PVP and PEG doped CuO nanoparticles are more biologically active: Antibacterial, antioxidant, antidiabetic and cytotoxic perspective

被引:127
作者
Javed, Rabia [1 ]
Ahmed, Madiha [2 ]
ul Haq, Ihsan [2 ]
Nisa, Sobia [3 ]
Zia, Muhammad [1 ]
机构
[1] Quaid I Azam Univ, Dept Biotechnol, Islamabad 45320, Pakistan
[2] Quaid I Azam Univ, Dept Pharm, Islamabad 45320, Pakistan
[3] Univ Haripur, Dept Microbiol, Haripur, Pakistan
来源
MATERIALS SCIENCE AND ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS | 2017年 / 79卷
关键词
Cupricoxide (CuO) nanoparticles; X-ray diffraction (XRD); Scanning electron microscopy (SEM); Reactive oxygen species (ROS); Biological activities; Antibacterial; cytotoxic and antidiabetic activities; COPPER-OXIDE NANOPARTICLES; ZNO NANOPARTICLES; BACTERIA;
D O I
10.1016/j.msec.2017.05.006
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
Search for biologically active nanoparticles is prerequisite for biomedical applications. CuO nanopartides synthesized by co-precipitation method are capped by polyethylene-glycol (PEG) and polyvinyl-pyrrolidone (PVP) on the surface by simple adsorption. Physical and chemical properties carried out by SEM, XRD and FTIR confirm nanometer in size and efficient capping of PVP and PEG on CuO NPs. Biological assays reveal higher activities of CuO-PEG and CuO-PVP as compared to the uncapped CuO nanoparticles. CuO-PEG shows better antitumor activity against Streptomyces as compared with CuO-PVP and CuO NPs. Both the capped NPs are significantly active for ot-amylase inhibition assay. CuO-PVP demonstrates significantly better activity against bacterial strains followed by CuO-PEG and uncapped CuO. PVP coated CuO NPs also shows strong DPPH based free radical scavenging activity, total reducing power potential, total antioxidative potential and also carries flavonoid and phenolics properties determines to querecetin and gallic acid equivalence, respectively. It can be concluded that PVP and PEG capped CuO NPs are more capable to be used in biomedical applications as drug and diagnostic carrier molecules. (C) 2017 Elsevier B.V. All tights reserved.
引用
收藏
页码:108 / 115
页数:8
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