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生物医学加速器质谱法中¹⁴C同位素测量的当前视角

Current perspectives of 14C-isotope measurement in biomedical accelerator mass spectrometry.

作者信息

Lappin Graham, Garner R Colin

机构信息

Xceleron Ltd, York Biocentre, Innovation Way, York, YO10 5NY, UK.

出版信息

Anal Bioanal Chem. 2004 Jan;378(2):356-64. doi: 10.1007/s00216-003-2348-5. Epub 2003 Nov 18.

Abstract

Accelerator mass spectrometry (AMS) is an extremely sensitive nuclear physics technique developed in the mid-70's for radiocarbon dating of historical artefacts. The technique centres round the use of a tandem Van de Graaff accelerator to generate the potential energy to permit separation of elemental isotopes at the single atom level. AMS was first used in the early 90's for the analysis of biological samples containing enriched 14C for toxicology and cancer research. Since that time biomedical AMS has been used in the study of (1) metabolism of xenobiotics in animals and humans (2) pathways of drug metabolism (3) biomarkers (4) metabolism of endogenous molecules including vitamins (5) DNA and protein binding studies and (6) clinical diagnosis. A new drug development concept which relies on the ultrasensitivity of AMS known as human microdosing (Phase 0) is being used to obtain early human metabolism information of candidate drugs arising out of discovery. These various aspects of AMS are reviewed in this article and a perspective on future applications of AMS provided.

摘要

加速器质谱法(AMS)是一种极其灵敏的核物理技术,于20世纪70年代中期开发,用于对历史文物进行放射性碳年代测定。该技术的核心是使用串联范德格拉夫加速器来产生势能,以便在单原子水平上分离元素同位素。AMS于20世纪90年代初首次用于分析含有富集14C的生物样品,用于毒理学和癌症研究。从那时起,生物医学AMS已被用于研究(1)动物和人类中异生素的代谢(2)药物代谢途径(3)生物标志物(4)包括维生素在内的内源性分子的代谢(5)DNA和蛋白质结合研究以及(6)临床诊断。一种依赖于AMS超灵敏度的新药开发概念,即人类微剂量给药(0期),正被用于获取发现阶段产生的候选药物的早期人体代谢信息。本文对AMS的这些不同方面进行了综述,并对AMS的未来应用提供了展望。

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