摘要
利用离子凝胶法和超临界强制分散悬浮液(Sp EDS)技术制备具有核壳型结构的壳聚糖纳米粒(CS NPs)/聚乳酸-聚乙二醇-聚乳酸三嵌段共聚物(PLLA-PEG-PLLA)复合微粒,考察和优化了壳聚糖纳米粒和复合微粒的制备条件,并对二者的理化性质和细胞毒性进行研究。结果表明,壳聚糖纳米粒的制备优化条件为壳聚糖浓度2mg·ml-1、p H 5.0、三聚磷酸钠浓度1 mg·ml-1。溶剂/非溶剂比为复合微粒粒径的显著影响因素,复合微粒的制备优化条件为油相浓度5 mg·ml-1、水油比0.75:10.00、溶液流速2 ml·min-1、溶剂/非溶剂比0.5:1.0。优化条件制得的复合微粒粒径为323.7 nm,透射电镜(TEM)显示其具有核壳型结构。理化表征结果显示壳聚糖与三聚磷酸钠发生作用,但制备工艺前后材料官能团未发生明显变化,而且复合微粒中PLLA-PEG-PLLA晶型更加均匀;不同浓度组的CS NPs/PLLA-PEG-PLLA复合微粒(0.25、0.50和1.00-g·ml-1)的细胞相对增殖率分别为105.3%、101.9%和100.9%,细胞毒性分级为0级,表明具有核壳结构的CS NPs/PLLA-PEG-PLLA复合微粒生物相容性良好,有望进一步应用于共载基因和抗癌药物的抗癌活性研究。
The carriers with core-shell structure have been widely used in the field of co-loading gene and drug. In this study, chitosan(CS) nanoparticles(CS NPs)/poly(L-lactide)-poly(ethylene glycol)-poly(L-lactide) triblock copolymer(PLLA-PEG-PLLA) composite microparticles(MPs) with core-shell structure were prepared by the combination of ion gelation and suspension-enhanced dispersion by supercritical fluids(Sp EDS). The conditions for preparation of CS NPs and MPs were investigated and optimized, and the physicochemical properties and cytotoxicity of MPs were studied. The optimized condition for CS NPs were chitosan solution concentration of 2 mg·ml-1, chitosan solution p H of 5.0, and tripolyphosphate(TPP) solution concentration of 1 mg·ml-1. The ratio of solvent/non-solvent was the significant factor affecting sizes of MPs, and the optimized conditions for MPs were oil concentration of 5 mg·ml-1, W/O ratio of 0.75:10.00, solution flow rate of 2 ml·min-1 and solvent/non-solvent of 0.5:1.0. The MPs from optimized conditions had a size of 323.7 nm and the CS NPs were encapsulated in MPs, as observed by TEM. The results of experiments about physicochemical properties revealed that a reaction happened between CS and TPP. Little change occurred in the functional groups of materials used in the two processes, while the crystal forms of PLLA-PEG-PLLA in MPs were more uniform. The relative growth rates of Bcap-37 cells co-cultured with MPs with different concentrations of 0.25, 0.50 and 1.00 -g·ml-1 for 3 d were 105.3%, 101.9% and 100.9%, respectively. The above results demonstrated that the MPs with good biocompatibility could be used in the field of co-delivery for gene and antitumor drug to evaluate the antitumor effect and would achieve a good synergistic effect in the treatment of cancer.
出处
《化工学报》
EI
CAS
CSCD
北大核心
2015年第4期1565-1576,共12页
CIESC Journal
基金
国家自然科学基金项目(31470927
31170939
51103049)~~