Preparation and pH Controlled Release of Fe3O4/Anthocyanin Magnetic Biocomposites

Anthocyanins are a class of antioxidants extracted from plants, with a variety of biochemical and pharmacological properties. However, the wide and effective applications of anthocyanins have been limited by their relatively low stability and bioavailability. In order to expand the application of anthocyanins, Fe3O4/anthocyanin magnetic biocomposite was fabricated for the storage and release of anthocyanin in this work. The magnetic biocomposite of Fe3O4 magnetic nanoparticle-loaded anthocyanin was prepared through physical intermolecular adsorption or covalent cross-linking. Scanning electron microscopy (SEM), Dynamic light scattering (DLS), Fourier-transform infrared spectroscopy (FTIR), X-ray diffractometry (XRD) and thermal analysis were used to characterize the biocomposite. In addition, the anthocyanin releasing experiments were performed. The optimized condition for the Fe3O4/anthocyanin magnetic biocomposite preparation was determined to be at 60 °C for 20 h in weak alkaline solution. The smooth surface of biocomposite from SEM suggested that anthocyanin was coated on the surface of the Fe3O4 particles successfully. The average size of the Fe3O4/anthocyanin magnetic biocomposite was about 222 nm. Under acidic conditions, the magnetic biocomposite solids could be repeatable released anthocyanin, with the same chemical structure as the anthocyanin before compounding. Therefore, anthocyanin can be effectively adsorbed and released by this magnetic biocomposite. Overall, this work shows that Fe3O4/anthocyanin magnetic biocomposite has great potential for future applications as a drug storage and delivery nanoplatform that is adaptable to medical, food and sensing.

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Functional Attributes of Myco-Synthesized Silver Nanoparticles from Endophytic Fungi: A New Implication in Biomedical Applications

Biology ◽

10.3390/biology10060473 ◽

2021 ◽

Vol 10 (6) ◽

pp. 473

Author(s):

Prabu Kumar Seetharaman ◽

Rajkuberan Chandrasekaran ◽

Rajiv Periakaruppan ◽

Sathishkumar Gnanasekar ◽

Sivaramakrishnan Sivaperumal ◽

...

Keyword(s):

Silver Nanoparticles ◽

Culture Filtrate ◽

Morphological Changes ◽

Xrd Analysis ◽

Penicillium Oxalicum ◽

Breast Cancer Cell Lines ◽

Face Centered Cubic ◽

Tem Analysis ◽

X Ray ◽

Average Size

To develop a benign nanomaterial from biogenic sources, we have attempted to formulate and fabricate silver nanoparticles synthesized from the culture filtrate of an endophytic fungus Penicillium oxalicum strain LA-1 (PoAgNPs). The synthesized PoAgNPs were exclusively characterized through UV–vis absorption spectroscopy, Fourier Transform Infra-Red spectroscopy (FT-IR), X-ray powder diffraction (XRD), and Transmission Electron Microscopy (TEM) with energy dispersive X-ray spectroscopy (EDX). The synthesized nanoparticles showed strong absorbance around 430 nm with surface plasmon resonance (SPR) and exhibited a face-centered cubic crystalline nature in XRD analysis. Proteins presented in the culture filtrate acted as reducing, capping, and stabilization agents to form PoAgNPs. TEM analysis revealed the generation of polydispersed spherical PoAgNPs with an average size of 52.26 nm. The PoAgNPs showed excellent antibacterial activity against bacterial pathogens. The PoAgNPs induced a dose-dependent cytotoxic activity against human adenocarcinoma breast cancer cell lines (MDA-MB-231), and apoptotic morphological changes were observed by dual staining. Additionally, PoAgNPs demonstrated better larvicidal activity against the larvae of Culex quinquefasciatus. Moreover, the hemolytic test indicated that the as-synthesized PoAgNPs are a safe and biocompatible nanomaterial with versatile bio-applications.

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Combustion and gasification characteristics of low-temperature pyrolytic semi-coke prepared through atmosphere rich in CH4 and H2

Green Processing and Synthesis ◽

10.1515/gps-2021-0015 ◽

2021 ◽

Vol 10 (1) ◽

pp. 189-200

Author(s):

Yuan She ◽

Chong Zou ◽

Shiwei Liu ◽

Keng Wu ◽

Hao Wu ◽

...

Keyword(s):

Functional Groups ◽

Chemical Structure ◽

Nitrogen Adsorption ◽

Inhibitory Effect ◽

X Ray ◽

Coke Reactivity ◽

Reducing Gas ◽

Reactivity Indexes ◽

Infrared Spectrometer ◽

Reducing Gases

Abstract Thermoanalysis was used in this research to produce a comparative study on the combustion and gasification characteristics of semi-coke prepared under pyrolytic atmospheres rich in CH4 and H2 at different proportions. Distinctions of different semi-coke in terms of carbon chemical structure, functional groups, and micropore structure were examined. The results indicated that adding some reducing gases during pyrolysis could inhibit semi-coke reactivity, the inhibitory effect of the composite gas of H2 and CH4 was the most observable, and the effect of H2 was higher than that of CH4; moreover, increasing the proportion of reducing gas increased its inhibitory effect. X-ray diffractometer and Fourier-transform infrared spectrometer results indicated that adding reducing gases in the atmosphere elevated the disordering degree of carbon microcrystalline structures, boosted the removal of hydroxyl- and oxygen-containing functional groups, decreased the unsaturated side chains, and improved condensation degree of macromolecular networks. The nitrogen adsorption experiment revealed that the types of pore structure of semi-coke are mainly micropore and mesopore, and the influence of pyrolytic atmosphere on micropores was not of strong regularity but could inhibit mesopore development. Aromatic lamellar stack height of semi-coke, specific surface area of mesopore, and pore volume had a favorable linear correlation with semi-coke reactivity indexes.

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The Effect of Surfactant-Modified Montmorillonite on the Cross-Linking Efficiency of Polysiloxanes

Materials ◽

10.3390/ma14102623 ◽

2021 ◽

Vol 14 (10) ◽

pp. 2623

Author(s):

Monika Wójcik-Bania ◽

Jakub Matusik

Keyword(s):

Total Pore Volume ◽

Cross Linking ◽

X Ray Diffraction ◽

X Ray ◽

Transmission Electron ◽

The Cross ◽

Chain Lengths ◽

First Time ◽

Substituent Influence ◽

Benzyl Substituent

Polymer–clay mineral composites are an important class of materials with various applications in the industry. Despite interesting properties of polysiloxanes, such matrices were rarely used in combination with clay minerals. Thus, for the first time, a systematic study was designed to investigate the cross-linking efficiency of polysiloxane networks in the presence of 2 wt % of organo-montmorillonite. Montmorillonite (Mt) was intercalated with six quaternary ammonium salts of the cation structure [(CH3)2R’NR]+, where R = C12, C14, C16, and R’ = methyl or benzyl substituent. The intercalation efficiency was examined by X-ray diffraction, CHN elemental analysis, and Fourier transform infrared (FTIR) spectroscopy. Textural studies have shown that the application of freezing in liquid nitrogen and freeze-drying after the intercalation increases the specific surface area and the total pore volume of organo-Mt. The polymer matrix was a poly(methylhydrosiloxane) cross-linked with two linear vinylsiloxanes of different siloxane chain lengths between end functional groups. X-ray diffraction and transmission electron microscopy studies have shown that the increase in d-spacing of organo-Mt and the benzyl substituent influence the degree of nanofillers’ exfoliation in the nanocomposites. The increase in the degree of organo-Mt exfoliation reduces the efficiency of hydrosilylation reaction monitored by FTIR. This was due to physical hindrance induced by exfoliated Mt particles.

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Fabrication and characterization of hexadecyl acrylate cross-linked phase change microspheres

e-Polymers ◽

10.1515/epoly-2020-0008 ◽

2020 ◽

Vol 20 (1) ◽

pp. 69-75

Author(s):

Haoran Yun ◽

Xingxiang Zhang

Keyword(s):

Phase Change ◽

Smooth Surface ◽

Bone Conduction ◽

Cross Linking ◽

Gravimetric Analysis ◽

Orthopedic Implant ◽

Thermal Gravimetric ◽

Fabrication And Characterization ◽

Fast Release

AbstractMicrospheres with phase change properties were fabricated by polymerization of hexadecyl acrylate (HA) and different cross-linking agents. The samples were characterized by scanning electron microscope (SEM), Fourier transform infrared spectroscopy (FTIR), thermal gravimetric analysis (TGA). The results show that, the samples that added cross-linking agents have a smooth surface and the latent heat of them is different. The experiments show that all of the cross-linked copolymer shells can be made into temperature controlled release microspheres. These materials can be potentially applied in the field of thermal energy storage. β-tricalcium phosphate was encapsulated in microspheres to obtain one with a fast release effect. It will effectively promote bone conduction when these microspheres were implanted into a bone defect. This microsphere can be used for orthopedic implant or coating of instrument in the future.

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Synthesis and Characterization of Clay Polymer Nanocomposites of P(4VP-co-AAm) and Their Application for the Removal of Atrazine

Polymers ◽

10.3390/polym11040721 ◽

2019 ◽

Vol 11 (4) ◽

pp. 721 ◽

Cited By ~ 3

Author(s):

Jorge A. Ramírez-Gómez ◽

Javier Illescas ◽

María del Carmen Díaz-Nava ◽

Claudia Muro-Urista ◽

Sonia Martínez-Gallegos ◽

...

Keyword(s):

Polymer Nanocomposites ◽

Nanocomposite Materials ◽

Synthesis And Characterization ◽

Cross Linking ◽

X Ray Diffraction ◽

Numerous Species ◽

X Ray ◽

Different Types ◽

Synthesized Materials

Atrazine (ATZ) is an herbicide which is applied to the soil, and its mechanism of action involves the inhibition of photosynthesis. One of its main functions is to control the appearance of weeds in crops, primarily in corn, sorghum, sugar cane, and wheat; however, it is very toxic for numerous species, including humans. Therefore, this work deals with the adsorption of ATZ from aqueous solutions using nanocomposite materials, synthesized with two different types of organo-modified clays. Those were obtained by the free radical polymerization of 4-vinylpyridine (4VP) and acrylamide (AAm) in different stoichiometric ratios, using tetrabutylphosphonium persulfate (TBPPS) as a radical initiator and N,N′-methylenebisacrylamide (BIS) as cross-linking agent. The structural, morphological, and textural characteristics of clays, copolymers, and nanocomposites were determined through different analytical and instrumental techniques, i.e., X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), and thermogravimetric analysis (TGA). Adsorption kinetics experiments of ATZ were determined with the modified and synthesized materials, and the effect of the ratio between 4VP and AAm moieties on the removal capacities of the obtained nanocomposites was evaluated. Finally, from these sets of experiments, it was demonstrated that the synthesized nanocomposites with higher molar fractions of 4VP obtained the highest removal percentages of ATZ.

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Water soluble biguanide salts and their 1,3,5-triazine derivatives as inhibitors of acetylcholinesterase and α-glucosidase

Zeitschrift für Kristallographie - Crystalline Materials ◽

10.1515/zkri-2020-0025 ◽

2020 ◽

Vol 235 (10) ◽

pp. 465-475

Author(s):

Ozge Gungor ◽

Seda Nur Kertmen Kurtar ◽

Muhammet Kose

Keyword(s):

Spectroscopic Method ◽

Substitute Aniline ◽

Water Soluble ◽

X Ray Diffraction ◽

Nucleophilic Reaction ◽

X Ray ◽

Triazine Derivatives ◽

Acidic Conditions ◽

Approved Drugs ◽

Solid State Structures

AbstractSeven biguanide derivatives were prepared by the nucleophilic reaction between dicyandiamide and p-substitute aniline derivatives or memantine or adamantine under acidic conditions. The cyclization of the biguanide compounds were also conducted via acetone to give 1,3,5-triazine derivatives. The structures of the synthesized compounds were characterized by analytical methods. The solid state structures of [HL5]Cl, [H2L7]Cl2, [HL1a]Cl and [HL5a]Cl were investigated by X-ray diffraction study. The acetylcholinesterase and α-glucosidase inhibitor properties of the compounds were then evaluated by the spectroscopic method. The compounds were found to show considerable acetylcholinesterase and α-glucosidase inhibitory activities compared to the approved drugs. The cyclization of biguanide derivatives with acetone did not affect inhibition of acetylcholinesterase, yet increased the α-glucosidase inhibition.

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Studies on Magnetron-Sputtered NiO/Si3N4 Thin Films

International Journal of Nanoscience ◽

10.1142/s0219581x17600390 ◽

2018 ◽

Vol 17 (03) ◽

pp. 1760039

Author(s):

K. M. Dhanisha ◽

M. Manoj Christopher ◽

M. Abinaya ◽

P. Deepak Raj ◽

M. Sridharan

Keyword(s):

Electron Microscopy ◽

Thin Films ◽

Smooth Surface ◽

Deposition Time ◽

Si Substrate ◽

X Ray ◽

Coating Time ◽

Deposited Films ◽

Nio Films ◽

Scanning Electron

The present work deals with NiO/Si3N4 layers formed by depositing nickel oxide (NiO) thin films over silicon nitrate (Si3N[Formula: see text] thin films. NiO films were coated on Si3N4-coated Si substrate using magnetron sputtering method by changing duration of coating time and were analyzed using X-ray diffractometer, field emission-scanning electron microscopy, UV–Vis spectrophotometer and four-point probe method to study the influence of thickness on physical properties. Crystallinity of the deposited films increases with increase in thickness. All films exhibited spherical-like structure, and with increase in deposition time, grains are coalesced to form smooth surface morphology. The optical bandgap of NiO films was found to decrease from 3.31[Formula: see text]eV to 3.22[Formula: see text]eV with upsurge in the thickness. The film deposited for 30[Formula: see text]min exhibits temperature coefficient resistance of [Formula: see text]1.77%/[Formula: see text]C as measured at 80[Formula: see text]C.

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Microwave-Assisted Combustion Synthesis of ZnO Nanoparticles

Journal of Chemistry ◽

10.1155/2013/562028 ◽

2013 ◽

Vol 2013 ◽

pp. 1-4 ◽

Cited By ~ 34

Author(s):

M. Kooti ◽

A. Naghdi Sedeh

Keyword(s):

Electron Microscopy ◽

Zno Nanoparticles ◽

Combustion Method ◽

Zinc Nitrate ◽

High Yield ◽

Fast Method ◽

Simple Method ◽

X Ray ◽

Microwave Assisted ◽

Average Size

A new and simple method was applied for the synthesis of ZnO nanoparticles with an average size of 20 nm. In this microwave-assisted combustion method, glycine as a fuel and zinc nitrate as precursor were used. The final product was obtained very fast with high yield and purity. The synthesized nanoscale ZnO was characterized by X-ray Diffraction (XRD), Energy Dispersive X-ray spectroscopy (EDX), and Fourier transform infrared spectroscopy (FT-IR). The size and morphology of the ZnO nanoparticles have been determined by field emission scanning electron microscopy (FESEM) and transmission electron microscopy (TEM) techniques. This is a simple and fast method for the preparation of ZnO nanoparticles with no need for expensive materials or complicated treatments.

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ZnWO4 Nanoparticle Scintillators for High Resolution X-ray Imaging

Nanomaterials ◽

10.3390/nano10091721 ◽

2020 ◽

Vol 10 (9) ◽

pp. 1721

Author(s):

Heon Yong Jeong ◽

Hyung San Lim ◽

Ju Hyuk Lee ◽

Jun Heo ◽

Hyun Nam Kim ◽

...

Keyword(s):

Particle Size ◽

Zinc Oxide ◽

High Resolution ◽

Tungsten Oxide ◽

Spatial Resolution ◽

High Spatial Resolution ◽

X Ray ◽

X Ray Imaging ◽

Average Size ◽

And Tungsten

The effect of scintillator particle size on high-resolution X-ray imaging was studied using zinc tungstate (ZnWO4) particles. The ZnWO4 particles were fabricated through a solid-state reaction between zinc oxide and tungsten oxide at various temperatures, producing particles with average sizes of 176.4 nm, 626.7 nm, and 2.127 μm; the zinc oxide and tungsten oxide were created using anodization. The spatial resolutions of high-resolution X-ray images, obtained from utilizing the fabricated particles, were determined: particles with the average size of 176.4 nm produced the highest spatial resolution. The results demonstrate that high spatial resolution can be obtained from ZnWO4 nanoparticle scintillators that minimize optical diffusion by having a particle size that is smaller than the emission wavelength.

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ANNEALING EFFECT ON THE INDUCED MAGNETISM OF PLATINUM IN FePt NANOPARTICLES

Modern Physics Letters B ◽

10.1142/s0217984907013894 ◽

2007 ◽

Vol 21 (18) ◽

pp. 1189-1196 ◽

Cited By ~ 4

Author(s):

F. WILHELM ◽

A. ROGALEV ◽

P. POULOPOULOS ◽

M. ANGELAKERIS ◽

J. TSIAOUSSIS ◽

...

Keyword(s):

Magnetic Properties ◽

Magnetic Circular Dichroism ◽

Annealing Effect ◽

Fept Nanoparticles ◽

X Ray ◽

Remanence Ratio ◽

Structural And Magnetic Properties ◽

Coercivity Field ◽

Average Size ◽

Magnetic Circular Dichroism Spectra

Effect of annealing on structural and magnetic properties of non-equatomic chemically synthesized FePt nanoparticles with an average size of 3.2 nm diameter is reported. Annealing of the particles at 700°C resulted in the increase of particles size and the enhancement of total magnetization and coercivity, the latter could be attributed to a transformation from disordered to ordered crystallographic phase. Although the system is far from optimum "equatomic" stoichiometry, coercivity field of 1.1 kOe was obtained at 10 K together with remanence ratio of 0.55. X-ray magnetic circular dichroism spectra recorded at the Pt L 2,3 edges on annealed samples revealed the enhancement of magnetic moment induced on Pt atom.

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