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首页> 外文期刊>Colloids and Surfaces, B. Biointerfaces >Controlled release of anticancer drug using graphene oxide as a drug-binding effector in konjac glucomannan/sodium alginate hydrogels
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Controlled release of anticancer drug using graphene oxide as a drug-binding effector in konjac glucomannan/sodium alginate hydrogels

机译:使用氧化石墨烯作为魔芋葡甘露聚糖/海藻酸钠水凝胶中的药物结合效应物来控制释放抗癌药物

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摘要

In order to find new composite materials for the controlled release of drugs, a series of novel pH sensitive konjac glucomannan/sodium alginate (KGM/SA) and KGM/SA/graphene oxide (KGM/SA/GO) hydrogels were prepared, using GO as a drug-binding effector for anticancer drug loading and release. The hydrogels were characterized using Fourier transform infrared spectroscopy (FTIR), and scanning electron microscopy (SEM). The effects of component ratio and pH on the swelling properties of hydrogels were studied. The release amount of 5-fluorouracil (5-FU) incorporated into KGM/SA/GO-3 hydrogels was about 38.02% at pH 1.2 and 84.19% at pH 6.8 after 6 h and 12 h, respectively. Therefore, the release rate of 5-FU from the functionalized KGM/SA using GO could be effectively controlled, Go has a great potential to be a promising drug-binding effector for hydrogel functionalization in drug delivery.
机译:为了找到用于药物控制释放的新复合材料,使用GO制备了一系列新型的pH敏感魔芋葡甘露聚糖/海藻酸钠(KGM / SA)和KGM / SA /氧化石墨烯(KGM / SA / GO)水凝胶作为抗癌药物负载和释放的药物结合效应物。使用傅里叶变换红外光谱(FTIR)和扫描电子显微镜(SEM)对水凝胶进行表征。研究了组分比和pH值对水凝胶溶胀性能的影响。在6小时和12小时后,掺入KGM / SA / GO-3水凝胶中的5-氟尿嘧啶(5-FU)的释放量分别在pH 1.2和pH 6.8下分别约为38.02%和84.19%。因此,可以有效地控制使用GO从功能化的KGM / SA中5-FU的释放速率,Go具有很大的潜力,有望成为有前景的药物结合效应物,用于水凝胶在药物递送中的功能化。

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