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In recent years, orally disintegrating films (ODFs) have been studied as alternative ways for drug administration. They can easily be applied into the mouth and quickly disintegrate, releasing the drug with no need of water ingestion and enabling absorption through the oral mucosa. The ODFs matrices are typically composed of hydrophilic polymers, in which the natural polymers are highlighted since they are polymers extracted from natural sources, non-toxic, biocompatible, biodegradable, and have favorable properties for this application. Besides that, natural polymers such as polysaccharides and proteins can be applied either alone or blended with other synthetic, semi-synthetic, or natural polymers to achieve better mechanical and mucoadhesive properties and fast disintegration. In this review, we analyzed ODFs developed using natural polymers or blends involving natural polymers, such as maltodextrin, pullulan, starch, gelatin, collagen, alginate, chitosan, pectin, and others, to overview the recent publications and discuss how natural polymers can influence ODFs properties.

In this study, we proposed the use of the biopolymers silk fibroin, chitosan and alginate, which are recognized for their biocompatibility and biodegradability, for the preparation of multilayer membranes aiming at high performance wound dressings with controlled drug delivery. The rationale was to combine in one material the mechanical properties of fibroin, the antimicrobial action of chitosan and the ideal exudate absorption of alginate, reaching a synergic effect of each biopolymer, without losing their individual intrinsic properties. The membranes were prepared by casting and diclofenac sodium was incorporated as model drug into the chitosan solution before the solvent evaporation, being retained in the middle layer of the membrane. Morphological, thermal, mechanical, solubility and barrier properties of the membranes were evaluated, as well as cytotoxicity and microbiological permeation. Results show that the incorporation of the drug did not affect mechanical and barrier properties, as well as microbiological permeation. Drug release was evaluated in vitro using simulated solution of wound exudate at 37 °C and diclofenac sodium was released from the multilayer membrane in 7 h, in which Fickian diffusion was the main mechanism associated. The results show the potential application of the biopolymer multilayer membranes as high-performance wound dressings.

Freezing is an interesting technique to modify the mechanical properties and morphology of hydrogels. Konjac glucomannan (KGM) is a polysaccharide that has potential use in cutting-edge areas as biomaterials and tissue engineering. In this work, we deeply investigated the influence of freezing on KGM. For that, KGM hydrogels were frozen at several freezing rates and temperatures. Results show that the freezing rate was the most important factor in the final physical properties of the KGM hydrogels. Slow freezing rate produced structures with isotropic and large pores, while fast freezing resulted in hydrogels with small and aligned pores. In addition, hydrogels frozen at high temperature (−8 °C) exhibited higher penetration modulus than hydrogels frozen at low temperature (−28 °C), since dense polymer regions are formed due to higher molecules dehydration caused by slow freezing. KGM hydrogels that underwent freezing can be explored as scaffolds for tissue engineering, with improved structural and mechanical properties.

A novel bilayer film of chitosan and konjac glucomannan were prepared by the two-step casting technique. Blend films were also prepared to investigate the interactions between the two polymers in the interfacial region of the bilayer structure. Scanning electron microscopy, Fourier transform infrared spectroscopy, and X-ray diffraction analysis showed that, unlike in the blends, the physicochemical properties of each biopolymer were preserved in the bilayer film. Differential scanning calorimetry and thermogravimetric analysis also indicated a good thermostability and miscibility for both polymers, probably due to strong hydrogen bonds between their polymer chains. Biological, mechanical and water vapor transmission tests showed a high biocompatibility, low cytotoxicity, and suitable mechanical and barrier properties of the bilayer films for wound dressing applications.

In this study, we proposed the use of the biopolymer alginate to produce membranes with diclofenac sodium incorporated as model-drug aiming at wound dressing application with drug delivery. The membranes were prepared by casting and the drug was incorporated directly into alginate solution, being retained within the membrane. Morphological, chemical, mechanical and barrier properties were evaluated, as well as the release kinetics in vitro using simulated exudate fluid at 37 °C. Results show that the membranes are malleable in the glycerol presence and more resistant to water after crosslinking. The incorporation of diclofenac sodium did not affect barrier properties, but influenced the mechanical properties, increasing the total thickness (from 0.108 to 0.209 mm) and reducing tensile strength (from 40.85 to 21.76 MPa). Drug release evaluation shows that anomalous transport is the major rate-controlling mechanism, where the swelling or erosion of the alginate matrix is the major responsible for the diclofenac sodium release, with a small contribution of Fickian diffusion mechanism. The results show the potential of application of the alginate membranes for wound dressings with drug delivery for enhancing healing process.

Films of silk fibroin (SF) and sodium alginate (SA) blends were prepared by solution casting technique. The miscibility of SF and SA in those blends was evaluated and scanning electron microscopy (SEM) revealed that SF/SA 25/75 wt.% blends underwent microscopic phase separation, resulting in globular structures composed mainly of SF. X-ray diffraction indicated the amorphous nature of these blends, even after a treatment with ethanol that turned them insoluble in water. Thermal analyses of blends showed the peaks of degradation of pristine SF and SA shifted to intermediate temperatures. Water vapor permeability, swelling capacity and tensile strength of SF films could be enhanced by blending with SA. Cell viability remained between 90 and 100%, as indicated by in vitro cytotoxicity test. The SF/SA blend with self-assembled SF globules can be used to modulate structural and mechanical properties of the final material and may be used in designing high performance wound dressing.

Chitin is a natural copolymer found in crustacean shells and has potential for use in a wide range of faculties. During the chitin obtainment process, effluents with high organic charge are generated. These should be treated before discharge in order to avoid environmental problems. This work aimed to investigate the treatment of effluents from chitin obtainment process using chitin (CH) and aluminum sulfate (Al 2 (SO 4 ) 3 ) as coagulants. The effects of coagulant type (CH and Al 2 (SO 4 ) 3 ), coagulant concentration (150 and 300 mg L −1 ) and pH (6.0 and 8.5) were evaluated by a full 2 3 experimental design. The considered responses were: total solids reduction (TSR), suspended solids reduction (SSR) and turbidity reduction (TR). It was found that the use of 300 mg L −1 of Al 2 (SO 4 ) 3 under pH 6.0 or 8.5 favored the treatment of effluents from chitin obtainment process. The proposed treatment provided reductions of 20, 89 and 85% in the total solids, suspended solids and turbidity respectively.

Silk fibroin (SF) hydrogels were obtained from the dialysis of a SF metastable solution. Temperature and calcium concentration in SF solution/hydrogel were measured, as critical variables for SF gelation phenomenon. Gelation time of SF solution was increased by decreasing the dialysis temperature, whereas the residual calcium concentration was higher when higher dialysis temperatures were applied. Hydrogels obtained at 20 °C were characterized after freeze-drying. SEM micrographs showed porous structures, of ca. 20 μm (in cross-sectional area) and 5 μm (on surface). XRD indicated the presence of a β-sheet structure that is formed during SF gelation. In hydrogel formation, SF molecules in solution are dehydrated and interact by intra and intermolecular hydrogen bonds, forming a stable hydrogel. DSC measurements showed the decomposition peak for SF at 290 °C, characteristic of SF β-sheet structure, which is in accordance with the XRD results and demonstrate its high thermal resistance. SF hydrogels were found not to be toxic to cells using in vitro cytotoxicity tests. Results indicate that silk fibroin hydrogels hold promise for use in the biomaterial field.

The moisture equilibrium isotherms of chitosan were determined at 20, 30, 40, 50 and 60 � C, using the gravimetric static method. Experimental data were analyzed by the GAB, Oswin, Halsey and Smith equations. Isosteric heat and differential entropy of sorption were determined from the GAB model using the Clausius-Clapeyron and Gibbs-Helmholtz equations, and pore size distribution was calculated by the Kelvin and Halsey equations. The GAB and Oswin equations showed best fit to the experimental data with R 2 z 99% and low mean relative deviation values (E% < 10%). Monolayer moisture content values (from 0.12 to 0.20 kg kg � 1 ) and water surface area values (from 450 to 700 m 2 g �1 ) decrease with increasing temperature. Isosteric heat and differential entropy of sorption were estimated as a function of moisture content. The Kelvin and Halsey equations were adequate for calculation of pore size distribution, which varied from 0.5 to 30 nm.