RESUMEN
The study investigates the potential of Rhizoclonium hieroglyphicum as a novel source for synthesizing nickel oxide nanoparticles (RH-NiONPs) and evaluates its biological applications. Phytochemicals in the algal extract serve as capping, reducing and stabilizing agent for nickel oxide nanoparticles. The process variables were optimized using BBD based RSM to obtain maximum RH-NiONPs. Characterization of RH-NiONPs using UV-Vis and FT-IR spectroscopy reveals the plasmon resonance peak at 340 nm and the functional groups responsible for reduction and stabilization. XRD confirmed the crystalline nature while the stability and size of the RH-NiONPs were determined by DLS and zeta potential. Toxicity assessments demonstrated the effect of RH-NiONPs against Vigna radiata, Allium cepa and Artemia salina was low. RH-NiONPs revealed significant zone of inhibition against the selected bacteria and fungi. The results of larvicidal activity showed that RH-NiONPs are toxic to 4th instar larvae of Daphnis nerii. Also, RH-NiONPs efficiently decolorized Reactive Violet 13 (92%) under sunlight irradiation and the experimental data well fits to Langmuir isotherm along with pseudo second order kinetic model. The thermodynamic studies enunciate the exothermic and non-spontaneous photocatalytic decolorization of reactive violet 13. Thus, the current study assesses the eco-friendly and cost-effective nature of RH-NiONPs along with its biological applications.
Asunto(s)
Artemia , Nanopartículas del Metal , Níquel , Extractos Vegetales , Níquel/química , Níquel/farmacología , Animales , Extractos Vegetales/química , Extractos Vegetales/farmacología , Nanopartículas del Metal/química , Artemia/efectos de los fármacos , Cebollas/química , Cebollas/efectos de los fármacos , Daphnia/efectos de los fármacos , Vigna/química , Propiedades de Superficie , Larva/efectos de los fármacos , Tamaño de la Partícula , Pruebas de Sensibilidad Microbiana , Antibacterianos/farmacología , Antibacterianos/química , Antibacterianos/síntesis químicaRESUMEN
The present study is the first attempt to utilize the root extracts of Glycyrrhiza glabra as a novel biological route for the synthesis of iron oxide nanoparticles (Fe2O3NPs) under optimized conditions. The process variables namely concentration of ferric chloride, root extract of G. glabra and temperature were optimized using Response Surface Methodology (RSM) to obtain high yield. Phytochemicals mediated the reduction process and served as capping and stabilizing agent. The biosynthesized Fe2O3NPs characterized using UV-Vis spectroscopy exhibited a prominent peak at 350 nm. The crystallinity and valence state of Fe2O3NPs was confirmed by XRD and XPS. The surface functionalization of the nanoparticles was confirmed from the presence of functional groups in the FT-IR spectrum. The FESEM analysis revealed the biosynthesized Fe2O3NPs are irregular and the EDX spectrum recorded the presence of iron and oxygen in the synthesized nanoparticles. The biosynthesized Fe2O3NPs exhibited an appreciable photocatalytic activity against methylene blue under sunlight with a maximum decolorisation efficiency of 92% within 180 min of reaction time. The experimental data of adsorption studies well fitted with Langmuir isotherm and pseudo-second order kinetic model. The thermodynamic study proved to be spontaneous, feasible and endothermic in nature. The phytotoxicity study revealed 92% germination and increased seedling growth in the green gram seeds exposed to Fe2O3NPs. Hence the study established the efficiency of biosynthesized of Fe2O3NPs in photocatalytic and phytotoxic activities.
Asunto(s)
Alcaloides , Glycyrrhiza , Nanopartículas del Metal , Nanopartículas , Espectroscopía Infrarroja por Transformada de Fourier , Nanopartículas/química , Extractos Vegetales/farmacología , Extractos Vegetales/química , Nanopartículas Magnéticas de Óxido de Hierro , Nanopartículas del Metal/químicaRESUMEN
The present study was investigated to synthesis the iron nanoparticles (FeNPs) using the leaf extract of Phyllanthus reticulatus. The phytosynthesized FeNPs exhibited UV-visible absorption peaks at 229 nm and its crystalline nature was confirmed through XRD. FT-IR analysis revealed the presence of various functional groups which are responsible for the bioreduction of FeNPs. The SEM results showed that FeNPs were aggregated, irregular sphere shaped with rough surfaces and EDX spectrum recorded densely occupied iron nanoparticles region. The particle size range of the synthesized iron nanoparticles was 185.6 nm. The FeNPs showed potential methylene blue decolourisation activity which was visually observed by gradual colour change in the dye solution from deep blue to colorless. The control exhibited no change in coloration during exposure to sunlight and the iron nanoparticles completely disintegrated the methylene blue within 10 s in 10 mg/L methylene blue (98%), whereas the color change was decreased when the concentration of the dye increased. In addition, the phyto-synthesized FeNPs exhibited extensive antibacterial and antifungal activity against the selected pathogens. Phytotoxicity assay confirms the potential of biosynthesized iron nanoparticles as a fertilizer for the growth of green gram seeds. Thus the present study leads to development of cost-effective green synthesis, reduction of toxic chemicals and its extensive applications in the biological sciences.
RESUMEN
The present investigation is an attempt to assess the impact of untreated methyl orange and Oedogonium subplagiostomum AP1 treated methyl orange dye solutions on Labeo rohita. The behavioural response, mortality, haematological (red blood corpuscles (RBC), packed cell volume (PCV), haemoglobin (Hb), white blood corpuscles (WBC), mean corpuscular volume (MCV), mean corpuscular haemoglobin (MCH) and mean corpuscular haemoglobin concentration (MCHC)), biochemical (plasma glucose and protein), enzymological (aspartate amino transaminases (AST) and alanine amino transaminases (ALT)) and histological examination (gills, liver and kidney) of Labeo rohita are exposed to untreated and treated methyl orange dye solutions were assessed on 7th day. The fish exposed to tap water and treated dye solution showed normal behavioural response whereas abnormal behaviour was noted in fish exposed to untreated dye solution. Similar trend was recorded in the mortality rate of the fishes. Fish exposed to untreated dye solution showed reduction in RBC, PCV, Hb, MCHC, plasma glucose and plasma protein, increased level of WBC, MCV and MCH and also alteration in AST and ALT thereby indicating the toxicity of the dye. No such reduction and alteration were observed in haematological, biochemical and enzymological levels of fishes exposed to tap water and treated dye solution indicating the non-toxic nature of the degraded metabolites of dye. Histological examination of fishes exposed to methyl orange dye revealed necrosis and haemorrhage in the gills and hepatocytes, congested and shrunken glomeruli in kidney thereby indicating the toxicity of the dye. The histoarchitecture of control and algae-treated fishes showed no structural changes indicating the non-toxic nature of the degraded metabolites of the dye. The results concluded that methyl orange dye solution treated with O. subplagiostomum AP1 can be explored for aquacultural purposes owing to its non-toxic nature.