PAMAM-modified citric acid-coated magnetic nanoparticles as pH sensitive biocompatible carrier against human breast cancer cells

被引:69
作者
Nosrati, Hamed [1 ]
Adibtabar, Maral [2 ]
Sharafi, Ali [3 ,4 ]
Danafar, Hossein [3 ,5 ]
Kheiri, Manjili Hamidreza [3 ,4 ]
机构
[1] Zanjan Univ Med Sci, Sch Pharm, Dept Pharmaceut Biomat, Zanjan, Iran
[2] Islamic Azad Univ, Fac Genet, Dept Biol, East Tehran Branch, Tehran, Iran
[3] Zanjan Univ Med Sci, Canc Gene Therapy Res Ctr, Zanjan 4513956184, Iran
[4] Zanjan Univ Med Sci, Zanjan Pharmaceut Biotechnol Res Ctr, Zanjan, Iran
[5] Zanjan Univ Med Sci, Zanjan Pharmaceut Nanotechnol Res Ctr, Zanjan, Iran
关键词
Citric acid; curcumin; drug delivery; iron oxide; magnetic nanoparticles; PAMAM; denderimer; IRON-OXIDE NANOPARTICLES; DRUG-DELIVERY; CURCUMIN; NANOCARRIERS; METHOTREXATE; RELEASE;
D O I
10.1080/03639045.2018.1451881
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Dendenmer-modified magnetic nanoparticles are a promising drug delivery nanosystem which can improve the therapeutic efficacy of chemotherapy drugs and can also be beneficial as magnetic resonance (MR) images contrast agent. The present study introduces the preparation and characterization of the potential therapeutic efficiency of curcumin (CUR)-loaded denderimer-modified citric acid coated Fe3O4 NPs. Polyamidoamine (PAMAM, generation G(5)) was used to encapsulate citric acid coated Fe3O4 nanoparticles. The successful preparation of CUR-loaded nanocarriers were confirmed by X-ray diffraction (XRD), thermogravimetric analysis (TGA), Fourier transform infrared spectroscopy (FTIR), vibrating sample magnetometer (VSM), and transmission electron microscopy (TEM) techniques. The loading capacity and encapsulation efficiency of CUR molecules were 12 +/- 0.03% and 45.58 +/- 0.41%, respectively. The anticancer effect of void CUR and CUR-loaded nanocarriers were compared to each other by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay on treated MCF-7 cell line. It can be concluded that application of nanoparticles can be more effective strategy for controlled and slow release of CUR in human breast cancer treatment.
引用
收藏
页码:1377 / 1384
页数:8
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