Doolaanea Abd Almonem, Mansor Nur 'Izzati, Mohd Nor Nurul Hafizah, Mohamed Farahidah
Department of Pharmaceutical Technology, Faculty of Pharmacy, International Islamic University Malaysia (IIUM) , Kuantan , Malaysia .
J Microencapsul. 2014;31(6):600-8. doi: 10.3109/02652048.2014.898709. Epub 2014 Apr 3.
The aim of this study is to investigate the cell uptake of Nigella sativa oil (NSO)-PLGA microparticle by neuron-like PC-12 cells in comparison to surfactants; hydrophilic (Tween 80 & Triton X100) and hydrophobic (Span 80). Solvent evaporation was used to precisely control the size, zeta potential and morphology of the particle. The results revealed varying efficiencies of the cell uptake by PC-12 cells, which may be partially attributed to the surface hydrophobicity of the microparticles. Interestingly, the uptake efficiency of PC-12 cells was higher with the more hydrophilic microparticle. NSO microparticle showed evidence of being preferably internalised by mitotic cells. Tween 80 microparticle showed the highest cell uptake efficiency with a concentration-dependent pattern suggesting its use as uptake enhancer for non-scavenging cells. In conclusion, PC-12 cells can take up NSO-PLGA microparticle which may have potential in the treatment of neurodegenerative disease.
本研究的目的是研究与表面活性剂相比,黑种草籽油(NSO)-聚乳酸-羟基乙酸共聚物(PLGA)微粒被类神经元PC-12细胞摄取的情况;表面活性剂包括亲水性的(吐温80和曲拉通X100)和疏水性的(司盘80)。采用溶剂蒸发法精确控制微粒的大小、zeta电位和形态。结果显示PC-12细胞摄取的效率各不相同,这可能部分归因于微粒的表面疏水性。有趣的是,亲水性更强的微粒被PC-12细胞的摄取效率更高。NSO微粒显示出被有丝分裂细胞优先内化的证据。吐温80微粒显示出最高的细胞摄取效率,且呈浓度依赖性,表明其可用作非吞噬细胞的摄取增强剂。总之,PC-12细胞可以摄取NSO-PLGA微粒,这在神经退行性疾病的治疗中可能具有潜力。