Yao Renhua, Yu Xiaoqin, Deng Rui, Zou Huarong, He Qingwen, Huang Wenfeng, Li Chunxiao, Zou Kun
Hubei Key Laboratory of Natural Products Research and Development, College of Biological and Pharmaceutical Sciences, China Three Gorges University, Yichang 443002, China.
Hubei Hongyu New Packing Material Co., Ltd., 1 Juxiang Avenue, Jiaqueling Town, Yiling District, Yichang 443000, China.
Gels. 2023 Mar 14;9(3):221. doi: 10.3390/gels9030221.
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.
魔芋葡甘聚糖(KGM)可在结肠环境中被结肠特异性酶降解,这使其成为治疗结肠疾病的材料之一,已受到越来越多的关注。然而,在给药过程中,尤其是在胃环境中,由于其易于溶胀,KGM的结构通常会被破坏,药物会释放出来,从而降低药物的生物利用度。为了解决这个问题,通过制备互穿聚合物网络水凝胶来避免KGM水凝胶的易溶胀和药物释放特性。在本研究中,首先在交联剂的作用下将N-异丙基丙烯酰胺(NIPAM)形成水凝胶骨架以稳定凝胶形状,然后在碱性条件下加热凝胶,使KGM分子包裹在NIPAM骨架周围。使用傅里叶变换红外光谱(FT-IR)和X射线衍射仪(XRD)对IPN(KGM/NIPAM)凝胶的结构进行了确认。在胃和小肠中,发现该凝胶的释放率和溶胀率分别为30%和100%,低于KGM凝胶的60%和180%。实验结果表明,这种双网络水凝胶具有良好的结肠靶向释放特性和优良的药物载体能力。这为魔芋葡甘聚糖结肠靶向水凝胶的开发提供了新思路。