Stavchansky S, Loper A
J Pharm Sci. 1982 Feb;71(2):194-6. doi: 10.1002/jps.2600710214.
A method for quantitating phencyclidine in the blood serum of rhesus monkeys with a solvent extraction procedure followed by gas chromatography with nitrogen-phosphorous detection is reported. Phencyclidine was extracted with ether from 0.5 ml of serum (pH 13.5) made basic with 2M NaOH, followed by back-extraction into 0.5 M sulfuric acid. After the addition of 2 M sodium hydroxide, phencyclidine was extracted into a small volume of ether for concentration and injection into the gas chromatograph. The limit of quantitation of phencyclidine in serum was 5 ng/ml. Recovery averaged 51.9 +/- 4.3%. Standard curves were linear between 5-50 ng/ml and 100-2000 ng/ml. Comparison between serum and aqueous standards indicated no interference by serum components in the extraction procedure. Pentobarbital, caffeine, and the monohydroxy metabolites of phencyclidine did not interfere with the analysis. This procedure is a rapid and sensitive method for determination of serum phencyclidine levels in animal studies requiring analysis of large numbers of samples.
报道了一种用溶剂萃取法随后进行氮磷检测气相色谱法测定恒河猴血清中苯环利定的方法。用2M氢氧化钠将0.5ml血清(pH 13.5)碱化后,用乙醚萃取苯环利定,然后反萃取到0.5M硫酸中。加入2M氢氧化钠后,将苯环利定萃取到少量乙醚中进行浓缩并注入气相色谱仪。血清中苯环利定的定量限为5ng/ml。回收率平均为51.9±4.3%。标准曲线在5-50ng/ml和100-2000ng/ml之间呈线性。血清标准品与水标准品的比较表明,血清成分在萃取过程中无干扰。戊巴比妥、咖啡因和苯环利定的单羟基代谢物不干扰分析。该方法是一种快速、灵敏的方法,用于在需要分析大量样品的动物研究中测定血清苯环利定水平。