Zhu Zuoyin, Guo Wenbo, Zhao Hanke, Wang Jie, Yang Junhua, Zhou Xinli
1. Institute for Agro-Food Standards and Testing Technology, Shanghai Academy of Agricultural Sciences, Shanghai 201403, China.
2. School of Health Science and Engineering, University of Shanghai for Science and Technology, Shanghai 200093, China.
Se Pu. 2024 Apr;42(4):345-351. doi: 10.3724/SP.J.1123.2023.09016.
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 () 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 (<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.
建立了一种基于超高效液相色谱 - 三重四极杆质谱联用仪(UPLC-MS/MS)的方法,并对其进行了验证,该方法能够快速、准确地测定心脏组织中的腺苷(Ado),具有高灵敏度和特异性。将样品溶解于1 mL含10 μmol/L盐酸2 - 羟基 - 3 - 壬基腺嘌呤(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,流速为0.4 mL/min,柱温为40℃,进样量为3 μL。采用电喷雾电离(ESI)正离子切换多反应监测(MRM)模式对心脏组织中的Ado进行定性和定量分析。采用溶剂标准曲线和外标法对Ado进行准确定量。结果表明,Ado在心脏组织中的基质效应非常低。在0.1 - 160 ng/mL范围内获得了良好的线性关系,相关系数()为0.9930。检测限(LOD)和定量限(LOQ)分别为0.03和0.1 ng/mL。在小鼠心脏组织中,Ado在低、中、高三个加标水平下的加标回收率分别为113.6%、96.3%和102.9%。日内重复性(RSDs)为1.7% - 8.4%,日间重现性(RSDs)为2.6% - 7.4%。基于相关性和一致性结果,所提出的UPLC-MS/MS方法与双抗体夹心法之间存在正偏差。此外,这两种方法检测的Ado含量呈显著正相关(<0.0001)。从17只小鼠和17只大鼠中采集心脏组织样本并在本实验室进行检测。采用所建立的UPLC-MS/MS方法测定小鼠和大鼠心脏组织中Ado的含量范围分别为3.25 - 8.78 mg/kg和10.24 - 15.19 mg/kg(平均腺苷含量分别为5.37和12.60 mg/kg)。所建立的方法简单、准确、灵敏,适用于心脏组织中Ado的测定。它也为心脏临床研究和疾病诊断提供了重要的技术支持。