Roscoe R M, Cooper J K, Hawes E M, Midha K K
J Pharm Sci. 1982 Jun;71(6):625-7. doi: 10.1002/jps.2600710607.
A GLC-nitrogen phosphorous detector (NPD) method for the quantitative determination of trifluoperazine in plasma is described. It depends on an organic extraction of trifluoperazine and the internal standard prochlorperazine from basified plasma. Following the extraction, the organic solvent is evaporated to dryness and the residue is reconstituted in a small volume of methyl alcohol. GLC analysis of aliquots of the methanolic solution using a NPD permitted the determination of 0.5 ng/ml of trifluoperazine in plasma. Standard curves for trifluoperazine over a concentration range of 0.5 to 15 ng/ml of plasma were linear with an overall variation coefficient of 5.3%. In isolated samples obtained from a normal healthy volunteer, application of this method to plasma concentration determinations after oral administration of a 5-mg trifluoperazine tablet, is demonstrated and compared with the concentrations obtained by GLC-mass spectrometry and radioimmunoassay procedures.
本文描述了一种用气相色谱 - 氮磷检测器(NPD)定量测定血浆中三氟拉嗪的方法。该方法基于从碱化血浆中对三氟拉嗪和内标物氯丙嗪进行有机萃取。萃取后,将有机溶剂蒸发至干,残余物用少量甲醇复溶。使用NPD对甲醇溶液的等分试样进行气相色谱分析,可测定血浆中0.5 ng/ml的三氟拉嗪。三氟拉嗪在血浆浓度范围为0.5至15 ng/ml时的标准曲线呈线性,总变异系数为5.3%。在从正常健康志愿者获取的分离样本中,展示了该方法在口服5 mg三氟拉嗪片剂后用于血浆浓度测定的情况,并与通过气相色谱 - 质谱联用和放射免疫测定法获得的浓度进行了比较。