Impact Mineralization of Chokeberry and Cranberry Fruit Juices Using a New Functional Additive on the Protection of Bioactive Compounds and Antioxidative Properties
Abstract
:1. Introduction
2. Results and Discussion
2.1. Determination of Basic Physicochemical Parameters
2.2. Determination of Ash and Mineral Compounds
2.3. Determination of Polyphenolic Compounds
2.4. Determination of Antioxidant Activity
2.5. Determination of Sensory Evaluation
2.6. Principal Components Analysis
3. Materials and Methods
3.1. Reagent and Standard
3.2. Materials
3.3. Technology
3.4. Determination of Ash and pH
3.5. Determination of Color
3.6. Determination of Mineral Content by ICP-OES Analysis
3.7. Determination of Organic Acids
3.8. Determination of Polyphenolic Compounds
3.9. Determination of Antioxidant Activity
3.10. Sensorian Evaluation
3.11. Statistical Analysis
4. Conclusions
Supplementary Materials
Author Contributions
Funding
Conflicts of Interest
References
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Sample Availability: Samples of the compounds……are available from the authors. |
CESP [%] | Chokeberry Juice | Cranberry Juice | ||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
Unheated | Heated | Unheated | Heated | |||||||||
L* | a* | b* | L* | a* | b* | L* | a* | b* | L* | a* | b* | |
0.0 | 49.09 ± 0.101a2 | 60.80 ± 0.12a | 37.65 ± 0.08a | 49.52 ± 0.10a | 59.58 ± 0.12a | 35.70 ± 0.07c | 78.50 ± 0.16h | 33.68 ± 0.07a | 12.31 ± 0.02a | 76.74 ± 0.15h | 35.21 ± 0.07a | 13.01 ± 0.03a |
0.2 | 49.06 ± 0.10b | 58.81 ± 0.12b | 29.69 ± 0.06b | 37.26 ± 0.07d | 58.88 ± 0.12b | 43.32 ± 0.09a | 80.27 ± 0.16g | 29.96 ± 0.06b | 10.60 ± 0.02b | 79.62 ± 0.16g | 29.64 ± 0.06b | 10.36 ± 0.02b |
0.4 | 48.15 ± 0.10d | 56.56 ± 0.11i | 23.31 ± 0.05d | 39.53 ± 0.08c | 57.41 ± 0.11d | 30.31 ± 0.06e | 81.56 ± 0.16f | 26.81 ± 0.05c | 9.26 ± 0.02c | 82.27 ± 0.16f | 24.10 ± 0.05c | 8.39 ± 0.02c |
0.6 | 48.58 ± 0.10c | 55.03 ± 0.11k | 20.28 ± 0.04i | 29.79 ± 0.06i | 56.76 ± 0.11h | 37.68 ± 0.08b | 82.75 ± 0.17e | 24.07 ± 0.05d | 8.26 ± 0.02d | 83.06 ± 0.17e | 21.46 ± 0.04d | 7.45 ± 0.01d |
0.8 | 41.79 ± 0.08h | 58.63 ± 0.12c | 24.85 ± 0.05c | 40.53 ± 0.08b | 58.44 ± 0.12c | 25.05 ± 0.05j | 81.81 ± 0.16e | 21.62 ± 0.04e | 7.93 ± 0.02e | 84.41 ± 0.17d | 18.33 ± 0.04e | 6.56 ± 0.01e |
1.0 | 39.05 ± 0.08j | 57.87 ± 0.12h | 21.22 ± 0.04f | 35.78 ± 0.07e | 55.33 ± 0.11j | 23.07 ± 0.05k | 84.41 ± 0.17c | 20.40 ± 0.04f | 6.86 ± 0.01f | 85.28 ± 0.17c | 15.93 ± 0.03f | 5.96 ± 0.01f |
1.2 | 41.71 ± 0.08h | 58.35 ± 0.12d | 23.58 ± 0.05e | 32.45 ± 0.06f | 57.14 ± 0.11e | 27.70 ± 0.06g | 84.00 ± 0.17c | 18.61 ± 0.04g | 6.61 ± 0.01g | 85.66 ± 0.17c | 15.01 ± 0.03g | 5.58 ± 0.01h |
1.4 | 44.02 ± 0.09e | 57.05 ± 0.11g | 21.05 ± 0.04h | 29.01 ± 0.06j | 56.98 ± 0.11g | 33.87 ± 0.07d | 84.90 ± 0.17c | 18.00 ± 0.04h | 6.16 ± 0.01h | 84.29 ± 0.17d | 13.98 ± 0.03h | 5.61 ± 0.01g |
1.6 | 40.07 ± 0.08i | 58.02 ± 0.12e | 21.71 ± 0.04g | 27.90 ± 0.06k | 55.98 ± 0.11i | 29.40 ± 0.06f | 83.29 ± 0.17d | 13.29 ± 0.03j | 5.90 ± 0.01i | 87.20 ± 0.17a | 11.07 ± 0.02i | 4.89 ± 0.01j |
1.8 | 42.62 ± 0.09f | 55.99 ± 0.11j | 17.50 ± 0.04k | 30.74 ± 0.06h | 57.13 ± 0.11e | 27.19 ± 0.05h | 85.90 ± 0.17b | 15.17 ± 0.03i | 5.00 ± 0.01j | 86.91 ± 0.17b | 10.99 ± 0.02j | 4.81 ± 0.01k |
2.0 | 42.34 ± 0.08g | 56.67 ± 0.11h | 19.16 ± 0.04j | 31.29 ± 0.06g | 57.03 ± 0.11f | 27.05 ± 0.05i | 86.50 ± 0.17a | 13.77 ± 0.03j | 4.75 ± 0.01k | 84.42 ± 0.17d | 14.64 ± 0.03g | 5.09 ± 0.01i |
Process | CESP [%] | Chokeberry Juice | Cranberry Juice | ||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
OA | CA | ICA | MA | QA | FA | OA | GA | CA | ICA | MA | SA | ||
Unheated | 0.0 | 91.3 ± 0.0d | 322.3 ± 0.1m | 968.2 ± 0.2c | 15482.6 ± 3.1h | 3224.0 ± 0.6c | 677.9 ± 0.1f | 358.6 ± 0.1f | 161.3 ± 0.0e | 24364.4 ± 4.9h | 1666.4 ± 0.3h | 17435.9 ± 3.5h | 6162.2 ± 1.2f |
0.2 | 90.0 ± 0.0d | 236.0 ± 0.0l | 1022.8 ± 0.2b | 15256.7 ± 3.1i | 3221.8 ± 0.6c | 662.9 ± 0.1g | 359.0 ± 0.1f | 145.8 ± 0.0h | 24152.9 ± 4.8i | 1661.8 ± 0.3h | 17401.6 ± 3.5i | 6145.5 ± 1.2f | |
0.4 | 96.3 ± 0.0c | 268.6 ± 0.1p | 568.1 ± 0.1i | 16367.9 ± 3.3d | 3023.8 ± 0.6d | 736.4 ± 0.1d | 353.5 ± 0.1g | 160.6 ± 0.0e | 23755.8 ± 4.8j | 1648.6 ± 0.3i | 17137.4 ± 3.4j | 6026.9 ± 1.2g | |
0.6 | 85.8 ± 0.0e | 250.2 ± 0.1s | 486.6 ± 0.1o | 14462.8 ± 2.9l | 2938.9 ± 0.6e | 652.6 ± 0.1h | 344.8 ± 0.1h | 167.1 ± 0.0d | 23318.7 ± 4.7l | 1617.5 ± 0.3l | 16799.2 ± 3.4l | 5896.6 ± 1.2h | |
0.8 | 81.8 ± 0.0g | 387.0 ± 0.1i | 635.2 ± 0.1e | 14533.6 ± 2.9k | 2490.6 ± 0.5i | 635.2 ± 0.1i | 334.3 ± 0.1i | 145.3 ± 0.0h | 22677.7 ± 4.5m | 1573.5 ± 0.3n | 16334.9 ± 3.3o | 5729.6 ± 1.1i | |
1.0 | 76.0 ± 0.0i | 365.2 ± 0.1k | 477.8 ± 0.1 | 14364.9 ± 2.9m | 2454.0 ± 0.5i | 575.1 ± 0.1n | 337.9 ± 0.1i | 147.0 ± 0.0h | 22827.8 ± 4.6m | 1591.0 ± 0.3m | 16415.5 ± 3.3n | 5765.5 ± 1.2i | |
1.2 | 80.0 ± 0.0g | 381.1 ± 0.1j | 545.7 ± 0.1k | 13914.4 ± 2.8p | 2435.3 ± 0.5i | 602.9 ± 0.1k | 343.5 ± 0.1h | 154.3 ± 0.0g | 23244.9 ± 4.6l | 1632.4 ± 0.3j | 16660.7 ± 3.3m | 5858.0 ± 1.2h | |
1.4 | 75.7 ± 0.0i | 375.2 ± 0.1j | 543.5 ± 0.1k | 13269.0 ± 2.7r | 2267.0 ± 0.5k | 565.2 ± 0.1o | 345.1 ± 0.1h | 149.3 ± 0.0h | 23343.7 ± 4.7l | 1637.2 ± 0.3j | 16793.3 ± 3.4l | 5894.1 ± 1.2h | |
1.6 | 79.7 ± 0.0h | 477.4 ± 0.1e | 507.3 ± 0.1n | 14187.5 ± 2.8n | 2390.9 ± 0.5j | 577.9 ± 0.1n | 361.5 ± 0.1e | 176.5 ± 0.0c | 23650.2 ± 4.7k | 1620.7 ± 0.3k | 17152.3 ± 3.4j | 5890.2 ± 1.2h | |
1.8 | 73.9 ± 0.0j | 525.9 ± 0.1d | 558.8 ± 0.1j | 14979.5 ± 3.0j | 2384.9 ± 0.5j | 541.3 ± 0.1p | 352.7 ± 0.1g | 159.0 ± 0.0f | 23984.8 ± 4.8j | 1679.8 ± 0.3g | 17032.1 ± 3.4k | 6001.5 ± 1.2g | |
2.0 | 79.4 ± 0.0h | 557.8 ± 0.1c | 601.4 ± 0.1g | 14022.4 ± 2.8o | 2349.1 ± 0.5j | 580.6 ± 0.1m | 369.7 ± 0.1g | 169.2 ± 0.0f | 24484.1 ± 4.8j | 1790.2 ± 0.3g | 18012.2 ± 3.4k | 6211.2 ± 1.2g | |
Heated | 0.0 | 100.5 ± 0.0b | 354.6 ± 0.1r | 1065.0 ± 0.2a | 17030.9 ± 3.4b | 3546.4 ± 0.7a | 745.7 ± 0.1b | 394.5 ± 0.1a | 177.4 ± 0.0c | 26800.8 ± 5.4a | 1833.1 ± 0.4b | 19179.5 ± 3.8a | 6778.4 ± 1.4a |
0.2 | 99.0 ± 0.0b | 259.7 ± 0.1r | 1125.0 ± 0.2b | 16782.4 ± 3.4c | 3543.9 ± 0.7a | 729.2 ± 0.1c | 394.9 ± 0.1a | 160.3 ± 0.0e | 26568.1 ± 5.3b | 1828.0 ± 0.4b | 19141.7 ± 3.8a | 6760.0 ± 1.4a | |
0.4 | 105.9 ± 0.0a | 295.5 ± 0.1o | 624.9 ± 0.1e | 18004.7 ± 3.6a | 3326.2 ± 0.7b | 810.0 ± 0.2a | 388.8 ± 0.1b | 176.6 ± 0.0c | 26131.3 ± 5.2d | 1813.5 ± 0.4c | 18851.2 ± 3.8b | 6629.6 ± 1.3b | |
0.6 | 94.4 ± 0.0c | 275.2 ± 0.1p | 535.3 ± 0.1l | 15909.1 ± 3.2e | 3232.8 ± 0.6b | 717.9 ± 0.1d | 379.3 ± 0.1c | 183.8 ± 0.0b | 25650.6 ± 5.1e | 1779.2 ± 0.4e | 18479.1 ± 3.7d | 6486.3 ± 1.3c | |
0.8 | 90.0 ± 0.0d | 425.7 ± 0.1f | 698.8 ± 0.1d | 15987.0 ± 3.2e | 2739.6 ± 0.5f | 698.7 ± 0.1e | 367.7 ± 0.1e | 159.9 ± 0.0f | 24945.4 ± 5.0g | 1730.9 ± 0.3f | 17968.4 ± 3.6g | 6302.6 ± 1.3e | |
1.0 | 83.6 ± 0.0f | 401.7 ± 0.1h | 525.6 ± 0.1m | 15801.4 ± 3.2f | 2699.4 ± 0.5g | 632.6 ± 0.1i | 371.7 ± 0.1d | 161.7 ± 0.0e | 25110.6 ± 5.0f | 1750.1 ± 0.4f | 18057.1 ± 3.6f | 6342.1 ± 1.3e | |
1.2 | 88.0 ± 0.0e | 419.2 ± 0.1f | 600.3 ± 0.1g | 15305.8 ± 3.1i | 2678.8 ± 0.5g | 663.2 ± 0.1g | 377.9 ± 0.1c | 169.7 ± 0.0d | 25569.4 ± 5.1e | 1795.6 ± 0.4e | 18326.8 ± 3.7e | 6443.8 ± 1.3d | |
1.4 | 83.2 ± 0.0f | 412.7 ± 0.1g | 597.8 ± 0.1h | 14596.0 ± 2.9k | 2493.7 ± 0.5i | 621.7 ± 0.1j | 379.7 ± 0.1c | 164.2 ± 0.0e | 25678.1 ± 5.1e | 1800.9 ± 0.4d | 18472.6 ± 3.7d | 6483.5 ± 1.3c | |
1.6 | 87.7 ± 0.0e | 525.1 ± 0.1d | 558.1 ± 0.1j | 15606.3 ± 3.1g | 2629.9 ± 0.5g | 635.7 ± 0.1i | 397.6 ± 0.1a | 194.2 ± 0.0a | 26015.2 ± 5.2d | 1782.8 ± 0.4e | 18867.6 ± 3.8b | 6479.2 ± 1.3c | |
1.8 | 81.3 ± 0.0g | 578.5 ± 0.1b | 614.7 ± 0.1f | 16477.5 ± 3.3d | 2623.4 ± 0.5g | 595.4 ± 0.1l | 388.0 ± 0.1b | 174.9 ± 0.0c | 26383.3 ± 5.3b | 1847.7 ± 0.4a | 18735.4 ± 3.7c | 6601.6 ± 1.3b | |
2.0 | 87.3 ± 0.0e | 613.6 ± 0.1a | 661.6 ± 0.1e | 15424.6 ± 3.1h | 2584.0 ± 0.5h | 638.6 ± 0.1i | 398.0 ± 0.1b | 181.2 ± 0.0c | 27213.2 ± 5.3b | 1900.7 ± 0.4a | 19105.4 ± 3.7c | 6701.3 ± 1.3b |
Minerals | Sum [mg/100 g] | Ratio of Minerals [%] |
---|---|---|
Al | 0.00 | 0.00 |
As | 0.03 | 0.00 |
Ca | 27695.83 | 27.70 |
Cd | 0.01 | 0.00 |
Cr | 0.00 | 0.00 |
Cu | 0.08 | 0.00 |
Fe | 0.52 | 0.00 |
K | 57.59 | 0.06 |
Mg | 352.28 | 0.35 |
Mn | 0.12 | 0.00 |
Mo | 0.00 | 0.00 |
Na | 103.89 | 0.10 |
Ni | 0.00 | 0.00 |
P | 85.53 | 0.09 |
Pb | 0.00 | 0.00 |
S | 94.78 | 0.10 |
Sr | 22.35 | 0.02 |
Zn | 0.00 | 0.00 |
Tentative Identification | λmax [nm] | [H − M]− (m/z) | MS/MS Fragments (m/z) | Chokeberry | Cranberry |
---|---|---|---|---|---|
Cyanidin-3-hexoside-(epi)catechin | 520 | 737+ | 575/423/287 | x | |
Neochlorogenic acid | 323 | 353 | 191 | x | |
Cyanidin-3-pentoside-(epi)catechin | 520 | 707+ | 557/329/287 | x | |
( + )-catechin | 280 | 289 | 245/203 | x | |
Cyanidin-3-hexoside-(epi)cat-(epi)cat | 520 | 1025+ | 575/409/287 | x | |
3-O-p-Coumaroylquinic acid | 310 | 337 | 191 | x | x |
Delfinidyn-3-O-glucoside | 520 | 465+ | 303 | x | |
p-Coumaroyl-hexose isomer | 310 | 325 | 163 | x | |
p-Coumaroyl-hexose isomer | 310 | 325 | 163 | x | |
B-type procyanidin-dimer | 280 | 577 | 289 | x | |
Cyanidin-3-O-galactoside | 516 | 449+ | 287 | x | x |
Chlorogenic acid | 323 | 353 | 191 | x | x |
Cryptochlorogenic acid | 323 | 353 | 191 | x | |
Caffeoyl dihexoside | 320 | 503 | 341/179 | x | |
Caffeoyl hexoside | 320 | 341 | 179 | x | |
Caffeoyl hexoside isomer | 320 | 341 | 179 | x | |
Cyanidin-3-O-glucoside | 517 | 449+ | 287 | x | x |
Sinapoyl-hexose | 320 | 385 | 223 | x | |
Delphinidin-3-O-arabinoside | 520 | 435 | 303 | x | |
Peonidin-3-O-galactoside | 515 | 463+ | 301 | x | |
Cyanidin-3-O-arabinoside | 515 | 419+ | 287+ | x | x |
(−)-Epicatechin | 280 | 289 | 245/203 | x | |
A-type PA-trimer | 280 | 863 | 289 | x | |
Cyanidin-3-O-xyloside | 515 | 419+ | 287+ | x | |
Peonidin-3-O-glucoside | 515 | 463+ | 301 | x | |
Peonidin-3-O-arabinoside | 515 | 433+ | 301 | x | |
Malvidin-3-O-galactoside | 515 | 493 | 331 | x | |
Malwidin-3-O-arabinoside | 520 | 463+ | 331 | x | |
A-type PA-tetramer | 280 | 1151 | 289 | x | |
Quercetin-dihexoside | 352 | 625 | 445/301 | x | |
Quercetin-dihexoside | 352 | 625 | 445/301 | x | |
Quercetin-3-O-vicianoside | 353 | 595 | 432/301 | x | |
Quercetin-3-O-robinobioside | 353 | 609 | 463/301 | x | |
Quercetin-3-O-rutinoside | 353 | 609 | 463/301 | x | x |
Myricetin-3-O-arabinoside | 355 | 449 | 317 | x | |
Myricetin-3-O-galactoside | 355 | 479 | 317 | x | |
Quercetin-3-O-galactoside | 352 | 463 | 301 | x | x |
Quercetin-3-O-glucoside | 352 | 463 | 301 | x | x |
Myricetin-3-O-glucoside | 355 | 479 | 317 | x | |
Eriodictyol-glucuronide | 280 | 463 | 287 | x | |
Isorhamnetin pentosylhexoside | 352 | 609 | 315 | x | |
Quercetin-O-deoxyhexose-deoxyhexoside | 352 | 593 | 433/301 | x | |
Isorhamnetin rhamnosyl hexoside isomer | 352 | 623 | 463/315 | x | |
Isorhamnetin rhamnosyl hexoside isomer | 352 | 623 | 421/315 | x | |
Isorhamnetin-3-O-galactoside | 350 | 477 | 315 | x | |
Syringetin-3-O-galactoside | 358 | 507 | 330 | x | |
Methoxyquercetin-pentoside | 350 | 447 | 315 | x | |
Isorhamnetin-3-O-arabinoside | 352 | 447 | 315 | x | |
Quercetin-3-O-(6”p-coumaroyl)-galactoside | 350 | 609 | 301 | x |
Addition [%] | Antioxidant Activity [mmol TE/mL] | |||||||
---|---|---|---|---|---|---|---|---|
FRAP | ABTS | |||||||
Unheated | Heated | Unheated | Heated | |||||
Cranberry | Chokeberry | Cranberry | Chokeberry | Cranberry | Chokeberry | Cranberry | Chokeberry | |
0.0 | 1.38 ± 0.001a2 | 10.94 ± 0.02A | 1.31 ± 0.00b | 9.98 ± 0.02B | 1.48 ± 0.00a | 9.79 ± 0.02A | 1.41 ± 0.00b | 9.16 ± 0.02B |
0.2 | 1.01 ± 0.00g | 7.61 ± 0.02B | 1.00 ± 0.00g | 7.47 ± 0.01C | 1.16 ± 0.00d | 7.32 ± 0.01C | 1.03 ± 0.00g | 7.27 ± 0.02C |
0.4 | 1.19 ± 0.00c | 6.88 ± 0.01G | 1.18 ± 0.00c | 6.82 ± 0.01G | 1.25 ± 0.00c | 7.08 ± 0.01D | 1.21 ± 0.00c | 7.01 ± 0.01D |
0.6 | 1.03 ± 0.00g | 5.69 ± 0.01K | 1.00 ± 0.00c | 5.38 ± 0.01L | 1.15 ± 0.00d | 5.27 ± 0.01I | 1.05 ± 0.00g | 5.20 ± 0.01I |
0.8 | 1.18 ± 0.00c | 5.14 ± 0.01M | 1.11 ± 0.00e | 5.11 ± 0.01M | 1.09 ± 0.00f | 5.07 ± 0.01J | 1.01 ± 0.00gh | 5.05 ± 0.01J |
1.0 | 1.06 ± 0.00f | 6.45 ± 0.01I | 1.03 ± 0.00g | 6.05 ± 0.01J | 1.14 ± 0.00d | 4.95 ± 0.01J | 1.08 ± 0.00f | 4.58 ± 0.01K |
1.2 | 1.32 ± 0.00b | 6.10 ± 0.01J | 1.11 ± 0.00e | 5.64 ± 0.01K | 1.09 ± 0.00f | 5.53 ± 0.01H | 1.05 ± 0.00g | 5.22 ± 0.01I |
1.4 | 0.88 ± 0.00j | 7.29 ± 0.01D | 0.84 ± 0.00k | 7.20 ± 0.01D | 1.02 ± 0.00g | 7.06 ± 0.01D | 0.90 ± 0.00i | 7.03 ± 0.01D |
1.6 | 1.05 ± 0.00f | 7.04 ± 0.01F | 1.01 ± 0.00g | 6.55 ± 0.01H | 0.99 ± 0.00h | 6.42 ± 0.01F | 0.97 ± 0.00h | 6.38 ± 0.01F |
1.8 | 1.18 ± 0.00c | 7.44 ± 0.01C | 1.15 ± 0.00d | 7.21 ± 0.01D | 1.13 ± 0.00e | 7.07 ± 0.01D | 1.11 ± 0.00e | 7.03 ± 0.02D |
2.0 | 0.94 ± 0.00h | 7.11 ± 0.01E | 0.91 ± 0.00i | 6.63 ± 0.01H | 1.09 ± 0.00f | 6.50 ± 0.01E | 0.96 ± 0.00h | 6.25 ± 0.01G |
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Lachowicz, S.; Oszmiański, J.; Wilczyńska, M.; Zaguła, G.; Saletnik, B.; Puchalski, C. Impact Mineralization of Chokeberry and Cranberry Fruit Juices Using a New Functional Additive on the Protection of Bioactive Compounds and Antioxidative Properties. Molecules 2020, 25, 659. https://doi.org/10.3390/molecules25030659
Lachowicz S, Oszmiański J, Wilczyńska M, Zaguła G, Saletnik B, Puchalski C. Impact Mineralization of Chokeberry and Cranberry Fruit Juices Using a New Functional Additive on the Protection of Bioactive Compounds and Antioxidative Properties. Molecules. 2020; 25(3):659. https://doi.org/10.3390/molecules25030659
Chicago/Turabian StyleLachowicz, Sabina, Jan Oszmiański, Martyna Wilczyńska, Grzegorz Zaguła, Bogdan Saletnik, and Czesław Puchalski. 2020. "Impact Mineralization of Chokeberry and Cranberry Fruit Juices Using a New Functional Additive on the Protection of Bioactive Compounds and Antioxidative Properties" Molecules 25, no. 3: 659. https://doi.org/10.3390/molecules25030659
APA StyleLachowicz, S., Oszmiański, J., Wilczyńska, M., Zaguła, G., Saletnik, B., & Puchalski, C. (2020). Impact Mineralization of Chokeberry and Cranberry Fruit Juices Using a New Functional Additive on the Protection of Bioactive Compounds and Antioxidative Properties. Molecules, 25(3), 659. https://doi.org/10.3390/molecules25030659