AccScience Publishing / IJB / Online First / DOI: 10.36922/IJB026330354
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REVIEW ARTICLE

Sustainable ALMA from seaweed for DLP printing

Merve Ilgar1 Eylul Dila Carkci2 Elif Emekdar2 Oguzhan Gunduz3 Roger Narayan4*
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1 Department of Chemistry, İstanbul University-Cerrahpasa, Avcılar, İstanbul , Türkiye
2 Department of Bioengineering, Yıldız Technical University, Esenler, İstanbul , Türkiye
3 Department of Metallurgical and Materials Engineering, Marmara University, Maltepe, İstanbul , Türkiye
4 Department of Biomedical Engineering, North Carolina State University, Raleigh, North Carolina , United States of America
Received: 29 June 2026 | Revised: 10 August 2026 | Accepted: 19 August 2026 | Published online: 21 August 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

Alginate, which can be extracted from various brown seaweed species, is a sustainable biomaterial with several potential biomedical applications because of its biocompatibility and biodegradability. While alginate hydrogels are traditionally ionically crosslinked with divalent cations, this approach often produces hydrogels with low mechanical strength and poorly controlled degradation kinetics, limiting their suitability for biomedical applications. The chemical modification of alginate via methacrylation to produce alginate methacrylate (ALMA) allows the fabrication of photocrosslinkable hydrogels under ultraviolet (UV) light irradiation. This approach enables the fabrication of alginate-based hydrogels with superior physicochemical properties that can be tailored for specific biomedical areas. However, there is a relative lack of research related to the performance of ALMA bioinks in 3D printing using digital light processing (DLP). The research conducted to date indicates a connection between the choice of alginate source, methacrylation chemistry, and printing outcomes. This review directly addresses this topic by considering alginate extraction from brown seaweed, ALMA synthesis methods, and the biomedical applications of ALMA as a 3D hydrogel using DLP.  For this purpose, the focus has been on how each step in the process affects the performance of the materials used in final biomedical applications. The goal of this review is to provide researchers with a framework for optimizing ALMA-based bioinks for DLP-based biomedical fabrication.

Graphical abstract
Keywords
Brown seaweed
Alginate
Extraction methods
Bioink
Digital light processing
ALMA hydrogels
Funding
This work was supported by the Scientific and Technological Research Council of Türkiye (TÜBİTAK) under Project No. 224M659.
Conflict of interest
The authors declare they have no competing interests.
References
  1. Bi D, Yang X, Yao L, et al. Potential Food and Nutraceutical Applications of Alginate: A Review. Marine Drugs. 2022;20(9):564. doi: 10.3390/md20090564
  2. Wang Y, Lu Y. Sodium Alginate-Based Functional Materials toward Sustainable Applications: Water Treatment and Energy Storage. Ind Eng Chem Res. 2023;62(29):11279-11304. doi: 10.1021/acs.iecr.3c01082
  3. Jain D, Bar-Shalom D. Alginate drug delivery systems: Application in context of pharmaceutical and biomedical research. Drug Dev Ind Pharm. 2014;40(12):1576-1584. doi: 10.3109/03639045.2014.917657
  4. Farshidfar N, Iravani S, Varma RS. Alginate-Based Biomaterials in Tissue Engineering and Regenerative Medicine. Marine Drugs. 2023;21(3):189. doi: 10.3390/md21030189
  5. Li Y, Liao J, Li S, et al. Marine materials: New hope for biomedical applications. Cell Biomaterials. 2026;2(8):100370. doi: 10.1016/j.celbio.2026.100370
  6. Fernando IPS, Lee WW, Han EJ, Ahn G. Alginate-based nanomaterials: Fabrication techniques, properties, and applications. Chemical Engineering Journal. 2020;391(4472):123823. doi: 10.1016/j.cej.2019.123823
  7. Peteiro C. Alginate Production from Marine Macroalgae, with Emphasis on Kelp Farming. In: Springer Series in Biomaterials Science and Engineering. Singapore: Springer; 2017:27-66. doi: 10.1007/978-981-10-6910-9_2
  8. Saji S, Hebden A, Goswami P, Du C. A Brief Review on the Development of Alginate Extraction Process and Its Sustainability. Sustainability. 2022;14(9):5181. doi: 10.3390/su14095181
  9. Bojorges H, López-Rubio A, Martínez-Abad A, Fabra J. Overview of alginate extraction processes: Impact on alginate molecular structure and techno-functional properties. Trends Food Sci Technol. 2023;140:104142. doi: 10.1016/j.tifs.2023.104142
  10. Fawzy MA, Gomaa M, Hifney AF, Abdel-Gawad KM. Optimization of alginate alkaline extraction technology from Sargassum latifolium and its potential antioxidant and emulsifying properties. Carbohydr Polym. 2017;157:1903-1912. doi: 10.1016/J.CARBPOL.2016.11.077
  11. Stagnaro P, Schizzi I, Utzeri R, Marsano E, Castellano M. Alginate-polymethacrylate hybrid hydrogels for potential osteochondral tissue regeneration. Carbohydr Polym. 2018;185:56-62. doi: 10.1016/j.carbpol.2018.01.012
  12. Chou AI, Nicoll SB. Characterization of photocrosslinked alginate hydrogels for nucleus pulposus cell encapsulation. J Biomed Mater Res A. 2009;91A(1):187-194. doi: 10.1002/jbm.a.32191
  13. Wang X, Hao T, Qu J, Wang C, Chen H. Synthesis of Thermal Polymerizable Alginate‐GMA Hydrogel for Cell Encapsulation. J Nanomater. 2015;2015(1): 970619. doi: 10.1155/2015/970619
  14. Araiza-Verduzco F, Rodríguez-Velázquez E, Cruz H, et al. Photocrosslinked Alginate-Methacrylate Hydrogels with Modulable Mechanical Properties: Effect of the Molecular Conformation and Electron Density of the Methacrylate Reactive Group. Materials. 2020;13(3):534. doi: 10.3390/ma13030534
  15. Mishbak HH, Cooper G, Bartolo PJ. Development and characterization of a photocurable alginate bioink for three-dimensional bioprinting. Int J Bioprint. 2019;5(2):189. doi: 10.18063/ijb.v5i2.189
  16. Flórez-Fernández N, Domínguez H, Torres MD. A green approach for alginate extraction from Sargassum muticum brown seaweed using ultrasound-assisted technique. Int J Biol Macromol. 2019;124:451-459. doi: 10.1016/j.ijbiomac.2018.11.232
  17. Makoure D, Arhaliass A, Echchelh A, Baron R, Legrand J. Procédé d’extrusion réactive et/ou enzymatique pour l’extraction de phycocolloïdes: application aux produits de la mer [Reactive and/or enzymatic extrusion process for phycocolloids extraction: application to sea products]. STA. 2019;2(1). [In French] doi: 10.21494/iste.op.2021.0675
  18. Nesic A, De Bonis MV, Dal Poggetto G, Ruocco G, Santagata G. Microwave Assisted Extraction of Raw Alginate as a Sustainable and Cost-Effective Method to Treat Beach-Accumulated Sargassum Algae. Polymers. 2023;15(14). doi: 10.3390/polym15142979
  19. Ummat V, Zhao M, Sivagnanam SP, et al. Ultrasound-Assisted Extraction of Alginate from Fucus vesiculosus Seaweed By-Product Post-Fucoidan Extraction. Marine Drugs. 2024;22(11). doi: 10.3390/md22110516
  20. Ye S, Xie C, Agar OT, Barrow CJ, Dunshea FR, Suleria HAR. Alginates from Brown Seaweeds as a Promising Natural Source: A Review of Its Properties and Health Benefits. Food Reviews International. 2024;40(9):2682-2710. doi: 10.1080/87559129.2023.2279583
  21. Trica B, Delattre C, Gros F, et al. Extraction and Characterization of Alginate from an Edible Brown Seaweed (Cystoseira barbata) Harvested in the Romanian Black Sea. Marine Drugs. 2019;17(7). doi: 10.3390/md17070405
  22. Nøkling-Eide K, Langeng AM, Åslund A, Aachmann FL, Sletta H, Arlov Ø. An assessment of physical and chemical conditions in alginate extraction from two cultivated brown algal species in Norway: Alaria esculenta and Saccharina latissima. Algal Res. 2023;69(1-2):102951. doi: 10.1016/j.algal.2022.102951
  23. Wedlock DJ, Fasihuddin BA. Effect of formaldehyde pre-treatment on the intrinsic viscosity of alginate from various brown seaweeds. Food Hydrocoll. 1990;4(1):41-47. doi: 10.1016/S0268-005X(09)80326-3
  24. Shi Y, Dong M, Lei X, et al. Comparison of Flocculation Methods for Sodium Alginate and Characterization of Its Structure and Properties. Published online 2025. doi: 10.3390/foods14172970
  25. Qin Y. The Extraction of Alginate from Brown Seaweeds. In: Alginate Fibers and Wound Dressings. Hoboken, NJ: Wiley; 2023. doi: 10.1002/9783527845200.ch1
  26. Mohammed A, Bissoon R, Bajnath E, et al. Multistage extraction and purification of waste Sargassum natans to produce sodium alginate: An optimization approach. Carbohydr Polym. 2018;198:109-118. doi: 10.1016/J.CARBPOL.2018.06.067
  27. Vauchel P, Kaas R, Arhaliass A, Baron R, Legrand J. A New Process for Extracting Alginates from Laminaria digitata: Reactive Extrusion. Food Bioprocess Technol. 2008;1(3):297-300. doi: 10.1007/s11947-008-0082-x
  28. Baron R, Vauchel P, Kaas R, Arhaliass A, Legrand J. Dynamical modelling of a reactive extrusion process: Focus on residence time distribution in a fully intermeshing co-rotating twin-screw extruder and application to an alginate extraction process. Chem Eng Sci. 2010;65(10):3313-3321. doi: 10.1016/j.ces.2010.02.019
  29. Baron R, Vauchel P, Arhaliass A. Modeling of twin-screw reactive extrusion: application to alginate extraction. IFAC Proceedings Volumes. 2010;43(6):341-346. doi: 10.3182/20100707-3-BE-2012.0094
  30. Felicia WXL, Rovina K, Zuldin WH, Suriati L, Huda N, Nurdiani R. Sustainable Valorization of Alginate, a Review of Green Extraction, Structure–Function Relationships, and Next-Generation Food Applications. Food and Bioprocess Technology. 2026;19(2):97. doi: 10.1007/S11947-025-04096-X
  31. Savić Gajić IM, Savić IM, Ivanovska AM, Vunduk JD, Mihalj IS, Svirčev ZB. Improvement of Alginate Extraction from Brown Seaweed (Laminaria digitata L.) and Valorization of Its Remaining Ethanolic Fraction. Marine Drugs. 2024;22(6). doi: 10.3390/MD22060280
  32. Youssouf L, Lallemand L, Giraud P, et al. Ultrasound-assisted extraction and structural characterization by NMR of alginates and carrageenans from seaweeds. Carbohydr Polym. 2017;166:55-63. doi: 10.1016/J.CARBPOL.2017.01.041
  33. Dodero A, Vicini S, Castellano M. Depolymerization of sodium alginate in saline solutions via ultrasonic treatments: A rheological characterization. Food Hydrocoll. 2020;109:106128. doi: 10.1016/J.FOODHYD.2020.106128
  34. Yuan Y, Macquarrie D. Microwave assisted extraction of sulfated polysaccharides (fucoidan) from Ascophyllum nodosum and its antioxidant activity. Carbohydr Polym. 2015;129(10):101-107. doi: 10.1016/j.carbpol.2015.04.057
  35. Abdul Khalil HPS, Lai TK, Tye YY, et al. A review of extractions of seaweed hydrocolloids: Properties and applications. Express Polym Lett. 2018;12(4):296-317. doi: 10.3144/expresspolymlett.2018.27
  36. Nam H Bin, Lee KH, Yoo HY, Park C, Lim JM, Lee JH. Rapid and High-Yield Recovery of Sodium Alginate from Undaria pinnatifida via Microwave-Assisted Extraction. Processes. 2024;12(1). doi: 10.3390/pr12010208
  37. Sugiono S, Hidayat MT, Alrosyidi F, et al. Microwave-Assisted Extraction in A Sequential Biorefinery of Alginate and Fucoidan From Brown Alga Sargassum Cristaefolium. Food Sci Technol. Published online December 1, 2022:96-105. doi: 10.25139/fst.vi.4976
  38. Andriamanantoanina H, Rinaudo M. Characterization of the alginates from five madagascan brown algae. Carbohydr Polym. 2010;82(3):555-560. doi: 10.1016/j.carbpol.2010.05.002
  39. Sari-Chmayssem N, Taha S, Mawlawi H, Guégan JP, Jeftić J, Benvegnu T. Extracted and depolymerized alginates from brown algae Sargassum vulgare of Lebanese origin: chemical, rheological, and antioxidant properties. J Appl Phycol. 2016;28(3):1915-1929. doi: 10.1007/s10811-015-0676-4
  40. Khajouei RA, Keramat J, Hamdami N, et al. Extraction and characterization of an alginate from the Iranian brown seaweed Nizimuddinia zanardini. Int J Biol Macromol. 2018;118:1073-1081. doi: 10.1016/j.ijbiomac.2018.06.154
  41. Sugiono S, Masruri M, Estiasih T, Widjanarko SB. Optimization of extrusion-assisted extraction parameters and characterization of alginate from brown algae (Sargassum cristaefolium). J Food Sci Technol. 2019;56(8):3687-3696. doi: 10.1007/S13197-019-03829-Z
  42. Mohammed A, Rivers A, Stuckey DC, Ward K. Alginate extraction from Sargassum seaweed in the Caribbean region: Optimization using response surface methodology. Carbohydr Polym. 2020;245:116419. doi: 10.1016/J.CARBPOL.2020.116419
  43. Chica LR, Yamashita C, Nunes NSS, et al. Optimizing alginate extraction using Box-Behnken design: Improving yield and antioxidant properties through ultrasound-assisted citric acid extraction. Food Chem Adv. 2024;5:100813. doi: 10.1016/J.FOCHA.2024.100813
  44. Smith HA, Cabling LPB, Leonard NA, Dubrawski KL, Buckley HL. Green Alginate Extraction from Macrocystis pyrifera for Bioplastic Applications: Physicochemical, Environmental Impact, and Chemical Hazard Analyses. ACS Sustain Resour Manag. 2024;1(5):958-969. doi: 10.1021/acssusresmgt.4c00019
  45. Alboofetileh M, Jeddi S, Abdollahi M. Sequential recovery of alginate from fucoidan extraction by-products of Nizamuddinia zanardinii seaweed using green extraction methods. Ultrason Sonochem. 2025;117:107343. doi: 10.1016/J.ULTSONCH.2025.107343
  46. Varaprasad K, Jayaramudu T, Kanikireddy V, Toro C, Sadiku ER. Alginate-based composite materials for wound dressing application:A mini review. Carbohydr Polym. 2020;236:116025. doi: 10.1016/j.carbpol.2020.116025
  47. Jiao W, Chen W, Mei Y, et al. Effects of Molecular Weight and Guluronic Acid/Mannuronic Acid Ratio on the Rheological Behavior and Stabilizing Property of Sodium Alginate. Molecules. 2019;24(23). doi: 10.3390/molecules24234374
  48. Hernández-González AC, Téllez-Jurado L, Rodríguez-Lorenzo LM. Alginate hydrogels for bone tissue engineering, from injectables to bioprinting: A review. Carbohydr Polym. 2020;229:115514. doi: 10.1016/J.CARBPOL.2019.115514
  49. Axpe E, Oyen M. Applications of Alginate-Based Bioinks in 3D Bioprinting. Int J Mol Sci. 2016;17(12):1976. doi: 10.3390/ijms17121976
  50. Ching SH, Bansal N, Bhandari B. Alginate gel particles–A review of production techniques and physical properties. Crit Rev Food Sci Nutr. 2017;57(6):1133-1152. doi: 10.1080/10408398.2014.965773
  51. Liu J, Yang S, Li X, Yan Q, Reaney MJT, Jiang Z. Alginate Oligosaccharides: Production, Biological Activities, and Potential Applications. Compr Rev Food Sci Food Saf. 2019;18(6):1859-1881. doi: 10.1111/1541-4337.12494
  52. Hariyadi DM, Islam N. Current Status of Alginate in Drug Delivery. Adv Pharmacol Pharm Sci. 2020;2020:1-16. doi: 10.1155/2020/8886095
  53. Cardoso M, Costa R, Mano J. Marine Origin Polysaccharides in Drug Delivery Systems. Mar Drugs. 2016;14(2):34. doi: 10.3390/md14020034
  54. Deng Y, Shavandi A, Okoro OV, Nie L. Alginate modification via click chemistry for biomedical applications. Carbohydr Polym. 2021;270:118360. doi: 10.1016/j.carbpol.2021.118360
  55. Kumar B, Singh N, Kumar P. A review on sources, modification techniques, properties and potential applications of alginate-based modified polymers. Eur Polym J. 2024;213:113078. doi: 10.1016/J.EURPOLYMJ.2024.113078
  56. Jeon O, Bouhadir KH, Mansour JM, Alsberg E. Photocrosslinked alginate hydrogels with tunable biodegradation rates and mechanical properties. Biomaterials. 2009;30(14):2724-2734. doi: 10.1016/J.BIOMATERIALS.2009.01.034
  57. Wang H, Bu X, Huang Z, Yang J, Qiu T. Synthesis of Methacrylic Anhydride by Batch Reactive Distillation: Reaction Kinetics and Process. Ind Eng Chem Res. 2014;53(44):17317-17324. doi: 10.1021/IE501607V
  58. Habib M, Berthalon S, Leclercq L, Tourrette A, Sharkawi T, Blanquer S. Dual Cross-Linked Stimuli-Responsive Alginate-Based Hydrogels. Biomacromolecules. 2024;25(3):1660-1670. doi: 10.1021/ACS.BIOMAC.3C01201
  59. Hasany M, Talebian S, Sadat S, et al. Synthesis, properties, and biomedical applications of alginate methacrylate (ALMA)-based hydrogels: Current advances and challenges. Appl Mater Today. 2021;24:101150. doi: 10.1016/j.apmt.2021.101150
  60. Somo SI, Langert K, Yang CY, et al. Synthesis and evaluation of dual crosslinked alginate microbeads. Acta Biomater. 2018;65:53-65. doi: 10.1016/J.ACTBIO.2017.10.046
  61. Liang X, Chen S, Liang Y, et al. Alginate-Based Hydrogels: Recent Progress in Preparation, Property Tuning, and Multifunctional Applications. Gels. 2026;12(2):182. doi: 10.3390/gels12020182
  62. Ren Y, Wang Q, Xu W, et al. Alginate-based hydrogels mediated biomedical applications: A review. Int J Biol Macromol. 2024;279:135019. doi: 10.1016/J.IJBIOMAC.2024.135019
  63. Tansik G, Stowers R. Viscoelastic and phototunable GelMA-alginate hydrogels for 3D cell culture. MRS Advances. 2024;9(8):505-511. doi: 10.1557/S43580-024-00815-2
  64. Tavafoghi M, Sheikhi A, Tutar R, et al. Engineering tough, injectable, naturally-derived, bioadhesive composite hydrogels. Adv Healthc Mater. 2020;9(10):e1901722. doi: 10.1002/ADHM.201901722
  65. Yue H, Wang Y, Fernandes S, Vyas C, Bartolo P. Bioprinting of GelMA/PEGDA Hybrid Bioinks for SH-SY5Y Cell Encapsulation: Role of Molecular Weight and Concentration. Macromol Biosci. 2025;25(6). doi: 10.1002/MABI.202400587
  66. Yang W, Liu R, Qian K, et al. 3D-printed cell-free bioactive scaffolds from methacrylated hyaluronic acid and silk fibroin incorporating platelet-rich plasma for adipose tissue regeneration. Int J Biol Macromol. 2026;365:152341. doi: 10.1016/j.ijbiomac.2026.152341
  67. Gao Y, Jin X. Dual Crosslinked Methacrylated Alginate Hydrogel Micron Fibers and Tissue Constructs for Cell Biology. Mar Drugs. 2019;17(10):557. doi: 10.3390/MD17100557
  68. García-García A, Silván U, Pérez-Álvarez L, Lanceros S. Comparing the Printability, Biological and Physicochemical Properties of Bio-Based Photo-Crosslinkable Hydrogels. Polymers. 2025;17(21):2867. doi: 10.3390/POLYM17212867
  69. Augst AD, Kong HJ, Mooney DJ. Alginate hydrogels as biomaterials. Macromol Biosci. 2006;6(8):623-633. doi: 10.1002/MABI.200600069
  70. Masoumi Shahrbabak S, Jalali SM, Fathabadi MF, et al. Modified alginates for precision drug delivery: Advances in controlled-release and targeting systems. Int J Pharm X. 2025;10:100381. doi: 10.1016/J.IJPX.2025.100381
  71. Zoco de la Fuente A, García-García A, Pérez-Álvarez L, et al. Evaluation of Various Types of Alginate Inks for Light-Mediated Extrusion 3D Printing. Polymers. 2024;16(7):986. doi: 10.3390/POLYM16070986
  72. Chou AI, Akintoye SO, Nicoll SB. Photo-crosslinked alginate hydrogels support enhanced matrix accumulation by nucleus pulposus cells in vivo. Osteoarthritis Cartilage. 2009;17(10):1377-1384. doi: 10.1016/j.joca.2009.04.012
  73. Batool SR, Nazeer MA, Ekinci D, Sahin A, Kizilel S. Multifunctional alginate-based hydrogel with reversible crosslinking for controlled therapeutics delivery. Int J Biol Macromol. 2020;150:315-325. doi: 10.1016/J.IJBIOMAC.2020.02.042
  74. Tahir I, Floreani R. Dual-Crosslinked Alginate-Based Hydrogels with Tunable Mechanical Properties for Cultured Meat. Foods. 2022;11(18). doi: 10.3390/foods11182829
  75. Jalali Kandeloos A, Bastani S, Mashayekhan S. Architecting oxidized alginate methacrylate hydrogels with tunable characteristics by altering the sequence of the cross-linking steps, methacrylation reaction time, and polymer concentration. J Biomater Appl. 2023;38(1):25-38. doi: 10.1177/08853282231184294
  76. Mignon A, Zimmer J, Gutierrez Cisneros C, et al. Electron-Beam-Initiated Crosslinking of Methacrylated Alginate and Diacrylated Poly(ethylene glycol) Hydrogels. Polymers (Basel). 2023;15(24):4685. doi: 10.3390/POLYM15244685
  77. Lipari S, Sacco P, Marsich E, Donati I. Silk Fibroin-Enriched Bioink Promotes Cell Proliferation in 3D-Bioprinted Constructs. Published online 2024. doi: 10.3390/gels10070469
  78. Poshina D, Sokolova N, Nono-Tagne S, et al. Electrospinning of methacrylated alginate for tissue engineering applications. RSC Adv. 2024;14(52):38746-38756. doi: 10.1039/D4RA07559E
  79. Gutierrez Cisneros C, Agten H, Derveaux E, Adriaensens P, Bloemen V, Mignon A. Development of a biocompatible, low-cost reinforcement of methacrylated alginate hydrogels using synthetic crosslinking agents. React Funct Polym. 2025;214:106330. doi: 10.1016/J.REACTFUNCTPOLYM.2025.106330
  80. International Organization for Standardization. Additive manufacturing — General principles — Fundamentals and vocabulary. ISO/ASTM 52900:2021. Accessed July 26, 2026. https://www.iso.org/standard/74514.html
  81. Ng WL, An J, Chua CK. Process, Material, and Regulatory Considerations for 3D Printed Medical Devices and Tissue Constructs. Engineering. 2024;36:146-166. doi: 10.1016/J.ENG.2024.01.028
  82. Ng WL, Paula CTB, Serra AC, Coelho JFJ, Bartolo P. Vat photopolymerization-based bioprinting: Shaping next-generation tissues with light. Interdisciplinary Medicine. 2026;4(1):e70078. doi: 10.1002/INMD.70078
  83. Li Y, Zhang X, Zhang X, Zhang Y, Hou D. Recent Progress of the Vat Photopolymerization Technique in Tissue Engineering: A Brief Review of Mechanisms, Methods, Materials, and Applications. Polymers. 2023;15(19):3940. doi: 10.3390/POLYM15193940
  84. Islam A, Rahman MZ. Recent advances in additive manufacturing techniques: An in-depth review. Comprehensive Materials Processing: Volume 1-13, Second edition. 2024;13:352-378. doi: 10.1016/B978-0-323-96020-5.00187-4
  85. Li H, Dai J, Wang Z, et al. Digital light processing (DLP)‐based (bio)printing strategies for tissue modeling and regeneration. Aggregate. 2023;4(2). doi: 10.1002/agt2.270
  86. Zhao T, Liu Y, Wu Y, Zhao M, Zhao Y. Controllable and biocompatible 3D bioprinting technology for microorganisms: Fundamental, environmental applications and challenges. Biotechnol Adv. 2023;69:108243. doi: 10.1016/j.biotechadv.2023.108243
  87. Kowsari K, Zhang B, Panjwani S, et al. Photopolymer formulation to minimize feature size, surface roughness, and stair-stepping in digital light processing-based three-dimensional printing. Addit Manuf. 2018;24:627-638. doi: 10.1016/j.addma.2018.10.037
  88. Bhusal A, Dogan E, Nguyen HA, et al. Multi-material digital light processing bioprinting of hydrogel-based microfluidic chips. Biofabrication. 2022;14(1):014103. doi: 10.1088/1758-5090/ac2d78
  89. Goodarzi Hosseinabadi H, Nieto D, Yousefinejad A, Fattel H, Ionov L, Miri AK. Ink material selection and optical design considerations in DLP 3D printing. Appl Mater Today. 2023;30:101721. doi: 10.1016/j.apmt.2022.101721
  90. Grigoryan B, Paulsen SJ, Corbett DC, et al. Multivascular networks and functional intravascular topologies within biocompatible hydrogels. Science. 2019;364(6439):458-464. doi: 10.1126/science.aav9750
  91. He Y, Wang F, Wang X, Zhang J, Wang D, Huang X. A photocurable hybrid chitosan/acrylamide bioink for DLP based 3D bioprinting. Mater Des. 2021;202:109588. doi: 10.1016/j.matdes.2021.109588
  92. Na K, Shin S, Lee H, et al. Effect of solution viscosity on retardation of cell sedimentation in DLP 3D printing of gelatin methacrylate/silk fibroin bioink. J Ind Eng Chem. 2018;61:340-347. doi: 10.1016/j.jiec.2017.12.032
  93. Piras CC, Smith DK. Multicomponent polysaccharide alginate-based bioinks. J Mater Chem B. 2020;8(36):8171-8188. doi: 10.1039/D0TB01005G
  94. Ren X, Wang J, Wu Y, et al. One-pot synthesis of hydroxyapatite hybrid bioinks for digital light processing 3D printing in bone regeneration. J Mater Sci Technol. 2024;188:84-97. doi: 10.1016/J.JMST.2024.01.001
  95. Wan J, Xu Y, Qi T, et al. AG73-GelMA/AlgMA hydrogels provide a stable microenvironment for the generation of pancreatic progenitor organoids. J Nanobiotechnol. 2025;23(1):149. doi: 10.1186/S12951-025-03266-5
  96. Li Y, Mao Q, Yin J, Wang Y, Fu J, Huang Y. Theoretical prediction and experimental validation of the digital light processing (DLP) working curve for photocurable materials. Addit Manuf. 2021;37:101716. doi: 10.1016/j.addma.2020.101716
  97. Allen NS. Photoinitiators for UV and visible curing of coatings: Mechanisms and properties. J Photochem Photobiol A Chem. 1996;100(1-3):101-107. doi: 10.1016/S1010-6030(96)04426-7
  98. Tomal W, Ortyl J. Water-Soluble Photoinitiators in Biomedical Applications. Polymers. 2020;12(5):1073. doi: 10.3390/POLYM12051073
  99. Wang Y, Zhang S, Wang J. Photo-crosslinkable hydrogel and its biological applications. Chin Chem Lett. 2021;32(5):1603-1614. doi: 10.1016/j.cclet.2020.11.073
  100. Yagci Y, Jockusch S, Turro NJ. Photoinitiated Polymerization: Advances, Challenges, and Opportunities. Macromolecules. 2010;43(15):6245-6260. doi: 10.1021/MA1007545
  101. Dzwonkowska-Zarzycka M, Sionkowska A. Photoinitiators for Medical Applications—The Latest Advances. Molecules. 2024;29(16):3898. doi: 10.3390/MOLECULES29163898
  102. Elkhoury K, Zuazola J, Vijayavenkataraman S. Bioprinting the future using light: A review on photocrosslinking reactions, photoreactive groups, and photoinitiators. SLAS Technol. 2023;28(3):142-151. doi: 10.1016/J.SLAST.2023.02.003
  103. Kim M, Kang D, Han H, Jang J. Light-activated decellularized extracellular matrix-based bioinks for enhanced mechanical integrity. Mater Today Bio. 2025;32:101859. doi: 10.1016/J.MTBIO.2025.101859
  104. Enayati-Gerdroodbar A, Khayati A, Ahmadi M, Pourabbas B, Ali Aboudzadeh M, Salami-Kalajahi M. An overview on potential of novel photoinitiators for vat photopolymerization-based 3D/4D printing formulations. Eur Polym J. 2024;221:113552. doi: 10.1016/J.EURPOLYMJ.2024.113552
  105. Deng H, Yin J, Sun Y, et al. Application of new photoinitiating systems based on BODIPY derivatives in long-wavelength photo-induced free radical polymerization. Eur Polym J. 2025;228:113833. doi: 10.1016/J.EURPOLYMJ.2025.113833
  106. Rayat Pisheh H, Hoseinian MS, Dezfoulian D, et al. Digital light processing bioprinting: bioink innovations and applications in tissue and organ regeneration. J Biol Eng. Published online July 11, 2026. doi: 10.1186/s13036-026-00718-w
  107. Jacobs PF, Reid DT. Rapid Prototyping & Manufacturing: Fundamentals of Stereolithography. Society of Manufacturing Engineers in cooperation with the Computer and Automated Systems Association of SME; 1992.
  108. Zhu H, Yang H, Ma Y, et al. Spatiotemporally Controlled Photoresponsive Hydrogels: Design and Predictive Modeling from Processing through Application. Adv Funct Mater. 2020;30(32). doi: 10.1002/ADFM.202000639
  109. Danis K, Ilgar S, Saraj S, Topuzogullari M, Gunduz O, Ustundag CB. Influence of Light Exposure Time on the Vat Photopolymerization of Methacrylated PVA Microneedles. ACS Omega. 2026;11(29):44284-44293. doi: 10.1021/acsomega.6c04499
  110. Pagnotta G, Becconi M, Malferrari M, et al. Development of a tissue construct with spatially controllable stiffnessviaa one-step 3D bioprinting and dual-crosslinking process. Mater Adv. 2024;4(16):3491-3505. doi: 10.1039/D3MA00319A
  111. Sharifi S, Sharifi H, Akbari A, Chodosh J. Systematic optimization of visible light-induced crosslinking conditions of gelatin methacryloyl (GelMA). Scientific Reports. 2021;11(1):23276. doi: 10.1038/s41598-021-02830-x
  112. González G, Baruffaldi D, Martinengo C, et al. Materials Testing for the Development of Biocompatible Devices through Vat-Polymerization 3D Printing. Nanomaterials. 2020;10(9):1788. doi: 10.3390/NANO10091788
  113. Luo Z, Zhang H, Chen R, et al. Digital light processing 3D printing for microfluidic chips with enhanced resolution via dosing- and zoning-controlled vat photopolymerization. Microsyst and nanoeng. 2023;9(1):103. doi: 10.1038/s41378-023-00542-y
  114. Kashi PA, Bachlechner C, Huc-Mathis D, Jäger H, Shahbazi M. A porous 3D biofilm-inspired alginate/gellan hydrogel fabricated via dual-wavelength UV-crosslinking printer: Structural and rheological properties. Carbohydr Polym. 2025;370:124246. doi: 10.1016/J.CARBPOL.2025.124246
  115. Coser C, Ghaemmaghami AM, Yang J. Soft tissue-mimicking hydrogel stiffness modulates polarisation of human monocyte-derived macrophages. Biomater Sci. 2025;13(23):6637-6651. doi: 10.1039/d5bm01187f
  116. Mazzoli A, Greco S, Luzi F, et al. 3D-Printed Alginate-Based Hydrogels with Appropriate Rheological Properties and Efficient Development of Cell Spheroids. Polymers 2025, Vol 17, Page 1730. 2025;17(13):1730. doi: 10.3390/POLYM17131730
  117. Kim J, Choi YJ, Gal CW, Sung A, Park H, Yun HS. Development of an alginate-gelatin bioink enhancing osteogenic differentiation by gelatin release. Int J Bioprint. 2023;9(2):660. doi: 10.18063/IJB.V9I2.660
  118. Hazur J, Röder J, Czwalinna J, Schubert DW, Boccaccini AR. Pre-Crosslinking with Hydrogel Microparticles Enhances the Printability of Alginate-Based Inks. Macromol Mater Eng. 2023;308(12):2200675. doi: 10.1002/MAME.202200675
  119. Feng H, Song Y, Lian X, et al. Study on Printability Evaluation of Alginate/Silk Fibroin/Collagen Double-Cross-Linked Inks and the Properties of 3D Printed Constructs. ACS Biomater Sci Eng. 2024;10(10):6581-6593. doi: 10.1021/ACSBIOMATERIALS.4C01522
  120. Das S, Jegadeesan JT, Basu B. Gelatin Methacryloyl (GelMA)-Based Biomaterial Inks: Process Science for 3D/4D Printing and Current Status. Biomacromolecules. 2024;25(4):2156-2221. doi: 10.1021/ACS.BIOMAC.3C01271
  121. 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
  122. Mao Q, Wang Y, Li Y, et al. Fabrication of liver microtissue with liver decellularized extracellular matrix (dECM) bioink by digital light processing (DLP) bioprinting. Mat Sci Eng C-mater. 2020;109:110625. doi: 10.1016/j.msec.2020.110625
  123. Jeon O, Alt DS, Ahmed SM, Alsberg E. The effect of oxidation on the degradation of photocrosslinkable alginate hydrogels. Biomaterials. 2012;33(13):3503-3514. doi: 10.1016/J.BIOMATERIALS.2012.01.041
  124. Liu W, Madry H, Cucchiarini M. Application of Alginate Hydrogels for Next-Generation Articular Cartilage Regeneration. Int J Mol Sci. 2022;23(3):1147. doi: 10.3390/IJMS23031147
  125. Fenn SL, Miao T, Scherrer RM, Oldinski RA. Dual-Crosslinked Methacrylated Alginate Sub-Microspheres for Intracellular Chemotherapeutic Delivery. ACS Appl Mater Interfaces. 2016;8(28):17775. doi: 10.1021/ACSAMI.6B03245
  126. Román-Guerrero A, Cortés-Camargo S, Alpizar-Reyes E, et al. Chemically Modified Alginate-Based Hydrogel-Matrices in Drug Delivery. Macromol 2025, Vol 5, Page 36. 2025;5(3):36. doi: 10.3390/MACROMOL5030036
  127. da Silva CM, Reis RL, Correlo VM, Jahno VD. The efficient role of sodium alginate-based biodegradable dressings for skin wound healing application: a systematic review. J Biomater Sci Polym Ed. 2024;35(3):397-414. doi: 10.1080/09205063.2023.2289247
  128. Boddupalli A, Bratlie KM. Second harmonic generation microscopy of collagen organization in tunable, environmentally responsive alginate hydrogels. Biomater Sci. 2019;7(3):1188-1199. doi: 10.1039/C8BM01535J
  129. Vashishtha G, Chauhan S, Zimroz R, Yadav N, Kumar R, Gupta MK. Current Applications of Machine Learning in Additive Manufacturing: A Review on Challenges and Future Trends. Arch. Comput. Methods Eng. 2024;32(4):2635-2668. doi: 10.1007/S11831-024-10215-2
  130. Ma Y, Tian Z, Wang B, et al. Enhancing the 3D printing fidelity of vat photopolymerization with machine learning-driven boundary prediction. Mater Des. 2024;241:112978. doi: 10.1016/J.MATDES.2024.112978
  131. Standard Guide for Bioinks Used in Bioprinting. Published online March 15, 2024. doi: 10.1520/F3659-24
  132. Afshar AK, Mirshafiei M, Saberi A, et al. From light to life: Photocrosslinkable bioinks and their role in 3D bioprinting for shaping future regenerative medicine. Bioprinting. 2026;57:e00487. doi: 10.1016/j.bprint.2026.e00487
  133. U.S. Food and Drug Administration. Process of 3D Printing Medical Devices. Accessed July 28, 2026. https://www.fda.gov/medical-devices/3d-printing-medical-devices/process-3d-printing-medical-devices
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International Journal of Bioprinting, Electronic ISSN: 2424-8002 Print ISSN: 2424-7723, Published by AccScience Publishing