Abstract:To develop a soft-to-hard tissue interface, we made a decellularized dermis/poly(methyl methacrylate) (PMMA) complex by soaking the decellularized dermis in methyl methacrylate (MMA) and an initiator, and then polymerizing the MMA. The decellularized tissue was chosen because of its good biocompatibility and the easiness of suturing it, and MMA because of its hard tissue compatibility and wide use in the biomedical field. The MMA filled the cavities in the dermis and polymerized within 10 min. No leaking or po… Show more
“…The DD was prepared using the high‐pressure method that we previously reported . The dermis was placed into polyethylene bags containing PBS.…”
Section: Methodsmentioning
confidence: 99%
“…The fundamental idea is based on the articles by Nakabayashi research group, where they showed that the methyl methacrylate (MMA) can absorb the tissue and be polymerized . We previously reported a complex of decellularized dermis (DD) and PMMA for use as a tissue interface with similar methods . A tissue interface is a material that is placed at the interfaces between multiple types of tissue with different physical properties to facilitate regeneration of the damaged zone .…”
To develop a method for making percutaneous devices that have high biocompatibility and do not induce downgrowth of epidermal cells, we prepared a partial decellularized dermis (DD)/poly(methyl methacrylate) (PMMA) complex (PDPC) with a PMMA rod firmly stabilized inside. The porcine decellularized tissue was chosen because of its high biocompatibility and mechanical properties, and MMA was used because it would adhere firmly to a polymer such as a catheter. The MMA filled the cavities in the dermis and polymerized, anchoring to the collagenous fibrils inside the porcine DD. The PDPC was cemented to the PMMA rod tightly and it was integrated with the surrounding tissue within 12 weeks of implantation. Furthermore, no downgrowth of the epidermis, which may cause clinical problems, was observed. We consider that the tissue-polymer complex may be a suitable candidate for use in percutaneous devices.
“…The DD was prepared using the high‐pressure method that we previously reported . The dermis was placed into polyethylene bags containing PBS.…”
Section: Methodsmentioning
confidence: 99%
“…The fundamental idea is based on the articles by Nakabayashi research group, where they showed that the methyl methacrylate (MMA) can absorb the tissue and be polymerized . We previously reported a complex of decellularized dermis (DD) and PMMA for use as a tissue interface with similar methods . A tissue interface is a material that is placed at the interfaces between multiple types of tissue with different physical properties to facilitate regeneration of the damaged zone .…”
To develop a method for making percutaneous devices that have high biocompatibility and do not induce downgrowth of epidermal cells, we prepared a partial decellularized dermis (DD)/poly(methyl methacrylate) (PMMA) complex (PDPC) with a PMMA rod firmly stabilized inside. The porcine decellularized tissue was chosen because of its high biocompatibility and mechanical properties, and MMA was used because it would adhere firmly to a polymer such as a catheter. The MMA filled the cavities in the dermis and polymerized, anchoring to the collagenous fibrils inside the porcine DD. The PDPC was cemented to the PMMA rod tightly and it was integrated with the surrounding tissue within 12 weeks of implantation. Furthermore, no downgrowth of the epidermis, which may cause clinical problems, was observed. We consider that the tissue-polymer complex may be a suitable candidate for use in percutaneous devices.
“…Decellularized matrices are characterized by a low immunogenic potential and adequate mechanical properties (both on the macro-and micron-scale). Furthermore, they provide cells with natural adhesive ligands and open porosity, which make them perfect candidates to assess cell migration and invasion in vitro (DeQuach et al, 2011;Matsushima et al, 2014). Despite these unique features, the use of decellularized matrices requires that the complex and delicate chemical/physical processes that lead to the decellularization must be carefully undertaken to not affect the outcome of the subsequent cell cultures (Song and Ott, 2011).…”
Decellularized matrices are steadily gaining popularity to study the biology of cells and tissues, as they represent a biomimetic environment in which cells can recapitulate certain behaviours that share similarities with those observed in vivo. Basically, biochemistry, microstructure and mechanics of the decellularized matrices are the most valuable properties that differentiate these culturing systems from conventional bidimensional models. Several procedures to decellularize tissues have been proposed so far, with the common aim to preserve the tissue chemical/physical properties of the original tissue. However, these processes are complex, time-consuming and expensive. In this work, we propose a cost-effective, easy-to-produce decellularized dermal matrix, derived from animal skin. The chemical/physical processes to obtain the matrices proved to not alter matrix structure and did not induce cytotoxicity issues. To test the validity of the decellularized matrices as a model to study the behaviour of tumour cells in vitro, we performed microstructural and mechanical investigations as well as cell proliferation assays. In particular, three different tumour cell lines were used, which proliferated and invaded the matrix with no additional treatments. Decellularized skin scaffold, presented in this work, could be a strong competitor for conventional 3D systems like synthetic porous scaffolds or hydrogels.
“…Hard tissue applications include interactions of these materials with bones and teeth, and soft tissue applications may involve interactions of materials with human tissues such as blood and blood vessels [4][5][6]. These materials are used to treat, repair, or alter diseased tissues and organs to enhance functionality [7][8][9]. At present, most studies involving biomedical materials are focused on developing biodegradable materials based on polylactic acid (PLA), poly(hydroxyalkanoate) (PHA), and poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) [10][11][12].…”
Composite materials made from Ganoderma lucidum fibre (GLF) and poly(hydroxyalkanoate) (PHA) or acrylic acid-grafted PHA (PHA-g-AA) were characterised with regard to biocompatibility. GLF was homogeneously dispersed in the PHA-g-AA matrix as a result of condensation reactions. Mechanical characterisation indicated that the improved adhesion between GLF and PHA-g-AA enhanced the tensile strength of the composite compared with that of PHA/GLF. The PHA-g-AA/GLF composites were also more water resistant than the PHA/GLF composites. Human foreskin fibroblasts (FBs) were seeded on two series of these composites to assess biocompatibility. FB proliferation, collagen production, and the percentage of normal cells growing on the PHA/GLF composites were greater than those for the PHA-g-AA/GLF composites.
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