Renjing Wang, Yunxia Chen, Kyle R Phillips, Chuanshen Zhou, John-Thomas T Robinson, David B Iten, Dylan Z Ver Helst, Yong Huang
{"title":"可打印明胶复合材料-聚乙烯醇生物墨水的设计用于三维厚孔结构的自支撑制造。","authors":"Renjing Wang, Yunxia Chen, Kyle R Phillips, Chuanshen Zhou, John-Thomas T Robinson, David B Iten, Dylan Z Ver Helst, Yong Huang","doi":"10.1021/acsbiomaterials.5c00888","DOIUrl":null,"url":null,"abstract":"<p><p>The development of thick, permeable, three-dimensional (3D) constructs is essential for advancing tissue engineering applications that require efficient mass transport and prolonged cell viability. In this study, a printable gelatin composite-poly(vinyl alcohol) (PVA) bioink is designed and evaluated for the self-supported fabrication of 3D thick porous constructs with satisfactory permeability. The proposed bioink incorporates gelatin solution, gelatin microgels, and PVA, which is utilized as a sacrificial porogen to facilitate postprinting pore formation. The rheological properties of the bioink (the PVA-to-gelatin composite v/w ratio of 1:5) demonstrate suitable shear-thinning behavior and yield-stress fluid property for extrusion-based 3D printing, and the latter enables the jamming-based physical cross-linking mechanism during printing, which works with the thermal cross-linking of gelatin solution to retain the print shape for permanent enzymatic cross-linking. Printed constructs exhibit good print fidelity and structural integrity across both two-dimensional (2D) lattice and 3D tubular geometries. After PVA removal, the freeze-dried samples show large pores formed by removed PVA, as confirmed by scanning electron microscopy and pore size analysis. Permeability tests reveal that constructs fabricated with PVA porogen removal achieve a higher permeation rate of 1.39 mm/h. NIH 3T3 fibroblast-based cell viability studies demonstrate sustained cell survival in the 10.00 mm-thick porous constructs with cell viability above 75% over 7 days with the 2D cell viability control effect considered. Despite residual PVA detected postremoval, the porous network formed by PVA removal remains effective in supporting permeability and cellular function. These findings demonstrate the potential of the printable gelatin composite-PVA bioink for fabricating thick, permeable constructs suitable for cell culture and tissue engineering applications.</p>","PeriodicalId":8,"journal":{"name":"ACS Biomaterials Science & Engineering","volume":" ","pages":""},"PeriodicalIF":5.5000,"publicationDate":"2025-09-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Design of Printable Gelatin Composite-PVA Bioink for Self-Supported Fabrication of 3D Thick Porous Constructs.\",\"authors\":\"Renjing Wang, Yunxia Chen, Kyle R Phillips, Chuanshen Zhou, John-Thomas T Robinson, David B Iten, Dylan Z Ver Helst, Yong Huang\",\"doi\":\"10.1021/acsbiomaterials.5c00888\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The development of thick, permeable, three-dimensional (3D) constructs is essential for advancing tissue engineering applications that require efficient mass transport and prolonged cell viability. In this study, a printable gelatin composite-poly(vinyl alcohol) (PVA) bioink is designed and evaluated for the self-supported fabrication of 3D thick porous constructs with satisfactory permeability. The proposed bioink incorporates gelatin solution, gelatin microgels, and PVA, which is utilized as a sacrificial porogen to facilitate postprinting pore formation. The rheological properties of the bioink (the PVA-to-gelatin composite v/w ratio of 1:5) demonstrate suitable shear-thinning behavior and yield-stress fluid property for extrusion-based 3D printing, and the latter enables the jamming-based physical cross-linking mechanism during printing, which works with the thermal cross-linking of gelatin solution to retain the print shape for permanent enzymatic cross-linking. Printed constructs exhibit good print fidelity and structural integrity across both two-dimensional (2D) lattice and 3D tubular geometries. After PVA removal, the freeze-dried samples show large pores formed by removed PVA, as confirmed by scanning electron microscopy and pore size analysis. Permeability tests reveal that constructs fabricated with PVA porogen removal achieve a higher permeation rate of 1.39 mm/h. NIH 3T3 fibroblast-based cell viability studies demonstrate sustained cell survival in the 10.00 mm-thick porous constructs with cell viability above 75% over 7 days with the 2D cell viability control effect considered. Despite residual PVA detected postremoval, the porous network formed by PVA removal remains effective in supporting permeability and cellular function. 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Design of Printable Gelatin Composite-PVA Bioink for Self-Supported Fabrication of 3D Thick Porous Constructs.
The development of thick, permeable, three-dimensional (3D) constructs is essential for advancing tissue engineering applications that require efficient mass transport and prolonged cell viability. In this study, a printable gelatin composite-poly(vinyl alcohol) (PVA) bioink is designed and evaluated for the self-supported fabrication of 3D thick porous constructs with satisfactory permeability. The proposed bioink incorporates gelatin solution, gelatin microgels, and PVA, which is utilized as a sacrificial porogen to facilitate postprinting pore formation. The rheological properties of the bioink (the PVA-to-gelatin composite v/w ratio of 1:5) demonstrate suitable shear-thinning behavior and yield-stress fluid property for extrusion-based 3D printing, and the latter enables the jamming-based physical cross-linking mechanism during printing, which works with the thermal cross-linking of gelatin solution to retain the print shape for permanent enzymatic cross-linking. Printed constructs exhibit good print fidelity and structural integrity across both two-dimensional (2D) lattice and 3D tubular geometries. After PVA removal, the freeze-dried samples show large pores formed by removed PVA, as confirmed by scanning electron microscopy and pore size analysis. Permeability tests reveal that constructs fabricated with PVA porogen removal achieve a higher permeation rate of 1.39 mm/h. NIH 3T3 fibroblast-based cell viability studies demonstrate sustained cell survival in the 10.00 mm-thick porous constructs with cell viability above 75% over 7 days with the 2D cell viability control effect considered. Despite residual PVA detected postremoval, the porous network formed by PVA removal remains effective in supporting permeability and cellular function. These findings demonstrate the potential of the printable gelatin composite-PVA bioink for fabricating thick, permeable constructs suitable for cell culture and tissue engineering applications.
期刊介绍:
ACS Biomaterials Science & Engineering is the leading journal in the field of biomaterials, serving as an international forum for publishing cutting-edge research and innovative ideas on a broad range of topics:
Applications and Health – implantable tissues and devices, prosthesis, health risks, toxicology
Bio-interactions and Bio-compatibility – material-biology interactions, chemical/morphological/structural communication, mechanobiology, signaling and biological responses, immuno-engineering, calcification, coatings, corrosion and degradation of biomaterials and devices, biophysical regulation of cell functions
Characterization, Synthesis, and Modification – new biomaterials, bioinspired and biomimetic approaches to biomaterials, exploiting structural hierarchy and architectural control, combinatorial strategies for biomaterials discovery, genetic biomaterials design, synthetic biology, new composite systems, bionics, polymer synthesis
Controlled Release and Delivery Systems – biomaterial-based drug and gene delivery, bio-responsive delivery of regulatory molecules, pharmaceutical engineering
Healthcare Advances – clinical translation, regulatory issues, patient safety, emerging trends
Imaging and Diagnostics – imaging agents and probes, theranostics, biosensors, monitoring
Manufacturing and Technology – 3D printing, inks, organ-on-a-chip, bioreactor/perfusion systems, microdevices, BioMEMS, optics and electronics interfaces with biomaterials, systems integration
Modeling and Informatics Tools – scaling methods to guide biomaterial design, predictive algorithms for structure-function, biomechanics, integrating bioinformatics with biomaterials discovery, metabolomics in the context of biomaterials
Tissue Engineering and Regenerative Medicine – basic and applied studies, cell therapies, scaffolds, vascularization, bioartificial organs, transplantation and functionality, cellular agriculture