Yang Qiong, Xing Maochen, Wang Ke, Wei Qiang, Zhao Jiarui, Wang Yuan, Ji Kai, Song Shuliang
Marine College, Shandong University, Weihai 264209, China.
Department of Plastic Surgery, China-Japan Friendship Hospital, Beijing 100029, China.
Pharmaceuticals (Basel). 2022 Mar 30;15(4):418. doi: 10.3390/ph15040418.
The Caco-2 model is a common cell model for material intestinal absorption in vitro, which usually takes 21 days to establish. Although some studies have shown that adding puromycin (PM) can shorten the model establishment period to 7 days, this still requires a long modeling time. Therefore, exploring a shorter modeling method can reduce the experimental costs and promote the development and application of the model. Fucoidan is an acidic polysaccharide with various biological activities. Our study showed that the transepithelial electrical resistance (TEER) value could reach 600 Ω·cm2 on the fourth day after the addition of fucoidan and puromycin, which met the applicable standards of the model (>500 Ω). Moreover, the alkaline phosphatase (AKP) activity, fluorescein sodium transmittance, and cell morphology of this model all met the requirements of model establishment. Fucoidan did not affect the absorption of macromolecular proteins and drugs. The results indicate that fucoidan can be applied to establish the Caco-2 model and can shorten the model establishment period to 5 days.
Caco-2模型是一种常见的体外物质肠道吸收细胞模型,通常需要21天来建立。尽管一些研究表明添加嘌呤霉素(PM)可将模型建立周期缩短至7天,但这仍需要较长的建模时间。因此,探索更短的建模方法可以降低实验成本并促进该模型的开发与应用。岩藻多糖是一种具有多种生物活性的酸性多糖。我们的研究表明,添加岩藻多糖和嘌呤霉素后第四天,跨上皮电阻(TEER)值可达600Ω·cm²,符合模型适用标准(>500Ω)。此外,该模型的碱性磷酸酶(AKP)活性、荧光素钠透过率及细胞形态均符合模型建立要求。岩藻多糖不影响大分子蛋白质和药物的吸收。结果表明,岩藻多糖可用于建立Caco-2模型,并可将模型建立周期缩短至5天。