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Silk Sericin as an industrial wastewater with valuable biomedical potential

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Enhancing Wound Healing: A Comprehensive Review of Sericin and Chelidonium majus L. as Potential Dressings
Publication . Borges, Ana Margarida; Calvo, María Luisa Martín; Vaz, Josiana A.; Calhelha, Ricardo C.
Wound healing, a complex physiological process orchestrating intricate cellular and molecular events, seeks to restore tissue integrity. The burgeoning interest in leveraging the therapeutic potential of natural substances for advanced wound dressings is a recent phenomenon. Notably, Sericin, a silk-derived protein, and Chelidonium majus L. (C. majus), a botanical agent, have emerged as compelling candidates, providing a unique combination of natural elements that may revolutionize conventional wound care approaches. Sericin, renowned for its diverse properties, displays unique properties that accelerate the wound healing process. Simultaneously, C. majus, with its diverse pharmacological compounds, shows promise in reducing inflammation and promoting tissue regeneration. As the demand for innovative wound care solutions increases, understanding the therapeutic potential of natural products becomes imperative. This review synthesizes current knowledge on Sericin and C. majus, envisioning their future roles in advancing wound management strategies. The exploration of these natural substances as constituents of wound dressings provides a promising avenue for developing sustainable, effective, and biocompatible materials that could significantly impact the field of wound healing.
Chemical characterization and bioactivities of sericin extracted from silkworm cocoons from two regions of Portugal
Publication . Reis, Sara Filipa Gomes; Vaz, Josiana A.
Along the years, sericin has been undervalued and discarded as waste from the textile silk industry. However, recent studies have shown that sericin has great potential for biomedical applications. The potential for medicinal applications depends on its physicochemical properties and molecular heterogeneity. In addition, the characteristics of sericin are influenced by its extraction method, its origin and the variety of cocoon. This work aimed to characterize the biochemical and bioactivities of sericin from Bragança and Castelo Branco. Sericin was extracted using the autoclave method, and its physicochemical properties were then characterized by analyzing its amino acid content by HPLC. In addition, its potential for antioxidant by TBARS and CAA assays, anti- inflammatory by NO inhibition, antimicrobial by microdilution method, anti-proliferative by SBR assay, and anticoagulant activities by APTT method was evaluated. In its pure state, sericin did not have a high content of free amino acids, with tyrosine being identified as the most abundant. On the other hand, when hydrolyzed sericin showed a higher content of amino acids and serine was the most abundant. In terms of bioactivities, the sericin tested did not show antioxidant or anti-inflammatory potential in the tests carried out. Despite this, it showed anti-proliferative activity in contact with human tumor cell lines and in non-tumor cell lines at a minimum concentration of 0.52 and 0.32 mg /mL, respectively. As far as antimicrobial activity is concerned, sericin proved capable of inhibiting the growth of the bacteria and fungi tested at concentrations between 5 and 10 mg/mL. Finally, sericin was also shown to be able to prolong the coagulation time in adult mice plasma, presenting anticoagulant potential. The sericin from Bragança and Castelo Branco, collected in 2019, did not differ greatly, differences in amino acid composition were identified. In addition, the sericin collected in Bragança in 2021 and 2022, S3 and S4, respectively, showed differences compared to the other samples and showed the best antiproliferative, antibacterial and anticoagulant potential. Additionally, there are also differences between extracted and commercial samples.

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Entidade financiadora

Fundação para a Ciência e a Tecnologia

Programa de financiamento

3599-PPCDT

Número da atribuição

PTDC/BTA-BTA/0696/2020

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