scholarly journals Hydrophobic and hydrophilic drug loading capacity of micro diatom frustule from diatomite

2021 ◽  
pp. 35-40
Author(s):  
Le Thi Duy Hanh
Keyword(s):  
Photoelectron Spectroscopy ◽  
Drug Loading ◽  
Porous Silica ◽  
Loading Capacity ◽  
Diatom Frustule ◽  
Promising Candidate ◽  
X Ray ◽  
Hydrophilic Drugs ◽  
Hydrophilic Drug ◽  
Bet Method

The aim of this work was to strengthen the evidence of using micro diatom frustule as a promising candidate for drug loading materials for both hydrophobic and hydrophilic drug models. The morphological, surface elemental composition of diatomite powder, a raw source of micro diatom frustules and purified diatomite to collect micro diatom frustule were investigated. Scanning electron microscope (SEM) and X-ray photoelectron spectroscopy (XPS) confirmed again the porous silica structure of micro diatom structure as well as validated a necessity of raw diatomite purification before using. UV- vis was used to measure drug loading content of untreated and treated surface of micro diatom frustule with maximum loading for hydrophobic and hydrophilic drugs after 24 hours were at 5.48 ± 0.42% and 5.70 ± 0.34, respectively. Moreover, we also proved that the ability of drug adsorption on materials surface by the reduction of specific surface area and pore size of micro diatom frustule after loading using a (Brunauer–Emmett–Teller) BET method. Besides, the hydrophobic loading capacity of materials was affected by surface modification. Based on the results, micro diatom frustule showed a potential for a drug delivery system.

scholarly journals Fabrication and Characterization of Al/NiO Energetic Nanomultilayers

2015 ◽  
Vol 2015 ◽  
pp. 1-6 ◽  
Author(s):  
YiChao Yan ◽  
Wei Shi ◽  
HongChuan Jiang ◽  
Jie Xiong ◽  
WanLi Zhang ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Total Thickness ◽  
X Ray Diffraction ◽  
Dc Magnetron Sputtering ◽  
Metallic Oxide ◽  
Promising Candidate ◽  
X Ray ◽  
Thermal Boundary Conductance ◽  
Fabrication And Characterization

The redox reaction between Al and metallic oxide has its advantage compared with intermetallic reaction and Al/NiO nanomutlilayers are a promising candidate for enhancing the performance of energetic igniter. Al/NiO nanomutlilayers with different modulation periods are prepared on alumina substrate by direct current (DC) magnetron sputtering. The thicknesses of each period are 250 nm, 500 nm, 750 nm, 1000 nm, and 1500 nm, respectively, and the total thickness is 3 μm. The X-ray diffraction (XRD) and scanning electron microscope (SEM) results of the as-deposited Al/NiO nanomutlilayers show that the NiO films are amorphous and the layered structures are clearly distinguished. The X-ray photoelectron spectroscopy (XPS) demonstrates that the thickness of Al2O3increases on the side of Al monolayer after annealing at 450°C. The thermal diffusion time becomes greater significantly as the amount of thermal boundary conductance across the interfaces increases with relatively smaller modulation period. Differential scanning calorimeter (DSC) curve suggests that the energy release per unit mass is below the theoretical heat of the reaction due to the nonstoichiometric ratio between Al and NiO and the presence of impurities.

scholarly journals Solvent-Tuned Synthesis of Mesoporous Nickel Cobaltite Nanostructures and Their Catalytic Properties

2019 ◽  
Vol 9 (6) ◽  
pp. 1100 ◽  
Author(s):  
Xiangfeng Guan ◽  
Peihui Luo ◽  
Yunlong Yu ◽  
Xiaoyan Li ◽  
Dagui Chen
Keyword(s):  
Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
X Ray Diffraction ◽  
X Ray ◽  
Catalytic Activities ◽  
Transmission Electron ◽  
Nickel Cobaltite ◽  
Solvent Type ◽  
Bet Method ◽  
Mesoporous Nico2o4

In this paper, we prepared mesoporous nickel cobaltite (NiCo2O4) nanostructures with multi-morphologies by simple solvothermal and subsequent heat treatment. By adjusting the solvent type, mesoporous NiCo2O4 nanoparticles, nanorods, nanowires, and microspheres were easily prepared. The as-prepared products were systematically characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), and Brunauer–Emmett–Teller (BET) method. Furthermore, the catalytic activities towards the thermal decomposition of ammonium perchlorate (AP) of as-prepared NiCo2O4 nanostructures were investigated.

scholarly journals Icariin/Aspirin Composite Coating on TiO2 Nanotubes Surface Induce Immunomodulatory Effect of Macrophage and Improve Osteoblast Activity

Coatings ◽  
2020 ◽  
Vol 10 (4) ◽  
pp. 427
Author(s):  
Aobo Ma ◽  
Yapeng You ◽  
Bo Chen ◽  
Wanmeng Wang ◽  
Jialin Liu ◽  
...  
Keyword(s):  
Composite Coating ◽  
Photoelectron Spectroscopy ◽  
Tio2 Nanotubes ◽  
Immunomodulatory Effect ◽  
Surface Scanning ◽  
Promising Candidate ◽  
Implant Surface ◽  
X Ray ◽  
Osteoblast Activity ◽  
Modification Of Titanium

Surface coating modification of titanium-based alloys is an efficient way to accelerate early osseointegration in dental implant fields. Icariin (ICA) is a traditional Chinese medicine that has bone activating functions, while aspirin (ASP) is a classical non-steroidal anti-inflammatory drug with good antipyretic and analgesic capabilities. Moreover, poly(lactic–co–glycolic acid) (PLGA) has attracted great attention due to its excellent biocompatibility and biodegradability. We superimposed an ASP/PLGA coating onto ICA loaded TiO2 nanotubes structure so as to establish an icariin/aspirin composite coating on TiO2 nanotubes surface. Scanning electron microscopy, X-ray photoelectron spectroscopy, a contact angle test and a drug release test confirmed the successful preparation of the NT–ICA–ASP/PLGA substrate, with a sustained release pattern of both ICA and ASP. Compared to those cultured on the Ti surface, macrophage cells on the NT-ICA-ASP/PLGA substrate displayed decreased M1 proinflammatory and enhanced M2 proregenerative genes and proteins expression, which implied activated immunomodulatory effect. Moreover, when cultured with conditioned medium from macrophages, osteoblast cells on the NT-ICA-ASP/PLGA substrate revealed improved cell proliferation, adhesion and osteogenic genes and proteins expression, compared with those on the Ti surface. The abovementioned results suggest that the established NT-ICA-ASP/PLGA substrate is a promising candidate for functionalized coating material in Ti implant surface modification.

Magnetization of aminated lignin and characterization

TAPPI Journal ◽  
2019 ◽  
Vol 18 (01) ◽  
pp. 21-27 ◽  
Author(s):  
Xueqing Qiu ◽  
Yingzhi Ma ◽  
Dafeng Zheng
Keyword(s):  
Fourier Transform ◽  
Photoelectron Spectroscopy ◽  
Chemical Properties ◽  
Total Pore Volume ◽  
Vibrating Sample Magnetometer ◽  
X Ray Diffraction ◽  
X Ray ◽  
Physico Chemical ◽  
Bet Method ◽  
Scanning Electron

A magnetic lignin-based nanomaterial (MLN) was prepared from alkaline lignin through an amination and precipitation strategy and characterized with Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), thermogravimetric analysis (TG), Brunauer-Emmett-Teller (BET) method, scanning electron microscope (SEM), dynamic light scattering (DLS), and vibrating sample magnetometer (VSM). The results illustrated that MLN was thermostable and had an extensive degree of aminated lignin coating. The specific surface area of MLN was 65.43 m2/g, with the total pore volume of 0.311 cm3/g. The zeta potential of MLN was positive when pH was less than 2.9, and the saturation magnetization was 50.8 emu/g. The characterization data discovered that the physico-chemical properties of MLN were helpful for the adsorption application.

Mesoporous phosphated and sulphated silica as solid acid catalysts for glycerol acetylation

2014 ◽  
Vol 68 (9) ◽  
Author(s):  
Khadijeh Ghoreishi ◽  
Nilofar Asim ◽  
Mohd Yarmo ◽  
Mohd Samsudin
Keyword(s):  
Photoelectron Spectroscopy ◽  
Solid Acid ◽  
Sol Gel ◽  
Acid Catalysts ◽  
X Ray ◽  
Bet Method ◽  
Ft Ir ◽  
Temperature Programmed ◽  
Catalyst Acidity ◽  
Glycerol Esterification

AbstractSulphate- and phosphate-loaded silicas were synthesised using the sol-gel method with different sulphate and phosphate loadings. These catalysts were characterised using Fourier transform infrared spectroscopy (FT-IR), the Brunauer-Emmett-Teller (BET) method and X-ray photoelectron spectroscopy (XPS). Acidity was measured using the temperature-programmed desorption of ammonia (TPD-NH3) method. The results showed that glycerol esterification with acetic acid conversion decreased as follows: α(H2SO4) (100 %) > α(H3PO4) (99 %) > α(silica loaded with 20 % sulphuric acid) (SS-20; 98 %) > α(silica loaded with 20 % phosphoric acid) (PS-20; 83 %). These studies suggest that the solid acid catalytic activity in the esterification of glycerol is highly dependent on catalyst acidity strength, pore size and surface area.

scholarly journals Green Synthesis and Biomedical Applications of ZnO Nanoparticles: Role of PEGylated-ZnO Nanoparticles as Doxorubicin Drug Carrier against MDA-MB-231(TNBC) Cells Line

Crystals ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 344
Author(s):  
Madiha Batool ◽  
Shazia Khurshid ◽  
Walid M. Daoush ◽  
Sabir Ali Siddique ◽  
Tariq Nadeem
Keyword(s):  
Breast Cancer ◽  
Electron Microscopy ◽  
Zno Nanoparticles ◽  
Drug Loading ◽  
Loading Capacity ◽  
X Ray Diffraction ◽  
Zno Nps ◽  
X Ray ◽  
Drug Loading Efficiency

The present study aimed to develop the synthesis of zinc oxide nanoparticles (ZnO-NPs) using the green method, with Aloe barbadensis leaf extract as a stabilizing and capping agent. In vitro antitumor cytotoxic activity, as well as the surface-functionalization of ZnO-NPs and their drug loading capacity against doxorubicin (DOX) and gemcitabine (GEM) drugs, were also studied. Morphological and structural properties of the produced ZnO-NPs were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy dispersion X-ray diffraction (EDX), UV-Vis spectrophotometry, Fourier-transform infrared analysis (FTIR), and X-ray diffraction (XRD). The prepared ZnO-NPs had a hexagonal shape and average particle size of 20–40 nm, with an absorption peak at 325 nm. The weight and atomic percentages of zinc (50.58% and 28.13%) and oxygen (26.71% and 60.71%) were also determined by EDAX (energy dispersive x-ray analysis) compositional analysis. The appearance of the FTIR peak at 3420 m–1 confirmed the synthesis of ZnO-NPs. The drug loading efficiency (LE) and loading capacity (LC) of unstabilized and PEGylated ZnO-NPs were determined by doxorubicin (DOX) and gemcitabine (GEM) drugs. DOX had superior LE 65% (650 mg/g) and higher LC 32% (320 mg/g) than GEM LE 30.5% (30 mg/g) and LC 16.25% (162 mg/g) on ZnO-NPs. Similar observation was observed in the case of PEG-ZnO-NPs, where DOX had enhanced LE 68% (680 mg/g) and LC 35% (350) mg/g in contrast to GEM, which had LE and LC values of 35% (350 mg/g) and 19% (190 mg/g), respectively. Therefore, DOX was chosen to encapsulate nanoparticles, along with the untreated nanoparticles, to check their in vitro antiproliferative potential against the triple-negative breast cancer (TNBC) cell line (MDA-MB-231) through the MTT (3-(4,5-Dimethylthiazol-2-Yl)-2,5-Diphenyltetrazolium Bromide) assay. This drug delivery strategy implies that the PEGylated biogenically synthesized ZnO-NPs occupy an important position in chemotherapeutic drug loading efficiency and can improve the therapeutic techniques of triple breast cancer.

scholarly journals Development of Hydrophilic Drug Encapsulation and Controlled Release Using a Modified Nanoprecipitation Method

Processes ◽  
2019 ◽  
Vol 7 (6) ◽  
pp. 331
Author(s):  
Jiang Xu ◽  
Yuyan Chen ◽  
Xizhi Jiang ◽  
Zhongzheng Gui ◽  
Lei Zhang
Keyword(s):  
Lactic Acid ◽  
Controlled Release ◽  
Drug Loading ◽  
Continuous Phase ◽  
Poly Lactic Acid ◽  
Feed Concentration ◽  
Hydrophilic Drugs ◽  
Hydrophilic Drug ◽  
Nanoprecipitation Method

The improvement of the loading content of hydrophilic drugs by polymer nanoparticles (NPs) recently has received increased attention from the field of controlled release. We developed a novel, simply modified, drop-wise nanoprecipitation method which separated hydrophilic drugs and polymers into aqueous phase (continuous phase) and organic phase (dispersed phase), both individually and involving a mixing process. Using this method, we produced ciprofloxacin-loaded NPs by Poly (d,l-lactic acid)-Dextran (PLA-DEX) and Poly lactic acid-co-glycolic acid-Polyethylene glycol (PLGA-PEG) successfully, with a considerable drug-loading ability up to 27.2 wt% and an in vitro sustained release for up to six days. Drug content with NPs can be precisely tuned by changing the initial drug feed concentration of ciprofloxacin. These studies suggest that this modified nanoprecipitation method is a rapid, facile, and reproducible technique for making nano-scale drug delivery carriers with high drug-loading abilities

scholarly journals Copper Adsorption on Lignin for the Removal of Hydrogen Sulfide

Molecules ◽  
2020 ◽  
Vol 25 (23) ◽  
pp. 5577
Author(s):  
Miroslav Nikolic ◽  
Marleny Cáceres Najarro ◽  
Ib Johannsen ◽  
Joseph Iruthayaraj ◽  
Marcel Ceccato ◽  
...  
Keyword(s):  
Hydrogen Sulfide ◽  
Photoelectron Spectroscopy ◽  
Copper Ions ◽  
Porous Silica ◽  
Proton Transfer Reaction ◽  
Kraft Lignin ◽  
Copper Adsorption ◽  
X Ray ◽  
Removal Capacity ◽  
H2s Adsorption

Lignin is currently an underutilized part of biomass; thus, further research into lignin could benefit both scientific and commercial endeavors. The present study investigated the potential of kraft lignin as a support material for the removal of hydrogen sulfide (H2S) from gaseous streams, such as biogas. The removal of H2S was enabled by copper ions that were previously adsorbed on kraft lignin. Copper adsorption was based on two different strategies: either directly on lignin particles or by precipitating lignin from a solution in the presence of copper. The H2S concentration after the adsorption column was studied using proton-transfer-reaction mass spectrometry, while the mechanisms involved in the H2S adsorption were studied with X-ray photoelectron spectroscopy. It was determined that elemental sulfur was obtained during the H2S adsorption in the presence of kraft lignin and the differences relative to the adsorption on porous silica as a control are discussed. For kraft lignin, only a relatively low removal capacity of 2 mg of H2S per gram was identified, but certain possibilities to increase the removal capacity are discussed.

Mechanical Properties and Porosity of Organo-Silicate Glass (OSG) Low-k Dielectric Films

2001 ◽  
Vol 695 ◽  
Author(s):  
J. B. Vella ◽  
Q. Xie ◽  
N. V. Edwards ◽  
J. Kulik ◽  
K. H. Junker
Keyword(s):  
Mechanical Properties ◽  
Photoelectron Spectroscopy ◽  
Elastic Moduli ◽  
Porous Silica ◽  
Material Behavior ◽  
Dielectric Films ◽  
X Ray ◽  
Transmission Electron ◽  
Microelectronics Industry ◽  
Low K

ABSTRACTLow-k material integration issues that plague the microelectronics industry include the compromise in mechanical properties that one incurs in abandoning fully dense silica dieletrics. Typical elastic moduli of OSG low-k dieletric films are 2-10 GPa with corresponding hardnesses of 0.5 to 1.5 GPa. In the present study, the hardness and elastic modulus properties measured by nanoindentation of porous silica based low-k films are correlated with in initial estimates of density using a novel technique of spectroscopic ellispsometry. Transmission electron microscopy and X-ray photoelectron spectroscopy show the structural and chemical similarity of the films. Nanoindentation and spectroscopic ellipsometry results reflect significant deviations in material behavior from that expected from a simple model of silica (SiO2) with included voids or porosity, suggesting that the methyl groups are actively participating in the mechanical and optical properties of the material.

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