Surface modified silk fibroin nanoparticles for improved delivery of doxorubicin: Development, characterization, in-vitro studies

被引:42
作者
Pandey, Vikas [1 ]
Haider, Tanweer [1 ]
Chandak, Ashok R. [2 ]
Chakraborty, Avik [2 ]
Banerjee, Sharmila [2 ]
Soni, Vandana [1 ]
机构
[1] Dr Hari Singh Gour Vishwavidyalaya, Dept Pharmaceut Sci, Sagar 470003, Madhya Pradesh, India
[2] Bhabha Atom Res Ctr BARC, Radiat Med Ctr, Mumbai 400012, Maharashtra, India
关键词
Silk fibroin nanoparticles; Tween-80; Doxorubicin; DRUG; POLYSORBATE-80; FABRICATION; VIVO;
D O I
10.1016/j.ijbiomac.2020.07.326
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Silk fibroin nanoparticles possess the hydrophobic nature which assists them to become a good substrate for reticulo-endothelial system (RES) and macrophageal uptake. Surface coating of these nanoparticles with hydrophilic stabilizers, like Tween-80 make them long circulating and facilitate their uptake by low density lipoprotein (LDL) receptors to cross blood brain barrier (BBB). Surface modified silk fibroin nanoparticles bearing anti-cancer agent doxorubicin (DOX) were fabricated by desolvation method and coated with Tween-80 as surface modifier. The prepared nanoparticles were characterized for various physicochemical parameters, like particle size, surface charge, surface morphology by scanning electron microscope (SEM) and transmission electron microscopy (TEM), and in vitro drug release along with in vitro cell cytotoxicity, flow cytometry and cellular uptake studies by flourocytometry on glioblastoma cell lines. Entrapment efficiency for the silk fibroin nanoparticles were found to be >85% for coated and uncoated nanoparticles. Nanoparticles with average diameter less than 150 nm having negative charge were found to show no toxicity of its own. The pro-inflammatory response of nanoparticles was observed by determining the cytokines level, such as TNF-alpha and IL-1 beta. Sustained drug release pattern from the nanoparticles with better cytotoxicty as compared to free drug was observed, signifying their potential ability to work as a drug delivery system. (C) 2020 Elsevier B.V. All rights reserved.
引用
收藏
页码:2018 / 2027
页数:10
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