Nanomedicine (Lond). 2015 Nov;10(22):3373-89. doi: 10.2217/nnm.15.123.
To develop Finasteride-loaded self micro-emulsifying drug delivery systems (SMEDDS) for the treatment of hormonal associated problems.
MATERIALS & METHODS: Ternary phase diagrams were constructed to obtain self-emulsification regions. Multivariate statistical methods viz. Principal component analysis and agglomerative hierarchy clustering analysis were used to evaluate the microemulsions stability. In vitro redispersibility study was adopted and two formulations were selected for spray-drying. Further investigations were performed (Fourier transform infrared, x-ray diffraction and transmission electron microscopy). Finally, the in vivo performance was tested in human volunteers.
Multivariate statistical methods selected stable SMEDDS. Spray-drying utilizing maltodextrin/leucin carrier system yielded a flowable product. Selected solid SMEDDS scored 129.35% relative bioavailability compared with a commercial tablet.
The developed SMEDDS poses successful platform for glucosteroid analogs oral delivery.
开发用于治疗激素相关问题的非那雄胺负载自微乳药物传递系统 (SMEDDS)。
构建三元相图以获得自乳化区域。采用多元统计方法,如主成分分析和凝聚层次聚类分析,来评估微乳液的稳定性。采用体外再分散性研究,并选择两种制剂进行喷雾干燥。进一步进行傅里叶变换红外、X 射线衍射和透射电子显微镜研究。最后,在人体志愿者中测试体内性能。
多元统计方法选择了稳定的 SMEDDS。利用麦芽糊精/亮氨酸载体系统进行喷雾干燥可得到可流动的产品。与市售片剂相比,所选固体 SMEDDS 的相对生物利用度为 129.35%。
所开发的 SMEDDS 为糖皮质激素类似物的口服递送提供了成功的平台。