Björkman S, Stanski D R
Department of Anesthesia, Stanford University School of Medicine, CA 94305.
J Chromatogr. 1988 Dec 9;433:95-104. doi: 10.1016/s0378-4347(00)80588-5.
Fentanyl and alfentanil were determined in blood and in thirteen tissues from rats by gas chromatography, with splitless injections on a fused-silica capillary column and nitrogen-selective detection. Sufentanil was used as the internal standard for both drugs and the acetyl analogue of sufentanil was used as an external standard to quantitate extraction recoveries. The extraction solvent was isopentanol-pentane (1:49) and a back-extraction into 0.1 M hydrochloric acid was used for sample clean-up. The extraction recoveries from tissue homogenates averaged 88% for fentanyl, 72% for alfentanil and 87% for sufentanil. The standard curves were linear over a range of 0.5-800 ng per sample for both drugs and the coefficients of variation for eight determinations of the drugs in tissue homogenates were 2-9% at 0.8-32 ng per sample. Assays of tissues from rats treated with simultaneous intravenous infusions of fentanyl and alfentanil confirmed the high precision and sensitivity of the method, which should therefore prove feasible for studies of the tissue distribution of these opioids.
采用气相色谱法,在熔融石英毛细管柱上进行不分流进样并采用氮选择性检测,测定大鼠血液及13种组织中的芬太尼和阿芬太尼。舒芬太尼用作两种药物的内标,舒芬太尼的乙酰类似物用作外标以定量提取回收率。提取溶剂为异戊醇 - 戊烷(1:49),并采用反萃取至0.1 M盐酸中进行样品净化。组织匀浆中芬太尼的提取回收率平均为88%,阿芬太尼为72%,舒芬太尼为87%。两种药物的标准曲线在每个样品0.5 - 800 ng范围内呈线性,组织匀浆中药物八次测定的变异系数在每个样品0.8 - 32 ng时为2 - 9%。对同时静脉输注芬太尼和阿芬太尼的大鼠组织进行的测定证实了该方法的高精度和高灵敏度,因此该方法对于研究这些阿片类药物的组织分布应是可行的。