Whitmire D, Whitmire P S
Driftmier Engineering Center, University of Georgia, Athens 30602, USA.
Alcohol Alcohol. 1995 Sep;30(5):623-8.
Recovery of acetaldehyde (0-20 microM) or ethanol (0-50 mM) added to blood and subsequently treated with perchloric acid (PCA) was evaluated using head-space gas chromatography and compared with controls. Using blood from five dogs, < 100% of acetaldehyde and ethanol was recovered from PCA-treated samples. Mathematical models of putative binding mechanisms indicated acetaldehyde partitioned simply between supernatant and PCA-induced precipitate and occupied < 1% of acetaldehyde binding sites on precipitate; ethanol partitioned simply between supernatant and precipitate and occupied > 62% of ethanol binding sites. The mathematical model also indicated acetaldehyde binding is 2500-fold stronger than ethanol binding. These results indicate as much as 46.4% of acetaldehyde may be bound to PCA-induced precipitate formed in whole blood. This loss of acetaldehyde is 3- to 4-fold greater than acetaldehyde loss caused by evaporation from PCA-treated blood.
对添加到血液中随后用高氯酸(PCA)处理的乙醛(0 - 20微摩尔)或乙醇(0 - 50毫摩尔)的回收率进行了顶空气相色谱评估,并与对照组进行比较。使用五只狗的血液,PCA处理后的样品中乙醛和乙醇的回收率<100%。假定结合机制的数学模型表明,乙醛仅在上清液和PCA诱导的沉淀之间分配,且在沉淀上占据的乙醛结合位点<1%;乙醇仅在上清液和沉淀之间分配,且占据乙醇结合位点>62%。数学模型还表明乙醛结合比乙醇结合强2500倍。这些结果表明,高达46.4%的乙醛可能与全血中PCA诱导的沉淀结合。这种乙醛的损失比PCA处理血液蒸发导致的乙醛损失大3至4倍。