Islam Ariful, Sakamoto Takumi, Zhai Qing, Rahman Md Muedur, Mamun Md Al, Takahashi Yutaka, Kahyo Tomoaki, Setou Mitsutoshi
Department of Cellular & Molecular Anatomy, Hamamatsu University School of Medicine, Hamamatsu, Shizuoka 431-3192, Japan.
Preppers Co., Ltd., Hamamatsu University School of Medicine, Hamamatsu, Shizuoka 431-3192, Japan.
Pharmaceuticals (Basel). 2022 Oct 25;15(11):1314. doi: 10.3390/ph15111314.
Mass spectrometry imaging (MSI) is well-known for the non-labeling visualization of analytes, including drugs and their metabolites in biological samples. In this study, we applied three different tools of MSI, desorption electrospray ionization (DESI)-MSI, matrix-assisted laser desorption ionization (MALDI)-MSI, and a newly developed atmospheric pressure (AP)-MALDI-MSI known as iMScope QT for rapid mapping of imipramine, chloroquine, and their metabolites in C57BL/6 male wild-type mice. Among three MSI tools, better detection capability for targeted drugs at higher speed (up to 32 pixels/s) was observed in iMScope QT. It revealed that imipramine and its metabolites were significantly accumulated in the renal cortex of mice, but chloroquine and its metabolites were highly accumulated in the renal pelvis and renal medulla of mice. Additionally, a higher accumulation of imipramine was noted in the thalamus, hypothalamus, septum, and hindbrain of mice brains. However, chloroquine and its metabolites showed notable accumulation in the lateral ventricle, fourth ventricle, and fornix of the mice brains. These findings of our study can be helpful in understanding clinically relevant properties, efficacy, and potential side effects of these drugs. Our study also showed the potentiality of iMScope QT for rapid mapping of small drugs and their metabolites in biological samples.
质谱成像(MSI)以对生物样品中的分析物(包括药物及其代谢物)进行非标记可视化而闻名。在本研究中,我们应用了三种不同的MSI工具,解吸电喷雾电离(DESI)-MSI、基质辅助激光解吸电离(MALDI)-MSI以及一种新开发的大气压(AP)-MALDI-MSI,即iMScope QT,用于快速绘制C57BL/6雄性野生型小鼠体内的丙咪嗪、氯喹及其代谢物图谱。在这三种MSI工具中,iMScope QT在更高速度(高达32像素/秒)下对靶向药物具有更好的检测能力。结果显示,丙咪嗪及其代谢物在小鼠肾皮质中显著蓄积,但氯喹及其代谢物在小鼠肾盂和肾髓质中高度蓄积。此外,在小鼠脑的丘脑、下丘脑、隔区和后脑发现丙咪嗪有较高蓄积。然而,氯喹及其代谢物在小鼠脑的侧脑室、第四脑室和穹窿中显示出明显蓄积。我们的研究结果有助于理解这些药物的临床相关特性、疗效和潜在副作用。我们的研究还展示了iMScope QT在生物样品中快速绘制小分子药物及其代谢物图谱的潜力。