Radiation-induced crosslinking of collagen gelatin into a stable hydrogel

Gelatin, the low molecular weight collagen derivative from porcine skin was transformed into a stable permanent hydrogel by γ-radiation. A series of samples with 3% gelatin solution in water were irradiated at doses of 12, 25, 50, 100, 150, 200 kGy at room temperature in the absence of air with a dose rate of 2.2 kGy/h. At low dose gelatin hydrogels incorporating all the available water were obtained. At higher doses above 50 kGy, the gelatin hydrogel samples show a curious shrinking phenomenon due to the relatively high crosslinking density level achieved, so part of the available water is squeezed out from the gel cage. The gelatin hydrogel samples were studied by mass fractionation analysis, by spectrophotometric and polarimetric analysis. Further characterization was made by FT-IR spectroscopy and by thermal analysis (DSC, DTA and TGA) of the dried gelatin samples after irradiation in comparison to a reference untreated sample.     

Helix formation in the polymer brush

This work considers the physics of a brush formed by polymers capable of undergoing a helix-coil transition. A self-consistent field approximation for strongly stretched polymer chains is used in combination with a lattice model of the interaction energy in helix-coil mixtures. Crowding-induced chain stretching stabilizes helix formation at moderate tethering densities while high tethering density causes sufficiently strong stretching to unravel segments of the helix, resulting in distinct layers of monomer density and helical content. Compared to a random-coil brush at low-to-moderate tethering density, a helicogenic brush is less resistant to compression in the direction perpendicular to stretching due to easy alignment of helices and fewer unfavorable interactions between helical segments. At higher tethering density, the abovementioned stretch-induced decrease in helical content resists further compression. The proposed model is useful for understanding an emerging class of biomaterials that utilize helix-forming polymer brushes to induce shape changes or to stabilize biofunctional helical peptide sequences.     

Highly efficient alginate-based macromolecular photoinitiator for crosslinking and toughening gelatin hydrogels

Constructing gelatin hydrogels through photopolymerization is getting increasingly attractive due to their excellent biocompatibility and unparalleled flexibility in fabricating complex structures. In this study, an alginate-based macromolecular photoinitiator (Alg-2959) is synthesized by grafting Irgacure2959, a widely used hydrophilic small molecular photoinitiator, onto the framework of alginate. The characterization of Alg-2959 is carried out by ¹H nuclear magnetic resonance (¹HNMR), Fourier infrared spectroscopic (FTIR), Thermogravimetric analysis (TGA), and UV–Vis absorption spectrum. It is shown that Alg-2959 can induce the polymerization of acrylate monomer poly(ethylene glycol) diacrylate (PEGDA400) and glycidyl methacrylate modified gelatin (Gel-GM) with similar initiation efficiency as Irgacure2959. Compared with the pure hydrogels prepared using Irgacure2959, the hybrid hydrogels containing Alg-2959 can be further crosslinked by Ca²⁺ to form the double-network hydrogels, which exhibit enhanced toughness and elasticity. In addition, due to the introduction of alginate, the migration stability of Alg-2959 in the hydrogel networks is significantly improved compared with Irgacure2959. These results indicate the great potential of Alg-2959 in preparing biocompatible and resilient photopolymers.     

Some aspects of the crosslinking of gelatin by dextran dialdehydes

The present paper describes the formation of hydrogels by reaction of gelatins with periodate oxidized dextrans. The effect of a number of reaction parameters on the rate of gelation is investigated. It is demonstrated that the time to onset of gelation depends on the nature of the gelatin, the nature of the dextran dialdehyde, the type of buffer, the ionic strength and the presence of added salts. The gelation time decreases with increasing concentration of aldehydes, increasing pH and increasing molecular weight of the dextran dialdehyde. In general, the gelation occurs more rapidly with decreasing concentration of indifferent electrolytes, except for the reaction in phosphate buffer where an increase in gelation is observed with increasing buffer strength. Ammonium and calcium salts are found to retard significantly the crosslinking reaction.     

Overshoot and oscillation in surface tension of gelatin solutions

The experimental data of the surface tension of aqueous gelatin solution reported by Sato and Ueberreiter [H. Sato, K. Ueberreiter, Macromol. Chem. 180 (1979) 829; H. Sato, K. Ueberreiter, Macromol. Chem. 180 (1979) 1107; H. Sato, K. Ueberreiter, ACS Polym. Preprints 20 (1979) 907] were analyzed with a theory of adsorption kinetics with time delay. It is found that the observed overshoot and oscillation of the surface tension are well explained by the present theory. The delay time and the rate constants of adsorption and desorption of gelatin molecules onto the air/gelatin solution interface have been evaluated.     

Viscometric study of gelatin in dilute aqueous solutions

The viscosities of aqueous solutions of gelatin at different temperatures were carefully measured in a common glass‐capillary Ubbelohde viscometer at dilute to extremely dilute concentrations. The adsorption effect that occurred in the viscosity measurements was theoretically analyzed and discussed. A theory based on Langmuir isotherms could adequately describe the existing data. Some structural information was obtained by the use of an iterative fitting procedure to treat the reduced viscosity data, which disclosed that individual gelatin chains underwent a coil‐to‐helix transition as the solution cooled from 40 to 15 °C. © 2006 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 44: 1804–1812, 2006     

Kinetics of bond formation in cross-linked gelatin gels

In chemical cross-linking of gelatin solutions, two different time scales affect the kinetics of the gel formation in the experiments. We complement the experimental study with Monte Carlo numerical simulations of a lattice model. This approach shows that the two characteristic time scales are related to the formation of single bond cross-linker-chain and of bridges between chains. In particular, their ratio turns out to control the kinetics of the gel formation. We discuss the effect of the concentration of chains. Finally our results suggest that by varying the probability of forming bridges as an independent parameter, one can finely tune the kinetics of the gelation via the ratio of the two characteristic times.     

Helix formation in a pentapeptide: experiment and force-field dependent dynamics

We used a combined approach of experiment and simulation to determine the helical population and folding pathway of a small helix forming blocked pentapeptide, Ac-(Ala)(5)-NH(2). Experimental structural characterization of this blocked peptide was carried out with far UV circular dichroism spectroscopy, FTIR, and NMR measurements. These measurements confirm the presence of the α-helical state in a buffer solution. Direct molecular dynamics and replica-exchange simulations of the pentapeptide were performed using several popular force fields with explicit solvent. The simulations yielded statistically reliable estimates of helix populations, melting curves, folding, and nucleation times. The distributions of conformer populations are used to measure folding cooperativity. Finally, a statistical analysis of the sample of helix-coil transition paths was performed. The details of the calculated helix populations, folding kinetics and pathways vary with the employed force field. Interestingly, the helix populations, folding, and unfolding times obtained from most of the studied force fields are in qualitative agreement with each other and with available experimental data, with the deviations corresponding to several kcal/mol in energy at 300 K. Most of the force fields also predict qualitatively similar transition paths, with unfolding initiated at the C-terminus. Accuracy of potential energy parameters, rather than conformational sampling may be the limiting factor in current molecular simulations.     

Network formation by chain crosslinking photopolymerization and some applications in electronics

Two applications of photopolymerization are described, viz. the replication of optical discs and the manufacturing of aspherical lenses, used for the read-out of these discs. The development of these and similar processes has required a thorough understanding of the formation of densely crosslinked networks. Results on the evolution of crosslink density with conversion, the delay of shrinkage with respect to conversion and the occurrence and modelling of inhomogeneous network formation are presented.     

Computer simulation of network formation via crosslinking copolymerization

The topology of networks formed by radical crosslinking copolymerization is strongly dependent on the type of crosslinker chosen. By a series of computer simulations, the influence of the relative reactivities of crosslinker and monomer on the network properties was investigated. Basic condition of the simulation is the postulation of a diffusion process control of the polymerization reaction. The resulting networks are analyzed with respect to cycle rank, loop formation, dangling ends, sol fraction and crosslinker molecules reacted only by one double bond. The results of the computer simulations indicate that the reactivity of the crosslinker decisively affects the properties of the network. Particularly the cycle rank, which determines the elastic properties of the network, is influenced strongly by the reactivity of the crosslinker. A change of the cycle rank of approximately one decade was observed. The influence of the reactivity was found to be most important in the region where the reactivity of the crosslinker is less than the reactivity of the monomer.     

Monodisperse gelatin microspheres as a drug delivery vehicle: release profile and effect of crosslinking density

Uniform gelatin microspheres (GMS) of a wet size of 100 microm in diameter were fabricated by the electric field assisted precision particle fabrication (E-PPF) method and crosslinked with different glutaraldehyde (GA) concentrations to study the effect of the crosslinking density on drug release. The drug release profiles of the crosslinked GMS were studied along with the intraparticle drug distribution and the particle degradation characteristics. Due to the concentration gradient of GA along the diffusion path into the GMS, the crosslinking density is higher on the GMS surface, making it less susceptible to degradation. As a result, the GMS with higher GA concentrations (0.375-0.875%) exhibited a highly resistant surface toward enzymatic degradation. On the other hand, the amount of drug complexation at the surface decreases as the GA concentration increases, which can be attributed to the lowered basicity of gelatin caused by the increased crosslinking density. These factors collectively affect the drug release kinetics and give rise to similar release profiles for GMS above a GA concentration of 0.375%.     

Spectrophotometric determination of formaldehyde,furfural, and vanillin in bisulfite solutions

Formaldehyde, furfural, and vanillin are determined in solutions containing bisulfite. The interference of bisulfite is eliminated by oxidation with iodine before furfural and vanillin are determined spectrophotometrically in ultraviolet light. Formaldehyde is determined with chromotropic acid by a slightly modified procedure; bisulfite is not destroyed previously.     

Free-energy landscape of alcohol driven coacervation transition in aqueous gelatin solutions

Liquid-liquid phase separation of a homogeneous polyampholyte (gelatin) solution into a dense polymer-rich coacervate and the dilute supernatant phase is discussed through free-energy landscape formalism. We have evaluated the free energy and entropy of the system as it undergoes the phenomenon of simple coacervation, driven by the addition of a nonsolvent. Electrophoretic mobility (mu) and turbidity measurements were performed on 0.01% and 0.05% (w/v) aqueous gelatin solutions that were driven towards coacervation by the addition of ethanol. The mobility of the polyampholyte molecules, which was typically mu approximately 0.38+/-0.02 microm/s cm/V in water, gradually reduced for the soluble intermolecular complexes to a plateau value of mu approximately 0.11+/-0.01 microm/s cm/V as the ethanol volume fraction equaled phi(ns) approximately 0.47+/-0.03, which coincided with the first appearance of coacervate droplets (coacervation transition) observed from turbidity measurements, a behavior found to be invariant of gelatin concentration. These results were used as input to the theoretical model to explicitly construct the free-energy landscape for a single gelatin chain and the global system comprising the polymer-rich coacervate and the dilute supernatant phase.     

Quasielastic light scattering study of chemically crosslinked gelatin solutions and gels

Quasielastic light scattering measurements are reported for experiments performed on mixtures of gelatin and glutaraldehyde (GA) in the aqueous phase, where the gelatin concentration was fixed at 5 (w/v) and the GA concentration was varied from 1×10⁻⁵ to 1×10⁻³ (w/v). The dynamic structure factor, S(q,t), was deduced from the measured intensity autocorrelation function, g ₂(τ), with appropriate allowance for heterodyning detection in the gel phase. The S(q,t) data could be fitted to S(q,t)=Aexp(−D _f q ² t)+Bexp(−t/τ_c)^β, both in the sol (50 and 60 ^∘C) and gel states (25 and 40 ^∘C). The fast-mode diffusion coefficient, D _f showed almost negligible dependence on the concentration of the crosslinker GA; however, the resultant mesh size, ξ, of the crosslinked network exhibited strong temperature dependence, ξ∼(0.5−χ)^1/5exp(−A/RT) implying shrinkage of the network as the gel phase was approached. The slow-mode relaxation was characterized by the stretched exponential factor exp(−t/τ_c)^β. β was found to be independent of GA concentration but strongly dependent on the temperature as β=β₀+β₁ T+β₂ T ². The slow-mode relaxation time, τ_c, exhibited a maximum GA concentration dependence in the gel phase and at a given temperature we found τ_c(c)=τ₀+τ₁ c+τ₂ c ². Our results agree with the predictions of the Zimm model in the gel case but differ significantly for the sol state. Received: 25 May 1999 /Accepted in revised form: 27 July 1999