TY - JOUR
T1 - All natural mussel-inspired bioadhesives from soy proteins and plant derived polyphenols with marked water-resistance and favourable antibacterial profile for wound treatment applications
AU - Argenziano, R
AU - Viggiano, S
AU - Esposito, R
AU - Schibeci, M
AU - Gaglione, R
AU - Castaldo, R
AU - Fusaro, L
AU - BOCCAFOSCHI, FRANCESCA
AU - Arciello, A
AU - Della, Greca M
AU - Gentile, G
AU - Cerruti, P
AU - D'Errico, G
AU - Panzella, L
AU - Napolitano, A.
N1 - Publisher Copyright:
© 2023 Elsevier Inc.
PY - 2023
Y1 - 2023
N2 - Hypothesis: Implementation of tissue adhesives from natural sources endowed with good mechanical properties and underwater resistance still represents a challenging research goal. Inspired by the extraordinary wet adhesion properties of mussel byssus proteins resulting from interaction of catechol and amino residues, hydrogels from soy protein isolate (SPI) and selected polyphenols i.e. caffeic acid (CA), chlorogenic acid (CGA) and gallic acid (GA) under mild aerial oxidative conditions were prepared.
Experiments: The hydrogels were subjected to chemical assays, ATR FT-IR and EPR spectroscopy, rheological and morphological SEM analysis. Mechanical tests were carried out on hydrogels prepared by inclusion of agarose. Biological tests included evaluation of the antibacterial and wound healing activity, and hemocompatibility.
Findings: The decrease of free NH2 and SH groups of SPI, the EPR features, the good cohesive strength and excellent underwater resistance (15 days for SPI/GA) under conditions relevant to their use as surgical glues indicated an efficient interaction of the polyphenols with the protein in the hydrogels. The polyphenols greatly also improved the mechanical properties of the SPI/ agarose/polyphenols hydrogels. These latter proved biocompatible, hemocompatible, not harmful to skin, displayed durable adhesiveness and good water-vapour permeability. Excellent antibacterial properties and in some cases (SPI/CGA) a favourable wound healing activity on dermal fibroblasts was obtained.
Keywords: Antibacterial activity; Bioadhesives; Hydrogel; Polyphenols; Soy proteins; Surgical glues; Underwater resistance; Water-vapour permeability; Wound healing properties.
AB - Hypothesis: Implementation of tissue adhesives from natural sources endowed with good mechanical properties and underwater resistance still represents a challenging research goal. Inspired by the extraordinary wet adhesion properties of mussel byssus proteins resulting from interaction of catechol and amino residues, hydrogels from soy protein isolate (SPI) and selected polyphenols i.e. caffeic acid (CA), chlorogenic acid (CGA) and gallic acid (GA) under mild aerial oxidative conditions were prepared.
Experiments: The hydrogels were subjected to chemical assays, ATR FT-IR and EPR spectroscopy, rheological and morphological SEM analysis. Mechanical tests were carried out on hydrogels prepared by inclusion of agarose. Biological tests included evaluation of the antibacterial and wound healing activity, and hemocompatibility.
Findings: The decrease of free NH2 and SH groups of SPI, the EPR features, the good cohesive strength and excellent underwater resistance (15 days for SPI/GA) under conditions relevant to their use as surgical glues indicated an efficient interaction of the polyphenols with the protein in the hydrogels. The polyphenols greatly also improved the mechanical properties of the SPI/ agarose/polyphenols hydrogels. These latter proved biocompatible, hemocompatible, not harmful to skin, displayed durable adhesiveness and good water-vapour permeability. Excellent antibacterial properties and in some cases (SPI/CGA) a favourable wound healing activity on dermal fibroblasts was obtained.
Keywords: Antibacterial activity; Bioadhesives; Hydrogel; Polyphenols; Soy proteins; Surgical glues; Underwater resistance; Water-vapour permeability; Wound healing properties.
UR - https://iris.uniupo.it/handle/11579/169742
U2 - 10.1016/j.jcis.2023.08.170
DO - 10.1016/j.jcis.2023.08.170
M3 - Article
SN - 0021-9797
VL - 652
SP - 1308
EP - 1324
JO - Journal of Colloid and Interface Science
JF - Journal of Colloid and Interface Science
ER -