A mass spectrometry matrix factor compares analyte response in a sample matrix with response from an equal amount in a specified reference solution. For matched acquisition and blank-corrected peak areas, a common post-preparation comparison isThe post-preparation sample is a prepared blank matrix to which the analyte is added after extraction. This separates response from extraction recovery under the matching assumptions. MF below 1 indicates ion suppression relative to the reference; MF above 1 indicates enhanced response. The number is not an absolute ionization efficiency.
The original method study distinguishes matrix effects, recovery and variation across sample sources.[ref]
Strategies for the assessment of matrix effect in quantitative bioanalytical methods based on HPLC-MS/MS by B. K. Matuszewski and others. Abstract, absolute/relative matrix effects and recovery measurements.
For an invented example, take neat response , post-preparation response and response when the same nominal amount is added before preparation. Then MF is , the estimated recovery is , and mass spectrometry process efficiency is . The product identifies which two effects this model combines.An internal-standard-normalized matrix factor divides analyte MF by the corresponding MF for an internal standard. If both are , the normalized value is 1 even though both raw responses are suppressed. If the analyte MF is and the standard MF is , the normalized value is 2. Normalization can therefore fail when the two responses change differently.
Magnitude and variability are separate questions. Three matrices giving factors have a large common suppression but no between-matrix variation in this invented set. Factors differ between matrices despite their less suppressed mean. Report the reference, analyte level, sample preparation and response calculation; near-zero reference signals make a ratio unstable, and unmatched volumes or uncorrected offsets can invalidate its interpretation.
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