首页> 外文期刊>Forensic science international >Effect of post-mortem changes on peripheral and central whole blood and tissue clozapine and norclozapine concentrations in the domestic pig (Sus scrofa).
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Effect of post-mortem changes on peripheral and central whole blood and tissue clozapine and norclozapine concentrations in the domestic pig (Sus scrofa).

机译:验尸变化对家猪(Sus scrofa)外周和中央全血及组织中氯氮平和去氯氮平浓度的影响。

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Interpretation of the results of psychoactive or other drug measurements in post-mortem blood specimens may not be straightforward, in part because analyte concentrations in blood may change after death. There is also the issue of comparability of plasma (or serum) results to those obtained in whole blood. To investigate these problems with respect to clozapine, this drug (10mg/kg daily) was given orally to two pigs. Blood was collected 3h post-dose on day 7, the animals were sacrificed, and blood taken from central and peripheral veins for up to 48h after death. Tissue samples were also collected immediately after death and at 48h. Ante-mortem whole blood clozapine/N-desmethylclozapine (norclozapine) concentrations were 0.86/1.07 and 1.11/1.15mg/l in pigs 1 and 2, respectively. Blood clozapine and norclozapine concentrations generally increased after death (central vein: clozapine up to 300%, norclozapine up to 460%; peripheral vein: clozapine up to 155%, norclozapine up to 185%). Initial blood and kidney clozapine and norclozapine concentrations were comparable in both animals, but were some two-fold higher in heart, liver and striated muscle in pig 2. In both animals, the heart and striated muscle clozapine and norclozapine concentrations had increased some two- to three-fold at 48h, whilst the liver and kidney concentrations were essentially unchanged. The reason for the increase in heart and striated muscle concentrations at 48h is unclear, but could be simple variation in sample site. The plasma:whole blood distribution of clozapine and norclozapine was studied in vitro. In human blood (one volunteer donor, haematocrit 0.50) the plots of plasma versus whole blood concentration were linear for both analytes across the range 0.1-1.5mg/l, although clozapine favoured plasma (plasma:whole blood ratio=1.12), whereas norclozapine favoured whole blood (ratio 0.68). In pig blood, the plots of plasma versus whole blood were non-linear in both cases, although clozapine favoured plasma to a greater extent thannorclozapine. This may be due to lower plasma clozapine and norclozapine protein binding capacity in the pig as compared to man.
机译:死后血液样本中精神活性或其他药物测量结果的解释可能并不直接,部分原因是死后血液中的分析物浓度可能会发生变化。还存在血浆(或血清)结果与全血中获得的结果可比性的问题。为了研究氯氮平的这些问题,将这种药物(每天10mg / kg)口服给两只猪。给药后第3天,在第7天采血,处死动物,死后从中心静脉和外周静脉采血长达48小时。死后和第48小时也收集组织样本。猪1和2的宰前全血氯氮平/ N-去甲基氯氮平(去氯氮平)浓度分别为0.86 / 1.07和1.11 / 1.15mg / l。死亡后血液中的氯氮平和去甲氯氮平的浓度通常会增加(中心静脉:氯氮平高达300%,去甲氯氮平高达460%;外周静脉:氯氮平高达155%,去氯氮平高达185%)。两只动物的初始血液和肾脏的氯氮平和去氯氮平浓度相当,但是猪2的心脏,肝脏和横纹肌中的氯氮平和去甲氯氮平浓度高两倍。在两只动物中,氯氮平和去甲氯氮平的心脏和横纹肌浓度都增加了约两倍。在48h时达到3倍,而肝脏和肾脏的浓度基本不变。 48小时心脏和横纹肌浓度增加的原因尚不清楚,但可能是样品部位的简单变化。体外研究了氯氮平和去甲氯氮平的血浆:全血分布。在人血中(一名自愿供血者,血细胞比容为0.50),两种分析物的血浆浓度对全血浓度的曲线在0.1-1.5mg / l范围内呈线性关系,尽管氯氮平偏爱血浆(血浆:全血比= 1.12),而氯氮平偏爱偏爱全血(比率0.68)。在猪血中,两种情况下血浆与全血的关系图都是非线性的,尽管氯氮平比诺氯氮平更倾向于血浆。与人相比,这可能是由于猪中血浆氯氮平和去氯氮平的结合能力较低。

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