Bioinspired green synthesis of ZnO nanoparticles by marine-derived Streptomyces plicatus and its multifaceted biomedicinal properties.

The present study explores the bioinspired green synthesis of zinc oxide nanoparticles (ZnONPs) using marine Streptomyces plicatus and its potent antibacterial, antibiofilm activity against dental caries forming Streptococcus mutans MTCC and S. mutans clinical isolate (CI), cytotoxicity against oral KB cancer cells, hemolysis against blood erythrocytes and artemia toxicity. The bioinspired ZnONPs showed a distinctive absorption peak at 375 nm in UV-Vis spectra, the FT-IR spectra divulged the active functional groups, and XRD confirmed the crystalline nature of the nanoparticles with an average grain size of 41.76 nm. SEM analysis evidenced hexagonal morphology, and EDX spectra affirmed the presence of zinc. The ZnONPs exerted higher antagonistic activity against S. mutans MTCC (Inhibitory zone: 19 mm; MIC: 75 µg/ml) than S. mutans CI (Inhibitory zone: 17 mm; MIC: 100 µg/ml). Results of biofilm inhibitory activity showed a concentration-dependent reduction with S. mutans MTCC (15 %-95 %) more sensitive than S. mutans CI (13 %-89 %). The 50 % biofilm inhibitory concentration (BIC50) of ZnONPs against S. mutans MTCC was considerably lower (71.76 µg/ml) than S. mutans CI (78.13 µg/ml). Confocal Laser Scanning Microscopic visuals clearly implied that ZnONPs effectively distorted the biofilm architecture of both S. mutans MTCC and S. mutans CI. This was further bolstered by a remarkable rise in protein leakage (19 %-85 %; 15 %-77 %) and a fall in exopolysaccharide production (34 mg-7 mg; 49 mg-12 mg). MTT cytotoxicity of ZnONPs recorded an IC50 value of 22.06 µg/ml against KB cells. Acridine orange/ethidium bromide staining showed an increasing incidence of apoptosis in KB cells. Brine shrimp cytotoxicity using Artemia salina larvae recorded an LC50 value of 78.41 µg/ml. Hemolysis assay substantiated the biocompatibility of the ZnONPs. This study underscores the multifaceted application of bioinspired ZnONPs in dentistry.

Biosynthesis, characterization, and anticoagulant properties of copper nanoparticles from red seaweed of Acanthophora sp.

INTRODUCTION: In the last few decades, nanoparticles have found extensive use in a variety of biological applications. Traditional medicine widely uses Acanthophora sp., a marine macroalgae, to cure and prevent diabetes, skin disorders, and blood clotting. OBJECTIVE: The present study aims to investigate whether green-synthesized copper nanoparticles (CuNPs) might work as an anticoagulant. METHODOLOGY: The CuNPs were made using an environmentally friendly method that uses Acanthophora extract. We used UV-vis spectroscopy to assess the surface plasmon resonance of the material, scanning electron microscopy (SEM) to analyze its form, and energy dispersive X-ray (EDX) spectroscopy to identify the material's constituent elements. Furthermore, Fourier-transform infrared (FT-IR) determined the functional groups of the CuNPs. RESULTS: The biosynthesis of CuNPs was confirmed by UV-vis spectroscopy, which showed a surface plasmon resonance peak at 570 nm. The FT-IR analysis showed that certain functional groups are involved in the formation of CuNPs. These groups include OH stretching, C=O stretching, C-H bonding, C-N bonding, and Cu vibration. SEM analysis demonstrated the morphology of CuNPs synthesized, with a size of 0.5 µm, while EDS analysis confirmed their purity. The anticoagulant activity of prothrombin time (PT) and activated partial thromboplastin time (aPTT) assays showed that the clotting time got longer depending on the concentration. The CuNPs synthesized from Acanthophora had strong anticoagulant effects at 100 µg/mL, further suggesting that they might be useful as a natural blood thinner. CONCLUSION: The interesting thing we observed is that the green-synthesized CuNPs made from Acanthophora extract could be used in anticoagulation therapy.

Antifouling activity and biodegradable potential of the bioactive metabolites isolated from mangrove Avicennia officinalis L.

The present study explores the antifouling potentials of ethanol extract of mangrove Avicennia officinalis. Results of antibacterial activity inferred that extract had strongly inhibited the growth of fouling bacterial strains with significant differences in halos (9-16 mm) and showed minimal bacteriostatic (12.5-100 µg ml-1) and bactericidal (25-200µg ml-1) values. It had also strenuously suppressed fouling microalgae with appreciable MIC (12.5 and 50 µg ml-1). The extract had also effectively deterred settlement of larvae of Balanus amphitrite and byssal thread of mussel Perna indica with lower EC50 (11.67 and 37.43 µg ml-1) and higher LC50 (257.33 and 817 µg ml-1) values. Further 100% recuperation of mussels from toxicity assay and therapeutic ratio of >20 substantiated its non-toxicity. GC-MS profile of bioassay guided fraction showed four (M1-M4) major bioactive metabolites. In silico biodegradability study revealed that metabolites M1 (Pentanoic acid, 5-methoxy-, phenyl ester) and M3 (Benzaldehyde, methyl-) have rapid biodegradation rates and eco-friendly in nature.

Low cost and biocompatible Marine algae derived scaffolds: enhancing tissue regeneration in oral cancer surgery.

Efficient tissue regeneration following oral cancer surgery is crucial for maintaining function. Seaweed-derived scaffold materials, with their resemblance to oral tissue structure, promote cell adhesion and differentiation. Their high porosity aids in exudate absorption, reducing infection risks and tissue maceration. Further scaffold breakdown releases growth factors, aiding tissue regeneration. Easily integrated into dressings or gels, these scaffolds accelerate healing and protect against contaminants. Their biocompatibility and safety ensure minimal adverse effects. Seaweed-derived scaffolds offer a natural, sustainable approach to tissue repair, making them ideal for post-oral surgery dressing, facilitating effective tissue regeneration.

Unraveling bioactive metabolites of mangroves as putative inhibitors of SARS-CoV-2 Mpro and RBD proteins: molecular dynamics and ADMET analysis.

COVID-19 is a deadly pandemic caused by Corona virus leading to millions of deaths worldwide. Till today no medicine was available to cure this disease. This study selected 262 potential bioactive natural products derived from mangroves to inhibit the main protease (Mpro) and receptor-binding domain (RBD) protein of the COVID-19 virus. All the ligands were subjected to Adsorption Digestion Metabolism Excretion and Toxicity (ADMET) predictions and docking studies using AutodockVina. Among all the ligands, NP_143 (Shearinine A) and NP_242 (Amentoflavone), having the highest docking score of 10.2 and 10.1 Kj/mole, respectively, were picked for 100 ns of Molecular Dynamics using GROMACS. The trajectories generated were used to estimate Root mean square deviation (RMSD), Root mean square fluctuations (RMSF), Radius of Gyrations (RG), Solvent accessible surface area (SASA), and Hydrogen bonds. From the data generated, both the ligands have good binding ability at the active site of Mpro protein and do not deviate much. They have strong interactions with the amino acids during the 100 ns of simulations and can thus be considered potential drug candidates.Communicated by Ramaswamy H. Sarma.

HIGHLIGHTSSARS-CoV-2 Mpro plays a pivotal role in viral replication and serves as important drug target.Bioactive compounds of mangroves origin are promising source of antiviral drugs.ADMET and docking study explored two lead compounds from mangroves against Mpro.MD simulation validated ligands of lead compounds had stronger binding affinity with Mpro.