Mallet A I, Cunningham F M
Biochem Biophys Res Commun. 1985 Jan 16;126(1):192-8. doi: 10.1016/0006-291x(85)90590-x.
Platelet activating factor was isolated from the lesional scale of psoriatic patients using the method described by Bligh and Dyer (8). The extract was subjected to thin layer chromatography, and the region of the plate co-migrating with platelet activating factor removed. A portion of each sample was assayed for aggregating activity using washed guinea-pig platelets and the remainder treated with phospholipase C, derivatised, and subjected to reversed phase high performance liquid chromatography. Fractions were analysed for platelet activating factor using capillary gas chromatography-mass spectrometry. Nanogram quantities of platelet activating factor were recovered from 100 mg scale and both the C16 and C18 alkyl substituents were present in the ratio 3:1, C16:C18.
采用布莱和戴尔(8)描述的方法,从银屑病患者的皮损鳞屑中分离出血小板活化因子。提取物进行薄层层析,将薄板上与血小板活化因子共迁移的区域刮下。每个样品的一部分用洗涤过的豚鼠血小板检测聚集活性,其余部分用磷脂酶C处理、衍生化,然后进行反相高效液相色谱分析。用毛细管气相色谱-质谱法分析各馏分中的血小板活化因子。从100mg鳞屑中回收了纳克量的血小板活化因子,C16和C18烷基取代基的比例为3:1,即C16:C18。