| Autor: |
Purves RW; Centre for Veterinary Drug Residues, Canadian Food Inspection Agency, Saskatoon, SK S7N 2R3, Canada.; College of Pharmacy and Nutrition, University of Saskatchewan, Saskatoon, SK S7N 5E5, Canada., West M; Centre for Veterinary Drug Residues, Canadian Food Inspection Agency, Saskatoon, SK S7N 2R3, Canada., Vaghela R; Centre for Veterinary Drug Residues, Canadian Food Inspection Agency, Saskatoon, SK S7N 2R3, Canada., Kinar J; Centre for Veterinary Drug Residues, Canadian Food Inspection Agency, Saskatoon, SK S7N 2R3, Canada., Patel Y; Centre for Veterinary Drug Residues, Canadian Food Inspection Agency, Saskatoon, SK S7N 2R3, Canada., Belford MW; Thermo Fisher Scientific, San Jose, California 95134, United States., Shurmer BO; Centre for Veterinary Drug Residues, Canadian Food Inspection Agency, Saskatoon, SK S7N 2R3, Canada. |
| Abstrakt: |
Gestagens, a class of veterinary drugs also called progestogens, are synthetic hormones used to increase feed efficiency and rate of gain in heifers. The Canadian Food Inspection Agency analyzes progestogens melengestrol acetate (MGA), megestrol acetate, and chlormadinone acetate using liquid chromatography-mass spectrometry (LC-MS). Our conventional gestagen method for kidney fat has many time-consuming steps, including solid-phase extraction. A sample preparation procedure having fewer clean-up steps was developed for routine diagnostic analysis of kidney fat and provided similar results faster, and at lower cost. A confirmatory liver method for gestagens, developed using salt-assisted extraction, employed minimal clean-up steps that resulted in high chemical background at the desired lower limit of quantification (LLOQ). Differential ion mobility spectrometry, specifically high-field asymmetric waveform ion mobility spectrometry (FAIMS), was used to filter chemical background in the gas phase. The effect of the ionization probe position on FAIMS parameters, including sensitivity, is described. With LC-FAIMS-MS, chemical background for each gestagen was virtually eliminated, resulting in a quantitative liver method having the desired 0.6 ng/g LLOQ and estimated limits of detection (LODs) up to 140 times lower than LC-MS. Incurred MGA samples, analyzed using kidney fat and liver methods from the same animal, show levels within the quantitative ranges of both methods. |
