首页|蛛丝丝素蛋白膜的制备及其释药性能评价

蛛丝丝素蛋白膜的制备及其释药性能评价

Preparation and drug release evaluation of spider fibroin membrane

扫码查看
天然蜘蛛丝具有优越的力学性能,其多种剂型具有优异的抗菌活性、生物相容性及良好的导热性.开发具有良好生物相容性的纯天然生物载药材料,对于降低患者的强烈免疫原性反应具有重要意义.通过对蛛丝在不同溶剂中溶解及成膜方式的探索,优化反应条件:以六氟异丙醇做溶解溶剂,以 1∶1(mg∶mL)的料液质量体积比进行投料,在 60℃条件下溶解 8 h,通过溶剂浇铸法成膜,并结合相关表征探索其以罗丹明B为模型药物的体外释药规律.通过浸提法测试材料细胞毒性,将蛛丝丝素蛋白膜浸提液与细胞共培养显示其对小鼠胚胎成骨细胞无潜在细胞毒性.制得的载药蛛丝丝素蛋白膜产率高、厚度均一、操作简单,为天然蜘蛛丝丝素蛋白的溶解及其膜剂的制备提供了一项简单易行的技术.
Natural spider silk has superior mechanical properties,and its various forms have excellent antibacterial activity,biocompatibility,and good thermal conductivity.It is of great significance to develop natural biological drug-loaded materials with good biocompatibility for reducing the strong immunogenicity reaction of patients.By explor-ing the dissolution and membrane-forming methods of spider silk in different solvents,the reaction conditions were optimized,hexafluoroisopropanol was used as the dissolution solvent,the material ratio was 1∶1(mg∶mL),the spider silk was dissolved at 60℃for 8 h,and the membrane was formed by solvent casting,and the drug release in vitro of rhodamine B(RhB)as the model drug was explored with the correlation characterization.The cytotoxicity of the material was tested by extraction method.The spider fibroin membrane extract co-culture with cells showed that the material had no potential cytotoxicity to mouse embryonic osteoblasts cells.The drug-loaded spider silk fibroin mem-brane prepared by this method has high yield,uniform thickness and simple operation,which provides a simple and feasible technology for the dissolution of natural spider silk protein and the preparation of membrane agent.

spider silkhexafluoroisopropanolsilk fibroinsolvent casting methodsustained releaseRhB

刘欣欣、曾惠娜、纪晨然、高鹏飞、赵昱、张成桂

展开 >

大理大学 云南省昆虫生物医药研发重点实验室暨药学院, 大理 671000

大理大学 药用特种昆虫开发国家地方联合工程研究中心, 大理 671000

大理大学 中国西南药用昆虫及蛛形类资源开发利用协同创新中心,大理 671000

蜘蛛丝 六氟异丙醇 丝素蛋白 溶剂浇铸法 缓释 罗丹明B

国家自然科学基金重大科技专项(云南生物医药)

32160113202002AA100007

2024

复合材料学报
北京航空航天大学 中国复合材料学会

复合材料学报

CSTPCD北大核心
影响因子:0.933
ISSN:1000-3851
年,卷(期):2024.41(2)
  • 3