Locust bean gum hydrogels are bioadhesive and improve indole-3-carbinol cutaneous permeation: influence of the polysaccharide concentration

Abstract The locust bean gum (LBG) is a polysaccharide with thickening, stabilizing and gelling properties and it has been used in the preparation of pharmaceutical formulations. Hydrogels (HGs) are obtained from natural or synthetic materials that present interesting properties for skin application. This study aimed to develop HGs from LBG using indole-3-carbinol (I3C) as an asset model for cutaneous application. HGs were prepared by dispersing LBG (2%, 3% and 4% w/v) directly in cold water. The formulations showed content close to 0.5 mg/g (HPLC) and pH ranging from 7.25 to 7.41 (potentiometry). The spreadability factor (parallel plate method) was inversely proportional to LBG concentration. The rheological evaluation (rotational viscometer) demonstrated a non-Newtonian pseudoplastic flow behavior (Ostwald De Weale model), which is interesting for cutaneous application. The HET-CAM evaluation showed the non-irritating characteristic of the formulations. The bioadhesive potential demonstrated bioadhesion in a concentration-dependent manner. Permeation in human skin using Franz cells showed that the highest LBG concentration improved the skin distribution profile with greater I3C amounts in the viable skin layers. The present study demonstrated the feasibility of preparing HGs with LBG and the formulation with the highest polymer concentration was the most promising to transport active ingredients through the skin.

Fluoride Release from Restorative Materials

The aim of this study was to evaluate in vitro fluoride (F) release from 4 restorative materials (3M ESPE): Ketak Molar Easymix [KME - conventional glass ionomer cement (GIC)]; Rely-X luting 2 [RL2 - resin-modified GIC (RMGIC)]; Vitremer (VIT- RMGIC); and Filtek Z250 [Z250 - negative control]. Disc-shaped specimens were fabricated according to the manufacturer’s instructions and placed into 10 mL of reverse osmosis water at 37°C until the analyses were done using a liquid membrane for selective F ion electrode (Orion 710). F release was evaluated every 6 h in the first day and thereafter daily during 28 days (d). The results were analyzed statistically by two-way ANOVA and Tukey’s test (α=0.05). Mean F release and standard deviation values (in ppm) were: KME: 6 h- 0.34 ± 0.04; 24 h- 1.22 ± 0.30; 7 d- 0.29 ± 0.09; 14 d- 0.20 ± 0.04; 28 d- 0.16 ± 0.01; RL2: 6 h- 2.46 ± 0.48; 24 h-12.33 ± 2.93; 7 d- 1.37 ± 0.38; 14 d- 0.80 ± 0.13; 28 d- 0.80 ± 0.21; VIT: 6 h- 0.98 ± 0.35; 24 h- 4.35 ± 1.22; 7 d- 0.66 ± 0.23; 14 d- 0.40 ± 0.07; 28 d- 0.39 ± 0.08; Z250: 6 h- 0.029 ± 0.001; 24 h- 0.024 ± 0.009; 7 d- 0.023 ± 0.004; 14 d- 0.025 ± 0.001; 28 d- 0.028 ± 0.001. RL2 RMGIC released more F than the other materials in all periods. The greatest release of F occurred in the first 24 h.

O objetivo deste estudo foi avaliar, in vitro, a liberação de flúor (F) de 4 materiais restauradores (3M-ESPE): KME cimento de ionômero de vidro convencional (CIV) (Ketak Molar Easymix); RX2- GIC modificado por resina (RMGIC) (Rely-X luting 2); VIT-RMGIC (Vitremer); -resina composta Z250 (controle negativo) (Filtek Z250). As amostras foram confeccionadas de acordo com as instruções do fabricante e colocadas em 10 mL de água destilada 37°C até as leituras, que foram feitas utilizando um eletrodo de íon seletivo de fluoreto de membrana líquida (Orion 710). A liberação de flúor foi avaliada a cada 6 h no primeiro dia e, diariamente durante 28 dias (d). Os resultados foram analisados estatisticamente usando ANOVA a dois critérios e teste de Tukey. A média e desvio padrão de liberação de F, valores (em ppm) foram: KME: 6 h- 0,34 ± 0,04; 24 h- 1,22 ± 0,30; 7 d- 0,29 ± 0,09; 14 d- 0,20 ± 0,04; 28 d- 0,16 ± 0,01; RL2: 6 h- 2,46 ± 0,48; 24 h- 12,33 ± 2,93; 7 d- 1,37 ± 0,38; 14 d- 0,80 ± 0,13; 28 d- 0,80 ± 0,21; VIT: 6 h- 0,98 ± 0,35; 24 h- 4,35 ± 1,22; 7 d- 0,66 ± 0,23; 14 d- 0,40 ± 0,07; 28 d- 0,39 ± 0,08; Z250: 6 h- 0,029 ± 0,001; 24 h- 0,024 ± 0,009; 7 d- 0,023 ± 0,004; 14 d- 0,025 ± 0,001; 28 d- 0,028 ± 0,001. Concluiu-se que RL2 liberou mais F do que os outros materiais em todos os períodos. A maior liberação de F ocorreu nas primeiras 24 h.

Formation constants of 3,5,7,2',4', pentahydroxyflavone-Nd-III complexes by spectrophotometric and potentiometric studies

Complex formation of Nd [III] with 3,5,7,2',4'-pentahydroxyflavone has been studied by spectrophotometric and potentiometric methods at 25C and at mu = 0.1 M using NaClO4. The metal forms 1:1 and 1:2 complexes. The protonation constants of morin and the stepwise stability constants of its Nd complex have been determined. Free energy changes during protonation of the ligand as well as during complex formation are reported. The solid complex was prepared and studied to ascertain the mode of bonding

Potentiometric and spectrophotometric methods for determination of PKa, for weak acids Correlation of solvent properties with pKa values for phenol derivatives

The ionization of phenols, as weak acids, depends on the nature of the solvents used. Correlations between their pKa values and the solvent properties exist, but are mostly nonlinear. Free energies of ionization suggested the presence of solvent types of interactions