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1 its trolox equivalent antioxidant capacity (TEAC).
2 mug.mL(-1), and ABTS from 1.87 to 2.70 mmol TEAC.
3 ctivity of the oils reached up to 3.00 mM/kg TEAC.
4 t was observed in both assays, PCL and alpha-TEAC.
5 xidant capacity (AOC) by using PCL and alpha-TEAC.
9 ured by ORAC (20.6 +/- 3.9 muM TE) and alpha-TEAC (2.92 +/- 0.58 uM alpha-TE) assays and their in vit
10 termined by UPLC and antioxidant capacity by TEAC ABTS and FRAP methods) properties of plum powders.
11 ed polyphenol content (348-413 mg GAE/L) and TEAC activity (1.9-2.3 mmol L(-1) Trolox), with 3-propyl
12 ta-carotene were the primary contributors to TEAC activity, while lutein, beta-cryptoxanthin and beta
17 ise free radicals in different test systems (TEAC and ORAC assays), to form complexes with Fe(2+) and
18 and antioxidant capacity (total polyphenols, TEAC and ORAC) of plant-based beverages made from local
19 olic content (TPC) and antioxidant capacity (TEAC and ORAC) were studied from the food quality point
20 heating methods the TAC of HM, determined by TEAC and ORAC-FL assay, proved to be insensitive to temp
22 tion of PF and a direct relationship between TEAC and the total phenolic compounds (r(2)=0.9998) and
24 th the radical scavenging capacity (DPPH and TEAC) and the ferric reducing antioxidant power (FRAP).
25 ing, Trolox equivalent antioxidant capacity (TEAC), and the total oxidation (TOTOX) of encapsulated S
27 luated through both in vitro DPPH, FRAP, and TEAC anti-radical scavenging assays and cell-based OxHLI
29 the Trolox equivalent antioxidant capacity (TEAC), as assessed by the anionic DPPH and cationic ABTS
30 nt (TPC) and the total antioxidant activity (TEAC assay and EPR spectrometry) of each cultivar were d
31 idant activity than its racemate form in the TEAC assay at all pHs, with similar values in the FRAP a
32 HF) and its racemate [6R,S] form was made by TEAC assay at different pHs, FRAP assay, and ORAC assay.
33 tes observed in vitro, were slightly higher (TEAC assay for C(alc): 848.11 +/- 60.78 mumol TE/g prote
34 and DPPH assays were more suitable than the TEAC assay for predicting meat oxidation and any resulti
40 t, antioxidant capacity using DPPH, FRAP and TEAC assays, and specific anthocyanins were determined u
43 high antioxidant activity, the best value of TEAC being 2223+/-10.10muM, which means 91.1+/-0.43% oxi
50 ve analysis of antioxidant properties (DPPH, TEAC, FRAP), singlet oxygen production and intracellular
51 ed to determine total phenolic compounds and TEAC, FRAP, and ORAC were applied to determine the antio
52 and antioxidant capacity (DPPH 255.12 mumol TEAC g(-1), IC(50) 0.17 mg mL(-1), and ORAC 380.32 mumol
55 diphenyl-2-picrylhydrazyl (DPPH) (8.90 mumol TEAC/g) and 2,2'-Azino-bis (3-ethylbenzothiazoline-6-sul
56 (Mobola plum) had the highest FRAP (9.5 mmol TEAC/g) and DPPH (14.2 IC(50) ug/mL) scavenging activiti
58 od suggested TEAC(red wine) > TEAC(coffee) > TEAC(green tea), which is the same as DPPH, spectrophoto
59 rolox-equivalent antioxidant capacity assay (TEAC) in the second growing season, while the growing co
60 ng to the standard chosen, by analogy to the TEAC indice (Trolox Equivalent Antioxidant Capacity) alr
63 and trolox equivalent antioxidant capacity (TEAC) levels, and catalase (CAT) and glutathione peroxid
64 ME (GDE)-66.26 %; ABTS: FE (IDE)-1963.83 uM TEAC/mg extract; Phosphomolybdenum reduction: FE (IDE)-
65 +) scavenging activity ( approximately 232.3 TEAC, muM Trolox/g), whereas the ex vivo hydrolysate of
67 he color allows us to determine both TPC and TEAC of the sample by the analysis of a picture taken wi
68 The Trolox equivalent antioxidant capacity (TEAC) of each of these various alcoholic beverages is de
69 acity (DPPH) and trolox equivalent capacity (TEAC) of grape and acai pulps, with savings of time and
70 The Trolox equivalent antioxidant capacity (TEAC) of red wine, coffee and green tea determined using
72 tioxidant capacity (35.8%, 29.1%, 31.9%, for TEAC, ORAC and DPPH assay, respectively) compared to unt
74 ed significant correlations with DPPH, FRAP, TEAC (Pearson's r of 0.481, 0.331 and 0.417, respectivel
78 mely Trolox equivalent antioxidant capacity (TEAC), reducing power (RP) and metal chelation activity
80 d antioxidant activity was assayed using the TEAC system based on the 2,2'-azinobis(3-ethylbenzothiaz
82 rolox equivalent antioxidant capacity assay (TEAC), the 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical
85 system from protein isolate had the highest TEAC value and was shown to undergo single-electron tran
87 statistical analysis, it was found that the TEAC value significantly depends on the TP, production m
89 the proposed model for converting EC50 into TEAC values and TEAC into EC50 values works properly.
96 the main phenolic compounds associated with TEAC values were those extracted by SC-CO(2), which were
98 ween Trolox equivalent antioxidant capacity (TEAC) values and total anthocyanins, suggesting that the
99 The trolox equivalent antioxidant capacity (TEAC) values of various (hydrophilic and lipophilic) ant
101 med the degradation of phenols; however, its TEAC was significantly (p<0.01) increased following irra