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机构地区:[1]天津市中医医院,天津300140
出 处:《天津药学》2007年第3期25-26,共2页Tianjin Pharmacy
摘 要:目的:建立测定盐酸曲马朵血浆药物浓度的HPLC方法。方法:以非那西丁为内标,正己烷-乙酸乙酯(4:1)在碱性条件下提取血样中曲马朵,流动相为乙腈一KH2PO4(31:69),色谱柱为迪马C18柱,测定波长为218nm。结果:盐酸曲马朵在10—1000ng/nd范围内,标准曲线方程为Y=0.001392X-0.007136;提取血样中曲马朵平均回收率为(90.4±4.2)%;测定的日内和日问相对标准差(RSD)分别为3.0%-6.3%和4.4%-5.5%;室温(25℃)放置8h和冻融3次对血样中盐酸曲马朵测定没有明显影响。结论:本方法灵敏、准确、重复性好,可应用于含盐酸曲马朵制剂的临床药代动力学研究。OBJECTIVE To establish a HPLC method for determination of tramadol in plasma. Method : Plasma samples ( with phenacetin as internal standard ) were extracted with n - hexane/acetic ether ( 4 : 1 ) in alkaline condition and determining by HPLC. The mobile phase was composed of acetonitrile:buffer( 25 mmol/L KH2PO4 containing 0.15% triethylamine) = 31:69 ( V/V). The chromatographic procedure was carried out using Diamonsil C18 column(4.6 mm × 250 mm, 5 μm) and detection wavelength was at 218 nm. RESULT Tramadol HC1 concentration range was between 10 and 1 000 ng/ml, the average recoveries of tramadol HC1 were (90.4 ± 4.2 ) %. RSD of within day and between days were 3.0% - 6.3% and 4.4% - 5.5%. It had not significant influence that samples were stored in 25 ℃ for 8 h or freeze thawing three times. CONCLUSION The method was a sensitive, precise and repeatable. It could be applied in clinic pharmacokinetics.
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