Abstract
The application of biomimetic technologies to neural interfaces seeks to improve the long-term safety and performance of implantable systems. These biomimetic approaches encompass methods that alter the biological environment through mechanical, topographical and biological approaches. This chapter examines recent developments in bioinspired soft and functional materials designed for neural interfaces and their application to neuroprosthetic devices. Further approaches to engineering the neural interface, such as the application of tissue engineering and genetic engineering technologies, including their role in the development of next-generation neuroprosthetic devices are assessed.
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Abbreviations
- 3D:
-
Three Dimensional
- Ascl1:
-
Achaete-Scute Homolog 1
- AV8:
-
Adeno-Associated Viral Vector
- AVV2:
-
Adeno-Associated Viral Vector
- BAC:
-
Bacterial Artificial Chromosome
- Brn2:
-
Bearskin 2
- ChR2:
-
Channelrhodopsin2
- CHs:
-
Conducting Hydrogels
- CNS:
-
Central Nervous System
- CPs:
-
Conducting Polymers
- DCX+ :
-
Doublecortin
- Dlx2:
-
Distal-Less Homeobox 2
- ECM:
-
Extracellular Matrix
- EL222:
-
Erythrobacter Litoralis Protein
- GAGs:
-
Glycosaminoglycans
- GABA:
-
Gamma-Aminobutyric Acid
- GFAP:
-
Anti-Glial Fibrillary Acidic Protein
- GFP:
-
Green Fluorescent Protein
- LED:
-
Light Emitting Diode
- Myt1l:
-
Myelin Transcription Factor 1-Like
- NeuroD1:
-
Neuronal Differentiation 1
- Neurog2:
-
Neurogenin-2
- Pax6:
-
Paired Box Protein-6
- PBS:
-
Phosphate-Buffered Saline Solution
- Pt:
-
Platinum
References
Wang, M., et al.: Nanotechnology and nanomaterials for improving neural interfaces. Adv. Funct. Mater. 28, 1700905 (2018)
Chaudhary, U., Birbaumer, N., Ramos-Murguialday, A.: Brain–computer interfaces for communication and rehabilitation. Nat. Rev. Neurol. 12, 513 (2016)
Vallejo-Giraldo, C., et al.: Polyhydroxyalkanoate/carbon nanotube nanocomposites: flexible electrically conducting elastomers for neural applications. Nanomedicine. 11, 2547–2563 (2016)
Sofroniew, M.V.: Molecular dissection of reactive astrogliosis and glial scar formation. Trends Neurosci. 32, 638–647 (2009)
Hamzavi, N., Tsang, W. & Shim, V.: Nonlinear elastic brain tissue model for neural probe-tissue mechanical interaction. In: 2013 6th International IEEE/EMBS Conference on Neural Engineering (NER), pp. 1119–1122. IEEE (2013)
Miller, K., Chinzei, K., Orssengo, G., Bednarz, P.: Mechanical properties of brain tissue in-vivo: experiment and computer simulation. J. Biomech. 33, 1369–1376 (2000)
Palchesko, R.N., Zhang, L., Sun, Y., Feinberg, A.W.: Development of polydimethylsiloxane substrates with tunable elastic modulus to study cell mechanobiology in muscle and nerve. PLoS One. 7, e51499 (2012)
Kozai, T.D.Y., et al.: Ultrasmall implantable composite microelectrodes with bioactive surfaces for chronic neural interfaces. Nat. Mater. 11, 1065 (2012)
McClain, M.A., et al.: Highly-compliant, microcable neuroelectrodes fabricated from thin-film gold and PDMS. Biomed. Microdevices. 13, 361–373 (2011)
Heo, D.N., et al.: Flexible and highly biocompatible nanofiber-based electrodes for neural surface interfacing. ACS Nano. 11, 2961–2971 (2017)
Yu, Z., et al.: Monitoring hippocampus electrical activity in vitro on an elastically deformable microelectrode array. J. Neurotrauma. 26, 1135–1145 (2009)
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)
Goding, J., Gilmour, A., Martens, P., Poole-Warren, L., Green, R.: Interpenetrating conducting hydrogel materials for neural interfacing electrodes. Adv. Healthc. Mater. 6, 1601177 (2017)
Green, R.A., et al.: Conductive hydrogels: mechanically robust hybrids for use as biomaterials. Macromol. Biosci. 12, 494–501 (2012)
Boehler, C., Stieglitz, T., Asplund, M.: Nanostructured platinum grass enables superior impedance reduction for neural microelectrodes. Biomaterials. 67, 346–353 (2015)
Yiannakou, C., et al.: Cell patterning via laser micro/nano structured silicon surfaces. Biofabrication. 9, 025024 (2017)
Chung, C.-K., Tseng, S.-F., Hsiao, W.-T., Chiang, D., Lin, W.-C.: Laser micromachining of PEDOT: PSS/Graphene thin films by using beam shaping technology. J Laser Micro/Nanoeng. 11, 395–399 (2016)
Bass, R.B., Clark, W.W., Zhang, J.Z., Lichtenberger, A.W.: Use of a focused ion beam for characterizing SIS circuits. IEEE Trans. Appl. Supercond. 11, 92–94 (2001)
Hof, L., Guo, X., Seo, M., Wüthrich, R., Greener, J.: Glass imprint templates by spark assisted chemical engraving for microfabrication by hot embossing. Micromachines. 8, 29 (2017)
Hoshino, T., Miyazako, H., Nakayama, A., Wagatsuma, A., Mabuchi, K.: Electron beam induced fine virtual electrode for mechanical strain microscopy of living cell. Sensors Actuators B Chem. 236, 659–667 (2016)
Chapman, C.A., et al.: Nanoporous gold biointerfaces: modifying nanostructure to control neural cell coverage and enhance electrophysiological recording performance. Adv. Funct. Mater. 27, 1604631 (2017)
Turner, A., et al.: Attachment of astroglial cells to microfabricated pillar arrays of different geometries. J. Biomed. Mater. Res. 51, 430–441 (2000)
Qi, L., et al.: The effects of topographical patterns and sizes on neural stem cell behavior. PLoS One. 8, e59022 (2013)
Richardson-Burns, S.M., et al.: Polymerization of the conducting polymer poly (3, 4-ethylenedioxythiophene)(PEDOT) around living neural cells. Biomaterials. 28, 1539–1552 (2007)
Yang, J., Martin, D.C.: Microporous conducting polymers on neural microelectrode arrays: II. Physical characterization. Sensors Actuators A Phys. 113, 204–211 (2004)
Abidian, M.R., Kim, D.H., Martin, D.C.: Conducting-polymer nanotubes for controlled drug release. Adv. Mater. 18, 405–409 (2006)
HajjHassan, M., Chodavarapu, V., Musallam, S.: NeuroMEMS: neural probe microtechnologies. Sensors. 8, 6704–6726 (2008)
Uppalapati, D., Boyd, B.J., Garg, S., Travas-Sejdic, J., Svirskis, D.: Conducting polymers with defined micro-or nanostructures for drug delivery. Biomaterials. 111, 149–162 (2016)
Kotov, N.A., et al.: Nanomaterials for neural interfaces. Adv. Mater. 21, 3970–4004 (2009)
Pancrazio, J.J.: Neural interfaces at the nanoscale. Nanomedicine. 3, 823–830 (2008)
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, 8–18 (2001)
Biggs, M.J.P., Richards, R.G., Dalby, M.J.: Nanotopographical modification: a regulator of cellular function through focal adhesions. Nanomedicine. 6, 619–633 (2010)
Ballester-Beltrán, J., Biggs, M.J., Dalby, M.J., Salmeron-Sanchez, M., Leal-Egaña, A.: Sensing the difference: the influence of anisotropic cues on cell behavior. Front. Mater. 2, 39 (2015)
Yang, X., et al.: Bioinspired neuron-like electronics. Nat. Mater. 18, 510–517 (2019)
Zanganeh, S., et al.: Electrochemical approach for monitoring the effect of anti tubulin drugs on breast cancer cells based on silicon nanograss electrodes. Anal. Chim. Acta. 938, 72–81 (2016)
Pacelli, S., et al.: Nanodiamond-based injectable hydrogel for sustained growth factor release: preparation, characterization and in vitro analysis. Acta Biomater. 58, 479–491 (2017)
Collazos-Castro, J.E., Hernández-Labrado, G.R., Polo, J.L., García-Rama, C.: N-Cadherin-and L1-functionalised conducting polymers for synergistic stimulation and guidance of neural cell growth. Biomaterials. 34, 3603–3617 (2013)
Povlich, L.K., et al.: Synthesis, copolymerization and peptide-modification of carboxylic acid-functionalized 3, 4-ethylenedioxythiophene (EDOTacid) for neural electrode interfaces. Biochimica et Biophysica Acta (BBA)-General Sub. 1830, 4288–4293 (2013)
Park, S.J., et al.: Functional nerve cuff electrode with controllable anti-inflammatory drug loading and release by biodegradable nanofibers and hydrogel deposition. Sensors Actuators B Chem. 215, 133–141 (2015)
Boehler, C., et al.: Actively controlled release of Dexamethasone from neural microelectrodes in a chronic in vivo study. Biomaterials. 129, 176–187 (2017). https://doi.org/10.1016/j.biomaterials.2017.03.019
Catt, K., Li, H., Hoang, V., Beard, R., Cui, X.T.: Self-powered therapeutic release from conducting polymer/graphene oxide films on magnesium. Nanomedicine. 14, 2495–2503 (2018)
Castagnola, E. et al.: Nanostructured microsphere coated with living cells and tethered with low-stiffness wire: a possible solution to brain tissue reactions. In: 2015 7th International IEEE/EMBS Conference on Neural Engineering (NER), pp. 390–393. IEEE (2015)
Yue, Z., Moulton, S.E., Cook, M., O’Leary, S., Wallace, G.G.: Controlled delivery for neuro-bionic devices. Adv. Drug Deliv. Rev. 65, 559–569 (2013). https://doi.org/10.1016/j.addr.2012.06.002
Weaver, C.L., LaRosa, J.M., Luo, X., Cui, X.T.: Electrically controlled drug delivery from graphene oxide nanocomposite films. ACS Nano. 8, 1834–1843 (2014)
Boehler, C. et al.: In: Front. Bioeng. Biotechnol. Conference Abstract: 10th World Biomaterials Congress. https://doi.org/10.3389/conf.FBIOE.2016.01.01475. FBIOE
Jian, W.-H., et al.: Glycosaminoglycan-based hybrid hydrogel encapsulated with polyelectrolyte complex nanoparticles for endogenous stem cell regulation in central nervous system regeneration. Biomaterials. 174, 17–30 (2018)
Stevens, M.M., George, J.H.J.S.: Exploring and engineering the cell surface interface. Science. 310, 1135–1138 (2005)
Song, I., Dityatev, A.J.B.: Crosstalk between glia, extracellular matrix and neurons. Brain Res. Bull. 136, 101–108 (2018)
Righi, M., et al.: Peptide-based coatings for flexible implantable neural interfaces. Sci. Rep. 8, 502 (2018)
Rodda, A.E., Meagher, L., Nisbet, D.R., Forsythe, J.S.: Specific control of cell–material interactions: targeting cell receptors using ligand-functionalized polymer substrates. Prog. Polym. Sci. 39, 1312–1347 (2014)
Kim, S., et al.: Versatile biomimetic conductive polypyrrole films doped with hyaluronic acid of different molecular weights. Acta Biomater. 80, 258–268 (2018). https://doi.org/10.1016/j.actbio.2018.09.035
Mantione, D., et al.: Poly (3, 4-ethylenedioxythiophene): GlycosAminoGlycan aqueous dispersions: toward electrically conductive bioactive materials for neural. Interfaces. 16, 1227–1238 (2016)
Green, R.A., Baek, S., Poole-Warren, L.A., Martens, P.J.: Conducting polymer-hydrogels for medical electrode applications. Sci. Technol. Adv. Mater. 11, 014107 (2010)
Frantz, C., Stewart, K.M., Weaver, V.M.: The extracellular matrix at a glance. J. Cell Sci. 123, 4195–4200 (2010)
Xiao, Y., Li, C.M., Wang, S., Shi, J., Ooi, C.P.: Incorporation of collagen in poly (3, 4-ethylenedioxythiophene) for a bifunctional film with high bio-and electrochemical activity. J. Biomed. Mater. Res. A. 92, 766–772 (2010)
Wan, A.M.-D., et al.: 3D conducting polymer platforms for electrical control of protein conformation and cellular functions. J. Mater. Chem. B. 3, 5040–5048 (2015)
Baek, P., Voorhaar, L., Barker, D., Travas-Sejdic, J.: Molecular approach to conjugated polymers with biomimetic properties. Acc. Chem. Res. 51, 1581–1589 (2018)
Bhagwat, N., Murray, R.E., Shah, S.I., Kiick, K.L., Martin, D.C.: Biofunctionalization of PEDOT films with laminin-derived peptides. Acta Biomater. 41, 235–246 (2016)
Cui, X., et al.: Surface modification of neural recording electrodes with conducting polymer/biomolecule blends. J. Biomed. Mater. Res. 56, 261–272 (2001)
Xiao, Y., Martin, D.C., Cui, X., Shenai, M.: Surface modification of neural probes with conducting polymer poly (hydroxymethylated-3, 4-ethylenedioxythiophene) and its biocompatibility. Appl. Biochem. Biotechnol. 128, 117–129 (2006)
Green, R.A., Lovell, N.H., Poole-Warren, L.A.: Impact of co-incorporating laminin peptide dopants and neurotrophic growth factors on conducting polymer properties. Acta Biomater. 6, 63–71 (2010)
Green, R.A., Lovell, N.H., Poole-Warren, L.A.: Cell attachment functionality of bioactive conducting polymers for neural interfaces. Biomaterials. 30, 3637–3644 (2009)
Eles, J.R., et al.: Neuroadhesive L1 coating attenuates acute microglial attachment to neural electrodes as revealed by live two-photon microscopy. Biomaterials. 113, 279–292 (2017). https://doi.org/10.1016/j.biomaterials.2016.10.054
Trowbridge, J.M., Gallo, R.L.: Dermatan sulfate: new functions from an old glycosaminoglycan. Glycobiology. 12, 117R–125R (2002)
Asplund, M., et al.: Toxicity evaluation of PEDOT/biomolecular composites intended for neural communication electrodes. Biomed. Mater. 4, 045009 (2009)
Cheong, G.M., et al.: Conductive hydrogels with tailored bioactivity for implantable electrode coatings. Acta Biomater. 10, 1216–1226 (2014)
Papy-Garcia, D., et al.: Glycosaminoglycans, protein aggregation and neurodegeneration. Curr. Protein Pept. Sci. 12, 258–268 (2011)
Asplund, M., von Holst, H., Inganäs, O.: Composite biomolecule/PEDOT materials for neural electrodes. Biointerphases. 3, 83–93 (2008)
Wang, M., et al.: Glycosaminoglycans (GAGs) and GAG mimetics regulate the behavior of stem cell differentiation. Colloids Surf. B: Biointerfaces. 150, 175–182 (2017)
Wang, M., et al.: A new avenue to the synthesis of GAG-mimicking polymers highly promoting neural differentiation of embryonic stem cells. Chem. Commun. 51, 15434–15437 (2015)
Mehanna, A., et al.: Polysialic acid glycomimetic promotes functional recovery and plasticity after spinal cord injury in mice. Mol. Ther. 18, 34–43 (2010)
Winter, B. M. et al.: Control of cell fate and excitability at the neural electrode interface: Genetic reprogramming and optical induction. In: 2017 IEEE Life Sciences Conference (LSC), pp. 157–161. IEEE (2017). https://doi.org/10.1109/LSC.2017.8268167
Hong, G., Lieber, C.M.: Novel electrode technologies for neural recordings. Nat. Rev. Neurosci. 20, 330–345 (2019)
Rivnay, J., Wang, H., Fenno, L., Deisseroth, K., Malliaras, G.G.: Next-generation probes, particles, and proteins for neural interfacing. Sci. Adv. 3, e1601649 (2017)
Capadona, J.R., Shoffstall, A.J., Pancrazio, J.J.: Neuron-like neural probes. Nat. Mater. 18, 429–431 (2019)
Rajasethupathy, P., Ferenczi, E., Deisseroth, K.J.C.: Targeting neural circuits. Cell. 165, 524–534 (2016)
Green, R.A., Lovell, N.H., Wallace, G.G., Poole-Warren, L.A.: Conducting polymers for neural interfaces: challenges in developing an effective long-term implant. Biomaterials. 29, 3393–3399 (2008)
Ochiai, H., Shibata, H., Sawa, Y., Katoh, T.: “Living electrode” as a long-lived photoconverter for biophotolysis of water. Proc. Natl. Acad. Sci. U. S. A. 77, 2442–2444 (1980). https://doi.org/10.1073/pnas.77.5.2442
Ouyang, L., Shaw, C.L., Kuo, C.-c., Griffin, A.L., Martin, D.C.: In vivo polymerization of poly (3, 4-ethylenedioxythiophene) in the living rat hippocampus does not cause a significant loss of performance in a delayed alternation task. J. Neural Eng. 11, 026005 (2014)
Goding, J.A., Gilmour, A.D., Aregueta-Robles, U.A., Hasan, E.A., Green, R.A.: Living bioelectronics: strategies for developing an effective long-term implant with functional neural connections. Adv. Funct. Mater. 28, 1702969 (2018)
Aregueta-Robles, U.A., Martens, P.J., Poole-Warren, L.A., Green, R.A.: Tailoring 3D hydrogel systems for neuronal encapsulation in living electrodes. J. Polym. Sci. B Polym. Phys. 56, 273–287 (2018)
Green, R. A. et al.: Living electrodes: tissue engineering the neural interface. Conference proceedings: … Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual Conference 2013, pp. 6957–6960, https://doi.org/10.1109/embc.2013.6611158 (2013)
Liu, Y., et al.: Human embryonic stem cell-derived retinal pigment epithelium transplants as a potential treatment for wet age-related macular degeneration. Cell Discov. 4, 50 (2018)
Cai, L., Dewi, R.E., Heilshorn, S.C.: Injectable hydrogels with in situ double network formation enhance retention of transplanted stem cells. Adv. Funct. Mater. 25, 1344–1351 (2015)
Serruya, M.D., et al.: Engineered axonal tracts as “living electrodes” for synaptic-based modulation of neural circuitry. Adv. Funct. Mater. 28, 1701183 (2018)
Adewole, D.O., Serruya, M.D., Wolf, J.A., Cullen, D.K.: Bioactive neuroelectronic interfaces. Front. Neurosci. 13, 269 (2019)
Li, H., Nguyen, V. H. & Zhang, H.: {Nature Inspired Conceptual Design of a Micro Neural Probe for Deep Brain Stimulation}. In: International Conference on Sustainable Design and Manufacturing, pp. 31–40. Springer (2018)
Won, S.M., et al.: Recent advances in materials, devices, and systems for neural interfaces. Adv. Mater. 30, 1800534 (2018)
Shoffstall, A.J., Capadona, J.R.J.C.: Bioinspired materials and systems for neural interfacing. Curr Opin Biomed Eng. 6, 110–119 (2018)
Tian, B., et al.: Macroporous nanowire nanoelectronic scaffolds for synthetic tissues. Nat. Mater. 11, 986–994 (2012). https://doi.org/10.1038/nmat3404
de Mena, L., Rizk, P., Rincon-Limas, D.E.: Bringing light to transcription: the optogenetics repertoire. Front. Genet. 9, 518–518 (2018). https://doi.org/10.3389/fgene.2018.00518
Vierbuchen, T., Wernig, M.J.: Molecular roadblocks for cellular reprogramming. Mol. Cell. 47, 827–838 (2012)
Meas, S.J., Zhang, C.L., Dabdoub, A.: Reprogramming glia into neurons in the peripheral auditory system as a solution for sensorineural hearing loss: lessons from the central nervous system. Front. Mol. Neurosci. 11, 77 (2018). https://doi.org/10.3389/fnmol.2018.00077
Chouchane, M., et al.: Lineage reprogramming of astroglial cells from different origins into distinct neuronal subtypes. Stem Cell Rep. 9, 162–176 (2017)
Winter, B., Daniels, S., Salatino, J., Purcell, E.J.M.: Genetic modulation at the neural microelectrode interface: methods and applications. Micromachines. 9, 476 (2018)
Pinyon, J.L., et al.: Close-field electroporation gene delivery using the cochlear implant electrode array enhances the bionic ear. Sci. Transl. Med. 6, 233ra254 (2014). https://doi.org/10.1126/scitranslmed.3008177
Zhao, S., et al.: Cell type–specific channelrhodopsin-2 transgenic mice for optogenetic dissection of neural circuitry function. Nat. Methods. 8, 745–752 (2011)
Wang, L., Huang, K., Zhong, C., Wang, L., Lu, Y.J.: Fabrication and modification of implantable optrode arrays for in vivo optogenetic applications. Biophys. Rep. 4, 82–93 (2018)
Goncalves, S.B., et al.: LED optrode with integrated temperature sensing for optogenetics. Micromachines. 9, 473 (2018)
Khan, W., Setien, M., Purcell, E., Li, W.: Micro-reflector integrated multichannel μLED optogenetic neurostimulator with enhanced intensity. Front. Mech. Eng. 4 (2018). https://doi.org/10.3389/fmech.2018.00017
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Vallejo-Giraldo, C., Genta, M., Goding, J., Green, R. (2023). Biomimetic Approaches Towards Device-Tissue Integration. In: Thakor, N.V. (eds) Handbook of Neuroengineering. Springer, Singapore. https://doi.org/10.1007/978-981-16-5540-1_97
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