• Title of article

    Aptamer affinity chromatography for rapid assay of adenosine in microdialysis samples collected in vivo

  • Author/Authors

    Deng، نويسنده , , Qing and Watson، نويسنده , , Christopher J. and Kennedy، نويسنده , , Robert T.، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2003
  • Pages
    8
  • From page
    123
  • To page
    130
  • Abstract
    An anti-adenosine aptamer was evaluated as a stationary phase in packed capillary liquid chromatography. Using an aqueous mobile phase containing 20 mM Mg2+, adenosine was strongly retained on the column. A gradient of increasing Ni2+ (to 18 mM), which is presumed to complex with nitrogen atoms in adenosine involved in binding to the aptamer, eluted adenosine in a narrow zone. Up to 6 μl of 1.2 μM adenosine could be injected onto the 150-μm I.D.×7 cm long column without loss of adenosine. With UV absorbance detection, the detection limit was 30 nM or 120 fmol (4 μl injected). Samples could be repetitively injected with 4.6% relative standard deviation in peak area. Columns were stable to at least 200 injections. The adenosine assay, which required no sample preparation, was used on microdialysis samples collected from the somatosensory cortex of chloral hydrate anesthetized rats. Total analysis times were short enough that dialysate samples could be injected every 5 min. Basal dialysate concentrations of adenosine stabilized at 87±10 nM (n=5) with the probe operated at 0.6 μl/min.
  • Keywords
    adenosine , oligonucleotides
  • Journal title
    Journal of Chromatography A
  • Serial Year
    2003
  • Journal title
    Journal of Chromatography A
  • Record number

    1519379