AccScience Publishing / IJB / Online First / DOI: 10.36922/IJB026230240
Cite this article
20
Download
326
Views
Related Info Links
More by Authors Links
Journal Browser
Volume | Year
Issue
Search
News and Announcements
View All
REVIEW ARTICLE

Smart hydrogel bioinks integrated with two-dimensional nanomaterials for cardiovascular bioprinting and atherosclerosis modeling

Jiangzhou Chu1 Zhi Liu2 Zhongshan He3,4 Shengbin Liu2*
Show Less
1 School of Medicine and Health, College of Medicine and Health, Urban Vocational College of Sichuan, Chengdu, Sichuan, China
2 Department of Critical Care Medicine, Frontiers Science Center for Disease-related Molecular Network, State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University, Chengdu, Sichuan, China
3 Department of Molecular Physiology and Biological Physics, The Robert M. Berne Cardiovascular Research Center, University of Virginia, Charlottesville, Virginia, United States of America
4 Department of Biomedical Engineering, The Robert M. Berne Cardiovascular Research Center, University of Virginia, Charlottesville, Virginia, United States of America
Received: 6 June 2026 | Revised: 4 July 2026 | Accepted: 14 July 2026 | Published online: 15 July 2026
(This article belongs to the Special Issue 3D Bioprinting for Engineered Tissues and Organs)
© 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

Cardiovascular diseases remain the leading cause of mortality worldwide, and atherosclerosis underlies most ischemic cardiovascular events. However, conventional in vitro and in vivo models fail to fully reproduce the complex cellular interactions, extracellular matrix remodeling, oxidative stress, and hemodynamic microenvironment of human vascular lesions. This review summarizes recent advances in stimuli-responsive hydrogel bioinks for three-dimensional bioprinting of atherosclerosis models. We discuss how disease-responsive biomaterials can dynamically regulate the cellular microenvironment and improve the physiological relevance of engineered vascular tissues. Particular emphasis is placed on the integration of two-dimensional nanomaterials. Graphene-based materials provide electrical conductivity, mechanical reinforcement, and sensing capabilities; black phosphorus offers biodegradability, photothermal responsiveness, and reactive oxygen species-sensitive behavior; and emerging Xene materials such as germanene present additional opportunities for multifunctional bioink design. We compare their respective advantages and limitations for cardiovascular bioprinting. Finally, we discuss key translational challenges, including material standardization, long-term biosafety, biological validation, manufacturing scalability, and regulatory approval. We propose that multifunctional, disease-responsive bioinks combined with advanced biofabrication technologies will accelerate the development of physiologically relevant cardiovascular disease models and precision medicine platforms.

Graphical abstract
Keywords
Cardiovascular bioprinting
Atherosclerosis modeling
Stimuli-responsive hydrogel bioinks
2D nanomaterials
Organ-on-a-chip
Funding
This study was supported by a key research project grant from the Chengdu Technology Bureau (2026-YF05-00796-SN) and the Sichuan Province Science and Technology Major Special Project (2025ZDZX0039).
Conflict of interest
The authors declare they have no competing interests.
References
  1. Porsch F, Binder CJ. Autoimmune diseases and atherosclerotic cardiovascular disease. Nat Rev Cardiol. 2024;21(11):780-807. doi: 10.1038/s41569-024-01045-7
  2. Shoaran M, Maffia P. Tackling inflammation in atherosclerosis. Nat Rev Cardiol. 2024;21(7):442. doi: 10.1038/s41569-024-01007-z
  3. Libby P, Buring JE, Badimon L, et al. Atherosclerosis. Nat Rev Dis Prim 2019.51 2019;5(1):56. doi: 10.1038/s41572-019-0106-z
  4. Mach F, Baigent C, Catapano AL, et al. 2019 ESC/EAS guidelines for the management of dyslipidaemias: Lipid modification to reduce cardiovascular risk. Atherosclerosis. 2019;290(1):140-205. doi: 10.1016/j.atherosclerosis.2019.08.014
  5. Zhang L, Zhou J, Kong W. Extracellular matrix in vascular homeostasis and disease. Nat Rev Cardiol. 2025;22(5):333-353. doi: 10.1038/S41569-024-01103-0
  6. Lin A, Miano JM, Fisher EA, Misra A. Chronic inflammation and vascular cell plasticity in atherosclerosis. Nat Cardiovasc Res. 2024;3(12):1408-1423. doi: 10.1038/S44161-024-00569-Y
  7. Döring Y, van der Vorst EPC, Weber C. Targeting immune cell recruitment in atherosclerosis. Nat Rev Cardiol. 2024;21(11):824-840. doi: 10.1038/S41569-024-01023-Z
  8. Stroope C, Nettersheim FS, Coon B, et al. Dysregulated cellular metabolism in atherosclerosis: mediators and therapeutic opportunities. Nat Metab. 2024;6(4):617. doi: 10.1038/S42255-024-01015-W
  9. Tamargo IA, Baek KI, Kim Y, Park C, Jo H. Flow-induced reprogramming of endothelial cells in atherosclerosis. Nat Rev Cardiol. 2023;20(11):738-753. doi: 10.1038/S41569-023-00883-1
  10. Nam U, Lee S, Ahmad A, Yi HG, Jeon JS. Microphysiological Systems as Organ-Specific In Vitro Vascular Models for Disease Modeling. BioChip J. 2024;18(3):345-356. doi: 10.1007/S13206-024-00152-4
  11. Zhao Y, Landau S, Okhovatian S, et al. Integrating organoids and organ-on-a-chip devices. Nat Rev Bioeng. 2024;2(7):588-608. doi: 10.1038/s44222-024-00207-z
  12. Khosravi R, Radisic M. Heart-on-a-chip and vasculature-on-a-chip platforms as models of cardiovascular disease. Nat Rev Cardiol. 2026;23(8):537-554. doi: 10.1038/s41569-026-01255-1
  13. Huang MS, Christakopoulos F, Roth JG, Heilshorn SC. Organoid bioprinting: from cells to functional tissues. Nat Rev Bioeng. 2025;3(2):126-142. doi: 10.1038/s44222-024-00268-0
  14. Khanna A, Ayan B, Undieh AA, Yang YP, Huang NF. Advances in three-dimensional bioprinted stem cell-based tissue engineering for cardiovascular regeneration. J Mol Cell Cardiol. 2022;169:13-27. doi: 10.1016/j.yjmcc.2022.04.017
  15. Kim MS, Choi Y, Lee KY. Three-Dimensional Printing and Bioprinting Strategies for Cardiovascular Constructs: From Printing Inks to Vascularization. Polym. 2025;17(17):2337. doi: 10.3390/POLYM17172337
  16. Wang B, Zhang J, Jiang J, Cheng C, Zhao Y. Current trends, applications, and challenges in three-dimensional bioprinting for cardiovascular disease models and therapies. iScience. 2026;29(5):115519. doi: 10.1016/j.isci.2026.115519
  17. Ma D, Liu J, Lu WW, Liu W, Ruan C. Dynamic bioinks for tissue/organ bioprinting: Principle, challenge, and perspective. Prog Mater Sci. 2026;155:101527. doi: 10.1016/j.pmatsci.2025.101527
  18. Chandarana C, Sane D, Mishra S, Chaubey A, Gohil U, Prajapati B. Recent Advances in Bioink Research for Biomedical Applications. Biomed Mater Devices. 2026;4(4):3950–3981. doi: 10.1007/S44174-025-00478-Z
  19. Malekmohammadi S, Aminabad NS, Sabzi A, et al. Smart and Biomimetic 3D and 4D Printed Composite Hydrogels: Opportunities for Different Biomedical Applications. Biomedicines. 2021;9(11):1-46. doi: 10.3390/biomedicines9111537
  20. El-Husseiny HM, Mady EA, Hamabe L, et al. Smart/stimuli-responsive hydrogels: Cutting-edge platforms for tissue engineering and other biomedical applications. Mater Today Bio. 2022;13:100186. doi: 10.1016/j.mtbio.2021.100186
  21. Rahimnejad M, Jahangiri S, Zirak Hassan Kiadeh S, et al. Stimuli-responsive biomaterials: smart avenue toward 4D bioprinting. Crit Rev Biotechnol. 2024;44(5):860-891. doi: 10.1080/07388551.2023.2213398
  22. Kim J, D A G, Debnath P, Saha P. Smart Multi-Responsive Biomaterials and Their Applications for 4D Bioprinting. Biomimetics. 2024;9(8):484. doi: 10.3390/biomimetics9080484
  23. Yarali E, Mirzaali MJ, Ghalayaniesfahani A, Accardo A, Diaz-Payno PJ, Zadpoor AA. 4D Printing for Biomedical Applications. Adv Mater. 2024;36(31):e2402301. doi: 10.1002/adma.202402301
  24. Kandasamy M, Vijayananth K, Parasuraman A, Ayrilmis N. 3D Bioprinting of Biomaterials: A Review of Advances in Techniques, Materials, and Applications. Polym Adv Technol. 2025;36(9):1-17. doi: 10.1002/pat.70324
  25. Batty M, Bennett MR, Yu E. The Role of Oxidative Stress in Atherosclerosis. Cells. 2022;11(23):3843. doi: 10.3390/cells11233843
  26. Pu M, Cao H, Zhang H, et al. ROS-responsive hydrogels: from design and additive manufacturing to biomedical applications. Mater Horizons. 2024;11(16):3721-3746. doi: 10.1039/D4MH00289J
  27. Gaihre B, Potes MA, Serdiuk V, Tilton M, Liu X, Lu L. Two-dimensional nanomaterials-added dynamism in 3D printing and bioprinting of biomedical platforms: Unique opportunities and challenges. Biomaterials. 2022;284:121507. doi: 10.1016/j.biomaterials.2022.121507
  28. Zhang J, Eyisoylu H, Qin XH, Rubert M, Müller R. 3D bioprinting of graphene oxide-incorporated cell-laden bone mimicking scaffolds for promoting scaffold fidelity, osteogenic differentiation and mineralization. Acta Biomater. 2021;121:637-652. doi: 10.1016/j.actbio.2020.12.026
  29. Patil R, Alimperti S. Graphene in 3D Bioprinting. J Funct Biomater. 2024;15(4):82. doi: 10.3390/jfb15040082
  30. Edrisi F, Baheiraei N, Razavi M, Roshanbinfar K, Imani R, Jalilinejad N. Potential of graphene-based nanomaterials for cardiac tissue engineering. J Mater Chem B. 2023;11(31):7280-7299. doi: 10.1039/D3TB00654A
  31. Memarian P, Bagher Z, Asghari S, Aleemardani M, Seifalian A. Emergence of graphene as a novel nanomaterial for cardiovascular applications. Nanoscale. 2024;16(27):12793-12819. doi: 10.1039/d4nr00018h
  32. He Z, Chen W, Hu K, et al. Resolvin D1 delivery to lesional macrophages using antioxidative black phosphorus nanosheets for atherosclerosis treatment. Nat Nanotechnol. 2024;19(9):1386–1398. doi: 10.1038/S41565-024-01687-1
  33. He M, Zhang X, Ran X, et al. Black Phosphorus Nanosheets Protect Neurons by Degrading Aggregative α-syn and Clearing ROS in Parkinson’s Disease. Adv Mater. 2024;36(30):e2404576. doi: 10.1002/adma.202404576
  34. Huang W, Hu L, Tang Y, Xie Z, Zhang H. Recent Advances in Functional 2D MXene-Based Nanostructures for Next-Generation Devices. Adv Funct Mater. 2020;30(49):2005223. doi: 10.1002/adfm.202005223
  35. Wang M, Huang W. Emerging Xene-Related Nanostructures for Versatile Applications. Nanomaterials. 2023;13(3):517. doi: 10.3390/nano13030517
  36. Wang X, Sun X, Bu T, et al. Germanene-modified chitosan hydrogel for treating bacterial wound infection: An ingenious hydrogel-assisted photothermal therapy strategy. Int J Biol Macromol. 2022;221:1558-1571. doi: 10.1016/j.ijbiomac.2022.09.128
  37. Kang MS, Jang HJ, Jo HJ, Raja IS, Han DW. MXene and Xene: promising frontier beyond graphene in tissue engineering and regenerative medicine. Nanoscale Horizons. 2024;9(1):93-117. doi: 10.1039/D3NH00428G
  38. Bennett MR, Sinha S, Owens GK. Vascular Smooth Muscle Cells in Atherosclerosis. Circ Res. 2016;118(4):692-702. doi: 10.1161/CIRCRESAHA.115.306361
  39. Lambert J, Jørgensen HF. Epigenetic regulation of vascular smooth muscle cell phenotypes in atherosclerosis. Atherosclerosis. 2025;401:119085. doi: 10.1016/j.atherosclerosis.2024.119085
  40. Grootaert MOJ, Bennett MR. Vascular smooth muscle cells in atherosclerosis: time for a re-assessment. Cardiovasc Res. 2021;117(11):2326-2339. doi: 10.1093/CVR/CVAB046
  41. Chen R, McVey DG, Shen D, Huang X, Ye S. Phenotypic Switching of Vascular Smooth Muscle Cells in Atherosclerosis. J Am Heart Assoc. 2023;12(20):31121. doi: 10.1161/JAHA.123.031121
  42. Saraswathibhatla A, Indana D, Chaudhuri O. Cell-extracellular matrix mechanotransduction in 3D. Nat Rev Mol Cell Biol. 2023;24(7):495-516. doi: 10.1038/S41580-023-00583-1
  43. Kong P, Cui ZY, Huang XF, Zhang DD, Guo RJ, Han M. Inflammation and atherosclerosis: signaling pathways and therapeutic intervention. Signal Transduct Target Ther. 2022;7(1):131. doi: 10.1038/S41392-022-00955-7
  44. Ajoolabady A, Pratico D, Lin L, et al. Inflammation in atherosclerosis: pathophysiology and mechanisms. Cell Death Dis. 2024;15(11):817. doi: 10.1038/S41419-024-07166-8
  45. Hou P, Fang J, Liu Z, et al. Macrophage polarization and metabolism in atherosclerosis. Cell Death Dis. 2023;14(10):691. doi: 10.1038/S41419-023-06206-Z
  46. Chen R, Zhang H, Tang B, et al. Macrophages in cardiovascular diseases: molecular mechanisms and therapeutic targets. Signal Transduct Target Ther. 2024;9(1):130. doi: 10.1038/S41392-024-01840-1
  47. Wieland EB, Kempen LJAP, Donners MMPC, Biessen EAL, Goossens P. Macrophage heterogeneity in atherosclerosis: A matter of context. Eur J Immunol. 2024;54(1):e2350464. doi: 10.1002/EJI.202350464
  48. Li Q, Yu S, Wang Y, et al. Multiscale bioprinted arterial models recapitulate synergistic microenvironmental interactions in vascular disease. Cell Biomater. 2026;2(5):100257. doi: 10.1016/j.celbio.2025.100257
  49. Förstermann U, Xia N, Li H. Roles of Vascular Oxidative Stress and Nitric Oxide in the Pathogenesis of Atherosclerosis. Circ Res. 2017;120(4):713-735. doi: 10.1161/circresaha.116.309326
  50. Susser LI, Rayner KJ. Through the layers: how macrophages drive atherosclerosis across the vessel wall. J Clin Invest. 2022;132(9):e157011. doi: 10.1172/jcI157011
  51. Gastanadui MG, Margaroli C, Litovsky S, et al. Spatial Transcriptomic Approach to Understanding Coronary Atherosclerotic Plaque Stability. Arterioscler Thromb Vasc Biol. 2024;44(11):e264-e276. doi: 10.1161/atvbaha.123.320330
  52. Cole JE, Monaco C. Spatial Transcriptomics: A New Frontier in Atherosclerosis Research? Arterioscler Thromb Vasc Biol. 2024;44(11):2291-2293. doi: 10.1161/atvbaha.124.321652
  53. Yu H, Gao R, Liu Y, Fu L, Zhou J, Li L. Stimulus-Responsive Hydrogels as Drug Delivery Systems for Inflammation Targeted Therapy. Adv Sci. 2024;11(1):1-48. doi: 10.1002/advs.202306152
  54. Zhang J, Sun D, Liao Y, et al. Time-Released Black Phosphorus Hydrogel Accelerates Myocardial Repairing through Antioxidant and Motivates Macrophage Polarization Properties. Biomater Res. 2024;28:0029. doi: 10.34133/BMR.0029
  55. Zhang J, Sun D, Guo Y, et al. Targeted delivery of black phosphorus nanosheets by ROS responsive complex hydrogel based on angiogenesis and antioxidant promotes myocardial infarction repair. J Nanobiotechnology. 2024;22(1):433. doi: 10.1186/s12951-024-02685-0
  56. Di Nubila A, Dilella G, Simone R, Barbieri SS. Vascular Extracellular Matrix in Atherosclerosis. Int J Mol Sci. 2024;25(22):12017. doi: 10.3390/ijms252212017
  57. Alonso-Herranz L, Albarrán-Juárez J, Bentzon JF. Mechanisms of fibrous cap formation in atherosclerosis. Front Cardiovasc Med. 2023;10:1-7. doi: 10.3389/fcvm.2023.1254114
  58. Yan A, Gotlieb AI. The microenvironment of the atheroma expresses phenotypes of plaque instability. Cardiovasc Pathol. 2023;67:107572. doi: 10.1016/j.carpath.2023.107572
  59. Ruddy JM, Ikonomidis JS, Jones JA. Multidimensional Contribution of Matrix Metalloproteinases to Atherosclerotic Plaque Vulnerability: Multiple Mechanisms of Inhibition to Promote Stability. J Vasc Res. 2016;53(1-2):1-16. doi: 10.1159/000446703
  60. Wang X, Shen Y, Shang M, Liu X, Munn LL. Endothelial mechanobiology in atherosclerosis. Cardiovasc Res. 2023;119(8):1656-1675. doi: 10.1093/cvr/cvad076
  61. Cheng H, Zhong W, Wang L, et al. Effects of shear stress on vascular endothelial functions in atherosclerosis and potential therapeutic approaches. Biomed Pharmacother. 2023;158:114198. doi: 10.1016/j.biopha.2022.114198
  62. Wang WL, Shih YT, Wei SY, Chiu JJ. Impacts of aging and fluid shear stress on vascular endothelial metabolism and atherosclerosis development. J Biomed Sci. 2025;32(1):83. doi: 10.1186/s12929-025-01177-z
  63. He L, Zhang CL, Chen Q, Wang L, Huang Y. Endothelial shear stress signal transduction and atherogenesis: From mechanisms to therapeutics. Pharmacol Ther. 2022;235:108152. doi: 10.1016/j.pharmthera.2022.108152
  64. Liu Y, Huang T, Yap NA, Lim K, Ju LA. Harnessing the power of bioprinting for the development of next-generation models of thrombosis. Bioact Mater. 2024;42:328-344. doi: 10.1016/j.bioactmat.2024.08.040
  65. Maringanti R, Van Dijk CGM, Meijer EM, et al. Atherosclerosis on a Chip: A 3-Dimensional Microfluidic Model of Early Arterial Events in Human Plaques. Arterioscler Thromb Vasc Biol. 2024;44(12):2453-2472. doi: 10.1161/atvbaha.124.321332
  66. Gong S, Li Y, Yan K, et al. The Crosstalk Between Endothelial Cells, Smooth Muscle Cells, and Macrophages in Atherosclerosis. Int J Mol Sci. 2025;26(4):1457. doi: 10.3390/ijms26041457
  67. Vuong TNAM, Bartolf-Kopp M, Andelovic K, et al. Integrating Computational and Biological Hemodynamic Approaches to Improve Modeling of Atherosclerotic Arteries. Adv Sci (Weinh). 2024;11(26):e2307627. doi: 10.1002/advs.202307627
  68. Kim JJ, Cho DW. Advanced strategies in 3D bioprinting for vascular tissue engineering and disease modelling using smart bioinks. Virtual Phys Prototyp. 2024;19(1):e2395470. doi: 10.1080/17452759.2024.2395470
  69. Lu P, Ruan D, Huang M, et al. Harnessing the potential of hydrogels for advanced therapeutic applications: current achievements and future directions. Signal Transduct Target Ther. 2024;9(1):166. doi: 10.1038/S41392-024-01852-X
  70. Neumann M, di Marco G, Iudin D, et al. Stimuli-Responsive Hydrogels: The Dynamic Smart Biomaterials of Tomorrow. Macromolecules. 2023;56(21):8377-8392. doi: 10.1021/acs.macromol.3C00967
  71. Ikram M, Mahmud MAP, Kalyar AA, Alomayri T, Almahri A, Hussain D. 3D-bioprinting of MXenes: Developments, medical applications, challenges, and future roadmap. Colloids Surfaces B Biointerfaces. 2025;251:114568. doi: 10.1016/j.colsurfb.2025.114568
  72. Choi JH, Haizan I, Choi JW. Recent advances in two-dimensional materials for the diagnosis and treatment of neurodegenerative diseases. Discov Nano. 2024;19(1):151. doi: 10.1186/S11671-024-04099-1
  73. Cao H, Duan L, Zhang Y, Cao J, Zhang K. Current hydrogel advances in physicochemical and biological response-driven biomedical application diversity. Signal Transduct Target Ther. 2021;6(1):426. doi: 10.1038/S41392-021-00830-X
  74. Miao Y, Chen Y, Luo J, et al. Black phosphorus nanosheets-enabled DNA hydrogel integrating 3D-printed scaffold for promoting vascularized bone regeneration. Bioact Mater. 2023;21:97-109. doi: 10.1016/j.bioactmat.2022.08.005
  75. Wolf D, Ley K. Immunity and Inflammation in Atherosclerosis. Circ Res. 2019;124(2):315-327. doi: 10.1161/CIRCRESAHA.118.313591
  76. Su C, Menon NV, Xu X, et al. A novel human arterial wall-on-a-chip to study endothelial inflammation and vascular smooth muscle cell migration in early atherosclerosis. Lab Chip. 2021;21(12):2359-2371. doi: 10.1039/D1LC00131K
  77. Kort-Mascort J, Flores-Torres S, Peza-Chavez O, et al. Decellularized ECM hydrogels: prior use considerations, applications, and opportunities in tissue engineering and biofabrication. Biomater Sci. 2023;11(2):400-431. doi: 10.1039/D2BM01273A
  78. Wang Z, Hu C, Zhang W, et al. Dynamically crosslinked ECM-like hydrogels loaded with ROS-responsive drug nanoparticles for treating inflammation in myocardial infarction and stroke. Compos Part B Eng. 2024;285:111734. doi: 10.1016/j.compositesb.2024.111734
  79. Shakeri A, Wang Y, Zhao Y, et al. Engineering Organ-on-a-Chip Systems for Vascular Diseases. Arterioscler Thromb Vasc Biol. 2023;43(12):2241-2255. doi: 10.1161/atvbaha.123.318233
  80. Basatemur GL, Jørgensen HF, Clarke MCH, Bennett MR, Mallat Z. Vascular smooth muscle cells in atherosclerosis. Nat Rev Cardiol. 2019;16(12):727-744. doi: 10.1038/s41569-019-0227-9
  81. Synofzik J, Heene S, Jonczyk R, Blume C. Ink-structing the future of vascular tissue engineering: a review of the physiological bioink design. Bio-Design Manuf 2024.72 2024;7(2):181-205. doi: 10.1007/S42242-024-00270-W
  82. Zhou Z, Tang W, Yang J, Fan C. Application of 4D printing and bioprinting in cardiovascular tissue engineering. Biomater Sci. 2023;11(19):6403-6420. doi: 10.1039/D3BM00312D
  83. Motta I, Soccio M, Guidotti G, Lotti N, Pasquinelli G. Hydrogels for Cardio and Vascular Tissue Repair and Regeneration. Gels (Basel, Switzerland). 2024;10(3):196. doi: 10.3390/GELS10030196
  84. El-Husseiny HM, Mady EA, El-Dakroury WA, Doghish AS, Tanaka R. Stimuli-responsive hydrogels: smart state of-the-art platforms for cardiac tissue engineering. Front Bioeng Biotechnol. 2023;11(Jun 28):1-30. doi: 10.3389/fbioe.2023.1174075
  85. Kalhori D, Zakeri N, Zafar-Jafarzadeh M, Moroni L, Solati-Hashjin M. Cardiovascular 3D bioprinting: A review on cardiac tissue development. Bioprinting. 2022;28(2022):e00221. doi: 10.1016/j.bprint.2022.e00221
  86. Schwab A, Levato R, D’Este M, Piluso S, Eglin D, Malda J. Printability and Shape Fidelity of Bioinks in 3D Bioprinting. Chem Rev. 2020;120(19):11028-11055. doi: 10.1021/acs.chemrev.0C00084
  87. Kamboj D, Choudhary B, Singh G, Kumar N, Narwal S, Dhingra AK. Oxidative Stress in Cardiovascular Diseases: Mechanisms and Exploring Advanced Therapies. Cardiovasc Hematol Agents Med Chem. 2025;23(3):183-201. doi: 10.2174/0118715257344485250207074727
  88. Ungvari Z, Tarantini S, Donato AJ, Galvan V, Csiszar A. Mechanisms of vascular aging. Circ Res. 2018;123(7):849-867. doi: 10.1161/CIRCRESAHA.118.31137
  89. Ungvari Z, Tarantini S, Sorond F, Merkely B, Csiszar A. Mechanisms of Vascular Aging, A Geroscience Perspective: JACC Focus Seminar. J Am Coll Cardiol. 2020;75(8):931. doi: 10.1016/j.jacc.2019.11.061
  90. Yuan Z, Li Y, Sun M, et al. Recent progress in ROS-responsive biomaterials for the diagnosis and treatment of cardiovascular diseases. Theranostics. 2025;15(11):5172-5219. doi: 10.7150/thno.106991
  91. Tapeinos C, Gao H, Bauleth-Ramos T, Santos HA. Progress in Stimuli-Responsive Biomaterials for Treating Cardiovascular and Cerebrovascular Diseases. Small. 2022;18(36):e2200291. doi: 10.1002/smll.202200291
  92. Zhang Y, Jiang M, Wang T. Reactive oxygen species (ROS)-responsive biomaterials for treating myocardial ischemia-reperfusion injury. Front Bioeng Biotechnol. 2024;12:1469393. doi: 10.3389/fbioe.2024.1469393
  93. Shen Z, Guo Z, Tan T, Hu J, Zhang Y. Reactive Oxygen Species Scavenging and Biodegradable Peptide Hydrogel as 3D Culture Scaffold for Cardiomyocytes. ACS Biomater Sci Eng. 2020;6(7):3957-3966. doi: 10.1021/acsbiomaterials.0c00340
  94. Tong S, Chen J, Li Y, Zhao W. Emerging Gel Technologies for Atherosclerosis Research and Intervention. Gels. 2026;12(1):80. doi: 10.3390/GELS12010080
  95. Fu Y, Zhou Y, Wang K, Li Z, Kong W. Extracellular Matrix Interactome in Modulating Vascular Homeostasis and Remodeling. Circ Res. 2024;134(7):931-949. doi: 10.1161/CIRCRESAHA.123.324055
  96. Bräuninger H, Krüger S, Bacmeister L, et al. Matrix metalloproteinases in coronary artery disease and myocardial infarction. Basic Res Cardiol. 2023;118(1):18. doi: 10.1007/S00395-023-00987-2
  97. Chen W, Wang C, Liu W, et al. A Matrix-Metalloproteinase-Responsive Hydrogel System for Modulating the Immune Microenvironment in Myocardial Infarction. Adv Mater. 2023;35(13):2209041. doi: 10.1002/adma.202209041
  98. 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
  99. Zustiak SP, Leach JB. Hydrolytically degradable poly(ethylene glycol) hydrogel scaffolds with tunable degradation and mechanical properties. Biomacromolecules. 2010;11(5):1348-1357. doi: 10.1021/bm100137q
  100. Marder M, Remmert C, Perschel JA, et al. Stem cell-derived vessels-on-chip for cardiovascular disease modeling. Cell Rep. 2024;43(4):114008. doi: 10.1016/j.celrep.2024.114008
  101. Ajiteru O, Sultan MT, Lee YJ, et al. A 3D Printable Electroconductive Biocomposite Bioink Based on Silk Fibroin-Conjugated Graphene Oxide. Nano Lett. 2020;20(9):6873-6883. doi: 10.1021/acs.nanolett.0c02986
  102. Lee M, Park J, Choe G, et al. A Conductive and Adhesive Hydrogel Composed of MXene Nanoflakes as a Paintable Cardiac Patch for Infarcted Heart Repair. ACS Nano. 2023;17(13):12290-12304. doi: 10.1021/acsnano.3c00933
  103. Chong J, Sung C, Nam KS, et al. Highly conductive tissue-like hydrogel interface through template-directed assembly. Nat Commun. 2023;14(1):2206. doi: 10.1038/S41467-023-37948-1
  104. Grzelak KA, Westerfield AD, Kumar V, et al. Electrical stimulation directs formation of perfused vasculature in engineered tissues. bioRxiv Prepr Serv Biol. Published online September 3,.2025 doi: 10.1101/2025.08.28.672965
  105. Qian Y, Yao Y. Mechanobiological regulation of endothelial vascularization after myocardial infarction: matrix mechanics, hydrogel strategies and applications. Biomater Sci. Published online.2026 doi: 10.1039/D5BM01885D
  106. Tao Y, Chan HF, Shi B, Li M, Leong KW. Light: A Magical Tool for Controlled Drug Delivery. Adv Funct Mater. 2020;30(49):2005029. doi: 10.1002/adfm.202005029
  107. Luo R, Xiang X, Jiao Q, Hua H, Chen Y. Photoresponsive Hydrogels for Tissue Engineering. ACS Biomater Sci Eng. 2024;10(6):3612-3630. doi: 10.1021/acsbiomaterials.4c00314
  108. Zhang Y, Kumar P, Lv S, et al. Recent advances in 3D bioprinting of vascularized tissues. Mater Des. 2021;199:109398. doi: 10.1016/j.matdes.2020.109398
  109. Xian R, Xian H, Dong H, et al. Black Phosphorus-Loaded Gelatin Methacryloyl Hydrogels Enhance Angiogenesis via Activation of the PEAK1-MAPK Pathway. ACS Appl Mater Interfaces. 2025;17(18):26371-26385. doi: 10.1021/acsami.5C02054
  110. Zhang Y, Qi G, Zhang L, et al. Black phosphorus-based photothermal-responsive hydrogel enhanced osteoporotic bone injury regeneration by alleviating oxidative stress and remodeling bone homeostasis. J Nanobiotechnology. 2026;24(1):238. doi: 10.1186/s12951-026-04097-8
  111. Picos A, Seoane N, Campos-Toimil M, Viña D. Vascular senescence and aging: mechanisms, clinical implications, and therapeutic prospects. Biogerontology. 2025;26(3):118. doi: 10.1007/S10522-025-10256-5
  112. Herzog MJ, Müller P, Lechner K, et al. Arterial stiffness and vascular aging: mechanisms, prevention, and therapy. Signal Transduct Target Ther. 2025;10(1):282. doi: 10.1038/s41392-025-02346-0
  113. Zheng Y, Hong X, Wang J, et al. 2D Nanomaterials for Tissue Engineering and Regenerative Nanomedicines: Recent Advances and Future Challenges. Adv Healthc Mater. 2021;10(7):e2001743. doi: 10.1002/adhm.202001743
  114. Zorrón M, Cabrera AL, Sharma R, et al. Emerging 2D Nanomaterials-Integrated Hydrogels: Advancements in Designing Theragenerative Materials for Bone Regeneration and Disease Therapy. Adv Sci. 2024;11(31):e2403204-e2403204. doi: 10.1002/advs.202403204
  115. Qi W, Zhang R, Wang Z, et al. Advances in the Application of Black Phosphorus-Based Composite Biomedical Materials in the Field of Tissue Engineering. Pharmaceuticals (Basel). 2024;17(2):242. doi: 10.3390/ph17020242
  116. Lee H, Kim KS, Zare I, et al. Smart nanomaterials for multimodal theranostics and tissue regeneration. Coord Chem Rev. 2025;541:216801. doi: 10.1016/j.ccr.2025.216801
  117. Chen J, Deng M, Wang J, et al. Recent advances in injectable hydrogels for osteoarthritis treatments. Front Bioeng Biotechnol. 2025;13:1644222. doi: 10.3389/fbioe.2025.1644222
  118. Jalilinejad N, Rabiee M, Baheiraei N, et al. Electrically conductive carbon-based (bio)-nanomaterials for cardiac tissue engineering. Bioeng Transl Med. 2023;8(1):e10347. doi: 10.1002/btm2.10347
  119. Lee M, Kim MC, Lee JY. Nanomaterial-Based Electrically Conductive Hydrogels for Cardiac Tissue Repair. Int J Nanomedicine. 2022;17:6181-6200. doi: 10.2147/ijn.s386763
  120. Lisboa ES, Serafim C, Santana W, et al. Nanomaterials-combined methacrylated gelatin hydrogels (GelMA) for cardiac tissue constructs. J Control Release. 2024;365:617-639. doi: 10.1016/j.jconrel.2023.11.056
  121. Byrne R, Carrico A, Lettieri M, Rajan AK, Forster RJ, Cumba LR. Bioinks and biofabrication techniques for biosensors development: A review. Mater today Bio. 2024;28:101185. doi: 10.1016/j.mtbio.2024.101185
  122. Wang Z, Zhao J, Tang W, et al. Multifunctional Nanoengineered Hydrogels Consisting of Black Phosphorus Nanosheets Upregulate Bone Formation. Small. 2019;15(41):e1901560. doi: 10.1002/smll.201901560
  123. Li J, Liu X, Crook JM, Wallace GG. Development of 3D printable graphene oxide based bio-ink for cell support and tissue engineering. Front Bioeng Biotechnol. 2022;10:994776. doi: 10.3389/fbioe.2022.994776
  124. Shin SR, Zihlmann C, Akbari M, et al. Reduced Graphene Oxide-GelMA Hybrid Hydrogels as Scaffolds for Cardiac Tissue Engineering. Small. 2016;12(27):3677-3689. doi: 10.1002/smll.201600178
  125. Chen XB, Fazel Anvari-Yazdi A, Duan X, et al. Biomaterials / bioinks and extrusion bioprinting. Bioact Mater. 2023;28:511-536. doi: 10.1016/j.bioactmat.2023.06.006
  126. Santana MDV, Magulas MBS, Brito GC, et al. Cryogenic 3D Printing of GelMA/Graphene Bioinks: Improved Mechanical Strength and Structural Properties for Tissue Engineering. Int J Nanomedicine. 2024;19:10745-10765. doi: 10.2147/ijn.s486868
  127. Ni F, Chen Y, Wang Z, et al. Graphene derivative based hydrogels in biomedical applications. J Tissue Eng. 2024;15:20417314241282131. doi: 10.1177/20417314241282131
  128. Diez-Aldama I, Garcia-Villen F, Saenz-Del-Burgo L, Scaini D, Pedraz JL. Graphene Oxide Modified Bioink for 3D-Bioprinting of Vascular Graft. ACS Appl bio Mater. 2025;8(5):3858-3872. doi: 10.1021/acsabm.5c00004
  129. Liu N, Ye X, Yao B, et al. Advances in 3D bioprinting technology for cardiac tissue engineering and regeneration. Bioact Mater. 2021;6(5):1388-1401. doi: 10.1016/j.bioactmat.2020.10.021
  130. Shin SR, Aghaei-Ghareh-Bolagh B, Dang TT, et al. Cell-laden microengineered and mechanically tunable hybrid hydrogels of gelatin and graphene oxide. Adv Mater. 2013;25(44):6385-6391. doi: 10.1002/adma.201301082
  131. Zhou J, Yang X, Liu W, et al. Injectable OPF/graphene oxide hydrogels provide mechanical support and enhance cell electrical signaling after implantation into myocardial infarct. Theranostics. 2018;8(12):3317-3330. doi: 10.7150/THNO.25504
  132. Noor N, Shapira A, Edri R, Gal I, Wertheim L, Dvir T. 3D Printing of Personalized Thick and Perfusable Cardiac Patches and Hearts. Adv Sci. 2019;6(11):1900344. doi: 10.1002/advs.201900344
  133. Dai X, Zhang Y, Gao L, et al. A mechanically strong, highly stable, thermoplastic, and self-healable supramolecular polymer hydrogel. Adv Mater. 2015;27(23):3566-3571. doi: 10.1002/adma.201500534
  134. Bellet P, Gasparotto M, Pressi S, et al. Graphene-Based Scaffolds for Regenerative Medicine. Nanomater (Basel, Switzerland). 2021;11(2):1-41. doi: 10.3390/nano11020404
  135. Oubari H, Berkane Y, Jeljeli M, Lellouch AG, Smadja DM. Engineering the Future of Stem Cells in Vascular Reconstruction: A Leap Towards Functional Endothelialized Tissue-Engineered Vascular Conduits. Stem cell Rev reports. 2025;21(8):2796-2806. doi: 10.1007/s12015-025-10968-8
  136. Paul A, Hasan A, Kindi H Al, et al. Injectable graphene oxide/hydrogel-based angiogenic gene delivery system for vasculogenesis and cardiac repair. ACS Nano. 2014;8(8):8050-8062. doi: 10.1021/nn5020787
  137. Landau S, Okhovatian S, Zhao Y, et al. Bioengineering vascularization. Dev. 2024;151(23):dev204455. doi: 10.1242/dev.204455/363262
  138. Wang X, He B. Endothelial dysfunction: molecular mechanisms and clinical implications. MedComm. 2024;5(8):e651. doi: 10.1002/mcO2.651
  139. Lu Y, Yang G, Wang S, et al. Stretchable graphene–hydrogel interfaces for wearable and implantable bioelectronics. Nat Electron. 2024;7(1):51-65. doi: 10.1038/s41928-023-01091-y
  140. Cognetti JS, Moen MT, Brewer MG, et al. A photonic biosensor-integrated tissue chip platform for real-time sensing of lung epithelial inflammatory markers. Lab Chip. 2023;23(2):239-250. doi: 10.1039/d2lC00864e
  141. Shinde A, Illath K, Kasiviswanathan U, et al. Recent Advances of Biosensor-Integrated Organ-on-a-Chip Technologies for Diagnostics and Therapeutics. Anal Chem. 2023;95(6):3121-3146. doi: 10.1021/acs.analchem.2C05036
  142. Yang W, Li T, Liao S, Zhou J, Huang L. Organ-on-a-chip platforms integrated with biosensors for precise monitoring of the cells and cellular microenvironment. TrAC Trends Anal Chem. 2024;172:117569. doi: 10.1016/j.trac.2024.117569
  143. Kosowska K, Korycka P, Jankowska-Snopkiewicz K, et al. Graphene Oxide (GO)-Based Bioink with Enhanced 3D Printability and Mechanical Properties for Tissue Engineering Applications. Nanomater (Basel, Switzerland). 2024;14(9):760. doi: 10.3390/nano14090760
  144. Lee YJ, Ajiteru O, Lee JS, et al. Highly conductive, stretchable, and biocompatible graphene oxide biocomposite hydrogel for advanced tissue engineering. Biofabrication. 2024;16(4):045032. doi: 10.1088/1758-5090/ad6cf7
  145. Chen X, Manshaii F, Tioran K, et al. Wearable biosensors for cardiovascular monitoring leveraging nanomaterials. Adv Compos Hybrid Mater. 2024;7(3):97. doi: 10.1007/s42114-024-00906-6
  146. Coronado Reyes OI, Téllez Anguiano A del C, Gutiérrez Gnecchi JA, Castro Pimentel LA, García Rodríguez E. Comparison between mathematical methods to estimate blood glucose levels from ECG signals. Biosens Bioelectron X. 2024;18:100474. doi: 10.1016/j.biosx.2024.100474
  147. Li J, Zeng H, Zeng Z, Zeng Y, Xie T. Promising Graphene-Based Nanomaterials and Their Biomedical Applications and Potential Risks: A Comprehensive Review. ACS Biomater Sci Eng. 2021;7(12):5363-5396. doi: 10.1021/acsbiomaterials.1c00875
  148. Lin H, Buerki-Thurnherr T, Kaur J, et al. Environmental and Health Impacts of Graphene and Other Two-Dimensional Materials: A Graphene Flagship Perspective. ACS Nano. 2024;18(8):6038-6094. doi: 10.1021/acsnano.3c09699
  149. Donato KZ, Tan HL, Marangoni VS, et al. Graphene oxide classification and standardization. Sci Rep. 2023;13(1):6064. doi: 10.1038/S41598-023-33350-5
  150. Loret T, de Luna LAV, Lucherelli MA, et al. Lung Persistence, Biodegradation, and Elimination of Graphene-Based Materials are Predominantly Size-Dependent and Mediated by Alveolar Phagocytes. Small. 2023;19(39):e2301201. doi: 10.1002/smll.202301201
  151. Zhang Z, Schniepp HC, Adamson DH. Characterization of graphene oxide: Variations in reported approaches. Carbon N Y. 2019;154:510-521. doi: 10.1016/j.carbon.2019.07.103
  152. Tao W, Zhu X, Yu X, et al. Black Phosphorus Nanosheets as a Robust Delivery Platform for Cancer Theranostics. Adv Mater. 2017;29(1):1603276. doi: 10.1002/adma.201603276
  153. Wu J, Xu R, Shao M, Zhao L, Xu W, Guo Y. Phosphorus-Based Nanomaterials for Biomedical Applications: A Review. ACS Appl Nano Mater. 2024;7(10):11022-11036. doi: 10.1021/acsanm.4c00015
  154. Guo Y, Huang C, Zhang J, Wang Z, Guo X, Wei Y. Injectable Conductive Hydrogel Containing Black Phosphorus Nanosheets Inhibits the Oxidative Stress-Inflammation Chain during Myocardial Infarction. ACS Appl Nano Mater. 2023;6(18):16749-16767. doi: 10.1021/acsanm.3c02956
  155. Ling X, Wang H, Huang S, Xia F, Dresselhaus MS. The renaissance of black phosphorus. Proc Natl Acad Sci U S A. 2015;112(15):4523-4530. doi: 10.1073/pnas.1416581112
  156. Qian X, Gu Z, Chen Y. Two-dimensional black phosphorus nanosheets for theranostic nanomedicine. Mater Horizons. 2017;4(5):800-816. doi: 10.1039/c7mh00305f
  157. Sun Z, Xie H, Tang S, et al. Ultrasmall Black Phosphorus Quantum Dots: Synthesis and Use as Photothermal Agents. Angew Chem Int Ed Engl. 2015;54(39):11526-11530. doi: 10.1002/anie.201506154
  158. Shao J, Xie H, Huang H, et al. Biodegradable black phosphorus-based nanospheres for in vivo photothermal cancer therapy. Nat Commun. 2016;7:12967. doi: 10.1038/ncomms12967
  159. Li H xuan, Zhao K chi, Jiang J jia, Zhu Q san. Research progress on black phosphorus hybrids hydrogel platforms for biomedical applications. J Biol Eng. 2023;17(1):8. doi: 10.1186/s13036-023-00328-w
  160. Choi JR, Yong KW, Choi JY, et al. Black Phosphorus and its Biomedical Applications. Theranostics. 2018;8(4):1005-1026. doi: 10.7150/THNO.22573
  161. Bai X, Wang R, Hu X, et al. Two-Dimensional Biodegradable Black Phosphorus Nanosheets Promote Large Full-Thickness Wound Healing through In Situ Regeneration Therapy. ACS Nano. 2024;18(4):3553-3574. doi: 10.1021/acsnano.3c11177
  162. Wu N, Wang X, Das CM, et al. Bioengineering applications of black phosphorus and their toxicity assessment. Environ Sci Nano. 2021;8(12):3452-3477. doi: 10.1039/d1en00273b
  163. Zhang T, Wan Y, Xie H, et al. Degradation Chemistry and Stabilization of Exfoliated Few-Layer Black Phosphorus in Water. J Am Chem Soc. 2018;140(24):7561-7567. doi: 10.1021/jacs.8b02156
  164. Qiu Y, Yu C, Yue Z, et al. Chronological-Programmed Black Phosphorus Hydrogel for Responsive Modulation of the Pathological Microenvironment in Myocardial Infarction. ACS Appl Mater Interfaces. 2024;16(14):17323-17338. doi: 10.1021/acsami.4c01956
  165. Xiang Q, Yi X, Zhu XH, Wei X, Jiang DS. Regulated cell death in myocardial ischemia–reperfusion injury. Trends Endocrinol Metab. 2024;35(3):219-234. doi: 10.1016/j.tem.2023.10.010
  166. Qin L, Ling G, Peng F, et al. Black phosphorus nanosheets and gemcitabine encapsulated thermo-sensitive hydrogel for synergistic photothermal-chemotherapy. J Colloid Interface Sci. 2019;556:232-238. doi: 10.1016/j.jcis.2019.08.058
  167. Qiu M, Wang D, Liang W, et al. Novel concept of the smart NIR-light-controlled drug release of black phosphorus nanostructure for cancer therapy. Proc Natl Acad Sci U S A. 2018;115(3):501-506. doi: 10.1073/pnas.1714421115
  168. Chen J, Huan W, Mao L, et al. Impaired barrier integrity of endothelial cells induced by PEGylated black phosphorus nanosheets. Sci Total Environ. 2023;861:160645. doi: 10.1016/j.scitotenv.2022.160645
  169. Xu Y, Xu C, He L, et al. Stratified-structural hydrogel incorporated with magnesium-ion-modified black phosphorus nanosheets for promoting neuro-vascularized bone regeneration. Bioact Mater. 2022;16:271-284. doi: 10.1016/j.bioactmat.2022.02.024
  170. Cui H, Yu ZX, Huang Y, et al. 3D printing of thick myocardial tissue constructs with anisotropic myofibers and perfusable vascular channels. Biomater Adv. 2023;153:213579. doi: 10.1016/j.bioadv.2023.213579
  171. Sakamoto A, Suwa K, Kawakami R, et al. Significance of Intra-plaque Hemorrhage for the Development of High-Risk Vulnerable Plaque: Current Understanding from Basic to Clinical Points of View. Int J Mol Sci. 2023;24(17):13298. doi: 10.3390/ijms241713298
  172. Ugusman A, Hisam NSN, Othman NS, et al. Pharmacological interventions for intraplaque neovascularization in atherosclerosis. Pharmacol Ther. 2024;261:108685. doi: 10.1016/j.pharmthera.2024.108685
  173. Wang H, Gui B, Chen Y, et al. Black-Phosphorus-Reinforced Injectable Conductive Biodegradable Hydrogel for the Delivery of ADSC-Derived Exosomes to Repair Myocardial Infarction. ACS Appl Mater Interfaces. 2024;16(43):58286-58298. doi: 10.1021/acsami.4c12285
  174. Hasan MM, Ahmad A, Akter MZ, Choi YJ, Yi HG. Bioinks for bioprinting using plant-derived biomaterials. Biofabrication. 2024;16(4):042004. doi: 10.1088/1758-5090/ad6932
  175. Emebu S, Ogunleye RO, Achbergerová E, Vítková L, Ponížil P, Martinez CM. Review and proposition for model-based multivariable-multiobjective optimisation of extrusion-based bioprinting. Appl Mater Today. 2023;34:101914. doi: 10.1016/j.apmt.2023.101914
  176. Wang J, Cui Z, Maniruzzaman M. Bioprinting: A focus on improving bioink printability and cell performance based on different process parameters. Int J Pharm. 2023;640:123020. doi: 10.1016/j.ijpharm.2023.123020
  177. Cooke ME, Rosenzweig DH. The rheology of direct and suspended extrusion bioprinting. APL Bioeng. 2021;5(1):011502. doi: 10.1063/5.0031475
  178. Ribeiro A, Blokzijl MM, Levato R, et al. Assessing bioink shape fidelity to aid material development in 3D bioprinting. Biofabrication. 2018;10(1):014102. doi: 10.1088/1758-5090/aa90e2
  179. Groll J, Burdick JA, Cho DW, et al. A definition of bioinks and their distinction from biomaterial inks. Biofabrication. 2019;11(1):013001. doi: 10.1088/1758-5090/aaec52
  180. Guo J, Du L. An update on ox-LDL-inducing vascular smooth muscle cell-derived foam cells in atherosclerosis. Front Cell Dev Biol. 2024;12:1-12. doi: 10.3389/fcell.2024.1481505
  181. Kong Z, Wang X. Bioprinting Technologies and Bioinks for Vascular Model Establishment. Int J Mol Sci. 2023;24(1):891. doi: 10.3390/ijms24010891
  182. Ashtari K, Nazari H, Ko H, et al. Electrically conductive nanomaterials for cardiac tissue engineering. Adv Drug Deliv Rev. 2019;144:162-179. doi: 10.1016/j.addr.2019.06.001
  183. Luo X, Zhang M, Dai W, et al. Targeted nanoparticles triggered by plaque microenvironment for atherosclerosis treatment through cascade effects of reactive oxygen species scavenging and anti-inflammation. J Nanobiotechnology. 2024;22(1):440. doi: 10.1186/s12951-024-02652-9
  184. Chen X, Sun Z, Peng X, et al. Graphene Oxide/Black Phosphorus Functionalized Collagen Scaffolds with Enhanced Near-Infrared Controlled In Situ Biomineralization for Promoting Infectious Bone Defect Repair through PI3K/Akt Pathway. ACS Appl Mater Interfaces. 2024;16(38):50369-50388. doi: 10.1021/acsami.4c10284
  185. Akther F, Sajin D, Moonshi SS, et al. An intimal-lumen model in a microfluidic device: potential platform for atherosclerosis-related studies. Lab Chip. 2025;25(3):354-369. doi: 10.1039/d4lc00868e
  186. Chegel R, Behzad S. Tunable Electronic, Optical, and Thermal Properties of two- dimensional Germanene via an external electric field. Sci Rep. 2020;10(1):704. doi: 10.1038/S41598-020-57558-x
  187. Rohaizad N, Mayorga-Martinez CC, Fojtů M, Latiff NM, Pumera M. Two-dimensional materials in biomedical, biosensing and sensing applications. Chem Soc Rev. 2021;50(1):619-657. doi: 10.1039/d0CS00150c
  188. Tao W, Kong N, Ji X, et al. Emerging two-dimensional monoelemental materials (Xenes) for biomedical applications. Chem Soc Rev. 2019;48(11):2891-2912. doi: 10.1039/c8cs00823j
  189. Kang Y, Zhang H, Chen L, et al. The marriage of Xenes and hydrogels: Fundamentals, applications, and outlook. Innov. 2022;3(6):100327. doi: 10.1016/j.xinn.2022.100327
  190. Garg M, Thakur A. A review: Biomedical applications of phosphorene, antimonene, and germanene-based 2D material/hydrogel complexes. J Mater Sci. 2023;58(1):34-45. doi: 10.1007/S10853-022-07954-7
  191. Ge M, Zong M, Xu D, et al. Freestanding germanene nanosheets for rapid degradation and photothermal conversion. Mater Today Nano. 2021;15:100119. doi: 10.1016/j.mtnano.2021.100119
  192. Liu N, Bo G, Liu Y, Xu X, Du Y, Dou SX. Recent Progress on Germanene and Functionalized Germanene: Preparation, Characterizations, Applications, and Challenges. Small. 2019;15(32):1805147. doi: 10.1002/smll.201805147
  193. Ng S, Pumera M. 2D Functionalized Germananes: Synthesis and Applications. Adv Mater. 2023;35(7):1-37. doi: 10.1002/adma.202207196
  194. Kupchak I, Bechstedt F, Pulci O, Gori P. Tuning the optical absorption and exciton bound states of germanene by chemical functionalization. Sci Rep. 2024;14(1):25182. doi: 10.1038/S41598-024-75620-W
  195. Kovalska E, Antonatos N, Luxa J, Sofer Z. Edge-Hydrogenated Germanene by Electrochemical Decalcification-Exfoliation of CaGe2: Germanene-Enabled Vapor Sensor. ACS Nano. 2021;15(10):16709-16718. doi: 10.1021/acsnano.1c06675
  196. Miri AK, Khalilpour A, Cecen B, Maharjan S, Shin SR, Khademhosseini A. Multiscale bioprinting of vascularized models. Biomaterials. 2019;198:204-216. doi: 10.1016/j.biomaterials.2018.08.006
  197. Samal S, Sahoo SP, Acharya B. Nanotechnology-Driven cardiac tissue engineering and 3D bioprinting: Mechanistic insights into myocardial repair and regeneration. Nano Trends. 2025;12:100155. doi: 10.1016/j.nwnano.2025.100155
  198. 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
  199. Suzuki S, Katsube D, Yano M, et al. Germanene Reformation from Oxidized Germanene on Ag(111)/Ge(111) by Vacuum Annealing. Small methods. 2025;9(3):e2400863. doi: 10.1002/smtd.202400863
  200. Ouyang J, Feng C, Ji X, et al. 2D Monoelemental Germanene Quantum Dots: Synthesis as Robust Photothermal Agents for Photonic Cancer Nanomedicine. Angew Chem Int Ed Engl. 2019;58(38):13405-13410. doi: 10.1002/ANIE.201908377
  201. Geevarghese R, Żur-Pińska J, Parisi D, Włodarczyk-Biegun MK. A comprehensive protocol for hydrogel-based bioink design: balancing printability, stability, and biocompatibility. J Mater Chem B. 2025;13(42):13750-13768. doi: 10.1039/d5tb00737b
  202. 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
  203. Bianco E, Butler S, Jiang S, Restrepo OD, Windl W, Goldberger JE. Stability and Exfoliation of Germanane: A Germanium Graphane Analogue. ACS Nano. 2013;7(5):4414-4421. doi: 10.1021/nn4009406
  204. Wang H, Wang C, Zhang Y, et al. Recent Advances in Xenes Based FET for Biosensing Applications. Adv Sci (Weinh). 2025;12(21):e2500752. doi: 10.1002/advs.202500752
  205. Duan X, Liu Z, Xie Z, et al. Emerging monoelemental 2D materials (Xenes) for biosensor applications. Nano Res. 2023;16(5):7030-7052. doi: 10.1007/S12274-023-5418-3
  206. Dixit M, Shrestha LK, Ariga K, Pati F. Carbon-Based Nanoarchitectonics in Advancing Cardiac Tissue Bioprinting: A Review. ACS Appl Nano Mater. 2024;7(21):24638-24652. doi: 10.1021/acsanm.4C04441
  207. Ding Q, Sun T, Su W, et al. Bioinspired Multifunctional Black Phosphorus Hydrogel with Antibacterial and Antioxidant Properties: A Stepwise Countermeasure for Diabetic Skin Wound Healing. Adv Healthc Mater. 2022;11(12):e2102791. doi: 10.1002/adhm.202102791
  208. Wu Y, Okesola BO, Xu J, et al. Disordered protein-graphene oxide co-assembly and supramolecular biofabrication of functional fluidic devices. Nat Commun. 2020;11(1):1182. doi: 10.1038/S41467-020-14716-Z
  209. Kaviani S, Talebi A, Labbaf S, Karimzadeh F. Conductive GelMA/alginate/polypyrrole/graphene hydrogel as a potential scaffold for cardiac tissue engineering; Physiochemical, mechanical, and biological evaluations. Int J Biol Macromol. 2024;259(Pt 2):129276. doi: 10.1016/j.ijbiomac.2024.129276
  210. Liu F, Ding N, Huo D, et al. Surface-Engineered Monocyte Inhibits Atherosclerotic Plaque Destabilization via Graphene Quantum Dot-Mediated MicroRNA Delivery. Adv Healthc Mater. 2019;8(15):e1900386. doi: 10.1002/adhm.201900386
  211. Chung S, Revia RA, Zhang M. Graphene Quantum Dots and Their Applications in Bioimaging, Biosensing, and Therapy. Adv Mater. 2021;33(22):e1904362. doi: 10.1002/adma.201904362
  212. Yan Z, Liu Z, Yang B, Zhu X, Song E, Song Y. Long-term exposure of molybdenum disulfide nanosheets leads to hepatic lipid accumulation and atherogenesis in apolipoprotein E deficient mice. NanoImpact. 2023;30:100462. doi: 10.1016/j.impact.2023.100462
  213. Ge X, Cui H, Kong J, et al. A Non-Invasive Nanoprobe for In Vivo Photoacoustic Imaging of Vulnerable Atherosclerotic Plaque. Adv Mater. 2020;32(38):e2000037. doi: 10.1002/adma.202000037
  214. Bai Q, Lao X, Pang SY, et al. Plaque-Targeted Delivery of Fluoride-Free MXene Nanozyme for Alleviating Atherosclerosis via Sonocatalytic Therapy. Adv Mater. 2025;37(48):1-16. doi: 10.1002/adma.202420189
  215. Leung CM, de Haan P, Ronaldson-Bouchard K, et al. A guide to the organ-on-a-chip. Nat Rev Methods Prim. 2022;2(1):33. doi: 10.1038/s43586-022-00118-6
  216. Augustin HG, Koh GY. Organotypic vasculature: From descriptive heterogeneity to functional pathophysiology. Science. 2017;357(6353):1-12. doi: 10.1126/science.aal2379
  217. Li J, Chen X, Hu M, et al. The application of composite scaffold materials based on decellularized vascular matrix in tissue engineering: a review. Biomed Eng Online. 2023;22(1):62. doi: 10.1186/S12938-023-01120-z
  218. Ouyang Z, Zhong J, Shen J, Zeng Y. The cell origins of foam cell and lipid metabolism regulated by mechanical stress in atherosclerosis. Front Physiol. 2023;14:01-09. doi: 10.3389/fphys.2023.1179828
  219. Fernandez DM, Rahman AH, Fernandez NF, et al. Single-cell immune landscape of human atherosclerotic plaques. Nat Med. 2019;25(10):1576-1588. doi: 10.1038/S41591-019-0590-4
  220. La Chica Lhoëst MT, Martinez A, Claudi L, et al. Mechanisms modulating foam cell formation in the arterial intima: exploring new therapeutic opportunities in atherosclerosis. Front Cardiovasc Med. 2024;11:1381520. doi: 10.3389/fcvm.2024.1381520
  221. Chen J, Zhang X, Millican R, et al. Recent Progress in in vitro Models for Atherosclerosis Studies. Front Cardiovasc Med. 2021;8:1-23. doi: 10.3389/fcvm.2021.790529
  222. Wang R, Zhang H, Li S, et al. Current progress of in vitro vascular models on microfluidic chips. Biofabrication. 2025;17(2):022004. doi: 10.1088/1758-5090/adb182
  223. Garcia-Sabaté A, Mohamed WKE, Sapudom J, Alatoom A, Al Safadi L, Teo JCM. Biomimetic 3D Models for Investigating the Role of Monocytes and Macrophages in Atherosclerosis. Bioeng (Basel, Switzerland). 2020;7(3):1-20. doi: 10.3390/bioengineering7030113
  224. Akther F, Sajin D, Moonshi SS, Wu Y, Vazquez-Prada KX, Ta HT. Modeling Foam Cell Formation in A Hydrogel-Based 3D-Intimal Model: A Study of The Role of Multi-Diseases During Early Atherosclerosis. Adv Biol. 2024;8(4):e2300463. doi: 10.1002/adbi.202300463
  225. Naiyeju I, Lehoux S, Tabrizian M. Key parameters for designing robust 2D and 3D spheroid models for in vitro atherosclerosis research. Bioeng Transl Med. 2025;10(3):e10736. doi: 10.1002/btm2.10736
  226. Krug A, Inserra G, Drewes R, et al. Three-dimensional spheroid models for cardiovascular biology and pathology. Mechanobiol Med. 2025;3(3):100144. doi: 10.1016/j.mbm.2025.100144
  227. Parma L, Sachs N, Sobczak N, et al. CXCL12 Derived From ACKR1+ Intraplaque Neovessels Mediates CD8+ T Cell Recruitment in Human Atherosclerosis. Circulation. 2025;151(8):581-584. doi: 10.1161/CIRCULATIONAHA.124.072560
  228. Mallone A, Stenger C, Von Eckardstein A, Hoerstrup SP, Weber B. Biofabricating atherosclerotic plaques: In vitro engineering of a three-dimensional human fibroatheroma model. Biomaterials. 2018;150:49-59. doi: 10.1016/j.biomaterials.2017.09.034
  229. Wang Y, Liu A, Zhang X, et al. Microfluidic organ-on-a-chip for modeling coronary artery disease: Recent applications, limitations and potential. J Tissue Eng. 2025;16:20417314251394447. doi: 10.1177/20417314251394447
  230. Quintard C, Tubbs E, Jonsson G, et al. A microfluidic platform integrating functional vascularized organoids-on-chip. Nat Commun. 2024;15(1):1452. doi: 10.1038/s41467-024-45710-4
  231. Chandra Sekar N, Khoshmanesh K, Baratchi S. Bioengineered models of cardiovascular diseases. Atherosclerosis. 2024;393:117565. doi: 10.1016/j.atherosclerosis.2024.117565
  232. Chang SQ, Qiao L, Abodunrin OD, Zou L, Huang NP. Advanced technologies of artery-on-a-chip: a review of construction strategies and disease models. Angiogenesis. 2026;29(2):17. doi: 10.1007/S10456-026-10030-2
  233. Yarbrough D, Chen R, Katsouleas K, et al. Artery-on-Chip Demonstrates Mechanical and Functional Features of Healthy and Diseased Living Smooth Muscle Tissue. Adv Funct Mater. Published online July 1, 2026. 2026:e76324. doi: 10.1002/adfm.76324
  234. Gold KA, Saha B, Rajeeva Pandian NK, et al. 3D Bioprinted Multicellular Vascular Models. Adv Healthc Mater. 2021;10(21):e2101141. doi: 10.1002/adhm.202101141
  235. Wang Z, Lee SJ, Cheng HJ, Yoo JJ, Atala A. 3D bioprinted functional and contractile cardiac tissue constructs. Acta Biomater. 2018;70:48-56. doi: 10.1016/j.actbio.2018.02.007
  236. Dell AC, Maresca J, Davis BA, Isaji T, Dardik A, Geibel JP. Development and deployment of a functional 3D-bioprinted blood vessel. Sci Reports. 2025;15(1):11668. doi: 10.1038/s41598-025-93276-y
  237. Krajewska U, Chechli´nska C, Kurzyk A, Vascularisation in 3D bioprinted models: emerging solutions engineering functional tissues and tumour models. Biofabrication. 2026;18(2):022001. doi: 10.1088/1758-5090/AE2F02
  238. Liao Y, Gallegos-Martínez S, Kuang X, Du Y, Zhang YS, Zhang Y. Hybrid bioprinting of hierarchical vascular networks at capillary-scale resolution. Nat Chem Eng. 2026;3(6):328-339. doi: 10.1038/s44286-026-00396-x
  239. Chandra DK, Reis RL, Kundu SC, Kumar A, Mahapatra C. Nanomaterials-Based Hybrid Bioink Platforms in Advancing 3D Bioprinting Technologies for Regenerative Medicine. ACS Biomater Sci Eng. 2024;10(7):4145-4174. doi: 10.1021/acsbiomaterials.4c00166
  240. Jin X, Li Y, Ran H, Zhang Z, Cheng P, Wu Y. Smart nanomaterial-crosslinked hydrogels for biomedical applications. Smart Mater Med. 2025;6(3):417-433. doi: 10.1016/j.smaim.2025.11.001
  241. Ribezzi D, Zegwaart JP, Van Gansbeke T, et al. Multi-material Volumetric Bioprinting and Plug-and-play Suspension Bath Biofabrication via Bioresin Molecular Weight Tuning and via Multiwavelength Alignment Optics. Adv Mater. 2025;37(13):e2409355. doi: 10.1002/adma.202409355
  242. Aizarna-Lopetegui U, Größbacher G, Herrero-Ruiz A, et al. Hybrid Plasmonic Bioresins and dECM-Based Materials for Volumetric Bioprinting of Vascular-Inspired Architectures. ACS Appl Mater Interfaces. 2025;17(25):36982-36991. doi: 10.1021/acsami.5c03880
  243. Kong D, Ryu JC, Shin N, et al. In Vitro Modeling of Atherosclerosis Using iPSC-Derived Blood Vessel Organoids. Adv Healthc Mater. 2025;14(1):e2400919. doi: 10.1002/adhm.202400919
  244. Taylor CA, Figueroa CA. Patient-specific modeling of cardiovascular mechanics. Annu Rev Biomed Eng. 2009;11:109-134. doi: 10.1146/annurev.bioeng.10.061807.160521
  245. Jackson ML, Bond AR, George SJ. Mechanobiology of the endothelium in vascular health and disease: in vitro shear stress models. Cardiovasc drugs Ther. 2023;37(5):997-1010. doi: 10.1007/S10557-022-07385-1
  246. Aitken C, Mehta V, Schwartz MA, Tzima E. Mechanisms of endothelial flow sensing. Nat Cardiovasc Res. 2023;2(6):517-529. doi: 10.1038/S44161-023-00276-0
  247. Tabas I, Bornfeldt KE. Macrophage Phenotype and Function in Different Stages of Atherosclerosis. Circ Res. 2016;118(4):653-667. doi: 10.1161/CIRCRESAHA.115.306256
  248. De Meyer GRY, Zurek M, Puylaert P, Martinet W. Programmed death of macrophages in atherosclerosis: mechanisms and therapeutic targets. Nat Rev Cardiol. 2024;21(5):312-325. doi: 10.1038/S41569-023-00957-0
  249. Lee J, Choi JH. Deciphering Macrophage Phenotypes upon Lipid Uptake and Atherosclerosis. Immune Netw. 2020;20(3):1-21. doi: 10.4110/IN.2020.20.E22
  250. Moore KJ, Sheedy FJ, Fisher EA. Macrophages in atherosclerosis: a dynamic balance. Nat Rev Immunol. 2013;13(10):709-721. doi: 10.1038/NRI3520
  251. Roy P, Orecchioni M, Ley K. How the immune system shapes atherosclerosis: roles of innate and adaptive immunity. Nat Rev Immunol. 2022;22(4):251-265. doi: 10.1038/S41577-021-00584-1
  252. Guan Y, Racioppi L, Gerecht S. Engineering biomaterials to tailor the microenvironment for macrophage–endothelium interactions. Nat Rev Mater. 2023;8(10):688-699. doi: 10.1038/s41578-023-00591-9
  253. Imhof BA, Aurrand-Lions M. Adhesion mechanisms regulating the migration of monocytes. Nat Rev Immunol. 2004;4(6):432-444. doi: 10.1038/nri1375
  254. Whitworth CP, Polacheck WJ. Vascular organs-on-chip made with patient-derived endothelial cells: technologies to transform drug discovery and disease modeling. Expert Opin Drug Discov. 2024;19(3):339-351. doi: 10.1080/17460441.2023.2294947
  255. Jiang H, Li X, Chen T, et al. Bioprinted vascular tissue: Assessing functions from cellular, tissue to organ levels. Mater today Bio. 2023;23:100846. doi: 10.1016/j.mtbio.2023.100846
  256. Tabish TA, Zhu Y, Shukla S, et al. Graphene nanocomposites for real-time electrochemical sensing of nitric oxide in biological systems. Appl Phys Rev. 2023;10(4):041310. doi: 10.1063/5.0162640
  257. Ochieng BO, Zhao L, Ye Z. Three-Dimensional Bioprinting in Vascular Tissue Engineering and Tissue Vascularization of Cardiovascular Diseases. Tissue Eng Part B Rev. 2024;30(3):340-358. doi: 10.1089/TEN.TEB.2023.0175
  258. Lai J, Liu Y, Lu G, et al. 4D bioprinting of programmed dynamic tissues. Bioact Mater. 2024;37:348-377. doi: 10.1016/j.bioactmat.2024.03.033
  259. Liu J, Zhu M, Bai N, et al. Microfluidic Perfusable Pathological Vasculature for Atherosclerosis Drug Screening. Res (Washington, DC). 2025;8:0902. doi: 10.34133/research.0902
  260. Chae S, Ha DH, Lee H. 3D bioprinting strategy for engineering vascularized tissue models. Int J bioprinting. 2023;9(5):748. doi: 10.18063/ijb.748
  261. Kizhisseri M, Gharaie S, Schluter J. An analytical method informed by clinical imaging data for estimating outlet boundary conditions in computational fluid dynamics analysis of carotid artery blood flow. Sci Rep. 2023;13(1):14973. doi: 10.1038/S41598-023-42004-5
  262. Mir A, Lee E, Shih W, et al. 3D Bioprinting for Vascularization. Bioeng (Basel, Switzerland). 2023;10(5):606. doi: 10.3390/bioengineering10050606
  263. Zhou Y, Sekar NC, Thurgood P, et al. Bioengineered Vascular Model of Foam Cell Formation. ACS Biomater Sci Eng. 2023;9(12):6947-6955. doi: 10.1021/acsbiomaterials.3c01308
  264. Agarwal T, Onesto V, Banerjee D, et al. 3D bioprinting in tissue engineering: current state-of-the-art and challenges towards system standardization and clinical translation. Biofabrication. 2025;17(4):045001. doi: 10.1088/1758-5090/ade47a
  265. Wang Z, Hao Z, Yu S, Huang C, Pan Y, Zhao X. A Wearable and Deformable Graphene-Based Affinity Nanosensor for Monitoring of Cytokines in Biofluids. Nanomater (Basel, Switzerland). 2020;10(8):1-9. doi: 10.3390/nano10081503
  266. Sun Z, Zhao J, Leung E, et al. Three-Dimensional Bioprinting in Cardiovascular Disease: Current Status and Future Directions. Biomolecules. 2023;13(8):1180. doi: 10.3390/biom13081180
  267. Kim J. Characterization of Biocompatibility of Functional Bioinks for 3D Bioprinting. Bioeng (Basel, Switzerland). 2023;10(4):457. doi: 10.3390/bioengineering10040457
  268. Alves T, Mota WS, Barros C, et al. Review of scientific literature and standard guidelines for the characterization of graphene-based materials. J Mater Sci. 2024;59(32):14948-14980. doi: 10.1007/S10853-024-10061-4
  269. Bai M, Wan H, Zhang Y, et al. Two-dimensional nanomaterials based on rare earth elements for biomedical applications. Chem Sci. 2024;15(41):16887-16907. doi: 10.1039/d4sc02625j
  270. Wang Z, Guo H, Zhang J, Qian Y, Liu Y. Two-Dimensional Nanomaterials in Hydrogels and Their Potential Bio-Applications. Lubr. 2024;12(5):149. doi: 10.3390/lubricants12050149
  271. Libby P. The changing landscape of atherosclerosis. Nature. 2021;592(7855):524-533. doi: 10.1038/S41586-021-03392-8
  272. Ou L, Tan X, Qiao S, et al. Graphene-Based Material-Mediated Immunomodulation in Tissue Engineering and Regeneration: Mechanism and Significance. ACS Nano. 2023;17(19):18669-18687. doi: 10.1021/acsnano.3C03857
  273. Ding X, Pu Y, Tang M, Zhang T. Pulmonary hazard identifications of Graphene family nanomaterials: Adverse outcome pathways framework based on toxicity mechanisms. Sci Total Environ. 2023;857(Pt 1):159329. doi: 10.1016/j.scitotenv.2022.159329
  274. Smith LS, Haidari H, Amsalu A, et al. Black Phosphorus Nanoflakes: An Emerging Nanomaterial for Clinical Wound Management and Biomedical Applications. Int J Mol Sci. 2024;25(23):12824. doi: 10.3390/ijms252312824
  275. Yedgar S, Barshtein G, Gural A. Hemolytic Activity of Nanoparticles as a Marker of Their Hemocompatibility. Micromachines. 2022;13(12):2091. doi: 10.3390/mi13122091
  276. Kim Y, Chica-Carrillo EC, Lee HJ. Microfabricated sensors for non-invasive, real-time monitoring of organoids. Micro Nano Syst Lett. 2024;12(1):26. doi: 10.1186/S40486-024-00216-y
  277. Liu S, Kumari S, He H, et al. Biosensors integrated 3D organoid/organ-on-a-chip system: A real-time biomechanical, biophysical, and biochemical monitoring and characterization. Biosens Bioelectron. 2023;231:115285. doi: 10.1016/j.bios.2023.115285
  278. Flynn CD, Chang D, Mahmud A, et al. Biomolecular sensors for advanced physiological monitoring. Nat Rev Bioeng. 2023;1(8):560-575. doi: 10.1038/s44222-023-00067-z
  279. Wu J, Liu H, Chen W, Ma B, Ju H. Device integration of electrochemical biosensors. Nat Rev Bioeng. 2023;1(5):346-360. doi: 10.1038/S44222-023-00032-W
  280. Chen S, Sun Y, Fan X, et al. Review on two-dimensional material-based field-effect transistor biosensors: accomplishments, mechanisms, and perspectives. J Nanobiotechnology. 2023;21(1):144. doi: 10.1186/S12951-023-01898-z
  281. He W, Deng J, Ma B, et al. Recent Advancements of Bioinks for 3D Bioprinting of Human Tissues and Organs. ACS Appl Bio Mater. 2023;7(1):17-43. doi: 10.1021/acsabm.3C00806
  282. Havelikar U, Ghorpade KB, Kumar A, et al. Comprehensive insights into mechanism of nanotoxicity, assessment methods and regulatory challenges of nanomedicines. Discov Nano. 2024;19(1):165. doi: 10.1186/S11671-024-04118-1
  283. Shyam R, Palaniappan A. Effect of sterilization techniques on biomaterial inks’ properties and 3D bioprinting parameters. Bioprinting. 2023;33:e00294. doi: 10.1016/j.bprint.2023.E00294
  284. Liang K. Tissue Bioprinting: Promise and Challenges. Bioeng. 2023;10(12):1400. doi: 10.3390/bioengineering10121400
  285. Nahon DM, Moerkens R, Aydogmus H, et al. Standardizing designed and emergent quantitative features in microphysiological systems. Nat Biomed Eng. 2024;8(8):941-962. doi: 10.1038/S41551-024-01236-0
  286. Wang Y, Zhang X, Yue H. Two-dimensional nanomaterials induced nano-bio interfacial effects and biomedical applications in cancer treatment. J Nanobiotechnology. 2024;22(1):67. doi: 10.1186/S12951-024-02319-5
  287. Xu Y, Chen S, Zhang Y, et al. Antibacterial black phosphorus nanosheets for biomedical applications. J Mater Chem B. 2023;11(30):7069-7093. doi: 10.1039/D3TB00723E
  288. Chen X, He W, Liang Y, et al. Enhanced degradation of few-layer black phosphorus by fulvic acid: Processes and mechanisms. Water Res. 2023;238:120014. doi: 10.1016/j.watres.2023.120014
  289. Mandrycky CJ, Howard CC, Rayner SG, Shin YJ, Zheng Y. Organ-on-a-chip systems for vascular biology. J Mol Cell Cardiol. 2021;159:1-13. doi: 10.1016/j.yjmcc.2021.06.002
  290. Ingber DE. Human organs-on-chips for disease modelling, drug development and personalized medicine. Nat Rev Genet. 2022;23(8):467-491. doi: 10.1038/S41576-022-00466-9
  291. Wang D, Maharjan S, Kuang X, et al. Microfluidic bioprinting of tough hydrogel-based vascular conduits for functional blood vessels. Sci Adv. 2022;8(43):eabq6900. doi: 10.1126/sciadv.abq6900
  292. Grebenyuk S, Abdel Fattah AR, Kumar M, et al. Large-scale perfused tissues via synthetic 3D soft microfluidics. Nat Commun. 2023;14(1):193. doi: 10.1038/S41467-022-35619-1
  293. Huang Y, Liu T, Huang Q, Wang Y. From Organ-on-a-Chip to Human-on-a-Chip: A Review of Research Progress and Latest Applications. ACS Sensors. 2024;9(7):3466-3488. doi: 10.1021/acssensors.4c00004
  294. Zhang B, Korolj A, Lai BFL, Radisic M. Advances in organ-on-a-chip engineering. Nat Rev Mater. 2018;3(8):257-278. doi: 10.1038/s41578-018-0034-7
  295. Ugodnikov A, Persson H, Simmons CA. Bridging barriers: advances and challenges in modeling biological barriers and measuring barrier integrity in organ-on-chip systems. Lab Chip. 2024;24(13):3199-3225. doi: 10.1039/d3lc01027a
  296. Liu J, Han X, Zhang T, Tian K, Li Z, Luo F. Reactive oxygen species (ROS) scavenging biomaterials for anti-inflammatory diseases: from mechanism to therapy. J Hematol Oncol. 2023;16(1):116. doi: 10.1186/S13045-023-01512-7
  297. Liu J, Jia B, Li Z, Li W. Reactive oxygen species-responsive polymer drug delivery systems. Front Bioeng Biotechnol. 2023;11:01-11. doi: 10.3389/fbioe.2023.1115603
  298. Amirthalingam S, Rajendran AK, Moon YG, Hwang NS. Stimuli-responsive dynamic hydrogels: design, properties and tissue engineering applications. Mater Horizons. 2023;10(9):3325-3350. doi: 10.1039/d3mh00399J
  299. Chen S, Qiao Z, Niu Y, et al. Wearable flexible microfluidic sensing technologies. Nat Rev Bioeng. 2023;1(12):950-971. doi: 10.1038/s44222-023-00094-w
  300. Song JW, Munn LL. Fluid forces control endothelial sprouting. Proc Natl Acad Sci U S A. 2011;108(37):15342-15347. doi: 10.1073/pnas.1105316108
  301. Zhu W, Ma X, Gou M, Mei D, Zhang K, Chen S. 3D printing of functional biomaterials for tissue engineering. Curr Opin Biotechnol. 2016;40:103-112. doi: 10.1016/j.copbio.2016.03.014
  302. Wang Q, Zhang Y, Ma Y, Wang M, Pan G. Nano-crosslinked dynamic hydrogels for biomedical applications. Mater Today Bio. 2023;20:100640. doi: 10.1016/j.mtbio.2023.100640
Share
Back to top
International Journal of Bioprinting, Electronic ISSN: 2424-8002 Print ISSN: 2424-7723, Published by AccScience Publishing