摘要
目的:建立人血浆帕珠沙星检测的高效液相色谱方法。方法:血浆经高氯酸沉淀,以Agilent TC-C_(18)为色谱柱;流动相为乙腈-0.1%三氟乙酸-水体系,流速为0.8 ml·min^(-1);检测波长314 nm。结果:帕珠沙星浓度在0.10~20.00 mg·L^(-1)范围内线性关系良好(r=0.999 8);高中低三个浓度(0.25,5.00,15.00 mg·L^(-1))的相对回收率分别为(101.47±4.53)%、(99.50±3.63)%和(100.71±3.33)%;日内RSD分别为3.12%、2.85%和2.63%,日间RSD分别为4.18%、3.29%和2.81%。结论:该方法简便、快速、准确可靠,适用于人血浆帕珠沙星浓度的测定及其药物动力学研究。
Objective: To develop an HPLC method for the determination of pazufloxacin in human plasma. Method: The human plasma samples were precipitated by perchloric acid. The analytical column was packed with an Agilent TC-C18 column. The mobile phase was acetonitrile-0. 1% trifluoroacetic acid-water and the flow rate was 0. 8 ml·min^-1. The UV detection wavelength was 314 nm. Result: Excellent linear relationship was obtained within the range of 0. 10 mg·min^-1to 20. 00 mg. L^- 1 (r = 0. 999 8 ). The relative recovery was ( 101.47 ± 4. 53 ) % , (99. 50 ± 3.63 ) % and ( 100. 71 ± 3.33 ) % , respectively for three concentrations (0. 25,5.00, 15.00 mg.L^-1 ) ,the intra-day RSD was 3.12% ,2. 85% and 2. 63% ,and the inter-day RSD was 4. 18% ,3.29% and 2. 81% ,respectively. Conclusion: The method is simple, rapid and accurate which can be used to determine pazufloxacin in human plasma and study its nharmacokinetics.
出处
《中国药师》
CAS
2011年第9期1304-1305,共2页
China Pharmacist