dc.contributor.author | Salehiabar, M | |
dc.contributor.author | Nosrati, H | |
dc.contributor.author | Javani, E | |
dc.contributor.author | Aliakbarzadeh, F | |
dc.contributor.author | Manjili, HK | |
dc.contributor.author | Davaran, S | |
dc.contributor.author | Danafar, H | |
dc.date.accessioned | 2018-08-26T06:34:59Z | |
dc.date.available | 2018-08-26T06:34:59Z | |
dc.date.issued | 2018 | |
dc.identifier.uri | http://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/44114 | |
dc.description.abstract | This study described a curcumin (CUR) loaded bovine serum albumin nanoparticles (BSA@CUR NPs), which could solubilize the poorly water-soluble drug and increase the therapeutic efficacy of the drug. BSA@CUR NPs were synthesized by a simple coacervation procedure. The resultant BSA@CUR NPs showed a spherical shape, with a diameter of 92.59 +/- 16.75 nm (mean +/- SD) nm and a zeta-potential of - 9.19 my. The in vitro drug release study of CUR showed 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 for investigation of hemocompatibility. Hemolysis assay and cytotoxicity study results on HFF-2 cell line show that as prepared BSA NPs are biocompatible. The in vitro anticancer activity of the BSA@CUR NPs were performed by MTF assay on MCF-7 cancer cells. These results suggest that BSA@CUR NPs are a new drug delivery system for cancer therapy. (C) 2018 Elsevier B.V. All rights reserved. | |
dc.language.iso | English | |
dc.relation.ispartof | INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES | |
dc.subject | Albumin | |
dc.subject | BSA | |
dc.subject | Drug delivery | |
dc.subject | Controlled release | |
dc.subject | Curcumin | |
dc.subject | Protein | |
dc.title | Production of biological nanoparticles from bovine serum albumin as controlled release carrier for curcumin delivery | |
dc.type | Article | |
dc.citation.volume | 115 | |
dc.citation.spage | 83 | |
dc.citation.epage | 89 | |
dc.citation.index | Web of science | |
dc.identifier.DOI | https://doi.org/10.1016/j.ijbiomac.2018.04.043 | |