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For each patient, effective dose was evaluated using standard coefficients referring to a generic reference individual.
Moreover, the significance of solution pH, contact time, temperature, and adsorbent dose was evaluated.
Depectinization kinetics was also studied at optimum temperature and variation of kinetic constants with enzyme dose was evaluated.
Dependence of the D, G, and 2D Raman band parameters on the laser pulse energy and the irradiation dose was evaluated.
In addition, the UV-C dose was evaluated by calculation of the theoretical maximum UV-C energy input and actinometric measurements using iodide/iodate actinometry.
Following the recommendations of Publication 103 of the ICRP [14], these absorbed doses were then sex-averaged and the effective dose was evaluated using the tissue weighting factors of Publication 60 of the ICRP [15].
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In each session, the time-course of effects of a single drug dose are evaluated.
SUVs, normalized for patient weight and injected dose, were evaluated in the interval 40 50 and 50 60 min.
Different design parameters such as iron concentration, pH, temperature, flow conditions, UV irradiance and H2O2 addition strategy and dose were evaluated.
The effect of mass, type of catalyst clay and H2O2 dose were evaluated, and the photodegradation of ECs was followed by Ultra Performance Liquid Chromatography (UPLC) and Dissolved Organic Carbon content (DOC).
The safety data and pharmacokinetic data obtained at the lower dose were evaluated before increasing the dose to 3, 9, 15, or 25 mg.
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