自愈水凝胶
肿胀 的
药物输送
傅里叶变换红外光谱
材料科学
葡甘露聚糖
化学工程
控制释放
化学
高分子化学
纳米技术
复合材料
生物化学
工程类
作者
Renhua Yao,Xiaoqin Yu,Rui Deng,Huarong Zou,Qingwen He,Wenfeng Huang,Chunxiao Li,Kun Zou
出处
期刊:Gels
[Multidisciplinary Digital Publishing Institute]
日期:2023-03-14
卷期号:9 (3): 221-221
被引量:4
摘要
Konjac glucomannan (KGM) can be degraded by colon-specific enzymes in the colonic environment, making it one of the materials for treating colonic diseases, which has attracted more and more attention. However, during drug administration, especially in the gastric environment and due to its easy swelling, the structure of KGM is usually destroyed and the drug is released, thereby reducing the bioavailability of the drug. To solve this problem, the easy swelling and drug release properties of KGM hydrogels are avoided by creating interpenetrating polymer network hydrogels. In this study, N-isopropylacrylamide (NIPAM) is first formed into a hydrogel framework under the action of a cross-linking agent to stabilize the gel shape before the gel is heated under alkaline conditions to make KGM molecules wrap around the NIPAM framework. The structure of the IPN(KGM/NIPAM) gel was confirmed using Fourier transform infrared spectroscopy (FT-IR) and x-ray diffractometer (XRD). In the stomach and small intestine, it was found that the release rate and swelling rate of the gel were 30% and 100%, which were lower than 60% and 180% of KGM gel. The experimental results showed that this double network hydrogel has a good colon-directed release profile and fine drug carrier ability. This provides a new idea for the development of konjac glucomannan colon-targeting hydrogel.
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