首页> 外文期刊>Journal of inherited metabolic disease >A rapid screening procedure for the diagnosis of peroxisomal disorders: quantification of very long-chain fatty acids, as dimethylaminoethyl esters, in plasma and blood spots, by electrospray tandem mass spectrometry.
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A rapid screening procedure for the diagnosis of peroxisomal disorders: quantification of very long-chain fatty acids, as dimethylaminoethyl esters, in plasma and blood spots, by electrospray tandem mass spectrometry.

机译:诊断过氧化物酶体紊乱的快速筛选程序:通过电喷雾串联质谱法定量测定血浆和血斑中的长链脂肪酸,如二甲基氨基乙基酯。

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摘要

A rapid method with potential to screen for many of the peroxisomal disorders using 5 microl of plasma or a 3-mm blood spot (3.6 microl blood impregnated on filter paper) is described. Fatty acids are liberated from plasma or blood spots and converted to dimethylaminoethyl esters. Trideuterated fatty acids, added as internal standards, are used to quantify eicosanoic (C20:0), docosanoic (C22:0), tetracosanoic (C24:0) and hexacosanoic (C26:0) acids by electrospray tandem mass spectrometry. The C26:0/C22:0 and C24:0/C22:0 ratios are significantly greater in the plasma of patients with peroxisomal disorders compared to controls. The C20:0/C22:0 ratio is elevated in the plasma of peroxisomal patients who accumulate phytanic acid. Blood spots collected from four peroxisomal patients between 2 and 10 days after birth and stored for up to 17 years, were shown to give between 33% and 233% higher C26:0/C22:0 ratios compared to age-matched controls.
机译:描述了一种快速的方法,该方法具有使用5微升血浆或3毫米血斑(3.6微升血液浸渍在滤纸上)筛查许多过氧化物酶体异常的潜力。脂肪酸从血浆或血斑中释放出来并转化为二甲基氨基乙基酯。作为内部标准物添加的三氘代脂肪酸用于通过电喷雾串联质谱法定量二十烷酸(C20:0),二十烷酸(C22:0),十四烷酸(C24:0)和十六烷酸(C26:0)。与对照组相比,过氧化物酶体紊乱患者血浆中的C26:0 / C22:0和C24:0 / C22:0比率明显更高。过氧化物酶体累积植酸的患者血浆中C20:0 / C22:0比率升高。与年龄匹配的对照组相比,在出生后2至10天之间从四名过氧化物酶体血症患者中收集的血斑保存了长达17年,结果显示它们的C26:0 / C22:0比值高出33%至233%。

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