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首页> 外文期刊>International Journal of Biological Macromolecules: Structure, Function and Interactions >Effects of β-cyclodextrin on the intestinal absorption of berberine hydrochloride, a P-glycoprotein substrate
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Effects of β-cyclodextrin on the intestinal absorption of berberine hydrochloride, a P-glycoprotein substrate

机译:β-环糊精对盐酸小ber碱(一种P-糖蛋白底物)的肠道吸收的影响

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摘要

The major objective of this work is to investigate the enhancing effect of β-cyclodextrin on the intestinal absorption of berberine hydrochloride, a P-glycoprotein (Pgp) substrate. The inclusion complexation behavior of BBH with β-CD was investigated by phase-solubility diagram, Fourier transform infrared spectroscopy, differential scanning calorimetry, X-ray powder diffractometry, NMR spectroscopy, and molecular modeling studies. Results indicated that the 1,3-benzodioxole of BBH was included into the cavity of β-CD to form an inclusion complex which exhibited higher dissolution rate than BBH in vitro. The intestinal absorption of the inclusion complex in rats was significantly higher than the free drug due to its solubilizing effect and Pgp modulatory activity. The mechanisms of β-CD on Pgp modulation were demonstrated by modifying the Pgp ATPase activity, the Pgp mRNA level and the Pgp expression.
机译:这项工作的主要目的是研究β-环糊精对盐酸小ber碱(一种P-糖蛋白(Pgp)底物)的肠道吸收的增强作用。通过相溶解图,傅立叶变换红外光谱,差示扫描量热法,X射线粉末衍射,NMR光谱和分子模型研究研究了BBH与β-CD的夹杂物络合行为。结果表明,BBH的1,3-苯并二恶唑被包含在β-CD的腔中,形成包合物,其体外溶出速率高于BBH。由于其增溶作用和Pgp调节活性,包合物在大鼠中的肠道吸收明显高于游离药物。通过修饰Pgp ATPase活性,Pgp mRNA水平和Pgp表达,证明了β-CD对Pgp调节的机制。

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