Biosynthesis and biological activities of magnesium hydroxide nanoparticles using Tinospora cordifolia leaf extract.

The synthesis of magnesium hydroxide nanoparticles (Mg(OH)2 NPs) using plant extracts are known to be a practical, economical, and an environmentally friendly approach. In this work, Mg(OH)2 NPs were synthesized using aqueous leaf extract of Tinospora cordifolia, a medicinal plant commonly found in India. The synthesized Mg(OH)2 NPs were characterized using various spectroscopic techniques. The ultraviolet-visible (UV-Vis) absorption peak of the Mg(OH)2 NPs was detected at 289 nm, Fourier transform infrared (FTIR) analysis confirmed the presence of various functional groups, and X-ray diffraction (XRD) patterns revealed the well-crystallized structure of the Mg(OH)2 NPs. High-resolution transmission electron microscopy (HR-TEM) and scanning electron microscopy (SEM) analyses depicted spherical morphology and an average particle size (PS) of 27.71 nm. The energy-dispersive X-ray (EDX) analysis confirmed the presence of C, O, and Mg elements, and the X-ray photoelectron spectroscopy (XPS) survey spectrum confirmed the elements for the Su 1 s peak at 280.2 eV. The dynamic light scattering (DLS) analysis displayed an average PS of 54.3 nm, and the Zeta potential (ZP) was of 9.89 mV. The fabricated Mg(OH)2 NPs displayed notable antibacterial activity against S. epidermidis, E. coli, and S. aureus. In addition, these NPs exhibited strong antioxidant properties (> 75%) based on DPPH, ABTS, and hydrogen peroxide (H2O2) assays. Further, the same NPs exerted a potent anti-inflammatory activity (> 65%) based on COX-1 and COX-2 evaluations. The anti-Alzheimer' disease (AD) potential of Mg(OH)2 NPs was assessed through effective inhibition (> 70%) of acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) activities. Molecular docking (MD) studies confirmed that caryophyllene has higher binding affinity with AChE (-5.3 kcal/mol) and BuChE (-6.4 kcal/mol) enzymes. This study emphasizes the green synthesis of Mg(OH)2 NPs using T. cordifolia as a plant source and highlights their potential for biomedical applications.

Sustainable heavy metal (Cr(VI) ion) remediation: Ternary blend approach with chitosan, carboxymethyl cellulose, and bioactive glass.

Heavy metal pollution poses a significant environmental challenge to worldwide, especially in developing countries. This study focuses on eliminating the heavy metal chromium (VI) ion from wastewater, employing an eco-friendly and economical ternary blend composed of Chitosan (CS), Carboxymethyl cellulose (CMC), and bioactive glass (BAG). The innovative bioactive glass is crafted from biosilica extracted from biowaste of cow dung ash, calcium oxide from eggshell ash, and phosphorus pentoxide. The CS/CMC/BAG blend is prepared via sol-gel method and characterized using XRD, FT-IR, TGA, BET, TEM and SEM revealing a porous structural morphology during blending. Batch adsorption studies explore various parameters such as pH, adsorbent dose, contact time and initial metal ion concentrations. The results are then evaluated through adsorption kinetics and adsorption isotherms (Langmuir, Freundlich, D-R, and Temkin isotherm modeling). The investigation concludes that the optimal conditions for Cr (VI) removal are pH 3, contact time of 300 min, adsorbent dosage of 0.5 g, and an initial metal ion concentration of 50 ppm. The adsorption isotherm model indicates an excellent fit with the Freundlich isotherm (R2 = 0.9576) and pseudo-second-order kinetics (R2 = 0.981). In summary, the CS/CMC/BAG ternary blend exhibits a remarkable ability to effectively remove heavy metal Cr(VI) ions from industrial wastewater.

Sustainable Green Synthesis of Yttrium Oxide (Y2O3) Nanoparticles Using Lantana camara Leaf Extracts: Physicochemical Characterization, Photocatalytic Degradation, Antibacterial, and Anticancer Potency.

Due to their appropriate physicochemical properties, nanoparticles are used in nanomedicine to develop drug delivery systems for anticancer therapy. In biomedical applications, metal oxide nanoparticles are used as powerful and flexible multipurpose agents. This work described a green synthesis of Y2O3 nanoparticles (NPs) using the sol-gel technique with the use of aqueous leaf extracts of Lantana camara L (LC). These nanoparticles were characterized with the aid of different methods, including UV, X-ray diffraction (XRD), Fourier transformed infrared spectroscopy (FTIR), transmitted electron microscopy (TEM), and photocatalytic degradation. Y2O3 nanoparticles showed excellent antibacterial activity against Gram-positive Bacillus subtilis and Gram-negative Escherichia coli with a 10 to 15 mm inhibitory zone. Green Y2O3 NPs were released with a 4 h lag time and 80% sustained release rate, indicating that they could be used in drug delivery. In addition, the bioavailability of green Y2O3 NPs was investigated using cell viability in cervical cancer cell lines. These green-synthesized Y2O3 NPs demonstrated photocatalytic degradation, antibacterial, and anticancer properties.

Synthesis, characterization and pharmacological potential of green synthesized copper nanoparticles.

The phenomenal and astonishing properties and their different application in the field of pharmaceutical made copper nanoparticles (Cu-NPs) to be in the spotlight of the researcher's focus. In the present study, copper nanoparticles were biologically synthesized with the aqueous extract of the flower Millettia pinnata, and their corresponding characteristics were studied using UV-visible spectroscopy, XRD, FT-IR, SEM, TEM, and SAED analysis. Copper acetate was reduced to copper nanoparticles and is confirmed by UV-visible spectrophotometer analysis. The maximum absorption occurring at 384 nm at the visible spectrum of UV rays confirms the surface plasmon resonance of the nanoparticles. The result of the FTIR spectroscopy analysis of the nanoparticles complements the involvement of organic mioties of the flower extract in the synthesis. The synthesized particles were extremely durable, spherical with the average particle size in the range of 23 ± 1.10 nm. The Cu-NPs exhibited greater inhibition on DPPH radical and nitric oxide scavenging activities. The biologically synthesized Cu-NPs was receptive to the Gram-negative and Gram-positive bacteria as well. The Cu-NPs exhibited strong anti-inflammatory activity using albumin denaturation and membrane stabilization. The present study is the first effort done to synthesize of Cu-NPs from the extract of M. pinnata flower. Consequently, to authenticate the results and to establish the antioxidant, antibacterial, an anti-diabetic and anti-inflammatory agent, in vivo studies are made in the molecular level.

Green approach for synthesis of zinc oxide nanoparticles from Andrographis paniculata leaf extract and evaluation of their antioxidant, anti-diabetic, and anti-inflammatory activities.

Bio-mediated synthesis of zinc oxide nanoparticles (ZnO NPs) was carried out by utilizing the reducing and capping potential of Andrographis paniculata leaf extract. The capped ZnO NPs were characterized using UV-Vis, XRD, FTIR, SEM, TEM and SAED analyses. FTIR analysis suggested the role of phenolic compounds, terpenoids, and proteins of A. paniculata leaf extract, in nucleation and stability of ZnO NPs. XRD pattern compared with the standard confirmed spectrum of zinc oxide particles formed in the present experiments were in the form of nanocrystals, as evidenced by the peaks at 2θ values. SEM and TEM analysis of ZnO NPs reveals those spherical and hexagonal shapes and the sizes at the range of 96-115 and 57 ± 0.3 nm, respectively. The synthesized nanoparticles possess strong biological activities regarding anti-oxidant, anti-diabetic, and anti-inflammatory potentials which could be utilized in various biological applications by the cosmetic, food and biomedical industries.

Batch adsorption and desorption studies on the removal of lead (II) from aqueous solution using nanochitosan/sodium alginate/microcrystalline cellulose beads.

The feasibility of adsorption and desorption behavior of nanochitosan(NCS)/sodium alginate(SA)/microcrystalline cellulose (MC) bead prepared in 2:8:1 ratio for Pb(II) removal has been investigated through batch studies. The proof of adsorption of Pb(II) ions onto NCS/SA/MC beads was identified from FT-IR and EDX-SEM Studies. Studies of the effect of pH, adsorbent dose, metal ion concentration and temperature reveals that the optimum conditions for adsorption was found to be pH:6; adsorbent dose:4g; initial metal concentration: 62.5mg/L and temperature:50°C. Various equilibrium adsorption isotherm models namely Langmuir, Freundlich, Temkin and D-R applied for the analysis of isotherm data indicate that the Freundlich adsorption isotherm model was found to be followed. On the basis of kinetic studies, specific rate constants involved in the processes were calculated and the observed result shows that the pseudo second order kinetics was found to be a better fit. The desorption studies reveals that the recovery of Pb(II) from NCS/SA/MC bead was found to be effective by using 0.1M HCl solution. From the results it was evident that the NCS/SA/MC bead showed better Pb(II) uptake performance and regeneration for further use and hence it was found to be an efficient biosorbent for treating industrial effluent.

Fabrication of letrozole formulation using chitosan nanoparticles through ionic gelation method.

In this study, the anticancer drug letrozole (LTZ) was formulated using chitosan nanoparticles (CS-NPs) with the crosslinking agent sodium tripolyphosphate (TPP). The nano-formulation was optimized by varying the concentration of drug. The prepared particles were characterized using FTIR, TGA, XRD, SEM, TEM and DLS. From the FTIR results, the appearance of a new peak for CH, CC and CN confirms the formation of LTZ loaded chitosan nanoparticles. TEM images shows that the average particle size was in the range of 60-80nm and 20-40mm air dried and freeze dried samples respectively. Also the prepared formulation had been evaluated in vitro for determining its hemocompatability, biodegradability and serum stability. The preliminary studies supported that the chitosan nanoparticles formulation has biocompatibility and hemocompatible properties and it can act as an effective pharmaceutical excipient for letrozole.

Evaluation of anti-cholinesterase, antibacterial and cytotoxic activities of green synthesized silver nanoparticles using from Millettia pinnata flower extract.

The aim of this study is to develop an easy and eco-friendly method for the synthesis of Ag-NPs using extracts from the medicinal plant, Millettia pinnata flower extract and investigate the effects of Ag-NPs on acetylcholinesterase (AChE), butyrylcholinesterase (BChE), antibacterial and cytotoxicity activity. UV-Vis peak at 438 nm confirmed the Ag-NPs absorbance. The SEM analysis results confirmed the presence of spherical shaped Ag-NPs by a huge disparity in the particle size distribution with an average size of 49 ± 0.9 nm. TEM images revealed the formation of Ag-NPs with spherical shape and sizes in the range between 16 and 38 nm. The Ag-NPs showed an excellent inhibitory efficacy against AChE and BChE. The highest antibacterial activity was found against Escherichia coli (20.25 ± 0.91 mm). These nanoparticles showed the cytotoxic effects against brine shrimp (artemia saliana) nauplii with a LD50 value of 33.92.

Removal of Cr(VI) from aqueous solution using chitosan-g-poly(butyl acrylate)/silica gel nanocomposite.

The present work deals with the preparation of the novel sorbent, glutaraldehye crosslinked silica gel/chitosan-g-poly(butyl acrylate) (Cs-g-PBA/SG) nanocomposite by sol-gel method for removal of toxic chromium ion. Prepared nanosorbent was then characterized by FTIR, XRD, DLS, SEM, BET isotherm for its formation and suitability. Its sorption capacity and sorption isotherms were brought under batch mode to suit the optimal parameters viz., contact time, pH, adsorbent dose and initial metal ion concentration which influence the sorption. The theoretical modeling such as Langmuir and Freundlich isotherm adsorption were applied to describe isotherm constants. Equilibrium data agreed well with the Langmuir isotherm model (R(2)=0.9763) with maximum adsorption capacity of 55.71 (mg/g). The kinetic studies showed that the adsorption follows the pseudo-second-order kinetics (R(2)=0.9999). From the results, it was concluded that Cs-g-PBA/SG nanocomposite is an excellent biosorbent for Cr removal from wastewater.

Removal of copper(II) from aqueous solution using nanochitosan/sodium alginate/microcrystalline cellulose beads.

The present study was aimed to prepare the novel ternary biopolymeric beads of nanochitosan (NCS)/sodium alginate (SA)/microcrystalline cellulose (MC) for the removal of heavy metal copper from aqueous solution through batch adsorption mode. The polymeric beads were characterized before and after adsorption using FTIR, XRD and EDX-SEM studies. The efficiency of the adsorbent was analyzed by varying the parameters such as initial metal ion concentration, contact time, adsorbent dose and pH. The experimental data obtained were fitted in the isotherm models such as Langmuir, Freundlich and Tempkin models and in pseudo first and second order kinetics studies. The isotherm and kinetics models revealed that the adsorption was found to fit well with Freundlich isotherm and follows pseudo second-order kinetics.

Sunitinib loaded chitosan nanoparticles formulation and its evaluation.

The nano-polymeric pharmaceutical excipient such as chitosan nanoparticles (CS-NPs) were synthesized for formulating the anticancer drug Sunitinib (STB). The formulation was done through the simple ionic cross linking method. The prepared formulation was characterized by DLS, SEM, FT-IR and XRD. The DLS study reveals that the Sunitinib loaded chitosan nanoparticles (SNB-CS-NPs) were in the size range of < 200 nm. Encapsulation of Sunitinib and validation for the formulation was done using UV spectrophotometry. In vitro drug release and its cytotoxic studies were performed for STB-CS-NPs. This study implies the novel drug delivery system for Sunitinib for the effective sustained delivery.

Marine carbohydrates of wastewater treatment.

Our natural heritage (rivers, seas, and oceans) has been exploited, mistreated, and contaminated because of industrialization, globalization, population growth, urbanization with increased wealth, and more extravagant lifestyles. The scenario gets worse when the effluents or contaminants are discharged directly. So wastewater treatment is a very important and necessary in nowadays to purify wastewater before it enters a body of natural water, or it is applied to the land, or it is reused. Various methods are available for treating wastewater but with many disadvantages. Recently, numerous approaches have been studied for the development of cheaper and more effective technologies, both to decrease the amount of wastewater produced and to improve the quality of the treated effluent. Biosorption is an emerging technology, which uses natural materials as adsorbents for wastewater treatment. Low-cost adsorbents of polysaccharide-based materials obtained from marine, such as chitin, chitosan, alginate, agar, and carrageenan, are acting as rescue for wastewater treatment. This chapter reviews the treatment of wastewater up to the present time using marine polysaccharides and its derivatives. Special attention is paid to the advantages of the natural adsorbents, which are a wonderful gift for human survival.

Comparative studies on the removal of heavy metals ions onto cross linked chitosan-g-acrylonitrile copolymer.

The graft copolymerization of acrylonitrile onto cross linked chitosan was carried out using ceric ammonium nitrate as an initiator. The prepared cross linked chitosan-g-acrylonitrile copolymer was characterized using FT-IR and XRD studies. The adsorption behavior of chromium(VI), copper(II) and nickel(II) ions from aqueous solution onto cross linked chitosan graft acrylonitrile copolymer was investigated through batch method. The efficiency of the adsorbent was identified from the varying the contact time, adsorbent dose and pH. The results evident that the adsorption of metal ions increases with the increase of shaking time and metal ion concentration. An optimum pH was found to be 5.0 for both Cr(VI) and Cu(II), whereas the optimum pH is 5.5 for the adsorption of Ni(II) onto cross linked chitosan-g-acrylonitrile copolymer. The Langmuir and Freundlich adsorption models were applied to describe the isotherms and isotherm constants. Adsorption isothermal data could be well interpreted by the Freundlich model. The kinetic experimental data properly correlated with the second-order kinetic model. From the above results it was concluded that the cross linked chitosan graft acrylonitrile copolymer was found to be the efficient adsorbent for removing the heavy metals under optimum conditions.

Studies on drug-polymer interaction, in vitro release and cytotoxicity from chitosan particles excipient.

Nonobvious controlled polymeric pharmaceutical excipient, chitosan nanoparticles (CS-NPs) for lenalidomide encapsulation were geared up by the simple ionic cross linking method to get better bioavailability and to reduce under as well as overloading of hydrophobic and sparingly soluble drug lenalidomide towards cancer cells. Lenalidomide loaded chitosan nanoparticles (LND-CS-NPs) were in the size range of 220-295 nm and characterized by DLS, TEM, FT-IR, TGA and XRD. Encapsulation of lenalidomide over chitosan nanoparticles was observed about 99.35% using UV spectrophotometry method. In vitro release and the cytotoxic studies were performed using LND-CS-NPs. This study implies the new drug delivery route for lenalidomide and illustrates that the CS-NPs serves as the effective pharmaceutical carrier for sustained delivery of lenalidomide.

Preparation and characterization of nano chitosan for treatment wastewaters.

Chitosan nanorod with minimum particle size of <100 nm was prepared by crosslinking low molecular weight chitosan with polyanion sodium tripolyphosphate and physicochemically characterized (FT-IR, XRD, SEM, AFM, TGA and DSC) for waste water treatment. Its sorption capacity and sorption isotherms for chromium (Cr) were studied. The effect of initial concentration of Cr ions, sorbent amount, agitation period and pH of solution that influence sorption capacity were also investigated. It was found that nanochitosan in the solid state was rod shaped which could sorb Cr (VI) to Cr (III) ions effectively. Based on the Langmuir, the Freundlich and the Temkin sorption isotherms, the sorption capacity of chitosan nanoparticles is very high and the adsorbent favors multilayer adsorption. The kinetics studies show that the adsorption follows the pseudo-second-order kinetics, which infers the transformation of Cr (VI) to Cr (III). From the results it was concluded that nanochitosan is an excellent material as a biosorbent for Cr removal from water.