The synergistic effects of transition metal based nanocomposites are known to possess enhanced antibacterial activities. However, in‐depth analysis of the relative antibacterial performance of some of the prominent nanocomposites remains unavailable. This study compares the antibacterial activity of two separate nanocomposites, which are copper oxide with silver (CuO/Ag) and zinc oxide with silver (ZnO/Ag). The individual CuO/Ag and ZnO/Ag nanocomposites were synthesised by a mixed wet‐chemical method. The resulting particles were analysed by XRD, XRF, TEM, UV‐Vis spectrophotometer, BET, and FTIR. The antibacterial activity of the nanoparticles were tested on Gram‐negative and Gram‐positive bacteria, Escherichia coli (ATCC25922) and Staphylococcus aureus (ATCC25923), respectively, using the Kirby–Bauer disc diffusion and the microdilution methods. The Kirby–Bauer disc diffusion test results had the same minimum inhibition concentration (MIC) value for both CuO/Ag and ZnO/Ag against E. coli and S. aureus, which was 0.25 mg/ml. The applied nanocomposites using microdilution showed that CuO/Ag had approximately 98.8% and 98.7% efficiency on the respective Gram‐positive and Gram‐negative bacterial species, while ZnO/Ag achieved 91.7% and 89.3% efficiency, respectively, against the Gram‐positive and Gram‐negative bacterial species. This study presents a novel approach for relative analysis of the performance efficiency of transition metal based nanocomposites.

This paper presents the effect of modified halloysite nanotubes on the sustained drug release mechanisms of sodium salicylate. Acid treatment and composite polymer-halloysite modification techniques were adopted in this study. After each modification, sodium salicylate drug was loaded, and in vitro release properties were evaluated and compared with the raw unmodified halloysite nanotubes. The results obtained from SEM, TEM and FTIR analyses indicate that both acid treatment and composite formation have no effect on the tubular structure and morphology of halloysite. However, modification of the halloysite nanotubes did influence the drug release rate. In the acid treatment modification, there was an improved loading of sodium salicylate drug which resulted in the sustain release of large amount of the sodium salicylate. In the polymer/halloysite composite formation, a consistent layer of polymer was formed around the halloysite during the composite formation and thus delayed release providing sustained release of sodium salicylate drug over a longer period of time as compared to the acid treated and unmodified halloysite. The results from the invitro release were best fitted with the Higuchi and the Koresymer-Peppas models.