首页> 外文期刊>Journal of Pharmacological and Toxicological Methods >Mapping pharmaceuticals in tissues using MALDI imaging mass spectrometry.
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Mapping pharmaceuticals in tissues using MALDI imaging mass spectrometry.

机译:使用MALDI成像质谱法在组织中绘制药物图。

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摘要

During drug discovery and development stage, often the question is raised as to whether the drug can reach the site of action which helps researchers better assess the potential value of that compound as a pharmaceutical product and toxicological outcomes. High performance liquid chromatography coupled to a tandem mass spectrometer (HPLC-MS/MS) has totally replaced HPLC methods that use UV or other detectors for most drug analysis applications. However, HPLC-MS/MS approaches are not able to provide the answer to certain questions regarding the distribution of a drug in various organs or tissues from laboratory animal experiments. Whole body radioautography (WBA) normally provides a standard means to answer this question on the time course of the drug candidates. However, the major disadvantage in this radioautographic technique is to allow for visualization of total drug-related materials but to image the distribution of the administrated drugs and their metabolites in all tissues. In addition, the availability of radiolabeled compounds at drug discovery stage is another concern. To overcome these issues, matrix-assisted laser desorption/ionization-mass spectrometric method (MALDI-MS) has been developed to directly determine the distribution of pharmaceuticals in tissue sections which might unravel their disposition or biotransformation pathway for new drug development.
机译:在药物发现和开发阶段,通常会提出一个问题,即药物是否可以到达作用部位,这有助于研究人员更好地评估该化合物作为药物产品的潜在价值和毒理学结果。高效液相色谱联用串联质谱仪(HPLC-MS / MS)已完全取代了在大多数药物分析应用中使用UV或其他检测器的HPLC方法。但是,HPLC-MS / MS方法无法为实验室动物实验中有关药物在各种器官或组织中的分布的某些问题提供答案。全身放射自显影(WBA)通常提供一种标准方法来回答候选药物的时程问题。然而,这种放射自显影技术的主要缺点是允许可视化与药物有关的全部材料,但是对所给药的药物及其代谢物在所有组织中的分布成像。另外,在药物发现阶段放射性标记化合物的可用性是另一个问题。为克服这些问题,已开发出基质辅助激光解吸/电离质谱法(MALDI-MS),以直接确定药物在组织切片中的分布,这可能会破坏其处置方式或生物转化途径,从而开发新药物。

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