Abstract:Hydrogen sulfide (H 2 S) is a physiological gasotransmitter known to possess a regulatory role in several tissues, including bone. The exogenous administration by injection of solutions of H 2 S-releasing compounds (e.g., GYY4137) has been previously investigated as a novel therapeutic approach for the treatment of bone diseases. Here, GYY4137 was embedded into fibroin sponges, previously shown to be suitable as scaffolds for bone, thanks to their biocompatibility, scalable porous structure, and biodegradabili… Show more
“…Instead, in wet conditions both scaffold results to have a compressive strength at least one order of magnitude lower than the natural cartilage. However, it should be noticed that the value reported in wet conditions are like the one obtained in literature, for other biopolymer‐based scaffold proposed for cartilage applications (Gambari et al., 2019; Pulkkinen et al., 2006; Raggio et al., 2018). We performed also a mechanical test on the hydrogels just before the lyophilization to form the sponges.…”
Articular hyaline cartilage is an extremely hydrated, not vascularized tissue with a low‐cell density. The damage of this tissue can occur after injuries or gradual stress and tears (osteoarthritis), minor damages can be self‐healed in several weeks, but major injuries may eventually require surgery. In fact, in this case, because of nature of the cartilage (the absence of cells and vascularization) it is difficult to expect its natural regeneration in a reasonable amount of time. In recent years, cell therapy, in which cells are directly transplanted, has attracted attention. In this study, a scaffold for implanting chondrocytes was prepared. The scaffold was made as a sponge using the eggshell membrane and agarose. The eggshell membrane is structurally similar to the extracellular matrix and nontoxic due to its many collagen components and has good biocompatibility and biodegradability. However, scaffolds made of collagen only has poor mechanical properties. For this reason, the disulfide bond of collagen extracted from the insoluble eggshell membrane was cut, converted into water‐soluble, and then mixed with agarose to prepare a scaffold. Agarose is capable of controlling mechanical properties, has excellent biocompatibility, and is suitable for forming a hydrogel having a three‐dimensional porosity. The scaffold was examined for Fourier‐transform infrared, mechanical properties, biodegradability, and biocompatibility. In in vitro experiment, cytotoxicity, cell proliferation, and messenger RNA expression were investigated. The study demonstrated that the agarose/eggshell membrane scaffold can be used for chondrocyte transplantation.
“…Instead, in wet conditions both scaffold results to have a compressive strength at least one order of magnitude lower than the natural cartilage. However, it should be noticed that the value reported in wet conditions are like the one obtained in literature, for other biopolymer‐based scaffold proposed for cartilage applications (Gambari et al., 2019; Pulkkinen et al., 2006; Raggio et al., 2018). We performed also a mechanical test on the hydrogels just before the lyophilization to form the sponges.…”
Articular hyaline cartilage is an extremely hydrated, not vascularized tissue with a low‐cell density. The damage of this tissue can occur after injuries or gradual stress and tears (osteoarthritis), minor damages can be self‐healed in several weeks, but major injuries may eventually require surgery. In fact, in this case, because of nature of the cartilage (the absence of cells and vascularization) it is difficult to expect its natural regeneration in a reasonable amount of time. In recent years, cell therapy, in which cells are directly transplanted, has attracted attention. In this study, a scaffold for implanting chondrocytes was prepared. The scaffold was made as a sponge using the eggshell membrane and agarose. The eggshell membrane is structurally similar to the extracellular matrix and nontoxic due to its many collagen components and has good biocompatibility and biodegradability. However, scaffolds made of collagen only has poor mechanical properties. For this reason, the disulfide bond of collagen extracted from the insoluble eggshell membrane was cut, converted into water‐soluble, and then mixed with agarose to prepare a scaffold. Agarose is capable of controlling mechanical properties, has excellent biocompatibility, and is suitable for forming a hydrogel having a three‐dimensional porosity. The scaffold was examined for Fourier‐transform infrared, mechanical properties, biodegradability, and biocompatibility. In in vitro experiment, cytotoxicity, cell proliferation, and messenger RNA expression were investigated. The study demonstrated that the agarose/eggshell membrane scaffold can be used for chondrocyte transplantation.
“…The combinations of properties such as high mechanical strength, easy processability, and resorbability make this material unique among the other available biopolymers because of its exceptional versatility . In particular, in tissue engineering, silk fibroin in different structural forms is widely studied as a material for bone, − cartilage, − tendon, − skin, − and cornea regeneration − and, in minor part, for nerve, muscle, spinal cord, and liver regeneration . In addition, the possibility to produce different structures and to chemically modify the regenerated protein allows the use of silk fibroin in an increasing number of frontier applications in which traditional fields like electronics and optics encounter the integration with biology (bio-electronics − and bio-optics − ).…”
Silk
fibroin is a protein with a unique combination of properties
and is widely studied for biomedical applications. The extraction
of fibroin (degumming) from the silk filament impacts the properties
of the outcoming material. The degumming can be conducted with different
procedures. Among them, the most used and studied procedure in the
research field is the alkali degumming with sodium carbonate (Na2CO3). In this study, by the use of a statistical
method, namely, design of experiment (DOE), we characterized the Na2CO3 degumming, taking into consideration the main
process factors involved and changing them within a selected range
of values. We considered the process temperature and time, the salt
concentration, and the number of baths used, testing the impact of
these variables on the fibroin properties by building empirical models.
These models not only took into consideration the direct effect of
the process factors but also their combined effect, which are not
conventionally detectable with other methods. The weight loss and
the amount of sericin removed in the process were determined and used
as a measure of the effectiveness of the process. The secondary structure,
the molecular weight, the diameter of fibers, and their morphology
and mechanical properties were studied with the intent to correlate
the macroscopical properties with the structural changes. We report,
for the first time, the possibility to effectively remove all sericin
from the silk fibroin using Na2CO3, using a
process that requires less salt, water, and energy, in comparison
with the standard alkali protocol, making this technique overall more
environmentally sustainable; in addition, we have demonstrated the
possibility to tune the material properties by varying the degumming
conditions and even to optimize them with empirical statistically
based equations that allow one to directly set the optimal process
parameters. The major effect on the macroscopical properties (such
as the ultimate strength and Young’s modulus) has been proved
to be correlated with the removal of sericin instead of the microstructural
variations. Finally, a ready-to-use table with a set of optimized
degumming procedures to maximize or minimize the studied properties
was provided.
“…The single steps are described in the following. Silk fibroin solution preparation. Bombyx mori cocoons (purchased from Chul Thai SilkCo., Phetchabun, Thailand) were degummed by treating twice with Na 2 CO 3 aqueous solution (1.1 g/L) at 98 °C (1.5 h for each treatment) and rinsed with distilled water. The degummed silk fibroin was dissolved in 9.3 M LiBr solution (1 g/10 mL) at 65 °C for 4 h. The solution was dialyzed in a Slide-A-Lyzer Cassette (ThermoScientific), MWCO 3500 Da, against distilled water for 3 days. Diazonium coupling reaction.…”
A bio-inspired multifunctionalized silk fibroin (BMS) was synthesized in order to mimic the interaction of nidogen with the type IV collagen and laminin of basement membranes. The designed BMS consists of a motif of laminin αchain-derived, called IK peptide, and type IV collagen covalently bound to the silk fibroin (SF) by using EDC/NHS coupling and a Cu-free click chemistry reaction, respectively. Silk fibroin was chosen as the main component of the BMS because it is versatile and biocompatible, induces an in vivo favorable bioresponse, and moreover can be functionalized with different methods. The chemical structure of BMS was analyzed by using X-ray photoelectron spectroscopy, attenuated total reflection−Fourier transform infrared, cross-polarization magic angle spinning nuclear magnetic resonance techniques, and colorimetric assay. The SF and BMS solutions were cross-linked by sonication to form hydrogels or casted to make films in order to evaluate and compare the early adhesion and viability of MRC5 cells. BMS hydrogels were also characterized by rheological and thermal analyses.
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