Composites of inherently conductive polypyrrole (PPy) within highly hydrophilic poly(2‐hydroxyethyl methacrylate)‐based hydrogels (p(HEMA)) have been fabricated and their electrochemical properties investigated. The electrochemical characteristics observed by cyclic voltammetry suggest less facile reduction of PPy within the composite hydrogel compared to electropolymerized PPy, as shown by the shift in the reduction peak potential from ?472 mV for electropolymerized polypyrrole to ?636 mV for the electroconductive composite gel. The network impedance magnitude for the electroconductive hydrogel remains quite low, ca. 100 Ω, even upon approach to DC, over all frequencies and at all offset potentials suggesting retained electronic (bipolaronic) conductivity within the composite. In contrast, sustained application of +0.7 V (vs. Ag/AgCl, 3 M Cl?) for typically 100 min. (conditioning) to reduce the background amperometric current to <1.0 μA, resulted in complete loss of electroactivity. Nyquist plots suggest that sustained application of such a modest potential to the composite hydrogel results in impedance characteristics that resembles p(HEMA) without evidence of the conducting polymer component. PPy composite gels supported a larger ferrocene monocarboxylate diffusivity (Dappt=7.97×10?5 cm2 s?1) compared to electropolymerized PPy (Dappt=5.56×10?5 cm2 s?1), however a marked reduction in diffusivity (Dappt=1.01×10?5 cm2 s?1) was observed with the conditioned hydrogel composite. Cyclic voltammograms in buffer containing H2O2 showed an absence of redox peaks for electrodes coated with PPy‐containing membranes, suggesting possible chemical oxidation of polypyrrole by the oxidant 相似文献
The development of electro-stimulated drug release devices is an innovative approach to attain the drug delivery in accurate doses at target sites in a programmed manner. In this work, novel electroactive nanocomposite hydrogels were prepared by encapsulating green-synthesized polypyrrole (PPy) colloids within chondroitin sulfate (CS) networks during the self-crosslinking of CS via N-ethyl-N′-(3-dimethylaminopropyl) carbodiimide chemistry. The structural and morphological properties of CS/PPy hydrogels were studied by Fourier-transformed infrared spectroscopy, scanning electron microscopy, and swelling kinetic measurements. The chemotherapeutic agent 5-fluorouracil (5-FU) was loaded into CS/PPy samples by hydrogel swelling method, or alternatively, by pre-incubating the drug in polymer mixture before crosslinking. Different electrical stimulations can be used to switch ON and accurately tune the 5-FU delivery from GG/PPy hydrogels. A single pulse potential of 5 V switched on the drug delivery up to 90% from nanocomposite hydrogel, in contrast to the low 5-FU amount released in a passive form (< 20%). PPy electroactive behavior played a determining role as the main driving force in 5-FU release activation. Cytotoxicity of hydrogels with and without 5-FU was examined in normal and cancer cells. Considering the high cytotoxicity of 5-FU, the ON/OFF 5-FU release patterns evidenced the potential of CS/PPy hydrogels for electrically controlled drug delivery in implantable or transdermal drug release devices. 相似文献
Nanostructured conductive polymers can offer analogous environments for extracellular matrix and induce cellular responses by electric stimulation, however, such materials often lack mechanical strength and tend to collapse under small stresses. We prepared electrically conductive nanoporous materials by coating nanoporous cellulose gels (NCG) with polypyrrole (PPy) nanoparticles, which were synthesized in situ from pyrrole monomers supplied as vapor. The resulting NCG/PPy composite hydrogels were converted to aerogels by drying with supercritical CO2, giving a density of 0.41–0.53 g cm?3, nitrogen adsorption surface areas of 264–303 m2 g?1, and high mechanical strength. The NCG/PPy composite hydrogels exhibited an electrical conductivity of up to 0.08 S cm?1. In vitro studies showed that the incorporation of PPy into an NCG enhances the adhesion and proliferation of PC12 cells. Electrical stimulation demonstrated that PC12 cells attached and extended longer neurites when cultured on NCG/PPy composite gels with DBSA dopant. These materials are promising candidates for applications in nerve regeneration, carbon capture, catalyst supports, and many others. 相似文献
Multifunctional graphene hydrogels have attracted great attention aimed at practical applications. Herein, the novel and bifunctional composite hydrogel containing reduced graphene‐oxide nanosheets (RGO) and V2O5 nanobelts (RGO/V2O5) is successfully prepared for the first time. Surprisingly, tridimensional (3D) RGO/V2O5 composite hydrogels cannot only be used as high‐performance electromagnetic (EM) wave absorbents; they also exhibit excellent properties suitable for supercapacitor electrodes. The composites exhibit a maximum absorption of up to ?21.5 dB. In particular, a composite hydrogel showed a bandwidth of 6.63 GHz, corresponding to a reflection loss at ?10 dB, which opens the possibility for the use of 3D graphene with other functional nanomaterials as lightweight and high‐performance EM wave absorption materials. Remarkably, the composite hydrogel is capable of delivering a high specific capacitance of about 320 F g?1 at a current density of 1.0 A g?1. 相似文献
The size of silver nanoparticles (AgNPs) is the key factor that governs their antibacterial activity. However, the size of AgNPs is difficult to control because agglomeration and uneven dispersion often occur during the processing of AgNP-based products, which has impeded their applications in different areas. In this work, an efficient strategy was developed to overcome this difficulty and to prepare an antibacterial hydrogel comprising AgNPs and chitosan (CS) with dialdehyde xylan (DAX) as the crosslinking agent. The size of AgNPs was controlled successfully to an extremely fine level (<?9 nm) by reducing AgNO3 solution in a methanolic suspension of the metal organic framework (MOF) -UiO-66-NH2, and forming an Ag@UiO-66-NH2 core–shell structure which avoided the agglomeration of AgNPs. DAX played a dual role by forming a hydrogel structure with CS through crosslinking, but also by stabilizing the even dispersion of Ag@UiO-66-NH2 in the hydrogel. Accordingly, the as-prepared hydrogels showed excellent antibacterial properties and low cytotoxicity. The survival ratio of NIH/3T3 cells cultured in the hydrogel extract was more than 90%, even when the concentration of the hydrogel extract was as high as 10 mg/mL. In addition, the hydrogel exhibited good abilities of water absorption (swelling ratio was up to 1100%) and self-healing (efficiency was up to 88% after 5 h). The hydrogels with size-well-controlled AgNPs prepared in this work are expected to find broad applications, especially in the area of antibacterial medical auxiliaries.
Superabsorbent hydrogels based on the natural polymer chitosan and acrylic acid (CS/AAc) was prepared using 60Co gamma radiation as a source of initiation and crosslinking. The factors, which affect the preparation of CS/AAc hydrogels such as irradiation dose, CS/AAc ratios, and acrylic acid monomer concentrations, to get the best optimum conditions, were investigated. The kinetic studies of the swelling of CS/AAc hydrogel showed that it follows a Fickian type of water diffusion. The Fickian constant value ‘n’ was more than 0.5 with a high swelling capacity of 300 g/g as superabsorbent hydrogel. In addition, the suitability of CS/AAc hydrogel as carrier material for the drug Chlortetracycline-HCl has been investigated by adsorption isotherm studies. The performance of drug release from hydrogel systems, influenced by acrylic acid ratio and the effect of pH of the medium was studied. 相似文献
The effects of pH of the buffer solution and the composition of the hydrogel system on the bovine serum albumin (BSA) adsorption capacity of chitosan (CS)–polyvinyl pyrrolidone (PVP) (CSPVP) hydrogels and release of BSA were investigated. Poly-electrolyte CSPVP hydrogels with different compositions were prepared by irradiating CS/PVP/water mixtures with γ-rays at ambient temperature. The adsorption capacity of hydrogels was found to increase from 0 to 350 mg BSA/g dry gel, by changing external stimuli and hydrogel composition. The adsorption of BSA within CSPVP hydrogels increased with increase in CS content in the hydrogels. When the irradiation doses of hydrogel increased, the adsorption of BSA decreased. The maximum adsorption of BSA was observed at pH 5. A significant amount of the adsorbed BSA (up to 95%) was eluted in the phosphate medium containing 0.1 M NaCl at pH 7.4. 相似文献
The ability to create artificial thick tissues is a major tissue engineering problem,requiring the formation of a suitable vascular supply.In this work we examined the ability of inducing angiogenesis in a bioactive hydrogel.GYIGSRG(NH 2-Gly-Tyr-IleGly-Ser-Arg-Gly-COOH,GG) has been conjugated to sodium alginate(ALG) to synthesize a biological active biomaterial ALG-GG.The product was characterized by 1 H NMR,FT-IR and elemental analysis.A series of CaCO 3 /ALG-GG composite hydrogels were prepared by crosslinking ALG-GG with D-glucono-lactone/calcium carbonate(GDL/CaCO 3) in different molar ratios.The mechanical strength and swelling ratio of the composite hydrogels were studied.The results revealed that both of them can be regulated under different preparation conditions.Then,CaCO 3 /ALG-GG composite hydrogel was implanted in vivo to study the ability to induce angiogenesis.The results demonstrated that ALG-GG composited hydrogel can induce angiogenesis significantly compared with non-modified ALG group,and it may be valuable in the development of thick tissue engineering scaffold. 相似文献
A composite hydrogel based on, by introducing, polyvinyl alcohol, sodium alginate, and hyaluronic acid was fabricated using CaCl2 as a cross-linker. The physical properties including morphology, water vapor transmission rate, and hydrophilicity were investigated. All PVA/SA/HA composite hydrogels with different compositions had highly homogeneous and interconnected pores, and the morphologies of the PVA/SA/HA hydrogels ranged from fibrous structure to irregular structure with increasing content of SA. The introduction of sodium alginate enhanced the hydrophilicity and water vapor transmission capacity of the hydrogel; however, the hydrophilicity of the composite hydrogels decreased with the increasing cross-linker content. 相似文献
Electrically conductive biomaterials that can efficiently deliver electrical signals to cells or improve electrical communication among cells have received considerable attention for potential tissue engineering applications. Conductive hydrogels are desirable particularly for neural applications, as they can provide electrical signals and soft microenvironments that can mimic native nerve tissues. In this study, conductive and soft polypyrrole/alginate (PPy/Alg) hydrogels are developed by chemically polymerizing PPy within ionically cross‐linked alginate hydrogel networks. The synthesized hydrogels exhibit a Young's modulus of 20–200 kPa. Electrical conductance of the PPy/Alg hydrogels could be enhanced by more than one order of magnitude compared to that of pristine alginate hydrogels. In vitro studies with human bone marrow‐derived mesenchymal stem cells (hMSCs) reveal that cell adhesion and growth are promoted on the PPy/Alg hydrogels. Additionally, the PPy/Alg hydrogels support and greatly enhance the expression of neural differentiation markers (i.e., Tuj1 and MAP2) of hMSCs compared to tissue culture plate controls. Subcutaneous implantation of the hydrogels for eight weeks induces mild inflammatory reactions. These soft and conductive hydrogels will serve as a useful platform to study the effects of electrical and mechanical signals on stem cells and/or neural cells and to develop multifunctional neural tissue engineering scaffolds.
A series of granular pH-sensitive semi-interpenetrating polymer network (semi-IPN) hydrogels based on chitosan (CTS), acrylic acid (AA) and gelatine (GE) were utilized for the adsorption and recycle of Pb(II) from aqueous solutions. The composite hydrogels have been characterized by FT-IR and TGA. The effects of contact time, pH value and initial Pb(II) concentration on the adsorption were investigated. Results indicated that the adsorption capacity of the hydrogel increased with increasing pH value and initial Pb(II) concentration, and a pH-sensitive adsorption characteristic was presented. The adsorption rate of the semi-IPN hydrogels on Pb(II) is fast with an adsorption rate constant of 14.9790 mg/(g·s), and adsorption equilibrium could be reached within 10 min. The adsorption isotherms of the hydrogels for Pb(II) could be described well by the Langmuir equation, rather than the Freundlich equation. The as-prepared hydrogels showed good reusability with 0.05 mol/l HNO3 solutions as the desorbing agent and 0.1 mol/l NaOH solutions as the regeneration agent, respectively. After five consecutive adsorption-desorption processes, the semi-IPN hydrogel with 20 wt% GE may reach 85.26% of its initial adsorption capacity. In addition, the adsorbed Pb(II) can be quantitatively recovered by simply eluting the hydrogel with dilute HNO3 solution, and a recovery ratio of 89.27% was reached for the semi-IPN hydrogel. The satisfactory adsorption amount is mainly derived from the chelating of functional groups (i.e. –COO? and –NH2) with Pb(II) ions. The hydrogel adsorbents exhibited excellent affinity for Pb(II), and can be applied to treat wastewater containing heavy metal ion and simultaneously recover the valuable metal sources. 相似文献
Conducting polymer composites of polyvinylferrocene and polypyrrole (PVF/PPy) were synthesized chemically by the in situ polymerization of pyrrole in the presence of PVF using FeCl3 as oxidant. Acetic (CH3COOH) and boric (H3BO3) acids were used as the synthesis medium. Effects of the synthesis medium on the properties of the PVF/PPy composite were investigated. The PVF/PPy composites and homopolymers were characterized by fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS) and magnetic susceptibility techniques. Conductivity measurements were performed using the four‐probe technique. We found that the conductivities of PVF/PPy‐H3BO3 (1.19 S cm?1) and PVF/PPy‐CH3COOH (4.5×10?1 S cm?1) increased relative to those of the homopolymers of PPy‐H3BO3 (2.1×10?2 S cm?1) and PPy‐CH3COOH (1.2×10?2 S cm?1) due to the interaction of PVF with the pyrrole moiety. The stability of all homopolymers and composites were investigated by thermogravimetric analysis and by conductivity measurements during heating‐cooling cycles. There was a small drop in conductivity caused by the annealing of PVF/PPy composites at 70°C. The conductivity of all samples increased with temperature and exhibited stable electrical behavior with increasing temperature. TGA analysis of samples showed that the composites were more stable than the homopolymers or PVF separately. The magnetic susceptibility values of samples were negative, except for PVF/PPy‐H3BO3. Morphology changes of the composites investigated by scanning electron microscopy (SEM), attributed to synthesis conditions, have a significant effect on their conductivity. 相似文献
Bacterial infections and oxidative damage caused by various reactive oxygen species (ROS) pose a significant threat to human health. It is highly desirable to find an ideal biomaterial system with broad spectrum antibacterial and antioxidant capabilities. A new supramolecular antibacterial and antioxidant composite hydrogel made of chiral L-phenylalanine-derivative (LPFEG) as matrix and Mxene (Ti3C2Tx) as filler material is presented. The noncovalent interactions (H-bonding and π–π interactions) in between LPFEG and Mxene and the inversion of LPFEG chirality are verified by Fourier transform infrared and circular dichroism spectroscopy. The composite hydrogels show improved mechanical properties revealed by rheological analysis. The composite hydrogel system exhibits photothermal conversion efficiency (40.79%), which enables effective photothermal broad-spectrum antibacterial activities against both Gram-positive (Staphylococcus aureus) and Gram-negative (Escherichia coli, Pseudomonas aeruginosa) bacteria. Furthermore, the Mxene also enables the composite hydrogel to exhibit excellent antioxidant activity by efficiently scavenging free radicals like DPPH•, ABTS•+, and •OH. These results indicate that the Mxene-based chiral supramolecular composite hydrogel, with improved rheological, antibacterial, and antioxidant properties has a great potential for biomedical applications. 相似文献
Composite hydrogels—macroscopic hydrogels with embedded microgel particles—are expected to respond to external stimuli quickly because microgels swell much faster than bulky gels. In this work, the kinetics of the pH‐induced swelling of a composite hydrogel are studied using turbidity measurements. The embedded microgel is a pH‐ and thermosensitive poly(N‐isopropylacrylamide‐co‐acrylic acid) microgel and the hydrogel matrix is polyacrylamide. A rapid pH‐induced swelling of the embedded microgel particles is observed, confirming that composite hydrogels respond faster than ordinary hydrogels. However, compared with the free microgels, the swelling of the embedded microgel is much slower. Diffusion of OH? into the composite hydrogel film is identified as the main reason for the slow swelling of the embedded microgel particles, as the time of the pH‐induced swelling of this film is comparable to that of OH? diffusion into the film. The composition of the hydrogel matrix does not significantly change the characteristic swelling time of the composite hydrogel film. However, the swelling pattern of the film changes with composition of the hydrogel matrix. 相似文献