In vitro degradation and antibacterial activity of bacterial cellulose deposited flax fabric reinforced with polylactic acid and polyhydroxybutyrate.

The objective of this study was to prepare biocomposites through the solution casting method followed by compression moulding in which bacterial cellulose (BC) deposited flax fabric (FF) produced through fermentation is coated with minimal amount of polylactic acid (PLA) and polyhydroxybutyrate (PHB). Biocomposites incorporated with 60 % of PLA or PHB (% w/w) show enhanced tensile strength. Cross-sectional morphology showed good superficial interaction of these biopolymers with fibres of FF thereby filling up the gaps present between the fibres. The tensile strength of biocomposites at 60 % PLA and 60 % PHB improved from 37.97 MPa (i.e., BC deposited FF produced in presence of honey) to 67.17 MPa and 56.26 MPa, respectively. Further, 0.25 % of nalidixic acid (NA) (% w/w) and 6 % of oleic acid (OA) (% w/w) incorporation into the biocomposites imparted prolonged antibacterial activity against Escherichia coli, Staphylococcus aureus and Pseudomonas aeruginosa. The in vitro cytotoxicity of biocomposites was determined using L929 mouse fibroblast cells. The 3-(4,5-cime- thylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide cytotoxicity tests showed that the PHB derived biocomposites along with antibacterial compounds in it were non-toxic. In vitro degradation of biocomposites was measured for up to 8 weeks in the mimicked physiological environment that showed a gradual rate of degradation over the period.

Structural, material and antibacterial properties of quercetin incorporated soy protein isolate films and its binding behavior through molecular docking.

This study aimed to investigate the three different methods for the fabrication of quercetin (1%-3% w/w of protein) incorporated soy protein isolate (SPI) films and their effect on material properties. The quercetin incorporated SPI films prepared by these methods were characterized by Fourier transform infrared (FTIR) spectroscopy, UV-Vis spectrophotometer, tensile properties, and water uptake and leaching properties. The cross-linking pattern was revealed by the FTIR spectrum that showed formation of an ester group because of interaction between the quercetin hydroxyl group and the carboxyl side chain of SPI amino acids. The tensile strength of SPI films were enhanced with the addition of quercetin as it increased to a maximum of 6.17 MPa while neat SPI film had tensile strength 4.13 MPa. The prepared films exhibit significant antibacterial activity against Listeria monocytogenes and Escherichia coli. The In-silico docking analysis demonstrates that covalent and non-covalent forces play crucial roles in binding interaction. It shows the formation of four hydrogen bonds, two salt bridges along with one pi-alkyl interaction. The simulation studies reflect the crucial amino acid residues involved in SPI-quercetin binding. The effect of quercetin binding with SPI on its stability and compactness is revealed by Root mean square deviation (RMSD) and radius of gyration studies.

Selective Orientation of Needlelike Sepiolite Nanoclay in Polymer Blend for Controlled Properties.

Sepiolite nanoclay needles have been selectively localized either in the natural rubber (NR) phase or in the carboxylated nitrile rubber (XNBR) phase of the XNBR/NR (50/50) blend prepared by the solution casting method. In a systematic manner, the role of the difference value between the interaction parameter of individual blend components (NR or XNBR)/solvent and the interaction parameter of sepiolite nanoclay/solvent in selectively localizing the sepiolite nanoclay to the NR phase or the XNBR phase of the XNBR/NR (50/50) blend has been explored. A higher percentage of sepiolite nanoclay resides in the dispersed NR phase when the difference value between the interaction parameter of NR/solvent and the interaction parameter of sepiolite nanoclay/solvent is lower than the difference value between the interaction parameter of XNBR/solvent and the interaction parameter of sepiolite nanoclay/solvent. On the other hand, a higher percentage of sepiolite nanoclay resides in the continuous XNBR phase when the difference value between the interaction parameter of XNBR/solvent and the interaction parameter of sepiolite nanoclay/solvent is lower than the difference value between the interaction parameter of NR/solvent and the interaction parameter of sepiolite nanoclay/solvent. It has been shown that by judiciously choosing different solvent combinations to prepare the blend and to disperse nanoclay, it is possible to fine-tune the difference value between the interaction parameter of individual blend components (NR or XNBR)/solvent and the interaction parameter of sepiolite nanoclay/solvent and dictate the selective localization of sepiolite nanoclay to the NR phase or the XNBR phase of XNBR/NR (50/50) blend. This study shows that it is possible to generate a rubber blend with controlled properties by selectively localizing needlelike sepiolite nanoclay in the dispersed phase or the continuous phase of the rubber blend prepared by the solution casting method.