An interface for direct analysis of (14)c in nonvolatile samples by accelerator mass spectrometry

We describe here apparatus and methods for direct analysis of (14)C in biological specimens by accelerator mass spectrometry (AMS). Liquid samples, including plasma and urine, are deposited by pipet into a bed of CuO powder that fills a space within a rigid, refractory support. Volatile components a...

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Veröffentlicht in:Analytical chemistry (Washington) 2004-01, Vol.76 (2), p.328-334
Hauptverfasser: Liberman, Rosa G, Tannenbaum, Steven R, Hughey, Barbara J, Shefer, Ruth E, Klinkowstein, Robert E, Prakash, Chandra, Harriman, Shawn P, Skipper, Paul L
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container_end_page 334
container_issue 2
container_start_page 328
container_title Analytical chemistry (Washington)
container_volume 76
creator Liberman, Rosa G
Tannenbaum, Steven R
Hughey, Barbara J
Shefer, Ruth E
Klinkowstein, Robert E
Prakash, Chandra
Harriman, Shawn P
Skipper, Paul L
description We describe here apparatus and methods for direct analysis of (14)C in biological specimens by accelerator mass spectrometry (AMS). Liquid samples, including plasma and urine, are deposited by pipet into a bed of CuO powder that fills a space within a rigid, refractory support. Volatile components are removed under reduced pressure prior to analysis. The CuO matrix is locally heated with an infrared laser while it is contained within a sealed chamber that is swept with He carrier gas. Heating induces combustion of the applied sample, and the carrier gas transports the CO(2) that is formed to the AMS instrument's ion source, which is appropriately modified for use with CO(2). A rodent study of drug clearance with [(14)C]-acetaminophen was performed to provide plasma and urine specimens, which were analyzed with this overall approach and by liquid scintillation counting for comparison. Results presented here confirm the potential utility of laser-induced sample combustion as an alternative to graphite production for AMS analysis of (14)C. Anticipated benefits of the present approach include reduced risk of sample cross-contamination, decreased analysis time, and greater compatibility with robotics.
doi_str_mv 10.1021/ac030181y
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subjects Acetaminophen - blood
Acetaminophen - pharmacokinetics
Acetaminophen - urine
Animals
Carbon Dioxide - chemistry
Carbon Radioisotopes - blood
Carbon Radioisotopes - pharmacokinetics
Carbon Radioisotopes - urine
Copper - chemistry
Female
Heating - methods
Lasers
Male
Mass Spectrometry - instrumentation
Mass Spectrometry - methods
Oxidation-Reduction
Rats
Rats, Sprague-Dawley
Reproducibility of Results
Scintillation Counting
title An interface for direct analysis of (14)c in nonvolatile samples by accelerator mass spectrometry
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