Ohkubo T, Osanai T, Sugawara K, Ishida M, Otani K, Mihara K, Yasui N
Department of Pharmacy, Hirosaki University Hospital, Japan.
J Pharm Pharmacol. 1995 Apr;47(4):340-4. doi: 10.1111/j.2042-7158.1995.tb05806.x.
A high-performance liquid chromatographic (HPLC) assay was developed for the determination of trazodone and its metabolite, 1-m-chlorophenylpiperazine (m-CPP), in plasma. The high level of trazodone in plasma was detected by ultraviolet absorbance at 254 nm and the low level of m-CPP in plasma was detected by coulometric electrochemical detection at 840 mV on the series arrangement of two detectors. Pilsicainide as an internal standard for both compounds was monitored by both detectors. Trazodone and m-CPP in plasma were extracted by a rapid and simple procedure based on CN bonded-phase extraction, and C8 reversed-phase HPLC separation. Determination was possible for trazodone in the concentration range 100-2000 ng mL-1 and for m-CPP in the concentration range 5-100 ng mL-1. The recoveries of trazodone and m-CPP added to plasma were 81.0-84.2 and 68.0-73.2%, respectively, with coefficients of variation of less than 7.3 and 8.2%, respectively. The method is applicable to high level monitoring of trazodone and low level monitoring of m-CPP in plasma of healthy volunteers and patients treated with trazodone.
建立了一种高效液相色谱(HPLC)法,用于测定血浆中曲唑酮及其代谢物1-间氯苯基哌嗪(m-CPP)。血浆中高浓度的曲唑酮通过在254nm处的紫外吸光度检测,血浆中低浓度的m-CPP通过在两个检测器串联配置下840mV的库仑电化学检测来测定。两种化合物均以吡西卡尼作为内标,由两个检测器进行监测。血浆中的曲唑酮和m-CPP采用基于氰基键合相萃取和C8反相HPLC分离的快速简便方法进行萃取。曲唑酮在100-2000 ng mL-1浓度范围内、m-CPP在5-100 ng mL-1浓度范围内均可进行测定。添加到血浆中的曲唑酮和m-CPP的回收率分别为81.0-84.2%和68.0-73.2%,变异系数分别小于7.3%和8.2%。该方法适用于健康志愿者和接受曲唑酮治疗患者血浆中曲唑酮的高浓度监测及m-CPP的低浓度监测。