Dual-Crosslinking of Gelatin-Based Hydrogels: Promising Compositions for a 3D Printed Organotypic Bone Model

Gelatin-based hydrogels have emerged as a popular scaffold material for tissue engineering applications. The introduction of variable crosslinking methods has shown promise for fabricating stable cell-laden scaffolds. In this work, we examine promising composite biopolymer-based inks for extrusion-based 3D bioprinting, using a dual crosslinking approach. A combination of carefully selected printable hydrogel ink compositions and the use of photoinduced covalent and ionic crosslinking mechanisms allows for the fabrication of scaffolds of high accuracy and low cytotoxicity, resulting in unimpeded cell proliferation, extracellular matrix deposition, and mineralization. Three selected bioink compositions were characterized and the respective cell-laden scaffolds were bioprinted. Temporal stability, morphology, swelling, and mechanical properties of the scaffolds were thoroughly studied and the biocompatibility of the constructs was assessed using rat mesenchymal stem cells while focusing on osteogenesis. Experimental results showed that the composition of 1% alginate, 4% gelatin, and 5% (w/v) gelatine methacrylate, was found to be optimal among the examined, with shape fidelity of 88%, large cell spreading area and cell viability at around 100% after 14 days. The large pore diameters that exceed 100 µm, and highly interconnected scaffold morphology, make these hydrogels extremely potent in bone tissue engineering and bone organoid fabrication.

[1]  D. Berillo,et al.  Macroporous 3D printed structures for regenerative medicine applications , 2022, Bioprinting.

[2]  Feiyang Zhang,et al.  Unraveling of Advances in 3D-Printed Polymer-Based Bone Scaffolds , 2022, Polymers.

[3]  Xiaokun Fan,et al.  A 4arm-PEG macromolecule crosslinked chitosan hydrogels as antibacterial wound dressing. , 2021, Carbohydrate polymers.

[4]  P. Nair,et al.  Dual crosslinked pullulan–gelatin cryogel scaffold for chondrocyte-mediated cartilage repair: synthesis, characterization and in vitro evaluation , 2021, Biomedical materials.

[5]  Zhenjiang Ma,et al.  3D bioprinting of proangiogenic constructs with induced immunomodulatory microenvironments through a dual cross-linking procedure using laponite incorporated bioink , 2021, Composites Part B: Engineering.

[6]  Chang Liu,et al.  Magnesium Ammonium Phosphate Composite Cell-Laden Hydrogel Promotes Osteogenesis and Angiogenesis In Vitro , 2021, ACS omega.

[7]  J. Fisher,et al.  Impact of cell density on the bioprinting of gelatin methacrylate (GelMA) bioinks , 2021, Bioprinting.

[8]  Y. Iwamura,et al.  Gelatin Methacryloyl–Riboflavin (GelMA–RF) Hydrogels for Bone Regeneration , 2021, International journal of molecular sciences.

[9]  J. Kulbacka,et al.  A Review on the Adaption of Alginate-Gelatin Hydrogels for 3D Cultures and Bioprinting , 2021, Materials.

[10]  J. Mano,et al.  GelMA/bioactive silica nanocomposite bioinks for stem cell osteogenic differentiation , 2021, Biofabrication.

[11]  Huazhe Yang,et al.  Applications of Gelatin Methacryloyl (GelMA) Hydrogels in Microfluidic Technique-Assisted Tissue Engineering , 2020, Molecules.

[12]  Zhenjiang Ma,et al.  Three-dimensional bioprinting of multicell-laden scaffolds containing bone morphogenic protein-4 for promoting M2 macrophage polarization and accelerating bone defect repair in diabetes mellitus , 2020, Bioactive materials.

[13]  Philippe Bédard,et al.  Innovative Human Three-Dimensional Tissue-Engineered Models as an Alternative to Animal Testing , 2020, Bioengineering.

[14]  A. C. Jayasuriya,et al.  Hydrogel-based 3D bioprinting: A comprehensive review on cell-laden hydrogels, bioink formulations, and future perspectives. , 2020, Applied materials today.

[15]  D. Losic,et al.  3D Bioprinting of Methylcellulose/Gelatin-Methacryloyl (MC/GelMA) Bioink with High Shape Integrity. , 2020, ACS applied bio materials.

[16]  Luis M. Rodríguez-Lorenzo,et al.  Alginate hydrogels for bone tissue engineering, from injectables to bioprinting: A review. , 2020, Carbohydrate polymers.

[17]  Lisa Moncrieff,et al.  Bone Regeneration, Reconstruction and Use of Osteogenic Cells; from Basic Knowledge, Animal Models to Clinical Trials , 2020, Journal of clinical medicine.

[18]  Geunhyung Kim,et al.  Collagen/bioceramic-based composite bioink to fabricate a porous 3D hASCs-laden structure for bone tissue regeneration , 2019, Biofabrication.

[19]  R. Hubrecht,et al.  The 3Rs and Humane Experimental Technique: Implementing Change , 2019, Animals : an open access journal from MDPI.

[20]  Jianhua Zhang,et al.  Alginate dependent changes of physical properties in 3D bioprinted cell-laden porous scaffolds affect cell viability and cell morphology , 2019, Biomedical materials.

[21]  Shan Huang,et al.  Enzymatically degradable alginate/gelatin bioink promotes cellular behavior and degradation in vitro and in vivo , 2019, Biofabrication.

[22]  Yogendra Pratap Singh,et al.  3D Bioprinting using Cross-Linker Free Silk-Gelatin Bioink for Cartilage Tissue Engineering. , 2019, ACS applied materials & interfaces.

[23]  T. Woodfield,et al.  Osteogenic and angiogenic tissue formation in high fidelity nanocomposite Laponite-gelatin bioinks , 2019, Biofabrication.

[24]  A. Feinberg,et al.  Cryopreserved cell-laden alginate microgel bioink for 3D bioprinting of living tissues. , 2019, Materials today. Chemistry.

[25]  M. Endres,et al.  Photopolymerizable gelatin and hyaluronic acid for stereolithographic 3D bioprinting of tissue‐engineered cartilage , 2019, Journal of biomedical materials research. Part B, Applied biomaterials.

[26]  Yibing Wu,et al.  The influence of the stiffness of GelMA substrate on the outgrowth of PC12 cells , 2019, Bioscience reports.

[27]  Cheng-Ting Shih,et al.  Osteogenic and angiogenic potentials of the cell-laden hydrogel/mussel-inspired calcium silicate complex hierarchical porous scaffold fabricated by 3D bioprinting. , 2018, Materials science & engineering. C, Materials for biological applications.

[28]  Xin Bai,et al.  Bioactive hydrogels for bone regeneration , 2018, Bioactive materials.

[29]  Ali Khademhosseini,et al.  Bioinks for 3D bioprinting: an overview. , 2018, Biomaterials science.

[30]  Jianzhong Fu,et al.  3D Bioprinting of Low-Concentration Cell-Laden Gelatin Methacrylate (GelMA) Bioinks with a Two-Step Cross-linking Strategy. , 2018, ACS applied materials & interfaces.

[31]  G. Tovar,et al.  Quantification of Substitution of Gelatin Methacryloyl: Best Practice and Current Pitfalls. , 2018, Biomacromolecules.

[32]  Ali Khademhosseini,et al.  Extrusion Bioprinting of Shear‐Thinning Gelatin Methacryloyl Bioinks , 2017, Advanced healthcare materials.

[33]  Ibrahim T. Ozbolat,et al.  The bioink: A comprehensive review on bioprintable materials. , 2017, Biotechnology advances.

[34]  Liliang Ouyang,et al.  A Generalizable Strategy for the 3D Bioprinting of Hydrogels from Nonviscous Photo‐crosslinkable Inks , 2017, Advanced materials.

[35]  Xiaodong Cao,et al.  3D Bioplotting of Gelatin/Alginate Scaffolds for Tissue Engineering: Influence of Crosslinking Degree and Pore Architecture on Physicochemical Properties , 2016 .

[36]  Kang Zhang,et al.  3D printing of functional biomaterials for tissue engineering. , 2016, Current opinion in biotechnology.

[37]  Pamela Habibovic,et al.  Calcium phosphates in biomedical applications: materials for the future? , 2016 .

[38]  Wenmiao Shu,et al.  Three-dimensional bioprinting of complex cell laden alginate hydrogel structures , 2015, Biofabrication.

[39]  Qun Wang,et al.  Ex Vivo Culture of Primary Intestinal Stem Cells in Collagen Gels and Foams. , 2015, ACS biomaterials science & engineering.

[40]  G. Spinks,et al.  Mechanical properties of interpenetrating polymer network hydrogels based on hybrid ionically and covalently crosslinked networks , 2013 .

[41]  Wim E Hennink,et al.  25th Anniversary Article: Engineering Hydrogels for Biofabrication , 2013, Advanced materials.

[42]  A. Khademhosseini,et al.  Transdermal regulation of vascular network bioengineering using a photopolymerizable methacrylated gelatin hydrogel. , 2013, Biomaterials.

[43]  J. Gorski Biomineralization of bone: a fresh view of the roles of non-collagenous proteins. , 2011, Frontiers in bioscience.

[44]  Sheng Lin-Gibson,et al.  The effect of 3D hydrogel scaffold modulus on osteoblast differentiation and mineralization revealed by combinatorial screening. , 2010, Biomaterials.

[45]  M. Hincke,et al.  Fibrin: a versatile scaffold for tissue engineering applications. , 2008, Tissue engineering. Part B, Reviews.

[46]  L. Shea,et al.  Physical properties of alginate hydrogels and their effects on in vitro follicle development. , 2007, Biomaterials.

[47]  Shelly R. Peyton,et al.  Intrinsic mechanical properties of the extracellular matrix affect the behavior of pre-osteoblastic MC3T3-E1 cells. , 2006, American journal of physiology. Cell physiology.

[48]  P. Esposito,et al.  Osteogenesis Imperfecta. , 1928, Proceedings of the Royal Society of Medicine.