Dual-Functional Iron Oxide Nanoparticles Coated with Polyvinyl Alcohol/5-Fluorouracil/Zinc-Aluminium-Layered Double Hydroxide for a Simultaneous Drug and Target Delivery System

被引:20
作者
Ebadi, Mona [1 ]
Bullo, Saifullah [1 ,2 ]
Buskaran, Kalaivani [3 ]
Hussein, Mohd Zobir [1 ]
Fakurazi, Sharida [3 ,4 ]
Pastorin, Giorgia [5 ]
机构
[1] Univ Putra Malaysia, Inst Adv Technol ITMA, Mat Synth & Characterizat Lab, Serdang 43400, Malaysia
[2] Univ Sukkur, Dept Management Sci & Technol, Begum Nusrat Bhutto Women, Sindh 65200, Pakistan
[3] Univ Putra Malaysia, Inst Biosci, Lab Vaccine & Immunotherapeut, Serdang 43400, Malaysia
[4] Univ Putra Malaysia, Fac Med & Hlth Sci, Dept Human Anat, Serdang 43400, Malaysia
[5] Natl Univ Singapore, Dept Pharm, Singapore 117543, Singapore
关键词
nanoparticles; Fe3O4; layered double hydroxide; polymeric coating; MAGNETIC NANOPARTICLES; RELEASE; NANOCARRIERS; THERAPY; CO;
D O I
10.3390/polym13060855
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Iron oxide nanoparticles are suitable for biomedical applications owing to their ability to anchor to various active agents and drugs, unique magnetic properties, nontoxicity, and biocompatibility. In this work, the physico-chemical and magnetic properties, as well as the cytotoxicity, of Fe3O4 nanoparticles coated with a polymeric carrier and loaded with a 5-fluorouracil (5-FU) anti-cancer drug are discussed. The synthesized Fe3O4 nanoparticles were coated with polyvinyl alcohol and Zn/Al-layered double hydroxide as the drug host. The XRD, DTA/TG, and FTIR analyzes confirmed the presence of the coating layer on the surface of nanoparticles. The results showed a decrease in saturation magnetization of bare Fe3O4 nanoparticles after coating with the PVA/5FU/Zn/Al-LDH layer. In addition, the presence of the coating prevented the agglomeration of nanoparticles. Furthermore, the pseudo-second-order equation governed the kinetics of drug release. Finally, the coated nanoparticles showed stronger activity against liver cancer cells (HepG2) compared to that of the naked 5-FU drug, and displayed no cytotoxicity towards 3T3 fibroblast cell lines. The results of the present study demonstrate the potential of a nano delivery system for cancer treatment.
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页数:18
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