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Quantitative MALDI Imaging of Spatial Distributions and Dynamic Changes of Tetrandrine in Multiple Organs of Rats

机译:粉防己碱在大鼠多器官中的空间分布和动态变化的定量MALDI成像

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摘要

Detailed spatio-temporal information on drug distribution in organs is of paramount importance to assess drug clinically-relevant properties and potential side-effects. Matrix-assisted laser desorption/ionization mass spectrometry imaging (MALDI MSI) as a label-free and sensitive imaging modality provides an additional means of accurately visualizing drug and its metabolites distributions in tissue sections. However, technical limitations, complex physiochemical environment of surface and low abundance of target drugs make quantitative MALDI imaging of drug and its metabolites quite challenging.>Methods: In this study, an internal standard correction strategy was applied for quantitative MALDI imaging of tetrandrine in multiple organs of rats including lung, liver, kidney, spleen, and heart. The feasibility and reliability of the developed quantitative MSI method were validated by conventional liquid chromatography-tandem MS (LC-MS/MS) analysis, and the two methods showed a significant correlation.>Results: The quantitative MALDI imaging method met the requirements of specificity, sensitivity and linearity. Tissue-specific spatio-temporal distribution patterns of tetrandrine in different organs were revealed after intravenous administration in the rat. Moreover, demethylated metabolite was detected in liver tissues.>Conclusions: The current work illustrates that quantitative MALDI imaging provides an alternative means of accurately addressing the problem of drug and its metabolites distribution in tissues, complementary to traditional LC-MS/MS of tissue homogenates and whole-body autoradiography (WBA). Quantitative spatio-chemical information obtained here can improve our understanding of pharmacokinetics (PK), pharmacodynamics (PD), and potential transient toxicities of tetrandrine in organs, and possibly direct further optimization of drug properties to reduce drug-induced organ toxicity.
机译:关于器官中药物分布的详细时空信息对于评估药物临床相关特性和潜在副作用至关重要。基质辅助激光解吸/电离质谱成像(MALDI MSI)作为无标签且灵敏的成像方式,提供了一种精确可视化组织切片中药物及其代谢物分布的附加手段。但是,由于技术限制,表面复杂的物理化学环境以及目标药物的丰度低,使得药物及其代谢物的定量MALDI成像颇具挑战性。>方法:在本研究中,采用了内标校正策略进行定量粉防己碱在大鼠多个器官(包括肺,肝,肾,脾和心脏)中的MALDI成像。通过常规液相色谱-串联质谱(LC-MS / MS)分析验证了所开发的定量MSI方法的可行性和可靠性,并且两种方法显示出显着的相关性。>结果:MALDI定量成像该方法满足了特异性,灵敏度和线性的要求。大鼠静脉内注射粉防己碱后不同器官的组织特异性时空分布规律。此外,在肝脏组织中检测到了脱甲基代谢物。>结论:当前工作表明,定量MALDI成像提供了另一种准确解决药物及其代谢物在组织中分布问题的方法,与传统的LC-组织匀浆和全身放射自显影(WBA)的MS / MS。此处获得的定量时空化学信息可以增进我们对粉防己碱在器官中的药代动力学(PK),药效学(PD)和潜在的瞬时毒性的了解,并可能直接指导进一步的药物性能优化以降低药物诱导的器官毒性。

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