利多卡因
肿胀 的
明胶
海藻酸钙
微球
钙
控制释放
止血剂
生物医学工程
化学
壳聚糖
药理学
药品
止血
材料科学
医学
外科
化学工程
复合材料
生物化学
有机化学
工程类
作者
Rongrong Ma,Hui-Xian Xu,Li Ni,Jia-Min Xiong,Yilin Chen,Jia-Yuan He,Qin Li,Lili Yang,Lian‐Di Zhou,Qi‐Hui Zhang,Ling Luo
标识
DOI:10.1142/s0192415x22500896
摘要
The development of effective drug-loaded dressings has been considered a hot research topic for biomedical therapeutics, including the use of botanical compounds. For wound healing, adequate dressings can provide a good microenvironment for drug release, such as lidocaine. Biological macromolecular materials such as alginate show excellent properties in wound management. This study involves the preparation and evaluation of biocompatible multilayered-structure microspheres composed of chitosan, porous gelatin, and calcium alginate microspheres. The multilayered structure microspheres were named chitosan@ porous gelatin@ calcium alginate microspheres (CPAMs) and the drugs were rapidly released by the volume expansion of the calcium alginate microspheres. The in vitro release curve revealed that the peak release of lidocaine from CPAMs was reached within 18[Formula: see text]min. After 21[Formula: see text]min, the remaining lidocaine was then slowly released, and the active drug release was converted to a passive drug release phase. The initial release effect of lidocaine was much better than that reported in the published studies. Additionally, blood coagulation experiments showed that CPAMs coagulated blood in 60[Formula: see text]s, and the blood liquidity of the CPAMs group was worse than that of the woundplast group. Therefore, the coagulation characteristics of CPAMs were superior to the commonly used woundplast containing lidocaine healing gel. These study outcomes indicated that the CPAMs acted as fast-release dressings for faster pain control and better coagulation properties.
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