Hydroxy-tyrosol as a Free Radical Scavenging Molecule in Polymeric Hydrogels Subjected to Gamma-Ray Irradiation

Abstract

Biomedical engineering is employing hydrogels with increasingly exciting possibilities for the treatment and regeneration of pathologically altered, degenerated, or traumatized tissues. Still, the sterilization processes may undesirably change the chemical and physical properties of hydrogels through cross-linking reactions. This work aims to characterize a new method of producing polyethylene oxide (PEO) hydrogels exploiting hydroxy-tyrosol (HT), an anti-oxidant molecule derived from olive leaf and olive oil, as a free radical scavenger to either prevent or limit gamma-ray-induced cross-linking. For this purpose, we produced hydrogels with PEO with two different buffer solutions (phosphate and citrate), varying HT concentration. We analyzed hydrogel preparations before and after gamma-ray irradiation, assessing the viscosity through rheological analysis and the chemical changes through IR analysis. We performed high-performance liquid chromatography (HPLC) analysis to measure residual HT in hydrogels after irradiation. The obtained results show that radiation-induced cross-linking and increase in viscosity of PEO hydrogels can be prevented by tailoring the concentration of HT as a free radical scavenging agent. Irradiation only consumes small amounts of HT; its presence in polymeric hydrogels can significantly impact biomedical applications by its anti-oxidant and anti-microbial activities.

1. Introduction

Hydrogels are three-dimensional polymeric networks with the ability to hold water within a porous structure. Thanks to their biocompatibility and mechanical properties, hydrogels are ideal scaffolds for tissue engineering, regenerative medicine, and drug delivery applications [1,2]. With this significant relevance in the biomedical field, sterilization of hydrogels is a conditio sine qua non to avoid any pathogen contamination risk and to fulfill medical device production requirements. However, sterilization may alter the structure and the characteristics of hydrogels inducing changes in the chemical and physical properties. Specifically, irradiation can cause cross-linking and polymerization reactions in conventional hydrogels, i.e., polyvinyl acetate (PVA), polyvinyl pyrrolidone (PVP), and polyethylene oxide (PEO) based synthetic formulations. As a consequence, these hydrogels undergo undesirable effects such as embrittlement, solidification, plasticization, or viscosity increase [3].

Compounds with anti-oxidant and free radical scavenging properties have been explored to limit cross-linking phenomena. Vitamin C can prevent irradiation-induced cross-linking of PVA solutions and decrease the viscosity of irradiated hydrogels, thus enhancing the stability and injectability of PVA-based medical formulations [4]. Vitamin E reduces cross-linking efficiency in ultrahigh molecular weight polyethylene during irradiation with the possibility of controlling the cross-link density distribution by tailoring the Vitamin E concentration profile [5].

Hydroxy-tyrosol (HT) is a phenylethanoid derived from olive leaf and olive oil with an extreme anti-oxidant efficiency, higher than Vitamin C [6]. Its high anti-oxidant activity is due to its free radical scavenging activity, attributed to the presence of the o-dihydroxyphenyl moiety which can release protons and promotes structural conjugation with radical species (Scheme 1) [7,8]. Notably, HT can inhibit low-density lipoprotein peroxidation chain reaction, which is a critical step in the development of atherosclerosis [9]. Moreover, HT shows biological impact against cancer development, osteoporosis, inflammation, bacteria proliferation, and virus infection [10,11].

On the basis of these considerations, we hypothesized that HT could be a molecule of interest in preventing or limiting irradiation-induced cross-linking of hydrogels. This work aims to characterize the rheological and chemical properties after gamma-ray irradiation of both citrate and phosphate buffer PEO-based hydrogel with tailored concentration of HT.

2. Materials and Methods

2.1. Hydrogels Preparation

For the production of hydrogels, PEO 600 kDa, 4% w/w (182028, Sigma-Aldrich, St. Louis, MO, USA) was mixed with either Phosphate Buffer Solution or Citrate Buffer Solution. Phosphate Buffer Solution was bought ready to use (PBS; pH 6.00 1X; TL1102, HiMedia, Mumbai, India) and 1 L of 10 mM of Citrate Buffer Solution has been prepared by mixing 0.86 g of Citric Acid (PM = 210.14 g/mol, C0759 Sigma-Aldrich, St. Louis, MO, USA), 1.74 g of Sodium Citrate Dihydrate (PM = 294.12 g/mol, W302600 Sigma-Aldrich, St. Louis, MO, USA) and 997.4 g of bi-distilled water with a high degree of purity (ELGA system). Samples of 100 g of both buffer-based hydrogels were prepared with HT concentrations equal to 0 mM (0 g HT), 1 mM (0.0154 g HT), 2 mM (0.0308 g HT), 5 mM (0.0771 g HT), 10 mM (0.1542 g HT), 50 mM (0.7708 g HT), and 100 mM (1.5416 g HT). Since PEO has been kept constant (4% w/w), the grams of Phosphate Buffer Solution or Citrate Buffer Solution to be added in each different solution were calculated accordingly. Mixture of components was prepared with a magnetic stirrer (Joan-SH-2, BIPEE, Shenzen, China) for 0 mM HT hydrogels and with a mechanical stirrer (AM20-D, ArgoLab, Carpi, Italy) for all other hydrogel preparations. Solvation occurred for at least 24 h.

2.2. Gamma-Ray Irradiation

The irradiation of HT-based hydrogels was carried out by Gammatom S.r.l. (Guanzate, Italy), at 25 kGy of intensity. Samples were placed in 50 mL Falcon tubes.

2.3. Rheological Analysis

In order to measure the viscosity and to study the rheological properties of the prepared hydrogels, the rheometer RM 200 PLUS (Lamy Rheology, Champagne au Mont d’Or, France) was used. 25 mL of sample was put into tubes with the corresponding coaxial cylinder measuring systems suitable for the control of homogeneous products, with liquid aspect and with or without particles. RheoTex software PN N311000 (Lamy Rheology, Champagne au Mont d’Or, France) was used for measurements, choosing the “Viscosity” program with the following set-up: pre-shearing time of 10 s with a shear rate of 10 s⁻¹, then the analysis was conducted with a shear rate fixed at 50 s^–1 for 60 s; within this time, 100 points have been recorded.

2.4. IR Chemical Analysis

In order to perform the chemical analysis of the hydrogels, one drop of each sample was put on aluminum plates at 55 °C for 24 h to avoid IR water interference. The FT-IR analysis was performed with the FT-IR spectrometer Spectrum Two (Perkin Elmer, Waltham, MA, USA) equipped with an ATR module, using the dedicated Spectrum 10 Software Suite (Perkin Elmer, Waltham, MA, USA). To analyze chemical changes, an assessment of the areas of peaks of interest has been carried out to obtain a direct measurement of the area under the peaks corresponding to the molar extinction coefficient.

2.5. HT Extraction and HPLC Quantification

Hydrogels were sonicated (DK-80, DK Sonic, Shenzen, China) for 30 min in extraction solvent 70:30 (v/v) ethanol:water to extract HT. Sonicated solution was filtered (0.22 μm) before liquid chromatography. The HPLC analysis was performed using Flexar LC (Perkin Elmer, Waltham, MA, USA) equipped with a binary pump and a DAD detector. Chromatographic conditions were: isocratic 70% (0.1% acetic acid) 30% (acetonitrile); temperature: 21 °C (±1 °C); flux and runtime: 1.6 mL/min for 10.0 min; absorbance: wavelength of 280 nm with an analytical bandwidth of 5 nm; injection Volume: 1.0 μL; column: HC-C18 Agilent 5 μm, 4.6 × 150 mm.

2.6. Statistical Analysis

When applicable, samples were compared with untreated samples (either with HT 0 mM or before irradiation) in the corresponding buffer and differences were tested with Student’s t-tests.

3. Results

3.1. Effects of Hydroxytyrosol on Rheological Properties of PEO Hydrogels

Rheological analysis was performed before and after gamma-ray irradiation on all formulations of citrate and phosphate buffer-based PEO 4% hydrogels, with increasing concentration of HT. HT addition decreases the viscosity of both phosphate and citrate buffer PEO 4% hydrogels in a concentration-dependent manner (Figure 1a). After gamma-ray irradiation, hydrogel viscosity highly increases; irradiated formulations with less than 10 mM HT concentration could not be analyzed with the rheometer because of their extreme density. Increasing doses of HT reduces the irradiation-induced viscosity with greater dose-dependent effects on citrate buffer-based hydrogels in comparison to phosphate buffer samples (Figure 1b).

3.2. Effects of Citrate and Phosphate Buffer Solutions on the Chemical Structure of Irradiated PEO Hydrogels

IR spectra were analyzed to observe chemical changes of hydrogels after gamma-ray irradiation. Bi-distilled water PEO 4% hydrogel was used as a control sample to compare the different chemical formulations of phosphate and citrate buffers. Bi-distilled and citrate buffer samples have similar IR spectra before and after irradiation with no evidence of new chemical bond formation. Only an overall reduction in molar extinction coefficients is observable in irradiated samples, indicating a decrease in the vibrational capacity of the chemical bonds (Figure 2a,b). Interestingly, analysis of the fingerprint region of the IR spectrum of the phosphate buffer PEO 4% hydrogel sample reveals new chemical bond formation showing new peaks at 1260 cm⁻¹, 802 cm⁻¹, and 660 cm⁻¹ (Figure 2c).

3.3. Hydroxytyrosol Protects PEO Hydrogels from Gamma Ray Irradiation-Induced Polymerization

The chemical formulations of citrate buffer PEO 4% hydrogels were analyzed before and after irradiation when increasing HT concentration. Addition of HT increases the vibrational capacity of chemical bonds in both non-irradiated and irradiated samples, although there is a general decrease in the molar extinction coefficients above 20 mM of HT concentration. Irradiation decreases areas of each peaks at 1241 cm^–1 (C-O-C stretching), 1098 cm^–1 (C-O stretching) and 841 cm^–1 (C-O-C stretching) in all hydrogel preparations, as an evidence of stiffening of the polymer structure (Figure 3a). The fold change in the area of the peaks of interest between non-irradiated and irradiated samples decreases with HT concentration higher than 10 mM (Figure 3b).

3.4. Hydroxytyrosol Protects PEO Hydrogels from Gamma Ray Irradiation-Induced Cross-Linking

The chemical formulations of phosphate buffer PEO 4% hydrogels were analyzed before and after irradiation when increasing HT concentration. In the phosphate buffer-based hydrogels, the addition of HT prevents the irradiation-induced formation of new chemical bonds (1260 cm⁻¹, 802 cm^–1, and 660 cm⁻¹) in a dose-dependent manner; above 10 mM of HT there is no evidence of new chemical bond formation (Figure 4a).

3.5. Quantification of Residual Hydroxytyrosol in PEO Hydrogels after Sterilization by Gamma Irradiation

HPLC quantification of residual HT in irradiated hydrogels was performed to test the consumption of HT after gamma-ray-induced oxidation. Averagely, HT concentrations are highly preserved in irradiated citrate buffer hydrogels in comparison with the not-irradiated samples, showing only little consumption of the molecule. On the other hand, HT concentrations are almost halved after irradiation in phosphate buffer hydrogel formulations (

Table 1. High-performance liquid chromatography (HPLC) quantification of residual HT in phosphate and citrated buffer PEO 4% hydrogels after gamma-ray irradiation.

HT Starting Concentration	Citrate Buffer-Based Polyethylen Oxide (PEO) Hydrogel		Phosphate Buffer-Based PEO Hydrogel
	(HT) Before Irradiation	(HT) After Irradiation	(HT) Before Irradiation	[HT] After Irradiation
1 mM	0.999	/	0.849	/
2 mM	1.823	/	1.734	/
5 mM	4.835	4.301	4.785	/
10 mM	9.867	9.411	8.913	5.761
20 mM	19.852	19.432	17.881	11.327
50 mM	49.926	48.966	42.859	28.059
100 mM	99.918	98.998	91.875	56.107

), probably due to the HT consumption exerting its anti-oxidative activity.

4. Discussion

We found that the addition of HT in PEO hydrogels can prevent cross-linking phenomena and the increase of viscosity caused by gamma-ray irradiation. Gamma-rays induce the creation of radical species interacting with water (H•, OH•), buffer components (ROO•), and polymers. We hypothesized that free radicals could break the polymer chains, thus enhancing their reactivity and either triggering interchain polymerization (Figure 5a), intrachain cross-linking (Figure 5b), or cross-linking with phosphate (Figure 5c). The proposed underlying mechanism is likely to be the following: in hydrogels, HT exerts anti-oxidant activity by scavenging free radicals through proton release and structural conjugation [7,8]. The free radical scavenging activity, which is possible for the highly reactive structure of o-quinone derived from HT (Scheme 1), limits or even prevents polymerization and cross-linking phenomena.

This protective effect is concentration-dependent; moreover, it maintains the rheological properties of hydrogels even after sterilization, being suitable for the production of medical devices. Indeed, hydrogels have different clinical applications that rely on their mechanical properties [1,2]; thus, these structural characteristics should not be altered in order to preserve the benefits of biocompatibility, scaffolding, or injectability.

The cross-linking phenomenon causes embrittlement and stiffness in hydrogels which consequently lose their mechanical properties. This was observed in IR analysis of phosphate buffer-based PEO hydrogels where irradiation of the polymer structure generates free radicals that rearrange C-O-C chemical bonds (1260 cm⁻¹) between the polymeric chains. Moreover, new phosphate bonds formation was observed at 802 cm⁻¹ and 660 cm⁻¹, corresponding to the C-O-P stretching and scissoring [12]. The chemical structure of HT can stop the chain propagation reactions by scavenging the free radicals [7,8,13]. Even if HT can prevent cross-linking reactions, these chemical changes suggest that other buffer solutions rather than phosphate buffer may be preferred for the production of medical-grade hydrogels to avoid any biological unpredictable interaction. Indeed, citrate buffer-based hydrogels are more stable according to the results obtained. One reason could be that citrate buffer stabilizes pH condition for HT molecules without altering hydrogel mechanical properties, as confirmed by rheological analysis. In IR analysis of citrate buffer-based hydrogels, only an overall decrease in the molar extinction coefficients is observed, suggesting a polymerization reaction between chains. HT can prevent polymerization by exerting its free radical scavenger activity, as shown by HT concentration higher than 10 mM. However, HT addition also decreases the viscosity and influences the vibrational capacity of the chemical bonds in non-irradiated samples, probably because HT surfactant properties may help the polymer hydration, therefore its solubilization [14]. Because of this activity, protection from polymerization reactions is not fully measurable in this experimental setting. However, rheological analysis shows that the presence of HT in citrate buffer-based hydrogels dramatically lowers the irradiation-induced increase in viscosity in a dose-dependent manner.

Other molecules, such as Vitamin C [4] or Vitamin E [5] have been explored as anti-oxidant agents in hydrogels preparation, but even if HT is a superior anti-oxidant and radical scavenger than Vitamin C [6], few data exist on this topic. HT is a remarkable molecule showing a broad spectrum of biological properties, e.g., anti-cancer, anti-microbial, anti-inflammatory, and anti-viral activities [7,10,13], which can be exploited in tissue engineering and medical application strategies. Our HPLC analysis shows that more than 50% of HT concentration is preserved after preventing cross-linking reactions in irradiated phosphate buffer-based PEO hydrogels, and HT is almost totally preserved in citrate buffer-based PEO hydrogels. The anti-microbial properties of HT are helpful against microbial agents typical of periodontal diseases [15] or infected chronic skin wounds [16], thus making the molecule an ideal ingredient for the preparation of medical-grade hydrogels.

A limitation of this first study is the impossibility of testing the viscosity of all hydrogel formulations within this experimental setting. The adopted rheometer cannot test semi-solid hydrogels obtained after irradiation in the absence of or with minimal amount of HT. Future characterization will involve the use of texture analyzer, i.e., relaxation tests with penetrating probes to provide information on the consistency, viscosity, and elasticity of all hydrogel formulations [17]. Moreover, future analyses can include irradiation-induced effects on swelling and gelation rate of hydrogels.

In conclusions, our findings suggest a novel exploitation of HT free radical scavenging activity to prevent irradiation-induced cross-linking reactions, thus helping the production of medical-grade polymeric hydrogels with optimized viscosity and injectability.