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For each compound, three mice bearing a tumour of ≈0.1 to 0.4 mL were selected randomly, weighed and bolus iv injected with lysine/gelofusine and the test item (5 mL/kg, 20 nmol/kg protein, ≈100 MBq) into each of the lateral tail veins.
A basal infusion of 3 mL/h and a bolus of 2 mL were selected.
Seven patients with ML were selected after several rounds of unsuccessful treatment and severe disease progression.
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So the volume of 400 ml was selected for further studies.
However, the addition of 0.25 mL was selected for a broader calibration range.
Given the data in this study, ML was selected as the estimation method for this analysis.
For the inoculum preparation, an ampule of API NaCl 0.85 % (2 ml) was selected and 1 4 colonies of bacteria were picked up using inoculation loop from the agar plate and then suspension was prepared with the turbidity equivalent to 0.5 McFarland.
The unusual 800-mL threshold for the definition of PPH, rather than 500 mL, was selected for active PPH.
The injection volume of 0.25 ml was selected by standardization with a dose dependent study and in that volume of high dose calcium chloride solution caused necrosis of entire testicular gland parenchyma without any leakage from the gland.
During the modification, an appropriate stirring rate of 300 r/min and a liquid solid ratio of 10 mL/g were selected.
To achieve optimum values for separation factors of all peak pairs, a TCA content of 0.025% (m/v), a gradient time of 10 min, and a flow rate of 3.5 mL min−1 were selected.
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CEO of Professional Science Editing for Scientists @ prosciediting.com