Layered double hydroxide modified by PEGylated hyaluronic acid as a hybrid nanocarrier for targeted drug delivery |
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Authors: | Anjie?Dong,Xue?Li,Weiwei?Wang,Shangcong?Han,Jianfeng?Liu,Jinjian?Liu,Junqiang?Zhao,Shuxin?Xu,Liandong?Deng author-information" > author-information__contact u-icon-before" > mailto:dengliandong@aliyun.com" title=" dengliandong@aliyun.com" itemprop=" email" data-track=" click" data-track-action=" Email author" data-track-label=" " >Email author |
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Affiliation: | 1.Key Laboratory of Systems Bioengineering of Ministry of Education, School of Chemical Engineering and Technology,Tianjin University,Tianjin,China;2.Collaborative Innovation Center of Chemical Science and Engineering(Tianjin),Tianjin,China;3.Tianjin Key Laboratory of Radiation Molecular and Molecular Nuclear Medicine, Institute of Radiation Medicine,Chinese Academy of Medical Science and Peking Union Medical College,Tianjin,China;4.Tianjin Key Laboratory of Biomaterial Research, Institute of Biomedical Engineering,Chinese Academy of Medical Science,Tianjin,China;5.School of Materials Science and Engineering,Tianjin Polytechnic University,Tianjin,China |
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Abstract: | In recent years, organic-inorganic hybrid nanocarriers are explored for effective drug delivery and preferable disease treatments. In this study, using 5-fluorouracil(5-FU)as electronegative model drug, a new type of organic-inorganic hybrid drug delivery system(LDH/HA-PEG/5-FU)was conceived and manufactured by the adsorption of PEGylated hyaluronic acid(HA-PEG)on the surface of layered double hydroxide(LDH, prepared via hydrothermal method)and the intercalation of 5-FU in the interlamination of LDH via ion exchange strategy. The drug loading amount of LDH/HA-PEG/5-FU achieved as high as 34.2%. LDH, LDH/5-FU and LDH/HA-PEG/5- FU were characterized by FT-IR, XRD, TGA, laser particle size analyzer and SEM. With the benefit of pHdegradable feature of LDH and enzyme-degradable feature of HA, LDH/HA-PEG/5-FU showed pH-degradable and enzyme-degradable capacity in in vitro drug release. Moreover, the drug carrier LDH/HA-PEG contained biocompatible PEG and tumor-targeted HA, resulting in lower cytotoxicity and better endocytosis compared with LDH in vitro. It was suggested that the organic-inorganic hybrid drug delivery system, which was endowed with the properties of controlled release, low toxicity and tumor-targeting delivery for ameliorative cancer therapy, was advisable and might be applied further to fulfill other treatments. |
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