Bovine serum albumin: An efficient biomacromolecule nanocarrier for improving the therapeutic efficacy of chrysin

被引:44
作者
Nosrati, Hamed [1 ,2 ]
Rakhshbahar, Akram [3 ]
Salehiabar, Marziyeh [1 ]
Afroogh, Saeed [1 ,3 ]
Manjili, Hamidreza Kheiri [3 ,4 ]
Danafar, Hossein [1 ,2 ,4 ]
Davaran, Soodabeh [5 ]
机构
[1] Zanjan Univ Med Sci, Zanjan Pharmaceut Nanotechnol Res Ctr, Zanjan, Iran
[2] Zanjan Univ Med Sci, Sch Pharm, Dept Pharmaceut Biomat, Zanjan, Iran
[3] Zanjan Univ Med Sci, Sch Med, Dept Med Biotechnol & Nanotechnol, Zanjan, Iran
[4] Zanjan Univ Med Sci, Sch Pharm, Dept Pharmaceut Biotechnol, Zanjan, Iran
[5] Tabriz Univ Med Sci, Drug Appl Res Ctr, Tabriz, Iran
关键词
Albumin; BSA; Drug delivery; Cancer; Chrysin; Protein; OXIDE MAGNETIC NANOPARTICLES; MOLECULAR DOCKING; DELIVERY; RELEASE; CARRIER; COPOLYMER; DESIGN;
D O I
10.1016/j.molliq.2018.06.066
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
This study manipulated a chrysin loaded bovine serum albumin nanoparticles (BSA NPs), which could solubilize the poorly water-soluble drug and increase the therapeutic efficacy of the drug. Chrysin (5, 7-dihydroxyflavone) is a natural flavonoid which have some significant biological effects on the processes of chemical defense. Chrysin loaded bovine serum albumin nanoparticles (Chrysin-BSA NPs) were synthesized by a simple desolvation procedure. The resultant Chrysin-BSA NPs showed a spherical shape, with a diameter of 97.5 +/- 5.75 nm (mean +/- SD) nm and zeta-potential of - 11 mV. The in vitro drug release study of chrysin presented a sustained and controlled release pattern. Cellular toxicity of BSA NPs was also investigated on HFF2 cell lines. Additionally, a hemolysis test of as prepared NPs were performed. Hemolysis assay and cytotoxicity study results on HFF-2 cell line show that as prepared BSA NPs are biocompatible. The in vitro cytotoxicity of the nanoparticles was performed by MTT assay on MCF-7 cancer cells. These results suggest that Chrysin-BSA NPs are a new drug delivery system for cancer therapy. (C) 2018 Published by Elsevier B.V.
引用
收藏
页码:639 / 646
页数:8
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