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作 者:李青翠[1,2] 张驰[1,2] 彭会明 夏桂珠[1,2]
机构地区:[1]北京医科大学药学院 [2]山西省药品检验所
出 处:《药学学报》1997年第8期635-637,共3页Acta Pharmaceutica Sinica
摘 要:毛细管气相色谱法测定人血清中二十二碳六烯酸的浓度李青翠张驰彭会明夏桂珠(北京医科大学药学院,北京100083;山西省药品检验所,太原030001)二十二碳六烯酸(cis4,7,10,13,16,19docosahexenoicacid,D...A reliable CGC method was developed for the determination of docosahexenoic acid (DHA) in human serum. The serum sample was acidified by adding two drops of 4 5 mol·L -1 H 2SO 4, and DHA was extracted from serum using ethyl acetate. The extract was evaporated to dryness under nitrogen stream. To each residue, 1 ml 1 3 mol·L -1 methanolic hydrogen chloride solution was added and the mixture was allowed to stand for 30 min in 60℃ water bath. After derivatization, the mixture was extracted with 1 ml of n hexane. The solvent was evaporated under a stream of nitrogen to dryness and the residue was dissolved in 30 μl n hexane and subjected to capillary GC, which was equipped with a fused silica capillary column (26 3 m×0 25 mm ID) coated with FFAP (free fatty acid phase, 0 1 μm film thickness). Tricosanoic acid was used as an internal standard. The retention time of DHA M and internal standard was 23 41 min and 20 79 min, respectively. The minimum detection concentration of DHA in serum was 40 ng·ml -1 with a serum volume of 200 μl and S/N value of 2. A good linear relationship between the peak area ratios and concentrations was found at the DHA concentrations ranging from 25 to 200 μg·ml -1 . The within day and between day precision was 5% and 9%, respectively.
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