AccScience Publishing / IJB / Online First / DOI: 10.36922/IJB026140127
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RESEARCH ARTICLE

Ta/PEEK cages with enhanced hydrophilicity and cell adhesion improve intervertebral fusion in a rabbit model of extreme lateral intervertebral fusion

Shaorong Li1 Han Wu1 Hongwei Gao1 Jianshi Song1 Xiuqi Shan1 Jiaqi Li1 Lei Ma1 Wei Zhang1*
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1 Department of Spinal Surgery, The Third Hospital of Hebei Medical University, Shijiazhuang, Hebei, China
Received: 1 April 2026 | Revised: 7 June 2026 | Accepted: 15 June 2026 | Published online: 15 June 2026
© 2026 by the Author(s). This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution 4.0 International License ( https://creativecommons.org/licenses/by/4.0/ )
Abstract

Conventional polyether ether ketone (PEEK) and titanium (Ti) cages for intervertebral fusion exhibit inherent limitations in bioactivity and elastic modulus, necessitating surface modification to enhance their performance. This study developed bioactive cages by fabricating hydroxyapatite-coated Ti (HA/Ti) and tantalum-coated PEEK (Ta/PEEK) cages and evaluated their physicochemical properties, cellular responses, and intervertebral fusion performance in a rabbit extreme lateral intervertebral fusion model. Both coatings improved surface wettability and maintained the intrinsic mechanical properties of the substrates. Ta/PEEK showed superior coating adhesion and enhanced expression of bone marrow-derived mesenchymal stem cell adhesion-related markers, whereas HA/Ti more strongly promoted osteogenic differentiation and matrix mineralization in vitro. In vivo, both coated cages significantly improved intervertebral fusion compared with uncoated Ti and PEEK cages. HA/Ti induced greater new bone formation, while Ta/PEEK enhanced cell adhesion and angiogenesis, as indicated by increased cadherin-1, integrin α2, cluster of differentiation 31, and hypoxia-inducible factor 1α expression. These findings suggest that Ta/PEEK cages provide a mechanically compatible and biologically active strategy for improving intervertebral fusion and represent a promising platform for next-generation printed spinal implants.

Graphical abstract
Keywords
Cage
Hydroxyapatite
Intervertebral fusion
Polyether ether ketone
Tantalum
Extreme lateral intervertebral fusion
Funding
This work was supported by the 2024 Hebei Provincial Traditional Chinese Medicine Scientific Research Project Plan [grant number 2024045]; 2025 Hebei Provincial Medical Applicable Technology Tracking Project [grant number GZ20250025]; and 2026 Hebei Provincial Higher Education Scientific Research Project [grant number CXZX2026045].
Conflict of interest
The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
References
  1. Kotheeranurak V, Jitpakdee K, Lin GX, et al. Subsidence of Interbody Cage Following Oblique Lateral Interbody Fusion: An Analysis and Potential Risk Factors. Global Spine J. 2023;13(7):1981-1991. doi: 10.1177/21925682211067210
  2. Xuan W, Cheng Q, Gao Y, Song Z, Gao Z. Early-stage lumbar paraspinal muscle injury: endoscopic versus transforaminal lumbar interbody fusion: a retrospective comparative analysis. J Orthop Surg Res. 2025;20(1):841. doi: 10.1186/s13018-025-06235-8
  3. Zhou H, Bian H, Zhang Y, et al. Evaluation of Indirect Decompression Effect After Extreme Lateral Lumbar Interbody Fusion Using Three-Dimensional Volumetric Measurements-A Retrospective Study. Orthop Surg. 2025;17(9):2558-2569. doi: 10.1111/os.70108
  4. Wu H, Shan Z, Zhao F, Cheung JPY. Poor Bone Quality, Multilevel Surgery, and Narrow and Tall Cages Are Associated with Intraoperative Endplate Injuries and Late-onset Cage Subsidence in Lateral Lumbar Interbody Fusion: A Systematic Review. Clin Orthop Relat Res. 2022;480(1):163-188. doi: 10.1097/corr.0000000000001915
  5. Burkhard MD, Guven AE, Demopoulos B, et al. 3D-Printed Titanium: Game-Changer for Standalone Lateral Lumbar Interbody Fusion? An Analysis of Risk Factors for Revision Surgery. Global Spine J. 2025:21925682251383879. doi: 10.1177/21925682251383879
  6. Schnake KJ, Fleiter N, Hoffmann C, et al. PLIF with titanium-coated versus uncoated PEEK cages: a prospective randomized clinical trial. Eur Spine J. 2021;30(1):114-121. doi: 10.1007/s00586-020-06642-x
  7. Jain S, Eltorai AE, Ruttiman R, Daniels AH. Advances in Spinal Interbody Cages. Orthop Surg. 2016;8(3):278-284. doi: 10.1111/os.12264
  8. Zhang Y, Yang J, Wan W, et al. Evaluation of biological performance of 3D printed trabecular porous tantalum spine fusion cage in large animal models. J Orthop Translat. 2025;50:185-195. doi: 10.1016/j.jot.2024.10.010
  9. He X, Li Y, Zou D, Zu H, Li W, Zheng Y. An overview of magnesium-based implants in orthopaedics and a prospect of its application in spine fusion. Bioact Mater. 2024;39:456-478. doi: 10.1016/j.bioactmat.2024.04.026
  10. Zhang H, Gao G, Wang L, et al. Innovative 3D-printed porous piezoelectric poly(vinylidene fluoride) cages with accelerated spinal fusion. Mater Today Bio. 2025;35:102333. doi: 10.1016/j.mtbio.2025.102333
  11. Wu H, Dong H, Tang Z, et al. Electrical stimulation of piezoelectric BaTiO3 coated Ti6Al4V scaffolds promotes anti-inflammatory polarization of macrophages and bone repair via MAPK/JNK inhibition and OXPHOS activation. Biomaterials. 2023;293:121990. doi: 10.1016/j.biomaterials.2022.121990
  12. Zheng H, Cheng F, Guo D, He X, Zhou L, Zhang Q. Nanoenzyme-Reinforced Multifunctional Scaffold Based on Ti(3)C(2)Tx MXene Nanosheets for Promoting Structure-Functional Skeletal Muscle Regeneration via Electroactivity and Microenvironment Management. Nano Lett. 2023;23(16):7379-7388. doi: 10.1021/acs.nanolett.3c01784
  13. Luo L, Zheng W, Li J, et al. 3D-Printed Titanium Trabecular Scaffolds with Sustained Release of Hypoxia-Induced Exosomes for Dual-Mimetic Bone Regeneration. Adv Sci (Weinh). 2025;12(23):e2500599. doi: 10.1002/advs.202500599
  14. Lin R, Wang Z, Li Z, Gu L. A two-phase and long-lasting multi-antibacterial coating enables titanium biomaterials to prevent implants-related infections. Mater Today Bio. 2022;15:100330. doi: 10.1016/j.mtbio.2022.100330
  15. Coppola B, Montanaro L, Palmero P. DLP Fabrication of Zirconia Scaffolds Coated with HA/β-TCP Layer: Role of Scaffold Architecture on Mechanical and Biological Properties. J Funct Biomater. 2022;13(3):148. doi: 10.3390/jfb13030148
  16. Sun T, Huang H, Zhao Y, Li Z, Wang H, Zhou G. Low-Temperature Deposited Amorphous Poly(aryl ether ketone) Hierarchically Porous Scaffolds with Strontium-Doped Mineralized Coating for Bone Defect Repair. Adv Healthc Mater. 2024;13(23):e2400927. doi: 10.1002/adhm.202400927
  17. Durham JW 3rd, Rabiei A. Deposition, Heat Treatment And Characterization of Two Layer Bioactive Coatings on Cylindrical PEEK. Surf Coat Technol. 2016;301:106-113. doi: 10.1016/j.surfcoat.2015.12.045
  18. Torstrick FB, Lin ASP, Potter D, et al. Porous PEEK improves the bone-implant interface compared to plasma-sprayed titanium coating on PEEK. Biomaterials. 2018;185:106-116. doi: 10.1016/j.biomaterials.2018.09.009
  19. Li J, Zhao B, Wang W, Xu Y, Wu H, Zhang W. Improved intervertebral fusion in LLIF rabbit model with a novel titanium cage. Spine J. 2024;24(6):1109-1120. doi: 10.1016/j.spinee.2023.12.011
  20. Guillot R, Pignot-Paintrand I, Lavaud J, et al. Assessment of a polyelectrolyte multilayer film coating loaded with BMP-2 on titanium and PEEK implants in the rabbit femoral condyle. Acta Biomater. 2016;36:310-322. doi: 10.1016/j.actbio.2016.03.010
  21. Zhang J, Ma T, Liu X, Zhang X, Meng W, Wu J. Multifunctional surface of the nano-morphic PEEK implant with enhanced angiogenic, osteogenic and antibacterial properties. Regen Biomater. 2024;11:rbae067. doi: 10.1093/rb/rbae067
  22. An J, Shi X, Zhang J, et al. Dual aldehyde cross-linked hyaluronic acid hydrogels loaded with PRP and NGF biofunctionalized PEEK interfaces to enhance osteogenesis and vascularization. Mater Today Bio. 2024;24:100928. doi: 10.1016/j.mtbio.2023.100928
  23. Adl Amini D, Okano I, Oezel L, et al. Evaluation of cage subsidence in standalone lateral lumbar interbody fusion: novel 3D-printed titanium versus polyetheretherketone (PEEK) cage. Eur Spine J. 2021;30(8):2377-2384. doi: 10.1007/s00586-021-06912-2
  24. Mahjoubi H, Buck E, Manimunda P, et al. Surface phosphonation enhances hydroxyapatite coating adhesion on polyetheretherketone and its osseointegration potential. Acta Biomater. 2017;47:149-158. doi: 10.1016/j.actbio.2016.10.004
  25. Zhang W, Shi D, Huang S, Li S, Zeng M, Wei Y. Personalised 3D-printed bioactive peek bone plate scaffold for treating femoral defects. RSC Adv. 2025;15(7):5060-5072. doi: 10.1039/d4ra07573k
  26. Xu J, Wu D, Ge B, et al. Selective Laser Melting of the Porous Ta Scaffold with Mg-Doped Calcium Phosphate Coating for Orthopedic Applications. ACS Biomater Sci Eng. 2024;10(3):1435-1447. doi: 10.1021/acsbiomaterials.3c01503
  27. Zhu C, He M, Mao L, et al. Titanium interlayer-mediated hydroxyapatite-coated polyetheretherketone cage in transforaminal lumbar interbody fusion surgery. BMC Musculoskelet Disord. 2021;22(1):918. doi: 10.1186/s12891-021-04803-7
  28. Jia CQ, Zhang Z, Cao SQ, et al. A biomimetic gradient porous cage with a micro-structure for enhancing mechanical properties and accelerating osseointegration in spinal fusion. Bioact Mater. 2022;23:234-246. doi: 10.1016/j.bioactmat.2022.11.003
  29. Ragni E, Perucca Orfei C, Bidossi A, et al. Superior Osteo-Inductive and Osteo-Conductive Properties of Trabecular Titanium vs. PEEK Scaffolds on Human Mesenchymal Stem Cells: A Proof of Concept for the Use of Fusion Cages. Int J Mol Sci. 2021;22(5):2379. doi: 10.3390/ijms22052379
  30. Laubach M, Kobbe P, Hutmacher DW. Biodegradable interbody cages for lumbar spine fusion: Current concepts and future directions. Biomaterials. 2022;288:121699. doi: 10.1016/j.biomaterials.2022.121699
  31. Mobbs RJ, Phan K, Assem Y, Pelletier M, Walsh WR. Combination Ti/PEEK ALIF cage for anterior lumbar interbody fusion: Early clinical and radiological results. J Clin Neurosci. 2016;34:94-99. doi: 10.1016/j.jocn.2016.05.028
  32. Park PJ, Lehman RA. Optimizing the Spinal Interbody Implant: Current Advances in Material Modification and Surface Treatment Technologies. Curr Rev Musculoskelet Med. 2020;13(6):688-695. doi: 10.1007/s12178-020-09673-5
  33. Lu T, Wen J, Qian S, et al. Enhanced osteointegration on tantalum-implanted polyetheretherketone surface with bone-like elastic modulus. Biomaterials. 2015;51:173-183. doi: 10.1016/j.biomaterials.2015.02.018
  34. Hwangbo H, Lee J, Kim G. Mechanically and biologically enhanced 3D-printed HA/PLLA/dECM biocomposites for bone tissue engineering. Int J Biol Macromol. 2022;218:9-21. doi: 10.1016/j.ijbiomac.2022.07.040
  35. Blom AM, Petersen EB, Grieser-Yoder RA, Olinger CR, Fredericks DC. A Novel Nano-Synthetic Hydrophilic Bone Graft (OsteoFlo HydroFiber) Is a Non-inferior Alternative to Iliac Crest Autograft in a Rabbit Posterolateral Fusion Model. Global Spine J. 2026. doi: 10.1177/21925682261442308
  36. Jin YZ, Zheng GB, Cho M, Lee JH. Effect of Whitlockite as a new bone substitute for bone formation in spinal fusion and ectopic ossification animal model. Biomater Res. 2021;25(1):34. doi: 10.1186/s40824-021-00237-3
  37. Ryan DA, Cheng J, Masuda K, Cashman JR. Role of Curcuminoids and Tricalcium Phosphate Ceramic in Rat Spinal Fusion. Tissue Eng Part C Methods. 2020;26(11):577-589. doi: 10.1089/ten.TEC.2020.0217
  38. Sun J, Liu SS, Zou D, et al. A novel porous interbody fusion cage modified by microarc oxidation and hydrothermal treatment technology accelerate osseointegration and spinal fusion in sheep. RSC Adv. 2024;14(44):31966-31978. doi: 10.1039/d3ra08185k
  39. Tian L, Zhang Z, Tian B, Zhang X, Wang N. Study on antibacterial properties and cytocompatibility of EPL coated 3D printed PCL/HA composite scaffolds. RSC Adv. 2020;10(8):4805-4816. doi: 10.1039/c9ra10275b
  40. Liu B, Ma Z, Li J, et al. Experimental study of a 3D printed permanent implantable porous Ta-coated bone plate for fracture fixation. Bioact Mater. 2022;10:269-280. doi: 10.1016/j.bioactmat.2021.09.009
  41. Liu T, Li B, Chen G, Ye X, Zhang Y. Nano tantalum-coated 3D printed porous polylactic acid/beta-tricalcium phosphate scaffolds with enhanced biological properties for guided bone regeneration. Int J Biol Macromol. 2022;221:371-380. doi: 10.1016/j.ijbiomac.2022.09.003
  42. Tao Y, Jia M, Shao-Qiang Y, et al. A novel fluffy PLGA/HA composite scaffold for bone defect repair. J Mater Sci Mater Med. 2024;35(1):16. doi: 10.1007/s10856-024-06782-2
  43. Duan W, Chen C, Haque M, Hayes D, Lopez MJ. Polymer-mineral scaffold augments in vivo equine multipotent stromal cell osteogenesis. Stem Cell Res Ther. 2018;9(1):60. doi: 10.1186/s13287-018-0790-8
  44. Chi H, Chen G, He Y, et al. 3D-HA Scaffold Functionalized by Extracellular Matrix of Stem Cells Promotes Bone Repair. Int J Nanomedicine. 2020;15:5825-5838. doi: 10.2147/ijn.S259678
  45. Zhang K, Hu H, Sun Y, et al. The bio-functionalized membrane loaded with Ta/WH nanoparticles promote bone regeneration through neurovascular coupling. Colloids Surf B Biointerfaces. 2023;230:113506. doi: 10.1016/j.colsurfb.2023.113506
  46. Baldwin P, Li DJ, Auston DA, Mir HS, Yoon RS, Koval KJ. Autograft, Allograft, and Bone Graft Substitutes: Clinical Evidence and Indications for Use in the Setting of Orthopaedic Trauma Surgery. J Orthop Trauma. 2019;33(4):203-213. doi: 10.1097/bot.0000000000001420
  47. Gupta A, Kukkar N, Sharif K, Main BJ, Albers CE, El-Amin Iii SF. Bone graft substitutes for spine fusion: A brief review. World J Orthop. 2015;6(6):449-456. doi: 10.5312/wjo.v6.i6.449
  48. Zhang J, Tong D, Song H, et al. Osteoimmunity-Regulating Biomimetically Hierarchical Scaffold for Augmented Bone Regeneration. Adv Mater. 2022;34(36):e2202044. doi: 10.1002/adma.202202044
  49. Deshpande R, Shukla S, Kale A, Deshmukh N, Nisal A, Venugopalan P. Silk Fibroin Microparticle Scaffold for Use in Bone Void Filling: Safety and Efficacy Studies. ACS Biomater Sci Eng. 2022;8(3):1226-1238. doi: 10.1021/acsbiomaterials.1c01103
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International Journal of Bioprinting, Electronic ISSN: 2424-8002 Print ISSN: 2424-7723, Published by AccScience Publishing