Xia Tianyi, Gao Shouhong, Shu Chang, Wen Yan, Yun Yunlei, Tao Xia, Chen Wansheng, Zhang Feng
Department of Pharmacy, Changzheng Hospital, Second Military Medical University, Shanghai 200003, PR China.
Department of Pharmacy, Changzheng Hospital, Second Military Medical University, Shanghai 200003, PR China.
Clin Biochem. 2016 Dec;49(18):1372-1378. doi: 10.1016/j.clinbiochem.2016.09.018. Epub 2016 Sep 30.
To investigate potential interferences of two pre-analytical variables, the storage time and the vacutainer tube, on the quantification of 20 amino acids using a UHPLC-MS/MS method.
Blood samples from 25 apparently healthy subjects were collected into duplicate sets of EDTA-2K, EDTA-3K, coagulation, heparin and citrate tubes, and stored in capped vacutainer tubes at 4°C for 6h, 12h and 24h before sample analysis. A UHPLC-MS/MS method was established for simultaneous quantification of 20 amino acids. ANOVA for repeated measurement was conducted based on the model of Mauchly's test of Sphericity. Student's t-test was applied for comparison between amino acid concentrations obtained from different vacutainer tubes, and consistency of the results was checked through Bland-Altman difference plots and Passing-Bablok regression analysis.
Most of the 20 amino acids showed a least concentration fluctuation with storage time in heparin plasma, followed by EDTA-3K and citrate plasma. The amino acid concentrations were significantly lower in citrate plasma and slightly higher in serum, compared with those in heparin plasma. No fixed bias was observed for amino acid concentrations in EDTA and heparin plasma, but the differences were mostly of statistical significance. Amino acid concentrations in EDTA-3K plasma achieved a good consistency with those in heparin plasma by UHPLC-MS/MS analysis.
Storage time and vacutainer tube were important variables for amino acid analysis. They should draw researchers' attention and then be controlled in good laboratory practice to reduce pre-analytical errors.
采用超高效液相色谱-串联质谱法(UHPLC-MS/MS)研究两个分析前变量,即储存时间和真空采血管,对20种氨基酸定量分析的潜在干扰。
采集25名表面健康受试者的血液样本,分装至乙二胺四乙酸二钾(EDTA-2K)、乙二胺四乙酸三钾(EDTA-3K)、凝血、肝素和枸橼酸盐真空管中,并在样本分析前于4℃下在加盖的真空采血管中储存6小时、12小时和24小时。建立了同时定量20种氨基酸的UHPLC-MS/MS方法。基于球形度的Mauchly检验模型进行重复测量方差分析。应用学生t检验比较不同真空采血管中获得的氨基酸浓度,并通过Bland-Altman差异图和Passing-Bablok回归分析检查结果的一致性。
在肝素血浆中,20种氨基酸中的大多数随储存时间的浓度波动最小,其次是EDTA-3K血浆和枸橼酸盐血浆。与肝素血浆相比,枸橼酸盐血浆中的氨基酸浓度显著降低,血清中的氨基酸浓度略高。在EDTA和肝素血浆中未观察到氨基酸浓度的固定偏差,但差异大多具有统计学意义。通过UHPLC-MS/MS分析,EDTA-3K血浆中的氨基酸浓度与肝素血浆中的氨基酸浓度具有良好的一致性。
储存时间和真空采血管是氨基酸分析的重要变量。它们应引起研究人员的注意,并在良好实验室规范中加以控制,以减少分析前误差。