Green synthesis, characterization, and anticancer activity of hyaluronan/zinc oxide nanocomposite

被引:62
作者
Namvar, Farideh [1 ,2 ]
Azizi, Susan [3 ]
Rahman, Heshu Sulaiman [4 ,5 ,6 ]
Mohamad, Rosfarizan [1 ,3 ]
Rasedee, Abdullah [4 ]
Soltani, Mozhgan [2 ]
Rahim, Raha Abdul [7 ]
机构
[1] Univ Putra Malaysia, Inst Trop Forestry & Forest Prod INTROP, Upm Serdang, Selangor, Malaysia
[2] Islamic Azad Univ, Mashhad Branch, Res Ctr Anim Dev Appl Biol, Mashhad, Iran
[3] Univ Putra Malaysia, Fac Biotechnol & Biomol Sci, Dept Bioproc Technol, Upm Serdang 43400, Selangor, Malaysia
[4] Univ Putra Malaysia, Fac Vet Med, Dept Vet Lab Diag, Upm Serdang, Selangor, Malaysia
[5] Univ Sulaimani, Coll Vet Med, Dept Clin & Internal Med, Sulaimani City, Kurdistan Regio, Iraq
[6] Komar Univ Sci & Technol, Dept Lab Med Sci, Sulaimani City, Kurdistan Regio, Iraq
[7] Univ Putra Malaysia, Fac Biotechnol & Biomol Sci, Dept Cell & Mol Biol, Upm Serdang, Selangor, Malaysia
关键词
green synthesis; hyaluronan; zinc oxide nanocomposite; anticancer activity; NANOSTRUCTURED LIPID CARRIER; WEIGHT HYALURONIC-ACID; MOLECULAR-WEIGHT; NANOPARTICLES; BIOSYNTHESIS; APOPTOSIS; CULTURE; OXYGEN;
D O I
10.2147/OTT.S95962
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
The study describes an in situ green biosynthesis of zinc oxide nanocomposite using the seaweed Sargassum muticum water extract and hyaluronan biopolymer. The morphology and optical properties of the hyaluronan/zinc oxide (HA/ZnO) nanocomposite were determined by Fourier transform infrared spectroscopy, X-ray diffraction, field emission scanning electron microscopy, transmission electron microscopy, and ultraviolet-vis analysis. Electron microscopy and X-ray diffraction analysis showed that the zinc oxide nanoparticles were polydispersed with a mean size of 10.2 +/- 1.5 nm. The nanoparticles were mostly hexagonal in crystalline form. The HA/ZnO nanocomposite showed the absorption properties in the ultraviolet zone that is ascribed to the band gap of zinc oxide nanocomposite. In the cytotoxicity study, cancer cells, pancreatic adenocarcinoma (PANC-1), ovarian adenocarcinoma (CaOV-3), colonic adenocarcinoma (COLO205), and acute promyelocytic leukemia (HL-60) cells were treated with HA/ZnO nanocomposite. At 72 hours of treatment, the half maximal inhibitory concentration (IC50) value via the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay was 10.8 +/- 0.3 mu g/mL, 15.4 +/- 1.2 mu g/mL, 12.1 +/- 0.9 mu g/mL, and 6.25 +/- 0.5 mu g/mL for the PANC-1, CaOV-3, COLO-205, and HL-60 cells, respectively, showing that the composite is most toxic to the HL-60 cells. On the other hand, HA/ZnO nanocomposite treatment for 72 hours did not cause toxicity to the normal human lung fibroblast (MRC-5) cell line. Using fluorescent dyes and flow cytometry analysis, HA/ZnO nanocomposite caused G2/M cell cycle arrest and stimulated apoptosis-related increase in caspase-3 and -7 activities of the HL-60 cells. Thus, the study shows that the HA/ZnO nanocomposite produced through green synthesis has great potential to be developed into an efficacious therapeutic agent for cancers.
引用
收藏
页码:4549 / 4559
页数:11
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