A Rational Procedure to Increase Selectivity in the Determination of an Elicitor as Salicylic Acid in Polygala Extracts Using Capillary Electrophoresis

Considering the economic potential of secondary metabolites, researches have been focusing several strategies in order to explore and enhance the accumulation of these metabolites in plant matrices in a broad context. One of those strategies is the development of suitable methodologies for the determination of some elicitors, such as salicylic acid (SA). Since literature presents only a few analytical methods for the quantification of SA in plants, this study developed, validated and evaluated these metabolite contents in Polygala species using capillary zone electrophoresis with ultraviolet-visible detection. The background electrolyte (BGE) consisted of 15 mmol L-1 of hydroxymethyl-aminomethane and 30 mmol L-1 of 2-hydroxy-isobutyric acid, pH = 3.9. The BGE was chosen using a rational procedure to increase selectivity and reduce migration time. The method presented rapid performance, migration time less than 0.76 min for salicylic and phthalic acid (internal standard), precision results for peak area were better than 2.9% (intra-day) and 2.8% (inter-day) and the responses for the analytes were linear (range of 1-5 mg L-1), with limits of detection and quantification of 0.2 and 0.6 mg L-1, respectively. The developed method was applied for 39 samples of plant extracts.

Automated summary

Considering the economic potential of secondary metabolites, researchers have been focusing on various strategies to explore and enhance the accumulation of these metabolites in plant matrices. One of the strategies is the development of suitable methodologies for the determination of elicitors such as salicylic acid (SA). This study developed, validated, and evaluated a capillary zone electrophoresis method with ultraviolet-visible detection for the quantification of SA in Polygala species. The method showed rapid performance and accurate results.