文摘
Ionically crosslinked chitin microspheres were prepared by using electrostatic droplet method and the drug release from the microspheres was controlled by adjusting external pH. Specifically, chitin was dissolved in NaOH/urea solution at low temperature and functionalized with acrylamide moieties. Acrylamide-modified chitin microspheres with a diameter of 400-500 渭m can be obtained at the voltage of 6 kV and the pump speed of 5 mL h鈭?. The formed microspheres were ionically crosslinked with Fe3+ and then complexed with polycationic polysaccharide chitosan. The structure of the microspheres was characterized by FT IR, SEM, and EDS analyses. Besides, the drug release behavior of the microspheres exhibited a fast responsive and pH sensitive release of vancomycin. It took 30 h for complete release of vancomycin in pH 4.0 buffer and pH 1.2 HCl solution while a fast release (10 min) occurred in pH 7.4 buffer. The results showed that the microspheres could be used in drug delivery.