Anticancer activity of metal nanoparticles and their peptide conjugates against human colon adenorectal carcinoma cells

被引:60
作者
Aswathanarayan, Jamuna Bai [1 ]
Vittal, Ravishankar Rai [1 ]
Muddegowda, Umashankar [2 ]
机构
[1] Univ Mysore, Dept Studies Microbiol, Mysore 570006, Karnataka, India
[2] KSOU, Dept Studies Chem, Mysore, Karnataka, India
关键词
Cytotoxicity; metal nanoparticles; zinc oxide nanoparticle; hydrophobic peptides; anticancer activity; HT; 29; ZINC-OXIDE NANOPARTICLES; IRON-OXIDE; ZNO NANOPARTICLES; CANCER-CELLS; IN-VITRO; HYPERTHERMIA; APOPTOSIS;
D O I
10.1080/21691401.2017.1373655
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
In the present study, nanoparticles of gold, iron oxide and zinc oxide (ZnO) were studied for cytotoxicity in the colorectal cancer cell HT 29. The metallic nanoparticles in the range of <50 and <100nm were screened for anticancer activity by MTT assay. The nanoparticles were tested at concentrations ranging from 0.5 to 50 mu g/ml. Zinc oxide exhibited significant anti-cancer activity in comparison to other nanoparticles. It had an IC50 value of 17.12 mu g/ml. The mechanism of action was studied by fluorescence microscopy with acridine orange, propidium iodide and DAPI staining techniques. The ROS production of ZnO nanoparticles was determined by DCFH-DA. The ZnO nanoparticles were conjugated with novel hydrophobic peptides and evaluated for anticancer activity. It was observed that the nanoparticles peptide complex showed better cytotoxicity than either peptide or nanoparticle alone. Thus, the ZnO nanoparticles tested in our study has anticancer activity against colon cancer cells. It can also be conjugated with peptides and used for targeting cancer cells with higher efficacy.
引用
收藏
页码:1444 / 1451
页数:8
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