Detector resolution enhancement, HPLC

Because polyphenolics show chemical complexities and similar structures, isolation and quantification of the individual polyphenolic compounds have been challenging. Many traditional techniques (paper chromatography, thin-layer chromatography, column chromatography) have been used. HPLC, with its merits of exacting resolution, ease of use, and short analysis time, has the further advantage that separation and quantification occur simultaneously. A reversed-phase HPLC apparatus equipped with a diode array detector makes possible the easy isolation and separation of many polyphenolics. For enhanced performance of HPLC separation, the polyphenolics should first be isolated into several fractions to effectively separate the individual polyphenolics (Jaworski and Lee, 1987 Oszmianski and Lee, 1990). 

As shown in Figure 3.8, an increased injection volume can have a negative effect on the column efficiency. Therefore, the injection volume should be appropriately scaled down when an HPLC method is transferred to a UHPLC method or vice versa to achieve the same sensitivity and avoid overloading or detector saturation and extracolumn band-broadening. The scaling factor is mainly based on column dimension, as shown in Eq. (3.26). However, lower injection volumes than calculated can often be used on UHPLC to achieve the same sensitivity due to enhanced peak heights from use of the high-resolution columns and low carryover from the injector ... 

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