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壳寡糖对低分子肝素在大鼠肠道吸收的促进作用。

Absorption enhancing effects of chitosan oligomers on the intestinal absorption of low molecular weight heparin in rats.

机构信息

School of Pharmacy, Health Science Center, Xi'an Jiaotong University, Xi'an 710061, China.

Department of Pharmaceutics, Kyoto Pharmaceutical University, Misasagi, Yamashina-ku, Kyoto 607-8414, Japan.

出版信息

Int J Pharm. 2014 May 15;466(1-2):156-62. doi: 10.1016/j.ijpharm.2014.03.010. Epub 2014 Mar 11.

Abstract

Absorption enhancing effects of chitosan oligomers with different type and varying concentration on the intestinal absorption of low molecular weight heparin (LMWH) were examined by an in situ closed loop method in different intestinal sections of rats. Chitosan hexamer with the optimal concentration of 0.5% (w/v) showed the highest absorption enhancing ability both in the small intestine and large intestine. The membrane toxicities of chitosan oligomers were evaluated by morphological observation and determining the biological markers including amount of protein and activity of lactate dehydrogenase (LDH) released from intestinal epithelium cells. There was no obvious change both in levels of protein and LDH and morphology in the intestinal membrane between control and various chitosan oligomers groups, suggesting that chitosan oligomers did not induce any significant membrane damage to the intestinal epithelium. In addition, zeta potentials became less negative and amount of free LMWH gradually decreased when various chitosan oligomers were added to LMWH solution, revealing that electrostatic interaction between positively charged chitosan oligomers and negative LMWH was included in the absorption enhancing mechanism of chitosan oligomers. In conclusion, chitosan oligomers, especially chitosan hexamer, are safe and efficient absorption enhancers and can be used promisingly to improve oral absorption of LMWH.

摘要

采用在体肠袢法,考察了不同类型和不同浓度的壳聚糖低聚物对低分子肝素(LMWH)在大鼠不同肠段吸收的促进作用。壳六聚体在 0.5%(w/v)的最佳浓度下,在小肠和大肠均显示出最高的吸收促进能力。通过形态观察和测定从肠上皮细胞释放的蛋白质含量和乳酸脱氢酶(LDH)活性等生物标志物,评估了壳聚糖低聚物的膜毒性。在对照组和各种壳聚糖低聚物组之间,蛋白质和 LDH 的水平以及肠膜的形态均无明显变化,这表明壳聚糖低聚物不会引起肠上皮的任何明显的膜损伤。此外,当各种壳聚糖低聚物加入到 LMWH 溶液中时,zeta 电位变得不那么负,游离 LMWH 的量逐渐减少,这表明正电荷的壳聚糖低聚物和负电荷的 LMWH 之间的静电相互作用包含在壳聚糖低聚物的吸收增强机制中。总之,壳聚糖低聚物,特别是壳六聚体,是安全有效的吸收促进剂,可用于提高 LMWH 的口服吸收。

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