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神经科学与加速器质谱分析法

Neuroscience and accelerator mass spectrometry.

作者信息

Palmblad Magnus, Buchholz Bruce A, Hillegonds Darren J, Vogel John S

机构信息

Center for Accelerator Mass Spectrometry, Lawrence Livermore National Laboratory, Livermore, California 94551, USA.

出版信息

J Mass Spectrom. 2005 Feb;40(2):154-9. doi: 10.1002/jms.734.

Abstract

Accelerator mass spectrometry (AMS) is a mass spectrometric method for quantifying rare isotopes. It has had a great impact in geochronology and archaeology and is now being applied in biomedicine. AMS measures radioisotopes such as 3H, 14C, 26Al, 36Cl and 41Ca, with zepto- or attomole sensitivity and high precision and throughput, allowing safe human pharmacokinetic studies involving microgram doses, agents having low bioavailability or toxicology studies where administered doses must be kept low (<1 microg kg(-1)). It is used to study long-term pharmacokinetics, to identify biomolecular interactions, to determine chronic and low-dose effects or molecular targets of neurotoxic substances, to quantify transport across the blood-brain barrier and to resolve molecular turnover rates in the human brain on the time-scale of decades. We review here how AMS is applied in neurotoxicology and neuroscience.

摘要

加速器质谱法(AMS)是一种用于定量稀有同位素的质谱方法。它在地质年代学和考古学领域产生了重大影响,目前正在生物医学中得到应用。AMS可测量诸如³H、¹⁴C、²⁶Al、³⁶Cl和⁴¹Ca等放射性同位素,具有zepto或attomole级别的灵敏度、高精度和高通量,能够进行涉及微克剂量的安全人体药代动力学研究、生物利用度低的药物研究或毒理学研究(给药剂量必须保持在低水平,<1微克/千克⁻¹)。它用于研究长期药代动力学、识别生物分子相互作用、确定神经毒性物质的慢性和低剂量效应或分子靶点、量化血脑屏障的转运以及在数十年的时间尺度上解析人类大脑中的分子更新率。我们在此回顾AMS在神经毒理学和神经科学中的应用情况。

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