[超高效液相色谱-三重四极杆质谱法测定心脏组织中的腺苷含量]。

Zuoyin Zhu, Wenbo Guo, Hanke Zhao, Jie Wang, Junhua Yang, Xinli Zhou
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引用次数: 0

摘要

建立并验证了一种基于超高效液相色谱-三重四极杆质谱(UPLC-MS/MS)快速、准确测定心脏组织中腺苷(Ado)含量的方法,该方法灵敏度高、特异性强。将样品溶解在 1 mL 含有 10 μmol/L 2-hydroxy-3-nonyladenine hydrochloride (EHNA) 作为稳定剂的超纯水中,低温研磨 2 分钟,然后在冰水浴中以 60 Hz 超声提取 40 分钟。以甲醇和5 mmol/L乙酸铵溶液为流动相,流速0.4 mL/min,柱温40 ℃,进样量3 μL。在多反应监测(MRM)模式下,采用电喷雾离子化(ESI)正离子切换对心脏组织中的阿杜进行定性和定量分析。采用溶剂标准曲线和外标法对阿朵进行准确定量。结果表明,阿杜在心脏组织中的基质效应非常低。在 0.1-160 ng/mL 范围内线性关系良好,相关系数(r2)为 0.9930。检出限(LOD)和定量限(LOQ)分别为 0.03 和 0.1 ng/mL。在低、中、高三个加标水平下,小鼠心脏组织中阿杜的加标回收率分别为 113.6%、96.3% 和 102.9%。日内重复性(RSD)为 1.7%-8.4%,日间重现性(RSD)为 2.6%-7.4%。从相关性和一致性结果来看,拟议的 UPLC-MS/MS 方法与双抗体夹心法之间存在正偏差。此外,这两种方法检测到的阿朵含量呈显著正相关(P<0.0001)。本实验室采集了 17 只小鼠和 17 只大鼠的心脏组织样本并进行了检测。采用所开发的 UPLC-MS/MS 方法测定的小鼠和大鼠心脏组织中的阿杜含量范围分别为 3.25-8.78 mg/kg 和 10.24-15.19 mg/kg(腺苷平均含量分别为 5.37 和 12.60 mg/kg)。该方法简便、准确、灵敏,适用于心脏组织中阿杜的检测。它还为心脏临床研究和疾病诊断提供了重要的技术支持。
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[Determination of adenosine content in heart tissue by ultra performance liquid chromatography-triple quadrupole mass spectrometry].
A method based on ultra performance liquid chromatography-triple quadrupole mass spectrometry (UPLC-MS/MS) was developed and validated for the rapid and accurate determination of adenosine (Ado) in cardiac tissues with high sensitivity and specificity. The samples were dissolved in 1 mL of ultrapure water containing 10 μmol/L 2-hydroxy-3-nonyladenine hydrochloride (EHNA) as a stabilizer, ground at low temperature for 2 min, and then ultrasonically extracted at 60 Hz in an ice-water bath for 40 min. Methanol and 5 mmol/L ammonium acetate solution were used as the mobile phases under a flow rate of 0.4 mL/min, a column temperature of 40 ℃ and an injection volume of 3 μL. The Ado in cardiac tissue was qualitatively and quantitatively analyzed by electrospray ionization (ESI) positive-ion-switching in multiple reaction monitoring (MRM) mode. A solvent standard curve and the external standard method were used for the accurate quantification of Ado. The results showed that the matrix effect of Ado in cardiac tissue was very low. A good linear relationship was obtained in the range of 0.1-160 ng/mL, and the correlation coefficient (r2) was 0.9930. The limits of detection (LOD) and quantification (LOQ) were 0.03 and 0.1 ng/mL, respectively. The spiked recoveries of Ado in murine cardiac tissue were 113.6%, 96.3%, and 102.9% at three spiked levels of low, medium, and high, respectively. The intra-day repeatability (RSDs) were 1.7%-8.4%, and the inter-day reproducibility (RSDs) were 2.6%-7.4%. Based on the correlation and consistency results, a positive bias was observed between the proposed UPLC-MS/MS method and the double-antibody sandwich method. Moreover, the Ado contents detected by these two methods were significantly positively correlated (P<0.0001). Cardiac tissue samples were collected from 17 mice and 17 rats and detected in our laboratory. The content ranges of Ado in the cardiac tissues of mice and rats determined by the developed UPLC-MS/MS method were 3.25-8.78 mg/kg and 10.24-15.19 mg/kg, respectively (average adenosine contents: 5.37 and 12.60 mg/kg, respectively). The developed method is simple, accurate, sensitive, and it is suitable for the determination of Ado in cardiac tissues. It also provides important technical support for cardiac clinical research and disease diagnosis.
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