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All treatments of Bio-CuNPs (Cu) and Bio-ZnONPs (ZnO) at their total lethal concentration were administered and kept in observation for 28 days; N = 6 rats per group.
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Dispersion of epidermis, cortex and vascular cylinder was observed after higher concentration was administered (Figure 9).
During the materials tests in HELIOS, dissolved oxygen concentration was administered at the intended condition of 10−6 wt% by direct gas bubbling with Ar + 4%H2, Ar + 5%O2 and/or pure Ar while corrosion tests were conducted for up to 1000 h with inspection after each 333 h.
Each NO concentration was administered for 10min before the first measurement was taken.
An enhanced LPS concentration was administered to exclude a dose-dependent defect.
Protein G purified normal rabbit serum (Aphton, CA, USA), at the same protein concentration, was administered to control mice.
An effective 5-mM concentration was administered to 30 embryos per treatment group in a 96-well plate setup, and behaviors were recorded for at least 20 min in accordance with methods described previously (Baraban et al. 2005; Tiedeken and Ramsdell 2007, 2009).
Altered sucrose and mannitol concentrations were administered replacing the liquid layer of medium with medium containing the substance in question.
Two coelenterazine concentrations were administered intranasally (10 and 20 µg) and images were acquired at different time points over 3 h.
Test drug concentrations were administered in triplicate in six different concentrations: 0.85, 1.7, 3.4, 6.8 and 13.6, 27.2 μg ml−1 paclitaxel.
HeLa cells were subjected to severe hypoxia (≤0.1% O2) for 24 h, after which increasing drug concentrations were administered for an additional 24 h under the same conditions.
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