Quantitative Analysis of Tocopherol Degradation and Radical Scavenging Activity During Lipid Oxidation in Bulk Soybean and Corn Oils


Cantele C., BAYRAM İ., Nuccitelli A., Li S., Cardenia V., Decker E. A.

JOURNAL OF THE AMERICAN OIL CHEMISTS SOCIETY, vol.102, no.10, pp.1489-1499, 2025 (SCI-Expanded) identifier identifier

  • Publication Type: Article / Article
  • Volume: 102 Issue: 10
  • Publication Date: 2025
  • Doi Number: 10.1002/aocs.70006
  • Journal Name: JOURNAL OF THE AMERICAN OIL CHEMISTS SOCIETY
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus, ABI/INFORM, Agricultural & Environmental Science Database, Analytical Abstracts, Applied Science & Technology Source, Aquatic Science & Fisheries Abstracts (ASFA), BIOSIS, Business Source Elite, Business Source Premier, CAB Abstracts, Chemical Abstracts Core, Chimica, Compendex, Computer & Applied Sciences, Food Science & Technology Abstracts, INSPEC, Veterinary Science Database
  • Page Numbers: pp.1489-1499
  • Keywords: ABTS, DPPH, lipid oxidation, seeds oil, spectrophotometry, tocopherols
  • Middle East Technical University Affiliated: Yes

Abstract

Accurate shelf-life prediction for fats and oils is essential, yet traditional lipid oxidation models are often time-consuming and unreliable. Since antioxidants deplete as oxidation progresses, tracking their loss alongside oxidation products could improve lag phase predictions. This study investigates a rapid, cost-effective spectrophotometric test to quantify antioxidant depletion in soybean and corn oils for potential use in mathematical modeling. Results showed that alpha-tocopherol was fully degraded by the end of the oxidation lag phase, while (gamma + beta)- and delta-tocopherols concentrations remained at > 70% (soybean oil) and 65% (corn oil). DPPH scavenging activity initially declined with tocopherol loss but later increased (up to 79%), likely due to lipid radical interference. Further analysis confirmed DPPH reacts with free radicals, compromising its specificity to only detecting antioxidants. To address this, the ABTS assay was tested, requiring prior antioxidant extraction from oil due to its water-soluble nature. Unlike DPPH, ABTS inhibition dropped to zero once all tocopherols were depleted, confirming its higher specificity. However, this depletion did not align with the oxidation lag phase, as (gamma + beta)- and delta-tocopherols were not completely depleted at the end of the lag phase. These findings highlight three key insights: (i) (gamma + beta)- and delta-tocopherols are less effective than alpha-tocopherol in inhibiting lipid oxidation in commercial oils, persisting even after oxidation begins; (ii) the direct application of DPPH in lipid-containing matrices can yield misleading results, as it reacts with lipid radicals during oxidation; (iii) while ABTS specifically tracks antioxidant depletion, it might be unsuitable for kinetic modeling due to minimal change during the lag phase.