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首页> 外文期刊>International Journal of Biological Macromolecules: Structure, Function and Interactions >Graphene quantum dot cross-linked carboxymethyl cellulose nanocomposite hydrogel for pH-sensitive oral anticancer drug delivery with potential bioimaging properties
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Graphene quantum dot cross-linked carboxymethyl cellulose nanocomposite hydrogel for pH-sensitive oral anticancer drug delivery with potential bioimaging properties

机译:石墨烯量子点交联羧甲基纤维素纳米复合物水凝胶,用于pH敏感口腔抗癌药物递送潜在的生物分析性能

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Herein, graphene quantum dots (GQDs) were introduced as a novel and safe crosslinker for carboxymethyl cellulose to make biodegradable and biocompatible hydrogels. The casting was used as a simple method for the preparation of the CMC/GQDs films. Effects of the GQDs percentage on the physicochemical properties of the films were studied, and several characterizations were performed including Fourier transform infrared spectroscopy, UV-vis spectroscopy, scanning electron microscopy, gas permeability, and mechanical testing analysis. The CMC/GQDs showed a pH-sensitive swelling and degradation with improved tensile strength. Fluorescent properties were also studied to evaluate the potential of the prepared CMC/GQDs nanocomposite for fluorescent bioimaging applications. Drug delivery property of the CMC-GQDs were studied using doxorubicin (DOX) as a model anticancer drug. Cytotoxicity studies were carried out using human colon adenocarcinoma HT29 cells. The prepared CMC/GQDs exhibited biocompatibility and pH-sensitive drug delivery behavior which proposed the prepared nanocomposite hydrogel has the potential to be used as a pH-triggered site-specific drug delivery system. (C) 2019 Elsevier B.V. All rights reserved.
机译:这里,将石墨烯量子点(GQDs)作为羧甲基纤维素的新型和安全交联剂引入制造可生物降解和生物相容性水凝胶。铸件用作制备CMC / GQD膜的简单方法。研究了GQDS百分比对薄膜物理化学性质的影响,进行了几种特征,包括傅立叶变换红外光谱,UV-Vis光谱,扫描电子显微镜,透气性和机械测试分析。 CMC / GQD显示PH敏感溶胀和降解,具有改善的拉伸强度。还研究了荧光特性以评估制备的CMC / GQD纳米复合物用于荧光生物成像应用的潜力。使用多柔比星(DOX)作为模型抗癌药物研究了CMC-GQDS的药物递送性能。使用人结肠腺癌HT29细胞进行细胞毒性研究。制备的CMC / GQD表现出生物相容性和pH敏感的药物递送行为,其提出制备的纳米复合水凝胶具有用作pH-触发的位点特异性药物递送系统。 (c)2019 Elsevier B.v.保留所有权利。

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