Influence of glycidylmethacrylate functional groups attached to gelatin on the formation and properties of hydrogels

2015 ◽  
Vol 1718 ◽  
pp. 103-108 ◽  
Author(s):  
Candy Löwenberg ◽  
Konstanze K. Julich-Gruner ◽  
Axel T. Neffe ◽  
Andreas Lendlein
Keyword(s):  
Mechanical Properties ◽  
Glycidyl Methacrylate ◽  
Triple Helix ◽  
Polymer Concentration ◽  
Polymer Networks ◽  
Side Chain ◽  
Metathesis Reaction ◽  
Gelatin Films ◽  
Order Of Magnitude ◽  
Chain Organization

ABSTRACTGelatin functionalized with glycidyl methacrylate (GMA) has been shown to allow crosslinking by photopolymerization and metathesis reaction. However, side chain functionalization of gelatin might reduce triple helicalization, which influences mechanical properties of gelatin-based polymer networks. Here, the influence of glycidylmethycrylation of gelatin on the chain organization, swelling, and mechanical properties is investigated by comparing among each other physical gels prepared from GMA-gelatin solutions of different concentrations (5-20 wt.-%) by drying and rehydration. An increase of GMA-gelatin concentration from 5 wt.-% to 20 wt.-% led to an increased density of produced gelatin films and a decreasing water uptake of the films from 1160 wt.-% to 730 wt.-%, while the storage modulus was increasing about one order of magnitude from 440 Pa to 4090 Pa. The relative single and triple helix content was not influenced by the variation of polymer concentration.

Role of pH on stability and mechanical properties of gelatin films

2012 ◽  
Vol 27 (1) ◽  
pp. 67-77 ◽  
Author(s):  
Michela Gioffrè ◽  
Paola Torricelli ◽  
Silvia Panzavolta ◽  
Katia Rubini ◽  
Adriana Bigi
Keyword(s):  
Mechanical Properties ◽  
Young’S Modulus ◽  
Triple Helix ◽  
Young's Modulus ◽  
In Vitro Tests ◽  
Diffraction Reflection ◽  
X Ray Diffraction ◽  
Solution Ph ◽  
Gelatin Films

The effect of the film-forming solution pH on the triple-helix content, thermal stability, and mechanical properties of gelatin films was investigated. The films were prepared from solutions at different pHs of type A pigskin gelatin, and their mechanical characteristics were determined. At pHs higher than 9 and lower than 5, Young’s modulus, E, and the stress at break, σb, of the films decreased significantly. Cross-linking with genipin reduced deformation at break, ϵb, and increased Young’s modulus. The intensity of the 1.1-nm X-ray diffraction reflection and the denaturation enthalpy decreased at these pHs, indicating that the triple helix reduced. Preliminary in vitro tests on the cross-linked samples indicated good cell proliferation and viability.

Comparison of the Potency of 8-L-Arginine, 8-D-Arginine and 8-D-Homoarginine Vasopressin Analogs with Substituted Phenylalanine in Position 2

1994 ◽  
Vol 59 (6) ◽  
pp. 1439-1450 ◽  
Author(s):  
Miroslava Žertová ◽  
Jiřina Slaninová ◽  
Zdenko Procházka
Keyword(s):  
Amino Acid ◽  
Solid Phase Synthesis ◽  
Solid Phase ◽  
Basic Amino Acid ◽  
The Other ◽  
Side Chain ◽  
Inhibitory Potency ◽  
Phase Synthesis ◽  
Other Hand ◽  
Order Of Magnitude

An analysis of the uterotonic potencies of all analogs having substituted L- or D-tyrosine or -phenylalanine in position 2 and L-arginine, D-arginine or D-homoarginine in position 8 was made. The series of analogs already published was completed by the solid phase synthesis of ten new analogs having L- or D-Phe, L- or D-Phe(2-Et), L- or D-Phe(2,4,6-triMe) or D-Tyr(Me) in position 2 and either L- or D-arginine in position 8. All newly synthesized analogs were found to be uterotonic inhibitors. Deamination increases both the agonistic and antagonistic potency. In the case of phenylalanine analogs the change of configuration from L to D in position 2 enhances the uterotonic inhibition for more than 1 order of magnitude. The L to D change in position 8 enhances the inhibitory potency negligibly. Prolongation of the side chain of the D-basic amino acid in position 8 seems to decrease slightly the inhibitory potency if there is L-substituted amino acid in position 2. On the other hand there is a tendency to the increase of the inhibitory potency if there is D-substituted amino acid in position 2.

scholarly journals Protein Hydrogels: The Swiss Army Knife for Enhanced Mechanical and Bioactive Properties of Biomaterials

Nanomaterials ◽  
2021 ◽  
Vol 11 (7) ◽  
pp. 1656
Author(s):  
Carla Huerta-López ◽  
Jorge Alegre-Cebollada
Keyword(s):  
Mechanical Properties ◽  
Tissue Engineering ◽  
Polymer Networks ◽  
Biological Tissues ◽  
Modern Medicine ◽  
Body Parts ◽  
Biomedical Sciences ◽  
Protein Hydrogels ◽  
Large Water ◽  
Design Options

Biomaterials are dynamic tools with many applications: from the primitive use of bone and wood in the replacement of lost limbs and body parts, to the refined involvement of smart and responsive biomaterials in modern medicine and biomedical sciences. Hydrogels constitute a subtype of biomaterials built from water-swollen polymer networks. Their large water content and soft mechanical properties are highly similar to most biological tissues, making them ideal for tissue engineering and biomedical applications. The mechanical properties of hydrogels and their modulation have attracted a lot of attention from the field of mechanobiology. Protein-based hydrogels are becoming increasingly attractive due to their endless design options and array of functionalities, as well as their responsiveness to stimuli. Furthermore, just like the extracellular matrix, they are inherently viscoelastic in part due to mechanical unfolding/refolding transitions of folded protein domains. This review summarizes different natural and engineered protein hydrogels focusing on different strategies followed to modulate their mechanical properties. Applications of mechanically tunable protein-based hydrogels in drug delivery, tissue engineering and mechanobiology are discussed.

scholarly journals Internal constraints and arrested relaxation in main-chain nematic elastomers

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Takuya Ohzono ◽  
Kaoru Katoh ◽  
Hiroyuki Minamikawa ◽  
Mohand O. Saed ◽  
Eugene M. Terentjev
Keyword(s):  
Mechanical Properties ◽  
Main Chain ◽  
Polymer Networks ◽  
Nematic Order ◽  
Nematic Elastomers ◽  
Nematic Director ◽  
Highly Nonlinear ◽  
Nonlinear Mechanical ◽  
Liquid Crystal Elastomers ◽  
Memory Applications

AbstractNematic liquid crystal elastomers (N-LCE) exhibit intriguing mechanical properties, such as reversible actuation and soft elasticity, which manifests as a wide plateau of low nearly-constant stress upon stretching. N-LCE also have a characteristically slow stress relaxation, which sometimes prevents their shape recovery. To understand how the inherent nematic order retards and arrests the equilibration, here we examine hysteretic stress-strain characteristics in a series of specifically designed main-chain N-LCE, investigating both macroscopic mechanical properties and the microscopic nematic director distribution under applied strains. The hysteretic features are attributed to the dynamics of thermodynamically unfavoured hairpins, the sharp folds on anisotropic polymer strands, the creation and transition of which are restricted by the nematic order. These findings provide a new avenue for tuning the hysteretic nature of N-LCE at both macro- and microscopic levels via different designs of polymer networks, toward materials with highly nonlinear mechanical properties and shape-memory applications.

scholarly journals Decoupling of Mechanical and Transport Properties in Organogels via Solvent Variation

Gels ◽  
2021 ◽  
Vol 7 (2) ◽  
pp. 61
Author(s):  
Kenneth P. Mineart ◽  
Cameron Hong ◽  
Lucas A. Rankin
Keyword(s):  
Mechanical Properties ◽  
Mechanical Behavior ◽  
Transdermal Drug Delivery ◽  
Triblock Copolymer ◽  
Polymer Concentration ◽  
Mineral Oil ◽  
Solute Diffusion ◽  
Oil Viscosity ◽  
Chain Entanglement ◽  
Mineral Oils

Organogels have recently been considered as materials for transdermal drug delivery media, wherein their transport and mechanical properties are among the most important considerations. Transport through organogels has only recently been investigated and findings highlight an inextricable link between gels’ transport and mechanical properties based upon the formulated polymer concentration. Here, organogels composed of styrenic triblock copolymer and different aliphatic mineral oils, each with a unique dynamic viscosity, are characterized in terms of their quasi-static uniaxial mechanical behavior and the internal diffusion of two unique solute penetrants. Mechanical testing results indicate that variation of mineral oil viscosity does not affect gel mechanical behavior. This likely stems from negligible changes in the interactions between mineral oils and the block copolymer, which leads to consistent crosslinked network structure and chain entanglement (at a fixed polymer concentration). Conversely, results from diffusion experiments highlight that two penetrants—oleic acid (OA) and aggregated aerosol-OT (AOT)—diffuse through gels at a rate inversely proportional to mineral oil viscosity. The inverse dependence is theoretically supported by the hydrodynamic model of solute diffusion through gels. Collectively, our results show that organogel solvent variation can be used as a design parameter to tailor solute transport through gels while maintaining fixed mechanical properties.

Reply to the ‘Comment on “Relating side chain organization of PNIPAm with its conformation in aqueous methanol”’ by N. van der Vegt and F. Rodriguez-Ropero, Soft Matter, 2017, 13, DOI: 10.1039/C6SM02139E

Soft Matter ◽  
2017 ◽  
Vol 13 (12) ◽  
pp. 2292-2294 ◽  
Author(s):  
Debashish Mukherji ◽  
Manfred Wagner ◽  
Mark D. Watson ◽  
Svenja Winzen ◽  
Tiago E. de Oliveira ◽  
...  
Keyword(s):  
Soft Matter ◽  
Recent Article ◽  
Side Chain ◽  
Aqueous Methanol ◽  
Chain Organization

We provide a reply to comments by N. van der Vegt and F. Rodriguez-Ropero on our recent article in Soft Matter.

The Influence of the Addition of Ti on the Mechanical Properties of W-S-Ti Coatings

2006 ◽  
Vol 514-516 ◽  
pp. 687-691 ◽  
Author(s):  
Manuel Evaristo ◽  
Ana Nossa ◽  
Albano Cavaleiro
Keyword(s):  
Mechanical Properties ◽  
Friction Coefficient ◽  
Tribological Performance ◽  
The Self ◽  
Wear Coefficient ◽  
Gradual Loss ◽  
Order Of Magnitude ◽  
Amorphous Structures ◽  
Ti Content ◽  
Ti Films

In this work, W-S-Ti films were deposited by r.f. magnetron sputtering, using simultaneously WS2 and Ti targets. The atomic percentage of Ti in the coating was varied from 0 at.% up to 28 at.%. No significant variations in the S/W ratio with the increase of Ti content were observed. The increasing Ti contents in the films led to a gradual loss of crystallinity. Coatings with contents greater than ≈ 16 at.% only presents a broad peak characteristic of amorphous structures. Alloying the films with Ti led to significant improvements in the hardness (from 0.3 to 8.9 GPa). Also, the adhesive critical load continuously grew with the increase of the Ti content in the films. The wear coefficient of the films dropped more than one order of magnitude with the increase of Ti content whereas the friction coefficient was kept fairly constant with just a small increase in relation to single W-S film. In conclusion, to have a good tribological performance, the addition of Ti to the films should be balanced in order that the increase of the mechanical properties does not lead to severe loss of the self-lubricant properties.

Thermal and mechanical properties of simultaneous and sequential full-interpenetrating polymer networks

2004 ◽  
Vol 370 (1-2) ◽  
pp. 288-292 ◽  
Author(s):  
A Bartolotta ◽  
G Di Marco ◽  
M Lanza ◽  
G Carini ◽  
G D’Angelo ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
Polymer Networks ◽  
Interpenetrating Polymer Networks ◽  
Thermal And Mechanical Properties

Studies on Nanostructured Polyurethane/Clay Interpenetrating Polymer Networks

2005 ◽  
Vol 475-479 ◽  
pp. 1001-1004
Author(s):  
Ninglin Zhou ◽  
Xiao Xian Xia ◽  
Li Li ◽  
Shao Hua Wei ◽  
Jian Shen
Keyword(s):  
Mechanical Properties ◽  
Polymer Networks ◽  
Testing Machine ◽  
Physical And Mechanical Properties ◽  
Interpenetrating Polymer Networks ◽  
Absorption Properties ◽  
Tensile Testing Machine ◽  
Swelling Agent ◽  
Silicate Layers ◽  
Polyurethane Matrix

A novel exfoliated polyurethane (PU)/clay Interpenetrating Polymer Networks (IPNs) nanocomposite has been synthesized with polyurethane and organoclay. MTPAC is used as swelling agent to treat Na-montmorillonite for forming organoclay. The results indicate that there is very good compatibility between organoclay and PU. Nanoscale silicate dispersion was analyzed by XRD. The mechanical properties of the nanocomposites have been measured by tensile testing machine. The nanocomposites show obviously improved physical and mechanical properties when compared with the pure polymer. Additionally, PU /MTPAC- clay shows lower water absorption properties than pure PU do. In addition, the reinforcing and intercalating mechanism of silicate layers in polyurethane matrix are discussed.

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