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The buffer value was used to quantify the buffer capacity.
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A buffer solution of phosphate with a pH 4 value was used in the experiments.
The former value was used.
For other experiments different MOPS buffer concentrations and different initial pH-values were used and are mentioned in the respective experiment description.
Extrapolated retention parameters that correspond to pure buffer as the mobile phase, i.e., log kw values are used as chromatographic lipophilicities.
Acidogenicity values (AV) were higher when 20% strength buffer was used, while lowering buffer pH increased values, equally across all feeds.
The lyticase buffer was used instead of buffer P1.
A standard bicarbonate buffer was used as dialysate buffer.
A 100 mM phosphate buffer was used to maintain the pH value at 6.5.
Acetate buffer was used as the blank.
This buffer was used for all experiments.
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