Giese R W, Vouros P
Department of Medicinal Chemistry, Northeastern University, Boston, MA 02115.
Res Rep Health Eff Inst. 1993 Oct(61):1-25; discussion 27-36.
The measurement of DNA adducts in human samples is at an early stage. The accuracy of some of the current measurements is not defined, the structures are unknown for a significant number of the adducts that have been detected, and there is little information about how many adducts remain to be discovered. This is due largely to the trace amounts of human DNA adducts in any sample. A consequence of this is that the true potential of DNA adducts as indicators of exposure and risk in human toxicology is far from realized. Mass spectrometry, a powerful technique for organic analysis, is the key to exploiting fully the usefulness of human DNA adducts as biomarkers of human exposure and risk. Mass spectrometry can make accurate measurements, discover unknown compounds, and determine the structures of these unknown compounds. However, the trace (very small) amounts of human DNA adducts have limited mass spectrometry's usefulness in analyzing such samples. This project focused on increasing the sensitivity of mass spectrometry for measuring human DNA adducts. Advances in sensitivity have been achieved for two modes of mass spectrometry applied to standards related to DNA adducts: gas chromatography with electron-capture negative ion mass spectrometry, and fast-atom-bombardment mass spectrometry. These advances involve both sample preparation and instrument conditions.
人体样本中DNA加合物的测量尚处于早期阶段。目前一些测量方法的准确性尚未明确,大量已检测到的加合物结构未知,而且关于还有多少加合物有待发现的信息很少。这主要是由于任何样本中人体DNA加合物的含量都极少。其结果是,DNA加合物作为人体毒理学中暴露和风险指标的真正潜力远未实现。质谱分析法是一种强大的有机分析技术,是充分发挥人体DNA加合物作为人体暴露和风险生物标志物作用的关键。质谱分析法可以进行精确测量、发现未知化合物并确定这些未知化合物的结构。然而,痕量(非常少)的人体DNA加合物限制了质谱分析法在分析此类样本中的作用。该项目专注于提高质谱分析法测量人体DNA加合物的灵敏度。在应用于与DNA加合物相关标准物的两种质谱分析模式方面,灵敏度已取得进展:电子捕获负离子质谱气相色谱法和快原子轰击质谱分析法。这些进展涉及样品制备和仪器条件两方面。