<?xml version="1.0" encoding="utf-8"?>
<XML>
<ISCJOURNAL>
<YEAR>2022</YEAR>
<VOL>4</VOL>
<NO>10</NO>
<MOSALSAL>10</MOSALSAL>
<PAGE_NO>10</PAGE_NO>
<ARTICLES>

			<ARTICLE>
				<TitleF></TitleF>
				<TitleE>Piezoelectric composites in neural tissue engineering: material and fabrication techniques</TitleE>
				<TitleLang_ID>en</TitleLang_ID>
				<ABSTRACTS>
					<ABSTRACT>
						<Language_ID>en</Language_ID>
						<CONTENT>To date, there is no effective treatment for central or peripheral nervous system damage, which results in cognitive and/or sensory impairment. After a neural injury, tissue engineering can provide a scaffold for either transplanted or native cells. With the recent focus on stimuli sensitive scaffolds, sometimes referred to as smart scaffolds, tissue engineering is highly dependent on scaffolds for supporting cell differentiation and growth. Piezoelectric scaffolds are a representative of this class of materials because they can generate electrical charges when mechanically stimulated, creating a prospect their possible use in non-invasive therapy for neural tissue. Research on piezoelectric materials that can be utilized to enhance neural tissue engineering is summarized in this study. The most common employed materials for tissue engineering strategies are discussed, as well as the most significant accomplishments, difficulties, and unmet research and treatment needs that will be needed in the future. As a result, this study compiles the most relevant findings and strategies, and it serves as a starting point for new research in the most relevant and difficult related issues.</CONTENT>
					</ABSTRACT>
				</ABSTRACTS>
				<PAGES>
					<PAGE>
						<FPAGE>37</FPAGE>
						<TPAGE>46</TPAGE>
					</PAGE>
				</PAGES>
	
				<AUTHORS>
					<AUTHOR>
						<NameE>Shadi</NameE>
						<MidNameE></MidNameE>		
						<FamilyE>Askari</FamilyE>
						<Organizations>
							<Organization>Department of Biomedical Engineering</Organization>
						</Organizations>
						<Universities>
							<University>Amirkabir University of Technology</University>
						</Universities>
						<Countries>
							<Country>Iran</Country>
						</Countries>
						<EMAILS>
							<Email>mapa4753@aut.ac.ir</Email>			
						</EMAILS>
					</AUTHOR>
					<AUTHOR>
						<NameE>Zahra</NameE>
						<MidNameE></MidNameE>		
						<FamilyE>Amerei Bozcheloei</FamilyE>
						<Organizations>
							<Organization>Department of Science Laboratory</Organization>
						</Organizations>
						<Universities>
							<University>Tehran University of Medical Sciences</University>
						</Universities>
						<Countries>
							<Country>Iran</Country>
						</Countries>
						<EMAILS>
							<Email>info@jourcc.com</Email>			
						</EMAILS>
					</AUTHOR>
				</AUTHORS>
				<KEYWORDS>
					<KEYWORD>
						<KeyText>Piezoelectric composite</KeyText>
					</KEYWORD>
					<KEYWORD>
						<KeyText>Neural tissue engineering</KeyText>
					</KEYWORD>
					<KEYWORD>
						<KeyText>β-phase induction</KeyText>
					</KEYWORD>
					<KEYWORD>
						<KeyText>Electrical stimulation</KeyText>
					</KEYWORD>
					</KEYWORDS>
				<PDFFileName>Article5.pdf</PDFFileName>
				<REFRENCES>
				<REFRENCE>
					<REF>[1] J. Harrison, Z. Ounaies, Polymers, piezoelectric, Encyclopedia of Smart Materials (2002). ## [2] T.D. Usher, K.R. Cousins, R. Zhang, S. Ducharme, The promise of piezoelectric polymers, Polymer International 67(7) (2018) 790-798. ## [3] S. Mathur, J. Scheinbeim, B. Newman, Piezoelectric properties and ferroelectric hysteresis effects in uniaxially stretched nylon‐11 films, Journal of applied physics 56(9) (1984) 2419-2425. ## [4] Q. Jing, S. Kar-Narayan, Nanostructured polymer-based piezoelectric and triboelectric materials and devices for energy harvesting applications, Journal of Physics D: Applied Physics 51(30) (2018) 303001. ## [5] A. Kholkin, N. Amdursky, I. Bdikin, E. Gazit, G. Rosenman, Strong piezoelectricity in bioinspired peptide nanotubes, ACS nano 4(2) (2010) 610-614. ## [6] E.J. Curry, K. Ke, M.T. Chorsi, K.S. Wrobel, A.N. Miller, A. Patel, I. Kim, J. Feng, L. Yue, Q. Wu, Biodegradable piezoelectric force sensor, Proceedings of the National Academy of Sciences 115(5) (2018) 909-914. ## [7] G. Liu, W.-C. Tsen, S.-C. Jang, F. Hu, F. Zhong, B. Zhang, J. Wang, H. Liu, G. Wang, S. Wen, Composite membranes from quaternized chitosan reinforced with surface-functionalized PVDF electrospun nanofibers for alkaline direct methanol fuel cells, Journal of Membrane Science 611 (2020) 118242. ## [8] S.A. Haddadi, S. Ghaderi, M. Amini, S.A. Ramazani, Mechanical and piezoelectric characterizations of electrospun PVDF-nanosilica fibrous scaffolds for biomedical applications, Materials Today: Proceedings 5(7) (2018) 15710-15716. ## [9] P. Sengupta, A. Ghosh, N. Bose, S. Mukherjee, A. Roy Chowdhury, P. Datta, A comparative assessment of poly (vinylidene fluoride)/conducting polymer electrospun nanofiber membranes for biomedical applications, Journal of Applied Polymer Science 137(37) (2020) 49115. ## [10] C. Ribeiro, J. Panadero, V. Sencadas, S. Lanceros-Méndez, M. Tamaño, D. Moratal, M. Salmerón-Sánchez, J.G. Ribelles, Fibronectin adsorption and cell response on electroactive poly (vinylidene fluoride) films, Biomedical Materials 7(3) (2012) 035004. ## [11] S.M. Damaraju, Y. Shen, E. Elele, B. Khusid, A. Eshghinejad, J. Li, M. Jaffe, T.L. Arinzeh, Three-dimensional piezoelectric fibrous scaffolds selectively promote mesenchymal stem cell differentiation, Biomaterials 149 (2017) 51-62. ## [12] N. Meng, X. Zhu, R. Mao, M.J. Reece, E. Bilotti, Nanoscale interfacial electroactivity in PVDF/PVDF-TrFE blended films with enhanced dielectric and ferroelectric properties, Journal of Materials Chemistry C 5(13) (2017) 3296-3305. ## [13] B. Tandon, J.J. Blaker, S.H. Cartmell, Piezoelectric materials as stimulatory biomedical materials and scaffolds for bone repair, Acta biomaterialia 73 (2018) 1-20. ## [14] R.A. Surmenev, T. Orlova, R.V. Chernozem, A.A. Ivanova, A. Bartasyte, S. Mathur, M.A. Surmeneva, Hybrid lead-free polymer-based nanocomposites with improved piezoelectric response for biomedical energy-harvesting applications: A review, Nano Energy 62 (2019) 475-506. ## [15] F.O. Agyemang, F.A. Sheikh, R. Appiah-Ntiamoah, J. Chandradass, H. Kim, Synthesis and characterization of poly (vinylidene fluoride)–calcium phosphate composite for potential tissue engineering applications, Ceramics International 41(5) (2015) 7066-7072. ## [16] A.S. Zviagin, R.V. Chernozem, M.A. Surmeneva, M. Pyeon, M. Frank, T. Ludwig, P. Tutacz, Y.F. Ivanov, S. Mathur, R.A. Surmenev, Enhanced piezoelectric response of hybrid biodegradable 3D poly (3-hydroxybutyrate) scaffolds coated with hydrothermally deposited ZnO for biomedical applications, European Polymer Journal 117 (2019) 272-279. ## [17] S. Jalili-Firoozinezhad, F. Mirakhori, H. Baharvand, Nanotissue Engineering of Neural Cells, Stem Cell Nanoengineering 265 (2014). ## [18] H.T. Nguyen, C. Wei, J.K. Chow, L. Nguy, H.K. Nguyen, C.E. Schmidt, Electric field stimulation through a substrate influences Schwann cell and extracellular matrix structure, Journal of neural engineering 10(4) (2013) 046011. ## [19] J. Venugopal, S. Low, A.T. Choon, S. Ramakrishna, Interaction of cells and nanofiber scaffolds in tissue engineering, Journal of Biomedical Materials Research Part B: Applied Biomaterials 84(1) (2008) 34-48. ## [20] S. Heydarkhan-Hagvall, K. Schenke-Layland, A.P. Dhanasopon, F. Rofail, H. Smith, B.M. Wu, R. Shemin, R.E. Beygui, W.R. MacLellan, Three-dimensional electrospun ECM-based hybrid scaffolds for cardiovascular tissue engineering, Biomaterials 29(19) (2008) 2907-2914. ## [21] Y. Ting, H. Gunawan, A. Sugondo, C.-W. Chiu, A new approach of polyvinylidene fluoride (PVDF) poling method for higher electric response, Ferroelectrics 446(1) (2013) 28-38. ## [22] B. Bera, M.D. Sarkar, Piezoelectricity in PVDF and PVDF based piezoelectric nanogenerator: a concept, IOSR J. Appl. Phys 9(3) (2017) 95-99. ## [23] S.M. Damaraju, S. Wu, M. Jaffe, T.L. Arinzeh, Structural changes in PVDF fibers due to electrospinning and its effect on biological function, Biomedical Materials 8(4) (2013) 045007. ## [24] Ç. Defteralı, R. Verdejo, S. Majeed, A. Boschetti-de-Fierro, H.R. Méndez-Gómez, E. Díaz-Guerra, D. Fierro, K. Buhr, C. Abetz, R. Martínez-Murillo, In vitro evaluation of biocompatibility of uncoated thermally reduced graphene and carbon nanotube-loaded PVDF membranes with adult neural stem cell-derived neurons and glia, Frontiers in bioengineering and biotechnology 4 (2016) 94. ## [25] E. Fukada, I. Yasuda, On the piezoelectric effect of bone, Journal of the physical society of Japan 12(10) (1957) 1158-1162. ## [26] M.W. Johnson, D.A. Chakkalakal, R.A. Harper, J.L. Katz, Comparison of the electromechanical effects in wet and dry bone, Journal of biomechanics 13(5) (1980) 437-442. ## [27] S. Guerin, S.A. Tofail, D. Thompson, Organic piezoelectric materials: milestones and potential, NPG Asia Materials 11(1) (2019) 1-5. ## [28] P. Shafiee, M. Reisi Nafchi, S. Eskandarinezhad, S. Mahmoudi, E. Ahmadi, Sol-gel zinc oxide nanoparticles: advances in synthesis and applications, Synthesis and Sintering 1(4) (2021) 242-254. ## [29] D. Denning, M. Abu-Rub, D.I. Zeugolis, S. Habelitz, A. Pandit, A. Fertala, B.J. Rodriguez, Electromechanical properties of dried tendon and isoelectrically focused collagen hydrogels, Acta biomaterialia 8(8) (2012) 3073-3079. ## [30] P. Poillot, J. O’Donnell, D.T. O’Connor, E.U. Haq, C. Silien, S.A. Tofail, J.M. Huyghe, Piezoelectricity in the Intervertebral disc, Journal of Biomechanics 102 (2020) 109622. ## [31] S. Yi, L. Xu, X. Gu, Scaffolds for peripheral nerve repair and reconstruction, Experimental neurology 319 (2019) 112761. ## [32] N.B. Fadia, J.M. Bliley, G.A. DiBernardo, D.J. Crammond, B.K. Schilling, W.N. Sivak, A.M. Spiess, K.M. Washington, M. Waldner, H.-T. Liao, Long-gap peripheral nerve repair through sustained release of a neurotrophic factor in nonhuman primates, Science Translational Medicine 12(527) (2020) eaav7753. ## [33] T. Kornfeld, P.M. Vogt, C. Radtke, Nerve grafting for peripheral nerve injuries with extended defect sizes, Wiener Medizinische Wochenschrift 169(9) (2019) 240-251. ## [34] J.A. Frank, M.-J. Antonini, P. Anikeeva, Next-generation interfaces for studying neural function, Nature biotechnology 37(9) (2019) 1013-1023. ## [35] G. Thrivikraman, S.K. Boda, B. Basu, Unraveling the mechanistic effects of electric field stimulation towards directing stem cell fate and function: A tissue engineering perspective, Biomaterials 150 (2018) 60-86. ## [36] R. Balint, N.J. Cassidy, S.H. Cartmell, Electrical stimulation: a novel tool for tissue engineering, Tissue Engineering Part B: Reviews 19(1) (2013) 48-57. ## [37] X. Zhao, H. Wu, B. Guo, R. Dong, Y. Qiu, P.X. Ma, Antibacterial anti-oxidant electroactive injectable hydrogel as self-healing wound dressing with hemostasis and adhesiveness for cutaneous wound healing, Biomaterials 122 (2017) 34-47. ## [38] L. Ghasemi‐Mobarakeh, M.P. Prabhakaran, M. Morshed, M.H. Nasr‐Esfahani, H. Baharvand, S. Kiani, S.S. Al‐Deyab, S. Ramakrishna, Application of conductive polymers, scaffolds and electrical stimulation for nerve tissue engineering, Journal of tissue engineering and regenerative medicine 5(4) (2011) 17-35. ## [39] J. Gu, W. Hu, A. Deng, Q. Zhao, S. Lu, X. Gu, Surgical repair of a 30 mm long human median nerve defect in the distal forearm by implantation of a chitosan–PGA nerve guidance conduit, Journal of tissue engineering and regenerative medicine 6(2) (2012) 163-168. ## [40] N. Zhang, U. Milbreta, J.S. Chin, C. Pinese, J. Lin, H. Shirahama, W. Jiang, H. Liu, R. Mi, A. Hoke, Biomimicking fiber scaffold as an effective in vitro and in vivo microrna screening platform for directing tissue regeneration, Advanced science 6(9) (2019) 1800808. ## [41] O. Hasturk, K.E. Jordan, J. Choi, D.L. Kaplan, Enzymatically crosslinked silk and silk-gelatin hydrogels with tunable gelation kinetics, mechanical properties and bioactivity for cell culture and encapsulation, Biomaterials 232 (2020) 119720. ## [42] C. Xue, H. Zhu, D. Tan, H. Ren, X. Gu, Y. Zhao, P. Zhang, Z. Sun, Y. Yang, J. Gu, Electrospun silk fibroin‐based neural scaffold for bridging a long sciatic nerve gap in dogs, Journal of tissue engineering and regenerative medicine 12(2) (2018) e1143-e1153. ## [43] S. Aznar-Cervantes, M.I. Roca, J.G. Martinez, L. Meseguer-Olmo, J.L. Cenis, J.M. Moraleda, T.F. Otero, Fabrication of conductive electrospun silk fibroin scaffolds by coating with polypyrrole for biomedical applications, Bioelectrochemistry 85 (2012) 36-43. ## [44] M. Sarker, S. Naghieh, A.D. McInnes, D.J. Schreyer, X. Chen, Strategic design and fabrication of nerve guidance conduits for peripheral nerve regeneration, Biotechnology journal 13(7) (2018) 1700635. ## [45] L. Huang, L. Zhu, X. Shi, B. Xia, Z. Liu, S. Zhu, Y. Yang, T. Ma, P. Cheng, K. Luo, A compound scaffold with uniform longitudinally oriented guidance cues and a porous sheath promotes peripheral nerve regeneration in vivo, Acta biomaterialia 68 (2018) 223-236. ## [46] I. Jun, H.-S. Han, J.R. Edwards, H. Jeon, Electrospun fibrous scaffolds for tissue engineering: Viewpoints on architecture and fabrication, International journal of molecular sciences 19(3) (2018) 745. ## [47] Y. Wu, L. Wang, B. Guo, P.X. Ma, Interwoven aligned conductive nanofiber yarn/hydrogel composite scaffolds for engineered 3D cardiac anisotropy, Acs Nano 11(6) (2017) 5646-5659. ## [48] Y.-H. Zhao, C.-M. Niu, J.-Q. Shi, Y.-Y. Wang, Y.-M. Yang, H.-B. Wang, Novel conductive polypyrrole/silk fibroin scaffold for neural tissue repair, Neural regeneration research 13(8) (2018) 1455. ## [49] Y. Liu, J. Gao, M. Peng, H. Meng, H. Ma, P. Cai, Y. Xu, Q. Zhao, G. Si, A review on central nervous system effects of gastrodin, Frontiers in pharmacology 9 (2018) 24. ## [50] F. Schulte, A.S. Kunin-Batson, B.A. Olson-Bullis, P. Banerjee, M.C. Hocking, L. Janzen, L.S. Kahalley, H. Wroot, C. Forbes, K.R. Krull, Social attainment in survivors of pediatric central nervous system tumors: a systematic review and meta-analysis from the Children’s Oncology Group, Journal of Cancer Survivorship 13(6) (2019) 921-931. ## [51] A. Teo, A. Mishra, I. Park, Y. Kim, W. Park, Y. Yoon, Polymeric biomaterials for medical implants and devices. ACS Biomater Sci Eng 2: 454–472, 2016. ## [52] J. Wen, M. Liu, Piezoelectric ceramic (PZT) modulates axonal guidance growth of rat cortical neurons via RhoA, Rac1, and Cdc42 pathways, Journal of Molecular Neuroscience 52(3) (2014) 323-330. ## [53] L. Finci, Y. Zhang, R. Meijers, J.-H. Wang, Signaling mechanism of the netrin-1 receptor DCC in axon guidance, Progress in biophysics and molecular biology 118(3) (2015) 153-160. ## [54] J. Guo, C. Walss‐Bass, R.F. Ludueña, The β isotypes of tubulin in neuronal differentiation, Cytoskeleton 67(7) (2010) 431-441. ## [55] J.B. Lansman, Blockade of current through single calcium channels by trivalent lanthanide cations. Effect of ionic radius on the rates of ion entry and exit, The Journal of general physiology 95(4) (1990) 679-696. ## [56] E. Mercadelli, A. Sanson, C. Galassi, Porous piezoelectric ceramics, INTECH Open Access Publisher (2010). ## [57] W. Wersing, K. Lubitz, J. Mohaupt, Dielectric, elastic and piezoelectric properties of porous PZT ceramics, Ferroelectrics 68(1) (1986) 77-97. ## [58] E. Ringgaard, F. Lautzenhiser, L.M. Bierregaard, T. Zawada, E. Molz, Development of porous piezoceramics for medical and sensor applications, Materials 8(12) (2015) 8877-8889. ## [59] N.C. Carville, L. Collins, M. Manzo, K. Gallo, B.I. Lukasz, K.K. McKayed, J.C. Simpson, B.J. Rodriguez, B iocompatibility of ferroelectric lithium niobate and the influence of polarization charge on osteoblast proliferation and function, Journal of Biomedical Materials Research Part A 103(8) (2015) 2540-2548. ## [60] J.P. Ball, B.A. Mound, J.C. Nino, J.B. Allen, Biocompatible evaluation of barium titanate foamed ceramic structures for orthopedic applications, Journal of Biomedical Materials Research Part A 102(7) (2014) 2089-2095. ## [61] F.R. Baxter, C.R. Bowen, I.G. Turner, A.C. Dent, Electrically active bioceramics: a review of interfacial responses, Annals of biomedical engineering 38(6) (2010) 2079-2092. ## [62] G. Ciofani, L. Ricotti, V. Mattoli, Preparation, characterization and in vitro testing of poly (lactic-co-glycolic) acid/barium titanate nanoparticle composites for enhanced cellular proliferation, Biomedical microdevices 13(2) (2011) 255-266. ## [63] J. Wang, C.H. Lee, Y.K. Yap, Recent advancements in boron nitride nanotubes, Nanoscale 2(10) (2010) 2028-2034. ## [64] J.W. Rasmussen, E. Martinez, P. Louka, D.G. Wingett, Zinc oxide nanoparticles for selective destruction of tumor cells and potential for drug delivery applications, Expert opinion on drug delivery 7(9) (2010) 1063-1077. ## [65] S. Goel, B. Kumar, A review on piezo-/ferro-electric properties of morphologically diverse ZnO nanostructures, Journal of Alloys and Compounds 816 (2020) 152491. ## [66] M. Safaei, H.A. Sodano, S.R. Anton, A review of energy harvesting using piezoelectric materials: state-of-the-art a decade later (2008–2018), Smart Materials and Structures 28(11) (2019) 113001. ## [67] G. Ciofani, S. Danti, D. D’Alessandro, L. Ricotti, S. Moscato, G. Bertoni, A. Falqui, S. Berrettini, M. Petrini, V. Mattoli, Enhancement of neurite outgrowth in neuronal-like cells following boron nitride nanotube-mediated stimulation, ACS nano 4(10) (2010) 6267-6277. ## [68] A. Marino, S. Arai, Y. Hou, E. Sinibaldi, M. Pellegrino, Y.-T. Chang, B. Mazzolai, V. Mattoli, M. Suzuki, G. Ciofani, Piezoelectric nanoparticle-assisted wireless neuronal stimulation, ACS nano 9(7) (2015) 7678-7689. ## [69] G. Genchi, L. Ceseracciu, A. Marino, M. Labardi, S. Marras, F. Pignatelli, L. Bruschini, V. Mattoli, G. Ciofani, P (VDF-TrFE)/BaTiO3 Nanoparticle Composite Films Mediate Piezoelectric Stimulation and Promote Differentiation of SH-SY5Y Neuroblastoma Cells, Adv. Healthc. Mater. 5 (2016) 1808–1820. ## [70] D. Mondal, A. Gayen, B. Paul, P. Bandyopadhyay, D. Bera, D. Bhar, K. Das, P. Nandy, S. Das, Enhancement of β-phase crystallization and electrical properties of PVDF by impregnating ultra high diluted novel metal derived nanoparticles: Prospect of use as a charge storage device, Journal of Materials Science: Materials in Electronics 29(17) (2018) 14535-14545. ## [71] S. Mishra, L. Unnikrishnan, S.K. Nayak, S. Mohanty, Advances in piezoelectric polymer composites for energy harvesting applications: a systematic review, Macromolecular Materials and Engineering 304(1) (2019) 1800463. ## [72] M. Li, H.J. Wondergem, M.-J. Spijkman, K. Asadi, I. Katsouras, P.W. Blom, D.M. De Leeuw, Revisiting the δ-phase of poly (vinylidene fluoride) for solution-processed ferroelectric thin films, Nature materials 12(5) (2013) 433-438. ## [73] Y.-J. Yu, A.J. McGaughey, Energy barriers for dipole moment flipping in PVDF-related ferroelectric polymers, The Journal of chemical physics 144(1) (2016) 014901. ## [74] S. Weinhold, M. Litt, J. Lando, The crystal structure of the γ phase of poly (vinylidene fluoride), Macromolecules 13(5) (1980) 1178-1183. ## [75] K. Koga, H. Ohigashi, Piezoelectricity and related properties of vinylidene fluoride and trifluoroethylene copolymers, Journal of applied physics 59(6) (1986) 2142-2150. ## [76] C. Wan, C.R. Bowen, Multiscale-structuring of polyvinylidene fluoride for energy harvesting: the impact of molecular-, micro-and macro-structure, Journal of Materials Chemistry A 5(7) (2017) 3091-3128. ## [77] W. Xia, Z. Xu, Q. Zhang, Z. Zhang, Y. Chen, Dependence of dielectric, ferroelectric, and piezoelectric properties on crystalline properties of p (VDF‐co‐TrFE) copolymers, Journal of Polymer Science Part B: Polymer Physics 50(18) (2012) 1271-1276. ## [78] F.-C. Sun, A.M. Dongare, A.D. Asandei, S.P. Alpay, S. Nakhmanson, Temperature dependent structural, elastic, and polar properties of ferroelectric polyvinylidene fluoride (PVDF) and trifluoroethylene (TrFE) copolymers, Journal of Materials Chemistry C 3(32) (2015) 8389-8396. ## [79] J. Ai, A. Kiasat-Dolatabadi, S. Ebrahimi-Barough, A. Ai, N. Lotfibakhshaiesh, A. Norouzi-Javidan, H. Saberi, B. Arjmand, H.R. Aghayan, Polymeric scaffolds in neural tissue engineering: a review, Arch Neurosci 1(1) (2013) 15-20. ## [80] T.-H. Young, H.-H. Chang, D.-J. Lin, L.-P. Cheng, Surface modification of microporous PVDF membranes for neuron culture, Journal of Membrane Science 350(1-2) (2010) 32-41. ## [81] R.F. Valentini, T.G. Vargo, J.A. Gardella Jr, P. Aebischer, Electrically charged polymeric substrates enhance nerve fibre outgrowth in vitro, Biomaterials 13(3) (1992) 183-190. ## [82] Y.-S. Lee, T.L. Arinzeh, The influence of piezoelectric scaffolds on neural differentiation of human neural stem/progenitor cells, Tissue Engineering Part A 18(19-20) (2012) 2063-2072. ## [83] E.G. Fine, R.F. Valentini, R. Bellamkonda, P. Aebischer, Improved nerve regeneration through piezoelectric vinylidenefluoride-trifluoroethylene copolymer guidance channels, Biomaterials 12(8) (1991) 775-780. ## [84] K.K. Sappati, S. Bhadra, Piezoelectric polymer and paper substrates: A review, Sensors 18(11) (2018) 3605. ## [85] J. Kim, A.S. Campbell, B.E.-F. de Ávila, J. Wang, Wearable biosensors for healthcare monitoring, Nature biotechnology 37(4) (2019) 389-406. ## [86] X. Liu, J. Ma, X. Wu, L. Lin, X. Wang, Polymeric nanofibers with ultrahigh piezoelectricity via self-orientation of nanocrystals, ACS nano 11(2) (2017) 1901-1910. ## [87] S. Gong, B. Zhang, J. Zhang, Z.L. Wang, K. Ren, Biocompatible poly (lactic acid)‐based hybrid piezoelectric and electret nanogenerator for electronic skin applications, Advanced Functional Materials 30(14) (2020) 1908724. ## [88] R. Torah, J. Lawrie-Ashton, Y. Li, S. Arumugam, H.A. Sodano, S. Beeby, Energy-harvesting materials for smart fabrics and textiles, MRS Bulletin 43(3) (2018) 214-219. ## [89] F. Memarian, S. Rahmani, M. Yousefzadeh, M. Latifi, Wearable Technologies in Sportswear, Materials in Sports Equipment, Elsevier (2019), 123-160. ## [90] K.S. Ramadan, D. Sameoto, S. Evoy, A review of piezoelectric polymers as functional materials for electromechanical transducers, Smart Materials and Structures 23(3) (2014) 033001. ## [91] U. Gross, C. Muller-Mai, C. Voigt, The tissue response on cellulose cylinders after implantation in the distal femur of rabbits, Proceedings of the Fourth World Biomaterials Congress, Berlin, Germany, (1992), 19-24. ## [92] M. Märtson, J. Viljanto, T. Hurme, P. Saukko, Biocompatibility of cellulose sponge with bone, European surgical research 30(6) (1998) 426-432. ## [93] A. Bhatnagar, M. Sain, Processing of cellulose nanofiber-reinforced composites, Journal of reinforced plastics and composites 24(12) (2005) 1259-1268. ## [94] A. Svensson, E. Nicklasson, T. Harrah, B. Panilaitis, D.L. Kaplan, M. Brittberg, P. Gatenholm, Bacterial cellulose as a potential scaffold for tissue engineering of cartilage, Biomaterials 26(4) (2005) 419-431. ## [95] M.C. Tate, D.A. Shear, S.W. Hoffman, D.G. Stein, M.C. LaPlaca, Biocompatibility of methylcellulose-based constructs designed for intracerebral gelation following experimental traumatic brain injury, Biomaterials 22(10) (2001) 1113-1123. ## [96] S. Wang, C. Sun, S. Guan, W. Li, J. Xu, D. Ge, M. Zhuang, T. Liu, X. Ma, Chitosan/gelatin porous scaffolds assembled with conductive poly (3, 4-ethylenedioxythiophene) nanoparticles for neural tissue engineering, Journal of Materials Chemistry B 5(24) (2017) 4774-4788. ## [97] Y.S. Elnaggar, S.M. Etman, D.A. Abdelmonsif, O.Y. Abdallah, Intranasal piperine-loaded chitosan nanoparticles as brain-targeted therapy in Alzheimer’s disease: optimization, biological efficacy, and potential toxicity, Journal of pharmaceutical sciences 104(10) (2015) 3544-3556. ## [98] M. Rinaudo, Chitin and chitosan: Properties and applications, Progress in polymer science 31(7) (2006) 603-632. ## [99] S.V. Madihally, H.W. Matthew, Porous chitosan scaffolds for tissue engineering, Biomaterials 20(12) (1999) 1133-1142. ## [100] K. Ohkawa, D. Cha, H. Kim, A. Nishida, H. Yamamoto, Electrospinning of chitosan, Macromolecular rapid communications 25(18) (2004) 1600-1605. ## [101] A. Cooper, N. Bhattarai, M. Zhang, Fabrication and cellular compatibility of aligned chitosan–PCL fibers for nerve tissue regeneration, Carbohydrate polymers 85(1) (2011) 149-156. ## [102] Y. Liu, T. Nelson, J. Chakroff, B. Cromeens, J. Johnson, J. Lannutti, G.E. Besner, Comparison of polyglycolic acid, polycaprolactone, and collagen as scaffolds for the production of tissue engineered intestine, Journal of Biomedical Materials Research Part B: Applied Biomaterials 107(3) (2019) 750-760. ## [103] S. Radhakrishnan, S. Nagarajan, M. Bechelany, S.N. Kalkura, Collagen based biomaterials for tissue engineering applications: A review, Processes and phenomena on the boundary between biogenic and Abiogenic nature (2020) 3-22. ## [104] Y. Eguchi, M. Ogiue-Ikeda, S. Ueno, Control of orientation of rat Schwann cells using an 8-T static magnetic field, Neuroscience letters 351(2) (2003) 130-132. ## [105] F. Sharifianjazi, M. Moradi, N. Parvin, A. Nemati, A. Jafari Rad, N. Sheysi, A. Abouchenari, A. Mohammadi, S. Karbasi, Z. Ahmadi, A. Esmaeilkhanian, M. Irani, A. Pakseresht, S. Sahmani, M. Shahedi Asl, Magnetic CoFe2O4 nanoparticles doped with metal ions: A review, Ceramics International 46(11, Part B) (2020) 18391-18412. ## [106] C. Ribeiro, V. Sencadas, D.M. Correia, S. Lanceros-Méndez, Piezoelectric polymers as biomaterials for tissue engineering applications, Colloids and Surfaces B: Biointerfaces 136 (2015) 46-55. ## [107] E. Fukada, History and recent progress in piezoelectric polymers, IEEE Transactions on ultrasonics, ferroelectrics, and frequency control 47(6) (2000) 1277-1290. ## [108] D. Puppi, F. Chiellini, A.M. Piras, E. Chiellini, Polymeric materials for bone and cartilage repair, Progress in polymer Science 35(4) (2010) 403-440. ## [109] P. Nooeaid, V. Salih, J.P. Beier, A.R. Boccaccini, Osteochondral tissue engineering: scaffolds, stem cells and applications, Journal of cellular and molecular medicine 16(10) (2012) 2247-2270. ## [110] T.-M. De Witte, L.E. Fratila-Apachitei, A.A. Zadpoor, N.A. Peppas, Bone tissue engineering via growth factor delivery: from scaffolds to complex matrices, Regenerative biomaterials 5(4) (2018) 197-211. ## [111] C. Ribeiro, C.M. Costa, D.M. Correia, J. Nunes-Pereira, J. Oliveira, P. Martins, R. Goncalves, V.F. Cardoso, S. Lanceros-Mendez, Electroactive poly (vinylidene fluoride)-based structures for advanced applications, Nature protocols 13(4) (2018) 681-704. ## [112] N. Abzan, M. Kharaziha, S. Labbaf, N. Saeidi, Modulation of the mechanical, physical and chemical properties of polyvinylidene fluoride scaffold via non-solvent induced phase separation process for nerve tissue engineering applications, European Polymer Journal 104 (2018) 115-127. ## [113] J.T. Jung, J.F. Kim, H.H. Wang, E. Di Nicolo, E. Drioli, Y.M. Lee, Understanding the non-solvent induced phase separation (NIPS) effect during the fabrication of microporous PVDF membranes via thermally induced phase separation (TIPS), Journal of Membrane Science 514 (2016) 250-263. ## [114] S. Bodkhe, P. Ermanni, Challenges in 3D printing of piezoelectric materials, Multifunctional Materials 2(2) (2019) 022001. ## [115] K. Hon, L. Li, I. Hutchings, Direct writing technology—Advances and developments, CIRP annals 57(2) (2008) 601-620. ## [116] D.G. Tamay, T. Dursun Usal, A.S. Alagoz, D. Yucel, N. Hasirci, V. Hasirci, 3D and 4D printing of polymers for tissue engineering applications, Frontiers in Bioengineering and Biotechnology 7 (2019) 164. ## [117] E. Suaste-Gómez, G. Rodríguez-Roldán, H. Reyes-Cruz, O. Terán-Jiménez, Developing an ear prosthesis fabricated in polyvinylidene fluoride by a 3D printer with sensory intrinsic properties of pressure and temperature, Sensors 16(3) (2016) 332. ## [118] S.A. Bencherif, T.M. Braschler, P. Renaud, Advances in the design of macroporous polymer scaffolds for potential applications in dentistry, Journal of periodontal and implant science 43(6) (2013) 251-261. ## [119] D.M. Correia, C. Ribeiro, V. Sencadas, L. Vikingsson, M.O. Gasch, J.G. Ribelles, G. Botelho, S. Lanceros-Méndez, Strategies for the development of three dimensional scaffolds from piezoelectric poly (vinylidene fluoride), Materials and Design 92 (2016) 674-681. ## [120] A. Idris, Z. Man, A.S. Maulud, M.S. Khan, Effects of phase separation behavior on morphology and performance of polycarbonate membranes, Membranes 7(2) (2017) 21. ## [121] X. Wang, X. Li, J. Yue, Y. Cheng, K. Xu, Q. Wang, F. Fan, Z. Wang, Z. Cui, Fabrication of poly (vinylidene fluoride) membrane via thermally induced phase separation using ionic liquid as green diluent, Chinese Journal of Chemical Engineering 28(5) (2020) 1415-1423. ## [122] G. Ciofani, A. Menciassi, Piezoelectric nanomaterials for biomedical applications, Springer (2012). ## [123] X. Wang, F. Sun, G. Yin, Y. Wang, B. Liu, M. Dong, Tactile-sensing based on flexible PVDF nanofibers via electrospinning: A review, Sensors 18(2) (2018) 330. ## [124] D.H. Kang, H.W. Kang, Advanced electrospinning using circle electrodes for freestanding PVDF nanofiber film fabrication, Applied Surface Science 455 (2018) 251-257. ## [125] D. Lolla, L. Pan, H. Gade, G.G. Chase, Functionalized polyvinylidene fluoride electrospun nanofibers and applications, Electrospinning Method Used to Create Functional Nanocomposites Films, IntechOpen (2018), 69-89. ## [126] A.H. Rajabi, M. Jaffe, T.L. Arinzeh, Piezoelectric materials for tissue regeneration: A review, Acta biomaterialia 24 (2015) 12-23. ## [127] S. Danti, Boron nitride nanotubes as nanotransducers, Boron Nitride Nanotubes in Nanomedicine, Elsevier (2016), 123-138.</REF>
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