HPLC法检测人血浆中枸橼酸坦度螺酮的浓度  

HPLC determination of tandospirone citrate in human plasma

作　　者：胡爱萍[1] 

机构地区：[1]温州医学院药学院药理学教研室,温州325027

出　　处：《药物分析杂志》2006年第12期1751-1753,共3页Chinese Journal of Pharmaceutical Analysis

摘　　要：目的:建立反相高效液相色谱内标法测定人血浆中枸橼酸坦度螺酮的浓度。方法:枸橼酸坦度螺酮血浆样品加入奥卡西平内标液,经2 mol·L^(-1)碳酸钠碱化后用乙酸乙酯-正己烷(4:1)一步提取,上清液于50℃水浴氮气吹干。色谱柱:Hyper-sil C_(18)(4.6 mm×250 mm,5μm,Agilent);流动相:乙腈-水-0.15 mol·L^(-1)磷酸二氢钠缓冲液(pH=3.0)(33:62:5);流速:0.8 mL·min^(-1);检测波长:239 nm;柱温:35℃。结果:枸橼酸坦度螺酮在0.02～5.0μg·mL^(-1)范围内线性关系良好(r=0.9994),定量下限为0.02μg·mL^(-1)。相对回收率98.6%～99.8%,提取回收率83.2%～92.3%,日内和日间 RSD 分别为2.9%～4.9%和3.8%～5.1%。结论:本法简便、准确、灵敏度高,适用于枸橼酸坦度螺酮的临床血药浓度检测及药代动力学研究。Objective：To establish an RP - HPLC method for the determination of tandospirone citrate in human plasma. Methods： After addition of oxcarbazepine （ internal standard ） , tandospirone citrate was extracted from human plasma with ethyl acetate - n-hexane （4：1 ）after alkalified by 2 mol·L^-1 Na2 CO3, the supernatant was evaporated at 50℃. The analytical column was packed with Hypersil C18 （4.6 mm ×250mm,5μm,Agilent）. The mobile phase was acetonitrile - water - 0. 15 mol·L^- 1 NaH2PO4 solution （ pH = 3.0 ） （ 33 ： 62 ： 5 ）, the flow rate was 0.8 mL· min^-1 ,the UV absorbanee wavelength was 239 nm ,and the column temperature was 35 ℃. Results ：The calibration curve was in good linearity in the range of 0.02 - 5.0μg·mL^-1 （ r = 0. 9994 ）. The quantitation limit was 0.02 μg·mL^-1. The relative recovery of method was 98.6% -99. 8%. The extraction recovery was 83.2% - 92.3%. Within - day precision （RSD） was 2.9% -4.9%, between - day precision （RSD） was 3.8% - 5. 1%. Conclusion： The method is convenient, accurate, sensitive, and is suitable for the determination of tandospirone citrate in human plasma and pharmacokinetic studies.

关 键 词：枸橼酸坦度螺酮 药物动力学 血浆 高效液相色谱法 

分 类 号：R917[医药卫生—药物分析学]