2609005244
  • Open Access
  • Review

Polysaccharide-Based Biomaterials in Oral Regenerative Medicine: Mechanisms, Engineering Strategies, and Translational Perspectives

  • Dan Qiao 1,   
  • Xinyi Chen 2,   
  • Yanan Wei 1,   
  • Yangheng Zhang 2,*,   
  • Fuhua Yan 2,*

Received: 29 Aug 2026 | Revised: 14 Sep 2026 | Accepted: 21 Sep 2026 | Published: 29 Sep 2026

Abstract

Oral regenerative medicine seeks to repair or regenerate the pulp-dentin complex, periodontal tissues, jawbone, and oral mucosa. Nevertheless, this field confronts considerable challenges, including the intricate oral microenvironment, the body’s limited intrinsic regenerative capacity, and the requirement for coordinated regeneration across multiple tissue types. Natural and engineered polysaccharides have emerged as highly promising regenerative platforms, owing to their excellent biocompatibility, extracellular matrix-mimicking properties, chemical tunability, and capacity for local delivery. This review systematically highlights recent advances in polysaccharide-mediated regeneration of oral and craniofacial tissues. First, polysaccharides are classified into three categories: linear non-sulfated polysaccharides, nitrogen-containing cationic polysaccharides, and sulfated polysaccharides, with an analysis of their structure–function relationships. Second, the key mechanisms through which polysaccharides modulate cellular behavior, reshape the immune microenvironment, regulate biomineralization, and enable the spatiotemporal delivery of bioactive molecules and cell-free therapeutic cargo are clarified. Third, tissue-specific applications of polysaccharide-based materials in pulp-dentin complex regeneration, periodontal tissue regeneration, and craniofacial bone regeneration are systematically reviewed. Furthermore, engineering design strategies—including chemical functionalization, physical assembly, and smart and bioinstructive engineering—alongside advanced manufacturing technologies such as 3D printing, electrospinning, and microsphere-based delivery systems, are discussed. Finally, this review highlights critical challenges in clinical translation, including material standardization, manufacturability, and clinical validation, while proposing future directions centered on mechanism-guided rational design, personalized precision therapy, and AI-assisted development. These insights aim to provide a theoretical framework and practical guidance for advancing next-generation polysaccharide-based biomaterials in oral regenerative medicine.

Graphical Abstract

References 

  • 1.

    Mohabatpour, F.; Chen, X.; Papagerakis, S.; et al. Novel trends, challenges and new perspectives for enamel repair and regeneration to treat dental defects. Biomater. Sci. 2022, 10, 3062–3087. https://doi.org/10.1039/d2bm00072e.

  • 2.

    Kao, R.T.; Nares, S.; Reynolds, M.A. Periodontal Regeneration – Intrabony Defects: A Systematic Review from the AAP Regeneration Workshop. J. Periodontol. 2015, 86, S77–104. https://doi.org/10.1902/jop.2015.130685.

  • 3.

    Huang, X.; Lou, Y.; Duan, Y.; et al. Biomaterial scaffolds in maxillofacial bone tissue engineering: A review of recent advances. Bioact. Mater. 2024, 33, 129–156. https://doi.org/10.1016/j.bioactmat.2023.10.031.

  • 4.

    Hazrati, P.; Mirtaleb, M.H.; Boroojeni, H.S.H.; et al. Current Trends, Advances, and Challenges of Tissue Engineering-Based Approaches of Tooth Regeneration: A Review of the Literature. Curr. Stem Cell Res. Ther. 2024, 19, 473–496. https://doi.org/10.2174/1574888x17666220818103228.

  • 5.

    Fallacara, A.; Durini, E.; Vertuani, S.; et al. Hyaluronic Acid Fillers in Soft Tissue Regeneration. Facial Plast. Surg. 2017, 33, 087–096. https://doi.org/10.1055/s-0036-1597685.

  • 6.

    Jin, M.; Shi, J.; Zhu, W.; et al. Polysaccharide-Based Biomaterials in Tissue Engineering: A Review. Tissue Eng. Part B Rev. 2021, 27, 604–626. https://doi.org/10.1089/ten.teb.2020.0208.

  • 7.

    Ali, A.; Ahmed, S. A review on chitosan and its nanocomposites in drug delivery. Int. J. Biol. Macromol. 2018, 109, 273–286. https://doi.org/10.1016/j.ijbiomac.2017.12.078.

  • 8.

    Sodhi, H.; Panitch, A. Glycosaminoglycans in Tissue Engineering: A Review. Biomolecules 2020, 11, 29. https://doi.org/10.3390/biom11010029.

  • 9.

    Li, Z.W.; Du, Z.M.; Wang, Y.W.; et al. Chemical Modification, Characterization, and Activity Changes of Land Plant Polysaccharides: A Review. Polymers 2022, 14, 4161. https://doi.org/10.3390/polym14194161.

  • 10.

    Liu, Z.; Wang, S.; Yang, S.; et al. Bridging Gaps in Oral Mucosa Regeneration: Advances and Challenges. Tissue Eng. Part B Rev. 2025. 19373368251405708. https://doi.org/10.1177/19373368251405708.

  • 11.

    Constantin, V.; Luchian, I.; Virvescu, D.I.; et al. Hyaluronic Acid-Based Gels and Biomaterial Systems for Oral Wound Healing: Design and Clinical Translation. Gels 2026, 12, 262. https://doi.org/10.3390/gels12030262.

  • 12.

    Brovold, M.; Almeida, J.I.; Pla-Palacín, I.; et al. Naturally-Derived Biomaterials for Tissue Engineering Applications. Adv. Exp. Med. Biol. 2018, 1077, 421–449.

  • 13.

    Tavianatou, A.G.; Caon, I.; Franchi, M.; et al. Hyaluronan: molecular size‐dependent signaling and biological functions in inflammation and cancer. FEBS J. 2019, 286, 2883–2908. https://doi.org/10.1111/febs.14777.

  • 14.

    Gomez-Florit, M.; Pardo, A.; Domingues, R.M.A.; et al. Natural-Based Hydrogels for Tissue Engineering Applications. Molecules 2020, 25, 5858. https://doi.org/10.3390/molecules25245858.

  • 15.

    Ren, Y.; Wang, Q.; Xu, W.; et al. Alginate-based hydrogels mediated biomedical applications: A review. Int. J. Biol. Macromol. 2024, 279, 135019. https://doi.org/10.1016/j.ijbiomac.2024.135019.

  • 16.

    Rastogi, P.; Kandasubramanian, B. Review of alginate-based hydrogel bioprinting for application in tissue engineering. Biofabrication 2019, 11, 042001. https://doi.org/10.1088/1758-5090/ab331e.

  • 17.

    Holiel, A.A.; Mahmoud, E.M.; Abdel-Fattah, W.M. Tomographic evaluation of direct pulp capping using a novel injectable treated dentin matrix hydrogel: a 2-year randomized controlled clinical trial. Clin. Oral Investig. 2021, 25, 4621–4634. https://doi.org/10.1007/s00784-021-03775-1.

  • 18.

    Holiel, A.A.; Mahmoud, E.M.; Abdel-Fattah, W.M.; et al. Histological evaluation of the regenerative potential of a novel treated dentin matrix hydrogel in direct pulp capping. Clin. Oral Investig. 2021, 25, 2101–2112. https://doi.org/10.1007/s00784-020-03521-z.

  • 19.

    Bagio, D.A.; Lestari, N.A.; Putra, W.A.; et al. The effect of hyaluronic acid conditioned media on hDPSCs differentiation through CD44 and transforming growth factor-β1 expressions. J. Adv. Pharm. Technol. Res. 2023, 14, 89–93. https://doi.org/10.4103/japtr.japtr_649_22.

  • 20.

    Czajkowska, K.; Rybicki, M.; Kłosiński, K.K.; et al. Factors Determining the Antimicrobial Effectiveness of Chitosan: A Critical Analysis of the Impact of Molecular Weight and Degree of Deacetylation. Molecules 2026, 31, 2412. https://doi.org/10.3390/molecules31142412.

  • 21.

    Aghbashlo, M.; Amiri, H.; Moosavi Basri, S.M.; et al. Tuning chitosan’s chemical structure for enhanced biological functions. Trends Biotechnol. 2023, 41, 785–797. https://doi.org/10.1016/j.tibtech.2022.11.009.

  • 22.

    Pathak, K.; Misra, S.K.; Sehgal, A.; et al. Biomedical Applications of Quaternized Chitosan. Polymers 2021, 13, 2514. https://doi.org/10.3390/polym13152514.

  • 23.

    Alshahhoud, A.; Rikab, M.S.; Issa, N.; et al. A Comparison Between Three Types of Scaffolds for Pulp Regeneration: A Histological Study on Dogs. Clin. Exp. Dent. Res. 2024, 10, e70031. https://doi.org/10.1002/cre2.70031.

  • 24.

    Wu, J.; Wang, P.; Yin, Y.; et al. Cationic Biopolymeric Scaffold of Chelating Nanohydroxyapatite Self-Regulates Intraoral Microenvironment for Periodontal Bone Regeneration. ACS Appl. Mater. Interfaces 2023, 15, 55409–55422. https://doi.org/10.1021/acsami.3c13047.

  • 25.

    Alshahhoud, A.; Rekab, M.S.; Issa, N.; et al. Application of Three Types of Scaffolds in Pulp Regeneration for Permanent Mature Teeth with Periapical Lesions: A Randomized Controlled Trial. Eur. Endod. J. 2024, 9, 352–364. https://doi.org/10.14744/eej.2024.60783.

  • 26.

    Kang, Y.; Xu, J.; Meng, L.A.; et al. 3D bioprinting of dECM/Gel/QCS/nHAp hybrid scaffolds laden with mesenchymal stem cell-derived exosomes to improve angiogenesis and osteogenesis. Biofabrication 2023, 15, 024103. https://doi.org/10.1088/1758-5090/acb6b8.

  • 27.

    Huang, K.X.; Zhou, L.Y.; Chen, J.Q.; et al. Applications and perspectives of quaternized cellulose, chitin and chitosan: A review. Int. J. Biol. Macromol. 2023, 242, 124990. https://doi.org/10.1016/j.ijbiomac.2023.124990.

  • 28.

    Huang, L.; Wu, T.; Sun, J.; et al. Biocompatible chitin-based Janus hydrogel membranes for periodontal repair. Acta Biomater. 2024, 190, 219–232. https://doi.org/10.1016/j.actbio.2024.10.038.

  • 29.

    Alizadeh, S.; Ameri, Z.; Daemi, H.; et al. Sulfated polysaccharide as biomimetic biopolymers for tissue engineering scaffolds fabrication: Challenges and opportunities. Carbohydr. Polym. 2024, 336, 122124. https://doi.org/10.1016/j.carbpol.2024.122124.

  • 30.

    Mhanna, R.; Becher, J.; Schnabelrauch, M.; et al. Sulfated Alginate as a Mimic of Sulfated Glycosaminoglycans: Binding of Growth Factors and Effect on Stem Cell Behavior. Adv. Biosyst. 2017, 1, 1700043. https://doi.org/10.1002/adbi.201700043.

  • 31.

    Malaeb, W.; Bahmad, H.F.; Abou-Kheir, W.; et al. The sulfation of biomimetic glycosaminoglycan substrates controls binding of growth factors and subsequent neural and glial cell growth. Biomater. Sci. 2019, 7, 4283–4298. https://doi.org/10.1039/c9bm00964g.

  • 32.

    Freeman, I.; Kedem, A.; Cohen, S. The effect of sulfation of alginate hydrogels on the specific binding and controlled release of heparin-binding proteins. Biomaterials 2008, 29, 3260–3268. https://doi.org/10.1016/j.biomaterials.2008.04.025.

  • 33.

    Ye, J.; Huang, B.; Gong, P. Nerve growth factor-chondroitin sulfate/hydroxyapatite-coating composite implant induces early osseointegration and nerve regeneration of peri-implant tissues in Beagle dogs. J. Orthop. Surg. Res. 2021, 16, 51. https://doi.org/10.1186/s13018-020-02177-5.

  • 34.

    Liu, T.; Gao, Y.; Guo, Z.; et al. An injectable hyaluronic acid/chondroitin sulfate hydrogel capturing stem cell factors attenuates periodontitis. Colloids Surfaces B Biointerfaces 2026, 264, 115641. https://doi.org/10.1016/j.colsurfb.2026.115641.

  • 35.

    Jafari, A.; Farahani, M.; Sedighi, M.; et al. Carrageenans for tissue engineering and regenerative medicine applications: A review. Carbohydr. Polym. 2022, 281, 119045. https://doi.org/10.1016/j.carbpol.2021.119045.

  • 36.

    He, Z.; Zhou, X.; Wang, Y.; et al. Asymmetric barrier membranes based on polysaccharide micro-nanocomposite hydrogel: Synthesis, characterization, and their antibacterial and osteogenic activities. Carbohydr. Polym. 2021, 273, 118525. https://doi.org/10.1016/j.carbpol.2021.118525.

  • 37.

    Kikionis, S.; Iliou, K.; Karra, A.G.; et al. Development of Bi- and Tri-Layer Nanofibrous Membranes Based on the Sulfated Polysaccharide Carrageenan for Periodontal Tissue Regeneration. Mar. Drugs 2023, 21, 565. https://doi.org/10.3390/md21110565.

  • 38.

    Wahnou, H.; Chgari, O.; Ndayambaje, M.; et al. Carrageenan and TLR4 Crosstalk: A Comprehensive Review of Inflammatory Responses in Animal Models. Recent Adv. Inflamm. Allergy Drug Discov. 2025, 19, 5–17. https://doi.org/10.2174/0127722708303188240708071523.

  • 39.

    Guo, J.; Shang, X.; Chen, P.; et al. How does carrageenan cause colitis? A review. Carbohydr. Polym. 2022, 302, 120374. https://doi.org/10.1016/j.carbpol.2022.120374.

  • 40.

    Wang, Y.; Xing, M.; Cao, Q.; et al. Biological Activities of Fucoidan and the Factors Mediating Its Therapeutic Effects: A Review of Recent Studies. Mar. Drugs 2019, 17, 183. https://doi.org/10.3390/md17030183.

  • 41.

    Eshwar, S.; Konuganti, K.; Manvi, S.; et al. Evaluation of Osteogenic Potential of Fucoidan Containing Chitosan Hydrogel in the Treatment of Periodontal Intra-Bony Defects—A Randomized Clinical Trial. Gels 2023, 9, 573. https://doi.org/10.3390/gels9070573.

  • 42.

    Zayed, A.; Ulber, R. Fucoidan production: Approval key challenges and opportunities. Carbohydr. Polym. 2019, 211, 289–297. https://doi.org/10.1016/j.carbpol.2019.01.105.

  • 43.

    Zayed, A.; El-Aasr, M.; Ibrahim, A.R.S.; et al. Fucoidan Characterization: Determination of Purity and Physicochemical and Chemical Properties. Mar. Drugs 2020, 18, 571. https://doi.org/10.3390/md18110571.

  • 44.

    Wang, P.; Chi, L.; Zhang, Z.; et al. Heparin: An old drug for new clinical applications. Carbohydr. Polym. 2022, 295, 119818. https://doi.org/10.1016/j.carbpol.2022.119818.

  • 45.

    Ying, Y.; Li, B.; Liu, C.; et al. Shape-Memory ECM-Mimicking Heparin-Modified Nanofibrous Gelatin Scaffold for Enhanced Bone Regeneration in Sinus Augmentation. ACS Biomater. Sci. Eng. 2022, 8, 218–231. https://doi.org/10.1021/acsbiomaterials.1c01365.

  • 46.

    Litwiniuk, M.; Krejner, A.; Speyrer, M.S.; et al. Hyaluronic Acid in Inflammation and Tissue Regeneration.. Wounds 2016, 28, 78–88.

  • 47.

    Han, B.; Cao, C.; Wang, A.; et al. Injectable Double-Network Hydrogel-Based Three-Dimensional Cell Culture Systems for Regenerating Dental Pulp. ACS Appl. Mater. Interfaces 2023, 15, 7821–7832. https://doi.org/10.1021/acsami.2c20848.

  • 48.

    Zhang, S.; Jia, Y.; Liu, J.; et al. A viscoelastic alginate-based hydrogel network coordinated with spermidine for periodontal ligament regeneration. Regen. Biomater. 2023, 10, rbad009. https://doi.org/10.1093/rb/rbad009.

  • 49.

    Feng, Q.; Zhang, M.; Zhang, G.; et al. A whole-course-repair system based on ROS/glucose stimuli-responsive EGCG release and tunable mechanical property for efficient treatment of chronic periodontitis in diabetic rats. J. Mater. Chem. B 2024, 12, 3719–3740. https://doi.org/10.1039/d3tb02898d.

  • 50.

    Wang, D.; Lv, Y.; Xie, F.; et al. An antioxidant, injectable hydrogel with mitochondrial fusion effect promotes inflamed dental pulp repair via immunomodulation and reactive oxygen species scavenging. Biomaterials 2026, 329, 123985. https://doi.org/10.1016/j.biomaterials.2026.123985.

  • 51.

    Huangfu, Y.; Zhao, Z.; Liu, X.; et al. An Off‐the‐Shelf Artificial Blood Clot Hydrogel Neutralizing Multiple Proinflammatory Mediators for Pro‐Regenerative Periodontitis Treatment. Adv. Sci. 2025, 12, e04106. https://doi.org/10.1002/advs.202504106.

  • 52.

    Qiao, D.; Cheng, S.; Xing, Z.; et al. Bio-inspired glycosylated nano-hydroxyapatites enhance endogenous bone regeneration by modulating macrophage M2 polarization. Acta Biomater. 2023, 162, 135–148. https://doi.org/10.1016/j.actbio.2023.03.027.

  • 53.

    Qiao, D.; Cheng, S.; Song, S.; et al. Polarized M2 macrophages induced by glycosylated nano‐hydroxyapatites activate bone regeneration in periodontitis therapy. J. Clin. Periodontol. 2024, 51, 1054–1065. https://doi.org/10.1111/jcpe.13999.

  • 54.

    Wang, S.; Chen, X.; Li, Q.; et al. Longan polysaccharides promote Th1 and Treg cell differentiation via dendritic cells. Int. J. Biol. Macromol. 2025, 321, 146462. https://doi.org/10.1016/j.ijbiomac.2025.146462.

  • 55.

    Zhu, Y.; Ali, A.; Mulinari dos Santos, G.; et al. A Chitosan-based Hydrogel to Modulate Immune Cells and Promote Periodontitis Healing in the High-Fat Diet-induced Periodontitis Rat Model. Acta Biomater. 2025, 200, 452–463. https://doi.org/10.1016/j.actbio.2025.05.034.

  • 56.

    Romo, M.; López-Vicario, C.; Pérez-Romero, N.; et al. Small fragments of hyaluronan are increased in individuals with obesity and contribute to low-grade inflammation through TLR-mediated activation of innate immune cells. Int J Obes Lond 2022, 46, 1960–1969. https://doi.org/10.1038/s41366-022-01187-z.

  • 57.

    Han, W.; Lv, Y.; Sun, Y.; et al. The anti-inflammatory activity of specific-sized hyaluronic acid oligosaccharides. Carbohydr. Polym. 2021, 276, 118699. https://doi.org/10.1016/j.carbpol.2021.118699.

  • 58.

    Hadagalu Revana Siddappa, R.; Bishop, E.; Ali, A.; et al. Engineered Immunomodulatory Nanoparticles Inhibit Root Resorption and Ankylosis. J. Endod. 2024, 50, 1579–1592.e3. https://doi.org/10.1016/j.joen.2024.08.006.

  • 59.

    Wang, Z.; Zhang, A.; Chen, L.; et al. Preparation and anti-inflammation activity of λ-carrageenan oligosaccharides degraded by a novel λ-carrageenase Car3193. Int. J. Biol. Macromol. 2024, 293, 139282. https://doi.org/10.1016/j.ijbiomac.2024.139282.

  • 60.

    Yao, Z.; Xu, L.; Jin, L.; et al. κ-Carrageenan Oligosaccharides Inhibit the Inflammation of Lipopolysaccharide-Activated Microglia Via TLR4/NF-κB and p38/JNK MAPKs Pathways. Neurochem. Res. 2021, 47, 295–304. https://doi.org/10.1007/s11064-021-03443-6.

  • 61.

    Liu, Y.; Ji, L.; Zhu, F.; et al. Sulfated chitosan mitigates acute lung injury induced bone loss via immunoregulation. Bone Res. 2026, 14, 18. https://doi.org/10.1038/s41413-025-00475-4.

  • 62.

    Zhang, W.; Lee, P.C.W.; Jin, J.O. Anti-Inflammatory Effect of Fucoidan from Costaria costata Inhibited Lipopolysaccharide-Induced Inflammation in Mice. Mar. Drugs 2024, 22, 401. https://doi.org/10.3390/md22090401.

  • 63.

    Xie, Y.; Wang, Z.; Liu, L.; et al. Fucoidan-hybrid hydroxyapatite nanoparticles promote the osteogenic differentiation of human periodontal ligament stem cells under inflammatory condition. Int. J. Biol. Macromol. 2024, 270, 132416. https://doi.org/10.1016/j.ijbiomac.2024.132416.

  • 64.

    Zhai, J.; Yang, X.; Ren, S.; et al. Spatiotemporally programmable hydrogel enables NIR-triggered biofilm disruption and mitophagy-driven immunometabolic remodeling for periodontitis. Biomaterials 2026, 334, 124281. https://doi.org/10.1016/j.biomaterials.2026.124281.

  • 65.

    Liu, Y.; Li, J.; Guo, R.; et al. Bioinspired nanomicelles with octopus-like adhesion for microenvironmental reprogramming in periodontitis. J. Control. Release 2026, 392, 114649. https://doi.org/10.1016/j.jconrel.2026.114649.

  • 66.

    Cui, Z.; Liu, Z.; Zhang, Z.; et al. On-demand amorphous calcium phosphate-mediated regeneration of dentin and enamel using ion-regulated hydroxypropyl methylcellulose and carboxymethyl chitosan hydrogels. Carbohydr. Polym. 2026, 381, 125170. https://doi.org/10.1016/j.carbpol.2026.125170.

  • 67.

    Iwasaki, A.; Hatakeyama, M.; Liu, Q.; et al. Proliferation and differentiation of human dental pulp stem cells on phosphorylated cellulose nanofiber scaffolds. Carbohydr. Polym. 2025, 359, 123593. https://doi.org/10.1016/j.carbpol.2025.123593.

  • 68.

    Shamszadeh, S.; Asgary, S.; Akrami, M.; et al. Development of a Thermoresponsive Core–Shell Hydrogel for Sequential Delivery of Antibiotics and Growth Factors in Regenerative Endodontics. Front. Biosci.-Elite 2024, 16, 32. https://doi.org/10.31083/j.fbe1604032.

  • 69.

    Fei, Y.; Wang, X.; Ling, Z.; et al. Angiogenic apoptotic vesicle-laden silk fibroin /sodium alginate hydrogel for pulp regeneration. Mater. Today Bio 2025, 33, 102060. https://doi.org/10.1016/j.mtbio.2025.102060.

  • 70.

    Hoveizi, E.; Naddaf, H.; Ahmadianfar, S.; et al. Encapsulation of human endometrial stem cells in chitosan hydrogel containing titanium oxide nanoparticles for dental pulp repair and tissue regeneration in male Wistar rats. J. Biosci. Bioeng. 2023, 135, 331–340. https://doi.org/10.1016/j.jbiosc.2022.12.009.

  • 71.

    Singh, H.; Rathee, K.; Kaur, A.; et al. Pulp Regeneration in an Immature Maxillary Central Incisor Using Hyaluronic Acid Hydrogel. Contemp. Clin. Dent. 2021, 12, 94–98. https://doi.org/10.4103/ccd.ccd_149_20.

  • 72.

    Abdelsalam, M.; Elgendy, A.; Seida, A.; et al. Histological evaluation of the regenerative potential of injectable hyaluronic acid hydrogel or collagen with blood clot as scaffolds during revascularization of immature necrotic dog’s teeth. Open Vet. J. 2024, 14, 3004–3016. https://doi.org/10.5455/ovj.2024.v14.i11.29.

  • 73.

    Loukelis, K.; Machla, F.; Bakopoulou, A.; et al. Kappa-Carrageenan/Chitosan/Gelatin Scaffolds Provide a Biomimetic Microenvironment for Dentin-Pulp Regeneration. Int. J. Mol. Sci. 2023, 24, 6465. https://doi.org/10.3390/ijms24076465.

  • 74.

    Saravana Karthikeyan, B.; Madhubala, M.M.; Rajkumar, G.; et al. Physico-chemical and biological characterization of synthetic and eggshell derived nanohydroxyapatite/carboxymethyl chitosan composites for pulp-dentin tissue engineering. Int. J. Biol. Macromol. 2024, 271, 132620. https://doi.org/10.1016/j.ijbiomac.2024.132620.

  • 75.

    Atila, D.; Chen, C.Y.; Lin, C.P.; et al. In vitro evaluation of injectable Tideglusib-loaded hyaluronic acid hydrogels incorporated with Rg1-loaded chitosan microspheres for vital pulp regeneration. Carbohydr. Polym. 2022, 278, 118976. https://doi.org/10.1016/j.carbpol.2021.118976.

  • 76.

    Bordini, E.A.F.; Cassiano, F.B.; Bronze-Uhle, E.S.; et al. Chitosan in association with osteogenic factors as a cell-homing platform for dentin regeneration: Analysis in a pulp-in-a-chip model. Dent. Mater. 2022, 38, 655–669. https://doi.org/10.1016/j.dental.2022.02.004.

  • 77.

    Mirzaeei, S.; Pourfarzi, S.; Saeedi, M.; et al. Development of a PVA/PCL/CS-Based Nanofibrous Membrane for Guided Tissue Regeneration and Controlled Delivery of Doxycycline Hydrochloride in Management of Periodontitis: In Vivo Evaluation in Rats. AAPS PharmSciTech 2024, 25, 27. https://doi.org/10.1208/s12249-024-02735-8.

  • 78.

    Li, A.; Khan, I.N.; Khan, I.U.; et al. Gellan Gum-Based Bilayer Mucoadhesive Films Loaded with Moxifloxacin Hydrochloride and Clove Oil for Possible Treatment of Periodontitis. Drug Des. Dev. Ther. 2021, 15, 3937–3952. https://doi.org/10.2147/dddt.s328722.

  • 79.

    Eftimie Totu, E.; Mănuc, D.; Totu, T.; et al. Considerations on the Controlled Delivery of Bioactive Compounds through Hyaluronic Acid Membrane. Membranes 2022, 12, 303. https://doi.org/10.3390/membranes12030303.

  • 80.

    Xu, G.; Xi, L.; Huang, X.; et al. Anti-aging chitosan/gelatin film crosslinked by α-arbutin for bone regeneration by free radical scavenging to prevent osteoblast senescence. Biomed. Mater. 2025, 20, 025019. https://doi.org/10.1088/1748-605x/adae6d.

  • 81.

    Murali, V.P.; Guerra, F.D.; Ghadri, N.; et al. Simvastatin loaded chitosan guided bone regeneration membranes stimulate bone healing. J. Periodontal Res. 2021, 56, 877–884. https://doi.org/10.1111/jre.12883.

  • 82.

    Zhong, X.; Lu, Y.; Lin, H.; et al. Electrospun Nanofiber Membrane with Sustained Release of Mogroside V Enhances Alveolar Bone Defect Repair in Diabetic Rats. ACS Biomater. Sci. Eng. 2025, 11, 1660–1674. https://doi.org/10.1021/acsbiomaterials.4c01918.

  • 83.

    Li, M.; Cheng, G.; Xiao, S.; et al. Biomimetic Mineralized Hydroxyapatite–Fish-Scale Collagen/Chitosan Nanofibrous Membranes Promote Osteogenesis for Periodontal Tissue Regeneration. ACS Biomater. Sci. Eng. 2024, 10, 5108–5121. https://doi.org/10.1021/acsbiomaterials.4c00569.

  • 84.

    Barbosa, R.M.; da Rocha, D.N.; Bombaldi de Souza, R.F.; et al. Cell-Friendly Chitosan-Xanthan Gum Membranes Incorporating Hydroxyapatite Designed for Periodontal Tissue Regeneration. Pharmaceutics 2023, 15, 705. https://doi.org/10.3390/pharmaceutics15020705.

  • 85.

    Ge, X.; Hu, J.; Qi, X.; et al. An Immunomodulatory Hydrogel Featuring Antibacterial and Reactive Oxygen Species Scavenging Properties for Treating Periodontitis in Diabetes. Adv. Mater. 2025, 37, 2412240. https://doi.org/10.1002/adma.202412240.

  • 86.

    Yang, Y.; Zhu, Y.; Yuan, H.; et al. Asiatic Acid-Loaded Hydrogel Ameliorates Diabetic Periodontitis via Mitophagy-Mediated M2 Macrophage Polarization. ACS Omega 2026, 11, 12229–12241. https://doi.org/10.1021/acsomega.5c11543.

  • 87.

    Dobrzyńska-Mizera, M.; Knitter, M.; Kamińska, M.; et al. Thermosensitive hydrogel doped with osteoconductive fillers for the treatment of periodontitis periapicalis chronica: from synthesis to clinical trial. Biomater. Sci. 2024, 12, 6063–6081. https://doi.org/10.1039/d4bm00927d.

  • 88.

    Abdelrasoul, M.; El‐Fattah, A.A.; Kotry, G.; et al. Regeneration of critical-sized grade II furcation using a novel injectable melatonin-loaded scaffold. Oral Dis. 2023, 29, 3583–3598. https://doi.org/10.1111/odi.14314.

  • 89.

    Badr, A.M.; Shalaby, H.K.; Awad, M.A.; et al. Assessment of bone morphogenetic protein-7 loaded chitosan/β-Glycerophosphate hydrogel on periodontium tissues regeneration of class III furcation defects. Saudi Dent. J. 2023, 35, 760–767. https://doi.org/10.1016/j.sdentj.2023.05.027.

  • 90.

    Sun, Y.; Zhao, Z.; Qiao, Q.; et al. Injectable periodontal ligament stem cell-metformin-calcium phosphate scaffold for bone regeneration and vascularization in rats. Dent. Mater. 2023, 39, 872–885. https://doi.org/10.1016/j.dental.2023.07.008.

  • 91.

    Liu, S.; Wang, Z.; Li, Y.; et al. Erythropoietin‐Stimulated Macrophage‐Derived Extracellular Vesicles in Chitosan Hydrogel Rescue BMSCs Fate by Targeting EGFR to Alleviate Inflammatory Bone Loss in Periodontitis. Adv. Sci. 2025, 12, 2500554. https://doi.org/10.1002/advs.202500554.

  • 92.

    Zhu, Y.; Xiu, Z.; Jiang, X.; et al. Injectable hydrogels with ROS-triggered drug release enable the co-delivery of antibacterial agent and anti-inflammatory nanoparticle for periodontitis treatment. J. Nanobiotechnology 2025, 23, 205. https://doi.org/10.1186/s12951-025-03275-4.

  • 93.

    Tang, R.; Ren, Y.; Zhang, Y.; et al. Glucose-driven transformable complex eliminates biofilm and alleviates inflamm-aging for diabetic periodontitis therapy. Mater. Today Bio 2023, 20, 100678. https://doi.org/10.1016/j.mtbio.2023.100678.

  • 94.

    Xie, C.; Zhang, Q.; Bianco, A.; et al. H2S-Scavenging Hydrogel Alleviating Mitochondria Damage to Control Periodontitis. J. Dent. Res. 2025, 104, 172–182. https://doi.org/10.1177/00220345241291540.

  • 95.

    Chen, H.; Zhao, Z.; Zhang, R.; et al. Adaptable Hydrogel with Strong Adhesion of Wet Tissue for Long‐Term Protection of Periodontitis Wound. Adv. Mater. 2025, 37, 2413373. https://doi.org/10.1002/adma.202413373.

  • 96.

    Ma, S.; Lu, X.; Yu, X.; et al. An injectable multifunctional thermo-sensitive chitosan-based hydrogel for periodontitis therapy. Biomater. Adv. 2022, 142, 213158. https://doi.org/10.1016/j.bioadv.2022.213158.

  • 97.

    Chen, J.; Guan, X.; Chen, L.; et al. Customized Hydrogel System for the Spatiotemporal Sequential Treatment of Periodontitis Propelled by ZEB1. Adv. Sci. 2025, 12, 2503338. https://doi.org/10.1002/advs.202503338.

  • 98.

    Zhou, J.; Li, H.; Li, S.; et al. Convertible Hydrogel Injection Sequentially Regulates Diabetic Periodontitis. ACS Biomater. Sci. Eng. 2025, 11, 916–929. https://doi.org/10.1021/acsbiomaterials.4c01784.

  • 99.

    Klein, O.; Balta, M.G.; Wohlfahrt, J.C. Treatment of Residual Pockets in StageIIIandIVPeriodontitis Using an Oscillating Chitosan Device with or Without a Chitosan Gel—A Randomised Parallel‐Arms Clinical Trial. J. Clin. Periodontol. 2026, 53, 706–718. https://doi.org/10.1111/jcpe.70086.

  • 100.

    Wang, W.; Wang, A.; Hu, G.; et al. Potential of an Aligned Porous Hydrogel Scaffold Combined with Periodontal Ligament Stem Cells or Gingival Mesenchymal Stem Cells to Promote Tissue Regeneration in Rat Periodontal Defects. ACS Biomater. Sci. Eng. 2023, 9, 1961–1975. https://doi.org/10.1021/acsbiomaterials.2c01440.

  • 101.

    Zhang, L.; Dong, Y.; Liu, Y.; et al. Multifunctional hydrogel/platelet-rich fibrin/nanofibers scaffolds with cell barrier and osteogenesis for guided tissue regeneration/guided bone regeneration applications. Int. J. Biol. Macromol. 2023, 253, 126960. https://doi.org/10.1016/j.ijbiomac.2023.126960.

  • 102.

    Shirakata, Y.; Imafuji, T.; Nakamura, T.; et al. Cross‐linked hyaluronic acid gel with or without a collagen matrix in the treatment of class III furcation defects: A histologic and histomorphometric study in dogs. J. Clin. Periodontol. 2022, 49, 1079–1089. https://doi.org/10.1111/jcpe.13694.

  • 103.

    Staples, R.; Ivanovski, S.; Vaquette, C. Fibre-guiding biphasic scaffold for perpendicular periodontal ligament attachment. Acta Biomater. 2022, 150, 221–237. https://doi.org/10.1016/j.actbio.2022.07.023.

  • 104.

    Schüpbach, P.; Gaberthüel, T.; Lutz, F.; et al. Periodontal repair or regeneration: structures of different types of new attachment. J. Periodontal Res. 1993, 28, 281–293. https://doi.org/10.1111/j.1600-0765.1993.tb02095.x.

  • 105.

    Benatti, B.B.; Neto, J.B.C.; Casati, M.Z.; et al. Periodontal healing may be affected by aging: a histologic study in rats. J. Periodontal Res. 2006, 41, 329–333. https://doi.org/10.1111/j.1600-0765.2006.00872.x.

  • 106.

    Reynolds, M.A.; Kao, R.T.; Camargo, P.M.; et al. Periodontal Regeneration – Intrabony Defects: A Consensus Report From the AAP Regeneration Workshop. J. Periodontol. 2015, 86, S105–S107. https://doi.org/10.1902/jop.2015.140378.

  • 107.

    Rasperini, G.; Tavelli, L.; Barootchi, S.; et al. Interproximal attachment gain: The challenge of periodontal regeneration. J. Periodontol. 2020, 92, 931–946. https://doi.org/10.1002/jper.20-0587.

  • 108.

    Ke, S.; Sun, X.; Qian, J.; et al. The Experimental Study of Double‐Layer Heterogeneous CA Scaffold in Promoting the Surface Shape Recovery and Internal Osteogenesis of Alveolar Bone. Biotechnol. J. 2025, 20, e202400603. https://doi.org/10.1002/biot.202400603.

  • 109.

    Krishnamoorthy, E.; Purusothaman, B.; Subramanian, B. Productizing Nano-Bioactive Glass-Based Bilayer Scaffolds: A Graft for Reconstruction of Mandibular and Femoral Bone Defects. ACS Appl. Mater. Interfaces 2024, 16, 25317–25332. https://doi.org/10.1021/acsami.4c02689.

  • 110.

    Zhao, Q.; Yang, D.; Chen, S.; et al. Carbon nanotube bacterial cellulose polycaprolactone scaffolds for bone tissue engineering using top-heating fused deposition three-dimensional printing. Int. J. Biol. Macromol. 2025, 318, 144588. https://doi.org/10.1016/j.ijbiomac.2025.144588.

  • 111.

    Farsinezhad, H.; Niknafs, M.; Samieifard, M.; et al. Enhanced hemostasis and alveolar bone regeneration induced by sandwich like egg shell membrane-laponite-chitosan nanocomposite after tooth extraction. Int. J. Biol. Macromol. 2025, 330, 147923. https://doi.org/10.1016/j.ijbiomac.2025.147923.

  • 112.

    Vu, N.B.; Chuenchompoonut, V.; Jansisyanont, P.; et al. Acemannan-induced tooth socket healing: A 12-month randomized controlled trial. J. Dent. Sci. 2021, 16, 643–653. https://doi.org/10.1016/j.jds.2020.10.003.

  • 113.

    Machado, A.; Pereira, I.; Costa, F.; et al. Randomized clinical study of injectable dextrin-based hydrogel as a carrier of a synthetic bone substitute. Clin. Oral Investig. 2023, 27, 979–994. https://doi.org/10.1007/s00784-023-04868-9.

  • 114.

    Wu, T.; Liu, Y.; Wang, S.; et al. Light‐Switched Mesenchymal Stem Cells for In Situ Exosome Amplification in Craniofacial Bone Defect Reconstruction. Adv. Sci. 2026, 13, e75519. https://doi.org/10.1002/advs.75519.

  • 115.

    Tavakoli, M.; Salehi, H.; Emadi, R.; et al. 3D printed polylactic acid-based nanocomposite scaffold stuffed with microporous simvastatin-loaded polyelectrolyte for craniofacial reconstruction. Int. J. Biol. Macromol. 2024, 258, 128917. https://doi.org/10.1016/j.ijbiomac.2023.128917.

  • 116.

    Salehi, S.; Ghomi, H.; Hassanzadeh-Tabrizi, S.A.; et al. Antibacterial and osteogenic properties of chitosan-polyethylene glycol nanofibre-coated 3D printed scaffold with vancomycin and insulin-like growth factor-1 release for bone repair. Int. J. Biol. Macromol. 2025, 298, 139883. https://doi.org/10.1016/j.ijbiomac.2025.139883.

  • 117.

    Huang, Y.; Zhang, Y.; Feng, Y.; et al. A DNA Tetrahedron Delivery Asiatic Acid to Reprogram Mitochondrial Metabolism for Promoting Bone Regeneration via STAT3 Phosphorylation. Adv. Sci. 2026, 13, e18796. https://doi.org/10.1002/advs.202518796.

  • 118.

    Han, Y.; Wang, C.; Liu, M.; et al. EGCG-Loaded Zinc Ion-Cross-Linked Injectable Sodium Alginate Hydrogel for Extraction Socket Healing. ACS Biomater. Sci. Eng. 2025, 11, 7313–7328. https://doi.org/10.1021/acsbiomaterials.5c00824.

  • 119.

    Zhao, X.Y.; Lei, S.; Yan, M.; et al. Polyhedral oligomeric silsesquioxane-functionalized carboxymethyl chitin microspheres via irradiation-induced grafting for hemostasis and tissue repair in post-extraction sockets. Int. J. Biol. Macromol. 2026, 358, 151727. https://doi.org/10.1016/j.ijbiomac.2026.151727.

  • 120.

    Xu, C.; Li, W.; Mao, J.; et al. Using chondroitin sulfate lithium hydrogel for diabetic bone regeneration via regulation of macrophage polarization. Carbohydr. Polym. 2025, 347, 122787. https://doi.org/10.1016/j.carbpol.2024.122787.

  • 121.

    He, S.; Zhao, H.; Chen, M.; et al. Bioglass‐Integrated Dynamic Hydrogels Improve Matrix‐Directed Repair of Cranial Defects through Cooperative Mechano‐Biochemical Regulation. Adv. Healthc. Mater. 2025, 14, 2500134. https://doi.org/10.1002/adhm.202500134.

  • 122.

    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. prd.70019. https://doi.org/10.1111/prd.70019.

  • 123.

    Ren, Y.; Fan, L.; Alkildani, S.; et al. Barrier Membranes for Guided Bone Regeneration (GBR): A Focus on Recent Advances in Collagen Membranes. Int. J. Mol. Sci. 2022, 23, 14987. https://doi.org/10.3390/ijms232314987.

  • 124.

    Hou, H.; Lanzi, A.M.; Feng, Y.; et al. Alginate Hydrogels with Tunable Degradation. Macromol. Rapid Commun. 2025, 47, e00348. https://doi.org/10.1002/marc.202500348.

  • 125.

    Zhou, Y.; Li, M.; Zheng, H.; et al. A photothermal therapy-based composite hydrogel for sequential management of inflammation control and bone regeneration in severe periodontitis. J. Mater. Chem. B 2025, 13, 10225–10238. https://doi.org/10.1039/d5tb01510c.

  • 126.

    Hu, Z.; Zhou, Y.; Wu, H.; et al. An injectable photopolymerizable chitosan hydrogel doped anti-inflammatory peptide for long-lasting periodontal pocket delivery and periodontitis therapy. Int. J. Biol. Macromol. 2023, 252, 126060. https://doi.org/10.1016/j.ijbiomac.2023.126060.

  • 127.

    Liang, C.; Wu, S.; Huang, Z.; et al. Harnessing Oxidized Alginate Microgels for Rapid and Self‐Assembling Dental Tissue Organogenesis In Vitro and In Vivo. Small Sci. 2025, 5, e202500053. https://doi.org/10.1002/smsc.202500053.

  • 128.

    Nguyen, N.Q.T.; Luu, C.H.; Nguyen, N.D.H.; et al. Dual-functional injectable hydrogels as antimicrobial and angiogenic therapeutics for dental pulp regeneration. J. Mater. Chem. B 2025, 13, 6765–6783. https://doi.org/10.1039/d5tb00559k.

  • 129.

    Moreira, M.S.; Sarra, G.; Carvalho, G.L.; et al. Physical and Biological Properties of a Chitosan Hydrogel Scaffold Associated to Photobiomodulation Therapy for Dental Pulp Regeneration: An In Vitro and In Vivo Study. BioMed Res. Int. 2021, 2021, 6684667. https://doi.org/10.1155/2021/6684667.

  • 130.

    Ouyang, M.; Yu, X.; Zhong, J.; et al. Injectable sodium alginate/4-arm polyethylene glycol-lipoic acid double-network hydrogel loading Ca2+-tannic acid nanocomposite treats periodontitis via anti-bacteria, ROS scavenging and osteogenesis. Int. J. Biol. Macromol. 2025, 307, 141841. https://doi.org/10.1016/j.ijbiomac.2025.141841.

  • 131.

    Wang, X.; Peng, Y.; Wu, Y.; et al. Chitosan/silk fibroin composite bilayer PCL nanofibrous mats for bone regeneration with enhanced antibacterial properties and improved osteogenic potential. Int. J. Biol. Macromol. 2023, 230, 123265. https://doi.org/10.1016/j.ijbiomac.2023.123265.

  • 132.

    Wang, Y.; Qu, Y.; Liu, X.; et al. Dual-functional probiotic hydrogel with puerarin integration for microbiota-neuroimmune regulation in antibiotic-free periodontitis therapy. Bioact. Mater. 2025, 53, 72–83. https://doi.org/10.1016/j.bioactmat.2025.07.004.

  • 133.

    Mousavi Nejad, Z.; Zamanian, A.; Saeidifar, M.; et al. 3D Bioprinting of Polycaprolactone-Based Scaffolds for Pulp-Dentin Regeneration: Investigation of Physicochemical and Biological Behavior. Polymers 2021, 13, 4442. https://doi.org/10.3390/polym13244442.

  • 134.

    Leite, M.L.; Anselmi, C.; Soares, I.P.M.; et al. Calcium silicate-coated porous chitosan scaffold as a cell-free tissue engineering system for direct pulp capping. Dent. Mater. 2022, 38, 1763–1776. https://doi.org/10.1016/j.dental.2022.09.014.

  • 135.

    Li, N.; Jiang, L.; Jin, H.; et al. An enzyme-responsive membrane for antibiotic drug release and local periodontal treatment. Colloids Surfaces B Biointerfaces 2019, 183, 110454. https://doi.org/10.1016/j.colsurfb.2019.110454.

  • 136.

    Nnane, N.S.; Gaikwad, A.; Rahim, M.I.; et al. Synthesis of an Enzyme‐Triggered Chitosan‐Based Drug Delivery System for Peri‐Implantitis Prevention. Chem. – A Eur. J. 2026, 32, e01800. https://doi.org/10.1002/chem.202501800.

  • 137.

    Parisi, L.; Rivara, F.; Costa, C.A.; et al. Aptamers recognizing fibronectin confer improved bioactivity to biomaterials and promote new bone formation in a periodontal defect in rats. Biomed. Mater. 2020, 16, 015016. https://doi.org/10.1088/1748-605x/abb6b2.

  • 138.

    Liu, X.; Li, X.; Yue, Y.; et al. Selection of a novel MSC-targeted aptamer Pt-1 and its functionalized hydrogel for tissue regeneration. Mater. Today Bio 2026, 39, 103410. https://doi.org/10.1016/j.mtbio.2026.103410.

  • 139.

    Ning, X.; Zong, M.; Tong, J.; et al. Preliminary Study on Carboxymethyl Chitosan-Based Carbon Dots for Tracing and Promoting Osteogenic Differentiation. ACS Biomater. Sci. Eng. 2025, 11, 4087–4100. https://doi.org/10.1021/acsbiomaterials.5c00135.

  • 140.

    Elnawam, H.; Thabet, A.; Mobarak, A.; et al. Bovine pulp extracellular matrix hydrogel for regenerative endodontic applications: in vitro characterization and in vivo analysis in a necrotic tooth model. Head Face Med. 2024, 20, 61. https://doi.org/10.1186/s13005-024-00460-y.

  • 141.

    Khalil, M.M.; Ibrahim, M.; Rawat, S.S.; et al. Comparative evaluation of 3D culture strategies for pulp-dentin models. BMC Oral Health 2026, 26, 242. https://doi.org/10.1186/s12903-025-07561-3.

  • 142.

    Salar Amoli, M.; Anand, R.; EzEldeen, M.; et al. The development of a 3D printable chitosan-based copolymer with tunable properties for dentoalveolar regeneration. Carbohydr. Polym. 2022, 289, 119441. https://doi.org/10.1016/j.carbpol.2022.119441.

  • 143.

    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, 1062. https://doi.org/10.3390/biom13071062.

  • 144.

    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, 2402727. https://doi.org/10.1002/adhm.202402727.

  • 145.

    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, 6817–6829. https://doi.org/10.1021/acsabm.5c00561.

  • 146.

    Wang, T.; Zhang, M.; Guo, J.; et al. Alginate/bacterial cellulose/GelMA scaffolds with aligned nanopatterns and hollow channel networks for vascularized bone repair. Int. J. Biol. Macromol. 2025, 308, 142578. https://doi.org/10.1016/j.ijbiomac.2025.142578.

  • 147.

    Tu, X.; Guo, L.; Li, Y.; et al. 3D-printed gelatin/sodium alginate/58S bioactive glass scaffolds promote osteogenesis in vitro and in vivo. J. Biomater. Appl. 2023, 37, 1758–1766. https://doi.org/10.1177/08853282231152128.

  • 148.

    Li, S.; Liu, Z.; Gao, X.; et al. Preparation and properties of a 3D printed nHA/PLA bone tissue engineering scaffold loaded with a β-CD–CHX combined dECM hydrogel. RSC Adv. 2024, 14, 9848–9859. https://doi.org/10.1039/d4ra00261j.

  • 149.

    Ho, M.H.; Huang, K.Y.; Tu, C.C.; et al. Functionally graded membrane deposited with PDLLA nanofibers encapsulating doxycycline and enamel matrix derivatives-loaded chitosan nanospheres for alveolar ridge regeneration. Int. J. Biol. Macromol. 2022, 203, 333–341. https://doi.org/10.1016/j.ijbiomac.2022.01.147.

  • 150.

    Peng, W.; Ren, S.; Zhang, Y.; et al. MgO Nanoparticles-Incorporated PCL/Gelatin-Derived Coaxial Electrospinning Nanocellulose Membranes for Periodontal Tissue Regeneration. Front. Bioeng. Biotechnol. 2021, 9, 668428. https://doi.org/10.3389/fbioe.2021.668428.

  • 151.

    Huang, Q.; Han, L.; Wang, R.; et al. Electrospun Nanofibers Loaded with Concentrated Growth Factors and Nanohydroxyapatite for the Healing of Alveolar Bone in Tooth Extraction Wounds. ACS Biomater. Sci. Eng. 2025, 11, 5975–5990. https://doi.org/10.1021/acsbiomaterials.5c00159.

  • 152.

    Su, H.; Fujiwara, T.; Anderson, K.M.; et al. A comparison of two types of electrospun chitosan membranes and a collagen membrane in vivo. Dent. Mater. 2021, 37, 60–70. https://doi.org/10.1016/j.dental.2020.10.011.

  • 153.

    Feng, Z.; Qiu, S.; Michálek, M.; et al. Anti-inflammatory and osteogenic nanofibrous scaffolds of bioactive glass/carboxymethyl chitosan-reinforced PCL short fibers for alveolar bone regeneration. Int. J. Biol. Macromol. 2025, 323, 147197. https://doi.org/10.1016/j.ijbiomac.2025.147197.

  • 154.

    Helal, M.H.; Ali, A.N.; Hamdy, Y.; et al. β-tricalcium phosphate/gelatin composite scaffolds incorporated with gentamycin-loaded chitosan microspheres for periodontal regeneration in class II furcation defects in dogs. Clin. Oral Investig. 2025, 29, 540. https://doi.org/10.1007/s00784-025-06582-0.

  • 155.

    Song, C.; Huang, D.; Zhao, C.; et al. Abalone‐Inspired Adhesive and Photo‐Responsive Microparticle Delivery Systems for Periodontal Drug Therapy. Adv. Sci. 2022, 9, 2202829. https://doi.org/10.1002/advs.202202829.

  • 156.

    Liu, Z.; Zhang, H.; Gan, J.; et al. Black Phosphorus Tagged Responsive Strontium Hydrogel Particles for Bone Defect Repair. Adv. Sci. 2025, 12, 2408284. https://doi.org/10.1002/advs.202408284.

  • 157.

    Zhou, E.; He, P.; Yang, Z.; et al. 3D-printed GelMA-Alginate microsphere scaffold with staged dual-growth factor release for enhanced bone regeneration. Mater. Today Bio 2025, 35, 102422. https://doi.org/10.1016/j.mtbio.2025.102422.

  • 158.

    Chelu, M.; Popa, M.; Calderón Moreno, J.M. Next-Generation Natural Hydrogels in Oral Tissue Engineering. Pharmaceutics 2025, 17, 1256. https://doi.org/10.3390/pharmaceutics17101256.

  • 159.

    Barreiro Carpio, M.; Thompson, P.M.; Moody, C.; et al. A versatile and efficient method to quantify purity and degree of substitution in alginate derivatives. Carbohydr. Polym. 2025, 369, 124299. https://doi.org/10.1016/j.carbpol.2025.124299.

  • 160.

    Martel-Pelletier, J.; Farran, A.; Montell, E.; et al. Discrepancies in Composition and Biological Effects of Different Formulations of Chondroitin Sulfate. Molecules 2015, 20, 4277–4289. https://doi.org/10.3390/molecules20034277.

  • 161.

    Xu, J.; Tang, W.; Che, S.; et al. From nature to clinic: Lessons from successfully marketed polysaccharide drugs. Carbohydr. Polym. 2026, 381, 125147. https://doi.org/10.1016/j.carbpol.2026.125147.

  • 162.

    Qadir, B.H.; Mahmood, M.K.; Rasheed, T.A.; et al. Applications of chitosan in oral health and diseases. Front. Oral Health 2025, 6, 1632233. https://doi.org/10.3389/froh.2025.1632233.

  • 163.

    Capuana, E.; Lopresti, F.; Carfì Pavia, F.; et al. Solution-Based Processing for Scaffold Fabrication in Tissue Engineering Applications: A Brief Review. Polymers 2021, 13, 2041. https://doi.org/10.3390/polym13132041.

  • 164.

    Lin, A.; Yuan, S.; Liang, C.; et al. Scaffold-free cell sheet therapies: clinical advances, global approval landscapes, and strategic directions to address regenerative medicine barriers. Stem Cell Res. Ther. 2025, 17, 5. https://doi.org/10.1186/s13287-025-04818-0.

  • 165.

    Han, P.; Liu, C.; Abdal-Hay, A.; et al. Proteome and microbiome profiles of polymicrobial salivary biofilms on 3D MEW fibrous scaffolds: biomimetic ECM-inspired structures. J. Mater. Chem. B 2025, 13, 13434–13445. https://doi.org/10.1039/d5tb01410g.

  • 166.

    Utomo, R.N.C.; Palkowitz, A.L.; Gan, L.; et al. In vitro plaque formation model to unravel biofilm formation dynamics on implant abutment surfaces. J. Oral Microbiol. 2024, 16, 2424227. https://doi.org/10.1080/20002297.2024.2424227.

  • 167.

    Helbig, R.; Hannig, M.; Basche, S.; et al. Bioadhesion on Textured Interfaces in the Human Oral Cavity—An In Situ Study. Int. J. Mol. Sci. 2022, 23, 1157. https://doi.org/10.3390/ijms23031157.

  • 168.

    Asgary, S.; Shamszadeh, S. Immunomodulatory and angiogenic strategies in vital pulp therapy: a systematic review of scaffold-based, scaffold-free, and cell-laden interventions. Clin. Oral Investig. 2026, 30, 73. https://doi.org/10.1007/s00784-025-06737-z.

  • 169.

    Shanbhag, S.; Stødle, I.H.; Lie, S.A.; et al. Histological Outcomes of Root Coverage Procedures: A Systematic Review With Meta‐Analysis. J. Periodontal Res. 2026, 61, 9–29. https://doi.org/10.1111/jre.70043.

  • 170.

    Chinta, M.L.; Gandam, P.K.; Parcha, S.R. Design and optimization of tamarind seed polysaccharide-based scaffold for tissue engineering applications using statistical modeling and machine learning, and it's in-vitro validation. Int. J. Biol. Macromol. 2025, 301, 140411. https://doi.org/10.1016/j.ijbiomac.2025.140411.

  • 171.

    Alqarni, M.; Al Harthi, S.M.; Alzubaidi, M.A.; et al. Model development using hybrid method for prediction of drug release from biomaterial matrix. Chemom. Intell. Lab. Syst. 2024, 253, 105216. https://doi.org/10.1016/j.chemolab.2024.105216.

  • 172.

    Yin, X.; Hao, J.; Liu, S.; et al. Hybrid physics-informed and data-driven modeling of material–process–property relationships in extrusion-printed GelMA/alginate vascular scaffolds. Addit. Manuf. 2026, 125, 105251. https://doi.org/10.1016/j.addma.2026.105251.

  • 173.

    Ng, W.L.; Goh, G.L.; Goh, G.D.; et al. Progress and Opportunities for Machine Learning in Materials and Processes of Additive Manufacturing. Adv. Mater. 2024, 36, 2310006. https://doi.org/10.1002/adma.202310006.

  • 174.

    Liu, Y.; Xie, R.; Wang, L.; et al. Fully automatic AI segmentation of oral surgery-related tissues based on cone beam computed tomography images. Int. J. Oral Sci. 2024, 16, 34. https://doi.org/10.1038/s41368-024-00294-z.

  • 175.

    Omigbodun, F.T.; Oladapo, B.I. AI-Optimized Lattice Structures for Biomechanics Scaffold Design. Biomimetics 2025, 10, 88. https://doi.org/10.3390/biomimetics10020088.

  • 176.

    Chen, F.; Chen, H.; Hai, D.; et al. AI-assisted preoperative surgical planning for dental implant. J. Transl. Med. 2025, 24, 104. https://doi.org/10.1186/s12967-025-07584-y.

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Qiao, D.; Chen, X.; Wei, Y.; Zhang, Y.; Yan, F. Polysaccharide-Based Biomaterials in Oral Regenerative Medicine: Mechanisms, Engineering Strategies, and Translational Perspectives. Regenerative Medicine and Dentistry 2026, 3 (3), 14. https://doi.org/10.53941/rmd.2026.100014.
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