Engineering Dental Tissues Using Biomaterials with Piezoelectric Effect: Current Progress and Future Perspectives
Source abstract
Abstract
Dental caries and traumatic injuries to teeth may cause irreversible inflammation and eventual death of the dental pulp. Nevertheless, predictably, repair and regeneration of the dentin-pulp complex remain a formidable challenge. In recent years, smart multifunctional materials with antimicrobial, anti-inflammatory, and pro-regenerative properties have emerged as promising approaches to meet this critical clinical need. As a unique class of smart materials, piezoelectric materials have an unprecedented advantage over other stimuli-responsive materials due to their inherent capability to generate electric charges, which have been shown to facilitate both antimicrobial action and tissue regeneration. Nonetheless, studies on piezoelectric biomaterials in the repair and regeneration of the dentin-pulp complex remain limited. In this review, we summarize the biomedical applications of piezoelectric biomaterials in dental applications and elucidate the underlying molecular mechanisms contributing to the biological effect of piezoelectricity. Moreover, we highlight how this state-of-the-art can be further exploited in the future for dental tissue engineering.
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Research context
OpenAlex topics: Advanced Sensor and Energy Harvesting Materials · Polydiacetylene-based materials and applications · Electrospun Nanofibers in Biomedical Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Faculty of Dentistry, The University of Hong Kong, Hong Kong SAR, China
Department of Mechanical Engineering & Department of Materials Science and Engineering, City University of Hong Kong, Hong Kong, China
Oral Health Sciences Department, Kornberg School of Dentistry, Temple University, Philadelphia, PA 19140, USA
Bioengineering Department, College of Engineering, Temple University, Philadelphia, PA 19140, USA
Funding
University of Hong Kong
References (100+)
Show source-provided references
1. International Association of Dental Traumatology guidelines for the management of traumatic dental injuries: General introduction10.1111/edt.12574 ↗
2. Evaluation of ultrasonically placed MTA and fracture resistance with intracanal composite resin in a model of apexification10.1097/00004770-200403000-00010 ↗
3. Piezoelectric materials for tissue regeneration: A review10.1016/j.actbio.2015.07.010 ↗
4. Ultrasound-mediated piezoelectric differentiation of neuron-like PC12 cells on PVDF membranes10.1038/s41598-017-03992-3 ↗
5. Zinc oxide nanorod‚ based piezoelectric dermal patch for wound healing10.1002/adfm.201603497 ↗
6. The regulation of tendon stem cell differentiation by the alignment of nanofibers10.1016/j.biomaterials.2009.11.083 ↗
7. Piezoelectric nano-biomaterials for biomedicine and tissue regeneration10.1002/adfm.201909045 ↗
8. Remotely controlled self-powering electrical stimulators for osteogenic differentiation using bone inspired bioactive piezoelectric whitlockite nanoparticles10.1016/j.nanoen.2021.105901 ↗
9. Zaszczynska, A., Sajkiewicz, P., and Gradys, A. (2020). Piezoelectric scaffolds as smart materials for neural tissue engineering. Polymers, 12.10.3390/polym12010161 ↗
10. Emerging approaches of neural regeneration using physical stimulations solely or coupled with smart piezoelectric nano-biomaterials10.1016/j.ejpb.2022.02.016 ↗
11. Matichescu, A., Ardelean, L.C., Rusu, L.C., Craciun, D., Bratu, E.A., Babucea, M., and Leretter, M. (2020). Advanced biomaterials and techniques for oral tissue engineering and regeneration-a review. Materials, 13.10.3390/ma13225303 ↗
12. Wound healing promotion by the use of negative electric current
13. Advanced scaffolds for dental pulp and periodontal regeneration
14. Present and future of tissue engineering scaffolds for dentin‚ Äêpulp complex regeneration
15. β4-Integrin and epidermal growth factor coordinately regulate electric field-mediated directional migration via Rac110.1091/mbc.e06-05-0433 ↗
16. Antifungal Effect of Piezoelectric Charges on PMMA Dentures10.1021/acsbiomaterials.1c00926 ↗
17. Bimodal nanocomposite platform with antibiofilm and self-powering functionalities for biomedical applications10.1021/acsami.1c11791 ↗
18. Size-dependent cytotoxicity study of ZnO nanoparticles in HepG2 cells10.1016/j.ecoenv.2018.12.096 ↗
19. Electroactive barium titanate coated titanium scaffold improves osteogenesis and osseointegration with low-intensity pulsed ultrasound for large segmental bone defects
20. Optical measurement of the converse piezoelectric d 33 coefficients of bulk and microtubular zinc oxide crystals10.1063/1.2742587 ↗
21. Zinc oxide nanoparticles for selective destruction of tumor cells and potential for drug delivery applications10.1517/17425247.2010.502560 ↗
22. Pierre Curie, 1859–190610.3747/co.2007.110 ↗
23. Piezoelectric ceramics10.1111/j.1151-2916.1958.tb12903.x ↗
24. Phonon dispersions and piezoelectricity in bulk and multilayers of hexagonal boron nitride10.1103/PhysRevB.83.115328 ↗
25. Ridge waveguide using highly oriented BaTiO3 thin films for electro-optic application10.1016/j.jascer.2014.05.002 ↗
26. Recent advances of polymer-based piezoelectric composites for biomedical applications10.1016/j.jmbbm.2021.104669 ↗
27. High-performance piezoelectric energy harvesters and their applications10.1016/j.joule.2018.03.011 ↗
28. Dahiya, R.S., and Valle, M. (2013). Robotic Tactile Sensing: Technologies and System, Springer.10.1007/978-94-007-0579-1 ↗
29. Piezoelectric nanomaterials activated by ultrasound: The pathway from discovery to future clinical adoption10.1021/acsnano.1c03087 ↗
30. A bibiliometric analysis of the Journal of Infection and Public Health: 2008–201610.1016/j.jiph.2017.12.011 ↗
31. Global research output in antimicrobial resistance among uropathogens: A bibliometric analysis (2002–2016)10.1016/j.jgar.2017.11.017 ↗
32. Bibliometric analysis of global scientific activity on umbilical cord mesenchymal stem cells: A swiftly expanding and shifting focus10.1186/s13287-018-0785-5 ↗
33. Wang, X., Sun, F., Yin, G., Wang, Y., Liu, B., and Dong, M. (2018). Tactile-sensing based on flexible PVDF nanofibers via electrospinning: A review. Sensors, 18.10.3390/s18020330 ↗
34. Comparison of osteogenic differentiation potential of induced pluripotent stem cells on 2D and 3D polyvinylidene fluoride scaffolds10.1002/jcp.28415 ↗
35. In vivo generation of dental pulp-like tissue by using dental pulp stem cells, a collagen scaffold, and dentin matrix protein 1 after subcutaneous transplantation in mice10.1016/j.joen.2008.02.005 ↗
36. Natural Piezoelectric Biomaterials: A Biocompatible and Sustainable Building Block for Biomedical Devices10.1021/acsnano.2c08164 ↗
37. Piezoelectric material-a promising approach for bone and cartilage regeneration10.1016/j.mehy.2017.07.021 ↗
38. Effects of different aperture-sized type I collagen/silk fibroin scaffolds on the proliferation and differentiation of human dental pulp cells10.1093/rb/rbab028 ↗
39. Structural origins of silk piezoelectricity10.1002/adfm.201002077 ↗
40. Uchino, K. (2017). The development of piezoelectric materials and the new perspective. Advanced Piezoelectric Materials, Woodhead Publishing.10.1016/B978-0-08-102135-4.00001-1 ↗
41. PZT-epoxy piezoelectric transducers: A simplified fabrication procedure10.1016/0025-5408(81)90267-1 ↗
42. Recent progress in piezoelectric nanogenerators as a sustainable power source in self-powered systems and active sensors10.1016/j.nanoen.2014.11.038 ↗
43. Effects of barium titanate nanoparticles on proliferation and differentiation of rat mesenchymal stem cells10.1016/j.colsurfb.2012.08.001 ↗
44. Multifunctional Dental Composite with Piezoelectric Nanofillers for Combined Antibacterial and Mineralization Effects10.1021/acsami.1c06331 ↗
45. Zinc oxide nanoparticles induce toxic responses in human neuroblastoma SHSY5Y cells in a size-dependent manner10.2147/IJN.S149070 ↗
46. Role of surface modification in zinc oxide nanoparticles and its toxicity assessment toward human dermal fibroblast cells
47. Thermosensitive, stretchable, and piezoelectric substrate for generation of myogenic cell sheet fragments from human mesenchymal stem cells for skeletal muscle regeneration10.1002/adfm.201703853 ↗
48. The odontogenic differentiation of human dental pulp stem cells on nanofibrous poly (L-lactic acid) scaffolds in vitro and in vivo10.1016/j.actbio.2010.04.009 ↗
49. Role of Piezo channels in ultrasound-stimulated dental stem cells10.1016/j.joen.2017.02.022 ↗
50. Nanocomposites for improved physical durability of porous PVDF membranes10.3390/membranes4010055 ↗
51. Kalimuldina, G., Turdakyn, N., Abay, I., Medeubayev, A., Nurpeissova, A., Adair, D., and Bakenov, Z. (2020). A review of piezoelectric PVDF film by electrospinning and its applications. Sensors, 20.10.3390/s20185214 ↗
52. Effect of poling state and morphology of piezoelectric poly (vinylidene fluoride) membranes for skeletal muscle tissue engineering10.1039/c3ra43499k ↗
53. Dynamic piezoelectric stimulation enhances osteogenic differentiation of human adipose stem cells10.1002/jbm.a.35368 ↗
54. Surface-potential-controlled cell proliferation and collagen mineralization on electrospun polyvinylidene fluoride (PVDF) fiber scaffolds for bone regeneration10.1021/acsbiomaterials.8b01108 ↗
55. Modulation of piezoelectric properties in electrospun PLLA nanofibers for application-specific self-powered stem cell culture platforms10.1016/j.nanoen.2021.106444 ↗
56. Synergistic effects of polyaniline and pulsed electromagnetic field to stem cells osteogenic differentiation on polyvinylidene fluoride scaffold10.1080/21691401.2019.1645154 ↗
57. Piezoelectric characterization of PVDF-TrFE thin films enhanced with ZnO nanoparticles10.1109/JSEN.2011.2182043 ↗
58. Enhancement of adhesion and promotion of osteogenic differentiation of human adipose stem cells by poled electroactive poly (vinylidene fluoride)10.1002/jbm.a.35234 ↗
59. Dentin matrix proteins: Composition and possible functions in calcification10.1002/ar.1092240206 ↗
60. Enhanced piezoelectricity from highly polarizable oriented amorphous fractions in biaxially oriented poly (vinylidene fluoride) with pure Œ ≤ crystals10.1038/s41467-020-20662-7 ↗
61. Three-dimensional piezoelectric fibrous scaffolds selectively promote mesenchymal stem cell differentiation10.1016/j.biomaterials.2017.09.024 ↗
62. Human oral motion‚ powered smart dental implant (SDI) for in situ ambulatory photobiomodulation therapy10.1002/adhm.202000658 ↗
63. Human dental pulp stem cells expressing transforming growth factor Œ≤3 transgene for cartilage-like tissue engineering10.1016/j.jcyt.2013.01.012 ↗
64. Simvastatin and nanofibrous poly (l-lactic acid) scaffolds to promote the odontogenic potential of dental pulp cells in an inflammatory environment10.1016/j.actbio.2017.12.037 ↗
65. Direct observation of shear piezoelectricity in poly-l-lactic acid nanowires10.1063/1.4979547 ↗
66. Piezoelectricity of biopolymers
67. Proliferation of mature ex vivo human dental pulp using tissue engineering scaffolds10.1016/j.joen.2011.05.030 ↗
68. Biodegradable nanofiber bone-tissue scaffold as remotely controlled and self-powering electrical stimulator10.1016/j.nanoen.2020.105028 ↗
69. Biocompatibility, biodegradation and excretion of polylactic acid (PLA) in medical implants and theranostic systems10.1016/j.cej.2018.01.010 ↗
70. Fabrication of biodegradable polymer nanocomposite from copolymer synthesized by C. necator for bone tissue engineering
71. Tissue engineered cartilage on collagen and PHBV matrices10.1016/j.biomaterials.2005.01.037 ↗
72. Smart piezoelectric nanohybrid of poly (3-hydroxybutyrate-co-3-hydroxyvalerate) and barium titanate for stimulated cartilage regeneration10.1021/acsabm.9b00667 ↗
73. Collagen for bone tissue regeneration10.1016/j.actbio.2012.06.014 ↗
74. On the piezoelectricity of collagen–chitosan films10.1039/b100189m ↗
75. Effect of resin matrix composition on the translucency of experimental dental composite resins10.1016/j.dental.2009.07.011 ↗
76. Piezoelectric heterogeneity in collagen type I fibrils quantitatively characterized by piezoresponse force microscopy10.1021/acsbiomaterials.0c01314 ↗
77. Location, arrangement and possible function of interodontoblastic collagen fibres in association with calcium hydroxide-induced hard tissue bridges10.1046/j.1365-2591.2002.00606.x ↗
78. Performance of collagen sponge as a 3-D scaffold for tooth-tissue engineering10.1016/j.biomaterials.2006.01.055 ↗
79. Collagen-hydroxyapatite films: Piezoelectric properties10.1016/S0921-5107(01)00674-2 ↗
80. Chitosan/collagen scaffold containing bone morphogenetic protein‚ DNA supports dental pulp stem cell differentiation in vitro and in vivo10.1002/jbm.a.34064 ↗
81. Chitosan monomer promotes tissue regeneration on dental pulp wounds10.1002/jbm.a.30588 ↗
82. Marine collagen scaffolds in tissue engineering10.1016/j.copbio.2021.10.011 ↗
83. Chitosan/carboxymethyl cellulose polyelectrolyte complex scaffolds for pulp cells regeneration10.1177/0883911507081329 ↗
84. Effects of morphogen and scaffold porogen on the differentiation of dental pulp stem cells10.1016/j.joen.2010.08.031 ↗
85. A novel bioactive three-dimensional (tricalcium phosphate/chitosan scaffold for periodontal tissue engineering10.1007/s10856-009-3931-x ↗
86. In vitro comparative evaluation of antifungal efficacy of three endodontic sealers with and without incorporation of chitosan nanoparticles against Candida albicans10.4103/JCD.JCD_242_19 ↗
87. Photoactivated rose bengal functionalized chitosan nanoparticles produce antibacterial/biofilm activity and stabilize dentin-collagen10.1016/j.nano.2013.10.010 ↗
88. Investigations on the existence of piezoelectric property of a bio-polymer-chitosan and its application in vibration sensors10.1039/C7RA04752E ↗
89. Glycine–chitosan-based flexible biodegradable piezoelectric pressure sensor10.1021/acsami.9b21052 ↗
90. Recent advances in cellulose-based piezoelectric and triboelectric nanogenerators for energy harvesting: A review10.1039/D0TA08642H ↗
91. On the mechanism of dissolution of cellulose10.1016/j.molliq.2010.04.016 ↗
92. Cellulose: The structure slowly unravels10.1023/A:1018431705579 ↗
93. Zugenmaier, P. (2008). Crystalline Cellulose and Derivatives: Characterization and Structures, Springer Science & Business Media.10.1007/978-3-540-73934-0 ↗
94. Studies of microstructure in native celluloses using solid-state carbon-13 NMR10.1021/ma00138a009 ↗
95. Cellulose: Fascinating biopolymer and sustainable raw material10.1002/anie.200460587 ↗
96. Piezoelectricity of wood10.1143/JPSJ.10.149 ↗
97. Industrial-scale production and applications of bacterial cellulose10.3389/fbioe.2020.605374 ↗
98. An, S.J., Lee, S.H., Huh, J.B., Jeong, S.I., Park, J.S., Gwon, H.J., Kang, E.S., Jeong, C.M., and Lim, Y.M. (2017). Preparation and characterization of resorbable bacterial cellulose membranes treated by electron beam irradiation for guided bone regeneration. Int. J. Mol. Sci., 18.10.3390/ijms18112236 ↗
99. Improvement of silicate cement properties with bacterial cellulose powder addition for applications in dentistry10.1016/j.carbpol.2017.06.062 ↗
100. Human dental pulp stem cells and gingival fibroblasts seeded into silk fibroin scaffolds have the same ability in attracting vessels10.3389/fphys.2016.00140 ↗