The Aquilegia pubiflora (Himalayan columbine) mediated synthesis of nanoceria for diverse biomedical applications

被引:73
作者
Jan, Hasnain [1 ,4 ]
Khan, Muhammad Aslam [2 ]
Usman, Hazrat [1 ]
Shah, Muzamil [1 ]
Ansir, Rotaba [3 ]
Faisal, Shah [4 ]
Ullah, Niamat [3 ]
Rahman, Lubna [1 ]
机构
[1] Quaid I Azam Univ, Dept Biotechnol, Islamabad 45320, Pakistan
[2] Int Islamic Univ, Dept Biotechnol, Islamabad, Pakistan
[3] Quaid I Azam Univ, Dept Chem, Islamabad 45320, Pakistan
[4] Bacha Khan Univ, Dept Biotechnol, Charsadda, KP, Pakistan
关键词
CERIUM OXIDE NANOPARTICLES; ZINC-OXIDE; ANTIBACTERIAL PROPERTIES; ZNO NANOPARTICLES; MEDICINAL-PLANTS; GREEN SYNTHESIS; ANTIOXIDANT; MECHANISM; EXTRACTS; PREVALENCE;
D O I
10.1039/d0ra01971b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Herein, we report an eco-friendly, facile, one-pot, green synthesis of nanoceria for multiple biomedical applications. In the study, cerium oxide nanoparticles (CeO2-NPs) were synthesized using a simple aqueous extract of Aquilegia pubiflora as an effective reducing and capping agent. The biosynthesized nanoparticles were characterized via UV-vis spectroscopy, X-ray powder diffraction (XRD), high-performance liquid chromatography (HPLC), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and Raman spectroscopy. The NPs were highly stable, exhibited high purity, and had a spherical morphology and mean size of 28 nm. FTIR and HPLC studies confirmed the successful capping of bioactive compounds on the nanoparticles. The well-characterized NPs were evaluated for a number of biomedical applications, and their antimicrobial (antifungal, antibacterial, and antileishmanial), protein kinase inhibition, anticancer, antioxidant, anti-diabetic and biocompatibility properties were studied. Our results showed that the Aquilegia pubiflora mediated CeO2-NPs were highly active against fungal strains, compared to the tested bacterial strains, with Aspergillus niger resulting in the largest zone of inhibition (15.1 +/- 0.27 mm). The particles also exhibited dose dependent leishmanicidal activity with significant LC50 values toward both the amastigote (114 mu g mL(-1)) and promastigote (97 mu g mL(-1)) forms of the parasite Leishmania tropica (KWH23). The NPs were found to be moderately active against the HepG2 cell line, showing 26.78% +/- 1.16% inhibition at 200 mu g mL(-1). Last but not least, their highly biocompatible nature was observed with respect to freshly isolated human red blood cells (hRBCs), making the greenly synthesized CeO2-NPs a novel candidates for multidimensional medical applications.
引用
收藏
页码:19219 / 19231
页数:13
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