Swelling Ratio Of Hydrogels Research Articles

Effect of freeze-thawing conditions for preparation of chitosan-poly (vinyl alcohol) hydrogels and drug release studies

The freezing-thawing is an advantageous method to produce hydrogels without crosslinking agents. In this study chitosan-poly(vinyl alcohol) (CS-PVA) hydrogels were prepared by varying the freezing conditions and composition, which affect the final characteristics of the products. The swelling degree, morphology, porosity, and diflunisal drug loading, as well as the drug release profiles were evaluated. The hydrogel swelling ratio was found to be mainly affected by the CS content, the number of freezing cycles and the temperature. SEM micrographs and porosity data confirm that pore size increases with the chitosan content. However, the use of either lower temperatures or longer freezing times, results in higher porosity and smaller pores. The drug release times of the CS-PVA hydrogels were as long as 30 h, and according to the mathematical fitting, a simple diffusion mechanism dominates the process. Moreover, a mathematical model predicting the hydrogels physical and structural behavior is proposed.

Water based PHEMA hydrogels for controlled drug delivery

Abstract Objective In the scope of presented work, synthesis of water based acrylate hydrogels, characterization, and their usage in controlled drug release systems were aimed to investigate. Methods Synthesis of acrylate based hydrogels that have different properties was carried out by free radical photopolymerization using photoinitiator. Because of its high biocompatibility, 2-hydroxyethyl metacrylate (HEMA) was used as monomer. Then drug release experiments were performed in pH 7.4 and 1.2 buffer solutions with certain ionic strength while the dynamic swelling behaviors were also determined. In the last part of the work, drug activities of synthesized drug-loaded hydrogels were tested in mediums containing Staphylococcus aureus and Pseudomonas aeruginosa bacteria cultures. Results ATR-FTIR spectrums of all synthesized hydrogels were analyzed. The characteristic O-H, C-H, C=O, C-O tension vibrations bands were observed in the spectrums of the hydrogels. The rate of drug release in acidic pH 1.2 for two types of hydrogels was observed to be much faster than at pH 7.4. It was determined that hydrogel swelling ratio decrease with increasing monomer ratio. All drug loaded hydrogels were effective to inhibit the growth of both two bacterial strains. Conclusion Hydrogels synthesized were found to be suitable for the controlled drug delivery applications.

Model development and numerical simulation of magnetic-sensitive hydrogels subject to an externally applied magnetic field

Magentic-sensitive hydrogel is a novel smart composite that undergoes a large deformation, when subjected to an externally applied magnetic field. In this paper, a multi-effect-coupling magnetic-stimulus (MECm) model is developed for numerical simulation of the responsive behavior of the magnetic-sensitive hydrogel that is immersed in solvent surrounding, with the effects of magneto-chemo-mechanical coupled fields. The developed model covers both the hydrogel and the solvent domains, where the present governing equations consist of the conservations of mass for solvent diffusion, the conservation of moment for hydrogel deformation, and the Maxwell’s equations for the magnetic field distribution. By examination with the published experimental data in open literature, it is confirmed that the model can simulate well the performance of the magnetic hydrogel quantitatively. The parameter studies are then carried out for the influences of the magnetic intensity and shear modulus on the response of the magnetic hydrogel, for a deeper insight into the responsive mechanism of the magnetic hydrogel. It reveals that the externally applied magnetic field contributes to the elongation of the hydrogel along the field direction and contraction in the transverse direction, while it has insignificant on the hydrogel swelling ratio. Furthermore, it is also found that the increasing shear modulus leads to a decreasing hydrogel swelling ratio.

Gellan gum/clay hydrogels for tissue engineering application: Mechanical, thermal behavior, cell viability, and antibacterial properties

In this study, sodium montmorillonite (Na-MMT) was successfully modified by using n-hexadecyl trimethyl ammonium bromide (CTAB) via cationic exchange to obtain an organophilic-montmorillonite (CTAB-MMT). The Na-MMT, CTAB-MMT, and a commercial montmorillonite, that is, Cloisite15A were incorporated into gellan gum (GG) hydrogel and their mechanical, physical, thermal properties, biocompatibility, and antibacterial activities were investigated. The mechanical performance results show that the GG hydrogels containing Cloisite15A required smallest volume to achieve optimum compression stress, modulus, and compression strain at 5% (w/w) compared to both Na-MMT and CTAB-MMT at 10% (w/w). Swelling ratio of GG hydrogels increased upon addition of MMT, and water vapor transmission rate (WVTR) values of all hydrogels were in the range of 1106–1890 g m−2 d−1, which were comparable to WVTR values of commercial wound dressings. Thermal behavior shows that the inclusion of Cloisite15A in GG hydrogel improved the thermal stability than its counterparts. Cell studies exhibit that the GG incorporated with Na-MMT is non-cytotoxic to human skin fibroblast cells (CRL2522), and in contrast, the GG hydrogels incorporated CTAB-MMT and Cloisite15A revealed that the cells were dying and the cell growth depleted after being cultured for 72 h. Qualitative antibacterial study revealed that GG hydrogel containing CTAB-MMT only in the sample exhibits inhibition against the Gram-positive bacteria, that is, Staphylococcus aureus and Bacillus cereus, while there was no inhibition exhibited against Gram-negative bacteria ( Escherichia coli and Klebsiella pneumoniae).

Stimuli-Responsive Matrix-Assisted Colorimetric Water Indicator of Polydiacetylene Nanofibers.

An alternative signal transduction mechanism of polydiacetylene (PDA) sensors is devised by combining stimuli-responsive polymer hydrogel as a matrix and PDA sensory materials as a signal-generating component. We hypothesized that volumetric expansion of the polymer hydrogel matrix by means of external stimuli can impose stress on the imbedded PDA materials, generating a sensory signal. PDA assembly as a sensory component was ionically linked with the alginate hydrogel in order to transfer the volumetric expansion force of alginate hydrogel efficiently to the sensory PDA molecules. Under the same swelling ratio of alginate hydrogel, alginate gel having embedded 1-dimensional thin PDA nanofibers (∼20 nm diameter) presented a sharp color change while 0-dimensional PDA liposome did not give any sensory signal when it was integrated in alginate gel. The results implied that dimensionality is an important design factor to realize stimuli-responsive matrix-driven colorimetric PDA sensory systems; more effective contact points between 1-dimensional PDA nanofibers and the alginate matrix much more effectively transfer the external stress exerted by the volumetric expansion force, and thin PDA nanofibers respond more sensitively to the stress.

Effect of the hydrogel carrier structure on the Activity of immobilized trypsin

The dependence of the activity of trypsin immobilized in polyacrylamide hydrogel on the hydrogel swelling ratio, the size distribution of its pores, and the means of enzyme binding has been studied. It has been shown that the most favorable conditions for immobilized trypsin are provided upon its binding to hydrogel via trypsin macromonomer copolymerization with acrylamide and a linking agent in the presence of a modifier that limits polymer chain growth.

Dynamics in Stimuli-Responsive Poly(N-isopropylacrylamide) Hydrogel Layers As Revealed by Fluorescence Correlation Spectroscopy

We employ fluorescence correlation spectroscopy (FCS) to study the translational mobility of molecular tracers in stimuli-responsive grafted poly(N-isopropylacrylamide) (PNiPAAm) hydrogels, under variable solvency conditions. Tracer–matrix interactions were tuned by selecting three different molecular tracers. In contrast to a noninteracting tracer (Alexa 647), the mobility of a weakly (Alexa 488) and a strongly interacting (Rhodamine 6G) tracer deviates from a simple single Fickian diffusion. In addition to pure crowding effects, the mobility of both Alexa488 and Rhodamine 6G is influenced by tracer–polymer interactions. We interpret the observed trends in tracer mobility in terms of the interplay between Coulombic repulsions and short-range attractions. Although tracer dynamics and hydrogel swelling ratio are interdependent properties, their relation turns out to be nontrivial and does not allow predictions of tracer dynamics on the basis of polymer structural information. Hence, a universal scaling behavior is not possible, due to tracer–polymer interactions.

Synthesis, characterization, and properties of a kind of novel artificial cartilage

Objective To prepare a kind of novel artificial cartilage and study its cell biocopatibility.Methods Polyhydroxyethyl methacrylate (PHEMA),0.5％ silica and 1％-5％ hydroxyapatite were mixed to prepare the composites.The composites were characterized by Fourier transform infrared spectroscopy (FTIR),scanning electron microscopy (SEM),swelling ratio (SR) measurement and the absorption of bovine serum albumin (BSA).Results Inorganic particles were n nanoscopic diameter and uniformly dispersed on side of the matrices.The swelling ratio of hydrogels was 45％-50％.The absorption of BSA on the surface of composite membrane was about 5％,indicating the good biocompatibility.Conclusion A biocompatible organic/inorganic complex artificial cartilage was prepared. Key words: Polyhydroxyethyl methacrylate ; Hydroxyapatite ; Silica; Artificial cartilage

Culture of preantral follicles in poly(ethylene) glycol‐based, three‐dimensional hydrogel: a relationship between swelling ratio and follicular developments

This study was undertaken to examine how the softness of poly(ethylene) glycol (PEG)-based hydrogels, creating a three-dimensional (3D) microenvironment, influences the in vitro growth of mouse ovarian follicles. Early secondary, preantral follicles of 2 week-old mice were cultured in a crosslinked four-arm PEG hydrogel. The hydrogel swelling ratio, which relates to softness, was modified within the range 25.7–15.5 by increasing the reactive PEG concentration in the precursor solution from 5% to 15% w/v, but it did not influence follicular growth to form the pseudoantrum (60–80%; p = 0.76). Significant (p < 0.04) model effects, however, were detected in the maturation and developmental competence of the follicle-derived oocytes. A swelling ratio of > 21.4 yielded better oocyte maturation than other levels, while the highest competence to develop pronuclear and blastocyst formation was detected at 20.6. In conclusion, gel softness, as reflected in swelling ratio, was one of the essential factors for supporting folliculogenesis in vivo within a hydrogel-based, 3D microenvironment. © 2014 The Authors. Journal of Tissue Engineering and Regenerative Medicine published by John Wiley & Sons, Ltd.

Extracellular delivery of modified oligonucleotide and superparamagnetic iron oxide nanoparticles from a degradable hydrogel triggered by tumor acidosis

Chemically modified antisense RNA oligonucleotides (antagomir) offer promise for cancer therapies but suffer from poor therapeutic effect after systemic administration. Chemical modification or loading in degradable hydrogels can offer improvements in the accuracy and efficacy for sustained delivery at specific sites. In our approach, antagomir were entrapped with degradable poly(ethylene glycol) (PEG)-based hydrogels, with and without incorporation of imidazole. Superparamagnetic iron oxide nanoparticles (SPION) were simultaneously loaded with intent for magnetic resonance imaging (MRI). The incorporation of imidazole into the PEG hydrogels led to a tunable-pH-response that dictated hydrogel swelling ratio and release rate of antagomir and SPION. As a result, the PEG–imidazole hydrogel swelling ratio and degradation over a 5 week period changed up to 734% and 149% as the pH dropped from 7.4 to 6.7, respectively. The swelling ratio of PEG–imidazole hydrogels was completely reversible over repeatable cycles of pH change. The stimuli-responsive behavior of PEG–imidazole hydrogels was used for the release of antagomir and SPION under conditions consistent with tumor acidosis. This manuscript demonstrates feasibility in designing tunable-pH-responsive hydrogels for loading multimodality therapeutic and contrast agents to enhance the bioactivity of chemically modified antisense RNA oligonucleotide and SPION for acidosis-related tumor therapy and MRI imaging applications.

Synthesis and drug-release properties of biodegradable hydrogels having β-cyclodextrin

A new β-cyclodextrin (β-CD) methacrylated monomer was synthesized from the reaction of β-CD, glycidyl methacrylate. Based on inclusion character of β-CD, a series of hydrogels were prepared by irradiating the mixtures of β-CD methacrylate monomer (β-CD-Met), poly(ethylene glycol) monoacrylate, poly(ethylene glycol)diacrylate, fumaric acid monoethyl ester-functionalized poly(lactic-co-glycolic) acid, 1-vinyl-2-pyrrolidone, N,N′-methylene bisacrylamide, and the photoinitiator. Gel percentages and equilibrium swelling ratios (%) of hydrogels were investigated. It was observed that equilibrium-swelling ratio increased with increasing β-CD-Met content in the hydrogel composition. SEM images demonstrated that β-CD-Met-based hydrogel have lots of voids on the fractured surface. In this study, ibuprofen (IBU) which is capable of forming inclusion complex with β-CD was chosen. For the hydrogel with maximum CD content, the IBU drug loading was found as 9 mg/g dry gel. It can be concluded that the inclusion complex-formation capability of β-CD moiety increases the drug release by improving the aqueous solubility of hydrophilic drugs.

Preparation of Biocompatible Graphene Oxide Composite Hydrogel to Deliver Ophthalmic Drugs

Considering that conventional hydrogels showed limited capabilities of controlling hydrophobic drug loading and releasing and graphene materials had interactions with hydrophobic drugs, we designed a graphene oxide (GO) composite hydrogel for drug delivery. But GO could not disperse well in monomer solution and agglomerated badly. Thus, water-soluble GO (GO-tripolymer) was first prepared under the stabilization of amphiphilic polymer, Pluronic F-127. The GO-tripolymer showed good solubility in PBS with the increase of polymer concentration. All GO-tripolymer solutions had the same UV absorption peaks as GO. Then, GO composite hydrogels (HNG hydrogels) were formed by the polymerization of hydroxyethyl methacrylate (HEMA), N-Vinyl pyrrolidone (NVP) and GO-tripolymer mixture. The introduction of GO-tripolymer had little effect on the gelation time and equilibrium swelling ratio of hydrogel. The freeze-drying hydrogel showed porous structure. The pore size decreased and the rough surface was detected with the increase of GO concentration. HNG hydrogel could load more puerarin and norfloxacin than conventional hydrogel (HN hydrogel). Moreover, HNG hydrogel could control puerarin and norfloxacin release more steadily than HN hydrogel. HNG exhibited low cytotoxicity.

Synthesis of High Strength and Well-Defined PEG-Based Hydrogel Networks via Click Chemistry

Click Chemistry was used to synthesize a series of PEG-based hydrogel networks. Attributable to the controlled nature and the quantitative yields of Click Chemistry, the prepared PEG-based hydrogels have the well-defined structures, which resulted in the improved mechanical properties and the high swelling ratios of hydrogels

Nanofibrillated cellulose composite hydrogel for the replacement of the nucleus pulposus

The swelling and compressive mechanical behavior as well as the morphology and biocompatibility of composite hydrogels based on Tween® 20 trimethacrylate (T3), N-vinyl-2-pyrrolidone (NVP) and nanofibrillated cellulose (NFC) were assessed in the present study. The chemical structure of T3 was verified by Fourier transform infrared spectroscopy and proton nuclear magnetic resonance, and the degree of substitution was found to be around 3. Swelling ratios of neat hydrogels composed of different concentrations of T3 and NVP were found to range from 1.5 to 5.7 with decreasing concentration of T3. Various concentrations of cellulose nanofibrils (0.2–1.6 wt.%) were then used to produce composite hydrogels that showed lower swelling ratios than neat ones for a given T3 concentration. Neat and composite hydrogels exhibited a typical nonlinear response under compression. All composite hydrogels showed an increase in elastic modulus compared to neat hydrogel of about 3- to 8-fold, reaching 18 kPa at 0% strain and 62 kPa at 20% strain for the hydrogel with the highest NFC content. All hydrogels presented a porous and homogeneous structure, with interconnected pore cells of around 100 nm in diameter. The hydrogels are biocompatible. The results of this study demonstrate that composite hydrogels reinforced with NFC may be viable as nucleus pulposus implants due to their adequate swelling ratio, which may restore the annulus fibrosus loading, and their increased mechanical properties, which could possibly restore the height of the intervertebral discs.

Logic swelling response of DNA–polymer hybrid hydrogel

An oligonucleotide–polymer hybrid hydrogel displaying swelling response in a logical AND and OR fashion depending on specific stimuli by probe oligonucleotides was prepared. The hydrogel acts as a transducer of the specific recognition of DNA sequences into micro- and macroscale mechanics. Input oligonucleotide probes induce hydrogel swelling ratio at two signal levels.

Hydrogel protection: a novel approach to reduce bowel inflammation in experimental gastroschisis

Objective In gastroschisis there is herniation of the fetal bowel into the amniotic cavity that results in severe intestinal dysfunction. In order to reduce bowel exposure to amniotic fluid we used a hydrogel of N-isopropylacrylamide copolymerized with acrylic acid (P(NIPAAm-co-AAc)) to coat the herniated bowel through the use of a fibrin adhesive (Beriplast ®). Study design Gastroschisis was created in fetuses of 31 pregnant Sprague–Dawley rats by evisceration of the bowel through a right paramedian incision in the abdominal wall on day 18.5 of pregnancy. The fetuses were separated in four groups of 12 fetuses: control (C), gastroschisis (G), gastroschisis + fibrin adhesive (GA) and gastroschisis + fibrin adhesive + dry hydrogel (GAH). Animals were harvested at day 21.5 of pregnancy and the hydrogel was removed. Fetuses and bowels were weighed and morphometric analysis was performed. Isoelectric focusing of the amniotic fluid determined its electrical charge. We evaluated the hydrogel swelling ratio ( Q) in the amniotic fluid. Histological analysis and scanning electronic microscopy (SEM) of the bowel and hydrogel were performed. Our primary outcome was bowel intactness after hydrogel removal and our secondary outcome was the effectiveness of the hydrogel in protecting the bowel against amniotic fluid and its components. Differences among the groups were tested by the ANOVA and Tukey–Kramer post-test method and the statistical significance accepted was for p values <0.05. Results The mass of swollen hydrogel was 34 times the mass of dry hydrogel. Isoelectric focusing of the amniotic fluid showed that most of its proteins are negatively charged as the hydrogel. SEM showed that removal of the hydrogel did not damage bowel serosa. Bowel weight, diameter and wall thickness were similar between groups C and GAH but bowel diameter and wall thickness was significantly reduced in C and GAH compared to G and GA ( p < 0.001). Conclusion The P(NIPAAm-co-AAc) hydrogel does not harm the bowel and provides a safe effective protection with reduction of bowel damage in gastroschisis.

Synthesis and characterization of pH‐ and salt‐responsive hydrogels based on etherificated sodium alginate

AbstractHydrogels composed of etherificated sodium alginate (ESA), sodium acrylic acid (NaAA), and poly (vinyl alcohol) (PVA) were synthesized by aqueous solution polymerization. The effects of reaction variables such as terminal pH, ions, and ionic strength on hydrogel swelling ratio (SR) were determined and compared. SR was influenced strongly by pH and ionic strength. SR increased with increasing pH but tended to decrease with PVA content. At a given ionic strength, SR of ESA/NaAA/PVA hydrogel was dependent on the valence of anion; SR was higher in multivalent anion salt solution than in monovalent anion salt solution, i.e., SRK2SO4 &gt; SRKCl and SRNa2SO4 &gt; SRNaCl. The swelling kinetic of the hydrogels showed Fickian kinetic diffusion in acidic media and non‐Fickian behavior in alkaline media. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2010

Factorial analyses of photopolymerizable thermoresponsive composite hydrogels for protein delivery

A smart protein delivery system for wound healing applications was developed using composite nanoparticle hydrogels that can release protein in a temperature-responsive manner. This system can also be formed in situ in the presence of ultraviolet light and Irgacure 2959 photoinitiator. The system consists of temperature-sensitive poly( N-isopropylacrylamide-co-acrylamide) (PNIPAM-AAm) nanoparticles embedded in a poly(ethylene glycol) diacrylate (PEGDA) matrix. A factorial analysis was performed to evaluate the effects of PEGDA concentration (10% and 15% w/v) and PEGDA molecular weight (MW; 3.4 kDa and 8 kDa), as well as PNIPAM-AAm nanoparticle concentration (2% and 4% w/v) and temperature (23°C and 40°C) on the protein release profiles and swelling ratios of the hydrogels. Results indicate that PNIPAM-AAm nanoparticle concentration and temperature were the most important factors affecting the protein release during the burst release phase. Additionally, PEGDA MW was the most important factor affecting the protein release in the plateau region. It was also important in controlling the hydrogel swelling ratio. A dual-layered hydrogel was further developed to produce a protein delivery system with a better sustained release. These findings have improved our understanding of the composite hydrogel systems and will help in tailoring future systems with desired release profiles. From the Clinical Editor A smart protein delivery system for wound healing applications using composite nanoparticle hydrogels that can release protein in a temperature-responsive manner is reported in this paper. Systems like this may aid in optimal would healing in the surgical and trauma-related settings.

The fabrication of elastin-based hydrogels using high pressure CO 2

The aim of this study was to investigate the effect of high pressure CO 2 on the crosslinking of elastin-based polymers and the characteristics of the fabricated hydrogels. A hydrogel was fabricated by chemically crosslinking α-elastin with glutaraldehyde at high pressure CO 2. The effects of pressure, reaction time, and crosslinker concentration on the characteristics of the fabricated hydrogels were determined. The reaction time had negligible effect on either the swelling ratio or the pore size of the fabricated hydrogels. Increasing the processing pressure from 30 bar to 150 bar resulted in a 60% increase in the hydrogel swelling ratio. The crosslinked hydrogels displayed stimuli-responsive characteristics towards temperature and salt concentration. The dense gas process facilitated coacervation, expedited the crosslinking reaction, and dramatically affected the micro- and macrostructures of pores within the sample. The results of micro-CT scan and SEM images demonstrated that pore interconnectivity was substantially enhanced for α-elastin hydrogels fabricated using high pressure CO 2. Dense gas CO 2 reduced the wall thickness and size of the pores and importantly induced channels within the structure of the α-elastin hydrogels. In vitro cell culture studies demonstrated that the channels facilitated fibroblast penetration and proliferation within α-elastin structures.

Characterization of Poly(Vinyl Alcohol) and Poly(Vinyl Pyrrolidone) Co-polymer Blend Hydrogel Prepared by Application of Gamma Radiation

Hydrogel is prepared from a poly(vinyl pyrrolidone) (PVP) and poly(vinyl alcohol) (PVA) blend solution by gamma radiation with a 60Co λ source at room temperature. Properties of the prepared hydrogel, such as gel fraction, gel strength swelling ratio, equilibrium water content, and water absorption in room temperature, were investigated. Blending hydrogel with PVP and PVA obviously increased the gel strength and decreased the swelling ratio of hydrogel. It was observed that the gel fraction increased while the swelling ratio and water content decreased with increased radiation dose, but gel strength increased up to a certain radiation dose and then decreased. The percentage of water absorption at room temperature increased with time but after a certain time it became steady and decreased with radiation dose.