Cinética de secagem e difusividade efetiva em folhas de jenipapo (Genipa americana L. ) / Drying kinetics and effective diffusivity in jenipapo sheets (Genipa americana L. )

RESUMO O jenipapo (Genipa americana L.) é uma espécie nativa com importância medicinal, sendo amplamente utilizada no Brasil. Em função da necessidade de conhecimento à cerca do pré-processamento desta espécie, este trabalho foi desenvolvido com o objetivo de avaliar a cinética de secagem de folhas de jenipapo (G. americana L.), bem como determinar a difusividade efetiva da água durante o processo. As folhas foram coletadas com teor de água inicial de 2,30±0,05 (decimal b.s.), e submetidas à secagem em três condições de temperatura do ar (35,3; 46,0 e 65,0°C) até atingirem o teor de água de equilíbrio. Aos dados experimentais, ajustaram-se doze modelos matemáticos, recomendados para representar o processo de secagem de produtos agrícolas. As magnitudes do coeficiente de determinação (R2), do erro médio relativo (P), do erro médio estimado (SE) e do teste do qui-quadrado (χ2), foram utilizadas para verificar o grau de ajuste dos modelos. Os modelos de Henderson e Pabis modificado e Midilli apresentaram ajustes adequados aos dados experimentais, sendo o modelo de Midilli, em função de sua simplicidade, escolhido para representar a cinética de secagem das folhas de jenipapo. Aumentando a temperatura do ar de secagem de 35,3 para 46,0 e 65,0ºC houve redução no tempo de secagem das folhas de jenipapo de 91,1 para 62,5 e 24,2 horas, respectivamente. O coeficiente de difusão efetivo aumenta com a elevação da temperatura, e esta relação é descrita pela equação de Arrhenius, que apresenta energia de ativação para a difusão líquida de 33,9 kJ mol-1.

ABSTRACT The jenipapo (Genipa americana L.) is a native species with medicinal importance and is widely used in Brazil. Due to the need for knowledge about the preprocessing of this species, this work was developed to evaluate the drying kinetics of the jenipapo leaves (G. americana L.), and also to determine the effective diffusivity of water during the process. The leaves were collected with an initial moisture content of 2.30 ± 0.05 (decimal db), and dried in three conditions of air temperature (35.3, 46.0 and 65.0°C) until they reach the equilibrium moisture content. The experimental data set were twelve mathematical models, recommended to represent the drying process of agricultural products. The magnitudes of the coefficient of determination (R2), the mean relative error (P), the average estimated error (SE) and the chi-square (X2), were used in order to verify the adequacy level of the models. The Henderson, modified Pabis and Midilli models presented appropriate adjustments to the experimental data, with the model Midilli, due to its simplicity, chosen to represent the drying kinetics of the jenipapo leaves. By increasing the temperature of the drying air from 35.3 to 46.0 and 65.0ºC, there was a reduction in the drying time of the jenipapo leaves, from 91.1 to 62.5 and to 24.2 hours, respectively. The effective diffusion coefficient increases with the temperature’s raise, and this relationship is described by the Arrhenius equation, which shows activation energy for liquid diffusion of 33.9 kJ mol-1.

Encapsulation of trans-dehydrocrotonin in liposomes: an enhancement of the antitumor activity.

The aim of this study was the encapsulation of trans-dehydrocrotonin (t-DCTN) and its inclusion complexes with hydropropyl-beta-cyclodextrin (HP-beta-CD) in liposomes to improve t-DCTN antitumor activity. The in vitro kinetic profiles of t-DCTN-loaded liposomes (LD) and t-DCTN:HP-beta-CD-loaded liposomes (LC) were evaluated using the dialysis technique. The antitumor activity of LD and LC were investigated against Sarcoma 180 in Swiss mice. Histopathological and hematological analyses were carried out. The amounts of t-DCTN and t-DCTN:HP-beta-CD inclusion complex encapsulated in liposomes were equivalent to 1 mg of t-DCTN. The encapsulation efficiencies of LD and LC were 95.0 +/- 3.8% and 91.1 +/- 5.6%, respectively. In relation to kinetics, the drug release profiles of t-DCTN are in substantial agreement with the Fickian model. The treatment of animals with LD and LC produced tumor inhibitions of 79.4 +/- 9.6% and 63.5 +/- 5.5%, respectively. The liposomal encapsulation of t-DCTN by entrapment in the phospholipid bilayer increased at twice the antitumor activity. Moreover, the liposomal formulations reduced the hepatotoxicity effect of the drug and no significant hematological toxicity was observed in the treated animals. However, the counting of platelets was slightly decreased. Thus, the results show that the development of liposomal formulations containing t-DCTN or t-DCTN:HP-beta-CD is an important advance for enabling this drug to be use in therapy.

Equilibrium and kinetic analysis of methyl orange sorption on chitosan spheres.

Chitosan can be used as adsorbent in the treatment of effluents from the textile industry, especially for negatively charged dyes, due to its cationic polyelectrolyte nature. In this work, the sorption of a model dye, methyl orange, on chitosan hydrobeads is analyzed in terms of equilibrium and kinetic approaches. Equilibrium studies showed that dye adsorption had a mixed Freundlich-Langmuir behavior that had its Langmuir character increased as the pH was increased. In terms of adsorption kinetics, it was found to be of nth-pseudo-order, with fractional n increasing from approximately 2 to approximately 2.5 as pH and initial dye concentration in the continuous phase were increased. The increase in the apparent pseudo-order was related to changes in mathematical approximation for the solution of the sorption rate equation, which were the result of the decrease in the ratio (number of active sites for adsorption)/(number of adsorbate molecules).