Dawidowicz A L, Fornal E, Fijalkowska A
Department of Chemical Physics and Physicochemical Separation Methods, Faculty of Chemistry, Maria Curie Sklodowska University, 20-031 Lublin, pl. M. Curie-Sklodowskiej 3, Poland.
Biomed Chromatogr. 2000 Jun;14(4):249-55. doi: 10.1002/1099-0801(200006)14:4<249::AID-BMC981>3.0.CO;2-H.
Due to unsatisfactory equipment efficiency and the time consuming manual procedures of sample preparation, drug analyses in physiological fluids and tissues frequently have to be carried out a few days after the sample collection. This is especially the case with investigations which require the examination of materials for which a large number of samples is necessary. The paper deals with the influence of storing blood samples on the level of propofol in blood and plasma. Propofol (2,6-diisopropylphenol, Diprivan) is a very popular intravenous agent used both for the induction and the maintenance of anaesthesia in human and veterinary patients as well as in laboratory animals. The results obtained show that, due to distinct losses of propofol in samples during their storage, the comparison of data estimated for subsequent days after sampling can lead to misleading or even wrong conclusions. The speed of drug diminution depends both on the type of blood and the anticoagulant used. The established interdependencies between the change in the level of propofol in blood and plasma samples and their storage time show that analogous investigations of other pharmaceutical agents are necessary.
由于设备效率不尽人意以及样本制备的手工操作耗时,生理体液和组织中的药物分析常常不得不在样本采集几天后进行。对于那些需要检查大量样本材料的研究而言,情况尤其如此。本文探讨了血液样本储存对血液和血浆中丙泊酚水平的影响。丙泊酚(2,6 - 二异丙基苯酚,得普利麻)是一种非常常用的静脉麻醉剂,用于人类、兽医患者以及实验动物的麻醉诱导和维持。所得结果表明,由于样本储存期间丙泊酚明显损失,对采样后后续几天估计数据的比较可能会导致误导甚至错误的结论。药物减少的速度既取决于血液类型,也取决于所使用的抗凝剂。血液和血浆样本中丙泊酚水平变化与其储存时间之间已确定的相互关系表明,有必要对其他药剂进行类似研究。