15 research outputs found
Optimization and Validation of a Microwave Digestion Method for Multi-element Characterization of Vranec Wines
Extraction and evaluation of natural occurring bioactive compounds and change in antioxidant activity during red winemaking
Phenolic composition of red wines from Stanušina, a grape variety indigenous of the Republic of Macedonia, was compared with the regional Vranec and the international Cabernet Sauvignon. The extent of skin contact (i.e. maceration time) on levels of phenolic compounds and antioxidant activity of wines was evaluated. A total of 19 phenolic compounds were identified and quantified. Among these malvidin-3-glucoside and its derivatives were the major compounds, while caftaric acid was the predominant cinnamic acid derivative, followed by catechin, the main flavan-3-ol. The concentration of hydroxycinnamic acids, anthocyanins and (+)-catechin ranged from 224 to 511 mg/L, 22 to 360 mg/L and 26 20 to 375 mg/L, respectively and peaked at 3rd, 6th and 9th day of maceration, respectively. However, prolong maceration slightly decreased their concentration. Stanušina wines presented high levels of hydroxycinnamic acids and antioxidant activity
Geographic characterization of Greek wine by inductively coupled plasma–mass spectrometry macroelemental analysis
Determination of Pb and Cd in Macedonian Wines by Electrothermal Atomic Absorption Spectrometry (ETAAS)
Rapid Determination of Trace Elements in Macedonian Grape Brandies for Their Characterization and Safety Evaluation
Extraction and evaluation of natural occurring bioactive compounds and change in antioxidant activity during red winemaking
Application of a Novel Small-Scale Sample Cleanup Procedure Prior to MALDI-TOF-MS for Rapid Pigment Fingerprinting of Red Wines
This study evaluates the anthocyanin and derived
pigment composition of
Vitis vinifera
red wines of Vranec,
Merlot, and Cabernet Sauvignon produced in 2006, 2007, and
2008 vintages from the Tikve
š
wine region in the Republic of
Macedonia.Their profile was established using matrix-assisted
laser desorption/ionization time-of-flight mass spectrometry
(MALDI-TOF-MS) technique. A total of 22 anthocyanins
and derived pigments have been identified in the samples including 10 anthocyanins, 1 ethyl-bridged flavanol
–
anthocy-
anin adduct, and 11 pyranoanthocyanins. MALDI-TOF-MS
analysis was performed after solid-phase extraction of the
wines by using, for the first time, the Zip-Tip® C18 stationary
phase, introducing a novel small-scale sample cleanup proce-
dure prior to the rapid MALDI-TOF-MS fingerprinting of
wine samples. 2
′
,4
′
,6
′
-Trihydroxyacetophenone (dissolved in
acetonitrile/water 1:1,
v
/
v
) was used as a matrix. The qualitative
screening of anthocyanins and derived pigments with MALDI-
TOF-MS confirmed the presence of glucoside, acetylglucoside,
and
p
-coumaroylglucoside derivatives of anthocyanins in the
wine samples. Furthermore, pyranoanthocyanins formed by
reactions of anthocyanins with pyruvic acid and acetaldehyde,
as well as flavanol
–
pyranoanthocyanins and ethyl-bridged
flavan-3-ol-anthocyanin adduct pigments have been detected
in the samples
Fast Analysis of Total Polyphenol Content and Antioxidant Activity in Wines and Oenological Tannins Using a Flow Injection System with Tandem Diode Array and Electrochemical Detections
An analytical method for simultaneous determination of total polyphenol content (TPC) and antioxidant activity (AA) of wines (white and red wines) and oenological tannins, using a flow injection system with sequential diode array and electrochemical amperometry detectors (DAD-ECD), was proposed. The signal at 280 nm provided aggregate data for TPC. The anodic peak related to wine phenolic oxidation was scanned using pulsed integrated amperometry over the potential of 800 mV vs. Ag/AgCl, to obtain AA. Serial dilutions avoided the poisoning at the glassy carbon (GC) electrode and the linear response obtained with both detectors was compared with spectrophotometric assays commonly used in oenology laboratory. Intraday and interday analytical repetitions showed a good repeatability and reproducibility (relative standard deviation RSD < 6% for both detectors), and the satisfactory relationship between the proposed coupled flow injection/DAD-ECD and the classic UV methods (R2TPC = 0.9967; R2DPPH = 0.9621) confirmed the efficacy of flow injection analysis with a coupled detection system, for the reliable quality control of wine and wine-related products