Hydrotropic polymer-based paclitaxel-loaded self-assembled nanoparticles: preparation and biological evaluation
作者:Lipeng Gao、Liefang Gao、Mingxue Fan、Qilong Li、Jiyu Jin、Jing Wang、Weiyue Lu、Lei Yu、Zhiqiang Yan、Yiting Wang
DOI:10.1039/c7ra04563h
日期:——
The poor compatibility of carrier materials with drugs is one of the main obstacles in the drug encapsulation of nano-drug delivery system (NDDS), hindering the clinical translation of NDDS. In this study, using paclitaxel (PTX) as the insoluble model drug, we conjugated N,N-diethylniacinamide (DENA), a hydrotropic agent of PTX, to the backbone of poly(L-γ-glutamyl-glutamine) (PGG), a water-soluble
载体材料与药物的相容性差是纳米药物递送系统(NDDS)的药物封装中的主要障碍之一,从而阻碍了NDDS的临床翻译。在这项研究中,使用紫杉醇(PTX)作为不溶性模型药物,我们将PTX的亲水剂N,N-二乙基烟酰胺(DENA)与聚(L -γ-谷氨酰胺-谷氨酰胺)(PGG)的骨架缀合,水溶性聚合物,以制备“水溶聚合物” PGG-DENA,以提高其与PTX的相容性。凭借DENA基团的水溶作用,PTX被PGG-DENA封装,从而得到水溶聚合物纳米颗粒(PGG-DENA / PTX NPs)。PTX共轭聚(L先前报道的-γ-谷氨酰胺-谷氨酰胺酸(PGG-PTX)NP被用作研究的对照。PGG–DENA / PTX NPs的z平均流体动力学直径约为70 nm,并且在PBS溶液中4°C时具有良好的长期稳定性。PGG-DENA / PTX NPs在96 h时PTX的累积释放率为79.10%,而PGG-PTX NPs的PTX累积释放率为22