Borgeat P, Picard S
Inflammation and Immunology-Rheumatology Research Unit, Le Centre Hospitalier de l'Université Laval, Sainte-Foy, Quebec, Canada.
Anal Biochem. 1988 Jun;171(2):283-9. doi: 10.1016/0003-2697(88)90487-3.
Variable recovery of polar compounds is a potential pitfall in the on-line extraction-reversed-phase HPLC analysis of lipoxygenase products. Therefore, the addition of a polar internal standard to biological samples, which permits the assessment of the recovery of the polar components in individual samples, appears to be essential. 19-Hydroxyprostaglandin (PG) B2 was found to be a suitable compound for this application. It was easily prepared from deproteinized human semen by base-catalyzed dehydration of 19-hydroxy-PGE2, and purified in a single step by reversed-phase HPLC. Similarly to PGB2, already used as internal in HPLC, 19-hydroxy-PGB2 has excellent chemical stability and carries a strong uv chromophore that enables detection at 280 nm. Most importantly, it is eluted just prior to the polar arachidonic acid metabolites 20-hydroxy- and 20-carboxy-leukotriene B4, 12-oxo-dodecatrienoic acid and the lipoxines A and B. The measurement of the ratio of PGB2 and 19-hydroxy-PGB2 used in combination as internal standards in HPLC analysis of lipoxygenase products, provides a simple and reliable way to assess sample to sample recovery of the polar components when using on-line extraction procedures.
在脂氧合酶产物的在线萃取-反相高效液相色谱分析中,极性化合物回收率的变化是一个潜在的陷阱。因此,向生物样品中添加极性内标物显得至关重要,它可以评估各个样品中极性成分的回收率。19-羟基前列腺素(PG)B2被发现是适用于此应用的化合物。它可通过对去蛋白化的人类精液中的19-羟基-PGE2进行碱催化脱水反应轻松制备,并通过反相高效液相色谱一步纯化。与已用作高效液相色谱内标的PGB2类似,19-羟基-PGB2具有出色的化学稳定性,并带有一个强紫外发色团,能够在280nm处进行检测。最重要的是,它恰好在极性花生四烯酸代谢物20-羟基-和20-羧基-白三烯B4、12-氧代-十二碳三烯酸以及脂氧素A和B之前洗脱。在脂氧合酶产物的高效液相色谱分析中,将PGB2和19-羟基-PGB2组合用作内标物,通过测量它们的比例,为使用在线萃取程序时评估极性成分在样品间的回收率提供了一种简单可靠的方法。