Ultra High Performance Liquid Chromatography Method for the Determination of Two Recently FDA Approved TKIs in Human Plasma Using Diode Array Detection

<div>Accuracy profile for ibrutinib in human plasma; <i>β</i> expectation tolerance interval set at 95% and <i>λ</i> acceptance limits set at ±15%. All tested concentrations were validated (from 5 to 400 ng/mL).</div>

Journal of Analytical Methods in Chemistry

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Figure 5: Ultra High Performance Liquid Chromatography Method for the Determination of Two Recently FDA Approved TKIs in Human Plasma Using Diode Array Detection 

Figure 5 | Ultra High Performance Liquid Chromatography Method for the Determination of Two Recently FDA Approved TKIs in Human Plasma Using Diode Array Detection 