Metal oxide nanoparticles are gaining interest in recent years. The present paper explains about the green synthesis of zirconium oxide nanoparticles (ZrO NPs) mediated from the leaves of Lagerstroemia speciosa. The prepared ZrO NPs were characterized by UV–vis spectroscopy, FT-IR, X-ray diffraction analysis (XRD), Transmission Electron Microscopy (TEM), Scanning Electron Microscopy (SEM), Energy Dispersive X-ray spectroscopy (EDX) and Thermogravimetric Analysis (TGA). The photocatalytic activity of ZrO NPs was studied for azo dye by exposing to sunlight. The azo dye was degraded up to 94.58%. Also the ZrO NPs were studied for in vitro cytotoxicity activity against breast cancer cell lines-MCF-7 and evaluated by MTT assay. The cell morphological changes were recorded by light microscope. The cells viability was seen at 500 μg/mL when compared against control. Hence the research highlights, that the method was simple, eco-friendly towards environment by phytoremediation activity of the azo dye and cytotoxicity activity against MCF-7 cell lines. Hence the present paper may help to further explore the metal nanoparticle for its potential applications. © 2017 Elsevier B.V.

Sai Saraswathi V

Department of Chemistry

School of Advanced Sciences

Vellore Campus

Santhakumar K

Vellore Institute of Technology (VIT) is a private university located in&nbsp;Tamil Nadu, India. Founded in 1984, as Vellore Engineering College, the institution offers 20 undergraduate, 34 postgraduate, four integrated and four research programs. It has campuses in Vellore, Amravati, Bhopal and Chennai.

VIT is one of the top ranked private universities in India according to NIRF, THE and QS Rankings.&nbsp;Govt. of India has recognized&nbsp;VIT, Vellore as an&nbsp;Institution of Eminence. This has allowed VIT to take independent quality initiatives and move up in world ranking.

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VIT University

Journal of Photochemistry and Photobiology B: Biology

The investigation was aimed to quantify the Gallic acid present in Lagerstroemia speciosa leaves (Lythraceae). The High-Performance Thin Layer Chromatography (HPTLC) quantification was performed for acetone (AE), methanolic (ME) and chloroform (CE) extract of leaves of L. speciosa. The pre-coated silica gel 60 F254 was used for complete separation of compounds using the mobile phase pet. Ether: ethyl acetate: formic acid (5:5:1 v/v).The validation of the extracts was carried out using ICH guidelines for precision, repeatability and accuracy showing the Rf 0.49 against standard Gallic acid. Linearity range for Gallic acid was done from 200 to 1000 ng/spot (AE) and200 ng to 600 ng/spot (ME), with Correlation, coefficient r = 0.99 (AE) and 0.54 (ME) in the said concentrations. The composition in crude leaf extract was determined to be of 49.712 mg (AE) and 20.125 mg (ME), while it was not found in chloroform extract against standard Gallic acid. Hence the proposed method was very simple, precise, accurate and easy for the screening of the bioactive compounds present in the acetone and methanolic extracts of the leaves of L. speciosa. It was observed that the acetone extract subjected to cytotoxicity showed promising activity at higher concentrations (100 and 200 μg/ml) showed 92.9% and 87.13% inhibition against MCF-7 cell lines respectively. The photocatalytic activity of the acetone and methanolic extracts of methyl orange was found to be 90.25% (190 min) and 89.03% (180 min) respectively. Therefore this can be used as an indicator of purity of herbal drugs and formulation containing L. speciosa. © 2017 Elsevier B.V.

Solar catalysed activity against methyl orange dye, cytotoxicity activity of MCF-7 cell lines and identification of marker compound by HPTLC of Lagerstroemia speciosa

The investigation was conducted to analyse the bioactive compounds from the leaf extracts of L. speciosa by GC–MS. The extracts were screened for antibacterial and antibiofilm activities against potential clinical strains. The bioactive compounds from the leaves of L. speciosa were extracted by soxhlet continuous extraction method and their chemical composition was analysed by Gas Chromatography–Mass Spectroscopy (GC–MS). The antibacterial activity was evaluated against clinical strain like Staphylococcus aureus, Escherichia coli, P. aeruginosa and Salmonella typhi by well diffusion technique. We also screened for antibacterial property against common food borne pathogens namely Listeria monocytogenes and Bacillus cereus at varied concentration 250 μ ml− 1 to 1000 μ ml− 1. Thereafter antibiofilm assay was carried out at from 250 to 1000 μg/ml against P. aeruginosa (high biofilm forming pathogen) clinical strain by cover slip technique and the morphology of the pathogen was observed using Scanning Electron Microscopy-(SEM). It was observed that diverse class of secondary metabolites were found by GC–MS analysis for all the extracts upon the continuous extraction. It was found that only minimum inhibition was seen in alcoholic extract for antibacterial activity, whereas all other extracts showed negligible activity. P. aeruginosa biofilm inhibited to 93.0 ± 2% and 91 ± 2% at higher concentration (1000 μg/ml) for methanolic and ethanolic extract respectively. Absence of extracellular matrix structure and the surface cracking of biofilm were viewed by SEM, which confirmed the antibiofilm activity. Hence this study reveals that L. speciosa showed significant antibiofilm activity against P. aeruginosa due to the phytoconstituents present in the leaf extracts which was well documented in the alcoholic extracts by GC–MS analysis. The methanolic and ethanolic extract showed good photocatalytic activity of 77.44% and 96.66% against azo dye degradation respectively. Further, isolating the novel phyto-compounds would yield better promising biological activities. © 2017 Elsevier B.V.

Biofilm inhibition formation of clinical strains of Pseudomonas aeruginosa mutans, photocatalytic activity of azo dye and GC–MS analysis of leaves of Lagerstroemia speciosa

Synthesis of metal oxide nanoparticles using novel methodologies always attracts great importance in research. The use of plant extract to synthesize nano-particle has been considered as one of the eco-friendly methods. This paper describes the biosynthetic route of preparation of zinc oxide nanoparticles (ZnO NPs) from the Lagerstroemia speciosa leaf extract. This approach appears to be low-cost preparation and alternative method to conventional methods. Highly stable and hexagonal phase ZnO NPs with average particle size of 40nm were synthesized and characterized by UV-Vis absorption spectroscopy (surface Plasmon resonance), Fourier transform infrared spectroscopy (surface functionalities), X-ray Diffraction analysis (crystallinity), TEM and SEM (size and morphology), Energy Dispersive X-ray spectroscopy (elemental composition), Thermogravimetric analysis (weight loss) and Zeta potential (stability). The preliminary phytochemical experiments identify the possible chemical groups present in leaves extract. The photocatalytic properties of ZnO NPs were studied using UV-Vis spectroscopy by exposing methyl orange to sunlight and it is found to be degraded up to 93.5% within 2h. The COD values were significantly reduced from 5600mg/L to 374mg/L after 100min of solar radiation. The hemolytic activity of synthesized zinc oxide nanoparticles was performed on human erythrocyte cells. Thus the present study provides a simple and eco-friendly method for the preparation of multifunctional property of ZnO NPs utilizing the biosynthetic route.

Facile biosynthesis, characterization, and solar assisted photocatalytic effect of ZnO nanoparticles mediated by leaves of L. speciosa

The aim of this study was to prepare silver nanoparticles by a green method using the aqueous leaves extract of Lagerstroemia speciosa. The prepared silver nanoparticles were characterized, studied for its photocatalytic and biofilm inhibition studies. The maximum absorbance peak was found at 427 nm and thus confirming the formation of silver nanoparticles. The average size of silver nanoparticles synthesized was found to be 12 nm using XRD and it was spherical in shape. The nanoparticles synthesized was investigated for photocatalytic activity for to two different dye molecules, methyl orange and methylene blue showing 310 and 290 min degradation time respectively. The silver nanoparticles biofilm inhibition assay against clinical strains of Pseudomonas aeruginosa showed lowest accumulation at a lower concentration. The biofilm inhibition was also studied by visual interpretation through Scanning Electron Microscopy states that 50 μg mL− 1 exerts the highest inhibition compared against the control. This evident helps to analysis the silver nanoparticles for various applications in future. © 2017 Elsevier B.V.

Phytoremediation of dyes using Lagerstroemia speciosa mediated silver nanoparticles and its biofilm activity against clinical strains Pseudomonas aeruginosa

Twelve surfactant Schiff base ligands were synthesized from salicylaldehyde and its chloro-, bromo- and methoxy- derivatives by condensation with long-chain aliphatic primary amines, and a number of mixed ligand cobalt(III) surfactant Schiff base coordination complexes of the type [Co(trien)A] 2+ were synthesized from the corresponding dihalogeno complexes by ligand substitution. The Schiff bases and their complexes were characterized by physico-chemical and spectroscopic methods. The complexes form foams in aqueous solution upon shaking. The critical micelle concentration (CMC) values of the complexes in aqueous solution were obtained from conductance measurements. Specific conductivity data (at 303-323 K) served for the evaluation of the thermodynamics of micellization (δGmo, δH mo, δSmo). The complexes were tested for its antimicrobial activity. © 2009 Springer Science+Business Media B.V.

Transition Metal Chemistry

Metallosurfactant Schiff base cobalt(III) coordination complexes. Synthesis, characterization, determination of CMC values and biological activities

Kinetics of reduction of the surfactant complex ions, cis-chloro/bromo (dodecylamine)bis(ethylenediamine)cobalt(III) by iron(II) in aqueous solution was studied at 303, 308, and 313 K by spectrophotometry method under pseudo-first-order conditions, using an excess of the reductant. The second-order rate constant remains constant below critical micelle concentration (cmc), but increases with cobalt(III) concentration above cmc, and the presence of aggregation of the complex itself alters the reaction rate. The rate of reaction was not affected by the added [H+]. Variation of ionic strength (μ) influences the reaction rate. Activation and thermodynamic parameters have been computed. It is suggested that the reaction of Fe 2+ (aq) with cobalt(III) complex proceeds by the inner-sphere mechanism. © 2005 Wiley Periodicals.

International Journal of Chemical Kinetics

Kinetics of Fe(II) reduction ofcis-halogeno(dodecylamine) bis(ethylenediamine)- cobalt(III) complex ion in aqueous solutions

Photocatalytic activity against azo dye and cytotoxicity on MCF-7 cell lines of zirconium oxide nanoparticle mediated using leaves of Lagerstroemia speciosa

Journal	Data powered by TypesetJournal of Photochemistry and Photobiology B: Biology
Publisher	Data powered by TypesetElsevier BV
ISSN	1011-1344
Open Access	No