壳聚糖
磺胺嘧啶银
聚电解质
抗菌活性
肿胀 的
自愈水凝胶
材料科学
葡萄糖醛酸
磺胺嘧啶
控制释放
高分子化学
核化学
化学工程
化学
有机化学
多糖
聚合物
细菌
伤口愈合
纳米技术
复合材料
抗生素
生物化学
遗传学
工程类
免疫学
生物
作者
Shu‐Huei Yu,Fwu‐Long Mi,Yu‐Bey Wu,Chih‐Kang Peng,Shin‐Shing Shyu,Rong Huang
摘要
Abstract Hydrogel membranes prepared from polyelectrolyte complex (PEC) have been used for repair of wounds and controlled antibacterial release. A simple method, based on homogenizing interpolyelectrolyte complex, has been developed to prepare a chitosan–alginate sponge with high stability. The spongelike chitosan–alginate hydrogel can be used as a wound dressing for the sustained release of silver sulfadiazine (AgSD) in a controlled way. In this study, we evaluated the effect of electrolyteic properties of chitosan and alginate on the characteristics of the prepared chitosan–alginate PEC. All types of the spongelike chitosan–alginate hydrogels exhibited superabsorbent properties. However, only the chitosan–alginate hydrogel prepared by the interpolyelectrolyte complex of alginate with low pH of chitosan, and that prepared by the interpolyelectrolyte complex of chitosan with high pH of alginate, can keep their stability after swelling in PBS solution. FTIR analysis suggests that the protonated amino groups on chitosan and the ionized carboxylic groups on alginate should be responsible for the formation of a stable ladder‐type of chitosan–alginate PEC. Ionic crosslinking is helpful to increase the stability of the loop‐type of chitosan–alginate PEC. The release of AgSD from chitosan–alginate PEC sponges could be controlled by the variation of ladder‐loop structural transition of chitosan–alginate PEC and the ionic crosslinking of the chitosan–alginate complex. The antibacterial ability of AgSD‐incorporated PEC sponges was examined in agar plate against Pseudomonas aeruginosa and Staphylococcus aureus . The result suggests that the PEC sponges containing antimicrobial agents should effectively suppress bacterial proliferation to protect the wound from bacterial invasion. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 98: 538–549, 2005
科研通智能强力驱动
Strongly Powered by AbleSci AI