ΔE	Color difference against control samples, in the L*C*h* color space
a*	Redness color change in the CIEL*a*b* space
ABTS	2,2-azino-bis(ethylbenzothiazoline-6-sulfonic acid)
aw	Activity of water
ANC	Anthocyanins
b*	Yellowness color change in the CIEL*a*b* space
C*	Chroma
C3G	Cyanidin-3-O-glucoside
C3G-Mal	Cyanidin-3-(6′-malonylglucoside)
Caco-2	Human colorectal adenocarcinoma cells
cfu	Colony forming units
D3G	Delphinidin-3-O-glucoside
DM	Dry matter
DPPH	2,2-diphenyl-1-picrylhydrazyl
EC3G/L	Equivalents of C3G
EC50	Half-maximal effective concentration
EF	Electric field
EGCG	Epigallocatechin gallate
FRAP	Ferric ion reducing antioxidant power
FT-IR	Fourier Transform Infrared
GAE	Gallic acid equivalents
GC	Gas chromatography
GRAS	Generally recognized as safe
HepG2	Human hepatocellular carcinoma cells
HHPE	High hydrostatic pressure extraction
HPE	High-pressure-assisted extraction
IAT	Inlet air temperature
L*	Luminosity or lightness in the CIEL*a*b* space
MBC	Minimum bactericidal concentration
MCF-7	Human mammary gland/breast adenocarcinoma cells (derived from metastatic site)
MDA	Malonaldehyde
MDA-MB-231	Triple negative human mammary gland/breast adenocarcinoma cells
MIC	Minimum inhibitory concentration
OAT	Outlet air temperature
OH	Ohmic heating
P3G	Peonidin-3-(6′-malonylglucoside)
P3G-Mal	Pelargonidin-3-(6′-malonylglucoside)
PEF	Pulsed electric fields
Pr3G	Pelargonidin-3-O-glucoside
RSA	Radical scavenging activity (%)
SC-CO2	Supercritical carbon dioxide
SFC	Supercritical fluid chromatography
SFE	Supercritical fluid extraction
TAC	Total anthocyanin content
TBARS	Thiobarbituric acid reactive substances
TEAC	Trolox equivalent antioxidant capacity
TPC	Total phenolic compounds
VPR	Vine-pruning residues
XR	X-ray