A Variety of Agilent ZORBAX RRHD Phases Offers Selectivity Options for the Determination of Anthocyanins in Blueberries with UHPLC/MS

Blueberries are extracted into acidified methanol and analyzed for anthocyanins with a methanol/formic acid gradient via UHPLC/MS; four different Agilent ZORBAX RRHD stationary phases are quickly evaluated. The Phenyl-Hexyl column separates the most anthocyanin peaks from the blueberry sample, while the SB-Phenyl is the most orthogonal of the columns.

Advancements in liquid chromatography have led to significantly improved sample throughput. The Agilent 1290 Infinity UHPLC and Agilent ZORBAX Rapid Resolution High Definition (RRHD) columns are manufactured to withstand pressures up to 1200 bar. This allows the use of faster flow rates and rapid column screening to easily take advantage of stationary phase selectivity differences during method development.

Advancements in liquid chromatography have led to significantly improved sample throughput. The Agilent 1290 Infinity LC System and Agilent ZORBAX Rapid Resolution High Definition (RRHD) columns are manufactured to withstand pressures up to 1200 bar. This allows the use of faster flow rates and rapid column screening to easily take advantage of stationary phase selectivity differences during method development.

Two different phenyl columns are currently available within the ZORBAX RRHD family, Eclipse Plus Phenyl-Hexyl and StableBond SB-Phenyl. Both phases excel with the analysis of anthocyanins due to the compounds' abundant conjugation. The π electrons in double bonds in these compounds interact with the π electrons in the phenyl stationary phase, providing a unique selectivity mechanism over traditional alkyl phases, such as C18 (3). While the π-π interactions are not as strong as the hydrophobic interactions responsible for retention with alkyl phases, they may provide slight selectivity advantages for phenyl columns when analyzing closely related conjugated compounds.

Experimental

An Agilent 1290 Infinity LC System with an Agilent G6410A Triple Quadrupole Mass Spectrometer was used in this experiment.

Results and Discussion

Ten grams of blueberries are extracted into acidified methanol and analyzed by LC–MS. A rapid screening of these four columns is possible within this 1200 bar system and column pressure limit. With this methanol/formic acid gradient at 0.65 mL/min, the maximum pressure generated is 1020 bar, and each analysis is accomplished in only 15 min. Total ion chromatograms (TIC) are generated from a scan from 200–1000 with the blueberry extract on each column. Extracted ion chromatograms (EIC) reveal the glycosides and acylglocysides of five common anthocyanidins.

Figure 1: Chemical structures of five common anthocyanidins found in blueberry extract.

The EICs in Figure 1 clearly show the distinct glycosides and acylglycosides of the five different anthocyandins, each marked with a unique color. By looking at the EICs it is easy to see many of the smaller peaks in the chromatogram, several of which coelute with larger peaks which would not be recognizeable with UV or TIC chromatograms. From these EICs, the total number of resolved anthocyanin peaks is determined and summarized in Table I. This data shows that the Eclipse Plus Phenyl-Hexyl column resolves a few more anthocyanin peaks with this methanol/formic acid gradient than the other three phases. To see more details and exhibits, reference the full application note on www.agilent.com (publication 5990-8470EN).

Table I: Total number of blueberry anthocyanin peaks resolved by four Agilent ZORBAX RRHD columns with a methanol/formic acid gradient

Figure 2: Extracted ion chromatograms from LC–MS scan data of blueberry anthocyanins.

References

(1) R.L. Prior, S.A. Lazarus, G. Cao, et al., "Identification of procyanidins and anthocyanins in blueberries and cranberries (vaccinium spp.) using high performance liquid chromatography/mass spectrometry" J Agric. Food. Chem.49(3), 1270–6 (2001).

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