Isolation, stability and bioactivity of Jatropha curcas phorbol esters

Jatropha curcas seed oil, which can be utilized for biodiesel production upon transesterification, is also rich in phorbol esters (PEs). In this study, PEs from J. curcas oil (Jatropha factors C₁ and C₂ (purified to homogeneity), Jatropha factors C₃ and (C₄ + C₅) (obtained as mixtures) and PE-rich extract (containing all the above stated Jatropha factors) were investigated. The concentrations of Jatropha PEs were expressed equivalent to Jatropha factor C₁. In the snail (Physa fontinalis) bioassay, the order of potency (EC₅₀, μg/L) was: PE-rich extract < factor C₃ mixture < factor C₂ < factor C₁ < factor (C₄ + C₅). In the Artemia salina bioassay, the order of potency (EC₅₀, mg/L) was: factor C₂ < factor C₃ mixture < factor C₁ < factor (C₄ + C₅) mixture. In addition, Jatropha PEs exhibited platelet aggregation (ED₅₀, μM, factor C₂ < factor C₃ mixture < factor C₁ < factor (C₄ + C₅) mixture. The stability of a PE-rich extract was evaluated and found to be low at room temperature but favourable in ethanol over a range of temperatures. By integrating the isolation methodology developed in this study in the Jatropha biodiesel industry, PEs could be obtained as value-added co-products.