Tianjin Key Laboratory for Modern Drug Delivery & High-Efficiency, School of Pharmaceutical Science and Technology, Tianjin University, Tianjin 300072, PR China.
Carbohydr Polym. 2016 Aug 1;146:52-7. doi: 10.1016/j.carbpol.2016.03.042. Epub 2016 Mar 19.
To improve the aqueous solubility of the anticancer agent paclitaxel (PTX), a newly conformed bipolymer paclitaxel-nanoparticle using tea polysaccharide (TPS) and zein was prepared and characterized. Tea polysaccharide was used as a biopolymer shell and zein was as the core and the optimal formula was subjected to the characteristic study by TEM, DSC, FTIR and in vitro release study. Results showed that the optimal particle was acquired with particle yield at 40.01%, drug loading at 0.12% and diameters around 165nm when the concentration of tea polysaccharide was set at 0.2%, and the amount of PTX:zein=1:10. The particle was a nanoparticle with spherical surface and the encapsulated PTX was in an amorphous form rather than cystalline form. PTX was interacted with zein and polysaccharide through O H and CO groups and it had a sustained release. The results suggested that the novel bipolymer might be a promising agent for PTX delivery and tea polysaccharide was demonstrated its function in drug delivery system.
为提高抗癌药物紫杉醇(PTX)的水溶性,采用茶多糖(TPS)和玉米醇溶蛋白制备了一种新的紫杉醇纳米粒子两亲聚合物,并对其进行了表征。茶多糖作为生物聚合物壳,玉米醇溶蛋白作为核,采用 TEM、DSC、FTIR 和体外释放研究对最佳配方进行了特征研究。结果表明,当茶多糖浓度设定为 0.2%,PTX:玉米醇溶蛋白=1:10 时,最佳粒径为 165nm 左右,粒径收率为 40.01%,载药量为 0.12%。该粒子为表面呈球形的纳米粒子,包封的 PTX 呈无定形态而不是结晶态。PTX 通过 O H 和 CO 基团与玉米醇溶蛋白和多糖相互作用,具有缓释作用。结果表明,新型两亲聚合物可能是一种有前途的 PTX 给药载体,并且茶多糖在药物传递系统中表现出其功能。