
Why Reproducibility Starts with Sample Preparation
In this segment of his SciX interview, Marc Porter explains why every step matters when measuring at picomolar and femtomolar levels, and how switching to proteinase K helped make his group’s tuberculosis work more clinic-ready.
In this segment of his SciX interview with Spectroscopy, Marc Porter, a Distinguished Professor Emeritus in Chemistry and Chemical Engineering at the University of Utah, identified reproducibility as the central challenge facing his group’s work in ultrasensitive measurement. It is the first question everyone asks, he noted. When analyses push into the picomolar and femtomolar ranges, and sometimes below, every variable in the workflow can affect the result.
Much of that challenge, he explained, comes down to
Porter also stressed that analytical chemists need to consider what clinicians will realistically adopt in a
He closed the segment by reinforcing that reproducibility encompasses more than the measurement itself. His group is working at concentration levels that are new territory, Porter says, so every detail matters, from sample handling through pretreatment to the final readout. For analysts pursuing trace-level detection, his message was that reliability starts long before the instrument. Methods must be designed with both analytical rigor and the practical realities of the clinical laboratory in mind.
Further Reading
(1) Porter, M.; Workman, J., Jr.; Wetzel, W. Taming Serum Interference: Marc Porter on Moving SERS Immunoassays Toward the Clinic. Spectroscopy Online, 2026.
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