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Both nanoparticles were evaluated at concentrations ranging from 1 to 100 μg/mL.
Compounds with a growth inhibition rate of 50% were further evaluated at concentrations of 0.064, 0.32, 1.6, 8, and 40 μM in triplicate, with cisplatin and paclitaxel (Sigma, St . Louis MO, USA) as positive controls.
The impact of H1 and H2 on the biofilm formation of two staphylococcal reference strains, S. aureus ATCC 25923, and S. epidermidis ATCC 35984, were evaluated at concentrations of 3.2 and 1.5 mg/ml (well below the MIC values obtained against the planktonic forms) by staining with safranin adherent bacteria.
The recovery, limit of detection, accuracy and precision of this method were evaluated at concentrations from 0.025 to 250 µg/g.
Dose response for SP600125 was evaluated at concentrations of 20 and 35 µM, and for U0126 at 10 and 20 µM.
The antibiotics were evaluated at concentrations ranging from 512 to 0.5 mg/mL.
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The linearity of the method was evaluated at different concentrations.
tritici of compounds 10d, 10e, 10h, 10i and 10j were evaluated at lower concentrations (Table 2).
Subsequently algicidal activity of liposomal TD53 against harmful and nonharmful algae was evaluated at various concentrations.
The interaction of various surfactants and polymer solutions was evaluated at different concentrations.
The effectiveness of surfactants and MEs was evaluated at two concentrations from different sets of spontaneous imbibition tests and petrographic analyses.
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