4.8 Article

Mini 12, Miniature Mass Spectrometer for Clinical and Other Applications-Introduction and Characterization

Journal

ANALYTICAL CHEMISTRY
Volume 86, Issue 6, Pages 2909-2916

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ac403766c

Keywords

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Funding

  1. National Science Foundation [CHE 0847205, DBI 0852740]
  2. National Center for Research Resources [5R21RR031246-03]
  3. National Institute of General Medical Sciences from the National Institutes of Health [8 R21 GM103454, 1R01GM106016]
  4. Alfred Mann Institute at Purdue University

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A benchtop miniature mass spectrometer system, Mini 12, with ambient ionization source and tandem mass spectrometry capabilities has been developed and characterized. This instrument was developed as a self-contained system to produce quantitative results for unprocessed samples of small volumes including nonvolatile analytes. The ion processing system, vacuum system, and control system are detailed. An integrated sample loading system facilitates automated operation. A user interface has been developed to acquire and to interpret analytical results for personnel who have limited mass spectrometry knowledge. Peak widths of Delta m/z 0.6 Th (full width at half-maximum) and a mass range of up to m/z 900 are demonstrated with the rectilinear ion trap mass analyzer. Multistage experiments up to MS5 are accomplished. Consumable cartridges have been designed for use in ambient paper spray ionization, and the recently developed extraction spray ionization method has been employed to improve the quantitative performance. Monitoring of trace-levels of chemicals in therapeutic drugs, as well as in food safety and environmental protection operations is demonstrated. Dual MS/MS scans are implemented to obtain the intensities of the fragment ions from the analyte and its internal standard, and the ratio is used in quantitative analysis of complex samples: Limits of quantitation (LOQ) of 7.5 ng/mL, with relative standard deviations below 10%, have been obtained for selected therapeutic drugs in whole blood throughout their individual therapeutic ranges.

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