Fabrication of inorganic alumina particles at nanoscale by a pulsed laser ablation technique in liquid and exploring their protein binding,anticancer and antipathogenic activities

The interaction of nanoparticles with biological systems can provide useful information about their therapeutic applications. The aluminum nanoparticles (Al₂O₃ NPs) were synthesized by laser ablation technique and well-characterized by different methods. Fluorescence spectroscopy, circular dichroism (CD) spectroscopy, and molecular docking studies were employed to evaluate the effect of Al₂O₃ NPs on the protein structure. Growth inhibitory and apoptotic effects of the Al₂O₃ NPs against K562 cancer cells and lymphocyte cells were assessed using [3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide] (MTT), flow cytometry, and real time polymerase chain reaction (PCR) assays. The antipathogenic activity of Al₂O₃ NPs against a diverse range of Gram-negative and Gram-positive pathogens was explored through a disk diffusion method. The characterization techniques determined that the Al₂O₃ NPs were successfully synthesized in the nanoscales. Intrinsic, 1-anilino-8-naphthalenesulfonate (ANS) and acrylamide fluorescence spectroscopy studies disclosed that Al₂O₃ NPs can partially change the tertiary structure of human serum albumin (HSA), whereas CD spectroscopy investigation depicted that the secondary structure of HSA remained intact. Molecular docking investigation also manifest that the Al₂O₃ nano-clusters preferably bind to electrostatic residues. Al₂O₃ NPs exhibited promising and selective anticancer features through reactive oxygen species (ROS) production, apoptosis induction, and elevation of Bax/Bcl-2 mRNA ratio. Furthermore, the Al₂O₃ NP showed a remarkable antibacterial activity against both Gram-negative and Gram-positive pathogens. In conclusion, it may be suggested that the synthesized Al₂O₃ NPs can be integrated in the development of anticancer and antipathogenic agents.     

In situ synthesis of water dispersible bovine serum albumin capped gold and silver nanoparticles and their cytocompatibility studies

A simple and convenient one step room temperature method is described for the synthesis of bovine serum albumin (BSA) capped gold and silver nanoparticles. BSA reduces silver ions to silver nanoparticles but does not directly reduce gold ions to gold nanoparticles at room temperature and varying pH conditions. However, when silver and gold ions are simultaneously added to BSA, silver ions get reduced to metallic silver first and these in turn reduce gold ions to gold nanoparticles through a galvanic exchange reaction. The so synthesized silver and gold nanoparticles are easily water dispersible and can withstand addition of salt even at high concentrations. It is shown that the capped protein retains its secondary structure and the helicity to a large extent on the nanoparticles surface and that the protein capping makes the nanoparticles cytocompatible.