Abstract

Oral colon-targeted gel beads containing isoliquiritigenin (ISL) were successfully designed in our study. In order to further explore the targeting of the colon by the gel beads, a systematic study of their in vivo pharmacokinetics and colon targeting was performed in mice. Eighteen male mice were included in this study. The mice were separated into six groups at random. We collected blood, stomach, duodenum, jejunum, ileum, and colon tissues at 2, 4, 6, 8, 12, and 24h after oral administration of gel beads containing isoliquiritigenin at a dose of 20mg/kg. Gel beads in tissues were recorded and taken out to observe their swelling and erosion. The total ISL concentrations in different tissues and gel beads were analyzed by high-performance liquid chromatography. All gel beads reached the upper part of the stomach at 2h with no obvious swelling. Most of the gel beads were still in the lower part of stomach, while a small amount had reached the small intestine at 4h. A few gel beads reached the colon and swelled at 6h. Furthermore, the gel beads in the colon were swollen and erosive at 8h. Meanwhile, the plasma ISL concentration could be detected, which indicated that the ISL in the gel beads was absorbed. At 12h, the gel beads were almost dissolved and the plasma concentration was 8.33 times that at 8 h. At 24h, the gel beads had completely disappeared, and the plasma concentration was 2.55 times that at 12h. The gel beads containing ISL are a sustained, controlled, and colon-targeting delivery system that can alter the ISL distribution in the gastrointestinal tract.

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