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基质辅助激光解吸/电离质谱成像技术可视化非诺贝特在大鼠胃肠道中的转运过程。

Visualizing the Journey of Fenofibrate through the Rat Gastrointestinal Tract by Matrix-Assisted Laser Desorption/Ionization-Mass Spectrometry Imaging.

机构信息

Department of Pharmacy, Faculty of Health and Medical Sciences, University of Copenhagen, Universitetsparken 2, Copenhagen DK-2100, Denmark.

Bioneer: FARMA, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen DK-2100, Denmark.

出版信息

Mol Pharm. 2021 Jun 7;18(6):2189-2197. doi: 10.1021/acs.molpharmaceut.0c01043. Epub 2021 Apr 23.

Abstract

Mapping the spatial distribution of a drug throughout the gastrointestinal tract (GIT) after oral ingestion can provide novel insights into the interaction between the drug, the oral drug delivery system, and the GIT. Matrix-assisted laser desorption/ionization-mass spectrometry imaging (MALDI-MSI) is a molecular imaging technique that can analyze molecules in the cryosections of tissues, determining their localization with a spatial resolution of 10-100 μm. The overall aim of this study was to use MALDI-MSI to visualize the distribution and spatial location of a model prodrug (fenofibrate) through the rat GIT. Furthermore, the distribution and spatial colocalization of taurocholate and phospholipids in the rat GIT in relation to fenofibrate were investigated. Rats were given a fenofibrate suspension of 10 mg/mL by oral gavage. Blood samples were drawn, and the rats were euthanized at three different time points. The GIT was collected and frozen, and MALDI-MSI was applied on cross sections of the stomach and intestine. Fenofibrate was detected by MALDI-MSI throughout the GIT, which also revealed that fenofibrate was hydrolyzed to the active drug fenofibric acid already in the stomach. Furthermore, the presence of lyso-phosphatidylcholine (lyso-PC) and taurocholate was confirmed in the lumen of the small intestine. MALDI-MSI was shown to be a useful qualitative tool for localizing parent prodrugs and active drugs, with a possibility for gaining insight into not only the location for activation but also the role of endogenous molecules in the process.

摘要

口服后在整个胃肠道(GIT)中绘制药物的空间分布,可以为药物、口服药物传递系统和 GIT 之间的相互作用提供新的见解。基质辅助激光解吸/电离质谱成像(MALDI-MSI)是一种分子成像技术,可分析组织冷冻切片中的分子,以 10-100μm 的空间分辨率确定其定位。本研究的总体目标是使用 MALDI-MSI 可视化模型前药(非诺贝特)在大鼠 GIT 中的分布和空间位置。此外,还研究了牛磺胆酸盐和磷脂在大鼠 GIT 中的分布和空间共定位与非诺贝特的关系。大鼠通过口服灌胃给予 10mg/mL 的非诺贝特混悬液。抽取血液样本,并在三个不同时间点处死大鼠。收集 GIT 并冷冻,然后对胃和肠的横截面进行 MALDI-MSI 分析。通过 MALDI-MSI 在整个 GIT 中检测到非诺贝特,这也表明非诺贝特已经在胃中水解为活性药物非诺贝特酸。此外,在小肠腔中还证实了溶血磷脂酰胆碱(lyso-PC)和牛磺胆酸盐的存在。MALDI-MSI 被证明是一种有用的定性工具,可用于定位母体前药和活性药物,不仅有可能深入了解激活的位置,还可能了解内源性分子在该过程中的作用。

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