Engineered tubular constructs made from soft biomaterials are employed in a myriad of applications in biomedical science. Potential uses of these constructs range from vascular grafts to conduits for enabling perfusion of engineered tissues and organs. The fabrication of standalone tubes or complex perfusable constructs from biofunctional materials, including hydrogels, via rapid and readily accessible routes is desirable. Here we report a methodology in which customized coaxial nozzles are 3D printed using commercially available stereolithography (SLA) 3D printers. These nozzles can be used for the fabrication of hydrogel tubes via coextrusion of two shear-thinning hydrogels: an unmodified Pluronic F-127 (F127) hydrogel and an F127-bisurethane methacrylate (F127-BUM) hydrogel. We demonstrate that different nozzle geometries can be modeled via computer-aided design and 3D printed in order to generate tubes or coaxial filaments with different cross-sectional geometries. We were able to fabricate tubes with luminal diameters or wall thicknesses as small as ∼150 μm. Finally, we show that these tubes can be functionalized with collagen I to enable cell adhesion, and human umbilical vein endothelial cells can be cultured on the luminal surfaces of these tubes to yield tubular endothelial monolayers. Our approach could enable the rapid fabrication of biofunctional hydrogel conduits which can ultimately be utilized for engineering in vitro models of tubular biological structures.
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http://dx.doi.org/10.1088/1758-5090/ab2b4d | DOI Listing |
Polymers (Basel)
December 2024
School of Chemical Engineering, Pusan National University, Busan 46241, Republic of Korea.
In this study, a transient viscosity adjustment method using a coaxial nozzle was explored to fabricate nanofibers from non-spinnable -poly(hydroxyamide) (-PHA). Unlike conventional electrospinning methods that often require additives to induce fiber formation, this approach relies on a sheath-core configuration, introducing tetrahydrofuran (THF) to the sheath to temporarily adjust solution viscosity. The diffusion of THF into the core -PHA solution resulted in momentary solidification at the interface, promoting nanofiber formation without compromising polymer solubility.
View Article and Find Full Text PDFACS Appl Mater Interfaces
December 2024
Faculty of Materials Sciences and Engineering, Warsaw University of Technology, Warsaw 02-507, Poland.
The microvascular bed plays a crucial role in establishing nutrient exchange and waste removal, as well as maintaining tissue metabolic activity in the human body. However, achieving microvascularization of engineered 3D tissue constructs is still an unsolved challenge. In this work, we developed biomimetic cell-laden hydrogel microfibers recapitulating oriented microvascular capillary-like networks by using a 3D bioprinting technique combined with microfluidics-assisted coaxial wet-spinning.
View Article and Find Full Text PDFACS Appl Mater Interfaces
November 2024
Zhejiang Provincial Engineering Center of Integrated Manufacturing Technology and Intelligent Equipment, Hangzhou City University, Hangzhou 310015, China.
A strategy for fabrication of macroporous hydrogels through 3D printing assisted by molding and multiple microfluidic bubble-templating nozzles is proposed here. This approach aims to address the challenges faced by methods for 3D printing macroporous hydrogels, such as difficulties in precisely controlling the spatial distribution of macropores, limited porosity, and low resolution of external boundaries due to the poor mechanical properties of hydrogel solutions as printing ink. In this method, fast-switching microfluidic bubble-templating nozzles of varying sizes allowed for precise control of target pore sizes over a wide range.
View Article and Find Full Text PDFMaterials (Basel)
November 2024
Laboratory of Bioactive Polymers, Institute of Polymers, Bulgarian Academy of Sciences, Acad. G. Bonchev St, Bl. 103A, BG-1113 Sofia, Bulgaria.
The preparation of core-sheath fibers by electrospinning is a topic of significant interest for producing composite fibers with distinct core and sheath functionalities. Moreover, in core-sheath fibers, low-molecular-weight substances or nanosized inorganic additives can be deposited in a targeted manner within the core or the sheath. Commonly, for obtaining a core-sheath structure, coaxial electrospinning is used.
View Article and Find Full Text PDFCell Mol Bioeng
October 2024
Biomedical Engineering Department, Oregon Health and Science University, Portland, OR 97201 USA.
Introduction: Coaxial 3D bioprinting has advanced the formation of tissue constructs that recapitulate key architectures and biophysical parameters for in-vitro disease modeling and tissue-engineered therapies. Controlling gene expression within these structures is critical for modulating cell signaling and probing cell behavior. However, current transfection strategies are limited in spatiotemporal control because dense 3D scaffolds hinder diffusion of traditional vectors.
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