戊二醛
壳聚糖
凝聚
结晶度
微球
扫描电子显微镜
材料科学
形态学(生物学)
化学工程
核化学
化学
色谱法
复合材料
遗传学
生物
工程类
作者
Lizhi Xiong,Zeqiang He
标识
DOI:10.1080/00222348.2012.674817
摘要
Chitosan microspheres, with a size range of 20–550 μm, were obtained by using an emulsification–coacervation method. The surface morphology and the structure of microspheres were characterized by scanning electron microscopy and X-ray diffraction. The effects of process variables, including stirring rate, chitosan concentration, emulsifier concentration, and cross-linker (glutaraldehyde) concentration, on the diameter of chitosan microspheres were investigated. The results showed that spherical microspheres, without aggregation phenomena and with a very smooth and uniform surface, were obtained when emulsifier concentration, chitosan concentration, stirring rate, and glutaraldehyde concentration were kept at 0.010–0.025 mL/mL, 0.05–0.20 g/mL, 800–2400 rpm, and 0.5–1.5% (v/v) respectively. The chitosan microsphere crystallinity degree decreased after cross-linking. The microsphere size increased with decreasing of stirring rate, emulsifier, and cross-linker concentration; however, the microsphere size increased with increase of chitosan concentration. This indicated that different diameters of chitosan microspheres can be achieved by controlling process variables.
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