Mg Of Nanoparticles Research Articles

Catalytic Degradation Efficacy of Silver Nanoparticles Fabricated Using Actinidia deliciosa Peel Extract

The preparation of metallic nanoparticles using green synthetic approaches and its application toward the efficient degradation of environmentally hazardous dyes constitutes an attractive alternative to currently employed methods. In the current report, the green synthesis of silver nanoparticles (AgNPs) was successfully achieved using Actinidia deliciosa (kiwifruit) peel aqueous extract as a bioreducing agent under optimized synthesis conditions. The experimental parameters were optimized in terms of reactant ratio, reaction temperature, and reaction time. The biogenic nanoparticles exhibited SPR absorption band at λmax 480 nm. Transmission electron microscopy (TEM) and scanning electron microscopy (SEM) images revealed quasispherical monodisperse nanoparticles which were 36 nm in diameter. The hydrodynamic diameter of the nanoparticles was 106 nm as determined by dynamic light scattering, and the highly negative ζ-potential (−34 mV) supported its superior colloidal stability. Energy dispersive X-ray confirmed that silver is a major constituent of the nanoparticles. X-ray diffraction (XRD) diffractograms confirmed the crystallinity of the nanoparticles and its face-centered cubic (fcc) lattice structure. The functional groups in the plant’s phytochemicals facilitating the reduction of Ag+ ions and stabilization of the formed AgNPs were identified by fourier transform infrared (FTIR) spectroscopy. In specific, the bands in the FTIR spectra at 3,412, 1,618, 1,419, and 1,237 cm−1 suggested the presence of phenolic compounds. Phytochemical analysis by colorimetric assays revealed that the kiwifruit peel extract was rich in phenolic compounds. When evaluated in the catalytic degradation of organic dyes, the biosynthesized AgNPs induced instant and complete discoloration of the methylene blue dye when 1.6 mg of nanoparticles was used. At a lower dose of AgNPs (0.4 mg), 80% degradation of the dye occurred after 3 hr of treatment. The degradation reaction followed second-order kinetics with a rate constant of 0.01083 mM−1s−1. The current study highlights the immense potential of the prepared nanoparticles as efficient catalysts for the degradation of hazardous organic dyes such as methylene blue and presents an intriguing argument for investigating the catalytic efficiency of the biogenic AgNPs for the degradation of other structurally different dye pollutants.

Development of an innovative analytical method for forensic detection of cocaine, antidepressants, and metabolites in postmortem blood using magnetic nanoparticles.

Cocaine and antidepressants rank high globally in substance consumption, emphasizing their impact on public health. The determination of these compounds and related substances in biological samples is crucial for forensic toxicology. This study focused on developing an innovative analytical method for the determination of cocaine, antidepressants, and their related metabolites in postmortem blood samples, using unmodified commercial Fe3O4 nanoparticles as a sorbent for dispersive magnetic solid-phase extraction (m-d-SPE), coupled with liquid chromatography coupled with tandem mass spectrometry (LC-MS/MS) analysis. An aliquot of 100 µL of whole blood and 5 µL of the internal standard pool were added to 30mg of nanoparticles. The nanoparticles were separated from the sample using a neodymium magnet inserted into a 3D-printed microtube rack. The liquid was then discarded, followed by desorption with 300 µL of 1/1/1 acetonitrile/methanol/ethyl acetate. The sample was vortexed and separated, and 1.5 µL of the organic supernatant was injected into the LC-MS/MS. The method was acceptably validated and successfully applied to 263 postmortem blood samples. All samples evaluated in this study were positive for at least one substance. The most frequent analyte was benzoylecgonine, followed by cocaine and cocaethylene. The most common antidepressants encountered in the analyzed samples were citalopram and fluoxetine, followed by fluoxetine's metabolite norfluoxetine. This study describes the first report of this sorbent in postmortem blood analysis, demonstrating satisfactory results for linearity, precision, accuracy, and selectivity for all compounds. The method's applicability was confirmed, establishing it as an efficient and sustainable alternative to traditional techniques for forensic casework.

Study protective role Camellia sinensis L. (black tea) and silver, Zn oxide nanoparticles on antioxidant-oxidant enzymes and biochemical level against paracetamol overdose in adult male rats

This study aims to measure the preventive effect of the silver, Zn oxide nanoparticles, and Camellia sinensis L. (black tea) on liver toxicity caused by the paracetamol drug. The Nanomaterials, with a practical size range of 33–40nm, black tea was extracted by Soxhlet apparatus using methanol alcohol at a concentration (80%); design in this study, 60 adult male rats weighing between 195 and 330 g and aged 11 to 14 weeks were used. They were kept in a relatively regulated setting with a temperature of 25Co at the University of Karbala’s animal facility. They received food. There were eight rat group divisions. G1: just received saline solution (0,85%) as the control. G2: 250 milligrams of black tea and 250 milligrams of paracetamol per kilogram of body weight. G3: 400 milligrams of C. sinensis L. and 250 milligrams of paracetamol per kilogram of body weight. G4: injection of 0.3 milligrams of zinc nanoparticles and 250 milligrams of paracetamol per kilogram of body weight. G5: injection of 0.5 milligrams of zinc nanoparticles and 250 milligrams of paracetamol per kilogram of body weight. G6: injection of 0.3 milligrams of silver nanoparticles and 250 milligrams of paracetamol per kilogram of body G7: injection of 0.5 milligrams of silver nanoparticles and 250 milligrams of paracetamol per kilogram of body, G8: 250 milligrams of paracetamol per kilogram of body administered intravenously, the blood bled for 30 days after receiving all dosages orally once daily for 21 days. When rats were given injections of 0.5 mg of nanoparticles and when injections of 250 mg of a black tee., it was discovered that the concentration of Malondialdehyde MDA, Lipid Peroxidation LPO, Triacylglycerid, cholesterol levels, and glucose decreased significantly. In contrast, Glutathione peroxidase GPX and protein levels are increased considerably. This was due to the injections’ preventive and antioxidant action against the oxidative stress brought on by the paracetamol height dose. Keywords: silver nanoparticles, Zn oxide nanoparticles, Camellia sinensis L., paracetamol.

Development of an ID-LC–MS/MS method using targeted proteomics for quantifying cardiac troponin I in human serum

BackgroundCardiac troponin is a complex protein consisting of the three subunits I, T and C located in heart muscle cells. When the heart muscle is damaged, it is released into the blood and can be detected. Cardiac troponin I (cTnI) is considered the most reliable and widely accepted test for detecting and confirming acute myocardial infarction. However, there is no current standardization between the commercial assays for cTnI quantification. Our work aims to create a measurement procedure that is traceable to the International System of Units for accurately measuring cardiac cTnI levels in serum samples from patients.MethodsThe workflow begins with immobilizing anti-cTnI antibodies onto magnetic nanoparticles to form complexes. These complexes are used to isolate cTnI from serum. Next, trypsin is used to enzymatically digest the isolated cTnI. Finally, the measurement of multiple cTnI peptides is done simultaneously using isotope dilution liquid chromatography–tandem mass spectrometry (ID-LC–MS/MS).ResultsThe maximum antibody immobilization was achieved by combining 1 mg of nanoparticles with 100 μg of antibody, resulting in an average of 59.2 ± 5.7 μg/mg of immobilized antibody. Subsequently, the anti-cTnI-magnetic nanoparticle complex was utilized to develop and validate a method for quantifying cTnI in human serum using ID-LC–MS/MS and a protein calibration approach. The analytical method was assessed regarding linearity and recovery. The developed method enables the quantification of cTnI from 0.7 to 24 μg/L (R > 0.996). The limit of quantification was 1.8 μg/L and the limit of detection was 0.6 μg/L. Intermediate precision was ≤ 9.6% and repeatability was 2.0–8.7% for all quality control materials. The accuracy of the analyzed quality control materials was between 90 and 110%. Total measurement uncertainties for target value assignment (n = 6) were found to be ≤ 12.5% for all levels.ConclusionsThe analytical method demonstrated high analytical performance in accurately quantifying cardiac troponin I levels in human serum. The proposed analytical method has the potential to facilitate the harmonization of cTnI results between clinical laboratories, assign target values to secondary certified reference materials and support reliable measurement of cTnI.Graphical

Solid Phase Extraction Penicillin and Tetracycline in Human Serum Using Magnetic Graphene Oxide-Based Sulfide Nanocomposite

Herein, we report a procedure for separating and preconcentrating antibiotics from human serum using a novel adsorbent of magnetic graphene oxide (MGO) and cadmium sulfide (CdS) nanoparticles. The adsorbent (MGO@CdS) was characterized using Fourier transformed infrared spectrometry (FT-IR), energy dispersive X-ray spectroscopy (EDX), and field emission scanning electron microscopy (FE-SEM). The effective parameters for extraction efficiency were investigated, including the desorption solvent’s nature, pH, adsorbent dose, salt concentration, extraction time, and volume of sample solution and desorption solvent. The proposed procedure proved to be fast (20 min), simple (two stages), and cost-effective (20 mg of nanoparticles). Under the optimum conditions, satisfactory linearity (R2 > 0.992) was obtained, and limits of detection (LOD) were estimated as 4.5 µg L−1 (for tetracycline) and 5.7 µg L−1 (for penicillin) and a linear dynamic range (LDR) from 20 to 200 µg L−1. The magnetic solid phase extraction (MSPE) method based on MGO@CdS has achieved a satisfactory recovery (71.5–109.5%) in human serum for the selected antibiotics. Finally, the antibiotic’s release was studied in simulated fluids of the gastric (pH = 1.2) and intestine (pH = 7.4). In this light, we demonstrate that the newly introduced adsorbent can be used in drug extraction from different biological media.

Turning carbon dots into selenium bearing nanoplatforms with in vitro GPx-like activity and pro-oxidant activity

Selenium (Se) has been defined as the “Janus element”, with one face showing antioxidant activity and the other pro-oxidant activity. The biological effect of Se depends on both dose and speciation. Se nanoparticles are attracting major interest, although their large-scale preparation for biomedical applications is not trivial. We hypothesize that acid anhydride-coated carbon dots (AA-CD) are an attractive platform for preparing nanoparticles containing chemically defined Se. The reaction of AA-CD with 3-selenocyanatopropan-1-amine yields carbon dots bearing selenocyanate and carboxylate groups (CD-SeCN) that allow for tuning the hydrosolubility. CD-SeCN has a Se content of 0.36 µmol per mg of nanoparticles, and they show the typical photoluminescence of carbon dots. The selenocyanate groups (SeCN) exhibited glutathione peroxidase-like activity and cytotoxicity. Data show that antioxidant behavior differs between normal and tumor cells, and the evaluation on HEK293 and A549 cells reveals that the toxicity of CD-SeCN depends on dose, time, and intracellular glutathione (GSH) content. The toxicity of CD-SeCN decreases with the time of incubation and the cell death mechanism switches from necrosis to apoptosis, indicating that CD-SeCN is neutralized. Additionally, high levels of intracellular GSH exert a protective effect. These results support a pharmacological potential in cancers with low levels of intracellular GSH. The use of AA-CD as nanoplatforms is a general strategy that paves the way for the engineering of advanced nanosystems.

Neuroprotective Effects of Nano-Curcumin against Cypermethrin Associated Oxidative Stress and Up-Regulation of Apoptotic and Inflammatory Gene Expression in Rat Brains.

Cypermethrin (CPM) is the most toxic synthetic pyrethroid that has established neurotoxicity through oxidative stress and neurochemical agitation in experimental rats. The toxic effects are supposed to be mediated by modifying the sodium channels, reducing Na-K ATPase, acetylcholine esterase (AchE), and monoamine oxidase (MAO). The use of curcumin nanoparticles (NC) that have potent antioxidant, anti-inflammatory and antiapoptotic properties with improved bioavailability attenuates neurotoxicity in rat brains. To test this hypothesis, animals were divided into five groups, each having six animals. Group-I control received vehicle only, while Group-II was treated with 50 mg/kg CPM. Group-III and Group-IV received both CPM and NC 2.5 mg/kg and 5 mg/kg, respectively. Group-V received 5 mg of NC alone. The CPM and NC were given by oral route. Afterwards, brain antioxidant status was measured by assessing lipid peroxidation (LPO), 4-HNE, glutathione reduced (GSH), antioxidant enzyme catalase, and superoxide dismutase (SOD) along with neurotoxicity markers Na-K ATPase, AchE, and MAO. Inflammation and apoptosis indices were estimated by ELISA, qRT-PCR, and immunohistochemistry, while morphologic changes were examined by histopathology. Observations from the study confirmed CPM-induced neurotoxicity by altering Na-K ATPase, AchE, and MAO, and by decreasing the activity of antioxidant enzymes and GSH. Oxidative stress marker LPO and the level of inflammatory interleukins IL-6, IL-1β, and TNF-α were notably high, and elevated expressions of Bax, NF-kB, and caspase-3 and -9 were reported in CPM group. However, NC treatment against CPM offers protection by improving antioxidant status and lowering LPO, inflammation, and apoptosis. The neurotoxicity marker's enzyme successfully attenuated after NC treatment. Therefore, this study supports the administration of NC effectively ameliorated CPM-induced neurotoxicity in experimental rats.

Application of Algal Nanotechnology for Leather Wastewater Treatment and Heavy Metal Removal Efficiency

Wastewater from tanneries may ruin agricultural fields by polluting them with trace metals. The synthesis of nanoparticles (NPs) from algal sources and their application could help in decreasing hazardous materials, for environmental safety. The potential of zinc oxide nanoparticles made from Oedogonium sp. was evaluated for removal of heavy metals from leather industrial wastewater. Synthesized algal nanoparticles (0 (control), 0.1, 0.5, and 1 mg) were applied to treat wastewater by using different concentrations of leather industrial effluents (0%, 5%, 10%, 15%, and 100%) for 15, 30, and 45 d. The wastewater collected was dark brown to black in color with very high pH (8.21), EC (23.08 μs/cm), and TDS, (11.54 mg/L), while the chloride content was 6750 mg/L. The values of biological oxygen demand (BOD) and chemical oxygen demand (COD) ranged between 420 mg/L and 1123 mg/L in the current study. Prior to the application of nanoparticles, Cr (310.1), Cd (210.5), and Pb (75.5 mg/L) contents were higher in the leather effluents. The removal efficiency of TDS, chlorides, Cr, Cd, and Pb was improved by 46.5%, 43.5%, 54%, 57.6%, and 59.3%, respectively, following treatment with 1 mg of nanoparticles after 45 d. Our results suggested that the green synthesis of ZnO nanoparticles is a useful and ecofriendly biotechnological tool for treating tannery effluents, before they are discharged into water bodies, thus making the soil environment clean.

Green synthesis of ZnO nanoparticles and comparison of 2,4-dinitrophenol removal efficiency using photocatalytic, sonocatalytic, and adsorption processes

In the present work, the extract of a paper-flower species called Bougainvillea spectabilis was used to green synthesis of ZnO nanoparticles (NPs). The synthesized ZnO NPs was confirmed by XRD, SEM, TEM, EDS, and FTIR techniques. Then, the ability of ZnO NPs to remove 2,4-dinitrophenol from aqueous solutions was investigated using photocatalytic and sonocatalytic processes. All experiments were carried out in a batch system and the effects of pH, NPs dosage, concentration, and contact time were evaluated. The findings of this study showed that the pseudo-second-order kinetic model could well describe the removal of 2,4-dinitrophenol by ZnO NPs. Langmuir, Freundlich, Temkin, and BE-T isotherm models were also assessed in a dark condition. The Freundlich isotherm model was able to provide the best fit with the experimental data. Examination of the results showed that the degradation of 2,4-dinitrophenol at the presence of ultraviolet (UV) and ultrasonic (US) waves was able to increase the removal efficiency to about twice as much as removal by adsorption alone. Also, The obtained results showed that the maximum removal of 2,4-dinitrophenol under photocatalytic and sonocatalytic conditions occurred at the presence of 25 mg of NPs, solution pH of 4, and 2,4-dinitrophenol concentration of 20 ppm. The best rates of photocatalytic and sonocatalytic degradation under the optimal conditions were 84.42% and 77.13% during 60 min, respectively. Thermodynamic studies indicated that the degradation of 2,4-dinitrophenol by ZnO NPs is a spontaneous and endothermic process in the direction of increasing entropy. The zinc oxide NPs have better performance in the removal of 2,4-dinitrophenol at the presence of UV and US waves.

Synthesis and Application of Albumin Nanoparticles Loaded with Prussian Blue Nanozymes

Prussian blue nanozymes exhibit peroxidase-like catalytic activity and are therefore considered a stable and inexpensive alternative to natural peroxidases in the enzyme-linked immunosorbent assay (ELISA). In this work, we propose a robust method of Prussian blue nanozyme functionalization, which relies on the entrapment of nanozymes into albumin nanoparticles. The principle of the method is the addition of ethanol to a solution that contains albumin and nanozymes. At a high ethanol concentration solubility of albumin decreases, resulting in the formation of albumin nanoparticles loaded with nanozymes. The hydrodynamic diameter of nanoparticles was between 120 and 230 nm and depended on the nanozyme-to-BSA ratio. Encapsulation efficiency of nanozymes reached 96–99% and up to 190 μg of nanozymes were loaded per 1 mg of nanoparticles. Nanoparticles were stable at pH 5.5–7.5 and upon long-term storage in deionized water. Excellent reproducibility of the synthesis procedure was confirmed by the preparation of three individual batches of Prussian-blue-loaded BSA nanoparticles with almost identical properties. Nanoparticles were functionalized with monoclonal antibodies using glutaraldehyde cross-linking. The resulting conjugates were applied as labels in an ELISA-like assay of tumor marker prostate-specific antigen (PSA). The lower limit of detection was below 1 ng/mL, which enables measurement of PSA in the range of clinically relevant concentrations.

Influence of bionanoparticles to treat a slaughterhouse wastewater

ABSTRACT Treatment of effluents from animal slaughterhouse industries is indispensable, standing out coagulation/flocculation/sedimentation processes. Bionanoparticles (BioNPs) (nanoparticles (NPs) functionalized with Moringa extracts (MO)) were studied as an alternative natural coagulant that would contribute to the microbial load reduction, without increasing the treated effluent toxicity. MO extracts were prepared with different salts, and then, in a kinetics study, different NPs mass and coagulant dosages were evaluated. In the best-defined conditions, microbial load, toxicity tests for the bioindicator Lactuca sativa, and NPs reuse evaluation were performed. Removals of 96.14% turbidity and 43.63% UV254nm were achieved when using 500 mg L−1 of BioNPs containing 60 mg of NPs for every 20 mL of MO extract prepared with 0.1 M CaCl2. The BioNPs with an external magnetic field also decreased the sedimentation time from 140 to 10 min compared to MO, and the process efficiency did not expressively decrease after reusing the recovered NPs. Through toxicity tests, BioNPs were not considered to leave residuals toxic to the Lactuca sativa in the treated effluent. Besides, the microbial load reduction was 97.33% for heterotrophic microorganisms and total mesophiles and 99.25% for moulds/yeasts. Therefore, a satisfactory primary treatment was achieved, contributing to the sustainability of industries.

Biodiesel Trace Element Analysis by Energy Dispersive X-ray Fluorescence Spectrometry Using Magnetic Solid-Phase Microextraction

One parameter to examine biodiesel quality has to do with the existence of metals, given that their presence can negatively affect fuel stability, by virtue of the alteration to their physicochemical properties. Given the significance of monitoring the concentration of metals in biodiesel, this work is aimed at developing a different mode for multielement determination through the use of energy dispersive X-ray fluorescence (EDXRF) spectrometry. For this purpose, an extraction procedure using sample preparation by emulsification associated with magnetic solid-phase microextraction was proposed for separation of Cd, Pb, Cr, V, and Mo from biodiesel samples for posterior analysis using EDXRF spectrometry. The emulsion was prepared by mixing the sample with n-propyl alcohol and 0.01 mol L–1 nitric acid alongside subsequent contact with the solid phase (CoFe2O4 nanoparticles impregnated with alizarin fluorine blue). Constrained mixing design was used to optimize the emulsion composition, and the recommended conditions were 36% (v v–1) n-propyl alcohol, 42% (v v–1) biodiesel, and 22% (v v–1) nitric acid solution for a total volume of 10 mL, using 100 mg of nanoparticles. The proposed extraction allowed enrichment factors of 9.3, 23, 27, 9.7, and 10 for Cd, Cr, V, Pb, and Mo, respectively. The limits of detection were found to be 13, 32, 17, 14, and 25 μg kg–1 for Cd, Pb, Cr, V, and Mo, respectively. Recovery tests were performed by adding 200 μg kg–1 of all analytes in question to six varying biodiesel samples with outcomes that registered between 85 and 114%. The recommended procedure was applied in the analysis of biodiesel, and the highest concentrations observed were 166 μg kg–1 for Cd, 106 μg kg–1 for Cr, 137 μg kg–1 for Pb, 82 μg kg–1 for V, and 92 μg kg–1 for Mo.

Effect of surfactant coating of Fe3O4 nanoparticles on magnetic dispersive micro-solid phase extraction of tetracyclines from human serum

A procedure for separation and preconcentration of tetracyclines from human serum samples involving magnetic dispersive micro-solid phase extraction was proposed. The extraction efficiency of different tetracyclines was improved with the use of the surfactant coated Fe3O4 magnetic nanoparticles. Sorption mechanism was presented, and the potential use of magnetic Fe3O4 nanoparticles coated with different surfactants for tetracyclines adsorption was demonstrated for the first time. The procedure involved nanoparticle floating in a liquid sample phase for analyte extraction followed by elution and determination by high performance liquid chromatography with diode array detection. Influence of the main involved parameters was studied, the system was dimensioned accordingly. The analytical curves were linear in the ranges of 0.25–10 mg L−1 for tetracycline and 0.10–10 mg L−1 for oxytetracycline or doxycycline. Limits of detection were estimated (IUPAC, 3 concept) as 0.08 mg L−1 for tetracycline, and 0.03 mg L−1 for oxytetracycline or doxycycline. The proposed procedure proved to be fast (10 min), simple (two stages), inexpensive (10 mg of nanoparticles) and was applied to human serum samples. Unlike previously synthesized nanoparticles for tetracyclines separation, the surfactant-coated Fe3O4 nanoparticles can be easily prepared with widely available and low-cost reagents. Moreover, elution of the analytes was accomplished in absence of organic solvents by an aqueous chelating agent solution.

Comparison of Cadmium Cd2+ and Lead Pb2+ Binding by Fe2O3@SiO2‐EDTA Nanoparticles – Binding Stability and Kinetic Studies

AbstractThis study describes the synthesis and characterization of ethylenediaminetetraacetic acid (EDTA) functionalized magnetic nanoparticles of 20 nm in size – Fe3O4@SiO2‐EDTA – which were used as a novel magnetic adsorbent for Cd(II) and Pb(II) binding in aqueous medium. These nanoparticles were obtained in two‐stage synthesis: covering by tetraethyl orthosilicate and functionalization with EDTA derivatives. Nanoparticles were characterized using TEM, FT‐IR, and XPS methods. Metal ions were detected under optimized experimental conditions using Differential Pulse Anodic Stripping Voltammetry (DPASV) and Hanging Mercury Drop Electrode (HDME) techniques. We compared the ability of Fe3O4@SiO2‐EDTA to bind cadmium and lead in concentration of 553.9 μg L−1 and 647.5 μg L−1, respectively. Obtained results show that the adsorption rate of cadmium binding was very high. The equilibrium for Fe3O4@SiO2‐EDTA‐Cd(II) was reached within 19 min while for the Fe3O4@SiO2‐EDTA‐Pb(II) was reached within 25 minutes. About 2 mg of nanoparticles was enough to bind 87.5 % Cd(II) and 54.1 % Pb(II) content. In the next step the binding capacity of Fe3O4@SiO2‐EDTA nanoparticles was determined. Only 1.265 mg of Fe3O4@SiO2‐EDTA was enough to bind 96.14 % cadmium ions while 5.080 mg of nanoparticles bound 40.83 % lead ions. This phenomenon proves that the studied nanoparticles bind Cd(II) much better than Pb(II). The cadmium ions binding capacity of Fe3O4@SiO2‐EDTA nanoparticles decreased during storage in 0.5 M KCl solution. Two days of Fe3O4@SiO2‐EDTA storage in KCl solution caused the 32 % increase in the amount of nanoparticles required to bind 60 % of cadmium while eight‐days storage caused further increase to 328 %. The performed experiment confirmed that the storage of nanoparticles in solution without any surfactants reduced their binding capacity. The best binding capacity was observed for the nanoparticles prepared directly before the electrochemical measurements.

Enhancing the efficacy of fluocinolone acetonide by encapsulating with PLGA nanoparticles and conjugating with linear PEG polymer

Fluocinolone acetonide (FA), a glucocorticoid is used to treat inflammation in the posterior segment of the eye. Due to short half-life and body clearance, it will not be able to give therapeutic effect for long time with a single injection. Formulating FA nanoparticles (NPs) or PEG conjugates can be an effective way to overcome these disadvantages. We prepared two formulations, FA loaded in PLGA nanoparticles (NPs-FA) and FA conjugated to linear PEG (PEG-FA). The NPs-FA were characterised for size and zeta potential using particle size analyser and shape and morphology by using scanning electron microscope (SEM). The amount of drug loaded per mg of NPs and in-vitro release of FA from NPs were calculated using reverse phase high pressure liquid chromatography (RP-HPLC). NPs synthesis was optimized with factorial and Response Surface Methodology (RSM). Chemically synthesized PEG-FA conjugates were characterized using H-NMR and purity of the conjugate was analysed using RP-HPLC. Visualization of cellular uptake of NPs was done by coumarin-6 loaded NPs under fluorescent microscope. RAW 264.7 macrophages were treated with NPs-FA and PEG-FA conjugates to study their effectiveness in inhibiting TNF-α levels compared to free FA treatment. Stability test confirmed that FA is more stable within NPs than in free form. Particle size and zeta potential were found to be 183.6 ± 12.47nm and −25.6 ± 4.4mV, respectively. 149.58 ± 11.3µg of FA was encapsulated per mg of NPs and 61 µg of FA was present per mg of PEG-FA conjugate. In vitro drug release study showed a sustained release of FA from the NPs for a period of 30 days. Fluorescent microscope images showed uptake of NPs by RAW 264.7 cells. TNF-α assay confirmed that substantial inhibition of TNF-α levels from both formulations compared to free FA. From the results, we conclude that new formulations will greatly reduce drug dosage and frequency of administration for long term treatment of inflammation in posterior part of the eye.

Preparation of aCarrier to Achieve In Vivo Delivery of siRNA: The Example of Chitosan-Coated Poly(isobutylcyanoacrylate) Nanoparticles.

This chapter describes the preparation of chitosan-coated poly(isobutylcyanoacrylate) nanoparticles as a suitablecarrier to deliver siRNAs to two types of xenograft tumor models of mice. The nanoparticles are prepared by a method of emulsion polymerization that includes steps of polymerization and purification. The polymerization method is carried out in a single pot in an aqueous medium. siRNAs are coupled with the nanoparticles at the end of the preparation by adsorption. The protocol also explains how to determine optimum yield/the titer of association of siRNA with the nanoparticles. It is described for a preparation scale at 4mL of nanoparticle dispersion at a concentration of 42-46 mg nanoparticles/mL. Optimal loading capacity of the nanoparticles with the siRNA can be achieved by performing an association yield above 90% using a mass ratio of 1 mg siRNA/50 mg of nanoparticles (20μg siRNA/mg nanoparticles, 1nmol siRNA (Mw 14kDa)/mg nanoparticles).

Nano/microstructure decorated thin film composite poly (arylene sulfide sulfone) membrane constructed by induced fouling in organic solvent ultrafiltration

In this study, novel thin film composite membranes with nano/macrostructure decorated surface were fabricated by deposition of poly (arylene sulfide sulfone) (PASS) polymer chains on oxidized poly (arylene sulfide sulfone) (O-PASS) support membrane during organic solvent ultrafiltration. Interestingly, the obtained membranes exhibited a rough surface structure composed of ordered arranged polymeric nodules with size ranging from nanoscale (100 nm) to macroscale (5 μm). Additionally, these membranes showed an improved, ultrahigh rejection of direct red 23, reactive blue 2, demonstrating their potential application for the reuse of dyes in wastewater. Furthermore, this novel synthesis approach of thin film composite membranes has great advantages in incorporating nanoparticles because of the facile process, the low consumption of nanoparticles and the high content of nanoparticles in the thin layer. During the whole thin layer synthesis process, only 2 mg of nanoparticles were used and thin layers with nanoparticles content of 20% were obtained. After the incorporation of candle soot, SiO2 and ZIF-8 in the separation layer, both the water permeation and rejection of direct red 23, reactive blue 2 and reactive orange 16 were greatly improved. Therefore, this study provides a novel and simple fabrication method for thin film composite membranes, which has advantages in incorporating nanoparticles in the thin separation layer to endow the membrane with an improved performance.

Isolation of nematode DNA from 100 g of soil using Fe3O4 super paramagnetic nanoparticles

An economical method for extracting nematode DNA from 100 g of soil was developed to facilitate nematode detection and quantification, and tested using the Northern root-knot nematode,Meloidogyne hapla. The method utilised enzymatic laundry detergent lysis, Fe3O4super paramagnetic iron oxide nanoparticle (SPION) capture, and polyvinylpolypyrrolidone (PVPP) purification. Resultant DNA from this SPION capture method was approximately 100-fold less but of similar quality to DNA obtained from a standard phenol procedure and a commercial DNA extraction kit. An addition of 10 mg of nanoparticles to the extraction lysate was identified to maximise DNA yield while minimising co-capture of contaminants. The detection limit of the SPION capture method was approximately 100 nematodes (100 g soil)−1. The SPION capture method extracted nematode DNA from mineral soils but requires further optimisation for extraction from high organic matter (i.e., ‘muck’) soils. The benefits of this method compared to alternative techniques are discussed.

Nanopartículas de CuO y su propiedad antimicrobiana en cepas intrahospitalarias

Empleando un prototipo de reactor, se sintetizaron nanopartículas (NPs) de CuO a través del método de precipitación a partir de CuSO2·5H2O y de Cu(CH3COO)2·H2O. Las NPs obtenidas fueron caracterizadas mediante XRD, FT-IR, TEM y SEM. La actividad antimicrobiana de las NPs se determinó mediante el método de difusión en placa, colocando 20 mg de NPs de CuO sobre cuatro cepas intrahospitalarias o nosocomiales aisladas de la Unidad de Cuidados Intensivos de un hospital nacional de Lima norte (Staphylococcus epidermidis, Aerococcus viridans, Ochrobactrum anthropi y Micrococcus lylae). La caracterización de las NPs de CuO demostró que las sintetizadas a partir de acetato (CuO–Acet) presentaron una fase pura de CuO, mientras que las sintetizadas a partir de sulfato (CuO–Sulf) presentaron dos fases, donde la de CuO representó más del 84%. Los dominios cristalinos del CuO–Acet y CuO–Sulf fueron 15 y 19 nm, respectivamente. Los halos de inhibición de las cepas estudiadas fueron mayores para las NPs de CuO–Sulf que para las NPs de CuO–Acet; solo para la cepa chrobactrum anthropi se presentaron halos similares para ambos tipos de NPs.

2229

2229