R., Cima, M.J.: Long-term dopamine neurochemical monitoring in primates. Proc. Natl. Acad. Sci. 114(50), 13260–13265 (2017). https://doi.org/10.1073/pnas.1713756114
Schwerdt, H.N., Kim, M., Karasan, E., Amemori, S., Homma, D., Shimazu, H., Yoshida, T., Langer, R., Graybiel, A.M., Cima, M.J.: Subcellular electrode arrays for multisite recording of dopamine in vivo. In: 2017 IEEE 30th international conference on micro electro mechanical systems (MEMS), pp 549–552 (2017)
Patel, P.R., Na, K., Zhang, H., Kozai, T.D., Kotov, N.A., Yoon, E., Chestek, C.A.: Insertion of linear 8.4 μm diameter 16 channel carbon fiber electrode arrays for single unit recordings. J. Neural Eng. 12(4), 046009 (2015)
Constantin, C.P., Aflori, M., Damian, R.F., Rusu, R.D.: Biocompatibility of polyimides: a mini-review. Materials. 12(19), 3166 (2019)
Rossini, P.M., Micera, S., Benvenuto, A., Carpaneto, J., Cavallo, G., Citi, L., Cipriani, C., Denaro, L., Denaro, V., Di Pino, G.: Double nerve intraneural interface implant on a human amputee for robotic hand control. Clin. Neurophysiol. 121(5), 777–783 (2010)
Noh, K.N., Park, S.I., Qazi, R., Zou, Z., Mickle, A.D., Grajales-Reyes, J.G., Jang, K.I., Gereau IV, R.W., Xiao, J., Rogers, J.A.: Miniaturized, battery-free optofluidic systems with potential for wireless pharmacology and optogenetics. Small. 14(4), 1702479 (2018)
Ecker, M., Joshi-Imre, A., Modi, R., Frewin, C.L., Garcia-Sandoval, A., Maeng, J., Gutierrez-Heredia, G., Pancrazio, J.J., Voit, W.E.: From softening polymers to multimaterial based bioelectronic devices. Multifunct. Mater. 2(1), 012001 (2018)
Arreaga-Salas, D.E., Avendaño-Bolívar, A., Simon, D., Reit, R., Garcia-Sandoval, A., Rennaker, R.L., Voit, W.: Integration of high-charge-injection-capacity electrodes onto polymer softening neural interfaces. ACS Appl. Mater. Interfaces. 7(48), 26614–26623 (2015)
Shanmuganathan, K., Capadona, J.R., Rowan, S.J., Weder, C.: Stimuli-responsive mechanically adaptive polymer nanocomposites. ACS Appl. Mater. Interfaces. 2(1), 165–174 (2010)
Campbell, P.K., Jones, K.E., Huber, R.J., Horch, K.W., Normann, R.A.: A silicon-based, three-dimensional neural interface: manufacturing processes for an intracortical electrode array. IEEE Trans. Biomed. Eng. 38(8), 758–768 (1991)
Wise, K.D., Angell, J.B., Starr, A.: An integrated-circuit approach to extracellular microelectrodes. IEEE Trans. Biomed. Eng. 3, 238–247 (1970)
Yoo, J.-M., Song, J.-I., Tathireddy, P., Solzbacher, F., Rieth, L.W.: Hybrid laser and reactive ion etching of Parylene-C for deinsulation of a Utah electrode array. J. Micromech. Microeng. 22(10), 105036 (2012)
Musallam, S., Bak, M.J., Troyk, P.R., Andersen, R.A.: A floating metal microelectrode array for chronic implantation. J Neurosci Methods. 160, 122–127 (2007)
Nicolelis, M.A., Lebedev, M.A.: Principles of neural ensemble physiology underlying the operation of brain–machine interfaces. Nat. Rev. Neurosci. 10(7), 530–540 (2009)
De Vittorio, M., Martiradonna, L., Assad, J.: Nanotechnology and neuroscience: nano-electronic, photonic and mechanical neuronal interfacing, vol. 8. Springer, New York, Heidelberg, Dordrecht, London (2014)
Kim, D.-H., Viventi, J., Amsden, J.J., Xiao, J., Vigeland, L., Kim, Y.-S., Blanco, J.A., Panilaitis, B., Frechette, E.S., Contreras, D.: Dissolvable films of silk fibroin for ultrathin conformal bio-integrated electronics. Nat. Mater. 9(6), 511–517 (2010)
Minev, I.R., Musienko, P., Hirsch, A., Barraud, Q., Wenger, N., Moraud, E.M., Gandar, J., Capogrosso, M., Milekovic, T., Asboth, L.: Electronic dura mater for long-term multimodal neural interfaces. Science. 347(6218), 159–163 (2015)
Patil, A.C., Bandla, A., Liu, Y.-H., Luo, B., Thakor, N.V.: Nontransient silk sandwich for soft, conformal bionic links. Mater. Today. 32, 68–83 (2020). https://doi.org/10.1016/j.mattod.2019.08.007
Kim, Y., Zhu, J., Yeom, B., Di Prima, M., Su, X., Kim, J.-G., Yoo, S.J., Uher, C., Kotov, N.A.: Stretchable nanoparticle conductors with self-organized conductive pathways. Nature. 500(7460), 59 (2013)
Kim, B.J., Meng, E.: Review of polymer MEMS micromachining. J. Micromech. Microeng. 26(1), 013001 (2015)
Rubehn, B., Stieglitz, T.: In vitro evaluation of the long-term stability of polyimide as a material for neural implants. Biomaterials. 31(13), 3449–3458 (2010)
Wurth, S., Capogrosso, M., Raspopovic, S., Gandar, J., Federici, G., Kinany, N., Cutrone, A., Piersigilli, A., Pavlova, N., Guiet, R.: Long-term usability and bio-integration of polyimide-based intra-neural stimulating electrodes. Biomaterials. 122, 114–129 (2017)
Jiang, X., Sui, X., Lu, Y., Yan, Y., Zhou, C., Li, L., Ren, Q., Chai, X.: In vitro and in vivo evaluation of a photosensitive polyimide thin-film microelectrode array suitable for epiretinal stimulation. J. Neuroeng. Rehabil. 10(1), 48 (2013)
Rembado, I., Castagnola, E., Turella, L., Ius, T., Budai, R., Ansaldo, A., Angotzi, G.N., Debertoldi, F., Ricci, D., Skrap, M.: Independent component decomposition of human somatosensory evoked potentials recorded by micro-electrocorticography. Int. J. Neural Syst. 27(4), 1650052 (2017)
Petrini, F.M., Valle, G., Bumbasirevic, M., Barberi, F., Bortolotti, D., Cvancara, P., Hiairrassary, A., Mijovic, P., Sverrisson, A.Ö., Pedrocchi, A.: Enhancing functional abilities and cognitive integration of the lower limb prosthesis. Sci Transl Med. 11(512), eaav8939 (2019)
Petrini, F.M., Bumbasirevic, M., Valle, G., Ilic, V., Mijović, P., Čvančara, P., Barberi, F., Katic, N., Bortolotti, D., Andreu, D.: Sensory feedback restoration in leg amputees improves walking speed, metabolic cost and phantom pain. Nat. Med. 25(9), 1356–1363 (2019)
Tan, C.P., Craighead, H.G.: Surface engineering and patterning using parylene for biological applications. Materials. 3(3), 1803–1832 (2010)
Davis, E.M., Benetatos, N.M., Regnault, W.F., Winey, K.I., Elabd, Y.A.: The influence of thermal history on structure and water transport in Parylene C coatings. Polymer. 52(23), 5378–5386 (2011)
Meng, J.K.E.: Micromachining of Parylene C for bioMEMS Brian. Polym. Adv. Technol. 27, 564–576 (2016)
TECH P Parylene Properties. http://www.parylene.com/
Brancato, L., Decrop, D., Lammertyn, J., Puers, R.: Surface nanostructuring of Parylene-C coatings for blood contacting implants. Materials. 11(7), 1109 (2018)
Gołda, M., Brzychczy-Włoch, M., Faryna, M., Engvall, K., Kotarba, A.: Oxygen plasma functionalization of parylene C coating for implants surface: nanotopography and active sites for drug anchoring. Mater. Sci. Eng. C. 33(7), 4221–4227 (2013). https://doi.org/10.1016/j.msec.2013.06.014
Omnexus Comprehensive guide on Polyimide (PI). https://omnexus.specialchem.com/
Lee, C., Seo, J., Shul, Y., Han, H.: Optical properties of polyimide thin films. Effect of chemical structure and morphology. Polym. J. 35(7), 578–585 (2003). https://doi.org/10.1295/polymj.35.578
Xu, F.J., Zhao, J.P., Kang, E.T., Neoh, K.G.: Surface functionalization of polyimide films via chloromethylation and surface-initiated atom transfer radical polymerization. Ind. Eng. Chem. Res. 46(14), 4866–4873 (2007). https://doi.org/10.1021/ie0701367
Feng, B., Xu, K., Huang, A.: Synthesis of graphene oxide/polyimide mixed matrix membranes for desalination. RSC Adv. 7(4), 2211–2217 (2017)
McKeen, L.: 3 – introduction to the physical, mechanical, and thermal properties of plastics and elastomers. In: McKeen, L. (ed.) The effect of sterilization on plastics and elastomers, 3rd edn, pp. 57–84. William Andrew Publishing, Boston (2012). https://doi.org/10.1016/B978-1-4557-2598-4.00003-4
Xu, T., Yoo, J.H., Babu, S., Roy, S., Lee, J.-B., Lu, H.: Characterization of the mechanical behavior of SU-8 at microscale by viscoelastic analysis. J. Micromech. Microeng. 26(10), 105001 (2016). https://doi.org/10.1088/0960-1317/26/10/105001
Ayad Ghannam, C.V., Bourrier, D.: Thierry Parra dielectric microwave characterization of the SU-8 thick resin used in an above-IC process. In: European microwave conference, Rome, Sept 2009 (2016)
Blagoi, G., Keller, S., Johansson, A., Boisen, A., Dufva, M.: Functionalization of SU-8 photoresist surfaces with IgG proteins. Appl. Surf. Sci. 255(5 Part 2), 2896–2902 (2008). https://doi.org/10.1016/j.apsusc.2008.08.089
Gao, Z., Henthorn, D.B., Kim, C.-S.: Enhanced wettability of an SU-8 photoresist through a photografting procedure for bioanalytical device applications. J. Micromech. Microeng. 18(4), 045013 (2008)
Roch, I., Bidaud, P., Collard, D., Buchaillot, L.: Fabrication and characterization of an SU-8 gripper actuated by a shape memory alloy thin film. J. Micromech. Microeng. 13(2), 330–336 (2003). https://doi.org/10.1088/0960-1317/13/2/323
Lai, J.-L., Liao, C.-J., G-DJ, S.: Using an SU-8 photoresist structure and cytochrome C thin film sensing material for a microbolometer. Sensors (Basel). 12(12), 16390–16403 (2012). https://doi.org/10.3390/s121216390
Armani, D., Liu, C., Aluru, N.: Re-configurable fluid circuits by PDMS elastomer micromachining. In: Technical digest. IEEE international MEMS 99 conference. Twelfth IEEE international conference on micro electro mechanical systems (Cat. No. 99CH36291), 21 Jan, pp. 222–227 (1999). https://doi.org/10.1109/MEMSYS.1999.746817.
Mark, J.E.: Polymer data handbook. Oxford University Press, New York (2009)
Zhang, J., Chen, Y., Brook, M.A.: Facile functionalization of PDMS elastomer surfaces using Thiol–Ene click chemistry. Langmuir. 29(40), 12432–12442 (2013). https://doi.org/10.1021/la403425d
Frewin, C.L., Ecker, M., Joshi-Imre, A., Kamgue, J., Waddell, J., Danda, V.R., Stiller, A.M., Voit, W.E., Pancrazio, J.J.: Electrical properties of Thiol-ene-based shape memory polymers intended for flexible electronics. Polymers (Basel). 11(5), 902 (2019). https://doi.org/10.3390/polym11050902
Park, J.K., Kim, S.: Droplet manipulation on a structured shape memory polymer surface. Lab Chip. 17(10), 1793–1801 (2017)
Muller, R.S., Kim, J., Cho, D.-iD.: Why is (111) Silicon a better mechanical material for MEMS? Paper presented at the Transducers ‘01 Eurosensors XV. Berlin/Heidelberg (2001)
Tsuchiya, T.: Tensile testing of silicon thin films. Fatigue Fract. Eng. Mater. Struct. 28(8), 665–674 (2005). https://doi.org/10.1111/j.1460-2695.2005.00910.x
AZoM: Silicon (Si) semiconductors. https://www.azom.com/article.aspx?ArticleID=8346 (2013)
Golabchi, A., Woeppel, K.M., Li, X., Lagenaur, C.F., Cui, X.T.: Neuroadhesive protein coating improves the chronic performance of neuroelectronics in mouse brain. Biosens. Bioelectron. 155, 112096 (2020)
Golabchi, A., Wu, B., Cao, B., Bettinger, C.J., Cui, X.T.: Zwitterionic polymer/polydopamine coating reduce acute inflammatory tissue responses to neural implants. Biomaterials. 225, 119519 (2019)
Zheng, X.S., Snyder, N.R., Woeppel, K., Barengo, J.H., Li, X., Eles, J., Kolarcik, C.L., Cui, X.T.: A superoxide scavenging coating for improving tissue response to neural implants. Acta Biomater. 99, 72–83 (2019)
de la Oliva, N., Mueller, M., Stieglitz, T., Navarro, X., del Valle, J.: On the use of Parylene C polymer as substrate for peripheral nerve electrodes. Sci. Rep. 8(1), 5965 (2018). https://doi.org/10.1038/s41598-018-24502-z
Castagnola, V., Descamps, E., Lecestre, A., Dahan, L., Remaud, J., Nowak, L.G., Bergaud, C.: Parylene-based flexible neural probes with PEDOT coated surface for brain stimulation and recording. Biosens. Bioelectron. 67, 450–457 (2015)
Lecomte, A., Degache, A., Descamps, E., Dahan, L., Bergaud, C.: Biostability assessment of flexible parylene c-based implantable sensor in wireless chronic neural recording. Procedia Eng. 168, 189–192 (2016)
Nemani, K.V., Moodie, K.L., Brennick, J.B., Su, A., Gimi, B.: In vitro and in vivo evaluation of SU-8 biocompatibility. Mater. Sci. Eng. C. 33(7), 4453–4459 (2013)
Feng, R., Farris, R.J.: Influence of processing conditions on the thermal and mechanical properties of SU8 negative photoresist coatings. J. Micromech. Microeng. 13(1), 80 (2002)
Yang, X., Zhou, T., Zwang, T.J., Hong, G., Zhao, Y., Viveros, R.D., Fu, T.-M., Gao, T., Lieber, C.M.: Bioinspired neuron-like electronics. Nat. Mater. 18(5), 510–517 (2019)
Hong, G., Yang, X., Zhou, T., Lieber, C.M.: Mesh electronics: a new paradigm for tissue-like brain probes. Curr. Opin. Neurobiol. 50, 33–41 (2018)
Xie, C., Liu, J., Fu, T.-M., Dai, X., Zhou, W., Lieber, C.M.: Three-dimensional macroporous nanoelectronic networks as minimally invasive brain probes. Nat. Mater. 14(12), 1286–1292 (2015)
Mata, A., Fleischman, A.J., Roy, S.: Characterization of polydimethylsiloxane (PDMS) properties for biomedical micro/nanosystems. Biomed. Microdevices. 7(4), 281–293 (2005)
Jothimuthu, P., Carroll, A., Bhagat, A.A.S., Lin, G., Mark, J.E., Papautsky, I.: Photodefinable PDMS thin films for microfabrication applications. J. Micromech. Microeng. 19(4), 045024 (2009)
Tybrandt, K., Khodagholy, D., Dielacher, B., Stauffer, F., Renz, A.F., Buzsáki, G., Vörös, J.: High-density stretchable electrode grids for chronic neural recording. Adv. Mater. 30(15), 1706520 (2018)
Mazurek, P., Vudayagiri, S., Skov, A.L.: How to tailor flexible silicone elastomers with mechanical integrity: a tutorial review. Chem. Soc. Rev. 48(6), 1448–1464 (2019)
Poole-Warren, L., Martens, P., Green, R.: Biosynthetic polymers for medical applications. Woodhead Publishing (2015)
Samineni, V.K., Yoon, J., Crawford, K.E., Jeong, Y.R., McKenzie, K.C., Shin, G., Xie, Z., Sundaram, S.S., Li, Y., Yang, M.Y.: Fully implantable, battery-free wireless optoelectronic devices for spinal optogenetics. Pain. 158(11), 2108 (2017)
Mickle, A.D., Won, S.M., Noh, K.N., Yoon, J., Meacham, K.W., Xue, Y., McIlvried, L.A., Copits, B.A., Samineni, V.K., Crawford, K.E.: A wireless closed-loop system for optogenetic peripheral neuromodulation. Nature. 565(7739), 361 (2019)
Do, D.-H., Ecker, M., Voit, W.E.: Characterization of a thiol-ene/acrylate-based polymer for neuroprosthetic implants. ACS Omega. 2(8), 4604–4611 (2017)
González-González, M.A., Kanneganti, A., Joshi-Imre, A., Hernandez-Reynoso, A.G., Bendale, G., Modi, R., Ecker, M., Khurram, A., Cogan, S.F., Voit, W.E.: Thin film multi-electrode softening cuffs for selective neuromodulation. Sci. Rep. 8(1), 16390 (2018)
Garcia-Sandoval, A., Pal, A., Mishra, A.M., Sherman, S., Parikh, A.R., Joshi-Imre, A., Arreaga-Salas, D., Gutierrez-Heredia, G., Duran-Martinez, A.C., Nathan, J.: Chronic softening spinal cord stimulation arrays. J. Neural Eng. 15(4), 045002 (2018)
Hosseini, S.M., Rihani, R., Batchelor, B., Stiller, A.M., Pancrazio, J.J., Voit, W.E., Ecker, M.: Softening shape memory polymer substrates for bioelectronic devices with improved hydrolytic stability. Front. Mater. 5, 66 (2018)
Shanmuganathan, K., Capadona, J.R., Rowan, S.J., Weder, C.: Stimuli-responsive mechanically adaptive polymer nanocomposites. ACS Appl. Mater. Interfaces. 2(1), 165–174 (2009)
Liu, Y., Li, Y., Yang, G., Zheng, X., Zhou, S.: Multi-stimulus-responsive shape-memory polymer nanocomposite network cross-linked by cellulose nanocrystals. ACS Appl. Mater. Interfaces. 7(7), 4118–4126 (2015)
Rockwood, D.N., Preda, R.C., Yücel, T., Wang, X., Lovett, M.L., Kaplan, D.L.: Materials fabrication from Bombyx mori silk fibroin. Nat. Protoc. 6(10), 1612 (2011)
Tao, H., Kaplan, D.L., Omenetto, F.G.: Silk materials – a road to sustainable high technology. Adv. Mater. 24(21), 2824–2837 (2012)
Lu, Q., Hu, X., Wang, X., Kluge, J.A., Lu, S., Cebe, P., Kaplan, D.L.: Water-insoluble silk films with silk I structure. Acta Biomater. 6(4), 1380–1387 (2010)
Alba, N., Du, Z., Catt, K., Kozai, T., Cui, X.: In vivo electrochemical analysis of a PEDOT/MWCNT neural electrode coating. Biosensors. 5(4), 618–646 (2015)
Kozai, T.D., Alba, N.A., Zhang, H., Kotov, N.A., Gaunt, R.A., Cui, X.T.: Nanostructured coatings for improved charge delivery to neurons. In: Nanotechnology and neuroscience: nano-electronic, photonic and mechanical neuronal interfacing, pp. 71–134. Springer Science+Business Media, New York (2014)
Kolarcik, C.L., Luebben, S.D., Sapp, S.A., Hanner, J., Snyder, N., Kozai, T.D.Y., Chang, E., Nabity, J.A., Nabity, S.T., Lagenaur, C.F.: Elastomeric and soft conducting microwires for implantable neural interfaces. Soft Matter. 11(24), 4847–4861 (2015)
Castagnola, E., Ansaldo, A., Maggiolini, E., Angotzi, G.N., Skrap, M., Ricci, D., Fadiga, L.: Biologically compatible neural interface to safely couple nanocoated electrodes to the surface of the brain. ACS Nano. 7(5), 3887–3895 (2013)
Abidian, M.R., Martin, D.C.: Experimental and theoretical characterization of implantable neural microelectrodes modified with conducting polymer nanotubes. Biomaterials. 29(9), 1273–1283 (2008)
Ansaldo, A., Castagnola, E., Maggiolini, E., Fadiga, L., Ricci, D.: Superior electrochemical performance of carbon nanotubes directly grown on sharp microelectrodes. ACS Nano. 5(3), 2206–2214 (2011)
Fan, J.A., Yeo, W.-H., Su, Y., Hattori, Y., Lee, W., Jung, S.-Y., Zhang, Y., Liu, Z., Cheng, H., Falgout, L.: Fractal design concepts for stretchable electronics. Nat. Commun. 5, 3266 (2014)
Qi, D., Liu, Z., Liu, Y., Jiang, Y., Leow, W.R., Pal, M., Pan, S., Yang, H., Wang, Y., Zhang, X.: Highly stretchable, compliant, polymeric microelectrode arrays for in vivo electrophysiological interfacing. Adv. Mater. 29(40), 1702800 (2017)
Nimbalkar, S., Castagnola, E., Balasubramani, A., Scarpellini, A., Samejima, S., Khorasani, A., Boissenin, A., Thongpang, S., Moritz, C., Kassegne, S.: Ultra-capacitive carbon neural probe allows simultaneous long-term electrical stimulations and high-resolution neurotransmitter detection. Sci. Rep. 8(1), 1–14 (2018). https://doi.org/10.1038/s41598-41018-25198-x
Abidian, M.R., Martin, D.C.: Multifunctional nanobiomaterials for neural interfaces. Adv. Funct. Mater. 19(4), 573–585 (2009)
Yuk, H., Lu, B., Zhao, X.: Hydrogel bioelectronics. Chem. Soc. Rev. 48(6), 1642–1667 (2019)
Fallegger, F., Schiavone, G., Lacour, S.P.: Conformable hybrid systems for implantable bioelectronic interfaces. Adv. Mater. 32, 1903904 (2019)
Kozai, T.D., Gugel, Z., Li, X., Gilgunn, P.J., Khilwani, R., Ozdoganlar, O.B., Fedder, G.K., Weber, D.J., Cui, X.T.: Chronic tissue response to carboxymethyl cellulose based dissolvable insertion needle for ultra-small neural probes. Biomaterials. 35(34), 9255–9268 (2014)
Lacour, S.P., Chan, D., Wagner, S., Li, T., Suo, Z.: Mechanisms of reversible stretchability of thin metal films on elastomeric substrates. Appl. Phys. Lett. 88(20), 204103 (2006)
Zhu, B., Gong, S., Cheng, W.: Softening gold for elastronics. Chem. Soc. Rev. 48(6), 1668–1711 (2019)
Gray, D.S., Tien, J., Chen, C.S.: High-conductivity elastomeric electronics. Adv. Mater. 16(5), 393–397 (2004)
AZoM: Gold – properties and applications of gold. https://www.azom.com/article.aspx?ArticleID=598 (2001)
Johnson, P.B., Christy, R.W.: Optical constants of the noble metals. Phys. Rev. B. 6(12), 4370–4379 (1972). https://doi.org/10.1103/PhysRevB.6.4370
Knake, H., Merker, J., Lupton, D., Topfer, M.: High temperature mechanical properties of the platinum group metalselastic properties of platinum, rhodium and iridium and their alloys at high temperatures. Platinum Metals Rev. 45(2), 50–100 (2001)
AZoM: Platinum (Pt) – properties, applications. https://www.azom.com/article.aspx?ArticleID=9235 (2013)
Ambrosch-Draxl, C., Werner, W., Glantschnig, K.: Optical constants and inelastic electron-scattering data for 17 elemental metals. J. Phys. Chem. Ref. Data. 38, 1013–1092 (2009)
AZoM: Iridium – properties and applications. https://www.azom.com/article.aspx?ArticleID=1700 (2002)
Windt, D.L., Cash Jr., W.C., Scott, M., Arendt, P., Newnam, B., Fisher, R.F., Swartzlander, A.B.: Optical constants for thin films of Ti, Zr, Nb, Mo, Ru, Rh, Pd, Ag, Hf, Ta, W, Re, Ir, Os, Pt, and Au from 24 A to 1216 A. Appl. Opt. 27(2), 246–278 (1988). https://doi.org/10.1364/ao.27.000246
AZoM: Tungsten. https://www.azom.com/article.aspx?ArticleID=614 (2001)
Ordal, M.A., Bell, R.J., Alexander Jr., R.W., Newquist, L.A., Querry, M.R.: Optical properties of Al, Fe, Ti, Ta, W, and Mo at submillimeter wavelengths. Appl. Opt. 27(6), 1203–1209 (1988). https://doi.org/10.1364/ao.27.001203
Gong, S., Zhao, Y., Shi, Q., Wang, Y., Yap, L.W., Cheng, W.: Self-assembled ultrathin gold nanowires as highly transparent, conductive and stretchable supercapacitor. Electroanalysis. 28(6), 1298–1304 (2016)
Gong, S., Schwalb, W., Wang, Y., Chen, Y., Tang, Y., Si, J., Shirinzadeh, B., Cheng, W.: A wearable and highly sensitive pressure sensor with ultrathin gold nanowires. Nat. Commun. 5, 3132 (2014)
Guo, C.F., Sun, T., Liu, Q., Suo, Z., Ren, Z.: Highly stretchable and transparent nanomesh electrodes made by grain boundary lithography. Nat. Commun. 5, 3121 (2014)
Kozai, T.D., Catt, K., Du, Z., Na, K., Srivannavit, O., Razi-ul, M.H., Seymour, J., Wise, K.D., Yoon, E., Cui, X.T.: ChronicIn vivoevaluation of PEDOT/CNT for stable neural recordings. IEEE Trans. Biomed. Eng. 63(1), 111–119 (2015)
Luo, X., Weaver, C.L., Zhou, D.D., Greenberg, R., Cui, X.T.: Highly stable carbon nanotube doped poly (3, 4-ethylenedioxythiophene) for chronic neural stimulation. Biomaterials. 32(24), 5551–5557 (2011)
Castagnola, E., Maiolo, L., Maggiolini, E., Minotti, A., Marrani, M., Maita, F., Pecora, A., Angotzi, G.N., Ansaldo, A., Fadiga, L.: Ultra-flexible and brain-conformable micro-electrocorticography device with low impedance PEDOT-carbon nanotube coated microelectrodes. In: 2013 6th international IEEE/EMBS conference on neural engineering (NER), pp 927–930. IEEE (2013).
Cui, X.T., Zhou, D.D.: Poly (3, 4-ethylenedioxythiophene) for chronic neural stimulation. IEEE Trans. Neural Syst. Rehabil. Eng. 15(4), 502–508 (2007)
Cui, X., Martin, D.C.: Electrochemical deposition and characterization of poly (3, 4-ethylenedioxythiophene) on neural microelectrode arrays. Sensors Actuators B Chem. 89(1–2), 92–102 (2003)
Musk, E., Neuralink: An integrated brain-machine interface platform with thousands of channels. BioRXiv. https://doi.org/10.1101/703801 (2019)
Ouyang, L., Wei, B., Kuo, C.-c., Pathak, S., Farrell, B., Martin, D.C.: Enhanced PEDOT adhesion on solid substrates with electrografted P (EDOT-NH2). Sci. Adv. 3(3), e1600448 (2017)
Wei, B., Liu, J., Ouyang, L., Martin, D.C.: POSS-ProDOT crosslinking of PEDOT. J. Mater. Chem. B. 5(25), 5019–5026 (2017)
Wei, B., Liu, J., Ouyang, L., Kuo, C.-C., Martin, D.C.: Significant enhancement of PEDOT thin film adhesion to inorganic solid substrates with EDOT-acid. ACS Appl. Mater. Interfaces. 7(28), 15388–15394 (2015)
Charkhkar, H., Knaack, G.L., McHail, D.G., Mandal, H.S., Peixoto, N., Rubinson, J.F., Dumas, T.C., Pancrazio, J.J.: Chronic intracortical neural recordings using microelectrode arrays coated with PEDOT–TFB. Acta Biomater. 32, 57–67 (2016)
Carli, S., Lambertini, L., Zucchini, E., Ciarpella, F., Scarpellini, A., Prato, M., Castagnola, E., Fadiga, L., Ricci, D.: Single walled carbon nanohorns composite for neural sensing and stimulation. Sensors Actuators B Chem. 271, 280–288 (2018)
Mitchell Taylor, I., Patel, N.A., Freedman, N.C., Castagnola, E., Cui, X.T.: Direct in vivo electrochemical detection of resting dopamine using PEDOT/CNT functionalized microelectrodes. Anal. Chem. 91, 12917–12927 (2019)
Cui, X., Hetke, J.F., Wiler, J.A., Anderson, D.J., Martin, D.C.: Electrochemical deposition and characterization of conducting polymer polypyrrole/PSS on multichannel neural probes. Sensors Actuators A Phys. 93(1), 8–18 (2001)
Cui, X., Wiler, J., Dzaman, M., Altschuler, R.A., Martin, D.C.: In vivo studies of polypyrrole/peptide coated neural probes. Biomaterials. 24(5), 777–787 (2003)
Guitchounts, G., Cox, D.: 64-channel carbon fiber electrode arrays for chronic electrophysiology. Sci. Rep. 10(1), 1–9 (2020)
Xin Liu, Y.L.D.K.: High-density porous graphene arrays enable detection and analysis of propagating cortical waves and spirals. Sci. Rep. 8, 17089 (2018)
Lu, Y., Lyu, H., Richardson, A.G., Lucas, T.H., Kuzum, D.: Flexible neural electrode array based-on porous graphene for cortical microstimulation and sensing. Sci. Rep. 6, 33526 (2016)
Goshi, N., Castagnola, E., Vomero, M., Gueli, C., Cea, C., Zucchini, E., Bjanes, D., Maggiolini, E., Moritz, C., Kassegne, S.: Glassy carbon MEMS for novel origami-styled 3D integrated intracortical and epicortical neural probes. J. Micromech. Microeng. 28(6), 065009 (2018). https://doi.org/10.1088/1361-6439/aab061
Vomero, M., Castagnola, E., Ciarpella, F., Maggiolini, E., Goshi, N., Zucchini, E., Carli, S., Fadiga, L., Kassegne, S., Ricci, D.: Highly stable glassy carbon interfaces for long-term neural stimulation and low-noise recording of brain activity. Sci. Rep. 7, 40332 (2017)
Zestos, A.G.: Carbon nanoelectrodes for the electrochemical detection of neurotransmitters. Int. J. Electrochem. 2018, 1–19 (2018)
Puthongkham, P., Venton, B.J.: Recent advances in fast-scan cyclic voltammetry. Analyst. 145, 1087–1102 (2020)
Yang, C., Denno, M.E., Pyakurel, P., Venton, B.J.: Recent trends in carbon nanomaterial-based electrochemical sensors for biomolecules: a review. Anal. Chim. Acta. 887, 17–37 (2015)
Vomero, M., Castagnola, E., Ciarpella, F., Maggiolini, E., Goshi, N., Zucchini, E., Carli, S., Fadiga, L., Kassegne, S., Ricci, D.: Highly stable glassy carbon interfaces for long-term neural stimulation and low-noise recording of brain activity. Sci. Rep. 7(1), 1–14 (2017)
Castagnola, E., Ansaldo, A., Fadiga, L., Ricci, D.: Chemical vapour deposited carbon nanotube coated microelectrodes for intracortical neural recording. Phys. Status Solidi B. 247(11–12), 2703–2707 (2010)
Wang, K., Fishman, H.A., Dai, H., Harris, J.S.: Neural stimulation with a carbon nanotube microelectrode array. Nano Lett. 6(9), 2043–2048 (2006)
Thunemann, M., Lu, Y., Liu, X., Kılıç, K., Desjardins, M., Vandenberghe, M., Sadegh, S., Saisan, P.A., Cheng, Q., Weldy, K.L.: Deep 2-photon imaging and artifact-free optogenetics through transparent graphene microelectrode arrays. Nat. Commun. 9(1), 2035 (2018)
Castagnola, E., Vahidi, N.W., Nimbalkar, S., Rudraraju, S., Thielk, M., Zucchini, E., Cea, C., Carli, S., Gentner, T.Q., Ricci, D.: In vivo dopamine detection and single unit recordings using intracortical glassy carbon microelectrode arrays. MRS Adv. 3(29), 1629–1634 (2018)
Lang, U., Naujoks, N., Dual, J.: Mechanical characterization of PEDOT: PSS thin films. Synth. Met. 159(5–6), 473–479 (2009)
Okuzaki, H., Ishihara, M.: Spinning and characterization of conducting microfibers. Macromol. Rapid Commun. 24(3), 261–264 (2003)
Zhang, J., Seyedin, S., Qin, S., Lynch, P.A., Wang, Z., Yang, W., Wang, X., Razal Joselito, M.: Fast and scalable wet-spinning of highly conductive PEDOT:PSS fibers enables versatile applications. J. Mater. Chem. A. 7(11), 6401–6410 (2019). https://doi.org/10.1039/C9TA00022D
Yu, Z., Xia, Y., Du, D., Ouyang, J.: PEDOT:PSS films with metallic conductivity through a treatment with common organic solutions of organic salts and their application as a transparent electrode of polymer solar cells. ACS Appl. Mater. Interfaces. 8(18), 11629–11638 (2016). https://doi.org/10.1021/acsami.6b00317
Yang, Z., Fang, Z., Sheng, J., Ling, Z., Liu, Z., Zhu, J., Gao, P., Ye, J.: Optoelectronic evaluation and loss analysis of PEDOT:PSS/Si hybrid heterojunction solar cells. Nanoscale Res. Lett. 12(1), 26–26 (2017). https://doi.org/10.1186/s11671-016-1790-1
Li, C., Xian, G.: Experimental and modeling study of the evolution of mechanical properties of PAN-based carbon fibers at elevated temperatures. Materials (Basel). 12(5), 724 (2019). https://doi.org/10.3390/ma12050724
Wentzel, D., Sevostianov, I.: Electrical conductivity of unidirectional carbon fiber composites with epoxy-graphene matrix. Int. J. Eng. Sci. 130, 129–135 (2018). https://doi.org/10.1016/j.ijengsci.2018.05.012
Papageorgiou, D.G., Kinloch, I.A., Young, R.J.: Mechanical properties of graphene and graphene-based nanocomposites. Prog. Mater. Sci. 90, 75–127 (2017). https://doi.org/10.1016/j.pmatsci.2017.07.004
Marinho, B., Ghislandi, M., Tkalya, E., Koning, C.E., de With, G.: Electrical conductivity of compacts of graphene, multi-wall carbon nanotubes, carbon black, and graphite powder. Powder Technol. 221, 351–358 (2012). https://doi.org/10.1016/j.powtec.2012.01.024
Xu, J.: Linear optical characterization of graphene structure. UWSpace (2018).
Goding, J., Gilmour, A., Martens, P., Poole-Warren, L., Green, R.: Interpenetrating conducting hydrogel materials for neural interfacing electrodes. Adv. Healtcare Mater. 6(9), 1601177 (2017)
Goding, J., Gilmour, A., Martens, P., Poole-Warren, L., Green, R.: Interpenetrating conducting hydrogel materials for neural interfacing electrodes. Adv. Healthc. Mater. 6(9), 1601177 (2017)
Castagnola, E., Maggiolini, E., Ceseracciu, L., Ciarpella, F., Zucchini, E., De Faveri, S., Fadiga, L., Ricci, D.: pHEMA encapsulated PEDOT-PSS-CNT microsphere microelectrodes for recording single unit activity in the brain. Front. Neurosci. 10, 151 (2016)
Aregueta-Robles, U.A., Woolley, A.J., Poole-Warren, L.A., Lovell, N.H., Green, R.A.: Organic electrode coatings for next-generation neural interfaces. Front. Neuroeng. 7, 15 (2014)
Liu, Y., Liu, J., Chen, S., Lei, T., Kim, Y., Niu, S., Wang, H., Wang, X., Foudeh, A.M., Tok, J.B.-H., Bao, Z.: Soft and elastic hydrogel-based microelectronics for localized low-voltage neuromodulation. Nat. Biomed. Eng. 3, 58–68 (2019)
Heo, D.N., Song, S.-J., Kim, H.-J., Lee, Y.J., Ko, W.-K., Lee, S.J., Lee, D., Park, S.J., Zhang, L.G., Kang, J.Y.: Multifunctional hydrogel coatings on the surface of neural cuff electrode for improving electrode-nerve tissue interfaces. Acta Biomater. 39, 25–33 (2016)
Spencer, K.C., Sy, J.C., Ramadi, K.B., Graybiel, A.M., Langer, R., Cima, M.J.: Characterization of mechanically matched hydrogel coatings to improve the biocompatibility of neural implants. Sci. Rep. 7(1), 1952 (2017)
Lu, Y., Wang, D., Li, T., Zhao, X., Cao, Y., Yang, H., Duan, Y.Y.: Poly(vinyl alcohol)/poly(acrylic acid) hydrogel coatings for improving electrode–neural tissue interface. Biomaterials. 30(25), 4143–4151 (2009)
Azemi, E., Lagenaur, C.F., Cui, X.T.: The surface immobilization of the neural adhesion molecule L1 on neural probes and its effect on neuronal density and gliosis at the probe/tissue interface. Biomaterials. 32(3), 681–692 (2011)
Winter, J.O., Cogan, S.F., Rizzo, I.I.I.J.F.: Neurotrophin-eluting hydrogel coatings for neural stimulating electrodes. J. Biomed. Mater. Res. Part B: Appl. Biomater. 81(2), 551–563 (2007)
Zhong, Y., Bellamkonda, R.V.: Dexamethasone-coated neural probes elicit attenuated inflammatory response and neuronal loss compared to uncoated neural probes. Brain Res. 1148, 15–27 (2007)
Fattahi, P., Yang, G., Kim, G., Abidian, M.R.: Biomaterials: a review of organic and inorganic biomaterials for neural interfaces (Adv. Mater. 12/2014). Adv. Mater. 26(12), 1793–1793 (2014)
Kim, D.-H., Wiler, J.A., Anderson, D.J., Kipke, D.R., Martin, D.C.: Conducting polymers on hydrogel-coated neural electrode provide sensitive neural recordings in auditory cortex. Acta Biomater. 6(1), 57–62 (2010)
Vitale, F., Vercosa, D.G., Rodriguez, A.V., Pamulapati, S.S., Seibt, F., Lewis, E., Yan, J.S., Badhiwala, K., Adnan, M., Royer-Carfagni, G.: Fluidic microactuation of flexible electrodes for neural recording. Nano Lett. 18(1), 326–335 (2017)
Huang, X.: Materials and applications of bioresorbable electronics. J. Semicond. 39(1), 011003209 (2018)
Li, C., Guo, C., Fitzpatrick, V., Ibrahim, A., Zwierstra, M.J., Hanna, P., Lechtig, A., Nazarian, A., Lin, S.J., Kaplan, D.L.: Design of biodegradable, implantable devices towards clinical translation. Nat. Rev. Mater. 5, 1–21 (2019)
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.: Bioresorbable silicon electronics for transient spatiotemporal mapping of electrical activity from the cerebral cortex. Nat. Mater. 15(7), 782 (2016)
Hava, M.A.S.: Single-crystal silicon: electrical and optical properties. In: Springer handbook of electronic and photonic materials. Springer, Cham (2017)
Filmetrics: Refractive index of Mg – smooth. https://www.filmetrics.com/refractive-index-database/Mg+-+Smooth (2019)
Palik, E.D.: Handbook of optical constants of solids, vol. 3. Elsevier, Academic Press, San Diego (1997)
Wall DA: Zinc and its uses. https://www.azom.com/article.aspx?ArticleID=749 (1998)
AZoM: Molybdenum (Mo) – properties, applications. https://www.azom.com/article.aspx?ArticleID=616 (2001)
Koh, L.-D., Cheng, Y., Teng, C.-P., Khin, Y.-W., Loh, X.-J., Tee, S.-Y., Low, M., Ye, E., Yu, H.-D., Zhang, Y.-W., Han, M.-Y.: Structures, mechanical properties and applications of silk fibroin materials. Prog. Polym. Sci. 46, 86–110 (2015). https://doi.org/10.1016/j.progpolymsci.2015.02.001
Lee, J.H., Kwak, H.W., Park, M.H., Hwang, J., Kim, J.W., Jang, H.W., Jin, H.-J., Lee, W.H.: Understanding hydroscopic properties of silk fibroin and its use as a gate-dielectric in organic field-effect transistors. Org. Electron. 59, 213–219 (2018). https://doi.org/10.1016/j.orgel.2018.05.012
Perotto, G., Zhang, Y., Naskar, D., Patel, N., Kaplan, D.L., Kundu, S.C., Omenetto, F.G.: The optical properties of regenerated silk fibroin films obtained from different sources. Appl. Phys. Lett. 111(10), 103702 (2017). https://doi.org/10.1063/1.4998950
Qi, Y., Wang, H., Wei, K., Yang, Y., Zheng, R.Y., Kim, I.S., Zhang, K.Q.: A review of structure construction of silk fibroin biomaterials from single structures to multi-level structures. Int. J. Mol. Sci. 18(3), 237 (2017). https://doi.org/10.3390/ijms18030237
Warwicker, J.: The crystal structure of silk fibroin. Acta Crystallogr. 7(8–9), 565–573 (1954). https://doi.org/10.1107/S0365110X54001867
Rivnay, J., Wang, H., Fenno, L., Deisseroth, K., Malliaras, G.G.: Next-generation probes, particles, and proteins for neural interfacing. Sci. Adv. 3(6), e1601649 (2017). https://doi.org/10.1126/sciadv.1601649
Oh, Y., Park, C., Kim, D.H., Shin, H., Kang, Y.M., DeWaele, M., Lee, J., Min, H.-K., Blaha, C.D., Bennet, K.E.: Monitoring in vivo changes in tonic extracellular dopamine level by charge-balancing multiple waveform fast-scan cyclic voltammetry. Anal. Chem. 88(22), 10962–10970 (2016). https://doi.org/10.1021/acs.analchem.6b02605
Di Flumeri, G., Aricò, P., Borghini, G., Sciaraffa, N., Di Florio, A., Babiloni, F.: The dry revolution: evaluation of three different EEG dry electrode types in terms of signal spectral features, mental states classification and usability. Sensors. 19(6), 1365 (2019)
Norton, J.J., Lee, D.S., Lee, J.W., Lee, W., Kwon, O., Won, P., Jung, S.-Y., Cheng, H., Jeong, J.-W., Akce, A.: Soft, curved electrode systems capable of integration on the auricle as a persistent brain–computer interface. Proc. Natl. Acad. Sci. 112(13), 3920–3925 (2015)
Grozea, C., Voinescu, C.D., Fazli, S.: Bristle-sensors – low-cost flexible passive dry EEG electrodes for neurofeedback and BCI applications. J. Neural Eng. 8(2), 025008 (2011)
Gargiulo, G., Calvo, R.A., Bifulco, P., Cesarelli, M., Jin, C., Mohamed, A., van Schaik, A.: A new EEG recording system for passive dry electrodes. Clin. Neurophysiol. 121(5), 686–693 (2010)
Myers, A.C., Huang, H., Zhu, Y.: Wearable silver nanowire dry electrodes for electrophysiological sensing. RSC Adv. 5(15), 11627–11632 (2015)
Ferrari, L.M., Sudha, S., Tarantino, S., Esposti, R., Bolzoni, F., Cavallari, P., Cipriani, C., Mattoli, V., Greco, F.: Ultraconformable temporary tattoo electrodes for electrophysiology. Adv. Sci. 5(3), 1700771 (2018)
Leuthardt, E.C., Schalk, G., Moran, D., Ojemann, J.G.: The emerging world of motor neuroprosthetics: a neurosurgical perspective. Neurosurgery. 59(1), 1 (2006)
Leuthardt, E.C., Freudenberg, Z., Bundy, D., Roland, J.: Microscale recording from human motor cortex: implications for minimally invasive electrocorticographic brain-computer interfaces. Neurosurg. Focus. 27(1), E10 (2009)
Schwartz, A.B.: Cortical neural prosthetics. Annu. Rev. Neurosci. 27, 487–507 (2004)
Degenhart, A.D., Eles, J., Dum, R., Mischel, J.L., Smalianchuk, I., Endler, B., Ashmore, R.C., Tyler-Kabara, E.C., Hatsopoulos, N.G., Wang, W.: Histological evaluation of a chronically-implanted electrocorticographic electrode grid in a non-human primate. J. Neural Eng. 13(4), 046019 (2016)
Collinger, J.L., Wodlinger, B., Downey, J.E., Wang, W., Tyler-Kabara, E.C., Weber, D.J., McMorland, A.J., Velliste, M., Boninger, M.L., Schwartz, A.B.: High-performance neuroprosthetic control by an individual with tetraplegia. Lancet. 381(9866), 557–564 (2013)
Maiolo, L., Polese, D., Convertino, A.: The rise of flexible electronics in neuroscience, from materials selection to in vitro and in vivo applications. Adv. Phys.: X. 4(1), 1664319 (2019)
Pazzini, L., Polese, D., Weinert, J.F., Maiolo, L., Maita, F., Marrani, M., Pecora, A., Sanchez-Vives, M.V., Fortunato, G.: An ultra-compact integrated system for brain activity recording and stimulation validated over cortical slow oscillations in vivo and in vitro. Sci. Rep. 8(1), 16717 (2018)
Yi Qiang, P.A., Seo, K.J., Culaclii, S., Hogan, V., Zhao, X., Zhong, Y., Han, X., Wang, P.-M., Lo, Y.-K., Li, Y., Patel, H.A., Huang, Y., Sambangi, A., Chu, J.S.V., Liu, W., Fagiolini, M., Fang, H.: Transparent arrays of bilayer-nanomesh microelectrodes for simultaneous electrophysiology and two-photon imaging in the brain. Sci. Adv. 4(9), eaat0626 (2018)
Wonryung Lee, D.K., Matsuhisa, N., Nagase, M., Sekino, M., Malliaras, G.G., Yokota, T., Someya, T.: Transparent, conformable, active multielectrode array using organic electrochemical transistors. PNAS. 114(40), 10554–10559 (2017)
Kuzum, D., Takano, H., Shim, E., Reed, J.C., Juul, H., Richardson, A.G., De Vries, J., Bink, H., Dichter, M.A., Lucas, T.H.: Transparent and flexible low noise graphene electrodes for simultaneous electrophysiology and neuroimaging. Nat. Commun. 5, 5259 (2014)
Park, D.-W., Ness, J.P., Brodnick, S.K., Esquibel, C., Novello, J., Atry, F., Baek, D.-H., Kim, H., Bong, J., Swanson, K.I.: Electrical neural stimulation and simultaneous in vivo monitoring with transparent graphene electrode arrays implanted in GCaMP6f mice. ACS Nano. 12(1), 148–157 (2018)
Ledochowitsch, P., Yazdan-Shahmorad, A., Bouchard, K., Diaz-Botia, C., Hanson, T., He, J.-W., Seybold, B., Olivero, E., Phillips, E., Blanche, T.: Strategies for optical control and simultaneous electrical readout of extended cortical circuits. J. Neurosci. Methods. 256, 220–231 (2015)
Lu, Y., Liu, X., Hattori, R., Ren, C., Zhang, X., Komiyama, T., Kuzum, D.: Ultralow impedance graphene microelectrodes with high optical transparency for simultaneous deep two-photon imaging in transgenic mice. Adv. Funct. Mater. 28(31), 1800002 (2018)
Park, D.-W., Ness, J.P., Brodnick, S.K., Esquibel, C., Novello, J., Atry, F., Baek, D.-H., Kim, H., Bong, J., Swanson, K.I., Suminski, A.J., Otto, K.J., Pashaie, R., Williams, J.C., Ma, Z.: Electrical neural stimulation and simultaneous in vivo monitoring with transparent graphene electrode arrays implanted in GCaMP6f mice. ACS Nano. 12, 148–−157 (2018)
Lee, W., Kim, D., Matsuhisa, N., Nagase, M., Sekino, M., Malliaras, G.G., Yokota, T., Someya, T.: Transparent, conformable, active multielectrode array using organic electrochemical transistors. Proc. Natl. Acad. Sci. 114(40), 10554–10559 (2017)
Lee, H., Bellamkonda, R.V., Sun, W., Levenston, M.E.: Biomechanical analysis of silicon microelectrode-induced strain in the brain. J. Neural Eng. 2(4), 81 (2005)
Rousche, P.J., Pellinen, D.S., Pivin, D.P., Williams, J.C., Vetter, R.J., Kipke, D.R.: Flexible polyimide-based intracortical electrode arrays with bioactive capability. IEEE Trans. Biomed. Eng. 48(3), 361–371 (2001)
Chi Lu, S.P., Richner, T.J., Derry, A., Brown, I., Hou, C., Rao, S., Kang, J., Moritz, C.T., Fink, Y., Anikeeva, P.: Flexible and stretchable nanowire-coated fibers for optoelectronic probing of spinal cord circuits. Sci. Adv. 3(3), e1600955 (2017)
DeWaele, M., Oh, Y., Park, C., Kang, Y.M., Shin, H., Blaha, C.D., Bennet, K.E., Kim, I.Y., Lee, K.H., Jang, D.P.: A baseline drift detrending technique for fast scan cyclic voltammetry. Analyst. 142(22), 4317–4321 (2017)
Park, S., Guo, Y., Jia, X., Choe, H.K., Grena, B., Kang, J., Park, J., Lu, C., Canales, A., Chen, R.: One-step optogenetics with multifunctional flexible polymer fibers. Nat. Neurosci. 20(4), 612–619 (2017)
Liu, J., Fu, T.-M., Cheng, Z., Hong, G., Zhou, T., Jin, L., Duvvuri, M., Jiang, Z., Kruskal, P., Xie, C., Suo, Z., Fang, Y., Lieber, C.M.: Syringe-injectable electronics. Nat. Nanotechnol. 10, 629–636 (2015)
Liu, J.: Syringe injectable electronics. In: Biomimetics Through Nanoelectronics, pp. 65–93. Springer (2018)
Du, Z.J., Kolarcik, C.L., Kozai, T.D.Y., Luebben, S.D., Sapp, S.A., Zheng, X.S., Nabity, J.A., Cui, X.T.: Ultrasoft microwire neural electrodes improve chronic tissue integration. Acta Biomater. 53, 46–58 (2017)
Zhang, Y., Mickle, A.D., Gutruf, P., McIlvried, L.A., Guo, H., Wu, Y., Golden, J.P., Xue, Y., Grajales-Reyes, J.G., Wang, X., Krishnan, S., Xie, Y., Peng, D., Su, C.-J., Zhang, F., Reeder, J.T., Vogt, S.K., Huang, Y., Rogers, J.A., Gereau, R.W.: Battery-free, fully implantable optofluidic cuff system for wireless optogenetic and pharmacological neuromodulation of peripheral nerves. Science Advances. 5(7), eaaw5296 (2019). https://doi.org/10.1126/sciadv.aaw5296
Canales, A., Jia, X., Froriep, U.P., Koppes, R.A., Tringides, C.M., Selvidge, J., Lu, C., Hou, C., Wei, L., Fink, Y.: Multifunctional fibers for simultaneous optical, electrical and chemical interrogation of neural circuits in vivo. Nat. Biotechnol. 33(3), 277 (2015)
Lo, M.-c., Wang, S., Singh, S., Damodaran, V.B., Kaplan, H.M., Kohn, J., Shreiber, D.I., Zahn, J.D.: Coating flexible probes with an ultra fast degrading polymer to aid in tissue insertion. Biomed. Microdevices. 17(2), 34 (2015)
Felix, S.H., Shah, K.G., Tolosa, V.M., Sheth, H.J., Tooker, A.C., Delima, T.L., Jadhav, S.P., Frank, L.M., Pannu, S.S.: Insertion of flexible neural probes using rigid stiffeners attached with biodissolvable adhesive. J. Vis. Exp. 79, e50609 (2013)
Joo, H.R., Fan, J.L., Chen, S., Pebbles, J.A., Liang, H., Chung, J.E., Yorita, A.M., Tooker, A.C., Tolosa, V.M., Geaghan-Breiner, C.: A microfabricated, 3D-sharpened silicon shuttle for insertion of flexible electrode arrays through dura mater into brain. J. Neural Eng. 16(6), 066021 (2019)
Lee, J.M., Hong, G., Lin, D., Schuhmann Jr., T.G., Sullivan, A.T., Viveros, R.D., Park, H.-G., Lieber, C.M.: Nanoenabled direct contact interfacing of syringe-injectable mesh electronics. Nano Lett. 19(8), 5818–5826 (2019)
Szikszay, T., Hall, T., von Piekartz, H.: In vivo effects of limb movement on nerve stretch, strain, and tension: a systematic review. J. Back Musculoskelet. Rehabil. 30(6), 1171–1186 (2017). https://doi.org/10.3233/BMR-169720
Romero-Ortega, M.: Peripheral nerves, anatomy and physiology of. In: Jaeger, D., Jung, R. (eds.) Encyclopedia of computational neuroscience, pp. 1–5. Springer, New York (2013). https://doi.org/10.1007/978-1-4614-7320-6_214-1
Johnson Chad, R.P.D., Barr Roger, C.P.D., Klein Stephen, M.M.D.: A computer model of electrical stimulation of peripheral nerves in regional anesthesia. Anesthesiol.: J. Am. Soc. Anesthesiol. 106(2), 323–330 (2007)
Tyler, D.J., Durand, D.M.: Functionally selective peripheral nerve stimulation with a flat interface nerve electrode. IEEE Trans. Neural Syst. Rehabil. Eng. 10(4), 294–303 (2002). https://doi.org/10.1109/tnsre.2002.806840
González-González, M.A., Kanneganti, A., Joshi-Imre, A., Hernandez-Reynoso, A.G., Bendale, G., Modi, R., Ecker, M., Khurram, A., Cogan, S.F., Voit, W.E., Romero-Ortega, M.I.: Thin film multi-electrode softening cuffs for selective neuromodulation. Sci. Rep. 8(1), 16390 (2018). https://doi.org/10.1038/s41598-018-34566-6
Navarro, X., Lago, N., Vivo, M., Yoshida, K., Koch, K.P., Poppendieck, W., Micera, S.: Neurobiological evaluation of thin-film longitudinal intrafascicular electrodes as a peripheral nerve interface. In: 2007 IEEE 10th international conference on rehabilitation robotics, 13–15 June 2007. pp. 643–649 (2007). https://doi.org/10.1109/ICORR.2007.4428492
Wang, J., Thow, X.Y., Wang, H., Lee, S., Voges, K., Thakor, N.V., Yen, S.-C., Lee, C.: A highly selective 3D Spiked Ultraflexible Neural (SUN) interface for decoding peripheral nerve sensory information. Adv. Healthc. Mater. 7(5), 1700987 (2018). https://doi.org/10.1002/adhm.201700987
Zheng, X., Woeppel, K.M., Griffith, A.Y., Chang, E., Looker, M.J., Fisher, L.E., Clapsaddle, B.J., Cui, X.T.: Soft conducting elastomer for peripheral nerve interface. Adv. Healthc. Mater. 8(9), 1801311 (2019). https://doi.org/10.1002/adhm.201801311
Musick, K.M., Rigosa, J., Narasimhan, S., Wurth, S., Capogrosso, M., Chew, D.J., Fawcett, J.W., Micera, S., Lacour, S.P.: Chronic multichannel neural recordings from soft regenerative microchannel electrodes during gait. Sci. Rep. 5, 14363 (2015)
Clark, G.A., Ledbetter, N.M., Warren, D.J., Harrison, R.R.: Recording sensory and motor information from peripheral nerves with Utah slanted electrode arrays. In: 2011 Annual international conference of the IEEE engineering in medicine and biology society, pp. 4641–4644. IEEE (2011)
Wark, H.A.C., Mathews, K.S., Normann, R.A., Fernandez, E.: Behavioral and cellular consequences of high-electrode count Utah arrays chronically implanted in rat sciatic nerve. J. Neural Eng. 11(4), 046027 (2014). https://doi.org/10.1088/1741-2560/11/4/046027
Christensen, M., Pearce, S., Ledbetter, N., Warren, D., Clark, G., Tresco, P.: The foreign body response to the Utah slant electrode array in the cat sciatic nerve. Acta Biomater. 10(11), 4650–4660 (2014)
Campbell, A., Wu, C.: Chronically implanted intracranial electrodes: tissue reaction and electrical changes. Micromachines (Basel). 9(9), 430 (2018). https://doi.org/10.3390/mi9090430
Ordonez, J.S., Pikov, V., Wiggins, H., Patten, C., Stieglitz, T., Rickert, J., Schuettler, M.: Cuff electrodes for very small diameter nerves – prototyping and first recordings in vivo. In: 2014 36th annual international conference of the IEEE engineering in medicine and biology society, 26–30 Aug. 2014, pp. 6846–6849 (2014). https://doi.org/10.1109/EMBC.2014.6945201
Yu, H., Xiong, W., Zhang, H., Wang, W., Li, Z.: A Parylene self-locking cuff electrode for peripheral nerve stimulation and recording. J. Microelectromech. Syst. 23(5), 1025–1035 (2014). https://doi.org/10.1109/JMEMS.2014.2333733
Meyer, J.U., Stieglitz, T., Beutel, H.È., Schuettler, M.: Micromachined, polyimide-based devices for flexible neural interfaces. Biomed. Microdevices. 2(4), 283–294 (2000). https://doi.org/10.1023/A:1009955222114
Zhang, Y., Zheng, N., Cao, Y., Wang, F., Wang, P., Ma, Y., Lu, B., Hou, G., Fang, Z., Liang, Z., Yue, M., Li, Y., Chen, Y., Fu, J., Wu, J., Xie, T., Feng, X.: Climbing-inspired twining electrodes using shape memory for peripheral nerve stimulation and recording. Sci. Adv. 5(4), eaaw1066 (2019). https://doi.org/10.1126/sciadv.aaw1066
Mizisin, A.W.A.P.: The blood-nerve barrier: structure and functional significance. In: The blood-brain and other neural barriers (2010). https://doi.org/10.1007/978-1-60761-938-3_6
de la Oliva, N., Navarro, X., del Valle, J.: Time course study of long-term biocompatibility and foreign body reaction to intraneural polyimide-based implants. J. Biomed. Mater. Res. A. 106(3), 746–757 (2018). https://doi.org/10.1002/jbm.a.36274
Myllymaa, S., Myllymaa, K., Korhonen, H., Lammi, M.J., Tiitu, V., Lappalainen, R.: Surface characterization and in vitro biocompatibility assessment of photosensitive polyimide films. Colloids Surf. B: Biointerfaces. 76(2), 505–511 (2010)
Goda, T., Konno, T., Takai, M., Ishihara, K.: Photoinduced phospholipid polymer grafting on Parylene film: Advanced lubrication and antibiofouling properties. Colloids Surf. B: Biointerfaces. 54(1), 67–73 (2007)
Jones, J.A., Chang, D.T., Meyerson, H., Colton, E., Kwon, I.K., Matsuda, T., Anderson, J.M.: Proteomic analysis and quantification of cytokines and chemokines from biomaterial surface-adherent macrophages and foreign body giant cells. J. Biomed. Mater.Res. Part A. 83(3), 585–596 (2007)
Ghosh, I., Konar, J., Bhowmick, A.K.: Surface properties of chemically modified polyimide films. J. Adhes. Sci. Technol. 11(6), 877–893 (1997)
Chang, T.Y., Yadav, V.G., De Leo, S., Mohedas, A., Rajalingam, B., Chen, C.-L., Selvarasah, S., Dokmeci, M.R., Khademhosseini, A.: Cell and protein compatibility of parylene-C surfaces. Langmuir. 23(23), 11718–11725 (2007)
Stieglitz, T., Beutel, H., Meyer, J.U.: A flexible, light-weight multichannel sieve electrode with integrated cables for interfacing regenerating peripheral nerves. Sensors Actuators A Phys. 60(1), 240–243 (1997). https://doi.org/10.1016/S0924-4247(97)01494-5
MacEwan, M.R., Zellmer, E.R., Wheeler, J.J., Burton, H., Moran, D.W.: Regenerated sciatic nerve axons stimulated through a chronically implanted macro-sieve electrode. Front. Neurosci. 10, 557–557 (2016). https://doi.org/10.3389/fnins.2016.00557
Srinivasan, A., Tahilramani, M., Bentley, J.T., Gore, R.K., Millard, D.C., Mukhatyar, V.J., Joseph, A., Haque, A.S., Stanley, G.B., English, A.W., Bellamkonda, R.V.: Microchannel-based regenerative scaffold for chronic peripheral nerve interfacing in amputees. Biomaterials. 41, 151–165 (2015). https://doi.org/10.1016/j.biomaterials.2014.11.035
Fernandez-Leon, J.A., Parajuli, A., Franklin, R., Sorenson, M., Felleman, D.J., Hansen, B.J., Hu, M., Dragoi, V.: A wireless transmission neural interface system for unconstrained non-human primates. J. Neural Eng. 12(5), 056005 (2015)
Shepherd, R.K., Villalobos, J., Burns, O., Nayagam, D.A.X.: The development of neural stimulators: a review of preclinical safety and efficacy studies. J. Neural Eng. 15(4), 041004 (2018)
Author information
Authors and Affiliations
Corresponding authors
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2023 Springer Nature Singapore Pte Ltd.
About this entry
Cite this entry
Castagnola, E., Zheng, X.S., Cui, X.T. (2023). Flexible and Soft Materials and Devices for Neural Interface. In: Thakor, N.V. (eds) Handbook of Neuroengineering. Springer, Singapore. https://doi.org/10.1007/978-981-16-5540-1_5
Download citation
DOI: https://doi.org/10.1007/978-981-16-5540-1_5
Published:
Publisher Name: Springer, Singapore
Print ISBN: 978-981-16-5539-5
Online ISBN: 978-981-16-5540-1
eBook Packages: EngineeringReference Module Computer Science and Engineering