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用于黄连素负载与释放的改性海藻酸钠和NIPAM的温度与pH双重响应性纳米凝胶

Temperature and pH Dual Responsive Nanogels of Modified Sodium Alginate and NIPAM for Berberine Loading and Release.

作者信息

Chang Shuhua, Qin Dawei, Yan Rongjun, Zhang Mengli, Sui Binglin, Xu Hui, Zheng Zhaomin, Hou Xiaoli, Wang Yonggang, Qi Chenggang

机构信息

School of Chemistry and Chemical Engineering, Qilu University of Technology (Shandong Academy of Sciences), Jinan 250353, China.

Jinan International Travel Health Care Center, Jinan 250353, China.

出版信息

ACS Omega. 2021 Jan 4;6(2):1119-1128. doi: 10.1021/acsomega.0c03965. eCollection 2021 Jan 19.

DOI:10.1021/acsomega.0c03965
PMID:33490771
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7818125/
Abstract

pH- and temperature-sensitive nanogels (NGs) were prepared from sodium alginate (SA) and -isopropylacrylamide (NIPAM), as the sensitivity at pH 5.5 and 31 °C. SA was pH-modified with glutamic acid (Glu) and ethylenediamine (EDA). The products Glu-SA (Glu-modified SA) and EGSA (EDA- and Glu-modified SA) were characterized by ninhydrin color reaction, infrared spectroscopy, and zeta potential, and the best reactant ratio was selected. Moreover, temperature-sensitive, pH-sensitive EGSA-NGs possessing a semi-interpenetrating network structure were prepared by radical polymerization using -isopropylacrylamide. The morphology of EGSA-NGs was characterized by transmission electron microscopy (TEM), scanning electron microscopy (SEM), and atomic force microscopy (AFM). The cytotoxicity test shows the low cytotoxicity and high biocompatibility of the NGs. The newly prepared NGs were also subjected to pH-sensitive temperature-sensitive in vitro drug-loading and drug-release experiments. The pH-sensitive and temperature-sensitive experiments showed that the particle size of EGSA-NGs was reduced at pH 5.5 and above 31 °C. The drug-loading and drug-release experiments also confirmed this finding, indicating that the newly synthesized NGs could release the drug according to the environmental changes. Therefore, the material has potential application value in solid tumor targeted therapy.

摘要

采用海藻酸钠(SA)和N-异丙基丙烯酰胺(NIPAM)制备了对pH值和温度敏感的纳米凝胶(NGs),其在pH 5.5和31℃时具有敏感性。SA用谷氨酸(Glu)和乙二胺(EDA)进行pH修饰。通过茚三酮显色反应、红外光谱和zeta电位对产物Glu-SA(Glu修饰的SA)和EGSA(EDA和Glu修饰的SA)进行表征,并选择最佳反应物比例。此外,采用N-异丙基丙烯酰胺通过自由基聚合制备了具有半互穿网络结构的温度敏感、pH敏感的EGSA-NGs。通过透射电子显微镜(TEM)、扫描电子显微镜(SEM)和原子力显微镜(AFM)对EGSA-NGs的形态进行表征。细胞毒性试验表明NGs具有低细胞毒性和高生物相容性。对新制备的NGs还进行了pH敏感和温度敏感的体外载药和释药实验。pH敏感和温度敏感实验表明,EGSA-NGs在pH 5.5及31℃以上时粒径减小。载药和释药实验也证实了这一发现,表明新合成的NGs可根据环境变化释放药物。因此,该材料在实体肿瘤靶向治疗中具有潜在的应用价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/290d/7818125/643db1ab80a0/ao0c03965_0014.jpg
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