McCartt A D, Ognibene T, Bench G, Turteltaub K
Center for Accelerator Mass Spectrometry (CAMS), Lawrence Livermore National Laboratory, United States.
Biology and Biotechnology Division, Lawrence Livermore National Laboratory, United States.
Nucl Instrum Methods Phys Res B. 2015 Oct 15;361:277-280. doi: 10.1016/j.nimb.2015.05.036.
Accelerator Mass Spectrometry (AMS) is the most sensitive method for quantitation of C in biological samples. This technology has been used in a variety of low dose, human health related studies over the last 20 years when very high sensitivity was needed. AMS helped pioneer these scientific methods, but its expensive facilities and requirements for highly trained technical staff have limited their proliferation. Quantification of C by cavity ring-down spectroscopy (CRDS) offers an approach that eliminates many of the shortcomings of an accelerator-based system and would supplement the use of AMS in biomedical research. Our initial prototype, using a non-ideal wavelength laser and under suboptimal experimental conditions, has a 3.5-modern, 1- precision for detection of milligram-sized, carbon-14-elevated samples. These results demonstrate proof of principle and provided a starting point for the development of a spectrometer capable of biologically relevant sensitivities.
加速器质谱法(AMS)是定量分析生物样品中碳的最灵敏方法。在过去20年中,当需要极高灵敏度时,这项技术已被用于各种与低剂量人类健康相关的研究。AMS助力开创了这些科学方法,但其昂贵的设备以及对训练有素的技术人员的要求限制了它们的推广。采用光腔衰荡光谱法(CRDS)对碳进行定量分析提供了一种方法,该方法消除了基于加速器的系统的许多缺点,并将补充AMS在生物医学研究中的应用。我们最初的原型使用非理想波长的激光器,且在非最佳实验条件下,对于毫克级、碳-14含量升高的样品检测具有3.5倍现代水平、1倍精度。这些结果证明了原理的可行性,并为开发具有生物相关灵敏度的光谱仪提供了一个起点。