PCL loaded with sol-gel synthesized organic-inorganic hybrid fillers: From the analysis of 2D substrates to the design of 3D rapid prototyped composite scaffolds for tissue engineering

2012 ◽  
Author(s):  
R. De Santis ◽  
A. Gloria ◽  
T. Russo ◽  
U. D’Amora ◽  
V. D'Antò ◽  
...  
Keyword(s):  
Tissue Engineering ◽  
Sol Gel ◽  
Composite Scaffolds ◽  
Inorganic Hybrid ◽  
Hybrid Fillers

scholarly journals Poly(∊-Caprolactone) Reinforced with Sol-Gel Synthesized Organic-Inorganic Hybrid Fillers as Composite Substrates for Tissue Engineering

2010 ◽  
Vol 8 (3) ◽  
pp. 146-152 ◽  
Author(s):  
Teresa Russo ◽  
Antonio Gloria ◽  
Vincenzo D'Antò ◽  
Ugo D'Amora ◽  
Gianluca Ametrano ◽  
...  
Keyword(s):  
Tissue Engineering ◽  
Sol Gel ◽  
Inorganic Hybrid ◽  
Hybrid Fillers ◽  
Composite Substrates ◽  
Poly Caprolactone

UV Curable Organic-Inorganic Hybrid Materials

2000 ◽  
Vol 628 ◽  
Author(s):  
Guang-Way Jang ◽  
Ren-Jye Wu ◽  
Yuung-Ching Sheen ◽  
Ya-Hui Lin ◽  
Chi-Jung Chang
Keyword(s):  
Hybrid Materials ◽  
Colloidal Silica ◽  
Sol Gel ◽  
Solution Ph ◽  
Uv Curable ◽  
Inorganic Hybrid ◽  
Degradation Temperature ◽  
Sol Gel Process ◽  
The Stability ◽  
Thermal Degradation Temperature

This work successfully prepared an UV curable organic-inorganic hybrid material consisting of organic modified colloidal silica. Applications of UV curable organic-inorganic hybrid materials include abrasion resistant coatings, photo-patternable thin films and waveguides. Colloidal silica containing reactive functional groups were also prepared by reacting organic silane and tetraethyl orthosilicate (TEOS) using sol-gel process. In addition, the efficiency of grafting organic moiety onto silica nanoparticles was investigated by applying TGA and FTIR techniques. Experimental results indicated a strong interdependence between surface modification efficiency and solution pH. Acrylate-SiO2 hybrid formation could result in a shifting of thermal degradation temperature of organic component from about 200°C to near 400°C. In addition, the stability of organic modified colloidal silica in UV curable formula and the physical properties of resulting coatings were discussed. Furthermore, the morphology of organic modified colloidal silica was investigated by performing TEM and SEM studies‥

scholarly journals Three-dimensionally printed polycaprolactone/multicomponent bioactive glass scaffolds for potential application in bone tissue engineering

2020 ◽  
Vol 6 (1) ◽  
pp. 57-69
Author(s):  
Amirhosein Fathi ◽  
Farzad Kermani ◽  
Aliasghar Behnamghader ◽  
Sara Banijamali ◽  
Masoud Mozafari ◽  
...  
Keyword(s):  
Tissue Engineering ◽  
3D Printing ◽  
Bone Tissue Engineering ◽  
Bone Tissue ◽  
Three Dimensional ◽  
Layer By Layer ◽  
Composite Scaffolds ◽  
3D Printed ◽  
Co Doped

AbstractOver the last years, three-dimensional (3D) printing has been successfully applied to produce suitable substitutes for treating bone defects. In this work, 3D printed composite scaffolds of polycaprolactone (PCL) and strontium (Sr)- and cobalt (Co)-doped multi-component melt-derived bioactive glasses (BGs) were prepared for bone tissue engineering strategies. For this purpose, 30% of as-prepared BG particles (size <38 μm) were incorporated into PCL, and then the obtained composite mix was introduced into a 3D printing machine to fabricate layer-by-layer porous structures with the size of 12 × 12 × 2 mm3.The scaffolds were fully characterized through a series of physico-chemical and biological assays. Adding the BGs to PCL led to an improvement in the compressive strength of the fabricated scaffolds and increased their hydrophilicity. Furthermore, the PCL/BG scaffolds showed apatite-forming ability (i.e., bioactivity behavior) after being immersed in simulated body fluid (SBF). The in vitro cellular examinations revealed the cytocompatibility of the scaffolds and confirmed them as suitable substrates for the adhesion and proliferation of MG-63 osteosarcoma cells. In conclusion, 3D printed composite scaffolds made of PCL and Sr- and Co-doped BGs might be potentially-beneficial bone replacements, and the achieved results motivate further research on these materials.

scholarly journals Preparation and Electrochemical Characterization of Organic–Inorganic Hybrid Poly(Vinylidene Fluoride)-SiO2 Cation-Exchange Membranes by the Sol-Gel Method Using 3-Mercapto-Propyl-Triethoxyl-Silane

Materials ◽  
2019 ◽  
Vol 12 (19) ◽  
pp. 3265 ◽  
Author(s):  
Li ◽  
Li ◽  
Li ◽  
Guan ◽  
Zheng ◽  
...  
Keyword(s):  
Membrane Potential ◽  
Oxidative Stability ◽  
Water Uptake ◽  
Polyvinylidene Fluoride ◽  
Vinylidene Fluoride ◽  
Sol Gel ◽  
Synthesis Method ◽  
Co2 Production ◽  
Inorganic Hybrid ◽  
Poly Vinylidene Fluoride

A new synthesis method for organic–inorganic hybrid Poly(vinylidene fluoride)-SiO2 cation-change membranes (CEMs) is proposed. This method involves mixing tetraethyl orthosilicate (TEOS) and 3-mercapto-propyl-triethoxy-silane (MPTES) into a polyvinylidene fluoride (PVDF) sol-gel solution. The resulting slurry was used to prepare films, which were immersed in 0.01 M HCl, which caused hydrolysis and polycondensation between the MPTES and TEOS. The resulting Si-O-Si polymers chains intertwined and/or penetrated the PVDF skeleton, significantly improving the mechanical strength of the resulting hybrid PVDF-SiO2 CEMs. The -SH functional groups of MPTES oxidized to-SO3H, which contributed to the excellent permeability of these CEMs. The surface morphology, hybrid structure, oxidative stability, and physicochemical properties (IEC, water uptake, membrane resistance, membrane potential, transport number, and selective permittivity) of the CEMs obtained in this work were characterized using scanning electron microscope and Fourier transform infrared spectroscopy, as well as electrochemical testing. Tests to analyze the oxidative stability, water uptake, membrane potential, and selective permeability were also performed. Our organic–inorganic hybrid PVDF-SiO2 CEMs demonstrated higher oxidative stability and lower resistance than commercial Ionsep-HC-C membranes with a hydrocarbon structure. Thus, the synthesis method described in this work is very promising for the production of very efficient CEMs. In addition, the physical and electrochemical properties of the PVDF-SiO2 CEMs are comparable to the Ionsep-HC-C membranes. The electrolysis of the concentrated CoCl2 solution performed using PVDF-SiO2-6 and Ionsep-HC-C CEMs showed that at the same current density, Co2+ production, and current efficiency of the PVDF-SiO2-6 CEM membrane were slightly higher than those obtained using the Ionsep-HC-C membrane. Therefore, our novel membrane might be suitable for the recovery of cobalt from concentrated CoCl2 solutions.

Structure and Properties of Poly(α-hydroxyl acids)/Nano Hydroxyapatite Composite Scaffolds

2002 ◽  
Vol 735 ◽  
Author(s):  
Guobao Wei ◽  
Peter X. Ma
Keyword(s):  
Tissue Engineering ◽  
Pore Structure ◽  
The Body ◽  
Polymer Scaffolds ◽  
Composite Scaffolds ◽  
Average Pore ◽  
Thermally Induced ◽  
Tissue Engineering Approach ◽  
Biodegradable Poly ◽  
Organ Failures

ABSTRACTTissue losses and organ failures resulting from injuries or diseases remain frequent and serious health problems despite great advances in medical technologies. Transplantation and reconstructive surgeries are seriously challenged by donor tissue shortage. We take a tissue engineering approach to design 3D scaffolds for cells to grow and synthesize new tissues. The scaffolds are biodegradable and will be absorbed after fulfilling the purpose as 3D templates, leaving nothing foreign in the body. To better mimic natural bone structurally, mechanically and biologically, nano-sized hydroxyapatite particles (N-HAP) were formulated with biodegradable poly(α-hydroxyl acids) to form composite scaffolds with well-controlled pore structures using thermally induced phase separation (TIPS) in this work. The pore structure and mechanical properties of the scaffolds were optimized by the use of multiple solvent systems, different quenching rates and quenching depths. The fabricated scaffolds possessed porosities higher than 90% and average pore sizes ranging from 50 to 500 μm. The scaffolds containing N-HAP maintained open and regular 3D pore structure similar to those of plain polymer scaffolds, implying that N-HAP particles were dispersed within the polymer pore walls of the scaffolds. The addition of N-HAP increased the compressive modulus by 20∼80% over that of plain polymer scaffolds. These results indicate that poly(α-hydroxyl acids)/N-HAP scaffolds may provide excellent 3D substrates for bone tissue engineering.

Synthesis and Intermolecularly Mediated Assembly of Organic Pigment in Hybrid Coating Films

1998 ◽  
Vol 519 ◽  
Author(s):  
Y. Yan ◽  
Z. Duan ◽  
D.-G. Chen ◽  
S. Ray Chaudhuri
Keyword(s):  
Sol Gel ◽  
Hybrid Coating ◽  
Hypsochromic Shift ◽  
Hybrid Films ◽  
Coating Films ◽  
Organic Pigment ◽  
Inorganic Hybrid ◽  
Matrix Interactions ◽  
Sol Gel Process

AbstractThe insoluble, strongly hydrogen bonded organic pigment of 3,6-bis-(4-chlorphenyl)-l,4- diketopyrrolo [3,4-c] pyrrole was transiently blocked by adding carbamate groups, and consequently incorporated into organic-inorganic hybrid matrices by a sol-gel process. The homo- (pigment-pigment) and hetero-intermolecular (pigment-matrix) interactions were found to control both the assembly and dispersion of pigment molecules in the hybrid coating films. A weaker interaction between matrices and pigment molecules results in aggregation of the carbamate pigment in the methyl-silicate films. A stronger interaction forms a homogenous dispersion and coloration of the phenyl-silicate films. The as-prepared methyl- and phenylsilicate films doped with the organic pigment were distinguished by a morphology change and a blue (hypsochromic) shift in absorption from 550 to 460 nm. Thermal treatment can remove the carbamate groups and in-situ form the organic pigment in the hybrid films.

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