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机构地区:[1]济南军区总医院血液科,250031 [2]济南军区总医院神经内科,250031 [3]济南军区药检所
出 处:《中国微循环》1999年第1期55-56,共2页Journal of Chinese Microcirculation
摘 要:目的探讨红细胞膜磷脂组分的高效液相测定方法。方法选用 Spherisorb硅胶色谱柱,流动相为乙腈-甲醇-85%磷酸(100:10:1.8V/V/V),波长203nm。结果4分钟内完全分离膜的四种磷脂组分磷脂酰丝氨酸(PS)、磷脂酰乙醇胺(PE)、磷脂酰胆碱(PC)和神经鞘磷脂(SM),最低检出限为1μg/ml,至少在4μg-2000μg/ml范围内标准品浓度与峰面积积分值呈线性关系,PS、PE、PC、SM的回收率分别为98.1±2.3%、99.8±0.7%、99.4±1.8%、90.6±2.2%。结论本法适于临床检测和科研探索。Objective To study the method for the quantification of human erythrocyte membrane phospholipid classes by high performance liquid chromatography. Methods The separation was performed on Spherisorb SI silica gel columns with a mobile phase of acetonitrile-methanol -85% phosphoric acid (100: 10: 1. 8 V/V/V) and UV detection at 203nm. Results Complete separation of phosphatidylserine (PS), phosphatidylethanolamin (PE), phosphatidylcholine (PC) and sphingomyelin (SM) was achieved within 4 minutes. The detection limit is 1μg/ml. The phospholipid concentrations and the peak-area values exhibited a linear relationship at least in the range 4-2000μg/ml.The recoveries of PS,PE,PC and SM were 98.1±2.3%, 99.8±0.7%, 99.4±1.8% and 90.6±2.2% respectively. Conclusion This method is suitable for clinical determination and scientific research.
分 类 号:R329.26[医药卫生—人体解剖和组织胚胎学] Q545.03[医药卫生—基础医学]
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