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Evaluation of multilayer coated magnetic nanoparticles as biocompatible curcumin delivery platforms for breast cancer treatment
被引:46
作者:
Akrami, Mohammad
[1
]
Khoobi, Mehdi
[2
,3
,4
]
Khalilvand-Sedagheh, Masoud
[2
,3
]
Haririan, Ismaeil
[1
,4
]
Bahador, Abbas
[5
]
Faramarzi, Mohammad Ali
[4
]
Rezaei, Shahla
[4
]
Javar, Hamid Akbari
[1
]
Salehi, Fahimeh
[8
]
Ardestanie, Sussan Kabudanian
[6
,7
,8
]
Shafiee, Abbas
[2
,3
]
机构:
[1] Univ Tehran Med Sci, Fac Pharm, Dept Pharmaceut Biomat, Tehran 14176, Iran
[2] Univ Tehran Med Sci, Fac Pharm, Dept Med Chem, Tehran 14176, Iran
[3] Univ Tehran Med Sci, Pharmaceut Sci Res Ctr, Tehran 14176, Iran
[4] Univ Tehran Med Sci, Med Biomat Res Ctr, Tehran 14176, Iran
[5] Univ Tehran Med Sci, Sch Med, Dept Microbiol, Tehran 14176, Iran
[6] Univ Tehran Med Sci, Fac Pharm, Dept Pharmaceut Biotechnol, Tehran 14176, Iran
[7] Univ Tehran Med Sci, Biotechnol Res Ctr, Tehran 14176, Iran
[8] Univ Tehran, Dept Biochem, Inst Biochem & Biophys, Tehran, Iran
基金:
美国国家科学基金会;
关键词:
IRON-OXIDE NANOPARTICLES;
SUPERPARAMAGNETIC FE3O4 NANOPARTICLES;
BETA-CYCLODEXTRIN;
DRUG-DELIVERY;
SURFACE FUNCTIONALIZATION;
BIOMEDICAL APPLICATIONS;
LIPASE IMMOBILIZATION;
DNA DELIVERY;
HELA-CELLS;
IN-VITRO;
D O I:
10.1039/c5ra13838h
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
Biocompatible multi-layer iron oxide magnetic nanoparticles (MNPs) for drug delivery applications with increased loading capacity, sustained sensitive release profile, and high inherent magnetic properties as well as improved cellular uptake were prepared. In this approach, Fe3O4 MNPs were obtained by a co-precipitation method and functionalized using hydroxyapatite (HAP) and/or polyethyleneimine (PEI). They were then modified with beta-cyclodextrin (CD) to increase their loading capacity. These MNPs allowed suitable encapsulation of hydrophobic curcumin (CUR) in the CD shell and CUR adsorption into the polymeric layers. The dissolution profile of CUR showed pH sensitive release of CUR. The protein corona pattern of the MNPs by electrophoresis showed lower protein adsorption for CD modified MNPs than for other MNPs. No significant toxicity was observed for the target MNPs, whereas the CUR loaded MNPs inhibited MCF-7 breast cancer cells more efficiently than free CUR. Moreover, the negligible hemolytic activity of the target MNPs showed their excellent haemocompatibility for cancer treatment. The preferential uptake of the drug by MCF-7 cells was observed for CUR loaded MNPs in comparison with free CUR using flow cytometric analysis. As a result, the designed and prepared MNPs can be considered to be a promising CUR delivery platform.
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页码:88096 / 88107
页数:12
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