scholarly journals Curcumin Nanocrystals: Production, Physicochemical Assessment, and In Vitro Evaluation of the Antimicrobial Effects against Bacterial Loading of the Implant Fixture

2020 ◽  
Vol 10 (23) ◽  
pp. 8356
Author(s):  
Ramin Negahdari ◽  
Simin Sharifi ◽  
Mohammad Ali Ghavimi ◽  
Mohammad Yousef Memar ◽  
Bita Khaneshi ◽  
...  
Keyword(s):  
Removal Rate ◽  
Antimicrobial Effect ◽  
Drying Method ◽  
X Ray Diffraction ◽  
X Ray ◽  
E Coli ◽  
Colony Forming Unit ◽  
Implant Abutment ◽  
Scanning Electron

Background: This study aimed to prepare and study physicochemical properties as well as the antibacterial action of curcumin nanocrystals inside the implant fixture against Escherichia coli (E. coli), Staphylococcus aureus (S. aureus), and Enterococcus faecalis (E. faecalis). Methods: Curcumin nanocrystals were prepared via precipitation combined with the spray drying method. The produced curcumin nanocrystals were characterized by dynamic light scattering (DLS), scanning electron microscopy (SEM), powder X-ray diffraction (PXRD), and Fourier transform infrared spectroscopy (FTIR). Moreover, the in vitro antimicrobial effect of curcumin nanocrystals inside the implant fixture was assessed against E. coli, S. aureus, and E. faecalis. All implant-abutment assemblies were immersed in bacterial suspensions and were incubated at 24, 48, and 72 h. The contents of each implant were cultured to count the colony of bacteria at 37 °C for 24 h. Results: The prepared curcumin nanocrystals with a mean particle size of 95 nm and spherical morphology exhibited a removal rate of 99.99% for all bacteria. In addition, the colony-forming unit (CFU) of bacteria in exposure to nanocrystals significantly was reduced (p < 0.010) by increasing the time. Conclusions: Curcumin nanocrystals can be used inside the implant fixture as an antimicrobial agent in order to more stabilization of the implant.

Mesenchymal Stem Cell Response to Surface Altered Porous Ti

2015 ◽  
Vol 638 ◽  
pp. 67-72
Author(s):  
Ana Maria Salantiu ◽  
Florin Popa ◽  
Petru Pascuta ◽  
Olga Soritau ◽  
Noemi Dirzu ◽  
...  
Keyword(s):  
Stem Cell ◽  
X Ray Diffraction ◽  
X Ray ◽  
Chemically Modified ◽  
Porous Ti ◽  
Average Porosity ◽  
Ft Ir ◽  
Cell Testing ◽  
Scanning Electron

This work aims to investigate the influence of surface conditioning of porous Ti for enhancing its biological activity, as assessed by in vitro stem cell testing. Porous Ti samples with an average porosity of 32% were processed by Powder Metallurgy with dextrin as a space holder. The samples were subjected to H2O2 treatment to form an enhanced TiO2 film, followed by a heat treatment at 400°C and 600°C aiming to the crystallization of the as-formed amorphous titanium oxide. Samples characterization was performed by Scanning Electron Microscopy (SEM), Fourier Transform Infrared Spectroscopy (FT-IR) and X-Ray Diffraction (XRD). The treated surfaces revealed to be made of both anatase and rutile TiO2, with groove–shaped structure and cracks on the surface of the TiO2 film. The intrinsic biocompatibility of the chemically modified porous Ti surfaces was assessed in vitro. In our cell culture tests, stem cells were found to attach and proliferate better on the chemically treated Ti surfaces compared to the control untreated Ti surfaces.

scholarly journals Development of an Oxcarbazepine Solid Dispersion Using Skimmed Milk to Improve the Solubility and Dissolution Profile

2019 ◽  
Vol 11 (05) ◽  
Author(s):  
M. Shah ◽  
D. Patel
Keyword(s):  
Electron Microscopy ◽  
Solid Dispersion ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Infra Red ◽  
Crystalline Nature ◽  
Skimmed Milk ◽  
Scanning Electron

Oxcarbazepine has low solubility and low oral bioavailability, so it’s a challenge to formulate suitable dosage form. In this present investigation, to improve the dissolution rate and solubility, skimmed milk is used as a carrier. Physical mixers were prepared using various drugs to carrier ratio and spray drying technology was used to develop solid dispersion with the carrier. Various techniques were used to characterize the solid dispersion immediately after they were made which includes differential scanning calorimetry, scanning electron microscopy, fourier transform infra- red spectroscopy, X-ray diffraction and in-vitro dissolution profiles. The differential scanning calorimetry thermograms of raw drug indicated of its anhydrous crystalline nature. In thermograms of solid dispersion, the characteristic peak was absent suggesting the change from crystalline nature to amorphous form. X-ray diffraction confirmed those results. X-ray diffraction results of raw drug showed highly intense peak characteristic of its crystalline nature where solid dispersion showed less intense, more diffused peak indicating the change in crystalline form. Fourier transforms infra-red spectroscopy studies showed there was no interaction between drug and carrier. Scanning electron microscopy support the amorphous nature of mixer. The whole formulation showed distinct enhancement in the drug release behavior and solubility. The optimum oxcarbazepine to skimmed milk ratio 1:3 enhances the in-vitro drug release by 3.5 fold and also show distinct increase in solubility. It was concluded that for improvement of solubility of poorly water soluble oxcarbazepine, skimmed milk powder as a carrier can be utilize very well.

Bioactive Composite Materials for Bone Tissue Applications

2006 ◽  
Vol 514-516 ◽  
pp. 985-989
Author(s):  
B.J.M. Leite Ferreira ◽  
M.G.G.M. Duarte ◽  
M. Helena Gil ◽  
Rui N. Correia ◽  
J. Román ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Bone Tissue ◽  
Tissue Repair ◽  
Body Fluid ◽  
In Vitro Bioactivity ◽  
X Ray Diffraction ◽  
X Ray ◽  
Biodegradable Composite ◽  
Scanning Electron

Two materials with potential application in bone tissue repair have been developed: 1) a non-biodegradable composite based in a new methacrylic-co-acrylic matrix; and 2) a biodegradable composite based in a chitosan (Ch) matrix. Both matrices were reinforced with glass-ceramic particles of composition (mol%) 70 SiO2 – 30 CaO. The in vitro bioactivity of composites was assessed by soaking in simulated body fluid (SBF) for periods of up to 7 days at 37º C. X-ray diffraction (XRD) and scanning electron microscopy coupled with X-ray energy dispersive spectroscopy (SEM-EDS) were used for deposit identification after different soaking periods. Calcium phosphate particulate deposits were detected after 3 days of immersion, followed by growth and maturation towards apatite.

Formation de Weddellite (CaC2O4∙2H2O) extracellulaire en culture in vitro par Paxillus involutus; signification de cette production pour la symbiose ecto- mycorhizienne

1984 ◽  
Vol 62 (6) ◽  
pp. 1116-1121 ◽  
Author(s):  
F. Lapeyrie ◽  
Monique Perrin ◽  
R. Pepin ◽  
G. Bruchet
Keyword(s):  
Calcium Oxalate ◽  
Culture Medium ◽  
Calcium Content ◽  
Ectomycorrhizal Fungus ◽  
Paxillus Involutus ◽  
X Ray Diffraction ◽  
X Ray ◽  
High Calcium ◽  
Scanning Electron

Several forms of extracellular crystals have been observed in vitro on a semisynthetic culture medium. The conditions for their formation have not been determined. Their morphology and their localisation on the hyphal surface and in the culture medium have been investigated by means of scanning electron microscopy. These crystals have been identified as dehydrated calcium oxalate (Weddellite) using x-ray diffraction methods. Their high calcium content has been demonstrated with the scanning electron microprobe, by detecting the x-ray emission of calcium. The significance of calcium oxalate production by an ectomycorrhizal fungus is discussed.

Spray dried hydroxyapatite-polyvinyl alcohol biocomposites

2016 ◽  
Vol 36 (8) ◽  
pp. 795-804 ◽  
Author(s):  
Tuğba Başargan ◽  
Nalan Erdöl-Aydın ◽  
Gülhayat Nasün-Saygılı
Keyword(s):  
Electron Microscopy ◽  
Polyvinyl Alcohol ◽  
Spray Dryer ◽  
Drying Method ◽  
X Ray Diffraction ◽  
X Ray ◽  
Pva Solutions ◽  
Spray Dried ◽  
Scanning Electron

Abstract In this study, hydroxyapatite/polyvinyl alcohol (HAp-PVA) biocomposites were prepared using a spray drying method. HAp-PVA solutions fed to spray dryer were prepared by two different routes, namely, physical and in situ biomimetric methods. In the former method, HAp was synthesized without the presence of polymer and then HAp particles were incorporated into a PVA solution. In the second one, hydroxyapatite was in situ synthesized in the presence of PVA. Experiments were also run to investigate the effect of the molecular weight of PVA on the structure of spray-dried biocomposites. Fourier transform infrared spectroscopy, X-ray diffraction, scanning electron microscopy and particle size analyses were performed to characterize the produced HAp-PVA composites.

scholarly journals Preparation and Biocompatibility of Poly Methyl Methacrylate (PMMA)-Mesoporous Bioactive Glass (MBG) Composite Scaffolds

Gels ◽  
2021 ◽  
Vol 7 (4) ◽  
pp. 180
Author(s):  
Irina Atkinson ◽  
Ana Maria Seciu-Grama ◽  
Oana Catalina Mocioiu ◽  
Ana Maria Mocioiu ◽  
Luminita Predoana ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Composite Scaffold ◽  
Bone Diseases ◽  
X Ray Diffraction ◽  
Composite Scaffolds ◽  
X Ray ◽  
In Vitro Biocompatibility ◽  
Mesoporous Bioactive Glass ◽  
Scanning Electron

In recent years, the rising number of bone diseases which affect millions of people worldwide has led to an increased demand for materials with restoring and augmentation properties that can be used in therapies for bone pathologies. In this work, PMMA- MBG composite scaffolds containing ceria (0, 1, 3 mol%) were obtained by the phase separation method. The obtained composite scaffolds were characterized by X-ray diffraction, infrared spectroscopy, and scanning electron microscopy. UV–Vis measurement and EDX analysis confirmed the presence of cerium ions in the composite scaffolds. Evaluation of the in-vitro biocompatibility using MTT assay showed that composite scaffold containing 1 mol% of ceria presented higher viability than control cells (100%) for concentrations ranging between 5 and 50% after 96 h of incubation.

Degradation of Orange IV Catalyzed by Fe/S/GAC in the Presence of H2O2

2012 ◽  
Vol 466-467 ◽  
pp. 458-462
Author(s):  
Ying Jie Zhang ◽  
Shu Fen Xu ◽  
Xia Liao ◽  
Rong Yang ◽  
Da Peng Li
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Catalytic Activity ◽  
Activated Carbon ◽  
Removal Rate ◽  
X Ray Diffraction ◽  
Heterogeneous Fenton ◽  
X Ray ◽  
Catalytic Reactivity ◽  
Scanning Electron

A new heterogeneous Fenton-like catalyst of Fe/S/GAC was prepared by granular activated carbon (GAC) soaked in solution of (NH4)2S2O8 and Fe(NO3)3. The effect of the concentration of (NH4)2S2O8 , Fe(NO3)3, drying temperature and different catalysts on the catalytic reactivity of catalyst was discussed. The removal rate of Orange IV was used to express the catalytic reactivity of the catalyst. The prepared catalysts were characterized by X-ray diffraction (XRD), specific surface area (BET) and scanning electron microscopy (SEM). The removal rate of Orange IV followed second-order kinetics. The catalyst of Fe/S/GAC has higher catalytic activity than that of Fe/GAC.

scholarly journals Enhanced In-Vitro Hemozoin Polymerization by Optimized Process using Histidine-Rich Protein II (HRPII)

Polymers ◽  
2019 ◽  
Vol 11 (7) ◽  
pp. 1162 ◽  
Author(s):  
Ju Hun Lee ◽  
Hyeong Ryeol Kim ◽  
Ja Hyun Lee ◽  
Soo Kweon Lee ◽  
Youngsang Chun ◽  
...  
Keyword(s):  
Physical Properties ◽  
Functional Materials ◽  
Important Class ◽  
Reaction Conditions ◽  
In Vitro System ◽  
X Ray ◽  
E Coli ◽  
The Fourier Transform ◽  
Scanning Electron

Conductive biopolymers, an important class of functional materials, have received attention in various fields because of their unique electrical, optical, and physical properties. In this study, the polymerization of heme into hemozoin was carried out in an in vitro system by the newly developed heme polymerase (histidine-rich protein 2 (HRP-II)). The HRP-II was produced by recombinant E. coli BL21 from the Plasmodium falciparum gene. To improve the hemozoin production, the reaction conditions on the polymerization were investigated and the maximum production was achieved after about 790 μM at 34 °C with 200 rpm for 24 h. As a result, the production was improved about two-fold according to the stepwise optimization in an in vitro system. The produced hemozoin was qualitatively analyzed using the Fourier transform infrared (FTIR) spectroscopy, energy dispersive X-ray spectroscopy (EDS), and scanning electron microscopy (SEM). Finally, it was confirmed that the enzymatically polymerized hemozoin had similar physical properties to chemically synthesized hemozoin. These results could represent a significant potential for nano-biotechnology applications, and also provide guidance in research related to hemozoin utilization.

scholarly journals Nano-CL-20/HMX Cocrystal Explosive for Significantly Reduced Mechanical Sensitivity

2017 ◽  
Vol 2017 ◽  
pp. 1-7 ◽  
Author(s):  
Chongwei An ◽  
Hequn Li ◽  
Baoyun Ye ◽  
Jingyu Wang
Keyword(s):  
Spray Drying ◽  
Raw Materials ◽  
Drop Height ◽  
Drying Method ◽  
X Ray Diffraction ◽  
Mechanical Sensitivity ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Friction Sensitivity ◽  
Scanning Electron

Spray drying method was used to prepare cocrystals of hexanitrohexaazaisowurtzitane (CL-20) and cyclotetramethylene tetranitramine (HMX). Raw materials and cocrystals were characterized using scanning electron microscopy, X-ray diffraction, differential scanning calorimetry, Raman spectroscopy, and Fourier transform infrared spectroscopy. Impact and friction sensitivity of cocrystals were tested and analyzed. Results show that, after preparation by spray drying method, microparticles were spherical in shape and 0.5–5 µm in size. Particles formed aggregates of numerous tiny plate-like cocrystals, whereas CL-20/HMX cocrystals had thicknesses of below 100 nm. Cocrystals were formed by C–H⋯O bonding between –NO2 (CL-20) and –CH2– (HMX). Nanococrystal explosives exhibited drop height of 47.3 cm, and friction demonstrated explosion probability of 64%. Compared with raw HMX, cocrystals displayed significantly reduced mechanical sensitivity.

scholarly journals Host-guest interaction and properties of cucurbit[8]uril with chloramphenicol

2021 ◽  
Author(s):  
Lin Zhang ◽  
Jun Zheng ◽  
Guangyan Luo ◽  
Xiaoyue Li ◽  
Yunqian Zhang ◽  
...  
Keyword(s):  
Inhibitory Concentration ◽  
Slow Release ◽  
In Vitro Release ◽  
Titration Calorimetry ◽  
X Ray Diffraction ◽  
X Ray ◽  
E Coli ◽  
The Stability ◽  
Vitro Release

The interaction between cucurbit[8]uril (Q[8]) and chloramphenicol (CPE) was investigated using single-crystal X-ray diffraction, spectroscopy, isothermal titration calorimetry (ITC) and UV-Vis, NMR and IR spectroscopy. The effects of Q[8] on the stability, in vitro release performance and antibacterial activity of CPE were also studied. The results showed that CPE and Q[8] formed a 1:1 inclusion complex (CPE@Q[8]) with an inclusion constant of 5.4736 × 105 L/mol. The intervention of Q[8] did not affect the stability of CPE, but obviously reduced the release rate of CPE in artificial gastric and intestinal juice; Q[8] has a slow-release effect on CPE. The antibacterial results showed that the minimum inhibitory concentration (MIC) of CPE and CPE@Q[8] toward Escherichia coli (E. coli) was 1.5 × 10–3 and 1.0 × 10–3 mol/L, respectively, and toward Staphylococcus aureus (SA), the MIC was 2.0 × 10–3 mol/L for both CPE and CPE@Q[8]. Therefore, Q[8] enhanced the inhibitory activity of CPE against E. coli.

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