scholarly journals Surface Modification of the Ti-6Al-4V Alloy by Anodic Oxidation and Its Effect on Osteoarticular Cell Proliferation

Coatings ◽  
2020 ◽  
Vol 10 (5) ◽  
pp. 491
Author(s):  
Itzel P. Torres-Avila ◽  
Itzia I. Padilla-Martínez ◽  
Nury Pérez-Hernández ◽  
Angel E. Bañuelos-Hernández ◽  
Julio C. Velázquez ◽  
...  
Keyword(s):  
Cell Proliferation ◽  
Titanium Oxide ◽  
Anodic Oxidation ◽  
Ammonium Fluoride ◽  
Biological Evaluation ◽  
In Vitro Assays ◽  
X Ray Diffraction ◽  
Inner Diameter ◽  
Xrd Patterns

This investigation describes the formation of crystalline nanotubes of titanium oxide on the surface of a Ti-6Al-4V alloy and its biological evaluation. The formation of nanotubes was performed by the anodic oxidation technique with a constant work potential of 60 V but with different anodizing times of 10, 20, 30, 40, 50, and 60 min used to evaluate their effects on the characteristics of the nanotubes and their biological activity. A mixture of ethylene glycol, water, and ammonium fluoride (NH4F) was used as the electrolytic fluid. Scanning electron microscopy (SEM) and X-ray diffraction (XRD) were applied to determine the morphology and crystalline nature of the nanotubes, showing a well-defined matrix of nanotubes of titanium oxide with a crystalline structure and a diameter in the range of 52.5 ± 5.13 to 95 ± 11.92 nm. In contrast, the XRD patterns showed an increase of defined peaks that directly correlated with treatment times. Moreover, in vitro assays using an innovative cell culture device demonstrated that the inner diameter of the nanotubes directly correlated with cell proliferation.

scholarly journals PSMA-D4 Radioligand for Targeted Therapy of Prostate Cancer: Synthesis, Characteristics and Preliminary Assessment of Biological Properties

2021 ◽  
Vol 22 (5) ◽  
pp. 2731
Author(s):  
Piotr Garnuszek ◽  
Urszula Karczmarczyk ◽  
Michał Maurin ◽  
Arkadiusz Sikora ◽  
Jolanta Zaborniak ◽  
...  
Keyword(s):  
Prostate Cancer ◽  
Targeted Therapy ◽  
Ex Vivo ◽  
Specific Binding ◽  
Biological Evaluation ◽  
In Vitro Assays ◽  
The Novel ◽  
Distribution Profile ◽  
System L

A new PSMA ligand (PSMA-D4) containing the Glu-CO-Lys pharmacophore connected with a new linker system (L-Trp-4-Amc) and chelator DOTA was developed for radiolabeling with therapeutic radionuclides. Herein we describe the synthesis, radiolabeling, and preliminary biological evaluation of the novel PSMA-D4 ligand. Synthesized PSMA-D4 was characterized using TOF-ESI-MS, NMR, and HPLC methods. The novel compound was subject to molecular modeling with GCP-II to compare its binding mode to analogous reference compounds. The radiolabeling efficiency of PSMA-D4 with 177Lu, 90Y, 47Sc, and 225Ac was chromatographically tested. In vitro studies were carried out in PSMA-positive LNCaP tumor cells membranes. The ex vivo tissue distribution profile of the radioligands and Cerenkov luminescence imaging (CLI) was studied in LNCaP tumor-bearing mice. PSMA-D4 was synthesized in 24% yield and purity >97%. The radio complexes were obtained with high yields (>97%) and molar activity ranging from 0.11 to 17.2 GBq mcmol−1, depending on the radionuclide. In vitro assays confirmed high specific binding and affinity for all radiocomplexes. Biodistribution and imaging studies revealed high accumulation in LNCaP tumor xenografts and rapid clearance of radiocomplexes from blood and non-target tissues. These render PSMA-D4 a promising ligand for targeted therapy of prostate cancer (PCa) metastases.

scholarly journals The immunosuppressant SR 31747 blocks cell proliferation by inhibiting a steroid isomerase in Saccharomyces cerevisiae.

1996 ◽  
Vol 16 (6) ◽  
pp. 2719-2727 ◽  
Author(s):  
S Silve ◽  
P Leplatois ◽  
A Josse ◽  
P H Dupuy ◽  
C Lanau ◽  
...  
Keyword(s):  
Saccharomyces Cerevisiae ◽  
Cell Proliferation ◽  
Gene Product ◽  
In Vitro Assays ◽  
Gene Products ◽  
Yeast Saccharomyces Cerevisiae ◽  
Isomerase Activity ◽  
Encoding Gene ◽  
Resistant Mutants

SR 31747 is a novel immunosuppressant agent that arrests cell proliferation in the yeast Saccharomyces cerevisiae, SR 31747-treated cells accumulate the same aberrant sterols as those found in a mutant impaired in delta 8- delta 7-sterol isomerase. Sterol isomerase activity is also inhibited by SR 31747 in in vitro assays. Overexpression of the sterol isomerase-encoding gene, ERG2, confers enhanced SR resistance. Cells growing anaerobically on ergosterol-containing medium are not sensitive to SR. Disruption of the sterol isomerase-encoding gene is lethal in cells growing in the absence of exogenous ergosterol, except in SR-resistant mutants lacking either the SUR4 or the FEN1 gene product. The results suggest that sterol isomerase is the target of SR 31747 and that both the SUR4 and FEN1 gene products are required to mediate the proliferation arrest induced by ergosterol depletion.

Cell Proliferation on Titania Layer with In Vitro Apatite Forming Ability

2007 ◽  
Vol 330-332 ◽  
pp. 131-134
Author(s):  
S. Yabe ◽  
Kanji Tsuru ◽  
Satoshi Hayakawa ◽  
Akiyoshi Osaka ◽  
Y. Yoshida ◽  
...  
Keyword(s):  
Heat Treatment ◽  
Hydrogen Peroxide ◽  
Cell Proliferation ◽  
Body Fluid ◽  
Surface Hydrophobicity ◽  
Diffraction Intensity ◽  
Titania Layer ◽  
Xrd Patterns ◽  
Titanium Substrates

Titania layer was fabricated on the titanium substrates with chemical treatment with 20ml or 40ml of hydrogen peroxide solution and subsequent heat treatment at 400°C, coded as CHT20 and CHT40, respectively. CHT20 spontaneously deposited apatite on the surface in a simulated body fluid (SBF), while CHT40 did not. TF-XRD patterns showed that the diffraction intensity of anatase of CHT20 was higher than that of CHT40. It was suggested that the thicker titania layer indicated in vitro apatite forming ability. The cell proliferation of CHT20 and CHT40 were lower than NT and HT. Since the surface of titania layers became hydrophobic after autoclaving, we can suppose that the cell proliferation on CHT20 and CHT40 were lower than NT and HT due to their surface hydrophobicity.

scholarly journals Preparation and Characterization of Chitosan obtained from Pacific White Shrimp Shells and its in vitro Antifungal Activity

2020 ◽  
Vol 32 (10) ◽  
pp. 2515-2519
Author(s):  
Arnannit Kuyyogsuy
Keyword(s):  
Pacific White Shrimp ◽  
White Shrimp ◽  
X Ray Diffraction ◽  
Vitro Assay ◽  
Shrimp Shells ◽  
Xrd Patterns ◽  
Two Peaks ◽  
In Vitro Antifungal Activity

In this article, a method for the processing of chitosan from Pacific white shrimp shells is developed which involves three steps viz. demineralization, deproteinization, and deacetylation. The samples of chitosan with more than 90% degree of deacetylation (DD%) were obtained by FTIR. This indicated that the current processing method of shrimp shells was beneficial for chitosan production. The morphology of chitosan sample was determined using scanning electron microscopy (SEM). X-ray diffraction (XRD) patterns exhibited two peaks of crystalline character approximately at 10º and 20º (2θ). The effect of 0.1% (w/v) of chitosan on the growth of Penicillium digitatum was tested by an in vitro assay and the results showed an almost complete inhibition (98% ± 0.56).

scholarly journals Controlled Release of Ropivacaine from Single-Armed (1-PCL) and Four-Armed PCL (4-PCL) Microspheres

2019 ◽  
Vol 2019 ◽  
pp. 1-8
Author(s):  
Wei Xiong ◽  
Yue-kun Shen ◽  
Peng Dong ◽  
Ying Xiao ◽  
Xiong-qing Huang ◽  
...  
Keyword(s):  
Chronic Pain ◽  
Cell Proliferation ◽  
Mammalian Cells ◽  
Great Promise ◽  
X Ray Diffraction ◽  
X Ray ◽  
Initial Release ◽  
Release Assay ◽  
Ft Ir

Sustained release of anesthesia has shown great promise in the treatment of chronic pain in patients. In this research, we used neutralized ropivacaine as an anesthesia and poly(ε-caprolactone) (PCL) with different architectures to systematically study how these architectures affect the release of ropivacaine. After optimizing the parameters of the preparation of microspheres, ropivacaine-loaded 1-PCL microspheres and 4-PCL microspheres were obtained. Fourier Transform infrared spectra (FT-IR) and X-ray diffraction spectra (XRD) confirmed that ropivacaine was encapsulated within the microsphere rather than inserted on the surface of the microsphere. Ropivacaine was found to be buried deeper in the 1-PCL microsphere than in the 4-PCL microsphere. In vitro release assay revealed that small crystalline grains interfered with ropivacaine release in 4-PCL microspheres during the initial release period, but then two kinds of microspheres showed a similar ropivacaine release rate. We basically proved that the architecture of PCL has a negligible effect on ropivacaine release. Cell proliferation test revealed that the release of products from the microspheres resulted in insignificant toxicity towards mammalian cells.

Titanium Oxide (TiO2) Coatings Produced on Titanium by Oxygen-Plasma Immersion and Cell Behaviour on TiO2

2006 ◽  
Vol 309-311 ◽  
pp. 367-370 ◽  
Author(s):  
E.T. Uzumaki ◽  
A.R. Santos ◽  
C.S. Lambert
Keyword(s):  
Titanium Oxide ◽  
Oxygen Plasma ◽  
Three Dimensional ◽  
Titanium Substrate ◽  
X Ray Diffraction ◽  
Cell Behaviour ◽  
In Vitro Biocompatibility ◽  
Metallic Implants ◽  
Titanium Substrates

Plasma immersion process was investigated as a method for producing bioceramics coatings on metallic implants due to its advantages, which include the production of coatings on three-dimensional workpieces, with high density and superior adhesion. In this process, the oxygen plasma was utilized to form titanium oxide on titanium substrate. The structure, composition and surface morphology were studied using scanning electron microscopy (SEM) and X-ray diffraction. In addition a preliminary study has also been carried out, on TiO2-coated and uncoated titanium substrates, to analyse the in vitro biocompatibility (cytotoxicity evaluation and cell morphology).

scholarly journals Curcumin-Loaded Mixed Micelles: Preparation, Characterization, and In Vitro Antitumor Activity

2018 ◽  
Vol 2018 ◽  
pp. 1-9 ◽  
Author(s):  
Suping Ji ◽  
Xiao Lin ◽  
Enjiang Yu ◽  
Chengyang Dian ◽  
Xiong Yan ◽  
...  
Keyword(s):  
Mixed Micelles ◽  
Drug Loading ◽  
Molecular State ◽  
X Ray Diffraction ◽  
X Ray ◽  
Release Property ◽  
Mean Size ◽  
Xrd Patterns ◽  
Mcf 7

The objective of this study was to prepare curcumin-loaded mixed Soluplus/TPGS micelles (Cur-TPGS-PMs) for oral administration. The Cur-TPGS-PMs showed a mean size of 65.54 ± 2.57 nm, drug encapsulation efficiency over 85%, and drug loading of 8.17%. The Cur-TPGS-PMs were found to be stable in various pH media (pH 1.2 for 2 h, pH 6.8 for 2 h, and pH 7.4 for 6 h). The X-ray diffraction (XRD) patterns illustrated that curcumin was in the amorphous or molecular state within PMs. The In vitro release test indicated that Cur-TPGS-PMs possessed a significant sustained-release property. The cell viability in MCF-7 cells was found to be relatively lower in Cur-TPGS-PM-treated cells as compared to free Cur-treated cells. CLSM imaging revealed that mixed micelles were efficiently absorbed into the cytoplasm region of MCF-7 cells. Therefore, Cur-TPGS-PMs could have the significant value for the chronic breast cancer therapy.

scholarly journals Novel Nonsymmetrically p-Benzyl-Substituted (Benz)imidazole N-Heterocyclic Carbene-Silver(I) Acetate Complexes: Synthesis and Biological Evaluation

2012 ◽  
Vol 2012 ◽  
pp. 1-13 ◽  
Author(s):  
Frauke Hackenberg ◽  
Anthony Deally ◽  
Grainne Lally ◽  
Sina Malenke ◽  
Helge Müller-Bunz ◽  
...  
Keyword(s):  
Cancer Cell Line ◽  
Benzyl Bromide ◽  
Biological Evaluation ◽  
Diffusion Method ◽  
X Ray Diffraction ◽  
Gram Positive Bacteria ◽  
Acetate Complex ◽  
Renal Cancer Cell ◽  
Synthesis And Biological Evaluation

Nonsymmetrically substituted N-heterocyclic carbene (NHC) precursors 1a–d and 3a–d were synthesised by first reacting 1H-(benz)imidazole with p-cyanobenzyl bromide to give 4-(1H-imidazole-1-ylmethyl)benzonitrile (1) and 4-(1H-benzimidazole-1-ylmethyl)benzonitrile (3) and afterwards introducing benzyl bromide, 1-(bromomethyl)-4-methylbenzene, 1-(bromomethyl)-4-methoxybenzene, and methyl 4-(bromomethyl)benzoate. The NHC-silver(I) acetate complexes (1-benzyl-3-(4-cyanobenzyl)-2,3-dihydro-1H-imidazole-2-ylidene) silver(I) acetate (2a), (1-(4-cyanobenzyl)-3-(4-methylbenzyl)-2,3-dihydro-1H-imidazole-2-ylidene) silver(I) acetate (2b), (1-(4-cyanobenzyl)-3-[4-(methoxycarbonyl)benzyl]-2,3-dihydro-1H-imidazole-2-ylidene) silver(I) acetate (2c), (1-benzyl-3-(4-cyanobenzyl)-2,3-dihydro-1H-benzimidazole-2-ylidene) silver(I) acetate (4a), (1-(4-cyanobenzyl)-3-(4-methylbenzyl)-2,3-dihydro-1H-benzimidazole-2-ylidene) silver(I) acetate (4b), (1-(4-cyanobenzyl)-3-(4-methoxybenzyl)-2,3-dihydro-1H-benzimidazole-2-ylidene) silver(I) acetate (4c), and (1-(4-cyanobenzyl)-3-[4-(methoxycarbonyl)benzyl]-2,3-dihydro-1H-benzimidazole-2-ylidene) silver(I) acetate (4d) were yielded by reacting these NHC precursors with silver(I) acetate. The silver(I) acetate complex 4b was characterised by single crystal X-ray diffraction. Preliminary in vitro antibacterial studies against the Gram-positive bacteria Staphylococcus aureus and the Gram-negative bacteria Escherichia coli, using the Kirby-Bauer disc diffusion method, were carried out on the seven NHC-silver(I) acetate complexes 2a–c and 4a–d. Also the IC50 values of these seven complexes were determined by an MTT-based assay against the human renal cancer cell line Caki-1. The complexes 2a–c and 4a–c revealed the following IC50 values, respectively, 25 (±1), 15 (±2), 5.4 (±0.8), 16 (±2), 7.1 (±1), 20 (±4), and 14 (±1) μM.

scholarly journals Electrochemical Anodization and Characterization of Titanium Oxide Nanotubes for Photo Electrochemical Cells

2021 ◽  
Vol 2070 (1) ◽  
pp. 012073
Author(s):  
C U Bhadra ◽  
D Henry Raja ◽  
D Jonas Davidson
Keyword(s):  
Titanium Oxide ◽  
Oxygen Vacancies ◽  
Ammonium Fluoride ◽  
Band Gap Energy ◽  
Electrochemical Anodization ◽  
Nanotube Arrays ◽  
Photoluminescence Intensity ◽  
Titania Nanotube Arrays ◽  
Titanium Oxide Nanotubes ◽  
Inner Diameter

Abstract Due to its multitude of applications, titanium oxide is one of the most coveted and most sought-after materials. The above experiment demonstrated that TiO2 nanotube arrays might be formed by electrochemical anodization of titanium foil. The 0.25 wt% ammonium fluoride (NH4F) was added to a solution of 99% ethylene glycol. Anodization is carried out at a constant DC voltage of 12V for 1 hour. Then, the annealing process is carried out for 1 hour at 4800C, which is known as an annealing. FE-SEM were utilized to evaluate the surface morphology of the nanotube arrays that were made. At the wavelength of 405 nm, sharply peaked photoluminescence intensity was observed, which corresponded tothe band gap energy (3.2 eV) of the anatase TiO2 phase. Since free excitations appear at 391 and 496 nm, and since oxygen vacancies are developed on the surface of titania nanotube arrays, it is reasonable to conclude that free excitations and oxygen vacancies are the causes of humps at 391 and 496 nm, and that they may also be present at 412 and 450 nm. FESEM results showed uniformly aligned TiO2 nanotube arrays with an inner diameter of 100 nm and a wall thickness of 50 nm

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