3D-printed scaffolds for periodontitis therapy: Spatial programming and microenvironmental regulation
Periodontitis is a chronic inflammatory disease characterized by plaque biofilm dysbiosis, immune dysregulation, oxidative stress, alveolar bone resorption, and impaired wound healing. Although conventional periodontal therapies can reduce microbial burden and slow disease progression, predictable regeneration of the cementum-periodontal ligament (PDL)-alveolar bone complex remains difficult in irregular, infected, and inflammation-compromised defects. Three-dimensional (3D) printing offers a programmable strategy for fabricating periodontal scaffolds with patient-specific geometry, tunable pore architecture, spatially distributed materials, and region-specific biological functions. This review summarizes recent advances in 3D-printed scaffolds for periodontitis therapy and periodontal tissue regeneration, with emphasis on spatial programming and microenvironmental regulation. We first analyze the pathological barriers dictating scaffold design requirements, including persistent biofilms, unresolved inflammation, oxidative stress, disrupted bone homeostasis, and defective healing. We then discuss major printing modalities, material platforms, and biomimetic design strategies, including patient-specific customization, multiphasic compartmentalization, PDL fiber guidance, vascularization-oriented pore networks, and integrated barrier control. Functional strategies involving antibacterial activity, immuno-redox regulation, tissue-specific regenerative cues, neurovascular support, and spatiotemporal delivery are highlighted. Finally, we outline challenges in material optimization, disease-relevant modelling, functional evaluation, manufacturing standardization, and clinical translation. Future 3D-printed periodontal scaffolds should evolve from passive defect fillers into microenvironment-driven precision regenerative systems for functional periodontal reconstruction.
- Xu J, Lin Y, Tian M, et al. Periodontal ligament stem cell-derived extracellular vesicles enhance tension-induced osteogenesis. ACS Biomater Sci Eng. 2023;9(1):388-398. doi: 10.1021/acsbiomaterials.2c00717
- de Molon RS, Vernal R, Oliveira GE, et al. Inflammatory bone loss and signaling pathways in periodontitis: mechanistic insights and emerging therapeutic strategies. Bone Res. 2026;14(1):1. doi: 10.1038/s41413-025-00478-1
- Xu J, Yin Y, Lin Y, et al. Long non-coding RNAs: emerging roles in periodontitis. J Periodontal Res. 2021;56(5):848-862. doi: 10.1111/jre.12910
- Bernabe E, Marcenes W, Abdulkader RS, et al. Trends in the global, regional, and national burden of oral conditions from 1990 to 2021: a systematic analysis for the Global Burden of Disease Study 2021. Lancet. 2025;405(10482):897-910. doi: 10.1016/S0140-6736(24)02811-3
- Xu Z, Wang Y, Li S, et al. Advances of functional nanomaterials as either therapeutic agents or delivery systems in the treatment of periodontitis. Biomater Adv. 2025;175:214326. doi: 10.1016/j.bioadv.2025.214326
- Zhou T, Xie Y, Cheng A, et al. Nanotherapeutics for microenvironment modulation and immune homeostasis in periodontitis treatment. Biomaterials. 2026;326:123713. doi: 10.1016/j.biomaterials.2025.123713
- Molina A, Meyle J, Ram D, Chun Y-HP, Colmenares ME, Davidovich E. Periodontal diseases and conditions in children and adolescents associated with systemic disorders: a systematic review. J Clin Periodontol. 2026;53(7):1199-1225. doi: 10.1111/jcpe.70109
- Uzun EV, Aksaka N, Çelik M, Toygar HU, Balci N. Effect of periodontal disease on bite force and the temporomandibular joint disorders: a cross-sectional study. BMC Oral Health. 2026;26(1):539. doi: 10.1186/s12903-026-07896-5
- Leite FRM, Tay JRH, Chow DY, Ng E, Nascimento GG, Peres MA. Tooth loss and edentulism are associated with poorer quality of life: a systematic review and meta-analyses. J Periodontal Res. 2026. doi: 10.1111/jre.70121
- Tao J, Sun Y, Wang G, Sun J, Dong S, Ding J. Advanced biomaterials for targeting mature biofilms in periodontitis therapy. Bioact Mater. 2025;48:474-492. doi: 10.1016/j.bioactmat.2025.02.026
- Romandini M, Hajishengallis G, Curtis M, Baima G. Periodontal medicine rewired: mechanisms linking periodontitis to systemic diseases. J Periodontal Res. 2026. doi: 10.1111/jre.70099
- Duarte PM, Lazarin R, Vilela N, Feres M. Adjunctive antimicrobials and host modulators in nonsurgical periodontal therapy: focus on patients with diabetes and smokers. Periodontol 2000. 2025. doi: 10.1111/prd.70020
- Tomasi C, Abrahamsson KH, Apatzidou D. Subgingival instrumentation. Periodontol 2000. 2023. doi: 10.1111/prd.12485
- Chen D, Li D, Su L, et al. Stimuli-responsive, antimicrobial-loaded nanocarriers for oral biofilm control and microbiome restoration. Int J Oral Sci. 2026;18(1):17. doi: 10.1038/s41368-025-00422-3
- Tian M, Chen G, Xu J, et al. Epigallocatechin gallate-based nanoparticles with reactive oxygen species scavenging property for effective chronic periodontitis treatment. Chem Eng J. 2022;433:132197. doi: 10.1016/j.cej.2021.132197
- Chen S, Wu Z, Huang Z, Liang C, Lee SJ. Implantable dental barrier membranes as regenerative medicine in dentistry: a comprehensive review. Tissue Eng Regen Med. 2025;22(4):527-549. doi: 10.1007/s13770-025-00704-1
- Wen S, Zheng X, Yin W, et al. Dental stem cell dynamics in periodontal ligament regeneration: from mechanism to application. Stem Cell Res Ther. 2024;15(1):389. doi: 10.1186/s13287-024-04003-9
- Liu G, Xue J, Zhou X, et al. The paradigm shifts of periodontal regeneration strategy: from reparative manipulation to developmental engineering. Bioact Mater. 2025;49:418-436. doi: 10.1016/j.bioactmat.2025.03.009
- Li D, Wang Y, Tian Y, Zheng Y, Lv J, Zhang C. Electro-controlled assembled of biphasic guided bone regeneration membrane for healing of diabetic periodontal bone defects. J Nanobiotechnology. 2026;24(1):289. doi: 10.1186/s12951-026-04224-5
- Zhang X, Zhong Z, Zhan P, et al. Adhesive microneedle-nanosheets with temporally orchestrated antimicrobial, immunomodulatory, and osteogenic functions for periodontal regeneration. Adv Mater. 2026;38(24):e72919. doi: 10.1002/adma.72919
- Damiri F, Fatimi A, Liu Y, et al. Recent advances in 3D bioprinted polysaccharide hydrogels for biomedical applications: a comprehensive review. Carbohydr Polym. 2025;348:122845. doi: 10.1016/j.carbpol.2024.122845
- Li X, Zheng F, Wang X, et al. Biomaterial inks for extrusion-based 3D bioprinting: property, classification, modification, and selection. Int J Bioprint. 2023;9(2):649. doi: 10.18063/ijb.v9i2.649
- Huang D, Li Z, Li G, et al. Biomimetic structural design in 3D-printed scaffolds for bone tissue engineering. Mater Today Bio. 2025;32:101664. doi: 10.1016/j.mtbio.2025.101664
- Grinchevskaia LR, Kardosh AV, Izhbulatova VR, et al. Tiny bricks for oral bioprinting: exploring gingiva and dental pulp-derived organ building blocks. Int J Bioprint. 2026;12(2):026060050. doi: 10.36922/IJB026060050
- Daghrery A, Soares IPM, dos Reis‑Prado AH, de Souza Araújo IJ, Dal-Fabbro R, Bottino MC. Advances in 3D printed scaffolds for periodontal regeneration. Curr Oral Health Rep. 2026;13(1):1. doi: 10.1007/s40496-025-00421-7
- Chen H, Wang Y, Lai Y, et al. Advances of 3D bioprinting technology for periodontal tissue regeneration. iScience. 2025;28(6):112532. doi: 10.1016/j.isci.2025.112532
- Golafshan N, Castilho M, Daghrery A, et al. Composite graded melt electrowritten scaffolds for regeneration of the periodontal ligament-to-bone interface. ACS Appl Mater Interfaces. 2023;15(10):12735-12749. doi: 10.1021/acsami.2c21256
- Verykokou S, Ioannidis C, Angelopoulos C. CBCT-based design of patient-specific 3D bone grafts for periodontal regeneration. J Clin Med. 2023;12(15):5023. doi: 10.3390/jcm12155023
- Xu H, Zhang Y, Zhang Y, et al. 3D bioprinting advanced biomaterials for craniofacial and dental tissue engineering - a review. Mater Des. 2024;241:112886. doi: 10.1016/j.matdes.2024.112886
- Mathur V, Agarwal P, Kasturi M, Srinivasan V, Seetharam RN, Vasanthan KS. Innovative bioinks for 3D bioprinting: exploring technological potential and regulatory challenges. J Tissue Eng. 2025;16:20417314241308022. doi: 10.1177/20417314241308022
- Xu Z, Meng R, Wang Y, et al. Advances of functional two-dimensional nanomaterials in the treatment of oral diseases. Bioengineering (Basel). 2025;12(10):1021. doi: 10.3390/bioengineering12101021
- Jakubovics NS, Goodman SD, Mashburn-Warren L, Stafford GP, Cieplik F. The dental plaque biofilm matrix. Periodontol 2000. 2021;86(1):32-56. doi: 10.1111/prd.12361
- Flemming H-C, van Hullebusch ED, Neu TR, et al. The biofilm matrix: multitasking in a shared space. Nat Rev Microbiol. 2023;21(2):70-86. doi: 10.1038/s41579-022-00791-0
- Jo J, Price-Whelan A, Dietrich LEP. Gradients and consequences of heterogeneity in biofilms. Nat Rev Microbiol. 2022;20(10):593-607. doi: 10.1038/s41579-022-00692-2
- Manoil D, Parga A, Bostanci N, Belibasakis GN. Microbial diagnostics in periodontal diseases. Periodontol 2000. 2024;95(1):176-193. doi: 10.1111/prd.12571
- Akatsu T, Souno H, Fujii A, Minegishi Y, Ota N, Yamashita Y. Characteristics of subgingival plaque microbiome in Japanese older adults with healthy gingiva. J Clin Periodontol. 2025;52(9):1314-1326. doi: 10.1111/jcpe.14192
- Belibasakis GN, Belstrøm D, Eick S, Gursoy UK, Johansson A, Könönen E. Periodontal microbiology and microbial etiology of periodontal diseases: historical concepts and contemporary perspectives. Periodontol 2000. 2023. doi: 10.1111/prd.12473
- Zhang Y, Cai Y, Zhang B, Zhang Y-HPJ. Spatially structured exchange of metabolites enhances bacterial survival and resilience in biofilms. Nat Commun. 2024;15(1):7575. doi: 10.1038/s41467-024-51940-3
- Ugwu CN, Ezeibe EN, Emencheta SC, et al. Biofilms: structure, resistance mechanism, emerging control strategies, and applications. RSC Pharm. 2025;2(6):1376-1407. doi: 10.1039/D5PM00094G
- Wu H, Li Y, Shi L, Liu Y, Shen J. New advances in periodontal functional materials based on antibacterial, anti-inflammatory, and tissue regeneration strategies. Adv Healthc Mater. 2025;14(9):2403206. doi: 10.1002/adhm.202403206
- Wang Y, Xu J, Yu C, et al. Prevention of bacterial biofilm formation on orthodontic brackets by non-crosslinked chitosan coating. Int J Biol Macromol. 2023;251:126283. doi: 10.1016/j.ijbiomac.2023.126283
- Wu Q, Zhang W, Lu Y, et al. Association between periodontitis and inflammatory comorbidities: the common role of innate immune cells, underlying mechanisms and therapeutic targets. Int Immunopharmacol. 2024;128:111558. doi: 10.1016/j.intimp.2024.111558
- Liu A, Hayashi M, Ohsugi Y, et al. The IL-33/ST2 axis is protective against acute inflammation during the course of periodontitis. Nat Commun. 2024;15(1):2707. doi: 10.1038/s41467-024-46746-2
- Li D, Wu M. Pattern recognition receptors in health and diseases. Signal Transduct Target Ther. 2021;6(1):291. doi: 10.1038/s41392-021-00687-0
- Nieboga E, Schuster A, Drapala DM, et al. Synergistic induction of PGE2 by oral pathogens and TNF promotes gingival fibroblast-driven stromal-immune cross-talk in periodontitis. mBio. 2025;16(5):e0004625. doi: 10.1128/mbio.00046-25
- Kim TS, Moutsopoulos NM. Neutrophils and neutrophil extracellular traps in oral health and disease. Exp Mol Med. 2024;56(5):1055-1065. doi: 10.1038/s12276-024-01219-w
- Chen B, Song D, Cheng T, Jin L, Li Y, Liao C. Neutrophil extracellular traps aggravate periodontitis by disturbing regulatory t-cell differentiation. Genes Immun. 2025;26(5):475-485. doi: 10.1038/s41435-025-00350-6
- Mo K, Wang Y, Lu C, Li Z. Insight into the role of macrophages in periodontitis restoration and development. Virulence. 2024;15(1):2427234. doi: 10.1080/21505594.2024.2427234
- Wang Z, Zeng H, Wang C, et al. Tim4 deficiency reduces CD301b+ macrophage and aggravates periodontitis bone loss. Int J Oral Sci. 2024;16(1):20. doi: 10.1038/s41368-023-00270-z
- Hsiao P-Y, Huang R-Y, Huang L-W, et al. MyD88 exacerbates inflammation-induced bone loss by modulating dynamic equilibrium between Th17/Treg cells and subgingival microbiota dysbiosis. J Periodontol. 2024;95(8):764-777. doi: 10.1002/JPER.23-0561
- Sidharthan S, Gopalakrishnan D, Kheur S, Mohapatra S. Assessment of the role of Th17 cell and related biomarkers in periodontitis: a systematic review. Arch Oral Biol. 2025;175:106272. doi: 10.1016/j.archoralbio.2025.106272
- Kinane DF, Lappin DF, Culshaw S. The role of acquired host immunity in periodontal diseases. Periodontol 2000. 2024. doi: 10.1111/prd.12562
- Ahmad P, Slots J, Siqueira WL. Serum cytokines in periodontal diseases. Periodontol 2000. 2025;98(1):138-180. doi: 10.1111/prd.12629
- Jansson L, Lundmark A, Modin C, Gustafsson A, Yucel-Lindberg T. Levels of matrix metalloproteinase-1 (MMP-1), MMP-2, MMP-3, osteopontin, pentraxin-3, and thymic stromal lymphopoietin in crevicular fluid samples from peri-implantitis, periodontitis, and healthy sites. J Periodontal Res. 2025;60(5):473-483. doi: 10.1111/jre.13338
- Hu X, Qiu T, Xiao Y, Wang Y, Guo W, Chen Y. DLP 3D-printed biomimetic periodontium composite with xenogenic treated dentin matrix modulates periodontal regeneration and inflammatory response. Biomater Adv. 2026;182:214668. doi: 10.1016/j.bioadv.2025.214668
- Bullon P, Giampieri F, Bullon B, Battino M. The role of oxidative stress in periodontitis. J Periodontal Res. 2025. doi: 10.1111/jre.70016
- Mohideen K, Krithika C, Jeyanthikumari T, Vani NV, Dhungel S, Ghosh S. The assessment of glutathione, glutathione peroxidase, glutathione reductase, and oxidized glutathione in patients with periodontitis—a systematic review and meta-analysis. Clin Exp Dent Res. 2024;10(3):e907. doi: 10.1002/cre2.907
- Oner F, Soysal F, Gokmenoglu C, Serdar MA, Guney Z. Oxidative stress-driven alterations in FoxO-1 and MMP-9 activity in smoking-associated periodontitis. Oral Dis. 2026. doi: 10.1111/odi.70371
- Guan P, Ruan Q, Li J, et al. Ferroptosis in periodontitis: mechanisms, impacts, and systemic connections. Cell Death Discov. 2025;11(1):283. doi: 10.1038/s41420-025-02550-5
- Su B, Wang F, Liu R, Jiang Y, Zhang Z, Liu Y. Periodontitis aggravates atherosclerosis by inducing inflammatory response and macrophage pyroptosis through the NF-κB/NLRP3/caspase-1 pathway. J Periodontol. Published online May 21, 2026. doi: 10.1002/jper.70146
- Qiu W, Sun Q, Li N, et al. Superoxide dismutase 2 scavenges ROS to promote osteogenic differentiation of human periodontal ligament stem cells by regulating Smad3 in alveolar bone-defective rats. J Periodontol. 2024;95(5):469-482. doi: 10.1002/JPER.23-0469
- Fu E, Kuo C-Y, Hsia Y-J, et al. Role of ferroptosis in periodontitis: an animal study in rats. J Periodontal Res. 2023;58(5):1031-1040. doi: 10.1111/jre.13165
- Zhou Q, Meng Y, Le J, et al. Ferroptosis: mechanisms and therapeutic targets. MedComm (2020). 2024;5(12):e70010. doi: 10.1002/mco2.70010
- Zhang M, Zhai X, Ma T, et al. Sequential therapy for bone regeneration by cerium oxide-reinforced 3D-Printed bioactive glass scaffolds. ACS Nano. 2023;17(5):4433-4444. doi: 10.1021/acsnano.2c09855
- Alghamdi B, Jeon HH, Ni J, et al. Osteoimmunology in periodontitis and orthodontic tooth movement. Curr Osteoporos Rep. 2023;21(2):128-146. doi: 10.1007/s11914-023-00774-x
- Wang Y, Nakagawa M, Luo C, et al. Cellular senescence of RANKL+ osteoblasts and Th17 cells in severe periodontitis with occlusal trauma. J Prosthodont Res. 2025;69(4):533-542. doi: 10.2186/jpr.JPR_D_24_00294
- Uchinuma M, Taketani Y, Kanaya R, et al. Role of Piezo1 in modulating the RANKL/OPG ratio in mouse osteoblast cells exposed to Porphyromonas gingivalis lipopolysaccharide and mechanical stress. J Periodontal Res. 2024;59(4):749-757. doi: 10.1111/jre.13265
- Lv D, Zhang J, Zhang Y, et al. Th17/IL-17A drives alveolar bone loss via the JAK/STAT3-RANKL axis in the periodontal ligament. Oral Dis. 2025. doi: 10.1111/odi.70154
- Veis DJ, O'Brien CA. Osteoclasts, master sculptors of bone. Annu Rev Pathol. 2023;18:257-281. doi: 10.1146/annurev-pathmechdis-031521-040919
- Gao J, Wu Z. M2 macrophage-derived exosomes enable osteogenic differentiation and inhibit inflammation in human periodontal ligament stem cells through promotion of CXCL12 expression. BMC Oral Health. 2024;24(1):1070. doi: 10.1186/s12903-024-04831-4
- Chi J, Yu X, Zhang H, et al. Astaxanthin reverses oxidative stress-induced dysfunction in human periodontal ligament stem cells by activating the Nrf2/ARE pathway. Stem Cells Int. 2026;2026(1):1662288. doi: 10.1155/sci/1662288
- Purwaningrum M, Giachelli CM, Osathanon T, Rattanapuchpong S, Sawangmake C. Dissecting specific wnt components governing osteogenic differentiation potential by human periodontal ligament stem cells through interleukin-6. Sci Rep. 2023;13(1):9055. doi: 10.1038/s41598-023-35569-8
- Sam YH, Nibali L, Ghuman M. Periodontal granulation tissue - to remove or not to remove, that is the question. J Periodontal Res. 2024;59(4):636-646. doi: 10.1111/jre.13261
- Miron RJ. Optimized bone grafting. Periodontol 2000. 2024;94(1):143-160. doi: 10.1111/prd.12517
- Saito MM, Onuma K, Yamakoshi Y. Cementum is key to periodontal tissue regeneration: a review on apatite microstructures for creation of novel cementum-based dental implants. Genesis. 2023;61(3-4):e23514. doi: 10.1002/dvg.23514
- Liu J, He J, Zhang Z, et al. Single-cell transcriptomics identifies PDGFRA+ progenitors orchestrating angiogenesis and periodontal tissue regeneration. Int J Oral Sci. 2025;17(1):56. doi: 10.1038/s41368-025-00384-6
- Gavriiloglou M, Hammad M, Iliopoulos JM, Layrolle P, Apatzidou DA. Bioengineering the junctional epithelium in 3D oral mucosa models. J Funct Biomater. 2024;15(11):330. doi: 10.3390/jfb15110330
- Zhan H, Shi R, Ni H, et al. Functional requirements for guided bone regeneration/guided tissue regeneration membrane design: progress and challenges. Periodontol 2000. 2025. doi: 10.1111/prd.70019
- Wen X, Pei F, Jin Y, Zhao Z. Exploring the mechanical and biological interplay in the periodontal ligament. Int J Oral Sci. 2025;17(1):23. doi: 10.1038/s41368-025-00354-y
- Zhu X, Xiang D, Huo Y, et al. Progress in basic research and clinical strategies for cementum regeneration. Int Dent J. 2025;75(3):1566-1584. doi: 10.1016/j.identj.2025.02.017
- Zuo W, Pan X, Liu Z, He Z, Zhou X, Qian Y. Bioactive scaffolds for periodontal tissue regeneration: synergistic strategies in controlled active ingredient delivery and pathologically responsive microenvironment modulation. ACS Appl Bio Mater. 2025;8(11):9589-9601. doi: 10.1021/acsabm.5c01545
- Fischer NG, de Souza Araújo IJ, Daghrery A, et al. Guidance on biomaterials for periodontal tissue regeneration: fabrication methods, materials and biological considerations. Dent Mater. 2025;41(3):283-305. doi: 10.1016/j.dental.2024.12.019
- Gharraei R, Bergstrom DJ, Chen X. Extrusion bioprinting from a fluid mechanics perspective. Int J Bioprint. 2024;10(6):3973. doi: 10.36922/ijb.3973
- Raghuvaran G, Nitschke BM, Roberts CT, Grunlan MA, Pentzer E. Direct ink writing of porous shape memory polyesters. Mater Adv. 2024;5(14):5763-5771. doi: 10.1039/D4MA00137K
- Peluso V, De Santis R, Gloria A, et al. Design of 3D additive manufactured hybrid scaffolds for periodontal repair strategies. ACS Appl Bio Mater. 2025;8(8):6817-6829. doi: 10.1021/acsabm.5c00561
- Wei P, Cipriani C, Hsieh C-M, Kamani K, Rogers S, Pentzer E. Go with the flow: rheological requirements for direct ink write printability. J Appl Phys. 2023;134(10):100701. doi: 10.1063/5.0155896
- Zhang C, Elvitigala KCML, Mubarok W, Okano Y, Sakai S. Machine learning-based prediction and optimisation framework for as-extruded cell viability in extrusion-based 3D bioprinting. Virtual Phys Prototyp. 2024;19(1):e2400330. doi: 10.1080/17452759.2024.2400330
- Lee SY, Phuc HD, Um SH, Mongrain R, Yoon J-K, Bhang SH. Photocuring 3D printing technology as an advanced tool for promoting angiogenesis in hypoxia-related diseases. J Tissue Eng. 2024;15:20417314241282476. doi: 10.1177/20417314241282476
- Alparslan C, Bayraktar Ş. Advances in digital light processing (DLP) bioprinting: a review of biomaterials and its applications, innovations, challenges, and future perspectives. Polymers (Basel). 2025;17(9):1287. doi: 10.3390/polym17091287
- Yang X, Ma Y, Wang X, et al. A 3D-Bioprinted functional module based on decellularized extracellular matrix bioink for periodontal regeneration. Adv Sci (Weinh). 2023;10(5):2205041. doi: 10.1002/advs.202205041
- Dogan E, Austin A, Pourmostafa A, Yogeshwaran S, Hosseinabadi HG, Miri AK. Design considerations for photoinitiator selection in cell-laden gelatin methacryloyl hydrogels. Biomater Sci. 2026;14(3):807-816. doi: 10.1039/D5BM00550G
- Qian Y, Gong J, Lu K, et al. DLP printed hDPSC-loaded GelMA microsphere regenerates dental pulp and repairs spinal cord. Biomaterials. 2023;299:122137. doi: 10.1016/j.biomaterials.2023.122137
- Jia J, Lei Q, Liu Z, et al. Advances in melt-electrowriting of fibrous bioscaffolds: a high-resolution manufacturing strategy for tissue regeneration. Adv Fiber Mater. 2026;8(2):499-525. doi: 10.1007/s42765-025-00658-y
- Yin Y, Yang H, Han W, et al. Melt electrowriting for biomimetic tissue engineering: advances in scaffold design, materials, and multifunctional applications. Polym Adv Technol. 2025;36(1):e70067. doi: 10.1002/pat.70067
- Devlin BL, Allenby MC, Ren J, et al. Materials design innovations in optimizing cellular behavior on melt electrowritten (MEW) scaffolds. Adv Funct Mater. 2024;34(18):2313092. doi: 10.1002/adfm.202313092
- Jones LS, Rodriguez Cetina Biefer H, Mekkattu M, et al. Volumetric 3D printing and melt-electrowriting to fabricate implantable reinforced cardiac tissue patches. Adv Mater. 2025;37(45):2504765. doi: 10.1002/adma.202504765
- Chen S, Sun J, Wu W, Chen Z. Advances in 3D bioprinting of scaffolds for dental tissue engineering and regeneration. Adv Funct Mater. 2025;35(38):2505258. doi: 10.1002/adfm.202505258
- Miao G, Liang L, Li W, et al. 3D bioprinting of a bioactive composite scaffold for cell delivery in periodontal tissue regeneration. Biomolecules. 2023;13(7):1062. doi: 10.3390/biom13071062
- Tavakoli S, Kocatürkmen A, Oommen OP, Varghese OP. Ultra-fine 3D bioprinting of dynamic hyaluronic acid hydrogel for in vitro modeling. Adv Mater. 2025;37(30):2500315. doi: 10.1002/adma.202500315
- Hu C, Wang C, Bian S, et al. In situ bioprinting: tailored printing strategies for regenerative medicine. Int J Bioprint. 2024;10(5):3366. doi: 10.36922/ijb.3366
- Ivanovski S, Staples R, Arora H, Vaquette C, Alayan J. Alveolar bone regeneration using a 3D-printed patient-specific resorbable scaffold for dental implant placement: a case report. Clin Oral Implants Res. 2024;35(12):1655-1668. doi: 10.1111/clr.14340
- Yogeshwaran S, Goodarzi Hosseinabadi H, Gendy DE, Miri AK. Design considerations and biomaterials selection in embedded extrusion 3D bioprinting. Biomater Sci. 2024;12(18):4506-4518. doi: 10.1039/D4BM00550C
- Arif ZU, Khalid MY, Noroozi R, et al. Recent advances in 3D-printed polylactide and polycaprolactone-based biomaterials for tissue engineering applications. Int J Biol Macromol. 2022;218:930-968. doi: 10.1016/j.ijbiomac.2022.07.140
- Yang H, Lu C, Xu B, et al. Research progress of 3D-printed PLGA scaffolds for the treatment of bone defects. Biomed Eng Online. 2026;25(1):14. doi: 10.1186/s12938-025-01505-2
- Golubchikov DO, Petrov AK, Popkov VA, Evdokimov PV, Putlayev VI. Advances in the fabrication of polycaprolactone-based composite scaffolds for bone tissue engineering: from chemical composition to scaffold architecture. ACS Biomater Sci Eng. 2025;11(6):3201-3227. doi: 10.1021/acsbiomaterials.5c00205
- Zhong Q, Huang S, Huang W, et al. Polydopamine-modified 3D-printed polycaprolactone scaffolds for promoting bone regeneration. Int J Bioprint. 2024;11(1):4995. doi: 10.36922/ijb.4995
- Bahraminasab M, Arabhalvaei M, Ghanbari MA. Indirect 3D printing in tissue engineering: expanding materials used for improved scaffold functionality. Biomed Eng Online. 2025;24(1):147. doi: 10.1186/s12938-025-01475-5
- Mohan T, Gürer F, Bračič D, et al. Functionalization of polycaprolactone 3D scaffolds with hyaluronic acid glycine-peptide conjugates and endothelial cell adhesion. Biomacromolecules. 2025;26(3):1771-1787. doi: 10.1021/acs.biomac.4c01559
- Zhang J-J, Li X, Tian Y, et al. Harnessing mechanical stress with viscoelastic biomaterials for periodontal ligament regeneration. Adv Sci (Weinh). 2024;11(18):2309562. doi: 10.1002/advs.202309562
- Ollier RC, Webber MJ. Mechanoresponsive hydrogels emerging from dynamic and non-covalent interactions. Adv Mater. 2025;37(40):2507397. doi: 10.1002/adma.202507397
- Shao H, Wen K, Liu R, et al. 3D printing of bioceramic multifunctional scaffolds for bone tissue engineering. Adv Funct Mater. 2025;35(49):e09039. doi: 10.1002/adfm.202509039
- Li S, Cui Y, Liu H, et al. Application of bioactive metal ions in the treatment of bone defects. J Mater Chem B. 2022;10(45):9369-9388. doi: 10.1039/D2TB01684B
- Ho C-C, Hsu T-T, Chiu Y-C, Lin Y-H, Xie P-C, Wang C-Y. 3D-printed magnesium/strontium-co-doped calcium silicate scaffolds promote angiogenesis and bone regeneration through synergistic bioactive ion stimulation. J Biol Eng. 2025;19(1):58. doi: 10.1186/s13036-025-00528-6
- Dedeloudi A, Bertelli PM, Martinez-Marcos L, et al. Development of bioceramic bone-inspired scaffolds through single-step melt-extrusion 3D printing for segmental defect treatment. J Funct Biomater. 2025;16(10):358. doi: 10.3390/jfb16100358
- Zhao X, Liu J, Li L. Research progress and challenges in 3D printing of bioceramics and bioceramic matrix composites. Biomimetics (Basel). 2025;10(7):428. doi: 10.3390/biomimetics10070428
- Pádua AS, Graça MP, Silva JC. Polycaprolactone/doped bioactive glass composite scaffolds for bone regeneration. J Funct Biomater. 2025;16(6):200. doi: 10.3390/jfb16060200
- Bilgili HK, Aydin MS, Sahin M, Sahin SB, Cetinel S, Kiziltas G. 3D-Printed functionally graded PCL-HA scaffolds with multi-scale porosity. ACS Omega. 2025;10(7):6502-6519. doi: 10.1021/acsomega.4c06820
- Ghezzi B, Matera B, Meglioli M, et al. Composite PCL scaffold with 70% β-TCP as suitable structure for bone replacement. Int Dent J. 2024;74(6):1220-1232. doi: 10.1016/j.identj.2024.02.013
- Ni X, Cui Y, Salehi M, et al. Piezoelectric biomaterials for bone regeneration: roadmap from dipole to osteogenesis. Adv Sci (Weinh). 2025;12(32):e14969. doi: 10.1002/advs.202414969
- Chen A, Li K, Li Y, et al. Occlusion-activated autonomous piezoelectric implants for adaptive prevention of peri-implantitis. Nat Commun. 2026;17(1):5017. doi: 10.1038/s41467-026-71556-z
- Khazani Y, Rafiee E, Samadi A, Mahmoodi M. Alginate-PVDF piezoelectric hydrogel containing calcium copper titanate- hydroxyapatite as a self-powered scaffold for bone tissue engineering and energy harvesting. Colloids Surf A Physicochem Eng Asp. 2024;687:133537. doi: 10.1016/j.colsurfa.2024.133537
- Li B, Ma Y, Fatima K, et al. 3D printed shape-memory piezoelectric scaffolds with in-situ self-power properties for bone defect repair. J Nanobiotechnology. 2025;23(1):244. doi: 10.1186/s12951-025-03325-x
- Resende MAA, Rigo ECS, Vercik A. Printability of bioinks: a consolidated definition for additive manufacturing. ACS Omega. 2025;10(48):58110-58122. doi: 10.1021/acsomega.5c00727
- Rea M, Di Lisa L, Pagnotta G, et al. Establishing a bioink assessment protocol: GelMA and collagen in the bioprinting of a potential in vitro intestinal model. ACS Biomater Sci Eng. 2025;11(4):2456-2467. doi: 10.1021/acsbiomaterials.5c00034
- Qiu J, Ma S, Qu X. Challenges and innovative strategies in 3D printing of natural biomolecular hydrogels. Nano Select. 2025;6(6):e202400149. doi: 10.1002/nano.202400149
- de Souza Araújo IJ, Perkins RS, Ibrahim MM, Huang GTJ, Zhang W. Bioprinting PDLSC-laden collagen scaffolds for periodontal ligament regeneration. ACS Appl Mater Interfaces. 2024;16(44):59979-59990. doi: 10.1021/acsami.4c13830
- Banigo AT, Nauta L, Zoetebier B, Karperien M. Hydrogel-based bioinks for coaxial and triaxial bioprinting: a review of material properties, printing techniques, and applications. Polymers (Basel). 2025;17(7):917. doi: 10.3390/polym17070917
- Sharma A, Puri V, Huanbutta K, Sangnim T. The role of 3D printing in regenerative medicine: a game-changer in tissue engineering. Int J Mol Sci. 2026;27(6):2589. doi: 10.3390/ijms27062589
- Xu J, Chang L, Xiong Y, Peng Q. Chitosan-based hydrogels as antibacterial/antioxidant/anti-inflammation multifunctional dressings for chronic wound healing. Adv Healthc Mater. 2024;13(30):2401490. doi: 10.1002/adhm.202401490
- Upton A, Mylona A, Zimbitas G. Utilising design of experiment to design an optimised bioink for 3D bioprinting. J Mater Sci. 2025;60(25):10467-10477. doi: 10.1007/s10853-025-11076-1
- Sasikumar SC, Goswami U, Raichur AM. Mucin-based dual cross-linkable IPN hydrogel bioink for 3D bioprinting and cartilage tissue engineering. ACS Appl Bio Mater. 2025;8(2):1186-1200. doi: 10.1021/acsabm.4c01505
- Zhang H, Wang Y, Zheng Z, et al. Strategies for improving the 3D printability of decellularized extracellular matrix bioink. Theranostics. 2023;13(8):2562-2587. doi: 10.7150/thno.81785
- Golebiowska AA, Intravaia JT, Sathe VM, Kumbar SG, Nukavarapu SP. Decellularized extracellular matrix biomaterials for regenerative therapies: advances, challenges and clinical prospects. Bioact Mater. 2024;32:98-123. doi: 10.1016/j.bioactmat.2023.09.017
- Han H, Kim M, Yong U, et al. Tissue-specific gelatin bioink as a rheology modifier for high printability and adjustable tissue properties. Biomater Sci. 2024;12(10):2599-2613. doi: 10.1039/D3BM02111D
- Rosadas M, Silva IV, Costa JB, Ribeiro VP, Oliveira AL. Decellularized dermal matrices: unleashing the potential in tissue engineering and regenerative medicine. Front Mater. 2024;10:1285948. doi: 10.3389/fmats.2023.1285948
- Norahan MH, Sivarasu S, Fayzullin A, et al. Bioengineering of periodontal tissues: cell therapy and biomaterials application. Bioengineering (Basel). 2025;12(11):1213. doi: 10.3390/bioengineering12111213
- Zhao F, Zhang Z, Guo W. The 3-dimensional printing for dental tissue regeneration: the state of the art and future challenges. Front Bioeng Biotechnol. 2024;12:1356580. doi: 10.3389/fbioe.2024.1356580
- Wei Q, An Y, Zhao X, Li M, Zhang J, Cui N. Optimal design of multi-biomaterials mixed extrusion nozzle for 3D bioprinting considering cell activity. Virtual Phys Prototyp. 2025;20(1):e2438897. doi: 10.1080/17452759.2024.2438897
- Wu D, Zhu D, Zhou X, et al. Development of intervertebral disc organoids through directed differentiation of mesenchymal stem cells and hierarchical 3D printing. ACS Nano. 2026;20(12):9619-9637. doi: 10.1021/acsnano.5c14391
- Zhao X, Li N, Zhang Z, et al. Beyond hype: unveiling the real challenges in clinical translation of 3D printed bone scaffolds and the fresh prospects of bioprinted organoids. J Nanobiotechnology. 2024;22(1):500. doi: 10.1186/s12951-024-02759-z
- Gutthedhar M, Hazarika K, Kumawat VS, et al. Beyond graphene: the MXene era in bioprinting. Biomed Eng Online. 2026;25(1):42. doi: 10.1186/s12938-026-01520-x
- Kamaraj M, Moghimi N, Joshi A, et al. Recent advances in handheld and robotic bioprinting approach for tissue engineering. Adv Mater Technol. 2025;10(15):2500206. doi: 10.1002/admt.202500206
- Richards D, Jia J, Yost M, Markwald R, Mei Y. 3D bioprinting for vascularized tissue fabrication. Ann Biomed Eng. 2017;45(1):132-147. doi: 10.1007/s10439-016-1653-z
- Xu Z, Xu J, Wu H, et al. Covalent organic framework-based nanozymes: from physicochemical properties to biomedical applications. Inorg Chem Commun. 2026;191:117126. doi: 10.1016/j.inoche.2026.117126
- Pi Y, Ganabady K, Celiz AD. Enzyme-responsive biomaterials for biomedical applications. Commun Mater. 2025;6(1):263. doi: 10.1038/s43246-025-00983-0
- Ding A, Tang F, Alsberg E. The emerging 4D printing of shape-memory thermomorphs for self-adaptative biomedical implants. Adv Funct Mater. 2025;35(28):2418348. doi: 10.1002/adfm.202418348
- Song W, Huang W, Qu J, et al. The application prospects of 4D printing tissue engineering materials in oral bone regeneration. Int J Bioprint. 2024;11(1). doi: 10.36922/ijb.4450
- Yamada S, Shanbhag S, Mustafa K. Scaffolds in periodontal regenerative treatment. Dent Clin North Am. 2022;66(1):111-130. doi: 10.1016/j.cden.2021.06.004
- Chen TS, Sung ND, Fok MR, Tarce M, Tavedhikul K, Pelekos G. Evaluation of periodontal infrabony defect topography via CBCT and comparisons with direct intrasurgical measurements. Bioengineering (Basel). 2025;12(7):780. doi: 10.3390/bioengineering12070780
- Verykokou S, Ioannidis C, Soile S, et al. The role of cone beam computed tomography in periodontology: from 3D models of periodontal defects to 3D-Printed scaffolds. J Pers Med. 2024;14(2):207. doi: 10.3390/jpm14020207
- Mangano C, Luongo G, Luongo F, et al. Custom-made computer-aided-design/ computer-assisted-manufacturing (CAD/CAM) synthetic bone grafts for alveolar ridge augmentation: a retrospective clinical study with 3 years of follow-up. J Dent. 2022;127:104323. doi: 10.1016/j.jdent.2022.104323
- Blume O, Back M, Dinya E, Palkovics D, Windisch P. Efficacy and volume stability of a customized allogeneic bone block for the reconstruction of advanced alveolar ridge deficiencies at the anterior maxillary region: a retrospective radiographic evaluation. Clin Oral Investig. 2023;27(7):3927-3935. doi: 10.1007/s00784-023-05015-0
- Anderson M, Dubey N, Bogie K, et al. Three-dimensional printing of clinical scale and personalized calcium phosphate scaffolds for alveolar bone reconstruction. Dent Mater. 2022;38(3):529-539. doi: 10.1016/j.dental.2021.12.141
- Daghrery A, Dal-Fabbro R, dos Reis-Prado AH, et al. Guidance on the assessment of the functionality of biomaterials for periodontal tissue regeneration: methodologies and testing procedures. Dent Mater. 2025;41(3):306-318. doi: 10.1016/j.dental.2024.12.018
- Pantazos I, Kapourani A, Chortis A, et al. Personalized drug-loaded 3D-printed scaffolds for periodontal bone repair: structural, mechanical, and controlled release properties. J Pharm Sci. 2025;114(7):103807. doi: 10.1016/j.xphs.2025.103807
- Puleio F, Lo Giudice G, Marenzi G, Bucci R, Nucera R, Lo Giudice R. Digitally designed bone grafts for alveolar defects: a scoping review of CBCT-based CAD/CAM workflows. J Funct Biomater. 2025;16(9):310. doi: 10.3390/jfb16090310
- Dai Y, Wang P, Mishra A, et al. 3D bioprinting and artificial intelligence-assisted biofabrication of personalized oral soft tissue constructs. Adv Healthc Mater. 2025;14(13):2402727. doi: 10.1002/adhm.202402727
- Raju R, Oshima M, Inoue M, et al. Three-dimensional periodontal tissue regeneration using a bone-ligament complex cell sheet. Sci Rep. 2020;10(1):1656. doi: 10.1038/s41598-020-58222-0
- Santos MS, Silva JC, Carvalho MS. Hierarchical biomaterial scaffolds for periodontal tissue engineering: recent progress and current challenges. Int J Mol Sci. 2024;25(16):8562. doi: 10.3390/ijms25168562
- Staples RJ, Ivanovski S, Vaquette C. Fiber guiding scaffolds for periodontal tissue engineering. J Periodontal Res. 2020;55(3):331-341. doi: 10.1111/jre.12729
- Gómez-Cerezo MN, Lozano D, Arcos D, Vallet-Regí M, Vaquette C. The effect of biomimetic mineralization of 3D-printed mesoporous bioglass scaffolds on physical properties and in vitro osteogenicity. Mater Sci Eng C Mater Biol Appl. 2020;109:110572. doi: 10.1016/j.msec.2019.110572
- Daghrery A, Ferreira JA, Xu J, et al. Tissue-specific melt electrowritten polymeric scaffolds for coordinated regeneration of soft and hard periodontal tissues. Bioact Mater. 2023;19:268-281. doi: 10.1016/j.bioactmat.2022.04.013
- Vaquette C, Fan W, Xiao Y, Hamlet S, Hutmacher DW, Ivanovski S. A biphasic scaffold design combined with cell sheet technology for simultaneous regeneration of alveolar bone/periodontal ligament complex. Biomaterials. 2012;33(22):5560-5573. doi: 10.1016/j.biomaterials.2012.04.038
- Fang L, Lin X, Xu R, et al. Advances in the development of gradient scaffolds made of nano-micromaterials for musculoskeletal tissue regeneration. Nano Micro Lett. 2024;17(1):75. doi: 10.1007/s40820-024-01581-4
- Wang D, Ker DFE, Ng KW, et al. Combinatorial mechanical gradation and growth factor biopatterning strategy for spatially controlled bone-tendon-like cell differentiation and tissue formation. NPG Asia Mater. 2021;13(1):26. doi: 10.1038/s41427-021-00294-z
- Santos MS, Cordeiro R, Moura CS, et al. Bioactive nanofibrous scaffolds incorporating decellularized cell-derived extracellular matrix for periodontal tissue engineering. ACS Appl Nano Mater. 2024;7(4):4501-4517. doi: 10.1021/acsanm.4c00140
- Hua W, Xiang J, Wu Y, Yang W, Zhao L. Growth factor-encapsulated triphasic scaffolds of electrospun polylactic acid-polycaprolactone (PLA-PCL) nanofibrous mats combined with a directionally freeze-dried chitosan hydrogel for periodontal tissue regeneration. Mater Adv. 2023;4(20):4798-4811. doi: 10.1039/D3MA00465A
- Costa PF, Vaquette C, Zhang Q, Reis RL, Ivanovski S, Hutmacher DW. Advanced tissue engineering scaffold design for regeneration of the complex hierarchical periodontal structure. J Clin Periodontol. 2014;41(3):283-294. doi: 10.1111/jcpe.12214
- Staples R, Ivanovski S, Vaquette C. Fiber-guiding biphasic scaffold for perpendicular periodontal ligament attachment. Acta Biomater. 2022;150:221-237. doi: 10.1016/j.actbio.2022.07.023
- Staples R, Ivanovski S, Vaswani K, Vaquette C. Melt electrowriting scaffolds with fiber-guiding features for periodontal attachment. Acta Biomater. 2024;180:337-357. doi: 10.1016/j.actbio.2024.04.006
- Lin H-H, Chao P-HG, Tai W-C, Chang P-C. 3D-Printed collagen-based waveform microfibrous scaffold for periodontal ligament reconstruction. Int J Mol Sci. 2021;22(14):7725. doi: 10.3390/ijms22147725
- Shao L, Jiang J, Yuan C, Zhang X, Gu L, Wang X. Omnidirectional anisotropic embedded 3D bioprinting. Mater Today Bio. 2024;27:101160. doi: 10.1016/j.mtbio.2024.101160
- Lee U-L, Yun S, Cao H-L, et al. Bioprinting on 3D printed titanium scaffolds for periodontal ligament regeneration. Cells. 2021;10(6):1337. doi: 10.3390/cells10061337
- Sadtler K, Estrellas K, Allen BW, et al. Developing a pro-regenerative biomaterial scaffold microenvironment requires t helper 2 cells. Science. 2016;352(6283):366-370. doi: 10.1126/science.aad9272
- Li W, Dai F, Zhang S, et al. Pore size of 3D-Printed polycaprolactone/polyethylene glycol/hydroxyapatite scaffolds affects bone regeneration by modulating macrophage polarization and the foreign body response. ACS Appl Mater Interfaces. 2022;14(18):20693-20707. doi: 10.1021/acsami.2c02001
- Chen Z, Yan X, Yin S, et al. Influence of the pore size and porosity of selective laser melted Ti6Al4V ELI porous scaffold on cell proliferation, osteogenesis and bone ingrowth. Mater Sci Eng C Mater Biol Appl. 2020;106:110289. doi: 10.1016/j.msec.2019.110289
- Daghrery A, Ferreira JA, de Souza Araújo IJ, et al. A highly ordered, nanostructured fluorinated CaP-Coated melt electrowritten scaffold for periodontal tissue regeneration. Adv Healthc Mater. 2021;10(21):2101152. doi: 10.1002/adhm.202101152
- Chang PC, Lin ZJ, Luo HT, et al. Degradable RGD-functionalized 3D-Printed scaffold promotes osteogenesis. J Dent Res. 2021;100(10):1109-1117. doi: 10.1177/00220345211024634
- Shan E, Chamorro C, Ferrández-Montero A, et al. In vitro biological properties assessment of 3D-Printed hydroxyapatite-polylactic acid scaffolds intended for bone regeneration. J Funct Biomater. 2025;16(6):218. doi: 10.3390/jfb16060218
- Zhu M, Li X, Xiao L, et al. 3D-printed microfibers encapsulating stem cells in scaffold with tri-culture and two-stage metformin release for bone/vasculature/nerve regeneration in rats. Bioact Mater. 2025;51:399-413. doi: 10.1016/j.bioactmat.2025.05.011
- Zhang Y, Chen Y, Ding T, et al. Janus porous polylactic acid membranes with versatile metal-phenolic interface for biomimetic periodontal bone regeneration. NPJ Regen Med. 2023;8(1):28. doi: 10.1038/s41536-023-00305-3
- Vaquette C, Saifzadeh S, Farag A, Hutmacher DW, Ivanovski S. Periodontal tissue engineering with a multiphasic construct and cell sheets. J Dent Res. 2019;98(6):673-681. doi: 10.1177/0022034519837967
- Wang D, Zhou X, Cao H, et al. Barrier membranes for periodontal guided bone regeneration: a potential therapeutic strategy. Front Mater. 2023;10:1220420. doi: 10.3389/fmats.2023.1220420
- Vahdatinia F, Hooshyarfard A, Jamshidi S, et al. 3D-Printed soft membrane for periodontal guided tissue regeneration. Materials (Basel). 2023;16(4):1364. doi: 10.3390/ma16041364
- dos Santos DM, Moon J-I, Kim D-S, et al. Hierarchical chitin nanocrystal-based 3D printed dual-layer membranes hydrogels: a dual drug delivery nano-platform for periodontal tissue regeneration. ACS Nano. 2024;18(35):24182-24203. doi: 10.1021/acsnano.4c05558
- Abtahi S, Chen X, Shahabi S, Nasiri N. Resorbable membranes for guided bone regeneration: critical features, potentials, and limitations. ACS Mater Au. 2023;3(5):394-417. doi: 10.1021/acsmaterialsau.3c00013
- Wang C-Y, Chiu Y-C, Lee AK, Lin Y-A, Lin P-Y, Shie M-Y. Biofabrication of gingival fibroblast cell-laden collagen/strontium-doped calcium silicate 3D-Printed bi-layered scaffold for osteoporotic periodontal regeneration. Biomedicines. 2021;9(4):431. doi: 10.3390/biomedicines9040431
- Liu P, Li Q, Yang Q, et al. Evaluation of the effect of 3D-bioprinted gingival fibroblast-encapsulated ADM scaffolds on keratinized gingival augmentation. J Periodontal Res. 2023;58(3):564-574. doi: 10.1111/jre.13126
- Li W, Li M, Cai T, Ding Y, Tian W, Guo S. Intelligent biomaterials for periodontitis and peri-implantitis therapies: stimuli-responsive strategies targeting inflammation and regeneration. J Mater Chem B. 2025;13(47):15167-15189. doi: 10.1039/D5TB01852H
- Wang Y, Qiao J, Xu Z, Sun Y, Chang L, Peng Q. 2D Ti3C2Tx MXene-based photothermal therapy for eradicating oral bacterial biofilms. J Photochem Photobiol A Chem. 2026;481:117411. doi: 10.1016/j.jphotochem.2026.117411
- Theodoridis K, Arampatzis AS, Liasi G, et al. 3D-Printed antibacterial scaffolds for the regeneration of alveolar bone in severe periodontitis. Int J Mol Sci. 2023;24(23):16754. doi: 10.3390/ijms242316754
- Li C, Xu X, Gao J, et al. 3D printed scaffold for repairing bone defects in apical periodontitis. BMC Oral Health. 2022;22(1):327. doi: 10.1186/s12903-022-02362-4
- Suo L, Wu H, Wang P, Xue Z, Gao J, Shen J. The improvement of periodontal tissue regeneration using a 3D-printed carbon nanotube/chitosan/sodium alginate composite scaffold. J Biomed Mater Res B Appl Biomater. 2023;111(1):73-84. doi: 10.1002/jbm.b.35133
- Nie Z, Qu Z, Wu S, et al. 3D-printed antimicrobial scaffolds for tissue repair: intrinsic, stimuli-responsive, and topographical strategies. Int J Bioprint. 2026. doi: 10.36922/IJB026230232.
- Chen S, Saeed AFUH, Liu Q, et al. Macrophages in immunoregulation and therapeutics. Signal Transduct Target Ther. 2023;8(1):207. doi: 10.1038/s41392-023-01452-1
- Sanati M, Pieterman I, Levy N, et al. Osteoimmunomodulation by bone implant materials: harnessing physicochemical properties and chemical composition. Biomater Sci. 2025;13(11):2836-2870. doi: 10.1039/D5BM00357A
- Hooshiar MH, Ostadsharifmemar N, Javaheri T, et al. Functionalized 3D-printed scaffolds for enhanced osteogenesis and guided bone regeneration. J Mater Chem B. 2025;13(22):6493-6507. doi: 10.1039/D4TB02788D
- Nie Z, Sun Y, Li K, et al. Non-destructive debridement and tuneable ion release via magnesium abrasion and electro-dissolution promote bone regeneration and osseointegration of infected implants. Mater Today Bio. 2026;38:103183. doi: 10.1016/j.mtbio.2026.103183
- Zheng Y, Mao L, Wang Q, et al. Mitochondria-targeted ROS scavenging natural enzyme cascade nanogels for periodontitis treatment via hypoxia alleviation and immunomodulation. Adv Sci (Weinh). 2025;12(29):e07481. doi: 10.1002/advs.202507481
- Wang H, Chang X, Ma Q, et al. Bioinspired drug-delivery system emulating the natural bone healing cascade for diabetic periodontal bone regeneration. Bioact Mater. 2023;21:324-339. doi: 10.1016/j.bioactmat.2022.08.029
- Whitaker R, Hernaez-Estrada B, Hernandez RM, Santos-Vizcaino E, Spiller KL. Immunomodulatory biomaterials for tissue repair. Chem Rev. 2021;121(18):11305-11335. doi: 10.1021/acs.chemrev.0c00895
- Bousnaki M, Beketova A, Kontonasaki E. A review of in vivo and clinical studies applying scaffolds and cell sheet technology for periodontal ligament regeneration. Biomolecules. 2022;12(3):435. doi: 10.3390/biom12030435
- Venkataiah VS, Handa K, Njuguna MM, et al. Periodontal regeneration by allogeneic transplantation of adipose tissue derived multi-lineage progenitor stem cells in vivo. Sci Rep. 2019;9(1):921. doi: 10.1038/s41598-018-37528-0
- Wang H, Yang L, Huang X, et al. Cementum regeneration strategies: insights from development and periodontal microenvironment. Front Cell Dev Biol. 2025;13:1685609. doi: 10.3389/fcell.2025.1685609
- Tang H, Bi F, Chen G, et al. 3D-bioprinted recombination structure of Hertwig’s epithelial root sheath cells and dental papilla cells for alveolar bone regeneration. Int J Bioprint. 2022;8(3):512. doi: 10.18063/ijb.v8i3.512
- Blaudez F, Ivanovski S, Vaquette C. Harnessing the native extracellular matrix for periodontal regeneration using a melt electrowritten biphasic scaffold. J Funct Biomater. 2023;14(9):479. doi: 10.3390/jfb14090479
- Han P, Raveendran N, Liu C, et al. 3D bioprinted small extracellular vesicles from periodontal cells enhance mesenchymal stromal cell function. Biomater Adv. 2024;158:213770. doi: 10.1016/j.bioadv.2024.213770
- Mei N, Wu Y, Chen B, et al. 3D-printed mesoporous bioactive glass/GelMA biomimetic scaffolds for osteogenic/cementogenic differentiation of periodontal ligament cells. Front Bioeng Biotechnol. 2022;10:950970. doi: 10.3389/fbioe.2022.950970
- Wang Y, Liu M, Zhang W, et al. Mechanical strategies to promote vascularization for tissue engineering and regenerative medicine. Burns Trauma. 2024;12:tkae039. doi: 10.1093/burnst/tkae039
- Mukasheva F, Adilova L, Dyussenbinov A, Yernaimanova B, Abilev M, Akilbekova D. Optimizing scaffold pore size for tissue engineering: insights across various tissue types. Front Bioeng Biotechnol. 2024;12:1444986. doi: 10.3389/fbioe.2024.1444986
- Li S, Wang Z, Wu Z, et al. 3D-bioprinted RGD-Alg/GelMA/PCL scaffolds laden with Schwann-like cells for peripheral nerve reconstruction. Int J Bioprint. 2024;10(4):2908. doi: 10.36922/ijb.2908
- Saleh-Bey-Kinj Z, Heller Y, Socratous G, Christodoulou P. 3D printing in oral drug delivery: technologies, clinical applications and future perspectives in precision medicine. Pharmaceuticals (Basel). 2025;18(7):973. doi: 10.3390/ph18070973
- Denizhan D, Buke AN, Kilicarslan M, Orhan K, Erol HB, Kaskatepe B. Effect of chitosan-alginate polyelectrolyte complex formation and multilayer polymer configuration on the characteristics of 3D-Printed metronidazole-loaded periodontal films. Biopolymers. 2026;117(4):e70107. doi: 10.1002/bip.70107
- Lee S, Choi D, Shim J-H, Nam W. Efficacy of three-dimensionally printed polycaprolactone/beta tricalcium phosphate scaffold on mandibular reconstruction. Sci Rep. 2020;10(1):4979. doi: 10.1038/s41598-020-61944-w
- Liu H, Wang C, Sun X, et al. Silk fibroin/collagen/hydroxyapatite scaffolds obtained by 3D printing technology and loaded with recombinant human erythropoietin in the reconstruction of alveolar bone defects. ACS Biomater Sci Eng. 2022;8(12):5245-5256. doi: 10.1021/acsbiomaterials.2c00690
- Sun X, Mao Y, Liu B, et al. Mesenchymal stem cell-derived exosomes enhance 3D-Printed scaffold functions and promote alveolar bone defect repair by enhancing angiogenesis. J Pers Med. 2023;13(2):180. doi: 10.3390/jpm13020180
- Wang Q, Sun J, Jiang H, Yu M. Emerging roles of extracellular vesicles in oral and maxillofacial areas. Int J Oral Sci. 2025;17(1):11. doi: 10.1038/s41368-024-00341-9
- Kapoor DU, Pareek A, Uniyal P, Prajapati BG, Thanawuth K, Sriamornsak P. Innovative applications of 3D printing in personalized medicine and complex drug delivery systems. iScience. 2025;28(10):113505. doi: 10.1016/j.isci.2025.113505
- Li H, Li B, Lv D, Li W, Lu Y, Luo G. Biomaterials releasing drug responsively to promote wound healing via regulation of pathological microenvironment. Adv Drug Deliv Rev. 2023;196:114778. doi: 10.1016/j.addr.2023.114778
- Yuan X, Wang Z, Che L, et al. Recent developments and challenges of 3D bioprinting technologies. Int J Bioprint. 2024;10(2):1752. doi: 10.36922/ijb.1752
- Karvinen J, Kellomäki M. Design aspects and characterization of hydrogel-based bioinks for extrusion-based bioprinting. Bioprinting. 2023;32:e00274. doi: 10.1016/j.bprint.2023.e00274
- Ji Y, Lv Z, Jin H, Chen J, Tang X. Three-dimensional bioprinting in tendon/ ligament-bone interface regeneration: from design innovations to performance enhancement. Int J Bioprint. 2025;12(1):1-18. doi: 10.36922/ijb025410419
- Ibrahimi S, D’Andrea L, Gastaldi D, Rivolta MW, Vena P. Machine learning approaches for the design of biomechanically compatible bone tissue engineering scaffolds. Comput Methods Appl Mech Eng. 2024;423:116842. doi: 10.1016/j.cma.2024.116842
- Grinchevskaia L, Revokatova D, Norahan MH, et al. Recent advances in periodontal regenerative medicine: a focus on the role of mechanical stimulation. Biomedicines. 2025;13(11):2839. doi: 10.3390/biomedicines13112839
- Sun Q, Li Y, Luo P, He H. Animal models for testing biomaterials in periodontal regeneration. Biomater Transl. 2023;4(3):142-150. doi: 10.12336/biomatertransl.2023.03.003
- Sriram G, Makkar H. Microfluidic organ-on-chip systems for periodontal research: advances and future directions. Front Bioeng Biotechnol. 2024;12:1490453. doi: 10.3389/fbioe.2024.1490453
- Adalbert L, Kanti SP, Jójárt-Laczkovich O, Akel H, Csóka I. Expanding quality by design principles to support 3D printed medical device development following the renewed regulatory framework in Europe. Biomedicines. 2022;10(11):2947. doi: 10.3390/biomedicines10112947
- Guo Y, Shi Z, Han L, et al. Infection-sensitive SPION/PLGA scaffolds promote periodontal regeneration via antibacterial activity and macrophage-phenotype modulation. ACS Appl Mater Interfaces. 2024;16(32):41855-41868. doi: 10.1021/acsami.4c06430
- Jiang Y, Li X, Li Z, Jiang H, Wang B, Xiang L. Smart stimuli-responsive biomaterials for oral and maxillofacial tissue repair and regeneration. Chem Eng J. 2025;524:168339. doi: 10.1016/j.cej.2025.168339
