Hipps P P, Eveland M R, Meyer E R, Sherman W R, Cicero T J
J Pharmacol Exp Ther. 1976 Mar;196(3):642-8.
Morphine levels in rat brain were measured by the multiple ion detection method (mass fragmentography), using a computer-controlled gas chromatograph-mass spectrometer, and were correlated with the analgesic activity of the narcotic at intervals up to 6 hours after the injection. Morphine levels in brain reached a peak of 346 ng/g of tissue wet weight 30 minutes after the subcutaneous injection of 10 mg/kg of morphine sulfate and then declined rapidly over the next 3 hours. Between 3 and 6 hours after the injection of morphine, the brain concentration decreased slightly but was still readily detectable at 6 hours after injection. An excellent correlation (r = 0.923) was found between the concentration of morphine in brain and analgesic activity, as measured by the hot plate method. The multiple ion detection method for the measurement of morphine appears to meet all of the criteria necessary for any drug assay: sensitivity, specificity and ease of analysis.
采用计算机控制的气相色谱 - 质谱仪,通过多离子检测法(质量碎片分析法)测定大鼠脑内的吗啡水平,并在注射后长达6小时的时间间隔内,将其与麻醉剂的镇痛活性进行关联。皮下注射10mg/kg硫酸吗啡后30分钟,脑内吗啡水平达到峰值,为346ng/g组织湿重,随后在接下来的3小时内迅速下降。注射吗啡后3至6小时,脑内浓度略有下降,但在注射后6小时仍可轻易检测到。通过热板法测定发现,脑内吗啡浓度与镇痛活性之间存在极好的相关性(r = 0.923)。用于测定吗啡的多离子检测法似乎满足任何药物分析所需的所有标准:灵敏度、特异性和分析简便性。