Laboratory of Pharmaco-Toxicological Analysis, Department of Pharmaceutical Sciences, Faculty of Pharmacy, Alma Mater Studiorum-University of Bologna, Via Belmeloro 6, I-40126 Bologna, Italy.
J Chromatogr B Analyt Technol Biomed Life Sci. 2011 Jan 15;879(2):167-73. doi: 10.1016/j.jchromb.2010.11.033. Epub 2010 Dec 4.
Risperidone is currently one of the most frequently prescribed atypical antipsychotic drugs; its main active metabolite 9-hydroxyrisperidone contributes significantly to the therapeutic effects observed. An original analytical method is presented for the simultaneous analysis of risperidone and the metabolite in plasma, urine and saliva by high-performance liquid chromatography coupled to an original sample pre-treatment procedure based on micro-extraction by packed sorbent (MEPS). The assays were carried out using a C8 reversed-phase column and a mobile phase composed of 73% (v/v) acidic phosphate buffer (30 mM, pH 3.0) containing 0.23% triethylamine and 27% (v/v) acetonitrile. The UV detector was set at 238 nm and diphenhydramine was used as the internal standard. The sample pre-treatment by MEPS was carried out on a C8 sorbent. The extraction yields values were higher than 92% for risperidone and 90% for 9-hydroxyrisperidone, with RSD for precision always lower than 7.9% for both analytes. Limit of quantification values in the different matrices were 4 ng/mL or lower for risperidone and 6 ng/mL or lower for the metabolite. The method was successfully applied to plasma, urine and saliva samples from psychotic patients undergoing therapy with risperidone, with satisfactory accuracy results (recovery>89%) and no interference from other drugs. Thus, the method seems to be suitable for the therapeutic drug monitoring of schizophrenic patients using the three different biological matrices plasma, urine and saliva.
利培酮是目前最常被开的非典型抗精神病药物之一;其主要的活性代谢物 9-羟基利培酮对观察到的治疗效果有重要贡献。本研究提出了一种新的分析方法,用于通过高效液相色谱法结合基于填充吸附剂微萃取(MEPS)的原始样品预处理程序,同时分析血浆、尿液和唾液中的利培酮和代谢物。该测定使用 C8 反相柱和由 73%(v/v)酸性磷酸盐缓冲液(30 mM,pH 3.0)组成的流动相进行,其中含有 0.23%三乙胺和 27%(v/v)乙腈。UV 检测器设置为 238nm,并用苯海拉明作为内标。MEPS 的样品预处理在 C8 吸附剂上进行。利培酮和 9-羟基利培酮的提取产率均高于 92%,精密度的 RSD 始终低于 7.9%。在不同基质中的定量限均为利培酮 4ng/mL 或更低,代谢物 6ng/mL 或更低。该方法成功应用于接受利培酮治疗的精神病患者的血浆、尿液和唾液样本,具有令人满意的准确度结果(回收率>89%),且无其他药物干扰。因此,该方法似乎适用于使用三种不同生物基质(血浆、尿液和唾液)对精神分裂症患者进行治疗药物监测。