Usnic acid-incorporated alginate and gelatin sponges prepared by freeze-drying for biomedical applications

Autor: Francilene Amaral da Silva, Adriano Antunes de Souza Araújo, Paula dos Passos Menezes, Aldino do Nascimento Porto Neto, Charlene R. S. Matos, Yasmim Maria Barbosa Gomes de Carvalho, Pedro José Rolim Neto, Paula Santos Nunes, Juliana Cordeiro Cardoso, Carla Francisca dos Santos Cruz, Mairim Russo Serafini, Ricardo Luiz Cavalcanti de Albuquerque Júnior
Rok vydání: 2016
Předmět:
Zdroj: Journal of Thermal Analysis and Calorimetry. 127:1707-1713
ISSN: 1588-2926
1388-6150
DOI: 10.1007/s10973-016-5760-8
Popis: There is considerable interest in the pharmaceutical and biomedical areas in the use of sponges, produced with biopolymers, as matrices for the controlled release of drugs. The objective of this work was to evaluate the physicochemical characterization of alginate–gelatin (ALG–GEL) sponges containing usnic acid (UA), by thermogravimetric analysis (TG/DTG), differential scanning calorimetry (DSC) and scanning electron microscopy (SEM). The macroscopic aspect showed a flexible structure, with variations in coloration depending on the concentration of UA in the sponges. The TG/DTG curves of ALG–GEL sponges and sponges containing 1 and 5 % of UA showed similar profiles and percentages of loss of mass. The DSC curves of both the sponges showed similar profiles, with two events involving a variation of enthalpy being observed, the first an endothermic event and the latter exothermic events, typical of decomposition. These curves show the absence of an endothermic peak of UA at 201 °C, indicating that the drug was present in the polymeric system. The SEM showed the ALG–GEL sponge to have the largest average pore diameter and a more heterogeneous arrangement of polymeric fibers, while sponges incorporated with UA showed more homogeneous arrangement of polymeric fibers. In conclusion, the incorporation of UA did not change the thermal stability of the sponges. Furthermore, the sponges incorporated with the drug showed a microstructural organization suitable for drug release systems.
Databáze: OpenAIRE