Gold nanoparticles show potential in vitro antiviral and anticancer activity

被引:34
|
作者
Babaei, Abouzar [1 ,2 ]
Mousavi, Seyed Mahmoud [3 ]
Ghasemi, Marzie [4 ]
Pirbonyeh, Neda [1 ,5 ]
Soleimani, Masoud [6 ,7 ]
Moattari, Afagh [1 ]
机构
[1] Shiraz Univ Med Sci, Dept Bacteriol & Virol, Shiraz, Iran
[2] Tarbiat Modares Univ, Fac Med Sci, Dept Virol, Tehran, Iran
[3] Shiraz Univ Med Sci, Dept Parasitol & Mycol, Shiraz, Iran
[4] Ahvaz Jundishapur Univ Med Sci, Sch Med, Dept Biochem, Ahvaz, Iran
[5] Shiraz Univ Med Sci, Burn & Wound Healing Res Ctr, Microbiol Dept, Shiraz, Iran
[6] Tarbiat Modares Univ, Dept Hematol & Cell Therapy, Tehran, Iran
[7] Shahid Beheshti Univ Med Sci, Nano Med & Tissue Engn Res Ctr, Tehran, Iran
关键词
AuNPs; Glioblastoma cancer; Influenza A virus; Therapeutic agent; INFLUENZA-VIRUS INFECTION; FUNCTIONALIZED GOLD; SILVER NANOPARTICLES; APOPTOSIS; INHIBITION; CELLS; TOXICITY; BREAST; SIZE;
D O I
10.1016/j.lfs.2021.119652
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Aims: Gold nanoparticles (AuNPs) have been attracted interests in the various areas of clinical therapeutics. In this study, we investigated the anticancer and antiviral potential activity of AuNPs against influenza A virus and human glioblastoma (GMB) U-87 and U-251 cell lines. Main methods: Gold nanoparticles (AuNPs) were synthesized by citrate reduction method. Then, ultravioletvisible spectrophotometry (UV-vis spectra) and electron microscopy analysis confirmed the type, size (mean diameter of 17 nm) and distribution of the particles. The AuNPs in vitro antiviral and anticancer effects was evaluated by hemagglutination inhibition (HAI), tissue culture infectious dose 50 (TCID50), real-time PCR, MTT, flow cytometry, and scratch assays. Key findings: The AuNPs were synthesized in spherical with a mean diameter of 17 +/- 2 nm and an absorbance peak at 520 nm. The AuNPs were well tolerable by MDCK cells at concentrations up to 0.5 mu g/ml and they significantly inhibited the hemagglutination and virus infectivity, particularly when added pre- or during virus infection. Furthermore, anticancer results indicated that AuNPs treatment caused the marked induction of apoptosis and reduced growth and migration capability of U-87 and U-251 cell lines in a time-dependent manner. Significance: The present results suggest that AuNPs provide promising antiviral and anticancer approaches. Further research is needed to fully elucidate the mode of antiviral and anticancer action of AuNPs against influenza virus infection and human glioblastoma cell lines.
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页数:8
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