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This study explains the development of eco-friendly polyvinyl alcohol (PVA)/oxidized maize starch (OMS)/Betel leaves extract (BLE) blend films by employing a cost effective technique. The influence of BLE on structural, Thermal, Mechanical, Morphological, Optical, Antibacterial, and Antioxidant properties of PVA/OMS blend were investigated successfully by applying FTIR, TGA, DSC, UTM, SEM, UV spectroscopy, In vitro antibacterial and DPPH scavenging activity. The hydrogen bonding interaction among the components of the blend films led to enhance thermal stability, miscibility, mechanical properties, smooth surface morphology and UV blocking properties of the blend films. The addition of BLE enormously improved the antibacterial and antioxidant properties of PVA/OMS blend films. Moreover, the water contact angle, solubility, biodegradability, Water vapour transmission rate, oxygen permeability properties of blend films were analyzed, which illustrates that the obtained films were hydrophilic, water soluble and biodegradable in nature. With regard to barrier properties the WVTR and oxygen permeability of the blend films were enhanced after doping of BLE. These experimental outcomes suggest that the BLE containing PVA/OMS films can be used for the expansion of active packaging material.

Beta-aryl keto hexanoic acids (5a-l) were synthesized efficiently, followed by esterification that afforded beta-aryl keto methylhexanoates (6a-l). The chemo-selective ketoxime beta-aryl methyl hexanoates (7a-l) were isolated in good yields. Spectroscopic methods were used to characterize the obtained moieties. The antioxidant, anti-inflammatory, and antibacterial properties of the effectively synthesized compounds 7a-l were also investigated. The anti-inflammatory activity of the compounds 7c, 7f, 7i, and 7l was excellent, with a low IC50 value at micromolar concentration, which was much better than the reference diclofenac. All synthesized compounds 7a-l were assessed for their in vitro antibacterial activity against S. aureus, B. subtilis and E. coli.  Most of the compounds exhibited promising activity against Gram-positive bacterial strain, compound 7i showed excellent activity compared to standard streptomycin and in the case of E. coli, compounds 7b, 7c, 7j, 7k and 7l have shown moderate activity. Further, the cytotoxic activities of the compounds were assessed against lung cancer cells (A549) by using MTT assay. The possible interaction mechanism of the molecules 7c and 7g with Gram-negative strain E. coli DNA gyrase B in complex with PDB ID: 4DUH was studied.