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以甲基纤维素作为有效的电渗流抑制剂,通过短端进样毛细管电泳检测细胞内三磷酸腺苷、二磷酸腺苷和一磷酸腺苷

Intracellular adenosine 5'-triphosphate, adenosine 5'-diphosphate, and adenosine 5'-monophosphate detection by short-end injection capillary electrophoresis using methylcellulose as the effective electroosmostic flow suppressor.

作者信息

Zinellu Angelo, Sotgia Salvatore, Pasciu Valeria, Madeddu Manuela, Leoni Giovanni Giuseppe, Naitana Salvatore, Deiana Luca, Carru Ciriaco

机构信息

Department of Biomedical Sciences, University of Sassari, Sassari, Italy.

出版信息

Electrophoresis. 2008 Jul;29(14):3069-73. doi: 10.1002/elps.200800033.

Abstract

We present a new rapid CE method to measure adenine nucleotides adenosine 5'-triphosphate (ATP), adenosine 5'-diphosphate (ADP), and adenosine 5'-monophosphate (AMP) in cells. The short-end injection mode allows a decrease in the analysis time by injecting samples at the outlet end of a silica capillary closest to the detection window, reducing the migration distance. Moreover, the use of methylcellulose (MC) as run buffer additive to suppress EOF permits to further reduce the migration times of analytes. Thus, when a capillary with an effective length of 10.2 cm was used with a 60 mmol/L sodium acetate buffer pH 3.80 in the presence of 0.01% of MC, the migration time of analytes were 1.35 min for ATP, 1.85 min for ADP, and 4.64 min for AMP. These conditions gave a good reproducibility for intra- and interassay (CV <4 and 8%, respectively) and all the procedure demonstrated an excellent analytical recovery (from 98.3 to 99 %). The method suitability was proved both on red blood cells and in spermatozoa. We compared our proposed method to a spectrophotometric assay, by measuring ATP levels in 40 spermatozoa samples. The obtained data were analyzed by the Passing and Bablok regression and Bland-Altman test.

摘要

我们提出了一种新的快速毛细管电泳方法,用于测量细胞中的腺嘌呤核苷酸三磷酸腺苷(ATP)、二磷酸腺苷(ADP)和一磷酸腺苷(AMP)。短端进样模式通过在最靠近检测窗口的硅胶毛细管出口端进样,减少了迁移距离,从而缩短了分析时间。此外,使用甲基纤维素(MC)作为运行缓冲添加剂来抑制电渗流,可进一步缩短分析物的迁移时间。因此,当使用有效长度为10.2 cm的毛细管,在含有0.01% MC的60 mmol/L醋酸钠缓冲液(pH 3.80)中时,ATP的迁移时间为1.35分钟,ADP为1.85分钟,AMP为4.64分钟。这些条件在批内和批间均具有良好的重现性(CV分别<4%和8%),并且整个过程显示出优异的分析回收率(98.3%至99%)。该方法在红细胞和精子中均得到了验证。我们通过测量40个精子样本中的ATP水平,将我们提出的方法与分光光度法进行了比较。所得数据通过Passing和Bablok回归以及Bland-Altman检验进行分析。

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