Akeem Akinboro

Biogenic synthesis of silver nanoparticles using a pod extract of Cola nitida: Antibacterial and antioxidant activities and application as a paint additive

Abstract This work reports the biogenic synthesis of silver nanoparticles (AgNPs) using the pod extract of Cola nitida, the evaluation of their antibacterial and antioxidant activities, and their application as an antimicrobial additive in paint. The AgNPs were characterized with UV–Vis spectroscopy, Fourier-transform infrared (FTIR) spectroscopy, and transmission electron microscopy (TEM). The AgNP solution was dark brown with a maximum absorbance occurring at 431.5 nm. The FTIR spectrum showed strong peaks at 3336.85, 2073.48, and 1639.49 cm−1, indicating that proteins acted as the capping and stabilization agents in the synthesis of the AgNPs. The AgNPs were spherical, with sizes ranging from 12 to 80 nm. Energy dispersive X-ray (EDX) analysis showed that silver was the prominent metal present, while the selected area electron diffraction pattern conformed to the face-centred cubic phase and crystalline nature of AgNPs. At various concentrations between 50 and 150 μg/ml, the AgNPs showed strong inhibition of the growth of multidrug resistant strains of Klebsiella granulomatis, Pseudomonas aeruginosa, and Escherichia coli. In addition, at 5 μg/ml, the AgNPs completely inhibited the growth of Staphylococcus aureus, Escherichia coli, Pseudomonas aeruginosa, Aspergillus niger, A. flavus and A. fumigatus in a paint-AgNP admixture. The AgNPs exhibited a potent antioxidant activity with an IC50 of 43.98 μg/ml against 2,2-diphenyl-1-picrylhydrazyl and a ferric ion reduction of 13.62–49.96% at concentrations of 20–100 μg/ml. This study has demonstrated the biogenic synthesis of AgNPs that have potent antimicrobial and antioxidant activities and potential biomedical and industrial applications. To the best of our knowledge, this work is the first to use the pod extract of C. nitida for the green synthesis of nanoparticles.

Biomedical and Catalytic Applications of Gold and Silver-Gold Alloy Nanoparticles Biosynthesized Using Cell-Free Extract of Bacillus Safensis LAU 13: Antifungal, Dye Degradation, Anti-Coagulant and Thrombolytic Activities

This study investigated the green biosynthesis of gold (Au) and silver-gold alloy (Ag-Au) nanoparticles using cell-free extract of Bacillus safensis LAU 13 strain (GenBank accession No: KJ461434). The biosynthesized AuNPs and Ag-AuNPs were characterized using UV-Vis spectroscopy, Fourier-transform infrared spectroscopy, and transmission electron microscopy. Evaluation of the antifungal activities, degradation of malachite green, anti-coagulation of blood, and thrombolysis of human blood clot by the biosynthesized nanoparticles were investigated. The AuNPs and Ag-AuNPs had maximum absorbance at 561 and 545 nm, respectively. The FTIR peaks at 3318, 2378, 2114, 1998, 1636, 1287, 446, 421 cm-1 for AuNPs; and 3310, 2345, 2203, 2033, 1636, 1273, 502, 453, 424 cm-1 for Ag-AuNPs indicated that proteins were the capping and stabilization molecules in the biosynthesized nanoparticles. The particles were fairly spherical in shape with size of 10-45 nm for AuNPs and 13-80 nm for Ag-AuNPs. Moreover, energy dispersive X-ray analysis of AuNPs revealed gold as the most prominent metal in the AuNPs solution, while silver and gold were the most prominent in the case of Ag-AuNPs. Selected area electron diffraction showed the biosynthesized nanoparticles as crystal structures with ring shape pattern. AuNPs and Ag-AuNPs displayed growth inhibitions of 66.67-90.78% against strains of Aspergillus fumigatus and A. niger at concentration of 200 μg/ml, and remarkable degradation (> 90%) of malachite green after 48 h. Furthermore, the nanoparticles prevented coagulation of blood, and also completely dissolved blood clots, indicating the biomedical potential of AuNPs and Ag-AuNPs in the management of blood coagulation disorders. This is the first report of the synthesis of AuNPs and Ag-AuNPs using a strain of B. safensis for biomedical and catalytic applications.

Enterococcus species for the one-pot biofabrication of gold nanoparticles: Characterization and nanobiotechnological applications

In the current work, cell-free extracts of four strains of non-pathogenic Enterococcus species of food origin, were studied for the green synthesis of gold nanoparticles (AuNPs), and characterized by UV-Vis absorption spectroscopy, Fourier transform infrared spectroscopy (FTIR), and transmission electron microscopy (TEM). The AuNPs were evaluated for their Anopheles gambiae larvicidal, dye degradation, antioxidant and thrombolytic activities. The blue-black colloidal AuNPs which absorbed maximally at 549-552nm were nearly spherical in shape, and crystalline in nature with size of 8-50nm. The EDX spectra showed formation of AuNPs to the tune of 89-94%. The prominent FTIR peaks obtained at 3251-3410, 2088 and 1641-1643cm-1 alluded to the fact that proteins were involved in the biofabrication and capping of AuNPs. AuNPs degraded methylene blue and malachite green by 24.3-57.6%, and 88.85-97.36% respectively in 24h, whereas at 12h, larvicidal activities with LC50 of 21.28-42.33μg/ml were obtained. DPPH scavenging activities of 33.24-51.47% were obtained for the biosynthesized AuNPs. The AuNPs prevented coagulation of blood and also achieved 9.4-94.6% lysis of blood clot showing potential nanomedical applications. This study has presented an eco-friendly and economical synthesis of AuNPs by non-pathogenic strains of Enterococcus species for various nanobiotechnological applications.

Safety evaluation of green synthesized Cola nitida pod, seed and seed shell extract-mediated silver nanoparticles (AgNPs) using an Allium cepa assay

Abstract The increase in the use of nanoparticles in various fields of human endeavours calls for the need to understand the toxic potential of green synthesized nanoparticles. Cytogenotoxic potentials of green synthesized Cola pod (Cp-AgNPs), seed (Cs-AgNPs) and seed shell (Css-AgNPs) silver nanoparticles and silver nitrate salts (Ags) were evaluated using an A. cepa assay. Twenty onion bulbs were exposed to 0.01, 0.10, 1.0, 10.0, and 100.0 μg/ml AgNPs and Ags solutions. Microscopic evaluation was performed at 24, 48 and 72 h with 5000 cells per concentration scored for chromosomal aberrations, while the effects on the root growth were evaluated at 72 h. The observed dividing cells and mitotic inhibition were dose-dependent for the three AgNPs and Ags at 24, 48 and 72 h. Mitotic index obtained for 1.0, 10 and 100 μg/mL at all times of evaluation were less than half the value of the negative control, while cell arrest was only observed at 72 h at a concentration of 100 μg/mL for the three AgNPs. The chromosomal aberrations observed were c-mitosis, a chromosome bridge, a vagrant chromosome, and a sticky chromosome, which indicate the potential of AgNPs for genotoxicity. The mean root length of A. cepa treated with AgNPs showed a dose-dependent significant decrease compared to the control, indicating their inhibitory potential, but the mean root lengths were found to be lower at all concentrations compared to those treated with Ags, thus showing the attenuation of growth inhibition. The EC50 values revealed the order of growth inhibition as Ags>Cp-AgNPs>Css-AgNPs>Cs-AgNPs. The cytogenotoxic potential of the AgNPs suggests that caution should be exercised in their usage to prevent environmental pollution.