State Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing, 210009, China.
School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing, 211198, China.
Theranostics. 2019 Jan 25;9(4):932-944. doi: 10.7150/thno.30408. eCollection 2019.
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. : 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. : 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. : 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.
详细的药物在器官中的分布时空信息对于评估药物的临床相关性质和潜在的副作用至关重要。基质辅助激光解吸/电离质谱成像(MALDI MSI)作为一种无标记和敏感的成像方式,为准确观察组织切片中的药物及其代谢物分布提供了额外的手段。然而,技术限制、表面复杂的物理化学环境和低丰度的靶药物使得药物及其代谢物的定量 MALDI 成像具有相当的挑战性。在这项研究中,应用内标校正策略对大鼠的多个器官(包括肺、肝、肾、脾和心脏)中的汉防己甲素进行定量 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,两种方法具有显著相关性。定量 MALDI 成像方法具有特异性、灵敏度和线性要求。在大鼠静脉给药后,揭示了汉防己甲素在不同器官中的组织特异性时空分布模式。此外,还在肝组织中检测到去甲基代谢物。目前的工作表明,定量 MALDI 成像提供了一种准确解决药物及其代谢物在组织中分布问题的替代方法,补充了组织匀浆的传统 LC-MS/MS 和全身放射自显影(WBA)。这里获得的定量时空化学信息可以提高我们对汉防己甲素在器官中的药代动力学(PK)、药效学(PD)和潜在瞬时毒性的理解,并可能直接指导进一步优化药物性质以减少药物引起的器官毒性。