Chitosan-laponite nanocomposite scaffolds for wound dressing application.

The pivotal issue of skin regeneration research is the development of effective biomaterials that exhibit biological activities as fungicide and bactericide, combining simple and low cost manufacturing technologies. In this context, nanocomposite scaffolds based on chitosan (Ch)/Laponite (Lap) were produced by using different concentrations of Lap via freeze-drying process for potential application in skin regeneration. The influence of Lap concentration on the scaffold properties was evaluated. The prepared scaffolds were characterized by x-ray diffraction (XRD), scanning electron microscopy (SEM), porosity, swelling capacity, and mechanical analyses. The results revealed that the scaffolds exhibited a porous architecture, besides the increase in the clay content, leads to an increase in the porosity, an improvement of mechanical strength, and a decrease of swelling capacity. In vitro tests were also carried out to evaluate the biocompatibility of the materials, such as bioadhesion, antibacterial activity, viability, and cell adhesion. Viability and cell adhesion demonstrated that all scaffolds were not cytotoxic and the fibroblast cells readily attached on the surface of the scaffolds. Thereby, the results suggested that the nanocomposite scaffolds are biomaterials potentially useful as wound dressings.

Photochemical synthesis of silver nanoparticles on chitosans/montmorillonite nanocomposite films and antibacterial activity.

Silver nanoparticles (AgNPs) were synthetized on chitosans/montmorillonite nanocomposite films by photochemical method. Nanocomposites were prepared using chitosans with different molar masses and deacetylation degrees, as well as modified with diethylaminoethyl (DEAE) and dodecyl groups. AgNPs formation on the films was followed by the appearance of the plasmon band around 440nm as a function of irradiation time. TEM images revealed AgNPs with spherical morphology for all nanocomposites. For nanocomposites using modified chitosans, the AgNPs synthesis occurred quickly (1.5h) while for the others films it was above 11h. The film of modified chitosan with dodecyl and DEAE groups presented smaller and more uniform nanoparticles size along mixture of exfoliated and intercalated structures. This modified chitosan is an amphiphilic compound that can act controlling the size/shape of the AgNPs. The results of antibacterial activity suggested that all nanocomposite-AgNPs films inhibited the growth of Escherichia coli and Bacillus subtilis.

Photophysical Behavior of Isocyanine/Clay Hybrids in the Solid State †.

In the present study, we have attempted to investigate, for the first time, the photophysical behavior of 1,1'-diethyl-2,4'-cyanine (ICY)/clay mineral hybrids in the solid state. The effects promoted by ICY loading and clay type on the spectroscopic properties were studied by UV-vis diffuse reflectance spectroscopy (DR) and different fluorescence techniques. The hybrids were characterized by X-ray diffraction (XRD) and thermogravimetric analysis (TGA). UV-vis-DR revealed the formation of ICY H-aggregates in Wyoming montmorillonite (SWy-1) and Laponite (Lap); however, J-aggregates were predominant for ICY on Arizona (SAz-1) and Barasym (SYn-1) montmorillonites. The formation of J-aggregates was favored on clays with a high layer charge density (SAz-1 and SYn-1). Increasing ICY loading leads to an increase in H-aggregates, which become predominant in all of the samples. The fluorescence spectra of ICY-Lap and ICY-SYn-1 hybrids showed two emissive bands, and they were assigned to the monomeric and J-aggregate species. The fluorescence lifetime showed consistent and distinct values for the two species. The longer fluorescence lifetime can be assigned to the ICY monomers, while the second component has a short lifetime value and may be attributed to J-aggregate emission species. Moreover, confocal fluorescence micrographs showed two different fluorescent domains; monomers (greenish domain) and J-aggregates (orange domain) can be clearly distinguished. For ICY adsorbed on SWy-1 and SAz-1, the intensities of the fluorescence spectra were very low, and it was not possible to measure the fluorescence lifetimes due to high iron content in these clays, which acts as an efficient quencher of the excited singlet state of the dye molecules. XRD and TGA curves showed that the intercalation of ICY into the interlayer regions of SWy-1, SAz-1, and SYn-1 occurred for high dye concentration only. In the case of Laponite, ICY adsorbs on the external surface of the layer. Our studies indicate that the ICY-clays, in particular, ICY-SYn-1 and ICY-Lap, are promising hybrid materials with interesting optical and photophysical properties.

Photochemical Deposition of Silver Nanoparticles on Clays and Exploring Their Antibacterial Activity.

Photochemical method was used to synthesize silver nanoparticles (AgNPs) in the presence of citrate or clay (SWy-1, SYn-1, and Laponite B) as stabilizers and Lucirin TPO as photoinitiator. During the photochemical synthesis, an appearance of the plasmon absorption band was seen around 400 nm, indicating the formation of AgNPs. X-ray diffraction results suggested that AgNPs prepared in SWy-1 were adsorbed into interlamellar space, and moreover, showed some clay exfoliation. In the case of SYn-1, AgNPs was not intercalated. For the AgNP/Lap B sample, the formation of an exfoliated structure occurred. Transmission electron microscopy revealed the spherical shape of AgNPs for all samples. The particle sizes obtained for AgNP/SWy-1, AgNP/SYn-1, and AgNP/Lap B were 2.6, 5.1, and 3.8 nm, respectively. AgNPs adsorbed on SYn-1 reveal nonuniform size and aggregation of some particles. However, AgNP/SWy-1 and AgNP/Lap B samples are more uniform and have diameters smaller than those prepared with SYn-1. This behavior is due to the ability to exfoliate these clays. The antibacterial activities of pure clays, AgNP/citrate, and AgNP/clays were investigated against Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus). AgNPs in the presence of clays (AgNPs/SYn-1 and AgNPs/SWy-1) showed a lower survival index percentage compared to those obtained for pure clays and AgNPs. The AgNP/SWy-1 sample showed good antibacterial activity against both tested species and the lowest survival index of 3.9 and 4.3 against E. coli and S. aureus, respectively. AgNPs are located in the interlayer region of the SWy-1, which has acid sites. These acidic sites may contribute to the release of Ag(+) ions from the surface of AgNPs. On the other hand, Laponite B and AgNP/Lap B samples did not demonstrate any bactericidal activity.

Effect of sonication on the particle size of montmorillonite clays.

This paper reports on the effect of sonication on SAz-1 and SWy-1 montmorillonite suspensions. Changes in the size of the particles of these materials and modifications of their properties have been investigated. The variation of the particle size has been analyzed by DLS (dynamic light scattering). In all cases the clay particles show a bimodal distribution. Sonication resulted in a decrease of the larger modal diameter, as well as a reduction of its volume percentage. Simultaneously, the proportion of the smallest particles increases. After 60 min of sonication, SAz-1 presented a very broad particle size distribution with a modal diameter of 283 nm. On the other hand, the SWy-1 sonicated for 60 min presents a bimodal distribution of particles at 140 and 454 nm. Changes in the properties of the clay suspensions due to sonication were evaluated spectroscopically from dye-clay interactions, using Methylene Blue. The acidic sites present in the interlamellar region, which are responsible for dye protonation, disappeared after sonication of the clay. The changes in the size of the scattering particles and the lack of acidic sites after sonication suggest that sonication induces delamination of the clay particles.

SDS (sodium dodecyl sulfate) effect on the autoxidation of the Glossoscolex paulistus giant extracellular hemoglobin: kinetic studies at pH 7.0 and 9.0.

The effect of the anionic surfactant sodium dodecyl sulfate (SDS) on the autoxidation process of the giant extracellular hemoglobin of Glossoscolex paulistus (HbGp) is addressed in the present work. The complex oligomeric assembly of hemoglobin subunits may influence the autoxidation rate and the exponential decay behavior. Kinetic studies were developed using UV-vis measurements at 415 nm. These spectroscopic measurements are analyzed at two pH values, 7.0 and 9.0, where the hemoglobin presents different oligomeric assembly. At pH 7.0 a high stability of the native form of the oxy-hemoglobin is observed, while at pH 9.0 an intense dissociation of the oligomer is promoted by alkalization. This difference is evident by comparison of the rate constants in the absence of surfactant: at pH 7.0 the kinetics presents a mono-exponential behavior with a rate constant of 0.27 x 10(-4)s(-1) while at pH 9.0 a bi-exponential behavior was observed with rate constant increase to 7 x 10(-4)s(-1) (fast process) and 1 x 10(-4)s(-1) (slow process). In the autoxidation induced by SDS two factors affect significantly the process rate, namely, the oligomeric arrangement of the hemoglobin and the strength of the interaction between SDS and HbGp. At pH 7.0, for SDS concentrations up to 0.3mM, a mono-exponential behavior was observed, showing rate constants around 0.4 x 10(-4)s(-1), which suggest that the hemoglobin still maintains the more compact structure observed at this pH for the native protein. In the SDS concentration range 0.75-1.0mM, the mono-exponential process changes into a bi-exponential behavior with rate constants varying from 48 x 10(-4) up to 99 x 10(-4)s(-1) for the fast process and from 1.7 x 10(-4) up to 3.7 x 10(-4)s(-1) for the slow process, suggesting hemoglobin dissociation. At pH 9.0, a bi-exponential decay is observed for all studied SDS concentration range, presenting rate constants from 11.0 x 10(-4) up to 179 x 10(-4)s(-1) for the fast process and from 1.0 x 10(-4) up to 8 x 10(4)s(-1) for the slow process probably due to hemoglobin dissociation, which is already present in the absence of surfactant. At pH 7.0, the highly packed native protein structure should inhibit the autoxidation process, but the SDS/HbGp interaction is more intense as compared to pH 9.0, due to the acid pI value, promoting oligomeric dissociation. So, the autoxidation process is regulated at pH 7.0 by the interaction with SDS, which triggers oligomeric dissociation and increase of autoxidation rate. At pH 9.0, the autoxidation process should be very fast, probably due to the oligomeric dissociation, which is already present in the absence of surfactant. At alkaline pH, the interaction with SDS seems be weaker than at pH 7.0. This behavior at pH 7.0 can be observed through the higher autoxidation rate for the faster chains and it is associated to the acid pI of the giant extracellular hemoglobins.