Absorption and excretion of iodixanol after intragastric administration to rats.

J A Dunkel, I F Helund, P B Jacobsen, D Grant, P Walday, H Refsum
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引用次数: 5

Abstract

Absorption and excretion of iodixanol 320 mg I/ml were investigated in rats after intragastric administration of 2.5 g I/kg b.w. Animals were observed for up to 96 hours after treatment, and blood, urine and feces taken at several time-points throughout the experiment. Concentrations of iodixanol in serum and urine were measured by means of reversed-phase high-performance liquid chromatography. Fecal concentrations of iodixanol, based on iodine measurements, were determined by X-ray fluorescence spectrometry. Serial radiographs were obtained and histopathological examination was performed on selected tissues. The results indicate that less than 1% of the intragastric dose of iodixanol is absorbed from the intestine into the blood stream. No adverse clinical signs were observed, and there were no treatment-related histomorphological findings.

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大鼠灌胃后碘沙醇的吸收和排泄。
以2.5 g I/kg b.w灌胃碘沙醇320 mg I/ml后,研究大鼠对碘沙醇的吸收和排泄情况。在给药后观察动物长达96小时,并在实验过程中的多个时间点采集血液、尿液和粪便。采用反相高效液相色谱法测定血清和尿液中碘沙醇的浓度。基于碘的测量,用x射线荧光光谱法测定了粪便中碘二醇的浓度。获得一系列x线片并对选定组织进行组织病理学检查。结果表明,只有不到1%的灌胃剂量的碘沙醇从肠道吸收进入血液。没有观察到不良临床症状,也没有治疗相关的组织形态学发现。
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