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1. Engineering a macroporous fibrin-based sequential interpenetrating polymer network for dermal tissue engineering

   https://doi.org/10.1039/D0BM01161D  

   Gsib, Olfat; Eggermont, Loek J.; Egles, Christophe; Bencherif, Sidi A. (December 2020, Biomaterials Science)

   null (Ed.)

   The success of skin tissue engineering for deep wound healing relies predominantly on the design of innovative and effective biomaterials. This study reports the synthesis and characterization of a new type of naturally-derived and macroporous interpenetrating polymer network (IPN) for skin repair. These biomaterials consist of a biologically active fibrous fibrin network polymerized within a mechanically robust and macroporous construct made of polyethylene glycol and biodegradable serum albumin (PEGDM- co -SAM). First, mesoporous PEGDM- co -SAM hydrogels were synthesized and subjected to cryotreatment to introduce an interconnected macroporous network. Subsequently, fibrin precursors were incorporated within the cryotreated PEG-based network and then allowed to spontaneously polymerize and form a sequential IPN. Rheological measurements indicated that fibrin-based sequential IPN hydrogels exhibited improved and tunable mechanical properties when compared to fibrin hydrogels alone. In vitro data showed that human dermal fibroblasts adhere, infiltrate and proliferate within the IPN constructs, and were able to secrete endogenous extracellular matrix proteins, namely collagen I and fibronectin. Furthermore, a preclinical study in mice demonstrated that IPNs were stable over 1-month following subcutaneous implantation, induced a minimal host inflammatory response, and displayed a substantial cellular infiltration and tissue remodeling within the constructs. Collectively, these data suggest that macroporous and mechanically reinforced fibrin-based sequential IPN hydrogels are promising three-dimensional platforms for dermal tissue regeneration. 

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2. Fabrication and Characterization of Quad-Component Bioinspired Hydrogels to Model Elevated Fibrin Levels in Central Nervous Tissue Scaffolds

   https://doi.org/10.3390/gels10030203  

   Diaz-Lasprilla, Ana M; McKee, Meagan; Jimenez-Vergara, Andrea C; Ravi, Swathisri; Bellamy, Devon; Ortega, Wendy; Crosby, Cody O; Steele, Jennifer; Plascencia-Villa, Germán; Perry, George; et al (March 2024, Gels)

   Kakehashi, Rie; Yamashita, Yuji (Ed.)

   Multicomponent interpenetrating polymer network (mIPN) hydrogels are promising tissue-engineering scaffolds that could closely resemble key characteristics of native tissues. The mechanical and biochemical properties of mIPNs can be finely controlled to mimic key features of target cellular microenvironments, regulating cell-matrix interactions. In this work, we fabricated hydrogels made of collagen type I (Col I), fibrin, hyaluronic acid (HA), and poly (ethylene glycol) diacrylate (PEGDA) using a network-by-network fabrication approach. With these mIPNs, we aimed to develop a biomaterial platform that supports the in vitro culture of human astrocytes and potentially serves to assess the effects of the abnormal deposition of fibrin in cortex tissue and simulate key aspects in the progression of neuroinflammation typically found in human pathologies such as Alzheimer’s disease (AD), Parkinson’s disease (PD), and tissue trauma. Our resulting hydrogels closely resembled the complex modulus of AD human brain cortex tissue (~7.35 kPa), promoting cell spreading while allowing for the modulation of fibrin and hyaluronic acid levels. The individual networks and their microarchitecture were evaluated using confocal laser scanning microscopy (CLSM) and scanning electron microscopy (SEM). Human astrocytes were encapsulated in mIPNs, and negligible cytotoxicity was observed 24 h after the cell encapsulation. 

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3. Influence of Short Fiber Encapsulated in Hybrid Hydrogel For 3d Bioprinting Process: Aspect of Rheological Properties

   Tuladhar, S.; Clark, S.; & Habib, M. A. (May 2023, Proceedings of the IISE Annual Conference & Expo 2023)

   Babski-Reeves, K; Eksioglu, B; Hampton, D. (Ed.)

   Extrusion-based three-dimensional (3D) bio-printing is one of the several 3D bioprinting methods that is frequently used in current times. This method enables the accurate deposition of cell-laden bio-ink while ensuring a predetermined scaffold architecture that may allow living tissue regeneration. Natural hydrogels are a strong choice for bio-ink formulation for the extrusion-based 3D bioprinting method because they have a combination of unique properties, which include biocompatibility, reduced cell toxicity, and high-water content. However, due to its low mechanical integrity, hydrogel frequently struggles to retain structural stability. To overcome this challenge, we evaluated the rheological characteristics of distinct hybrid hydrogels composed of carboxymethyl cellulose (CMC), a widely used alginate, and nanofibers generated from cellulose (TEMPO-mediated nano-fibrillated cellulose, TONFC). Therefore, to examine the rheological properties, a set of compositions was developed incorporating CMC (1%–4%), alginate (1%–4%), and higher and lower contents of TONFC (0.5%) and (0.005%) respectively. From the flow diagram, the shear thinning coefficients of n and K were calculated, which were later linked to the 3D printability. With the guidance of diverse nanofiber ratios, it is possible to regulate the rheological properties and create 3D bioprinted scaffolds with well-defined scaffold architecture. 

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4. Recent Progress in Biopolymer-Based Hydrogel Materials for Biomedical Applications

   https://doi.org/10.3390/ijms23031415  

   Mahmood, Ayaz; Patel, Dev; Hickson, Brandon; DesRochers, John; Hu, Xiao (February 2022, International Journal of Molecular Sciences)

   Hydrogels from biopolymers are readily synthesized, can possess various characteristics for different applications, and have been widely used in biomedicine to help with patient treatments and outcomes. Polysaccharides, polypeptides, and nucleic acids can be produced into hydrogels, each for unique purposes depending on their qualities. Examples of polypeptide hydrogels include collagen, gelatin, and elastin, and polysaccharide hydrogels include alginate, cellulose, and glycosaminoglycan. Many different theories have been formulated to research hydrogels, which include Flory-Rehner theory, Rubber Elasticity Theory, and the calculation of porosity and pore size. All these theories take into consideration enthalpy, entropy, and other thermodynamic variables so that the structure and pore sizes of hydrogels can be formulated. Hydrogels can be fabricated in a straightforward process using a homogeneous mixture of different chemicals, depending on the intended purpose of the gel. Different types of hydrogels exist which include pH-sensitive gels, thermogels, electro-sensitive gels, and light-sensitive gels and each has its unique biomedical applications including structural capabilities, regenerative repair, or drug delivery. Major biopolymer-based hydrogels used for cell delivery include encapsulated skeletal muscle cells, osteochondral muscle cells, and stem cells being delivered to desired locations for tissue regeneration. Some examples of hydrogels used for drug and biomolecule delivery include insulin encapsulated hydrogels and hydrogels that encompass cancer drugs for desired controlled release. This review summarizes these newly developed biopolymer-based hydrogel materials that have been mainly made since 2015 and have shown to work and present more avenues for advanced medical applications. 

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5. Dual Crosslinked Gelatin Methacryloyl Hydrogels for Photolithography and 3D Printing

   https://doi.org/10.3390/gels5030034  

   Basara, Gozde; Yue, Xiaoshan; Zorlutuna, Pinar (September 2019, Gels)

   Gelatin methacryloyl (GelMA) hydrogels have been used in tissue engineering and regenerative medicine because of their biocompatibility, photopatternability, printability, and tunable mechanical and rheological properties. However, low mechanical strength limits their applications in controlled drug release, non-viral gene therapy, and tissue and disease modeling. In this work, a dual crosslinking method for GelMA is introduced. First, photolithography was used to pattern the gels through the crosslinking of methacrylate incorporated amine groups of GelMA. Second, a microbial transglutaminase (mTGase) solution was introduced in order to enzymatically crosslink the photopatterned gels by initiating a chemical reaction between the glutamine and lysine groups of the GelMA hydrogel. The results showed that dual crosslinking improved the stiffness and rheological properties of the hydrogels without affecting cell viability, when compared to single crosslinking with either ultraviolet (UV) exposure or mTGase treatment. Our results also demonstrate that when treated with mTGase, hydrogels show decreased swelling properties and better preservation of photolithographically patterned shapes. Similar effects were observed when three dimensional (3D) printed and photocrosslinked substrates were treated with mTGase. Such dual crosslinking methods can be used to improve the mechanical properties and pattern fidelity of GelMA gels, as well as dynamic control of the stiffness of tissue engineered constructs. 

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