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Quantitative analysis of the flavonoid content of blueberry extracts by liquid chromatography – high resolution – mass spectrometry

Published online by Cambridge University Press:  20 June 2016

B. Mansoorian
Affiliation:
Institute of Cardiovascular and Medical Science, University of Glasgow, G12 8QQ
B. Nemzer
Affiliation:
FutureCeuticals, Inc, 2692 N State Rt. 1-17, Momence, IL 60954, USA University of Illinois at Urbana-Champaign, 1201 W Gregory Dr, Urbana, IL 61801USA
S. Silva
Affiliation:
IBET, Oeiras, Portugal ITQB, Oeiras, Portugal Pharmacy Faculty, University of Lisbon, Lisbon, Portugal
W. Mullen
Affiliation:
Institute of Cardiovascular and Medical Science, University of Glasgow, G12 8QQ
E. Combet
Affiliation:
Human Nutrition, School of Medicine, College of Medical, Veterinary & Life Sciences, University of Glasgow, Glasgow, G31 2ER
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Abstract

Type
Abstract
Copyright
Copyright © The Authors 2016 

Blueberries are a rich source of polyphenols, namely anthocyanins( Reference Mullen, Marks and Crozier 1 ). Polyphenols may be one of the key components playing a contributive role in the protective effect of fruits and vegetables against non-communicable diseases. However, the health impact of any compound is firstly dependent on i) its concentration in the food and ii) its bioavailability. The concentration of bioactives in food can be impacted on by a range of factors such as, variety, seasonal and climate changes, processing etc. Here, we carried out a quantitative analysis of phenolic compounds present in a range of blueberry varieties (Collins, Blue Crop, Spartan, Berkley and Blue Ray) collected over 3 consecutive years (2010, 2011 and 2012). Samples were analysed in triplicate using ultra performance liquid chromatography – photodiode array – high resolution – mass spectrometry (HPLC-PDA-HR-MS, Thermo Accella UPLC), injected onto a 100 × 2·1 mm C18 Hypersil Gold Column (Thermo Fisher) and eluted with a 5–40 % gradient of 1 % formic acid and methanol at 400 μL/min over 0–20 minutes. All samples were run in positive ion mode using high-resolution (50,000) exact mass for compound identification with a scan range of 250–1500 amu. A total of 28 compounds were detected and quantified (Fig. 1). The main components were anthocyanins with a minimum concentration of 8·9 ± 2·0 mg/g and maximum concentration of 19·8 ± 2·1 mg/g, corresponding to 55 %–64 % of total polyphenols, followed by flavonols with quercetin-3-galactoside the major flavonol in all the blueberries varieties. A trend was detected when comparing the three crop years, with 2011 as a better growing year in terms of polyphenolic content, with the exception of the Berkley variety.

Fig. 1. Mean total polyphenol content of blueberries analysed in triplicate with 3 year data; contribution from individual compounds.

It can be demonstrated that there is a variety in phenlolic content across the blueberry varieties as well as the year of crop. Although 2012 was reported as a year of crop failure, the polyphenolic content of the blueberries was not adversely affected. This could be interpreted in terms of these compounds being produced in times of attack or stress as a defense mechanism.

References

1. Mullen, W, Marks, SC, Crozier, A, (2007). Evaluation of phenolic compounds in commercial fruit juices and fruit drinks. Journal of Agricultural and Food Chemistry. 55(8), 3148–57.Google Scholar
Figure 0

Fig. 1. Mean total polyphenol content of blueberries analysed in triplicate with 3 year data; contribution from individual compounds.