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Exact(59)
Quantitative analysis is performed by preparing a working curve, at a specific retention time, by plotting the peak height or peak area of a series of standards as a function of the concentration of the component being assayed.
Calibration curves were generated by plotting the peak area of each enantiomer against its concentration.
Calibration curves were prepared by plotting the peak areas of the marker compounds versus the corresponding concentrations.
The calibration curve was established by plotting the peak area against the concentrations of the standards with linear regression analysis.
The calibration curves were constructed by plotting the peak areas (mAU) of the analytes versus the concentration (μg/ml).
The calibration curve was constructed by plotting the peak area ratio against the final concentration of the drug (μg/ml).
Standard curves were constructed by plotting the peak area against the corresponding concentration of the standard solutions.
The calibration graphs were obtained by plotting the peak area ratio against the concentration of the drugs.
Calibration curves for each compound were performed by plotting the peak area (y) against the concentrations (x, μg/ml).
Under the above described experimental conditions, a linear relationship was established by plotting the peak area ratio against the drug concentration.
Similar(1)
HPLC calibration curves were prepared by plotting the peak-area ratios (using naringin as an internal standard) against the corresponding concentrations.
More suggestions(15)
by plotting the cumulative
by calculating the peak
by shifting the peak
by plotting the efficient
by changing the peak
by normalizing the peak
by plotting the mean
by using the peak
by varying the peak
by finding the peak
by plotting the normalized
by plotting the theoretical
by comparing the peak
by plotting the entire
by plotting the Ct
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