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Blood samples for pharmacokinetic analyses were collected, and safety and tolerability were assessed.
Samples for RNA analyses were collected by filtration during fermentation after consumption of 15 g/L sugars.
To check for homogeneity at least 10 analyses were collected on the glass and at least 5 on the crystals.
Water samples (500 mL) for water quality analyses were collected at approximately 0.5 m above the lake bottom before sampling sediments.
After the CRRT initiation, arterial blood gas analyses were collected every hour; however, the highlighted points in the figure were the analyzed timepoints.
Water samples meant for hydrochemical analyses were collected from ten sampling points using two polyethylene bottles thoroughly rinsed with distilled water.
During two years, water samples for total and dissolved metal analyses were collected every third day at both the inlet and the outlet.
Water samples for metal analyses were collected into 100 ml plastic bottles and nitric acid (HNO3) added to the samples to bring the pH down to 2 for the metals to remain in solution.
Blood gas analyses were collected in from the earlobe in capillary tubes after pretreatment with an ointment containing 5% benzyl nicotinate (supplied by the hospital pharmacy) for 10 mins.
Over a 1 year period, gas samples for carbon dioxide (CO2) and oxygen (O2) analyses were collected from seven different soil depths (5 to 80 cm) at the shoulder- and footslope positions.
Cultured skin substitutes were grafted on full-thickness wounds in athymic mice, and biopsy samples for microarray analyses were collected at multiple in vitro and in vivo time points.
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