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新型 LC-MS/MS 测定法测定脓毒性休克时的血浆缓激肽浓度。

Plasma bradykinin concentrations during septic shock determined by a novel LC-MS/MS assay.

机构信息

HUSLAB, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.

Division of Intensive Care Medicine, Department of Anesthesiology, Intensive Care and Pain Medicine, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.

出版信息

Clin Chim Acta. 2019 Jun;493:20-24. doi: 10.1016/j.cca.2019.02.023. Epub 2019 Feb 22.

Abstract

BACKGROUND

Bradykinin is an important mediator of inflammation and vascular permeability and could have an important role in the development of septic shock. Measurement of bradykinin by immunological methods may suffer from interference and lack of specificity. We developed and validated a liquid chromatography mass spectrometry assay (LC-MS/MS) for plasma bradykinin.

METHODS

We used plasma samples from healthy volunteers (n = 19) and patients with septic shock (n = 47). Stable isotope bradykinin internal standard was added to samples before solid-phase extraction and quantification by LC-MS/MS. Stability of bradykinin was studied for 12 months.

RESULTS

Our assay has good sensitivity (0.1 nmol/l) and a wide linear range (0.1-1000 nmol/l). Bradykinin added to plasma was stable for 12 months at -20 °C when a mixture of protease inhibitors was added at sampling but degraded during repeated freezing and thawing. Bradykinin concentration in plasma from septic shock patients (<0.1-0.6 nmol/l) did not change significantly during shock and recovery but differed slightly from that in healthy individuals (0.5-1.1 nmol/l).

CONCLUSIONS

Our bradykinin assay was successfully used to determine bradykinin concentrations in plasma samples. Intensive care unit patients with septic shock had low concentrations of plasma bradykinin during both shock and recovery phases.

摘要

背景

缓激肽是炎症和血管通透性的重要介质,在脓毒性休克的发展中可能具有重要作用。免疫学法测量缓激肽可能会受到干扰和缺乏特异性的影响。我们开发并验证了一种用于检测血浆中缓激肽的液相色谱-质谱联用(LC-MS/MS)方法。

方法

我们使用了来自健康志愿者(n=19)和脓毒性休克患者(n=47)的血浆样本。在固相萃取和 LC-MS/MS 定量之前,向样本中加入稳定同位素标记的缓激肽内标。研究了缓激肽的稳定性达 12 个月。

结果

我们的检测方法具有良好的灵敏度(0.1 nmol/L)和宽线性范围(0.1-1000 nmol/L)。在采样时加入蛋白酶抑制剂混合物,缓激肽在 -20°C 下可稳定保存 12 个月,但在反复冷冻和解冻过程中会降解。脓毒性休克患者血浆中缓激肽浓度(<0.1-0.6 nmol/L)在休克和恢复期间没有明显变化,但略低于健康个体(0.5-1.1 nmol/L)。

结论

我们的缓激肽检测方法成功地用于确定血浆样本中的缓激肽浓度。脓毒性休克的重症监护病房患者在休克和恢复阶段血浆中缓激肽浓度均较低。

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