Glucosamine conjugated iron oxide and graphene oxide nanohybrid for smart drug delivery

被引:3
作者
Mousavi, Maedehsadat [1 ]
Salehi, Zeinab [1 ]
Rezvanpour, Alireza [2 ]
Mosayebi, Mehdi [1 ]
Farahani, Masoumeh [3 ]
Tokmedash, Mohammad Asadi [1 ]
Shokrgozar, Mohammad Ali [4 ]
机构
[1] Univ Tehran, Coll Engn, Sch Chem Engn, Tehran, Iran
[2] Carleton Univ, Dept Mech & Aerosp Engn, Ottawa, ON, Canada
[3] Shahid Beheshti Univ Med Sci, Prote Res Ctr, Tehran, Iran
[4] Pasteur Inst Iran IPI, New Res Technol Grp & Res Director, Natl Cell Bank Iran, Tehran, Iran
关键词
glucosamine; graphene oxide; iron oxide nanoparticles; nanohybrids; TARGETED DELIVERY; MAGNETIC NANOPARTICLES; FACILE PREPARATION; FOLIC-ACID; NANOCOMPOSITE; RELEASE; FABRICATION; ADSORPTION; TOXICITY; FUNCTIONALIZATION;
D O I
10.1002/cjce.24850
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Smart drug delivery systems have attracted a lot of attention as one of the new treatment methods for cancer. In this study, a smart drug delivery system carrying anticancer drugs was obtained by the intelligent synthesis of glucosamine (GA)-functionalized graphene oxide (GO)-based iron oxide nanoparticles (Fe3O4@GO-GA) using Hummers and chemical co-precipitation processes. Nanohybrids have a high surface area (280.26 m(2)/g) and superparamagnetic behaviour (Ms = 26.017 emu/g), indicating a significant loading capacity (373.78 mg/mg) and efficiency (96.3%) for pharmaceutical loading. An adsorption study of conventional daunorubicin (DNR) on this carrier showed that the drug release is more prone to occur under acidic conditions (pH = 5.5), at moderately high temperatures (T = 40 degrees C), and in the absence of smart carriers. The toxicity of the smart nanohybrids was examined using the sulphorhodamine B (SRB) assay in Michigan Cancer Foundation-7 (MCF-7) cell lines. The rate of death of cells exposed to smart drug-containing systems in comparison to the systems without GA shows that GA reduces the toxicity of Fe3O4@GO.
引用
收藏
页码:5482 / 5497
页数:16
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