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从生物活性杂环配体到银纳米颗粒的纳米金属表面能量转移(NSET)诱导了对革兰氏阳性细菌增强的抗菌活性。

Nanometal surface energy transfer (NSET) from biologically active heterocyclic ligands to silver nanoparticles induces enhanced antimicrobial activity against gram-positive bacteria.

作者信息

Sarkar Dilip, Manna Mihir, Adhikary Amisha, Reja Sahin, Ghosh Supriyo, Saha Tilak, Bhandari Satyapriya, Kumar Das Rajesh

机构信息

Department of Chemistry, University of North Bengal, Darjeeling, West Bengal, India.

Centre for Nano Technology, Indian Institute of Technology, Guwahati, Assam, India.

出版信息

Colloids Surf B Biointerfaces. 2024 Feb;234:113733. doi: 10.1016/j.colsurfb.2023.113733. Epub 2024 Jan 2.

Abstract

Herein we report the formation of a nanometal surface energy transfer (NSET) pair between a donor biologically active heterocyclic luminescent ligand such as 3-(1,3-Dioxoisoindolin-2-yl)-N, N-dimethylpropan-1-ammonium perchlorate (SPNL; λ-408 nm) and an acceptor silver nanoparticle (Ag NP; λ-406 nm). When the SPNL ligand interacts with Ag NPs, the quenching in their luminescence intensity at 408 nm is noticed, with a Stern-Volmer constant of 0.8 × 10 M. The present donor-acceptor pair displays a binding constant of 2.8 × 10 M and binding sites of 1.12. The current work shows the energy transfer from a molecular dipole (SPNL) to a nanometal surface (Ag NP) and thus follows the nanometal surface energy transfer (NSET) ruler with an energy transfer efficiency of 80.0%, 50% energy transfer efficiency distance (d) of 4.9 nm, donor-acceptor distance of 3.4 nm. The alteration in the zeta potential value of SPNL upon interaction with AgNP clearly demonstrates the strong electrostatic interaction between donor and acceptor. Importantly, the current NSET pair shows enhanced antimicrobial activity against gram-positive bacteria such as Bacillus cereus (B. cereus) in comparison to their parent components i.e. SPNL ligand and Ag NP. The NSET pair shows maximum inhibition against B. cereus (9202.21 ± 463.26 CFU/ml.) at 10% while minimum inhibition is observed at 0.01% of it (39,887.19 ± 242.67 CFU/ml.).

摘要

在此,我们报道了在供体生物活性杂环发光配体(如3-(1,3-二氧代异吲哚啉-2-基)-N,N-二甲基丙-1-铵高氯酸盐(SPNL;λ-408 nm))与受体银纳米颗粒(Ag NP;λ-406 nm)之间形成了纳米金属表面能量转移(NSET)对。当SPNL配体与Ag NPs相互作用时,可观察到其在408 nm处的发光强度猝灭,斯特恩-沃尔默常数为0.8×10 M。目前的供体-受体对显示出结合常数为2.8×10 M,结合位点为1.12。当前的工作表明了能量从分子偶极子(SPNL)转移到纳米金属表面(Ag NP),因此遵循纳米金属表面能量转移(NSET)规则,能量转移效率为80.0%,50%能量转移效率距离(d)为4.9 nm,供体-受体距离为3.4 nm。SPNL与AgNP相互作用时zeta电位值的变化清楚地证明了供体和受体之间的强静电相互作用。重要的是,与它们的母体成分即SPNL配体和Ag NP相比,当前的NSET对显示出对革兰氏阳性菌如蜡样芽孢杆菌(B. cereus)增强的抗菌活性。NSET对在10%时对蜡样芽孢杆菌显示出最大抑制(9202.21±463.26 CFU/ml.),而在0.01%时观察到最小抑制(39,887.19±242.67 CFU/ml.)。

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