LC–MS/MS quantification of free and Fab-bound colchicine in plasma, urine and organs following colchicine administration and colchicine-specific Fab fragments treatment in Göttingen minipigs.

Clinical evaluation of a colchicine specific antigen-binding fragment (Fab) in order to treat colchicine poisoning required the development of an accurate method allowing quantification of free and Fab-bound colchicine in plasma and urine, and free colchicine in tissues, to measure colchicine redistribution after Fab administration. Three methods have been developed for this purpose, and validated in plasma, urine and liver: total colchicine was determined after denaturation of Fab by dilution in water and heating; free colchicine was separated from Fab-bound colchicine by filtration with 30 KDa micro-filters; tissues were homogenized in a tissue mixer. Deuterated colchicine was used as internal standard. Samples were extracted by liquid–liquid extraction and analyzed with a LC–MS/MS. LOQ were 0.5 ng/mL in plasma and urine for free and total colchicine and 5 pg/mg in tissues. The methods were linear in the 0.5–100 ng/mL range in plasma and urine, and 5–300 pg/mg in tissues with determination coefficients > 0.99. Precision and accuracy of QC samples presented a CV < 9.4%. The methods require only 200 μL of sample and allow a high throughput due to short analytical run (2 min). These methods were successfully applied to a pig intoxicated with colchicine and treated with colchicine specific Fab fragments. [ABSTRACT FROM AUTHOR]