Song Steven, Hao Yuzhi, Yang Xiaoyan, Patra Prabir, Chen Jie
J Nanosci Nanotechnol. 2016 Mar;16(3):2582-6. doi: 10.1166/jnn.2016.12349.
Nanotechnology is an emerging paradigm for creating functional nanoscale materials for various biomedical applications. In this study, a new nanotechnology-based drug delivery method was developed using gold nanoparticles (GNPs) as a delivery vehicle to reduce adverse drug side effects. Fludarabine Phosphate is a commercial chemotherapy drug used in cancer treatment, and has ability to kill various cancer cells. KG-1 cell, a type of acute cancer leukemia cell, was selected as a proof-of-concept target in this study. Due to the small size of GNPs, they can help Fludarabine Phosphate enter cancer cells more efficiently and better interfere with DNA synthesis in the cancer cells. To enhance targeting ability, folic acid molecules were also covalently linked to GNPs, resulting in GNP-Fludarabine-folic acid (GNP-F/f). Compared to treatments with GNP-F or drugs on its own (Fludarabine Phosphate), the GNP-F/f achieves much improved cell-killing effects. The UV-Vis spectra results also revealed that the drugs had successfully bonded covalently to the GNPs. The higher cell-killing efficiency of GNP-F/f compared with GNP-Fludarabine (GNP-F) or drugs on their own further validates the effectiveness of both the vectors (GNPs) and folic acid in enhancing the drug delivery to the cancer cells. The MTT viability tests showed that the GNPs had no cytotoxicity.
纳米技术是一种新兴的范例,用于为各种生物医学应用创建功能性纳米级材料。在本研究中,开发了一种基于纳米技术的新型药物递送方法,使用金纳米颗粒(GNPs)作为递送载体以减少药物的不良副作用。氟达拉滨磷酸盐是一种用于癌症治疗的商业化疗药物,具有杀死各种癌细胞的能力。KG-1细胞,一种急性癌性白血病细胞,在本研究中被选为概念验证靶点。由于金纳米颗粒尺寸小,它们可以帮助氟达拉滨磷酸盐更有效地进入癌细胞,并更好地干扰癌细胞中的DNA合成。为了增强靶向能力,叶酸分子也共价连接到金纳米颗粒上,得到金纳米颗粒-氟达拉滨-叶酸(GNP-F/f)。与单独使用GNP-F或药物(氟达拉滨磷酸盐)治疗相比,GNP-F/f实现了大大提高的细胞杀伤效果。紫外-可见光谱结果还表明,药物已成功地共价结合到金纳米颗粒上。与金纳米颗粒-氟达拉滨(GNP-F)或单独的药物相比,GNP-F/f更高的细胞杀伤效率进一步验证了载体(金纳米颗粒)和叶酸在增强药物向癌细胞递送方面的有效性。MTT活力测试表明,金纳米颗粒没有细胞毒性。