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作 者:李天乐 仲慧 李小荣[2] 周静[3,4] 刘易鑫 胡卫成 程志鹏[2] 姚成[1] LI Tian-Le;ZHONG Hui;LI Xiao-Rong;ZHOU Jing;LIU Yi-Xin;HU Wei-Cheng;CHENG Zhi-Peng;YAO Cheng(College of Chemistry and Molecular Engineering,Nanjing Tech University,Nanjing 210000,China;Jiangsu Key Laboratory for Chemistry of Low-Dimensional Materials,School of Chemistry&Chemical Engineering,Huaiyin Normal University,Huaian,Anhui 223300,China;College of Food Science and Pharmacy,Xinjiang Agricultural University,Urumchi 830001,China;College of Life Science,Huaiyin Normal University,Huaian,Anhui 223300,China)
机构地区:[1]南京工业大学化学与分子工程学院,南京210000 [2]淮阴师范学院江苏低维材料化学重点实验室,淮安223300 [3]新疆农业大学食品科学与药学学院,乌鲁木齐830001 [4]淮阴师范学院生命科学学院,淮安223300
出 处:《无机化学学报》2021年第1期180-188,共9页Chinese Journal of Inorganic Chemistry
基 金:国家自然科学基金(No.21775051,51676082,21405055)资助。
摘 要:通过乳液聚合法制备了叶酸(FA)接枝的磁性FA-Fe3O4/凹凸棒土-聚(N-异丙基丙烯酰胺-丙烯酰胺)(FA-Fe3O4/ATPP(NIPAM-AAM))复合微凝胶(凹凸棒土=ATP,N-异丙基丙烯酰胺=NIPAM,丙烯酰胺=AAM),并通过X射线衍射(XRD)、振动样品磁强计(VSM)、热重(TG)、红外分析(IR)、紫外可见分光光度仪(UV)、扫描电子显微镜(SEM)和透射电子显微镜(TEM)对其进行表征。通过动态光散射(DLS)测定的低临界溶液温度(LCST)约为38.5℃,该温度适合于细胞实验。选择盐酸阿霉素(DOX)作为模型药物。药物负载和释放试验表明,ATP可以增加药物的负载和释放量。体外细胞毒性实验表明,与游离DOX相比,负载DOX的FA-Fe3O4/ATP-P(NIPAM-AAM)具有更好的生物相容性,并有望建立一个药物缓释系统。体外细胞摄取实验表明,FA-Fe3O4/ATP-P(NIPAM-AAM)具有靶向性,可用于靶向药物释放。The folic acid(FA)-grafted magnetic FA-Fe3O4/ATP-P(NIPAM-AAM)composite microgels(attapulgite=ATP,N-isopropyl acrylamide=NIPAM,acrylamide=AAM)were prepared via a method of emulsion copolymerization.The as-prepared microgels were characterized by X-ray diffraction(XRD),vibrating sample magnetometer(VSM),thermogravimetric analysis(TG),infrared spectroscopy(IR),UV-visible spectroscopy(UV),scanning electron microscope(SEM)and transmission electron microscope(TEM).The dynamic light scattering(DLS)results show that the low critical solution temperature(LCST)of microgel was about 38.5℃.The drug delivery ability of the as-prepared microgels was evaluated by using doxorubicin hydrochloride(DOX)as the model drug.Based on the drug loading and releasing results,the presence of ATP increased the amount of drug loading and releasing.Compared with free DOX,the in vitro cytotoxicity of DOX loaded FA-Fe3O4/ATP-P(NIPAM-AAM)was decreased and the biocompatibility was improved.Those results indicate that the microgels of FA-Fe3O4/ATP-P(NIPAM-AAM)can be used in potential as a slow-release drug system.The in vitro cellular uptake test revealed that the microgels of FA-Fe3O4/ATP-P(NIPAM-AAM)at the assigned site were significantly richer than that of other sites.This result indicates that the microgels of FA-Fe3O4/ATP-P(NIPAM-AAM)composite are targeting and expectable in the application of targeted drug releasing.
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