Functionalization of ZnO nanoparticles by 3-mercaptopropionic acid for aqueous curcumin delivery: Synthesis, characterization, and anticancer assessment

被引:76
|
作者
Ghaffari, Seyed-Behnam [1 ]
Sarrafzadeh, Mohammad-Hossein [1 ]
Fakhroueian, Zahra [1 ]
Shahriari, Shadab [2 ]
Khorramizadeh, M. Reza [2 ,3 ]
机构
[1] Univ Tehran, Coll Engn, Sch Chem Engn, Tehran, Iran
[2] Univ Tehran Med Sci, Endocrinol & Metab Res Ctr, Endocrinol & Metab Clin Sci Inst, Tehran, Iran
[3] Univ Tehran Med Sci, Endocrinol & Metab Mol Cellular Sci Inst, Biosensor Res Ctr, Tehran, Iran
基金
美国国家科学基金会;
关键词
ZnO nanoparticles; Surface functionalization; 3-Mercaptopropionic acid; Curcumin; Anticancer agent; ZINC-OXIDE NANOPARTICLES;
D O I
10.1016/j.msec.2017.05.065
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Inherent biocompatibility and stability of zinc oxide nanoparticles (ZnO-NPs) and their biomedical potentials make them an emerging candidate for drug delivery. The aim of this study was to develop and assess a simple procedure for surface functionalization of ZnO-NPs by 3-mercaptopropionic acid (MPA) for water-soluble curcumin delivery. Carboxyl-terminated ZnO nanoparticles were successfully made using ZnCl2 and NaOH in the presence of MPA. The functional groups were activated by 1,1'-carbonyldiimidazole (CDI) and the curcumin bonding was carried out at room temperature for 24 h. The core-shell nanocomposite had a significant better solubility versus free curcumin, as characterized by XRD, FTIR, UV-Vis spectrophotometry, DLS, and TEM, p < 0.005. In addition, MIT cytotoxicity assessment on MDA-MB-231 breast cancer cells revealed a drop of IC50 values from 5 mu g/mL to 3.3 mu g/mL for free curcumin and ZnO-MPA-curcumin complex, respectively. This result showed an augmented cancer-inhibitory effect of nanoconjugate complex. In conclusion, the presented improved solubility and elevated functionality of novel ZnO-MPA-curcumin nanoformula is promising, and could be considered for new therapeutic endeavors. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:465 / 472
页数:8
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