With the rapid development of modern science and technology, especially in materialscience and chemical science, the application of textile technique in pharmaceutics would becontinued exploited. Then as a new type of dosage form, drug-loaded fiber was fabricated.Currently, the main preparation of drug-loaded fiber was finishing method and blend spinningmethod. Evern though the process of drug-loaded fiber by finishing method was simple, therelease behavior was not good. Besides, drug-loaded fiber by blend wet-spinning technology wasvery popular in many studies, while it would cause mass drug lost and lower drug-loaded ratio.In order to enhance the drug loading capacity of drug-loaded fiber, nano-capsules wereprepared by sodium alginate, and subsequently mixed with sodium alginate solution to obtainspinning dope. Then drug-loaded alginate fiber was produced by wet-spinning through calciumchloride solution. This study had examined the rheological properties and spinnability ofsodium alginate solution; investigated the effect of spinning dope concentration, coagulationbath concentration, coagulation bath temperature and draft ratios on the fiber morphology,structure and mechanical properties; fabricated nano-capsules drug-loaded alginate fiber underthe optimiality spinning conditions, and investigated the effect of capsule dosage, pH andtemperature on the drug release behavior of drug-loaded alginate fiber, and tested the fibermoisture absorption and gel-forming properties. Finally, the results were showed as follows:1) The rheological properties and spinnability of sodium alginate solution: Sodium alginatesolution was typical pseudoplastic fluid. And, with the increasing of concentration, thenon-Newtonian index (n) was gradually reduced, while the structural viscosity index (Δη) wasgradually increased, resulting to the reduced of sodium alginate liquidity. Finally, the suitableconcentration for wet-spinning was obtained:0.5-4.5%.2) Fabricated alginate fiber and obtained optimal spinning parameters: System investigatedthe effect of spinning dope concentration, coagulation bath concentration, coagulation bathtemperature and draft ratios on the morphology, structure and mechanical properties of alginatefiber, and obtained the optimal spinning parameters: spinning dope concentration was3.5%,coagulation bath concentration was2.5%, coagulation bath temperture was30℃, and draft ratio was1.5. At this time, alginate fiber showed good morphology, and obtained max mechanicalproperties (tensile strength of18.90±0.90cN/tex, elongation at break of8.83±0.35%,respectively). Besides, with the increasing of draft ratios, the regularity of molecular chains wasgradually enhanced, and resulting to the better fiber orientation and crystallization.3) Fabricated and characterized drug-loaded alginate fiber: Calcium alginate nano-capsuleswere produced as methylene blue as drug model, and the max drug loaded ratio was70.1±1.3%.Drug-loaded alginate fiber was successfully wet-spun by mixing nano-capsules with sodiumalginate solution. Nano-capsules could be evenly present on the fiber surface and internal, andwould not significantly affect the fiber structure and mechanical properties. The drug capacity ofdrug-loaded alginate fiber by this method was two times than traditional drug-loaded fiber.Besides, it had confirmed that this preparation could effectively reduce the drug wastage in thespinning process, and improve the drug loaded ratio. Apart from this, drug-loaded alginate fibershowed more prominent sustained release function in vitro drug release. The moisture absorptionand gel-forming properties were also tested, and the results showed that the maximum waterabsorption was25.17g/g, and gelated just need4min, which had confirmed the possibility ofdrug-loaded alginate fiber as medical dressing. |