RESUMO
Smart hydrogels with dual network were presented since a new allylated chitosan was conceived. As a double network hydrogel, its first network consisted of poly(N-isopropylacrylamide) worked as the gel matrix, and its second network with Schiff base bond enabled itself function as a molecular switch through the formation and break of the bond. When only the intestinal fluid was used, the second network could provide efficient protection for the loaded drug, and the drug release mechanism conformed to the non-Fickian type diffusion. While pre-treated with simulated gastric fluid, the switch would be opened and the mechanism was the Fickian type, which increased the cumulative percentage of drug release by about 25% and the release time by about 300 min. Besides, the hydrogel was characterized by 1H NMR, FT-IR and SEM. The effects of allylated chitosan, pH and crosslinker on the swelling ratio and morphology of hydrogel were also studied.
Assuntos
Resinas Acrílicas/química , Anti-Inflamatórios não Esteroides/química , Quitosana/análogos & derivados , Diclofenaco/química , Hidrogéis/química , Resinas Acrílicas/síntese química , Quitosana/síntese química , Preparações de Ação Retardada/química , Difusão , Liberação Controlada de Fármacos , Hidrogéis/síntese química , Concentração de Íons de Hidrogênio , Cinética , PorosidadeRESUMO
Natural silk fiber spun by the silkworm Bombyx mori is widely used not only for textile materials, but also for biofunctional materials. In the present study, we genetically engineered an advanced silk material, named hSFSV, using a transgenic silkworm, in which the recombinant human acidic fibroblast growth factor (hFGF1) protein was specifically synthesized in the middle silk gland and secreted into the sericin layer to surround the silk fiber using our previously optimized sericin1 expression system. The content of the recombinant hFGF1 in the hSFSV silk was estimated to be approximate 0.07% of the cocoon shell weight. The mechanical properties of hSFSV raw silk fiber were enhanced slightly compared to those of the wild-type raw silk fiber, probably due to the presence of the recombinant of hFGF1 in the sericin layer. Remarkably, the hSFSV raw silk significantly stimulated the cell growth and proliferation of NIH/3T3 mouse embryonic fibroblast cells, suggesting that the mitogenic activity of recombinant hFGF1 was well maintained and functioned in the sericin layer of hSFSV raw silk. These results show that the genetically engineered raw silk hSFSV could be used directly as a fine biomedical material for mass application. In addition, the strategy whereby functional recombinant proteins are expressed in the sericin layer of silk might be used to create more genetically engineered silks with various biofunctions and applications.