In this study, a collagen hydrogel using collagen exclusively produced in Romania, was obtained by electron beam (e-beam) crosslinking. The purpose of our study is to obtain new experimental data on the crosslinking of collagen and to predict as faithfully as possible, its behavior at high irradiation doses and energies. To pursue this, the correlations between macromolecular structure and properties of collagen hydrogels were determined by rheological analysis, Fourier Transform Infrared Spectroscopy (FTIR), Scanning Electron Microscopy (SEM), and Differential Scanning Calorimetry (DSC), respectively. The gel fraction, swelling degree, and network parameters of the collagen hydrogels were also investigated at different irradiation doses. Through experimental exploration, we concluded that irradiation with e-beam up to 25 kGy induces crosslinking processes in collagen structure without producing advanced degradation processes. E-beam technology is a great method to develop new materials for medical applications without adding other chemical reagents harmful to human health. The future aim is to develop new wound dressings for rapid healing based on collagen, through irradiation technologies.

In the present study, we report on the complex hydrogels formulations based on collagen-poly(vinyl pyrrolidone) (PVP)-poly(ethylene oxide) (PEO) cross-linked by e-beam irradiation in an aqueous polymeric solution, aiming to investigate the influence of different PEO concentrations on the hydrogel properties. The hydrogel networks’ structure and their composition were investigated using equilibrium swelling degree, complex rheological analysis, and FT-IR spectroscopy. Rheological analysis was performed to determine the elastic (G′) and viscous (G″) moduli, the average molecular weight between cross-linking points (Mc), cross-link density (V_e), and the mesh size (ξ). The effect of the PEO concentration on the properties of the hydrogel was investigated as well. Depending on the PEO concentration added in their composition, the hydrogels swelling degree depends on the absorbed dose, being lower at low PEO concentrations. All hydrogel formulations showed higher G′ values (9.8 kPa) compared to G″ values (0.2 kPa), which shows that the hydrogels have a predominantly elastic behavior. They presented stability greater than 72 h in physiological pH buffers and reached equilibrium after 25 h. The Mc parameter is strongly dependent on the PEO concentration and the absorbed dose for all hydrogel compositions. The cross-linking density increased with the absorbed dose.

In this study, several superabsorbent hybrid hydrogel compositions prepared from xanthan gum (XG)/sodium carboxymethylcellulose (CMC)/graphene oxide (GO) were synthesized by e-beam radiation crosslinking. We studied and evaluated the effects of GO content from the chemical structure of the hydrogels according to: sol-gel analysis, swelling degree, diffusion of water, ATR-FTIR spectroscopy, network structure, and dynamic mechanical analysis. The gel fraction and swelling properties of the prepared hydrogels depended on the polymer compositions and the absorbed dose. The hybrid XGCMCGO hydrogels showed superabsorbent capacity and reached equilibrium in less than 6 h. In particular, the XGCMCGO (70:30) hydrogel reached the highest swelling degree of about 6000%, at an irradiation dose of 15 kGy. The magnitude of the elastic (G′) and viscous (G″) moduli were strongly dependent on the absorbed dose. When the degree of crosslinking was higher, the G′ parameter was found to exceed 1000 Pa. In the case of the XGCMCGO (80:20) hydrogel compositions, the Mc and ξ parameters decreased with the absorbed dose, while crosslinking density increased, which demonstrated that we obtained a superabsorbent hydrogel with a permanent structure.

The most widely occurring collagen in the extracellular matrix of the mammalian tissues – type I collagen has attracted huge interest from both theoretical and practical points of view. The results presented herein are mainly confined to a study of the thermal stability of type I collagen (CI) extracted from calfskin in acidic solutions (10⁻² M HCl). A two-step process associated with the heat-induced denaturation of CI was revealed by using ultra sensitive differential scanning calorimetry. The minor endothermic transition (peak temperatures of about 30.5–30.8 °C) has been assigned to the defibrillation of small supramolecular CI assemblies (occurring in solution) while the major endothermic transition (about 34.8–35.0 °C) has been ascribed to denaturation of CI, consisting of a complete unfolding of the native triple-helical conformation of the collagen molecule. The calorimetric data were supported by information obtained from capillary viscometry performed on the same solutions. The native state of CI (molecular integrity and triple-helical conformation) for all the systems studied in this paper was confirmed by transmission electron microscopy, ultraviolet circular dichroism and capillary viscometry. At the same time, based on the sodium dodecyl sulphate-polyacrylamide gel electrophoresis and an appropriate image processing of the corresponding electropherogram, a certain degree of intramolecular crosslinking of CI was detected, mainly between α1 and α2 chains of the collagen triple-helix. Such a feature seems to be caused by both the nature of the extraction procedure and the storage conditions.

Hydrogels containing both carboxyl and hydroxyl functional groups have been prepared by γ-irradiation of either aqueous solutions of acrylic acid (AA) and mixtures of AA and 2-hydroxyethyl methacrylate (HEMA) in different ratios, or aqueous solutions of poly(AA), PAA, and poly(AA-co-HEMA) obtained via solution polymerization. A higher absorbed dose is required in order to prepare hydrogels from monomer solutions, compared with those from polymer solutions. The range for the absorbed doses was chosen so that the probability of crosslinking reactions is higher than that of degradation ones. As the radiation energy deposited in a sample increases, the equilibrium swelling degree and the average molar mass between crosslinks diminishes. Chemical transformations induced by radiation were investigated by means of FTIR spectroscopy and thermal analysis of polymers before and after irradiation. For all these systems, the formation of a three-dimensional network enhances the glass transition temperature and thermal stability, but a further increase in the crosslinking degree may have the reverse effect on the glass transition temperature. Depending on the preparation protocol and/or hydrogel composition, superabsorbent materials that can bind different compounds throughout side functional groups may be obtained.

A new class of thermotropic lanthanidomesogens has been designed and prepared. They are based on 4-pyridone ligands that possess mesogenic cyanobiphenyl groups attached to the 4-pyridone unit via a flexible long alkyl spacer and show a very high thermal stability (decomposition temperatures near 300 °C). Depending on the alkyl length spacer, these complexes exhibit a SmA phase with transition temperatures influenced by the number of mesogenic groups employed and the spacer length.