4.6 Article

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

Journal

JOURNAL OF CHROMATOGRAPHY A
Volume 1005, Issue 1-2, Pages 123-130

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/S0021-9673(03)00812-4

Keywords

microdialysis; affinity adsorbents; adenosine; oligonucleotides

Funding

  1. NIBIB NIH HHS [R37 EB003320] Funding Source: Medline
  2. NINDS NIH HHS [R01 NS038476] Funding Source: Medline

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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 mul of 1.2 muM adenosine could be injected onto the 150-mum I.D. X 7 cm long column without loss of adenosine. With UV absorbance detection, the detection limit was 30 nM or 120 fmol (4 mul 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 mul/min. (C) 2003 Elsevier B.V. All rights reserved.

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