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Colloidal hydrogels, also known as microgels, are promising scaffold materials in the biomedical field. Microgels exhibit high biocompatibility, porosity, and mechanical stability, crucial in supporting cell development. Bio-based polymers, such as fibrin or dextran, are desirable for controlling the properties of microgels. The advantage of using these polymers includes producing degradable microgels that enable the release of active components. In this work, we fabricated fibrin-dextran-methacrylate (dextran-MA) interpenetrating polymer network microgels with tunable porosity, stiffness, and degradation profiles using droplet-based microfluidics. We incorporated fibrin to promote cell growth, while adding dextran-MA ensures improved structural stability of the microgels. By systematically varying the dextran-MA concentrations, we produced fibrin-dextran-MA microgels with a tunable range of stiffness, porosity, and degradation time, highlighting the material's versatility for biomedical applications. In particular, increasing the dextran-MA content reduced pore size, thereby offering a means to control the encapsulation and release of active components. Degradation studies using plasminogen and dextranase revealed that the degradation of the microgels strongly depended on the polymer concentration. This dependency allows controlling the degradation time and the release kinetics of active components, e.g., hepatocyte growth factor (HGF). HGF encapsulated in fibrin microgels was released rapidly through diffusion, while the release from fibrin-dextran microgels was delayed until enzymatic degradation. This delayed degradation of microgels demonstrates the potential to use the microgels for programmable release. Encapsulation of HGF in fibrin and fibrin-dextran-MA microgels promoted the spreading of human mesenchymal stem cells on the microgels, highlighting their potential for personalized Tissue Engineering applications. Our studies reveal that engineered microgels composed of fibrin and dextran-MA can be used as colloidal building blocks to design biomaterials with tailored stiffness, porosity, degradation, and programmed release behavior.
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http://dx.doi.org/10.1016/j.jcis.2025.138345 | DOI Listing |
Angiogenesis
September 2025
Division of Plastic Surgery, Department of Surgery, Penn State Health Milton S. Hershey Medical Center, Hershey, PA, 17033, USA.
Vascularization of implanted biomaterials is critical to reconstructive surgery and tissue engineering. Ultimately, the goal is to promote a rapidly perfusable hierarchical microvasculature that persists with time and can meet underlying tissue needs. We have previously shown that using a microsurgical technique, termed micropuncture (MP), in combination with porous granular hydrogel scaffolds (GHS) fabricated via interlinking hydrogel microparticles (microgels) results in a rapidly perfusable patterned microvasculature.
View Article and Find Full Text PDFACS Appl Bio Mater
September 2025
Department of Chemistry, Indian Institute of Technology Patna, Patna, Bihta, Bihar 801106, India.
Development of suitable carbohydrate-decorated, biocompatible, and stimuli-responsive fluorescent microgels that can selectively bind and detect proteins (such as lectins) is an important research topic. Herein, we report the development of mannose-decorated, dual-stimuli (temperature and pH)-responsive fluorescent poly(aminoamide) microgels, which can selectively bind to and thereby detect the presence of concanavalin A (Con A). The resultant stimuli-responsive microgels have a lower critical solution temperature (VPTT) of 37.
View Article and Find Full Text PDFInt J Pharm
September 2025
Laboratory of Advanced Theranostic Materials and Technology, Ningbo Institute of Materials Technology and Engineering, Chinese Academy of Sciences, Ningbo 315201, PR China; Zhejiang International Scientific and Technological Cooperative Base of Biomedical Materials and Technology, Ningbo Cixi Instit
Smart hydrogels have advanced rapidly in recent years. However, systems responsive to a single stimulus are typically triggered by specific cues, limiting their adaptability in complex and dynamic biological environments. To overcome this limitation, this study developed a dual-responsive hydrogel sensitive to both temperature and mechanical stress.
View Article and Find Full Text PDFACS Appl Mater Interfaces
September 2025
Department of Materials Science and Engineering, College of Engineering, Texas A&M University, College Station, Texas 77843, United States.
Hydrogel-based bioinks are widely adopted in digital light processing (DLP) 3D printing. Modulating their mechanical properties is especially beneficial in biomedical applications, such as directing cell activity toward tissue regeneration and healing. However, in both monolithic and granular hydrogels, the tunability of mechanical properties is limited to parameters such as cross-linking or packing density.
View Article and Find Full Text PDFMacromol Biosci
September 2025
Department of Chemistry, Korea Advanced Institute of Science and Technology (KAIST), Daejeon, Republic of Korea.
Conventional gelatin's gel-to-sol transition upon heating restricts its utility in biomedical applications that benefit from a gel state at physiological temperatures such as Pluronic F127 and poly(NIPAAm). Herein, we present "rev-Gelatin", a gelatin engineered with reverse thermo-responsive properties that undergoes a sol-to-gel transition as temperature rises from ambient to body temperature. Inspired by the phase dynamics of common materials like candy and ice cubes, whose surfaces soften or partially melt under warming, facilitating inter-object adhesion- rev-Gelatin leverages this concept to achieve fluidity at room temperature for easy injectability.
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