2607004547
  • Open Access
  • Review

From Nature to Implant: Biodegradable Piezoelectric Materials for Transient Biosensors

  • Min Kyeong Kim 1,2,   
  • Jinyi Xu 1,   
  • Hening Xing 1,   
  • Zhangsiyuan Jin 1,   
  • John Hong 2,   
  • Yuljae Cho 1,3,*

Received: 12 May 2026 | Revised: 22 Jun 2026 | Accepted: 06 Jul 2026 | Published: 13 Jul 2026

Abstract

Biodegradable piezoelectric materials are emerging as promising platforms for transient biosensors because they can mechanically interact with tissues, generate useful electrical signals, and degrade after a defined functional lifetime. Unlike conventional piezoelectric ceramics and fluorinated polymers, which raise concerns related to toxicity, persistence, or device retrieval, these materials aim to combine sensing performance with bioresorption and safer biological integration. This review distinguishes biodegradability from biocompatibility while examining how the two concepts intersect in the design of transient piezoelectric biosensors. It first discusses how the literature addresses degradation mechanisms, functional lifetime, byproduct safety, cytocompatibility, inflammatory response, and mechanical compatibility. It then surveys major material classes, including amino acid crystals, natural biopolymers, synthetic biodegradable polymers, and peptide-based self-assembling systems. Representative biosensing applications are considered, ranging from short-term implantable pressure monitoring to healing-related interfaces and therapy-adjacent transduction platforms. Finally, the review highlights key challenges, including the need for standardized degradation testing under physiologically relevant conditions, full-system biodegradable integration, and more rigorous evaluation of degradation products in realistic implant environments.

References 

  • 1.

    Chen, B.; Feng, Z.; Yao, F.-Z.; et al. Flexible piezoelectrics: Integration of sensing, actuating and energy harvesting. npj Flex. Electron. 2025, 9, 58. https://doi.org/10.1038/s41528-025-00432-5.

  • 2.

    Dinh, T.; Nguyen, T.; Phan, H.-P.; et al. Stretchable respiration sensors: Advanced designs and multifunctional platforms for wearable physiological monitoring. Biosens. Bioelectron. 2020, 166, 112460. https://doi.org/10.1016/j.bios.2020.112460.

  • 3.

    Hu, H.; Huang, H.; Li, M.; et al. A wearable cardiac ultrasound imager. Nature 2023, 613, 667–675. https://doi.org/10.1038/s41586-022-05498-z.

  • 4.

    Jin, H.; Kim, Y.; Youm, W.; et al. Highly pixelated, untethered tactile interfaces for an ultra-flexible on-skin telehaptic system. npj Flex. Electron. 2022, 6, 82. https://doi.org/10.1038/s41528-022-00216-1.

  • 5.

    Jin, H.; Zheng, Z.; Cui, Z.; et al. A flexible optoacoustic blood ‘stethoscope’ for noninvasive multiparametric cardiovascular monitoring. Nat. Commun. 2023, 14, 4692. https://doi.org/10.1038/s41467-023-40181-5.

  • 6.

    Kim, D.B.; Han, J.; Sung, S.M.; et al. Weave-pattern-dependent fabric piezoelectric pressure sensors based on polyvinylidene fluoride nanofibers electrospun with 50 nozzles. npj Flex. Electron. 2022, 6, 69. https://doi.org/10.1038/s41528-022-00203-6.

  • 7.

    Kim, Y.-G.; Song, J.-H.; Hong, S.; et al. Piezoelectric strain sensor with high sensitivity and high stretchability based on kirigami design cutting. npj Flex. Electron. 2022, 6, 52. https://doi.org/10.1038/s41528-022-00186-4.

  • 8.

    Kong, H.; Li, W.; Song, Z.; et al. Recent advances in multimodal sensing integration and decoupling strategies for tactile perception. Mater. Futures 2024, 3, 022501. https://doi.org/10.1088/2752-5724/ad305e.

  • 9.

    La, T.G.; Le, L.H. Flexible and wearable ultrasound device for medical applications: A review on materials, structural designs, and current challenges. Adv. Mater. Technol 2022, 7, 2100798. https://doi.org/10.1002/admt.202100798.

  • 10.

    Nag, A.; Mukhopadhyay, S.C.; Kosel, J. Wearable flexible sensors: A review. IEEE Sens. J. 2017, 17, 3949–3960. https://doi.org/10.1109/JSEN.2017.2705700.

  • 11.

    Seneviratne, S.; Hu, Y.; Nguyen, T.; et al. A survey of wearable devices and challenges. IEEE Commun. Surv. Tutor. 2017, 19, 2573–2620. https://doi.org/10.1109/COMST.2017.2731979.

  • 12.

    Sun, Z.; He, T.; Ren, Z.; et al. Moving toward human-like perception and sensation systems—From integrated intelligent systems to decentralized smart devices. SmartSys 2025, 1, e4. https://doi.org/10.1002/sys3.4.

  • 13.

    Vaghasiya, J.V.; Mayorga-Martinez, C.C.; Pumera, M. Wearable sensors for telehealth based on emerging materials and nanoarchitectonics. npj Flex. Electron. 2023, 7, 26. https://doi.org/10.1038/s41528-023-00261-4.

  • 14.

    Yin, J.; Hinchet, R.; Shea, H.; et al. Wearable soft technologies for haptic sensing and feedback. Adv. Funct. Mater. 2021, 31, 2007428. https://doi.org/10.1002/adfm.202007428.

  • 15.

    Yin, R.; Wang, D.; Zhao, S.; et al. Wearable sensors-enabled human-machine interaction systems: From design to application. Adv. Funct. Mater. 2021, 31, 2008936. https://doi.org/10.1002/adfm.202008936.

  • 16.

    Curry, E.J.; Ke, K.; Chorsi, M.T.; et al. Biodegradable piezoelectric force sensor. Proc. Natl. Acad. Sci. USA 2018, 115, 909–914. https://doi.org/10.1073/pnas.1710874115.

  • 17.

    Lu, J.; Xu, L.; Hazarika, D.; et al. Piezoelectric nanogenerator enabled fully self-powered instantaneous wireless sensor system. Nano Energy 2024, 129, 110022. https://doi.org/10.1016/j.nanoen.2024.110022.

  • 18.

    Ning, C.; Xiang, S.; Sun, X.; et al. Highly stretchable kirigami-patterned nanofiber-based nanogenerators for harvesting human motion energy to power wearable electronics. Mater. Futures 2024, 3, 025101. https://doi.org/10.1088/2752-5724/ad2f6a.

  • 19.

    Wang, H.; Li, S.; Zhang, Y.; et al. A self-powered, shapeable, and wearable sensor for effective hazard prevention and biomechanical monitoring. SmartSys 2025, 1, e3. https://doi.org/10.1002/sys3.3.

  • 20.

    Wu, P.; Chen, P.; Xu, C.; et al. Ultrasound-driven in vivo electrical stimulation based on biodegradable piezoelectric nanogenerators for enhancing and monitoring the nerve tissue repair. Nano Energy 2022, 102, 107707. https://doi.org/10.1016/j.nanoen.2022.107707.

  • 21.

    Wang, Z.; Chen, C.; Meng, H.; et al. Biodegradable piezoelectric materials: Powering the future of bioelectronic medicine. Adv. Funct. Mater. 2026, 36, e19501. https://doi.org/10.1002/adfm.202519501.

  • 22.

    Ali, M.; Bathaei, M.J.; Istif, E.; et al. Biodegradable piezoelectric polymers: Recent advancements in materials and applications. Adv. Healthc. Mater. 2023, 12, 2300318. https://doi.org/10.1002/adhm.202300318.

  • 23.

    Dai, F.; Geng, Q.; Hua, T.; et al. Organic biodegradable piezoelectric materials and their potential applications as bioelectronics. Soft Sci. 2023, 3, 7. https://doi.org/10.20517/ss.2022.30.

  • 24.

    Cung, K.; Han, B.J.; Nguyen, T.D.; et al. Biotemplated synthesis of PZT nanowires. Nano Lett. 2013, 13, 6197–6202. https://doi.org/10.1021/nl4035708.

  • 25.

    Ali, M.; Hoseyni, S.M.; Das, R.; et al. A flexible and biodegradable piezoelectric-based wearable sensor for non-invasive monitoring of dynamic human motions and physiological signals. Adv. Mater. Technol. 2023, 8, 2300347. https://doi.org/10.1002/admt.202300347.

  • 26.

    Stuber, V.L.; Deutz, D.B.; Bennett, J.; et al. Flexible lead-free piezoelectric composite materials for energy harvesting applications. Energy Technol. 2019, 7, 177–185. https://doi.org/10.1002/ente.201800419.

  • 27.

    Han, W.B.; Lee, J.H.; Shin, J.-W.; et al. Advanced materials and systems for biodegradable, transient electronics. Adv. Mater. 2020, 32, 2002211. https://doi.org/10.1002/adma.202002211.

  • 28.

    Ding, Z.; Qiao, J.; Gao, W.-C.; et al. A comprehensive review on biodegradable materials and technologies for transient electronics. Adv. Mater. Technol. 2026, 11, e01928. https://doi.org/10.1002/admt.202501928.

  • 29.

    Hwang, S.-W.; Tao, H.; Kim, D.-H.; et al. A physically transient form of silicon electronics. Science 2012, 337, 1640–1644. https://doi.org/10.1126/science.1226325.

  • 30.

    Shan, Y.; Wang, E.; Cui, X.; et al. A biodegradable piezoelectric sensor for real-time evaluation of the motor function recovery after nerve injury. Adv. Funct. Mater. 2024, 34, 2400295. https://doi.org/10.1002/adfm.202400295.

  • 31.

    Dai, F.; Cheng, H.; Qi, H.; et al. Rochelle salt-based biodegradable piezoelectric devices for nerve regeneration and intestinal motility monitoring. Nat. Commun. 2026, 17, 2169. https://doi.org/10.1038/s41467-026-68930-2.

  • 32.

    Chen, W.; Li, W.; Lai, P.; et al. Bioinspired hydrogel patch with controllable adhesion for soft tissue repair. Mater. Futures 2025, 4, 035002. https://doi.org/10.1088/2752-5724/adec0a.

  • 33.

    Lin, Q.; Zhang, Y.; Chen, L.; et al. Glycine/alginate-based piezoelectric film consisting of a single, monolithic β-glycine spherulite towards flexible and biodegradable force sensor. Regen. Biomater. 2024, 11, rbae047. https://doi.org/10.1093/rb/rbae047.

  • 34.

    Liu, J.; Li, S.; Zhou, S.; et al. A high-performance, biocompatible, and fully biodegradable piezo-triboelectric hybrid nanogenerator based on PVA/glycine/PVA heterostructured piezoelectric film. Nano Energy 2024, 122, 109310. https://doi.org/10.1016/j.nanoen.2024.109310.

  • 35.

    Xu, Q.; Gao, X.; Zhao, S.; et al. Construction of bio-piezoelectric platforms: From structures and synthesis to applications. Adv. Mater. 2021, 33, 2008452. https://doi.org/10.1002/adma.202008452.

  • 36.

    Chorsi, M.T.; Le, T.T.; Lin, F.; et al. Highly piezoelectric, biodegradable, and flexible amino acid nanofibers for medical applications. Sci. Adv. 2023, 9, eadg6075. https://doi.org/10.1126/sciadv.adg6075.

  • 37.

    Yu, Q.; Bai, Y.; Li, Z.; et al. Interface-induced high piezoelectric γ-glycine-based flexible biodegradable films. Nano Energy 2024, 121, 109196. https://doi.org/10.1016/j.nanoen.2023.109196.

  • 38.

    Zhang, Z.; Li, X.; Peng, Z.; et al. Active self-assembly of piezoelectric biomolecular films via synergistic nanoconfinement and in-situ poling. Nat. Commun. 2023, 14, 4094. https://doi.org/10.1038/s41467-023-39692-y.

  • 39.

    Guerin, S.; Stapleton, A.; Chovan, D.; et al. Control of piezoelectricity in amino acids by supramolecular packing. Nat. Mater. 2018, 17, 180–186. https://doi.org/10.1038/nmat5045.

  • 40.

    Zhang, Z.; Wang, Z.; Li, X.; et al. Design and manufacturing of piezoelectric biomaterials for bioelectronics and biomedical applications. Chem. Rev. 2025, 125, 9875–9929. https://doi.org/10.1021/acs.chemrev.5c00399.

  • 41.

    Wang, A.; Feng, S.; Xiao, T.; et al. Microenvironment-engineered piezoionic hydrogel nanogenerators for enhanced energy harvesting and sensing. SmartSys 2025, 1, e70004. https://doi.org/10.1002/sys3.70004.

  • 42.

    Li, T.; Yuan, Y.; Gu, L.; et al. Ultrastable piezoelectric biomaterial nanofibers and fabrics as an implantable and conformal electromechanical sensor patch. Sci. Adv 2024, 10, eadn8706. https://doi.org/10.1126/sciadv.adn8706.

  • 43.

    Xu, M.; Wen, Y.; Shi, Z.; et al. Piezoelectric biopolymers: Advancements in energy harvesting and biomedical applications. Polymers 2024, 16, 3314. https://doi.org/10.3390/polym16233314.

  • 44.

    Liu, T.; Wang, Y.; Hong, M.; et al. Advances in biodegradable piezoelectrics for medical implants. Nano Today 2023, 52, 101945. https://doi.org/10.1016/j.nantod.2023.101945.

  • 45.

    Yang, C.; Hou, X.; Zhang, L. Microfluidics-derived microfibers in flexible bioelectronics. Mater. Futures 2024, 3, 032401. https://doi.org/10.1088/2752-5724/ad667b.

  • 46.

    Chen, M.; Liu, J.; Hu, Y.; et al. Silk fibroin-based flexible pressure sensors: Processing and application. Mater. Futures 2024, 3, 032501. https://doi.org/10.1088/2752-5724/ad5f48.

  • 47.

    Li, Y.; Chen, J.; Liu, S.; et al. Biodegradable piezoelectric polymer for cartilage remodeling. Matter 2024, 7, 1631–1643. https://doi.org/10.1016/j.matt.2024.01.034.

  • 48.

    Dong, F.; Han, C.; Cai, S.T.; et al. Skin-integrated wearable electronics: A dual-interface perspective. SmartSys 2025, 1, e70013. https://doi.org/10.1002/sys3.70013.

  • 49.

    Khan, B.; Amara, U.; Khan, B.; et al. Next-generation piezoelectric materials in wearable and implantable devices for continuous physiological monitoring. Adv. Sci. 2025, 12, e07853. https://doi.org/10.1002/advs.202507853.

  • 50.

    Zhao, J.; Li, T.; Sun, H.; et al. Regulated crystallization and piezoelectric properties of bio-based poly(L-lactic acid)/diatomite composite fibers by electrospinning. Adv. Compos. Hybrid Mater. 2024, 7, 218. https://doi.org/10.1007/s42114-024-01034-x.

  • 51.

    Bernardo, M.P.; da Silva, B.C.R.; Hamouda, A.E.I.; et al. PLA/Hydroxyapatite scaffolds exhibit in vitro immunological inertness and promote robust osteogenic differentiation of human mesenchymal stem cells without osteogenic stimuli. Sci. Rep. 2022, 12, 2333. https://doi.org/10.1038/s41598-022-05207-w.

  • 52.

    Walton, M.; Cotton, N.J. Long-term in vivo degradation of poly-L-lactide (PLLA) in bone. J. Biomater. Appl. 2007, 21, 395–411. https://doi.org/10.1177/0885328206065125.

  • 53.

    Shi, J.; Zhang, J.; Zhang, Y.; et al. Crystallinity dependence of PLLA hydrophilic modification during alkali hydrolysis. Polymers 2023, 15, 75. https://doi.org/10.3390/polym15010075.

  • 54.

    Malone, L.P.; Best, S.M.; Cameron, R.E. Accelerated degradation testing impacts the degradation processes in 3D printed amorphous PLLA. Front. Bioeng. Biotechnol. 2024, 12, 1419654. https://doi.org/10.3389/fbioe.2024.1419654.

  • 55.

    Seddiqi, H.; Oliaei, E.; Honarkar, H.; et al. Cellulose and its derivatives: Towards biomedical applications. Cellulose 2021, 28, 1893–1931. https://doi.org/10.1007/s10570-020-03674-w.

  • 56.

    Hellmann, M.J.; Marongiu, G.L.; Gorzelanny, C.; et al. Hydrolysis of chitin and chitosans by the human chitinolytic enzymes: Chitotriosidase, acidic mammalian chitinase, and lysozyme. Int. J. Biol. Macromol. 2025, 297, 139789. https://doi.org/10.1016/j.ijbiomac.2025.139789.

  • 57.

    Li, M.; Ogiso, M.; Minoura, N. Enzymatic degradation behavior of porous silk fibroin sheets. Biomaterials 2003, 24, 357–365. https://doi.org/10.1016/S0142-9612(02)00326-5.

  • 58.

    Bergsma, J.E.; Rozema, F.R.; Bos, R.R.M.; et al. In vivo degradation and biocompatibility study of in vitro pre-degraded as-polymerized polylactide particles. Biomaterials 1995, 16, 267–274. https://doi.org/10.1016/0142-9612(95)93253-A.

  • 59.

    Antonaci, V.; de Marzo, G.; Blasi, L.; et al. Biodegradable chitosan-cellulose and sub-spherical nanocrystals composite piezoelectric thin film. npj Flex. Electron. 2026, 10, 55. https://doi.org/10.1038/s41528-026-00550-8.

  • 60.

    Hosseini, E.S.; Manjakkal, L.; Shakthivel, D.; et al. Glycine–chitosan-based flexible biodegradable piezoelectric pressure sensor. ACS Appl. Mater. Interfaces 2020, 12, 9008–9016. https://doi.org/10.1021/acsami.9b21052.

  • 61.

    de Marzo, G.; Mastronardi, V.M.; Algieri, L.; et al. Sustainable, flexible, and biocompatible enhanced piezoelectric chitosan thin film for compliant piezosensors for human health. Adv. Electron. Mater. 2023, 9, 2200069. https://doi.org/10.1002/aelm.202200069.

  • 62.

    D’Alessandro, D.; Ricci, C.; Milazzo, M.; et al. Piezoelectric signals in vascularized bone regeneration. Biomolecules 2021, 11, 1731. https://doi.org/10.3390/biom11111731.

  • 63.

    Basavalingappa, V.; Bera, S.; Xue, B.; et al. Diphenylalanine-derivative peptide assemblies with increased aromaticity exhibit metal-like rigidity and high piezoelectricity. ACS Nano 2020, 14, 7025–7037. https://doi.org/10.1021/acsnano.0c01654.

  • 64.

    Hu, P.; Hu, S.; Huang, Y.; et al. Bioferroelectric properties of glycine crystals. J. Phys. Chem. Lett. 2019, 10, 1319–1324. https://doi.org/10.1021/acs.jpclett.8b03837.

  • 65.

    Yang, F.; Li, J.; Long, Y.; et al. Wafer-scale heterostructured piezoelectric bio-organic thin films. Science 2021, 373, 337–342. https://doi.org/10.1126/science.abf2155.

  • 66.

    Yuan, H.; Han, P.; Tao, K.; et al. Piezoelectric peptide and metabolite materials. Research 2019, 2019, 9025939. https://doi.org/10.34133/2019/9025939.

  • 67.

    Guerin, S.; O’Donnell, J.; Haq, E.U.; et al. Racemic amino acid piezoelectric transducer. Phys. Rev. Lett. 2019, 122, 047701. https://doi.org/10.1103/PhysRevLett.122.047701.

  • 68.

    Shlapakova, L.E.; Shvartsman, V.V.; Slautin, B.N.; et al. Tailoring the topography, crystalline structure, and piezoelectric response of electrospun biodegradable poly(3-hydroxybutyrate) scaffolds by glycine loading. Adv. Compos. Hybrid Mater. 2025, 8, 424. https://doi.org/10.1007/s42114-025-01487-8.

  • 69.

    Wang, Y.; Liu, S.; Li, L.; et al. Manipulating the piezoelectric response of amino acid-based assemblies by supramolecular engineering. J. Am. Chem. Soc. 2023, 145, 15331–15342. https://doi.org/10.1021/jacs.3c02993.

  • 70.

    Maity, S.; Singh, R.K.; Gadhewal, M.; et al. Highly biodegradable piezoelectric flexible wearable tactile sensors with amino acid crystals: A paradigm shift towards smart transient electronics. Chem. Eng. J. 2025, 512, 162531. https://doi.org/10.1016/j.cej.2025.162531.

  • 71.

    Sencadas, V.; Garvey, C.; Mudie, S.; et al. Electroactive properties of electrospun silk fibroin for energy harvesting applications. Nano Energy 2019, 66, 104106. https://doi.org/10.1016/j.nanoen.2019.104106.

  • 72.

    Peng, Y.; Zhou, S.; Xing, X.; et al. Kinetically tuning the structural assembly of silk fibroin for highly piezoelectric wearable sensors. Langmuir 2025, 41, 32777–32789. https://doi.org/10.1021/acs.langmuir.5c04882.

  • 73.

    Minary-Jolandan, M.; Yu, M.-F. Uncovering nanoscale electromechanical heterogeneity in the subfibrillar structure of collagen fibrils responsible for the piezoelectricity of bone. ACS Nano 2009, 3, 1859–1863. https://doi.org/10.1021/nn900472n.

  • 74.

    Minary-Jolandan, M.; Yu, M.-F. Nanoscale characterization of isolated individual type I collagen fibrils: Polarization and piezoelectricity. Nanotechnology 2009, 20, 085706. https://doi.org/10.1088/0957-4484/20/8/085706.

  • 75.

    Kwon, J.; Cho, H. Piezoelectric heterogeneity in collagen type I fibrils quantitatively characterized by piezoresponse force microscopy. ACS Biomater. Sci. Eng. 2020, 6, 6680–6689. https://doi.org/10.1021/acsbiomaterials.0c01314.

  • 76.

    Chakraborty, S.; Debnath, S.; Mahipal Malappuram, K.; et al. Flexible and robust piezoelectric chitosan films with enhanced bioactivity. Biomacromolecules 2025, 26, 1128–1140. https://doi.org/10.1021/acs.biomac.4c01464.

  • 77.

    Curry, E.J.; Le, T.T.; Das, R.; et al. Biodegradable nanofiber-based piezoelectric transducer. Proc. Natl. Acad. Sci. USA 2020, 117, 214–220. https://doi.org/10.1073/pnas.1910343117.

  • 78.

    Che, X.; Fan, Y.; Su, Y.; et al. Performance improvement and application of degradable poly-L-lactide and yttrium-doped zinc oxide hybrid films for energy harvesting. ACS Appl. Mater. Interfaces 2024, 16, 33517–33526. https://doi.org/10.1021/acsami.4c05807.

  • 79.

    Smith, M.; Chalklen, T.; Lindackers, C.; et al. Poly-L-lactic acid nanotubes as soft piezoelectric interfaces for biology: Controlling cell attachment via polymer crystallinity. ACS Appl. Bio Mater. 2020, 3, 2140–2149. https://doi.org/10.1021/acsabm.0c00012.

  • 80.

    Strangis, G.; Labardi, M.; Gallone, G.; et al. 3D printed piezoelectric BaTiO3/polyhydroxybutyrate nanocomposite scaffolds for bone tissue engineering. Bioengineering 2024, 11, 193. https://doi.org/10.3390/bioengineering11020193.

  • 81.

    Qu, Y.; Shang, Y.; Luo, S.; et al. Biodegradable piezoelectric PHB-BT nanofiber scaffolds combined with ultrasound stimulation to accelerate bone regeneration by regulating Ca2+/CaN/NFAT. Theranostics 2026, 16, 4283–4303. https://doi.org/10.7150/thno.124648.

  • 82.

    More, N.; Srivastava, A.; Kapusetti, G. Graphene oxide reinforcement enhances the piezoelectric and mechanical properties of poly(3-hydroxybutyrate-co-3-hydroxy valerate)-based nanofibrous scaffolds for improved proliferation of chondrocytes and ECM production. ACS Appl. Bio Mater. 2020, 3, 6823–6835. https://doi.org/10.1021/acsabm.0c00765.

  • 83.

    Karanth, D.; Puleo, D.; Dawson, D.; et al. Characterization of 3D printed biodegradable piezoelectric scaffolds for bone regeneration. Clin. Exp. Dent. Res. 2023, 9, 398–408. https://doi.org/10.1002/cre2.712.

  • 84.

    U.S. Food and Drug Administration. Sculptra—P030050/S039. 2023. Available online: https://www.fda.gov/medical-devices/recently-approved-devices/sculptra-p030050s039 (accessed on 18 June 2026).

  • 85.

    Bera, S.; Guerin, S.; Yuan, H.; et al. Molecular engineering of piezoelectricity in collagen-mimicking peptide assemblies. Nat. Commun. 2021, 12, 2634. https://doi.org/10.1038/s41467-021-22895-6.

  • 86.

    Li, J.; Long, Y.; Yang, F.; et al. Natural piezoelectric biomaterials: A biocompatible and sustainable building block for biomedical devices. ACS Nano 2022, 16, 17708–17728. https://doi.org/10.1021/acsnano.2c08164.

  • 87.

    Lee, J.-H.; Lee, J.H.; Xiao, J.; et al. Vertical self-assembly of polarized phage nanostructure for energy harvesting. Nano Lett. 2019, 19, 2661–2667. https://doi.org/10.1021/acs.nanolett.9b00569.

  • 88.

    Park, H.; Kim, Y.; Kim, Y.; et al. Self-assembly of unidirectionally polarized piezoelectric peptide nanotubes using environmentally friendly solvents. Appl. Surf. Sci. 2023, 618, 156588. https://doi.org/10.1016/j.apsusc.2023.156588.

  • 89.

    Su, Y.; Liu, J.; Yang, D.; et al. Electric field-assisted self-assembly of diphenylalanine peptides for high-performance energy conversion. ACS Mater. Lett. 2023, 5, 2317–2323. https://doi.org/10.1021/acsmaterialslett.3c00664.

  • 90.

    Kim, Y.; Park, H.; Kim, Y.; et al. Control of the biodegradability of piezoelectric peptide nanotubes integrated with hydrophobic porphyrin. ACS Appl. Mater. Interfaces 2022, 14, 38778–38785. https://doi.org/10.1021/acsami.2c09751.

  • 91.

    Lee, B.Y.; Zhang, J.; Zueger, C.; et al. Virus-based piezoelectric energy generation. Nat. Nanotechnol. 2012, 7, 351–356. https://doi.org/10.1038/nnano.2012.69.

  • 92.

    Park, I.W.; Kim, K.W.; Hong, Y.; et al. Recent developments and prospects of M13-bacteriophage based piezoelectric energy harvesting devices. Nanomaterials 2020, 10, 93. https://doi.org/10.3390/nano10010093.

  • 93.

    Veronica, A.; Liu, S.; Yang, Z.; et al. Enhancing piezoelectricity of silk fibroin through in situ growth of metal-free perovskite for organic and eco-friendly wearable bioelectronics. Adv. Mater. Technol. 2024, 9, 2301320. https://doi.org/10.1002/admt.202301320.

  • 94.

    Pang, C.; Li, F.; Hu, X.; et al. Degradable silk fibroin based piezoresistive sensor for wearable biomonitoring. Discov. Nano 2024, 19, 55. https://doi.org/10.1186/s11671-024-04001-z.

  • 95.

    Lu, J.; Hu, S.; Li, W.; et al. A biodegradable and recyclable piezoelectric sensor based on a molecular ferroelectric embedded in a bacterial cellulose hydrogel. ACS Nano 2022, 16, 3744–3755. https://doi.org/10.1021/acsnano.1c07614.

  • 96.

    Sun, J.; Guo, H.; Ribera, J.; et al. Sustainable and biodegradable wood sponge piezoelectric nanogenerator for sensing and energy harvesting applications. ACS Nano 2020, 14, 14665–14674. https://doi.org/10.1021/acsnano.0c05493.

  • 97.

    Yogeswaran, N.; Hosseini, E.S.; Dahiya, R. Graphene based low voltage field effect transistor coupled with biodegradable piezoelectric material based dynamic pressure sensor. ACS Appl. Mater. Interfaces 2020, 12, 54035–54040. https://doi.org/10.1021/acsami.0c13637.

  • 98.

    Alvarez-Lorenzo, C.; Zarur, M.; Seijo-Rabina, A.; et al. Physical stimuli-emitting scaffolds: The role of piezoelectricity in tissue regeneration. Mater. Today Bio 2023, 22, 100740. https://doi.org/10.1016/j.mtbio.2023.100740.

  • 99.

    Liu, L.; Li, Z.; Zhu, T.; et al. Advances in applications of low-dimensional piezoelectric materials in musculoskeletal system. Mater. Today Bio 2025, 33, 102065. https://doi.org/10.1016/j.mtbio.2025.102065.

  • 100.

    Das, R.; Le, T.T.; Schiff, B.; et al. Biodegradable piezoelectric skin-wound scaffold. Biomaterials 2023, 301, 122270. https://doi.org/10.1016/j.biomaterials.2023.122270.

  • 101.

    Guillot-Ferriols, M.; Costa, C.M.; Correia, D.M.; et al. Piezoelectric stimulation induces osteogenesis in mesenchymal stem cells cultured on electroactive two-dimensional substrates. ACS Appl. Polym. Mater. 2024, 6, 13710–13722. https://doi.org/10.1021/acsapm.4c02485.

  • 102.

    Jeon, S.; Kim, D.; Jo, M.-Y.; et al. Wireless acousto-piezoelectric conduit with aligned nanofibers for neural regeneration. Adv. Mater. 2025, 37, 2503343. https://doi.org/10.1002/adma.202503343.

  • 103.

    Bianchini, M.; Iacoponi, F.; Battaglini, M.; et al. Piezoelectric chitosan microporous scaffolds for ultrasound-driven Schwann cell migration and enhanced neurotrophins production. ACS Biomater. Sci. Eng. 2026, 12, 461–475. https://doi.org/10.1021/acsbiomaterials.5c01086.

  • 104.

    Han, M.; Yildiz, E.; Bozuyuk, U.; et al. Janus microparticles-based targeted and spatially-controlled piezoelectric neural stimulation via low-intensity focused ultrasound. Nat. Commun. 2024, 15, 2013. https://doi.org/10.1038/s41467-024-46245-4.

  • 105.

    Bargero, A.; Battaglini, M.; Curiale, T.; et al. Ultrasound-responsive polymeric piezoelectric nanoparticles for remote activation and neuronal differentiation of human neural stem cells. Small Sci. 2025, 5, 2400354. https://doi.org/10.1002/smsc.202400354.

  • 106.

    Zhao, X.; Li, J.; Dai, J.; et al. Biodegradable piezoelectric implant for wirelessly delivering electrical stimulation to the heart under ultrasound stress. Adv. Funct. Mater. 2025, 35, 2418708. https://doi.org/10.1002/adfm.202418708.

  • 107.

    Rentero, C.; Amorín, H.; Jiménez, R.; et al. Key factors affecting the piezoelectric response of poly-L-lactic acid electrospun fibers. Polymer 2025, 325, 128286. https://doi.org/10.1016/j.polymer.2025.128286.

  • 108.

    Vishnoi, S.; Kumari, G.; Guest, R.; et al. High-throughput computational screening of small molecular crystals for sustainable piezoelectric materials. Angew. Chem. Int. Ed. 2025, 64, e202501232. https://doi.org/10.1002/anie.202501232.

  • 109.

    Stankiewicz, G.; Dev, C.; Weichelt, M.; et al. Towards advanced piezoelectric metamaterial design via combined topology and shape optimization. Struct. Multidisc. Optim. 2024, 67, 26. https://doi.org/10.1007/s00158-024-03742-w.

  • 110.

    Vannozzi, L.; Pucci, C.; Trucco, D.; et al. Biodegradable piezoelectric micro- and nanomaterials for regenerative medicine, targeted therapy, and microrobotics. Small Sci. 2025, 5, 2400439. https://doi.org/10.1002/smsc.202400439.

  • 111.

    Janićijević, Ž; Huang, T.; Sandoval Bojórquez, D.I.; et al. Design and development of transient sensing devices for healthcare applications. Adv. Sci. 2024, 11, 2307232. https://doi.org/10.1002/advs.202307232.

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How to Cite
Kim, M. K.; Xu, J.; Xing, H.; Jin, Z.; Hong, J.; Cho, Y. From Nature to Implant: Biodegradable Piezoelectric Materials for Transient Biosensors. Nanoenergy Communications 2026, 1 (1), 8. https://doi.org/10.53941/nc.2026.100008.
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