scholarly journals Mechanical properties of a bacterial cellulose/polyethylene glycol gel with a peripheral region crosslinked by polyethylene glycol diacrylate

2015 ◽  
Vol 48 (3) ◽  
pp. 317-321 ◽  
Author(s):  
Yukari Numata ◽  
Shiro Masaki ◽  
Kenji Tajima
Keyword(s):  
Mechanical Properties ◽  
Polyethylene Glycol ◽  
Bacterial Cellulose ◽  
Peripheral Region ◽  
Polyethylene Glycol Diacrylate ◽  
Glycol Diacrylate

Polyethylene glycol diacrylate scaffold filled with cell-laden methacrylamide gelatin/alginate hydrogels used for cartilage repair

2021 ◽  
pp. 088532822110448
Author(s):  
Xiang Zhang ◽  
Zhenhao Yan ◽  
Guotao Guan ◽  
Zijing Lu ◽  
Shujie Yan ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
Tissue Engineering ◽  
Polyethylene Glycol ◽  
Cartilage Tissue Engineering ◽  
Cartilage Tissue ◽  
High Concentration ◽  
Polyethylene Glycol Diacrylate ◽  
Low Concentration ◽  
Glycol Diacrylate

Natural cartilage tissue has excellent mechanical properties and has certain cellular components. At this stage, it is a great challenge to produce cartilage scaffolds with excellent mechanical properties, biocompatibility, and biodegradability. Hydrogels are commonly used in tissue engineering because of their excellent biocompatibility; however, the mechanical properties of commonly used hydrogels are difficult to meet the requirements of making cartilage scaffolds. The mechanical properties of high concentration polyethylene glycol diacrylate (PEGDA) hydrogel are similar to those of natural cartilage, but its biocompatibility is poor. Low concentration hydrogel has better biocompatibility, but its mechanical properties are poor. In this study, two different hydrogels were combined to produce cartilage scaffolds with good mechanical properties and strong biocompatibility. First, the PEGDA grid scaffold was printed with light curing 3D printing technology, and then the low concentration GelMA/Alginate hydrogel with chondral cells was filled into the PEGDA grid scaffold. After a series of cell experiments, the filling hydrogel with the best biocompatibility was screened out, and finally the filled hydrogel with cells and excellent biocompatibility was obtained. Cartilage tissue engineering scaffolds with certain mechanical properties were found to have a tendency of cartilage formation in in vitro culture. Compared with the scaffold obtained by using a single hydrogel, this molding method can produce a tissue engineering scaffold with excellent mechanical properties on the premise of ensuring biocompatibility, which has a certain potential application value in the field of cartilage tissue engineering.

scholarly journals Elucidating the Molecular Mechanisms for the Interaction of Water with Polyethylene Glycol-Based Hydrogels: Influence of Ionic Strength and Gel Network Structure

Polymers ◽  
2021 ◽  
Vol 13 (6) ◽  
pp. 845
Author(s):  
Xin Yang ◽  
Bronwin Dargaville ◽  
Dietmar Hutmacher
Keyword(s):  
Polyethylene Glycol ◽  
Ionic Strength ◽  
Molecular Mechanisms ◽  
Repeat Unit ◽  
Bound Water ◽  
Weight Fraction ◽  
Swelling Ratio ◽  
Polyethylene Glycol Diacrylate ◽  
Glycol Diacrylate ◽  
Hydrogel System

The interaction of water within synthetic and natural hydrogel systems is of fundamental importance in biomaterial science. A systematic study is presented on the swelling behavior and states of water for a polyethylene glycol-diacrylate (PEGDA)-based model neutral hydrogel system that goes beyond previous studies reported in the literature. Hydrogels with different network structures are crosslinked and swollen in different combinations of water and phosphate-buffered saline (PBS). Network variables, polyethylene glycol (PEG) molecular weight (MW), and weight fraction are positively correlated with swelling ratio, while “non-freezable bound water” content decreases with PEG MW. The presence of ions has the greatest influence on equilibrium water and “freezable” and “non-freezable” water, with all hydrogel formulations showing a decreased swelling ratio and increased bound water as ionic strength increases. Similarly, the number of “non-freezable bound water” molecules, calculated from DSC data, is greatest—up to six molecules per PEG repeat unit—for gels swollen in PBS. Fundamentally, the balance of osmotic pressure and non-covalent bonding is a major factor within the molecular structure of the hydrogel system. The proposed model explains the dynamic interaction of water within hydrogels in an osmotic environment. This study will point toward a better understanding of the molecular nature of the water interface in hydrogels.

scholarly journals Generation of Photopolymerized Microparticles Based on PEGDA Using Microfluidic Devices. Part 1. Initial Gelation Time and Mechanical Properties of the Material

Micromachines ◽  
2021 ◽  
Vol 12 (3) ◽  
pp. 293
Author(s):  
José M. Acosta-Cuevas ◽  
José González-García ◽  
Mario García-Ramírez ◽  
Víctor H. Pérez-Luna ◽  
Erick Omar Cisneros-López ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
Gelation Time ◽  
Mesh Size ◽  
Microfluidic Devices ◽  
Future Generation ◽  
Mechanical Tests ◽  
Continuous Systems ◽  
Polyethylene Glycol Diacrylate ◽  
Glycol Diacrylate ◽  
Close Relationship

Photopolymerized microparticles are made of biocompatible hydrogels like Polyethylene Glycol Diacrylate (PEGDA) by using microfluidic devices are a good option for encapsulation, transport and retention of biological or toxic agents. Due to the different applications of these microparticles, it is important to investigate the formulation and the mechanical properties of the material of which they are made of. Therefore, in the present study, mechanical tests were carried out to determine the swelling, drying, soluble fraction, compression, cross-linking density (Mc) and mesh size (ξ) properties of different hydrogel formulations. Tests provided sufficient data to select the best formulation for the future generation of microparticles using microfluidic devices. The initial gelation times of the hydrogels formulations were estimated for their use in the photopolymerization process inside a microfluidic device. Obtained results showed a close relationship between the amount of PEGDA used in the hydrogel and its mechanical properties as well as its initial gelation time. Consequently, it is of considerable importance to know the mechanical properties of the hydrogels made in this research for their proper manipulation and application. On the other hand, the initial gelation time is crucial in photopolymerizable hydrogels and their use in continuous systems such as microfluidic devices.

Polyacryloyl hydrazide based injectable & stimuli responsive hydrogels with tunable properties

2014 ◽  
Vol 2 (42) ◽  
pp. 7429-7439 ◽  
Author(s):  
Anuj Kumar ◽  
Sabindra K. Samal ◽  
Rupesh Dash ◽  
Umaprasana Ojha
Keyword(s):  
Polyethylene Glycol ◽  
Acrylic Acid ◽  
Diethyl Malonate ◽  
Synthesis And Characterization ◽  
Cross Linking ◽  
Stimuli Responsive ◽  
Polyethylene Glycol Diacrylate ◽  
Glycol Diacrylate ◽  
Responsive Hydrogels

The synthesis and characterization of a series of injectable and stimuli responsive hydrogels based on polyacryloyl hydrazide have been accomplished using dimethyl 2,2′-thiodiacetate, acrylic acid, diethyl malonate and polyethylene glycol diacrylate as cross-linkers through a chemical or dual cross-linking pathway.

Fabrication of PEG Hydrogel and PDMS Microstructures by a Simple UV Curing Process for Nanobio-Chip Applications

2014 ◽  
Vol 941-944 ◽  
pp. 404-410 ◽  
Author(s):  
Young Ho Kim ◽  
Jeong Woo Sohn ◽  
Youngjae Woo ◽  
Joo Hyun Hong ◽  
Juyoung Park
Keyword(s):  
Polyethylene Glycol ◽  
Uv Irradiation ◽  
Large Scale ◽  
Uv Light ◽  
Single Step ◽  
Polydimethyl Siloxane ◽  
Polyethylene Glycol Diacrylate ◽  
Glycol Diacrylate ◽  
Metal Mask ◽  
Glass Chip

Polyethylene glycol (PEG) hydrogel microstructures with various shapes and sizes on a glass chip were prepared by a simple and rapid ultraviolet (UV) irradiation method using a metal mask. Photocurable PEG solution prepared by mixing 95 wt.% polyethylene glycol diacrylate and 5 wt.% 2-hydroxy-2-methylpropiophenone as a photo-initiator was injected to the gap between bottom and upper glasses in a simply assembled glass chip. After a metal mask with line-and-space or complex patterns was placed on the glass chip, UV light from a spot UV irradiation device was exposed to the glass chip through the metal mask for 7 seconds at UV intensity of 26 mW/cm2. Then the PEG hydrogel micropatterns on the glass chip were obtained after removing unreacted PEG solution by air blowing. To prepare more rigid microstructure, the prepared PEG micropatterned chip was exposed under UV light for 20 seconds. Then the PEG hydrogel micropattern chip was fabricated by a simple and rapid procedure. Micropattern transferring was performed from the PEG hydrogel chip to polydimethyl siloxane (PDMS) replica by a solution casting. The prepared micropatterned PDMS replicas showed similar shape and size of microstructures compared to that of the corresponded PEG hydrogel chip. Thus the PEG hydrogel microstructures on a glass chip could be used as a mold to fabricate micropattern PDMS chips for nanobio-chip applications. Furthermore, the present method provides large scale chip fabrication, more than 4 cm-length and 4 cm-width in a single step, not only PEG hydrogel chips but also PDMS chips.

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