4.7 Article

In-situ polymerization of polycarbazole-zinc oxide nanocomposite: An in silico docking model and in vitro antibacterial biomaterial

Journal

EUROPEAN POLYMER JOURNAL
Volume 181, Issue -, Pages -

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.eurpolymj.2022.111701

Keywords

Nanocomposite; Molecular modelling; Binding affinity; Antibacterial activity; Zone of inhibition

Funding

  1. MoE (under the GATE scheme)

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This study focuses on the synthesis and characterization of polycarbazole-zinc oxide (PCz/ZnO) nanocomposite, and its applications in antibacterial biomaterial and molecular docking. The results showed successful polymerization of Cz on the surfaces of ZnO nanoparticles, and the PCz/ZnO nanocomposite exhibited better thermal stability compared to pristine PCz. The nanocomposite also demonstrated strong antibacterial activity against various bacteria, and the molecular docking suggested favorable binding affinity between PCz/ZnO and B-DNA.
The current study focuses on the synthesis of polycarbazole-zinc oxide (PCz/ZnO) nanocomposite and its application as an in vitro antibacterial biomaterial as well as an in silico docking model. The synthesized pristine polymer, polycarbazole (PCz) and its nanocomposite PCz/ZnO were characterized by Fourier transform infrared (FT-IR), Thermo-gravimetry/Differential Thermo-gravimetry (TG-DTG), X-ray diffraction (XRD), Field Emission Scanning Electron Microscopy (FE-SEM), Brunauer-Emmett-Teller (BET), Energy-dispersive X-ray (EDX), Raman and X-ray photoelectron spectroscopic (XPS) techniques. FT-IR, XRD, FE-SEM, and XPS studies revealed that the polymerization of Cz has been successfully achieved on the surfaces of ZnO nanoparticles, indicating the strong interfacial interaction between PCz and ZnO nanoparticles. However, TG-DTG studies revealed that the nano -composite, PCz/ZnO, proved thermally more stable compared to the pristine polymer, PCz. Further, the pristine PCz and PCz/ZnO nanocomposite were evaluated for antibacterial activity against Pseudomonas aeruginosa, Escherichia coli, Klebsiella pneumoniae, and Staphylococcus aureus. The nanocomposite PCz/ZnO showed the highest zone of inhibition against K. Pneumoniae (17 mm), followed by P. aeruginosa (16 mm), then S. aureus (14 mm) and E. coli (19 mm) at 80 mg ml -1. Significantly, the in silico molecular docking predicts the modes of interactions of PCz and PCz/ZnO with B-DNA. Briefly, the results obtained from in silico molecular docking studies of the pristine PCz and PCz/ZnO nanocomposite with negative free binding energies (-7.1 kcal mol-1 of PCz and-6.23 kcal mol-1 of PCz/ZnO) imply an excellent and favourable binding affinity vis-`a-vis interaction modes of both pristine PCz and PCz/ZnO nanocomposite (drugs) with B-DNA bases (target).

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