| Literature DB >> 28525943 |
Dalia Medhat1, Jihan Hussein1, Mehrez E El-Naggar2, Mohamed F Attia3, Mona Anwar1, Yasmine Abdel Latif1, Hoda F Booles4, Safaa Morsy1, Abdel Razik Farrag5, Wagdy K B Khalil4, Zakaria El-Khayat1.
Abstract
Dextran-capped gold nanoparticles (Au-dextran NPs) were prepared exploiting the natural polysaccharide polymer as both reducing and stabilizing agent in the synthesis process, aiming at studying their antitumor effect on solid carcinoma and EAC-bearing mice. To this end, Au-dextran NPs were designed via simple eco-friendly chemical reaction and they were characterized revealing the monodispersed particles with narrow distributed size of around 49nm with high negative charge. In vivo experiments were performed on mice. Biochemical analysis of liver and kidney functions and oxidation stress ratio in addition to histopathological investigations of such tumor tissues were done demonstrating the potentiality of Au-dextran NPs as antitumor agent. The obtained results revealed that EAC and solid tumors caused significant increase in liver and kidney functions, liver oxidant parameters, alpha feto protein levels and diminished liver antioxidant accompanied by positive expression of tumor protein p53 of liver while the treatment with Au-dextran NPs for both types caused improvement in liver and kidney functions, increased liver antioxidant, increased the expression level of B-cell lymphoma 2 gene and subsequently suppressed the apoptotic pathway. As a result, the obtained data provides significant antitumor effects of the Au-dextran NPs in both Ehrlich ascites and solid tumor in mice models.Entities:
Keywords: B-cell lymphoma 2; Caspase 3; Dextran; Ehrlich ascites carcinoma; Gold nanoparticles; Solid tumor
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Year: 2017 PMID: 28525943 DOI: 10.1016/j.biopha.2017.05.043
Source DB: PubMed Journal: Biomed Pharmacother ISSN: 0753-3322 Impact factor: 6.529