Why, when we study the Antioxidant Activity by différent méthodes( ABTS,DPPH,FRAP .....) for the différent variétés ,the order of Efficiency of thèse Samples It changes frome one way to another ?
An antioxidant can act through different mechanisms, and those tests should uncover partially the type of antioxidants contained in your samples, for example a sample could show strong scavenging activity but low iron chelating capacity which means that the sample's antioxidant molecules do not act as chelators or through chelating. Generally speaking ABTS and DPPH could give you an idea about your samples total activity but performing the other tests could add more information.
I fully concur with the above answers. No single assay can be regarded as the benchmark for the assessment of antioxidant capacity as each assay has its own limitations. Therefore I recommend that several antioxidant assays are used to give an overall picture of the antioxidant capacity of a sample. I suggest Total Phenol Content, FRAP, DPPH and Ferrous Ion Chelating Assay.