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An Interface for the Direct Coupling of Small Liquid Samples to AMS
T J Ognibene1, A T Thomas1, P F Daley1
1Center for Accelerator Mass Spectrometry, Lawrence Livermore National Laboratory, 7000 East Ave, Livermore, CA 94551.
A new moving wire interface enables Accelerator Mass Spectrometry (AMS) analysis of liquid samples. This technology precisely measures small amounts of carbon-14 (14C) in biochemical research, expanding capabilities for analyzing minute samples.
Area of Science:
- Analytical Chemistry
- Biochemistry
- Nuclear Science
Background:
- Accelerator Mass Spectrometry (AMS) is a powerful technique for isotope ratio measurements.
- Analysis of nonvolatile liquid samples, especially in biomedical research, presents unique challenges for AMS.
Purpose of the Study:
- To introduce and characterize a novel moving wire interface for AMS analysis of nonvolatile liquid samples.
- To enable the analysis of discrete liquid drops and direct output from chromatographic separations.
- To expand the capabilities of AMS for biomedical applications requiring the measurement of trace biochemicals.
Main Methods:
- Development and implementation of a moving wire interface coupled to a 1-MV AMS system.
- Analysis of discrete liquid samples and samples from high-performance liquid chromatography (HPLC).
- Quantification of carbon (C) and radiocarbon (14C) content with focus on precision and dynamic range.
Main Results:
- The system can measure discrete samples with as little as 50 zeptomoles (zmol) of 14C.
- Achieved precision of 3-5% for 14C measurements in minutes.
- Demonstrated a dynamic range of approximately three orders of magnitude.
- Minimized sample-to-sample memory effects through optimized procedures.
Conclusions:
- The moving wire interface is a viable technology for the AMS analysis of nonvolatile liquid samples.
- This advancement significantly enhances the capacity for low-level biochemical analysis in extremely small samples.
- The technology is expected to broaden the scope of biomedical AMS research, particularly for trace analyte detection.
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