Scaffolds For Skin Regeneration Research Articles

The role of BSA protein on the skin regeneration ability of electrospun PCL/HA scaffolds, kinetics of release and essential in vitro tests

This study focused on the skin regeneration ability of hybrid polycaprolactone (PCL) scaffolds incorporated by hydroxyapatite (HA) nanoparticles (NPs) and bovine serum albumin (BSA). The scaffolds were synthesized by the electrospinning method, and their microstructure, molecular groups, wettability, swelling, porosity, and mechanical properties were characterized. The results showed that the HA NPs and BSA protein could be incorporated within the PCL fibers without a significant effect on the main molecular groups of the PCL structure. Incorporation of both the HA NPs and BSA protein could reduce the superhydrophobicity of the PCL scaffold to the required amount for skin regeneration. It was also found that the incorporation of mentioned elements increased the water uptake by PCL fibrous scaffolds, and decreased the mechanical properties. The kinetics of BSA release from the hybrid scaffolds was also investigated. The Higuchi model was the best-fitting model to explain the protein release from the electrospun products. The cytocompatibility of scaffolds was evaluated by the human umbilical vein endothelial cells (HUVEC), and the higher ability of the PCL/BSA scaffold for skin regeneration was confirmed.

Current Biomaterials for Wound Healing.

Wound healing is the body's process of injury recovery. Skin healing is divided into four distinct overlapping phases: hemostasis, inflammation, proliferation, and remodeling. Cell-to-cell interactions mediated by both cytokines and chemokines are imperative for the transition between these phases. Patients can face difficulties in the healing process due to the wound being too large, decreased vascularization, infection, or additional burdens of a systemic illness. The field of tissue engineering has been investigating biomaterials as an alternative for skin regeneration. Biomaterials used for wound healing may be natural, synthetic, or a combination of both. Once a specific biomaterial is selected, it acts as a scaffold for skin regeneration. When the scaffold is applied to a wound, it allows for the upregulation of distinct molecular signaling pathways important for skin repair. Although tissue engineering has made great progress, more research is needed in order to support the use of biomaterials for wound healing for clinical translation.

Preparation and Characterization of Nanofibrous Membranes Electro-Spun from Blended Poly(l-lactide-co-ε-caprolactone) and Recombinant Spider Silk Protein as Potential Skin Regeneration Scaffold.

Biomaterial scaffolding serves as an important strategy in skin tissue engineering. In this research, recombinant spider silk protein (RSSP) and poly(L-lactide-co-ε-caprolactone) (PLCL) were blended in different ratios to fabricate nanofibrous membranes as potential skin regeneration scaffolds with an electro-spinning process. Scanning electron microscopy (SEM), water contact angles measurement, Fourier transform infrared (FTIR) spectroscopy, wide angle X-ray diffraction (WAXD), tensile mechanical tests and thermo-gravimetric analysis (TGA) were carried out to characterize the nanofibrous membranes. The results showed that the blending of RSSP greatly decreased the nanofibers' average diameter, enhanced the hydrophilicity, changed the microstructure and thermal properties, and could enable tailored mechanical properties of the nanofibrous membranes. Among the blended membranes, the PLCL/RSSP (75/25) membrane was chosen for further investigation on biocompatibility. The results of hemolysis assays and for proliferation of human foreskin fibroblast cells (hFFCs) confirmed the membranes potential use as skin-regeneration scaffolds. Subsequent culture of mouse embryonic fibroblast cells (NIH-3T3) demonstrated the feasibility of the blended membranes as a human epidermal growth factor (hEGF) delivery matrix. The PLCL/RSSP (75/25) membrane possessed good properties comparable to those of human skin with high biocompatibility and the ability of hEGF delivery. Further studies can be carried out on such membranes with chemical or genetic modifications to make better scaffolds for skin regeneration.

Preparation and in vitro characterization of electrospun scaffolds composed of chitosan, gelatin and 58S bioactive glass nanoparticles for skin tissue engineering

Background and aims: The presence of an appropriate scaffold at the wound site could significantly improve the healing process. In this study, we aimed to prepare a biomimetic nanocomposite scaffold composed of chitosan, gelatin, and 58S bioglass nanoparticles for skin tissue engineering. Methods: The nanocomposite scaffolds composed of chitosan, gelatin, and 58S bioglass nanoparticles were fabricated through electrospinning process. Then the cell viability assay was performed in order to evaluate the biological properties of the membranes. The optimum concentration of bioglass nanoparticles was determined for further studies. In vitro characterization was also performed to evaluate physicochemical properties of the scaffolds. Results: The chitosan/gelatin scaffold containing 2% of 58S bioglass nanoparticles showed no cell toxicity, and the dermal fibroblasts were found capable of proliferation on the membrane. The in vitro results obtained from the scanning electron microscopy (SEM), attenuated total reflectance-Fourier transform infrared spectroscopy (ATR-FTIR), and porosity tests demonstrated the appropriate properties of the membrane as a scaffold for skin regeneration. Conclusions: It was concluded that a chitosan-gelatin membrane containing 2% of 58S bioglass nanoparticles had the potential to function as a scaffold to accelerate wound healing due to its suitable properties, such as high porosity, high surface/volume ratio, and excellent biocompatibility.

Nanotechnology: A Promising Tool Towards Wound Healing.

Nanotechnology is an exciting emerging field with multiple applications in skin regeneration. Nanofibers have gained special attention in skin regeneration based on their structural similarity to the extracellular matrix. A wide variety of polymeric nanofibers with distinct properties have been developed and tested as scaffolds for skin regeneration. Besides providing support for tissue repair, nanofibrous materials can act as delivery systems for drugs, proteins, growth factors, and other molecules. Moreover, the morphology, biodegradability, and other functionalities of nanofibrous materials can be controlled towards specific conditions of wound healing. Other nanostructured drug delivery systems, such as nanoparticles, micelles, nanoemulsions, and liposomes, have been used to improve wound healing at different stages. These nanoscale delivery systems have demonstrated several benefits for the wound healing process, including reduced cytotoxicity of drugs, administration of poorly water-soluble drugs, improved skin penetration, controlled release properties, antimicrobial activity, and protection of drugs against light, temperature, enzymes or pH degradation, as well as stimulation of fibroblast proliferation and reduced inflammation.

3D-Printed FGF-incorporated silk scaffold for skin regeneration

Event Abstract Back to Event 3D-Printed FGF-incorporated silk scaffold for skin regeneration Shufang Zhang1, Si Xiong1, Ping Lu1, Yan Wu1, Quan Wang1, Xianzhu Zhang1, Heng Sun1 and Hong Wei Ouyang1 1 Center for Stem Cells and Tissue Engineering, School of Medicine, China The key problems hindering skin repair are deficiency of dermal vascularization and difficulty of epidermis regeneration, it is challenging to fabricate scaffolds that can biologically fulfill the requirements for regeneration of skin injuries. To solve this problem, we developed a three-dimensional printed hydrogel-silk fibroin (3DG-SF) matrix scaffold incorporated with basic fibroblast growth factor (FGF-2) through a sulfonic acid group (SO3). The efficacy and mechanism by which the 3DG-SF-SO3-FGF scaffolds promote skin regeneration were systematically investigated both in cell culture and a full-thickness skin defect models. The histological results showed that incorporation of FGF-2 into 3D scaffolds significantly enhanced the regeneration of skin-like tissues as compared to petroleum gauze, after implantation in rat skin defects for 14 and 28 days. Further investigations demonstrated that the 3DG-SF-FGF scaffolds might stimulate the vascularization of dermis. These findings suggest that the incorporation of FGF-2 into 3DG-SF-SO3 scaffolds is a viable strategy for skin regeneration. Keywords: Regenerative Medicine, Bioprinting, 3D scaffold, tissue niche Conference: 10th World Biomaterials Congress, Montréal, Canada, 17 May - 22 May, 2016. Presentation Type: Poster Topic: Regenerative medicine: biomaterials for control of tissue induction Citation: Zhang S, Xiong S, Lu P, Wu Y, Wang Q, Zhang X, Sun H and Ouyang H (2016). 3D-Printed FGF-incorporated silk scaffold for skin regeneration. Front. Bioeng. Biotechnol. Conference Abstract: 10th World Biomaterials Congress. doi: 10.3389/conf.FBIOE.2016.01.01297 Copyright: The abstracts in this collection have not been subject to any Frontiers peer review or checks, and are not endorsed by Frontiers. They are made available through the Frontiers publishing platform as a service to conference organizers and presenters. The copyright in the individual abstracts is owned by the author of each abstract or his/her employer unless otherwise stated. Each abstract, as well as the collection of abstracts, are published under a Creative Commons CC-BY 4.0 (attribution) licence (https://creativecommons.org/licenses/by/4.0/) and may thus be reproduced, translated, adapted and be the subject of derivative works provided the authors and Frontiers are attributed. For Frontiers’ terms and conditions please see https://www.frontiersin.org/legal/terms-and-conditions. Received: 27 Mar 2016; Published Online: 30 Mar 2016. Login Required This action requires you to be registered with Frontiers and logged in. To register or login click here. Abstract Info Abstract The Authors in Frontiers Shufang Zhang Si Xiong Ping Lu Yan Wu Quan Wang Xianzhu Zhang Heng Sun Hong Wei Ouyang Google Shufang Zhang Si Xiong Ping Lu Yan Wu Quan Wang Xianzhu Zhang Heng Sun Hong Wei Ouyang Google Scholar Shufang Zhang Si Xiong Ping Lu Yan Wu Quan Wang Xianzhu Zhang Heng Sun Hong Wei Ouyang PubMed Shufang Zhang Si Xiong Ping Lu Yan Wu Quan Wang Xianzhu Zhang Heng Sun Hong Wei Ouyang Related Article in Frontiers Google Scholar PubMed Abstract Close Back to top Javascript is disabled. Please enable Javascript in your browser settings in order to see all the content on this page.

Evaluation of a novel collagen-gelatin scaffold for achieving the sustained release of basic fibroblast growth factor in a diabetic mouse model

The objective of this study was to evaluate the ability of a scaffold, collagen-gelatin sponge (CGS), to release basic fibroblast growth factor (bFGF) in a sustained manner, using a pressure-induced decubitus ulcer model involving genetically diabetic mice. We confirmed that CGSs impregnated with a bFGF concentration of up to 50 µg/cm(2) were able to sustain the release of bFGF throughout their biodegradation. We prepared decubitus ulcers on diabetic mice. After debriding the ulcers, we implanted CGSs (diameter 8 mm) impregnated with normal saline solution (NSS) or bFGF solution (7, 14, 28 or 50 µg/cm(2)). At 1 and 2 weeks after implantation, the mice were sacrificed and tissue specimens were obtained. The wound area, neoepithelium length and numbers and total area of newly formed capillaries were evaluated. The CGSs impregnated with NSS became infected and degraded, whereas the CGSs impregnated with 7 or 14 µg/cm(2) bFGF displayed accelerated dermis-like tissue formation and the CGSs impregnated with 14 µg/cm(2) bFGF produced significant improvements in the remaining wound area, neoepithelium length and numbers and total area of newly formed capillaries compared with the NSS group. No significant difference was observed between the NSS and 50 µg/cm(2) bFGF groups. CGSs impregnated with 7-14 µg/cm(2) bFGF accelerated wound healing, and an excess amount of bFGF did not increase the wound-healing efficacy of the CGSs. Our CGS is a scaffold that can release positively charged growth factors such as bFGF in a sustained manner and shows promise as a scaffold for skin regeneration.