Distribution of quetiapine between serum and whole blood in therapeutic drug monitoring specimens

IF 2.3 3区 医学 Q3 CHEMISTRY, ANALYTICAL Journal of analytical toxicology Pub Date : 2024-02-23 DOI:10.1093/jat/bkae006
Håvard Breivik, Mette Elise Tunset, Morten Brix Schou, Joachim Frost
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Abstract

Quetiapine use is on the rise, leading to a corresponding increase in acute intoxications, some of which have fatal outcomes. When assessing whole blood quetiapine concentrations during forensic autopsies, interpretations are primarily based on toxicity data from studies of serum concentrations. To our knowledge, there are only two previous studies that have attempted to establish the ratio between whole blood and serum quetiapine concentrations, with limited populations and high variability of results. Paired specimens of whole blood and serum from 16 quetiapine users recruited from the Psychiatric Clinic, St. Olav University Hospital were analyzed using LC-MSMS. Quetiapine concentrations in both matrices were determined and compared. The mean blood:serum ratio of quetiapine was 0.74 (SD = 0.05, 95% CI 0.71-0.76, p < 0.001), range 0.66-0.85. Simple linear regression showed strong linear correlation between quetiapine concentrations in the two matrices (B=0.774, p>0.001, r=0.999). Our results imply that quetiapine occurs at lower concentrations within erythrocytes than in plasma. This is most likely due to a high degree of plasma protein binding. Other factors which may influence the distribution of quetiapine between these compartments are solubility, metabolism and passive or active efflux mechanisms. We did not observe any covariation between blood:serum ratios and serum concentrations. Quetiapine was consistently present at lower concentrations in whole blood than in serum. If so inclined to, a conversion factor of approximately 0.7 may be considered for extrapolation of concentrations from serum to whole blood, at least in cases with therapeutic quetiapine concentration levels.
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治疗药物监测样本中奎硫平在血清和全血中的分布情况
喹硫平的使用呈上升趋势,导致急性中毒事件相应增加,其中一些会造成致命后果。在法医尸检中评估全血奎硫平浓度时,主要是根据血清浓度研究中的毒性数据进行解释。据我们所知,此前只有两项研究试图确定全血和血清中奎硫平浓度的比例,但研究对象有限,结果差异很大。我们使用 LC-MSMS 分析了从圣奥拉夫大学医院精神病诊所招募的 16 名奎硫平使用者的全血和血清配对标本。测定并比较了两种基质中的喹硫平浓度。喹硫平的平均血药浓度比为 0.74(SD = 0.05,95% CI 0.71-0.76,p < 0.001),范围为 0.66-0.85。简单线性回归结果显示,两种基质中的喹硫平浓度之间具有很强的线性相关性(B=0.774,p>0.001,r=0.999)。我们的研究结果表明,喹硫平在红细胞中的浓度低于血浆。这很可能是由于血浆蛋白结合度较高所致。可能影响喹硫平在这些区室之间分布的其他因素包括溶解度、新陈代谢以及被动或主动外流机制。我们没有观察到血液:血清比率与血清浓度之间存在任何共变。全血中的喹硫平浓度始终低于血清中的浓度。如果愿意,至少在治疗性喹硫平浓度水平的病例中,可以考虑使用约 0.7 的换算系数将血清中的浓度外推至全血中。
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来源期刊
CiteScore
5.10
自引率
20.00%
发文量
92
审稿时长
6-12 weeks
期刊介绍: The Journal of Analytical Toxicology (JAT) is an international toxicology journal devoted to the timely dissemination of scientific communications concerning potentially toxic substances and drug identification, isolation, and quantitation. Since its inception in 1977, the Journal of Analytical Toxicology has striven to present state-of-the-art techniques used in toxicology labs. The peer-review process provided by the distinguished members of the Editorial Advisory Board ensures the high-quality and integrity of articles published in the Journal of Analytical Toxicology. Timely presentation of the latest toxicology developments is ensured through Technical Notes, Case Reports, and Letters to the Editor.
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