Hsu Y Y, Hao T, Hedley M L
Zycos, Inc., Cambridge, MA 02138, USA.
J Drug Target. 1999 Dec;7(4):313-23. doi: 10.3109/10611869909085514.
Poly(D,L-lactic-co-glycolic) acid (PLGA) microspheres containing plasmid DNA encoding the firefly luciferase gene were prepared using the water-in-oil-in-water (w/o/w) double emulsion and solvent evaporation method. In this study, we investigated the effects of three process parameters on DNA microencapsulation: (1) emulsification method used to generate the primary emulsion, (2) water/oil ratio during formation of the first emulsion, and (3) surfactant concentration used in the preparation of the second emulsion. The resulting formulations were also analyzed for microsphere size, encapsulation efficiency, and kinetics of DNA release. We found that although each process alteration resulted in encapsulation of biologically active, structurally intact DNA, the surfactant and water/oil ratio significantly affected the size, release kinetics and encapsulation efficiency of plasmid DNA.
采用水包油包水(w/o/w)双乳液和溶剂蒸发法制备了含有编码萤火虫荧光素酶基因的质粒DNA的聚(D,L-乳酸-共-乙醇酸)(PLGA)微球。在本研究中,我们研究了三个工艺参数对DNA微囊化的影响:(1)用于生成初级乳液的乳化方法,(2)第一乳液形成过程中的水/油比,以及(3)第二乳液制备中使用的表面活性剂浓度。还对所得制剂的微球大小、包封效率和DNA释放动力学进行了分析。我们发现,虽然每个工艺改变都导致了生物活性、结构完整的DNA的包封,但表面活性剂和水/油比对质粒DNA的大小、释放动力学和包封效率有显著影响。