Programmable flow system for automation of oxygen radical absorbance capacity assay using pyrogallol red for estimation of antioxidant reactivity

被引：16

作者：

Ramos, Ines I. ^{[1
]}

Gregorio, Bruno J. R. ^{[1
]}

Barreiros, Luisa ^{[1
]}

Magalhaes, Luis M. ^{[1
]}

Toth, Ildiko V. ^{[1
]}

Reis, Salette ^{[1
]}

Lima, Jose L. F. C. ^{[2
]}

Segundo, Marcela A. ^{[1
]}

机构：

[1] Univ Porto, Fac Farm, Dept Ciencias Quim, UCIBIO,REQUIMTE, Rua Jorge Viterbo Ferreira 228, P-4050313 Oporto, Portugal

[2] Univ Porto, Fac Farm, Dept Ciencias Quim, LAQV,REQUIMTE, Rua Jorge Viterbo Ferreira 228, P-4050313 Oporto, Portugal

来源：

TALANTA | 2016年 / 150卷

关键词：

Peroxyl radicals; Automation; Absorbance probe; Reaction kinetics; Flow injection analysis; HUMAN SERUM-ALBUMIN; SCAVENGING CAPACITY; IN-VITRO; PEROXYL RADICALS; ORAC VALUES; FOOD; FLUORESCEIN; INDEX; METHODOLOGIES; FLAVONOIDS;

D O I：

10.1016/j.talanta.2015.12.061

中图分类号：

O65 [分析化学];

学科分类号：

070302 ; 081704 ;

摘要：

An automated oxygen radical absorbance capacity (ORAC) method based on programmable flow injection analysis was developed for the assessment of antioxidant reactivity. The method relies on real time spectrophotometric monitoring (540 nm) of pyrogallol red (PGR) bleaching mediated by peroxyl radicals in the presence of antioxidant compounds within the first minute of reaction, providing information about their initial reactivity against this type of radicals. The ORAC-PGR assay under programmable flow format affords a strict control of reaction conditions namely reagent mixing, temperature and reaction timing, which are critical parameters for in situ generation of peroxyl radical from 2,2'-azobis(2-amidinopropane) dihydrochloride (AAPH). The influence of reagent concentrations and programmable flow conditions on reaction development was studied, with application of 37.5 mu M of PGR and 125 mM of AAPH in the flow cell, guaranteeing first order kinetics towards peroxyl radicals and pseudo-zero order towards PGR. Peroxyl-scavenging reactivity of antioxidants, bioactive compounds and phenolic-rich beverages was estimated employing the proposed methodology. Recovery assays using synthetic saliva provided values of 90 +/- 5% for reduced glutathione. Detection limit calculated using the standard antioxidant compound Trolox was 8 mu M. RSD values were <3.4 and <4.9%, for intra and inter-assay precision, respectively. Compared to previous batch automated ORAC assays, the developed system also accounted for high sampling frequency (29 h(-1)), low operating costs and low generation of waste. (C) 2015 Elsevier B.V. All rights reserved.

引用

页码：599 / 606

页数：8