Plasticizer concentration effect on films and coatings based on poly(vinyl alcohol) and cationic starch blends.

Films based on poly(vinyl alcohol) (PVA) and cationic starch (CS) were combined with different percentages of sorbitol (S; 15.0, 22.5, and 30.0% w v-1) to assess the effect of plasticizer on the films. Spectroscopic analyses confirmed the interaction between them. However, micrographs indicated the formation of sorbitol crystals on the surface of the films, especially at higher sorbitol concentrations. The blends presented low water vapor transmission rate values, reaching (7.703 ± 0.000) g h-1 m-2 (PVA75CS25S15), and low solubility values for the films containing higher CS amounts. The lack of statistical differences in most parameters suggests that no significant gain comes from increasing the amount of sorbitol at percentages higher than 15%. As a coating, the blend PVA75CS25S15 successfully decreased the loss of moisture content in acerolas by 1.15 times (compared to the control), confirming the suitability of this matrix as a fruit coating.

Hydrolysis effects on the water uptake of starch-g-glycidyl methacrylate (GMASt)/dimethylacrylamide (DMAAm)-based hydrogels for potential agricultural purposes.

This work assessed the effect of different hydrolysis periods on the properties of hydrogels based on 75 % w w-1 of N,N'-dimethyl acrylamide (DMAAm) and 25 % w w-1 of starch-g-(glycidyl methacrylate) (GMASt). FTIR results confirmed the conversion of ester groups into carboxylic acids and carboxylates, besides forming a keto-enol tautomer due to the peeling reaction of starch. For DMAAm, the hydrolysis mostly converted amide into carboxylate groups. The morphology, thermal stability, and the mechanical properties of the predominantly amorphous matrices (as confirmed by XRD results) did not drastically change even after 10 days of hydrolysis in alkali media. However, the thermogravimetric analysis results suggested that DMAAm partially protected GMASt from the hydrolysis. The swelling degree of the matrix increased from (10.1 ± 2.1) g g-1 to (61.9 ± 2.6) g g-1 after 1 day of hydrolysis, but no statistical differences (at 95 % of significance) were observed for the matrices hydrolyzed for longer periods, confirming that the maximum hydrolysis occurred within 24 h. The results confirmed that the hydrolysis increased the water uptake of the GMASt/DMAAm-based matrices, making appealing for uses as a water retentor for agricultural purposes.

A conventional and chemometric analytical approach to solving urea determination with accuracy and precision.

Urea is an essential molecule usually detected using spectroscopy, particularly ultraviolet and visible spectroscopy (UV-vis). However, its detection represents a not always fully acknowledged issue. Its concentration dependency has raised questions about the reliability of the UV-vis results. Derivatization reactions, common alternatives to achieve accuracy and precision with UV-vis measurements, still represent an additional step in the measurement process. Besides the problems mentioned earlier, urea forms complex mixtures in aqueous mediums. Therefore, this work proposes to investigate the accuracy and precision of urea determination by UV-vis spectroscopy in the pure form and derivatized with para-dimethylaminobenzaldehyde. The results show that UV-vis spectroscopy could not quantify urea in both forms with precision and accuracy. On the other hand, when applying multivariate curve resolution with alternating least squares (MCR-ALS) to the UV-vis data, the pure urea analytical signal is mathematically separated. Then, those parameters of merit were successfully achieved.

A comparative study of starch-g-(glycidyl methacrylate)/synthetic polymer-based hydrogels.

Chemical modification reactions and blending formation are two alternatives used to improve the properties of starch-based materials. This work used both approaches to evaluate how they would affect the properties of hydrogels. The hydrogels were based on corn starch (St), modified with glycidyl methacrylate (GMA; starch-g-GMA; GMASt), and blended with N,N'-dimethylacrylamide (DMAAm; GMAStxDMAAmy) or sodium acrylate (SA; GMAStxSAy). The results confirmed that the pure GMASt matrix had a low swelling degree (≈3 g g-1), but when blended with the synthetic polymers, this value reached ≈10 g g-1 (sample GMASt25DMAAm75). All matrices showed responsiveness towards pH variations. In general, they swelled more at pH 5 than at pH 7. While DMAAm had more influence on the swelling degree, SA was more efficient as a mechanical enhancer. Increasing 25 % of the amount of SA in the blend increased Young's Modulus by a factor of ≈10 times. It confirmed that both polymers effectively change the properties of GMASt, but in different ways.

Electrospun poly(lactic acid) (PLA)/poly(butylene adipate-co-terephthalate) (PBAT) nanofibers for the controlled release of cilostazol.

Drug delivery devices are attractive alternatives to drugs usually orally administrated. Therefore, this work aimed to produce PLA/PBAT-based nanofibers for the controlled release of cilostazol, evaluating the effect of different drug concentrations (20 and 30%) over the properties of the fibers. The fibers were characterized by scanning electron microscopy (SEM), Fourier Transform Infrared Spectroscopy (FTIR), x-ray diffraction (XRD), differential scanning calorimetry (DSC), thermogravimetric (TG/DTG), and mechanical analysis. SEM results indicated a high concentration of drug crystals on the surface of the fibers that contained 20% of cilostazol. These fibers were also thinner, more crystalline, less thermally stable, and less fragile in comparison to the fibers containing 30% of cilostazol, according to the XRD, DSC, TG/DTG, and mechanical results. The controlled release assays indicated that the fibers containing 20% of cilostazol would be attractive for short-term releases, reaching the equilibrium after approximately 6 h, while the ones containing 30% would ensure a slower release (~ 12 h). Despite the differences, both fibers would improve and enhance the efficiency of the treatment, and they would also prevent possible side effects caused by the drug to the gastric system.

Magnetic chitosan microgels: Synthesis, characterization, and evaluation of magnetic field effect over the drug release behavior.

Magnetic microgels based on chitosan, modified with glycidyl methacrylate (GMA) and activated with folic acid (FA), and cobalt ferrite nanoparticles, modified with GMA (GMACoFe2O4), were synthesized by emulsion polymerization. The size of the round-shaped microgels, with and without GMACoFe2O4, ranged from (1.62 ± 0.38) µm to (1.71 ± 0.61) µm, respectively. Their release behavior was evaluated in the presence and absence of a magnetic field (MF), using vitamin-B12 as a model drug. In the absence of MF, at pH 7.4, a fast release was observed, reaching the equilibrium after 30 min. In the MF presence, the alignment of the chains to it promoted an initial fast release, followed by a more controlled one, lasting for 50 min at pH 7.4. This type of release is attractive for the treatment of gastric wounds, which is improved by the presence of FA, conferring anti-oxidative and anti-secretory properties to the microgels.

Drug polarity effect over the controlled release in casein and chondroitin sulfate-based hydrogels.

This study compared the controlled release of two drugs: vitamin-B12, and l-dopa from hydrogels based on 50% of casein (CAS, a protein), 50% of chondroitin sulfate (CS, a polysaccharide) and different amounts of SiO2. The results indicated that the incorporation of 5% of SiO2 to the materials, allowed the best organization, distribution, and diameter of the pores, which are responsible for ensuring a more controlled release. Also, the matrices were not efficient in releasing vitamin-B12, but it successfully released l-dopa. It happened because vitamin-B12 is highly hydrophilic, interacting more with the medium than with the CAS/CS matrix, while l-dopa is less polar than vitamin-B12, interacting more with the CAS/CS matrix. It is worth mentioning that all synthesized hydrogels were non-toxic to the cells as showed by the in vitro assay. This work also demonstrated the importance of evaluating drug delivery devices using drugs of different polarities before stating if they are efficient or not.

pH-responsive hybrid hydrogels: Chondroitin sulfate/casein trapped silica nanospheres for controlled drug release.

In this study, the materials were synthesized by chemically crosslinking chondroitin sulfate (CS), casein (CAS), and silica nanospheres (SiO2), creating a highly crosslinked network. The hydrogel release profile was adaptable (that is, it could be faster or slower as needed) simply by changing the polymeric proportion. The incorporation of 5% of silica nanospheres, in mass, for all CAS/CS matrices promoted a better-controlled and sustained release of l-dopa, focusing on the matrix based on 70% of CAS, 30% of CS and 5% of silica, whose l-dopa release lasted for 87 h. Besides, hydrogels are cytocompatible. These new hydrogels can be considered highly attractive materials to be used for controlled and sustained drug release purposes, as well as scaffolds and wound dressing systems.