Key Laboratory of Eco-chemical Engineering Ministry of Education, College of Chemistry and Molecular Engineering, Qingdao University of Science and Technology, Zhengzhou Road 53, Sifang, Qingdao 266042, China.
J Chromatogr B Analyt Technol Biomed Life Sci. 2010 May 1;878(15-16):1093-7. doi: 10.1016/j.jchromb.2010.03.017. Epub 2010 Mar 18.
In this paper, the amount of ascorbic acid (AA) in single rat peritoneal mast cell was determined by the method of capillary electrophoresis (CE) with electrochemical detection (ED) at a carbon fiber microdisk bundle electrode. The CE-ED system and the single-cell injection system were rearranged to make the operation more convenient and efficient. In the experiment, a self-made holder made of foam was used to keep the capillary from swing, which kept the stability of the baseline of the electropherogram. The single cell was lysed completely within 5s using the 0.1% sodium dodecylsulfate (SDS) as the cell lysis solution together with the lysis voltage of 2 kV. The quantitation analysis was accomplished by the use of calibration curves, and the amount of AA in single rat peritoneal mast cell was from 2.4 to 7.1 fmol.
本文采用碳纤维微盘束电极电化学检测毛细管电泳法(CE-ED)测定了单个大鼠腹腔肥大细胞中的抗坏血酸(AA)含量。对 CE-ED 系统和单细胞进样系统进行了重新排列,使操作更加方便、高效。在实验中,使用自制的泡沫固定器来保持毛细管的稳定,防止其摆动,从而保持电泳图谱基线的稳定性。0.1%十二烷基硫酸钠(SDS)作为细胞裂解液,裂解电压为 2 kV,可在 5s 内完全裂解单个细胞。通过使用校准曲线进行定量分析,单个大鼠腹腔肥大细胞中的 AA 含量为 2.4 至 7.1 fmol。