Journal of Food Bioactives, ISSN 2637-8752 print, 2637-8779 online
Journal website www.isnff-jfb.com

Review

Volume 9, March 2020, pages 40-51


Blackberry polyphenols: review of composition, quantity, and health impacts from in vitro and in vivo studies

Figures

Figure 1.
Figure 1. Chemical structures of selected non-tannin polyphenolic antioxidants reported in blackberries. (a) protocatechuic acid glucoside; (b) ellagic acid; (c) hexahydroxydiphenic acid (HHDP); (d) cyanidin-3-O-glucoside (C3G); and (e) quercetin-3-O-galactoside.
Figure 2.
Figure 2. Chemical structures of selected tannin constituents reported in blackberries. (a) pedunculagin; (b) castalagin; (c) sanguiin H-6; (d) lambertianin C; and (e) procyanidin B-type dimer.

Tables

Table 1. Range of total phenolics content, total monomeric anthocyanin content, and total ellagitannins content in blackberries
 
ReferenceLocationTPC (mg GAE/100 g FW)TMAC (mg C3G eq./100 g FW)Total Ellagitannins (mg EAE/100 g FW)
Abbreviations: TPC, total phenolics content; GAE, gallic acid equivalents; FW, fresh weight; TMAC, total monomeric anthocyanins; C3G eq., cyanidin-3-O-glucoside equivalents; EAE, ellagic acid equivalents; –, not reported or measured.
Liao et al., 2020Georgia, USA409–459140–15010.4–27.8
Sellappan et al., 2002Georgia, USA418–555111–123
Siriwoharn & Wrolstad, 2004Oregon, USA822–844154–225
Siriwoharn et al., 2004Oregon, USA903–960131–22120.7–25.4
Fan-Chiang & Wrolstad, 2005Oregon, Oklahoma, France, Macedonia, Mexico and Chile70.3–201
Van de Velde et al., 2016Argentina140–162107–1248.9–10.3

 

Table 2. Content of dominant phenolic acids, anthocyanins, flavonols, and tannins reported in blackberries in mg/100 g fresh weight
 
Phenolic Acids
ellagic acidgallic acidp-coumaric acid
Abbreviations: –, not reported or measured; nd, not detectable but looked for; *, results reported on a dry weight have been converted to fresh weight according to the mass balance details.
Liao et al., 20200.55
Fan-Chiang & Wrolstad, 2005
Kolniak-Ostek et al., 20150.66–2.71nd–0.47
Mertz et al., 2007 *nd–0.240.06–0.220.50–0.76
Schulz et al., 2019 *0.09–0.18nd–0.03
Sellappan et al., 200230.01–33.814.12–6.420.4–2.08
Siriwoharn et al., 20041.64–3.62
Van de Velde et al., 2016
Anthocyanins and Flavonols
cyanidin-3-O-glucosidecyanidin-3-O-malonylglucosidecyanidin-3-O-rutinosidecyanidin-3-O-xylosidecyanidin-3-O-dioxalylglucosidequercetin-3-O-galactoside
Abbreviations: –, not reported or measured; nd, not detectable but looked for; *, results reported on a dry weight have been converted to fresh weight according to the mass balance details.
Liao et al., 202099.97.06
Fan-Chiang & Wrolstad, 200530.65–191.35nd–10.3nd–107.3nd–22.71nd–30
Kolniak-Ostek et al., 201525.15–122.540.96–3.34nd–4.66nd–6.37nd–3.030.72–2.56
Mertz et al., 2007 *45.6–81.6nd–4.8nd–75.6
Schulz et al., 2019 *
Sellappan et al., 2002nd
Siriwoharn et al., 200472.6–81.21.12–4.722.71–24.20.18–6.301.91–5.07
Van de Velde et al., 201691.4–107.35.8–7.10.8–2.92.94–4.02
Proanthocyanidin Monomer and Tannins
(−)-epicatechinlambertianin Csanguiin H-6
Abbreviations: –, not reported or measured; nd, not detectable but looked for; *, results reported on a dry weight have been converted to fresh weight according to the mass balance details.
Liao et al., 20205.47
Fan-Chiang & Wrolstad, 2005
Kolniak-Ostek et al., 20152.70–4.561.00–4.82
Mertz et al., 2007 *0.61–0.7662.4–71.850.4–294
Schulz et al., 2019 *0.03–0.05
Sellappan et al., 2002nd
Siriwoharn & Wrolstad, 20041.43–4.41
Van de Velde et al., 20163.8–4.7