Thi–Dan Thach

Recently, the waste agricultural materials have been widely considerable for green synthesis of noble metallic nanoparticles (MNPs) due to cost efficiency and environmental protection. This study has presented a simple method for the preparation of silver nanoparticles (AgNPs) and gold nanoparticles (AuNPs) utilizing aqueous extract of waste Passiflora edulis peel (PEP) as reducing and stabilizing agents. The formation of MNPs was optimized reaction conditions to obtain the best colloidal solutions. The characterizations of the biosynthesized MNPs were performed by analysis techniques such as Fourier transmission infrared spectroscopy (FTIR), X-ray diffraction (XRD), high-resolution transmission electron microscopy (HRTEM), selected area electron diffraction (SAED). The TEM data confirmed PEP-AgNPs and PEP-AuNPs in the spherical shape with mean size of 25 nm and 7 nm, respectively. The XRD and SAED patterns showed the synthesized nanoparticles existing in crystalline nature. Antibacterial and catalytic activities have been investigated for their applications. The PEP-AgNPs exhibited a strong antibacterial activity against three strains including Escherichia coli, Bacillus subtilis, and Staphylococcus aureus. The excellently catalytic activity of both the biosynthesized nanoparticles has been demonstrated for reduction of nitrophenols and degradation of toxic organic dyes via study on their kinetics.

The design of novel molecules is imperative for the discovery of potent drugs in the medicinal chemistry field. In this work, new 1,3,5-substituted pyrazoline sulphonamides were synthesised using a two-step process with microwave assistance and evaluated biologically for their antimicrobial, antiproliferative, and anti-inflammatory properties. Most of the sulphonamides bearing 3-OH or 4-Cl groups exhibited significant inhibition of two Gram-positive bacteria, Bacillus subtillis and Staphylococcus aureus, and the yeast Candida albicans. Six compounds showed good activity against the cancer cell lines cervix carcinoma (Hep-2C) and human lung carcinoma (A549) with IC50 in the range 16.03 ± 1.63 to 22.75 ± 0.19 μM and 18.64 ± 1.02 to 20.66 ± 2.09 μM, respectively, and exhibited low toxicity against mammalian Vero cells. In evaluating in vitro anti-inflammatory behaviour, five compounds showed high inhibition of NO production over the standard reference, with low toxicity against murine macrophage cell line RAW 264.7. Further investigation found that two compounds, 1b and 18b, exhibited the highest activity when testing mouse ear oedema. The findings are promising for the discovery of potent new drugs.

Two series of sulfonamides were synthesized from 4-hydrazinylbenzenesulfonamide as the key starting material. 1,3,5-Triarylpyrazoline sulfonamides (2a?i) were obtained by cyclocondensation of various chalcones in 53? ?64 % yields, while 4-thiazolidinone derivatives (4a?e) were synthesized by cyclocondensation between mercaptoacetic acid and different phenylhydrazones in 43?62 % yields. The synthesized compounds were characterized based on FTIR, 1H-NMR, 13C-NMR and HRMS data. The sulfonamides were evaluated for their in vitro antimicrobial activities against four bacterial strains (E. coli, P. aeruginosa, B. subtillis and S aureus), two filamentous fungal strains (A. niger and F. oxysporum) and two yeast strains (C. albicans and S. cerevisiae). Seven pyrazolines, 2a?c and 2e?h, exhibited significant inhibition of different microbial strains. Among them, compound 2b displayed good antifungal activity against A. niger (MIC value at 12.5 ?g mL-1) over the reference drug.