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논문명(한글), 논문명(영문), 성과주관부서, 품목코드, 학술지명, 주저자, 연도, 성과적용일, 첨부파일, 내용으로 구성된 글 상세입니다.
논문명(한글) |
Biological Synthesis of Copper Nanoparticles Using EdiblePlant Allium monanthum: Characterization of Antibacterial,Antioxidant, and Anti-Inflammatory Properties Using InSilico Molecular Docking Analysis |
논문명(영문) |
Biological Synthesis of Copper Nanoparticles Using EdiblePlant Allium monanthum: Characterization of Antibacterial,Antioxidant, and Anti-Inflammatory Properties Using InSilico Molecular Docking Analysis |
성과주관부서 |
국립축산과학원 축산자원개발부 초지사료과 |
품목코드 |
|
학술지명 |
Materials |
주저자 |
Hyo Shim Han |
성과년도 |
|
성과적용일 |
2023년11월 |
This study prepared copper nanoparticles using an edible leaf extract from A. monanthum
(AM-CuNPs) via eco-friendly green synthesis techniques. The size, shape, crystalline nature and functional
groups of the synthesized AM-CuNP particles were analyzed by a UV-VIS spectrophotometer
and SEM, EDX, TEM, XRD and FT-IR instrumentation. The synthesized AM-CuNPs had spherical
shapes with sizes in the range of 30–80 nm and were crystalline in nature. In addition, the AM-CuNPs
were synthesized using various bioactive sources, including flavonoids, phenolic acids, alkaloids and
sugars that were present in an aqueous broth of A. monanthum. Furthermore, the AM-CuNPs possessed
good antibacterial properties against selected major disease-causing pathogenic bacteria, such
as E. coli, Salmonella typhi, Pseudomonas aeruginosa and Staphylococcus aureus. The antioxidant activity
of AM-CuNPs exhibited potent free radical scavenging activities in DPPH, ABTS and H2O2 radical
assays. In addition, in silico analysis of the AM-CuNPs was performed, including ADME prediction,
and molecular simulation docking on the secondary metabolites identified in the edible plant extract
was used to evaluate their anti-inflammatory applications. In particular, the molecular docking scores
showed that alliin, apigenin, isorhamnetin, luteolin and myricetin have sufficient binding energy and
top values as inhibitors of the protein target involved in the inflammation signaling cascade