Jaesung Pyo* Pages 1 - 7 ( 7 )
Background: Since propofol is rapidly metabolized and excreted from the body, it is not easy to quantify its intake in blood or urine sample over the time. In this case, the hair sample would be more advantageous to estimate during the abuse period. However, presence of protein and lipid in the hair sample could interfere extraction and be problematic during mass spectrometric analysis.
Objective: The aim of this study is to develop the simple and less-time consuming method for extraction of propofol glucuronide by removing hair interferences with centrifugal filter.
Method: Hair samples were washed and dissolved with sodiumhydroxide solution. This dissolved hair solution was applied to centrifugal filter and centrifuged. The filtrate was extracted with ethyl acetate and evaporated to dryness. The residue was reconstituted with methanol and analyzed by liquid chromatography coupled with tandem mass spectrometry. This developed analytical method was validated by testing of linearity, selectivity, accuracy, precision, recovery, matrix effect and stability of propofol glucuronide.
Results and Discussion: The validation results showed good linearity over the concentration range of 0.5~500 pg/mg, with correlation coefficient of 0.9991. The LOD and LLOQ was 0.2 and 0.5 pg/mg, respectively. The intra-and inter-day precision and accuracy were acceptable within 14.5% for precision and 10.1% for accuracy. Similarly, the developed method revealed high sample recovery (>88%), low hair matrix effect (<10%) and highly-efficient extraction procedure.
Conclusion: This well validated procedure was successfully applied to determine propofol glucuronide in rat hair sample and can be applicable, with high potential, in the field of forensic toxicology especially with increasing abuse and accidental overdose of propofol.
Propofol glucuronide, hair sample, centrifugal devices, LC-MS/MS, forensic, analysis.
College of Pharmacy, Kyungsung University, Busan 48434