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作 者:喻振文 高欣[2] 房中则[3] 曹云峰[3] 孙晓宇[3] 洪沫 王东[1]
机构地区:[1]辽宁中医药大学药学院,辽宁大连116600 [2]军事医学科学院附属医院临床药理实验室,北京100071 [3]辽宁医学院附属第一医院转化医学中心,辽宁锦州121000
出 处:《转化医学电子杂志》2014年第3期129-132,共4页E-Journal of Translational Medicine
摘 要:目的:通过建立快速高效的UFLC—MS/MS方法同时检测分析胆汁酸类化合物,以便于更好地定量分析胆汁酸的在体水平.方法:以甘草次酸为内标,采用超高效液相与质谱联用技术同时测定13个胆汁酸类化合物,并评价该方法的精密度,准确度,及线性范围.结果:建立了能同时检测以甘草次酸为内标13个胆汁酸化合物的UFLC/MS/MS检测方法,各成分分离度好,13种胆汁酸的浓度在1~20000nmol/L的浓度范围有良好的线性关系;r在0.995—0.999之间;检出限为0.065—9.37nmol/L;方法的日内和日间准确度在97%-105%之间,日间日内精密度均小于8%.结论:建立的UFLC/MS/MS方法灵敏度高,特异性好,适用于胆汁酸体外的分析研究.AIM: To quantitative analyze the level of bile acids in vivo, a rapid and efficient UFLC-MS/MS analysis method was performed to detect multiple bile acids. METHODS: Compound glycyrrhetinic acid was used as the internal standard (IS). Ultrafast liquid chromatography-mass spectrometry technology was applied to simultaneously detect 13 bile acids compounds. Also the accuracy, precision and the linear range of the method was assessed. RESULTS: An UFLC/MS/MS analysis method which could respectively detect 13 bile acids and IS glycyrrhetinic was established. All 13 bile acids compounds were obtained well linear relationship with concentration range of 1 - 20000 nmol/L. The limit of detection (LOD) were defined 0. 065 - 9.37 nmol/L. The intra- and inter-day accuracy ranged from 97% - 105%, and the intra- and inter-day precision were all less than 8%. CONCLUSION: The UFLC/MS/MS method with good sensitivity and selectivity could be applied to investigate bile acids in vitro.
关 键 词:胆汁酸 超高效液相与质谱联用 分析方法开发
分 类 号:R917[医药卫生—药物分析学]
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