Subcritical Water Chromatography with Electrochemical Detection

被引:1
|
作者
Anderson, Heather [1 ]
Yang, Yu [1 ]
机构
[1] East Carolina Univ, Dept Chem, Sci & Technol Bldg 584, Greenville, NC 27858 USA
关键词
subcritical water chromatography; hot water chromatography; electrochemical detection; neurotransmitters; nucleic acids; heterocyclic bases; capsaicinoids; TEMPERATURE LIQUID-CHROMATOGRAPHY; MAGNETIC-RESONANCE-SPECTROSCOPY; SUPERHEATED DEUTERIUM-OXIDE; FLAME IONIZATION DETECTION; MOBILE-PHASE; SEPARATION;
D O I
10.3390/molecules22060962
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Reverse phase liquid chromatography (RPLC) is a commonly used separation and analysis technique. RPLC typically employs mixtures of organic solvents and water or aqueous buffers as the mobile phase. With RPLC being used on a global scale, enormous quantities of organic solvents are consumed every day. In addition to the purchasing cost of the hazardous solvents, the issue of waste disposal is another concern. At ambient temperature, water is too polar to dissolve many organic substances. Therefore, although water is nontoxic it cannot be used to replace the mobile phase in RPLC since organic analytes will not be eluted. Subcritical water chromatography may be an alternative. The characteristics of water, such as polarity, surface tension, and viscosity, can be altered by manipulating water's temperature, thus making it behave like an organic solvent. The aim of this study was to evaluate the feasibility of separation using water mobile phase and detection by an electrochemical (EC) detector. The classes of analytes studied were neurotransmitters/metabolites, nucleic acids/heterocyclic bases, and capsaicinoids. Both isothermal and temperature-programmed separations were carried out. The separation temperature ranged from 25 to 100 degrees C. For separations of all three classes of solutes, the retention time was decreased with increasing temperature, thus shortening the analysis time. The peaks also became narrower as temperature increased. The limit of detection of neurotransmitters/metabolites ranges from 0.112 to 0.224 ppm.
引用
收藏
页数:13
相关论文
共 50 条
  • [1] Subcritical water chromatography with flame ionization detection
    Miller, DJ
    Hawthorne, SB
    ANALYTICAL CHEMISTRY, 1997, 69 (04) : 623 - 627
  • [2] Flame ionization detection after splitting the water effluent in subcritical water chromatography
    Yang, Y
    Jones, AD
    Mathis, JA
    Francis, MA
    JOURNAL OF CHROMATOGRAPHY A, 2002, 942 (1-2) : 231 - 236
  • [3] The Method Development of Subcritical Water Chromatography
    Su Yisong
    Jen Jen-Fon
    Zhang Weibing
    CHINESE JOURNAL OF CHROMATOGRAPHY, 2005, 23 (03) : 238 - 242
  • [4] Carbon dioxide modified subcritical water chromatography
    Fogwill, Michael O.
    Thurbide, Kevin B.
    JOURNAL OF CHROMATOGRAPHY A, 2008, 1200 (01) : 49 - 54
  • [5] Rapid column heating method for subcritical water chromatography
    Fogwill, Michael O.
    Thurbide, Kevin B.
    JOURNAL OF CHROMATOGRAPHY A, 2007, 1139 (02) : 199 - 205
  • [6] Retention mechanism of phenolic compounds in subcritical water chromatography
    Yichao Wu
    Xiuqing Deng
    Yinchun Mao
    Yan Zhang
    Jiaqin Liu
    Li Rong
    Zhihong Xu
    Chemical Research in Chinese Universities, 2015, 31 : 103 - 106
  • [7] Retention Mechanism of Phenolic Compounds in Subcritical Water Chromatography
    Wu Yichao
    Deng Xiuqing
    Mao Yinchun
    Zhang Yan
    Liu Jiaqin
    Rong Li
    Xu Zhihong
    CHEMICAL RESEARCH IN CHINESE UNIVERSITIES, 2015, 31 (01) : 103 - 106
  • [8] Subcritical water chromatography: A green approach to high-temperature liquid chromatography
    Yang, Yu
    JOURNAL OF SEPARATION SCIENCE, 2007, 30 (08) : 1131 - 1140
  • [9] Off-line coupling of subcritical water extraction with subcritical water chromatography via a sorbent trap and thermal desorption
    Lamm, LJ
    Yang, Y
    ANALYTICAL CHEMISTRY, 2003, 75 (10) : 2237 - 2242
  • [10] Retention mechanisms in subcritical water reversed-phase chromatography
    Allmon, Steven D.
    Dorsey, John G.
    JOURNAL OF CHROMATOGRAPHY A, 2009, 1216 (26) : 5106 - 5111