The antibacterial activity of nanocomposites was determined by the disc diffusion method. For this, three 10-mm-diameter discs were created for each of the synthesized nanocomposites. The Staphylococcus aureus (ATCC 25,923) and Escherichia coli (ATCC 25,922) bacterial strains used in the study were enriched in peptone water. Suspensions were prepared at an average concentration of 106–107 CFU/mL by counting via the serial dilution method. Afterwards, incubation was carried out using 1 mL Petri dishes containing 25 mL Mueller-Hilton agar (Oxoid CM337). One day later, the prepared nanocomposite discs and the antibiotic (moxifloxacin, Oxoid) disc used for the control were placed in Petri dishes and incubated for 24 h at 37 °C in an oven. At the end of the incubation, the zones of inhibition (mm) formed around each disc were measured [23 (link)].
Cm337
The CM337 is a laboratory centrifuge designed for high-speed separation of samples. It is capable of reaching a maximum speed of 14,000 rpm and can accommodate a variety of rotor types and sample volumes. The CM337 is engineered for reliable and consistent performance in a wide range of laboratory applications.
Lab products found in correlation
2 protocols using cm337
Antimicrobial Activity of Nanocomposite Discs
The antibacterial activity of nanocomposites was determined by the disc diffusion method. For this, three 10-mm-diameter discs were created for each of the synthesized nanocomposites. The Staphylococcus aureus (ATCC 25,923) and Escherichia coli (ATCC 25,922) bacterial strains used in the study were enriched in peptone water. Suspensions were prepared at an average concentration of 106–107 CFU/mL by counting via the serial dilution method. Afterwards, incubation was carried out using 1 mL Petri dishes containing 25 mL Mueller-Hilton agar (Oxoid CM337). One day later, the prepared nanocomposite discs and the antibiotic (moxifloxacin, Oxoid) disc used for the control were placed in Petri dishes and incubated for 24 h at 37 °C in an oven. At the end of the incubation, the zones of inhibition (mm) formed around each disc were measured [23 (link)].
Antibacterial Activity of Verbascum lasianthum
The reference strains were counted with the nutrient broth serial dilution method. Suspensions were prepared so that the final bacteria concentration was 10 6 -10 7 cfu/mL. 250 µL bacteria culture was added to each petri dish that contained 25 mL of Mueller-Hilton agar (Oxoid CM337). 50 µL extract in four different concentrations (2.5%, 5%, 10% and 20%) in absolute methanol were added to discs.Gentamicin 10 µg (Oxoid CT0024B) and Ciprofloxacin 5 µg (Oxoid CT0425B) were used as positive controls. Later was incubated at 37±2 ºC for 18-24 hours. The zones formed around the discs after the incubation were measured (Bauer et al. 1966 , Ozkan et al. 2005) . All tests were performed in duplicates with 3 samples of each extract.
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