PHASE SEPARATION LIQUID-LIQUID EXTRACTION FOR THE QUANTIFICATION OF 8-ISO-PROSTAGLANDIN F2 ALPHA IN HUMAN PLASMA BY LC-MS/MS

Background: Reactive oxygen species (ROS) are produced in the body during normal metabolism by means of enzymes and non-enzymatic chemical reduction of molecular oxygen. In case of the prevalence of ROS formation over their elimination, highly reactive free radicals can be accumulated and can cause multiple damages to the biomolecules and cells. Determination of isoprostanes in biological matrices is most often used to register free radical damage and requires selective, sensitive and specific techniques. Methods: This study presents the development and validation of the LC-MS/MS method for the determination of 8-iso-Prostaglandin F2 alpha in human plasma utilising a modified liquid-liquid extraction procedure with phase separation. Results: Modified sample preparation procedure assured higher extraction yield, clear separation of organic layer from the plasma water phase and protein precipitates, and better-purified product for instrumental analysis. Linearity was validated in the range 0.1-5.0 mu g/L with R2 > 0.996; normalised matrix varied between 86.0% and 108.3%, accuracy ranged from 90.4 %to 113.9% and precision both within runs and between runs was less than 7%. With a run time of 10 min, a throughput of over 50 samples per working day could be performed. Conclusions: The method meets all the current industrial validation criteria and allows the accurate and precise determination of 8-iso-PGF(2 alpha) in human plasma at diagnostically significant concentration range.

Automated summary

This study developed and validated an LC-MS/MS method for determining 8-iso-Prostaglandin F2 alpha in human plasma using a modified liquid-liquid extraction procedure with phase separation. The modified sample preparation procedure resulted in higher extraction yield, clear separation of organic layer, and better-purified product for instrumental analysis. The method met industrial validation criteria and allowed accurate determination of 8-iso-PGF(2 alpha) in human plasma at a diagnostically significant concentration range.