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作 者:王晶[1,2] 董昕[3] 邹豪[1] 金磊[1] 张川
机构地区:[1]第二军医大学药学院新药研究中心,上海200433 [2]上海市中山医院青浦分院药剂科,上海201700 [3]第二军医大学药学院分析测试中心,上海200433
出 处:《药学实践杂志》2012年第1期52-54,共3页Journal of Pharmaceutical Practice
基 金:上海市中药现代化专项基金(08DZ1970802)
摘 要:目的建立液质联用色谱法(HPLC-MS/MS)测定SD大鼠肝脏组织中丹参素钠的浓度。方法肝脏组织样品制成匀浆后,加入内标酮洛芬,采用液液萃取方法进行预处理。色谱柱:Diamonsil C18柱(200 mm×4.6 mm,5μm);流动相:甲醇-水(含0.01‰甲酸)(80∶20);流速:1.0 ml/min;质谱条件:采用ESI离子源,负离子检测,选择MRM测定丹参素钠和酮洛芬197→135 m/z和253→209 m/z。结果丹参素钠在20.2~1 010 ng/ml检测浓度范围内呈良好的线性关系(r=0.999 8),最低定量限为20.2 ng/ml,日内精密度和日间精密度的RSD<10%,回收率在92%~107%之间。结论该方法灵敏度高、快速、简单、准确,适用于肝脏组织样品中丹参素钠的含量测定,可以满足药动学研究的需要。Objective To establish a HPLC-MS/MS method for determination of sodium Danshensu in SD rat liver. Methods Tissue samples were pretreated by liquid-liquid extraction method after homogenate, and ketoprofen was used as the internal standard. Analytical column was D iamonsil C18 (200 mm × 4.6 mm, 5 μm). The mobile phase was methanol: water(0.01%v formic acid) = 80 : 20 with flow rate as 1.0 ml/min. Mass spectrum determination was performed in the MRM mode with target ions m/z 197→135 (Sodium Danshensu) , m/z 253→209 (ketoprofen) , using ESI ion resource and negative ion detection. Results The calibration curve was linear over the range of 20.2 - 1 010 ng/ml. The LLOQ of sodium Danshensu in liver was 20.2 ng/ml. The intra-and inter-day RSD were both less than 10%. The extracted recovery rate ranged from 92% to 107%. Conclusion The method was sensitive, rapid, simple and accu- rate to determine sodium Danshensu distribution in rat liver and was suitable for preclinical test of Sodium Danshensu.
分 类 号:R917[医药卫生—药物分析学]
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