a Key Laboratory of Forest Plant Ecology , Northeast Forestry University, Ministry of Education , Harbin , China.
b College of Life Science , Northeast Forestry University , Harbin , China.
Artif Cells Nanomed Biotechnol. 2019 Dec;47(1):154-165. doi: 10.1080/21691401.2018.1548468.
This work investigated the preparation of specific targeted drug delivery systems in cancer chemotherapy by folate conjugated human serum albumin nanoparticles encapsulated resveratrol (RES) nanoparticles (FA-HSA-RESNPs). FA was coupled to HSA, and RES was encapsulated in FA-conjugated HSA by high pressure fluid nano-homogeneous emulsification. The average particle size and polydispersity index of NPs prepared under optimal conditions were 102.1 ± 4.9 nm and 0.001. The drug capsulation efficiency and drug loading efficiency were 98.36 and 14.66%, respectively. The analysis of the results of the physical characterization showed that the RES was present in the FA-HSA-RESNPs in an amorphous state. In vitro drug-release study showed that the NPs can release the drug persistently and slowly. The inhibition rate of FA-HSA-RESNPs and RES was detected using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-2H-tetrazolium bromide method to be 110.8 and 157.2 μM, respectively. The targeting ability of the FA-HSA-RESNPs for the HepG2 cell was measured by fluorescein isothiocyanate-modified albumin techniques. The uptake rate of FA-HSA-RESNPs was higher than that of the original RES. By using near-infrared imaging, in vivo activity was labeled with Cy5 fluorescent FA-HSA-RESNP confirmed FA-HSA-RESNP tumor-targeting ability. The intravenous administration bioavailability of FA-HSA-RESNPs was about 5.95-fold higher than that of the original RES.
本研究通过叶酸偶联人血清白蛋白纳米粒包载白藜芦醇纳米粒(FA-HSA-RESNPs)制备了用于癌症化疗的靶向药物传递系统。FA 与 HSA 偶联,RES 通过高压流体纳米均相乳化法包载于 FA 修饰的 HSA 中。在最佳条件下制备的 NPs 的平均粒径和多分散指数分别为 102.1±4.9nm 和 0.001。药物包封效率和载药效率分别为 98.36%和 14.66%。物理特性分析结果表明,RES 以无定形状态存在于 FA-HSA-RESNPs 中。体外药物释放研究表明,NPs 可以持续缓慢地释放药物。采用 3-(4,5-二甲基噻唑-2-基)-2,5-二苯基-2H-四唑溴盐法检测 FA-HSA-RESNPs 和 RES 的抑制率,分别为 110.8 和 157.2μM。通过荧光素异硫氰酸酯修饰白蛋白技术测量 FA-HSA-RESNPs 对 HepG2 细胞的靶向能力。FA-HSA-RESNPs 的摄取率高于原 RES。通过近红外成像,用 Cy5 荧光 FA-HSA-RESNP 标记体内活性,证实了 FA-HSA-RESNP 的肿瘤靶向能力。FA-HSA-RESNPs 的静脉注射生物利用度约为原 RES 的 5.95 倍。