دورية أكاديمية

Three-dimensional printing of cell-laden microporous constructs using blended bioinks.

التفاصيل البيبلوغرافية
العنوان: Three-dimensional printing of cell-laden microporous constructs using blended bioinks.
المؤلفون: Somasekhar L; Department of Biomedical, Chemical Engineering and Science, Florida Institute of Technology, Melbourne, Florida, USA., Huynh ND; Department of Biomedical, Chemical Engineering and Science, Florida Institute of Technology, Melbourne, Florida, USA., Vecheck A; Department of Biomedical, Chemical Engineering and Science, Florida Institute of Technology, Melbourne, Florida, USA., Kishore V; Department of Biomedical, Chemical Engineering and Science, Florida Institute of Technology, Melbourne, Florida, USA., Bashur CA; Department of Biomedical, Chemical Engineering and Science, Florida Institute of Technology, Melbourne, Florida, USA., Mitra K; Department of Biomedical, Chemical Engineering and Science, Florida Institute of Technology, Melbourne, Florida, USA.
المصدر: Journal of biomedical materials research. Part A [J Biomed Mater Res A] 2022 Mar; Vol. 110 (3), pp. 535-546. Date of Electronic Publication: 2021 Sep 05.
نوع المنشور: Journal Article; Research Support, U.S. Gov't, Non-P.H.S.
اللغة: English
بيانات الدورية: Publisher: John Wiley & Sons Country of Publication: United States NLM ID: 101234237 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4965 (Electronic) Linking ISSN: 15493296 NLM ISO Abbreviation: J Biomed Mater Res A Subsets: MEDLINE
أسماء مطبوعة: Original Publication: Hoboken, NJ : John Wiley & Sons, c2002-
مواضيع طبية MeSH: Bioprinting*/methods , Tissue Scaffolds*/chemistry, Alginates/chemistry ; Gelatin/chemistry ; Human Umbilical Vein Endothelial Cells ; Humans ; Hydrogels/chemistry ; Printing, Three-Dimensional ; Tissue Engineering/methods
مستخلص: Hydrogels such as alginate and gelatin have shown potential as biomaterials in various three-dimensional (3D) bioprinting applications. However, parameters such as viscosity, porosity, and printability influence the performance of hydrogel-based biomaterials, and there are limited characterization studies conducted on the behavior of these constructs. In this work, a syringe-based extrusion bioprinter was used to print 3D constructs with bioink composed of various concentrations of alginate and gelatin along with fibrinogen and human umbilical vein endothelial cells. Instead of crosslinking the gelatin, the gelatin was left uncrosslinked to provide microporosity within the system that can impact the cellular response. Mechanical and biochemical characterization was performed to evaluate the structural stability and integrity of the printed constructs along with viability of embedded cells. Bioprinted constructs of a higher total concentration of alginate and gelatin yielded better stability and structural integrity after culture. More importantly, higher amounts of gelatin (i.e., 1:9 instead of 2:3 alginate:gelatin) were shown to improve printability, which is different than most studies that instead use alginate to improve printability. In addition, higher amounts of gelatin impacted the changes in surface morphological features of the constructs after incubation, and ultimately improved biocompatibility with our system. Overall, this study demonstrated that an uncrosslinked gelatin system can provide flexible printing parameters and surface morphologies, but careful control over the printing parameters may be required. The bioink concentration of 10% (w/v) with minimum alginate and higher gelatin concentration exhibited the best printability, cell survival, and viability.
(© 2021 Wiley Periodicals LLC.)
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معلومات مُعتمدة: United States NASA NASA
فهرسة مساهمة: Keywords: endothelial cells; extrusion 3D bioprinting; fibrinogen; gelatin; porosity
المشرفين على المادة: 0 (Alginates)
0 (Hydrogels)
9000-70-8 (Gelatin)
تواريخ الأحداث: Date Created: 20210906 Date Completed: 20220331 Latest Revision: 20220401
رمز التحديث: 20231215
DOI: 10.1002/jbm.a.37303
PMID: 34486214
قاعدة البيانات: MEDLINE
الوصف
تدمد:1552-4965
DOI:10.1002/jbm.a.37303