Veigure Rūta, Aro Rudolf, Metsvaht Tuuli, Standing Joseph F, Lutsar Irja, Herodes Koit, Kipper Karin
University of Tartu, Institute of Chemistry, 14a Ravila Street, 50411 Tartu, Estonia.
Tartu University Hospital, Lunini 6, 51014 Tartu Estonia.
J Chromatogr B Analyt Technol Biomed Life Sci. 2017 May 1;1052:150-157. doi: 10.1016/j.jchromb.2017.03.007. Epub 2017 Mar 10.
In intensive care units, the precise administration of sedatives and analgesics is crucial in order to avoid under- or over sedation and for appropriate pain control. Both can be harmful to the patient, causing side effects or pain and suffering. This is especially important in the case of pediatric patients, and dose-response relationships require studies using pharmacokinetic-pharmacodynamic modeling. The aim of this work was to develop and validate a rapid ultra-high performance liquid chromatographic-tandem mass spectrometric method for the analysis of three common sedative and analgesic agents: morphine, clonidine and midazolam, and their metabolites (morphine-3-glucuronide, morphine-6-glucuronide and 1'-hydroxymidazolam) in blood plasma at trace level concentrations. Low concentrations and low sampling volumes may be expected in pediatric patients; we report the lowest limit of quantification for all analytes as 0.05ng/mL using only 100μL of blood plasma. The analytes were separated chromatographically using the C18 column with the weak ion-pairing additive 1,1,1,3,3,3-hexafluoro-2-propanol and methanol. The method was fully validated and a matrix matched calibration range of 0.05-250ng/mL was attained for all analytes In addition, between-day accuracy for all analytes remained within 93-108%, and precision remained within 1.5-9.6% for all analytes at all concentration levels over the calibration range.
在重症监护病房,精确给予镇静剂和镇痛药对于避免镇静不足或过度以及实现适当的疼痛控制至关重要。这两者对患者都可能有害,会导致副作用或疼痛与痛苦。这在儿科患者中尤为重要,剂量 - 反应关系需要采用药代动力学 - 药效学建模进行研究。本研究的目的是开发并验证一种快速超高效液相色谱 - 串联质谱法,用于分析血浆中痕量浓度的三种常见镇静和镇痛药物:吗啡、可乐定和咪达唑仑及其代谢物(吗啡 - 3 - 葡萄糖醛酸苷、吗啡 - 6 - 葡萄糖醛酸苷和1'-羟基咪达唑仑)。儿科患者可能预期有低浓度和低采样量;我们报告所有分析物仅使用100μL血浆时的最低定量限为0.05ng/mL。使用带有弱离子对添加剂1,1,1,3,3,3 - 六氟 - 2 - 丙醇和甲醇的C18柱对分析物进行色谱分离。该方法经过充分验证,所有分析物的基质匹配校准范围为0.05 - 250ng/mL。此外,在校准范围内所有浓度水平下,所有分析物的日间准确度保持在93 - 108%以内,精密度保持在1.5 - 9.6%以内。