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Subjects were studied during placebo and midazolam at 30 ng.mL -1) target effect site concentration.mL -1
Matsubu, J. C., Yang, V. N. & Christopher, P. Isolated metal active site concentration and stability control catalytic CO2 reduction selectivity.
Propofol predicted plasma concentration was calculated using a three-compartment model and the effect site concentration over time as the convolution between the predicted plasma concentration and the disposition function of the effect site concentration.
During each infusion, the effect site concentration was increased by a rate of 0.1, 0.3, 0.5, 0.7, or 0.9 microg.
There was an overall decrease in acid site concentration due to incorporation of inert silica pillars.
The selectivity to isomerization was constant for the catalysts with an acid site concentration >0.19 mmol/g.
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In all, we increased propofol effect-site concentration (Ce) until loss of response to the ARM occurred.
Objectives. – To determine the effect-site concentration (Ce) of propofol, required to achieving adequate sedation.
To investigate whether a patient's propofol effect-site concentration at return to consciousness (ROC) was related to the propofol effect-site concentration at loss of consciousness (LOC) and to patients' individual demographic parameters.
Subsequently, the propofol target effect-site concentration was increased by a designated increment (0.25 and 0.5 microg/ml) and the process repeated.
After a 15-min control period, propofol was infused to an initial target effect-site concentration of 0.0 microg/ml with N2O or 1.5 microg/ml with air.
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