Stretchable, Bio-Compatible, Antioxidant and Self-Powering Adhesives from Soluble Silk Fibroin and Vegetal Polyphenols Exfoliated Graphite.
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ABSTRACT:
SUBMITTER: Valentini L
PROVIDER: S-EPMC8472279 | biostudies-literature |
REPOSITORIES: biostudies-literature
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Project description:In search of a new way to fabricate graphene-like materials, isostatic graphite targets were ablated using high peak power with a nanosecond-pulsed infrared laser. We conducted dry ablations in an argon atmosphere and liquid-phase ablations in the presence of a liquid medium (water or toluene). After the dry ablation, the SEM images of the target showed carbon in the form of a volcano-like grain structure, which seemed to be the result of liquid carbon ejected from the ablation center. No graphite exfoliation could be achieved using dry ablation. When using liquid phase ablation with water or toluene as a liquid medium, no traces of the formation of liquid carbon were found, but cleaner and deeper craters were observed. In particular, when using toluene as a liquid medium, typical graphite exfoliation was found. We believe that due to the extremely high pressure and high temperature induced by the laser pulses, toluene was able to intercalate into the graphite layers. Between the laser pulses, the intercalated toluene was able to flash evaporate and blow-up the graphite, which resulted in exfoliated graphite. Exfoliated graphite was found on the ablated graphite surface, as well as in the toluene medium. The ablation experiments with toluene undertaken in this study demonstrated an effective method of producing micrometer-sized graphene material. When using water as a liquid medium, no massive graphite exfoliation was observed. This meant that under the used laser conditions, toluene was a better intercalant for graphite exfoliation than water.
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Project description:Binary-blended hydrogels fabricated from Bombyx mori silk fibroin (SF) and recombinant spider silk protein eADF4(C16) were developed and investigated concerning gelation and cellular interactions in vitro. With an increasing concentration of eADF4(C16), the gelation time of SF was shortened from typically one week to less than 48 h depending on the blending ratio. The biological tests with primary cells and two cell lines revealed that the cells cannot adhere and preferably formed cell aggregates on eADF4(C16) hydrogels, due to the polyanionic properties of eADF4(C16). Mixing SF in the blends ameliorated the cellular activities, as the proliferation of L929 fibroblasts and SaOS-2 osteoblast-like cells increased with an increase of SF content. The blended SF:eADF4(C16) hydrogels attained the advantages as well as overcame the limitations of each individual material, underlining the utilization of the hydrogels in several biomedical applications.
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Project description:As a functional biomaterial, silk fibroin has been widely used in drug release, cell encapsulation and tissue regeneration. To meet the requirements of these applications, the properties of silk fibroin-based materials should be finely tunable. Many useful properties of biomaterials emerge from the collective interactions among ordered and disordered domains. Thus, increasing subtle control of silk hierarchical structures is required. As a characteristic of ordered silk fibroin, crystalline silk fibroin (CSF) is an important part of silk fibroin-based biomaterials, but the preparation of CSF solution, especially high concentration CSF solution, remains a challenge. Here, a solution composed of β-sheet-rich silk fibroin is reported. These CSF were obtained by the sonication of silk fibroin hydrogel, destroying the hydrogel network, and turning silk fibroin hydrogels into CSF solution. These β-sheet-rich CSF solutions were stable enough for several days or even weeks. In addition, they were typically ordered crystalline domains, which could be mixed with disordered domains and fabricated into porous scaffolds, films, hydrogels and other silk fibroin-based scaffolds with different properties.
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