首页|白藜芦醇温敏凝胶的制备HepG-2人肝癌细胞的抑制作用

白藜芦醇温敏凝胶的制备HepG-2人肝癌细胞的抑制作用

扫码查看
以泊洛沙姆407(P407)、泊洛沙姆188(P188)为凝胶基质制备白藜芦醇温敏水凝胶,通过Box-Behnken Design(BBD)法优化处方后对其进行药剂学性质及质量评价,通过MTT法检测其对人肝癌HepG-2细胞的抑制活性.结果表明:确定的最优处方为P407质量分数为21.22%、P188质量分数为4.87%、P407与P188体积比为3:1、白藜芦醇质量为2.5 mg;电镜结果显示其具有均匀致密的孔道,胶凝温度为36.4℃,胶凝时间为230 s,pH为7.12,黏度为1784.6 mPa·s;溶蚀时间达6 h,溶蚀度为95.5%,药物释放可达到90%以上,凝胶系统稳定性良好,可稳定释放药物;MTT法检测发现能够有效抑制肿瘤细胞增长并有浓度依赖特性.制备的白藜芦醇温敏水凝胶具有良好的温敏效果,能够在局部形成药物储库,期待能为未来的临床应用及成果转化奠定基础.
Preparation of Resveratrol Thermosensitive Hydrogel and Its Inhibitory Effect on HepG-2 Human Hepatoma Cells
Resveratrol thermosensitive hydrogel was prepared with poloxamer 407 (P407) and poloxamer 188 (P188) as gel matrix. The formulation was optimized by box Behnken design (BBD) method, and its pharmaceutical properties and quality were evaluated. Its inhibitory activity on human hepatoma HepG-2 cells was detected by MTT method. The results showed that the optimal formula was as follows: P40721.22%, P1884.87%, volume ratio of P407 to P1883:1, resveratrol 2.5 mg. The results of electron microscope showed that it had uniform and dense pores, the gelation temperature was 36.4 ℃, the gelation time was 230 s, the pH was 7.12, and the viscosity was 1784.6 mPa·s. The dissolution time was 6 h, the dissolution degree was 95.5%, and the drug release could be more than 90%. The gel system is stable and can release the drug stably. MTT assay showed that it could effectively inhibit the growth of tumor cells in a concentration dependent manner. The prepared resveratrol thermosensitive hydrogel has good thermosensitive effect and can form a local drug repository. It is expected to lay a foundation for future clinical application and achievement transformation.

TumorRharmaceuticalsThermosensitive gelPolymers

高国铸、李磊、范郁琳、汪海峰、梁梦秋、鞠婉婷

展开 >

沈阳化工大学制药与生物工程学院,辽宁沈阳 110142

辽宁省制药化工过程专业技术创新中心,辽宁沈阳 110142

肿瘤 药物 温敏凝胶 聚合物

辽宁省教育厅一般项目辽宁省科技厅博士科研启动基金项目辽宁省教育厅面上项目沈阳化工大学重点攻关项目

L201602320141083LJKZ0427LDB2019001

2024

当代化工
中国石油抚顺石化公司,中国石化抚顺石油化工研究院,沈阳市医药和化工行业联合会

当代化工

CSTPCD
影响因子:0.412
ISSN:1671-0460
年,卷(期):2024.53(5)
  • 7