Faculty of Chemical Engineering, Universiti Teknologi Malaysia, Johor Bahru 81310 Johor, Malaysia.
Int J Biol Macromol. 2012 Jun 1;50(5):1334-40. doi: 10.1016/j.ijbiomac.2012.03.017. Epub 2012 Mar 30.
In this article, modified κ-carrageenan hydrogel nanocomposites were synthesized to increase the release ability of carrageenan hydrogels under gastrointestinal conditions. The effect of MgO nanoparticle loading in a model drug (methylene blue) release is investigated. Characterization of hydrogels were carried out using Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), Field Emission Scanning Electron Microscope (FESEM) and Differential Scanning Calorimetry (DSC). Genipin was used to increase the delivery performance in gastrointestinal tract delivery by decreasing release in simulated stomach conditions and increasing release in simulated intestine conditions. It is shown that the amount of methylene blue released from genipin-cross-linked nanocomposites can be 67.5% higher in intestine medium and 56% lower in the stomach compared to κ-carrageenan hydrogel. It was found that by changing the nanoparticle loading and genipin concentration in the composite, the amount of drug released can be monitored. Therefore, applying nanoparticles appears to be a potential strategy to develop controlled drug delivery especially in gastrointestinal tract studies.
在本文中,合成了改性 κ-卡拉胶水凝胶纳米复合材料,以提高卡拉胶水凝胶在胃肠道条件下的释放能力。研究了氧化镁纳米粒子负载对模型药物(亚甲蓝)释放的影响。使用傅里叶变换红外光谱(FTIR)、X 射线衍射(XRD)、场发射扫描电子显微镜(FESEM)和差示扫描量热法(DSC)对水凝胶进行了表征。京尼平通过降低模拟胃条件下的释放量和增加模拟肠条件下的释放量,用于提高胃肠道传递的递送性能。结果表明,与 κ-卡拉胶水凝胶相比,京尼平交联纳米复合材料在肠介质中的亚甲蓝释放量可提高 67.5%,在胃中的释放量可降低 56%。结果发现,通过改变复合材料中的纳米粒子负载量和京尼平浓度,可以监测药物的释放量。因此,应用纳米粒子似乎是开发特别是在胃肠道研究中控制药物释放的一种有潜力的策略。