College of Pharmacy, The Ohio State University, Columbus, OH 43210, USA.
Int J Oncol. 2010 Jul;37(1):177-85. doi: 10.3892/ijo_00000665.
The purpose of this work was to assess synergistic inhibitory responses of a novel chemopreventive combination regimen of drugs namely, aspirin in combination with calcium and folic acid on two human colon cancer cell lines, HT-29 and SW-480. Subsequently, based on positive responses, nanotechnology-based formulations were developed for the targeted delivery of these combinatorial regimens to the colon for the chemoprevention of colon cancer. Additionally, conventional drug formulations using controlled release polymers chitosan, pectin and hydroxypropyl methylcellulose (HPMC) were tested for release of the drugs, for comparison purposes. Chemopreventive combination regimens demonstrated significant synergistic efficacy in both cell lines from XTT assay studies, when compared to the effects of individual agents. Approximately 45% decrease in cell viability for aspirin (15 mM) and calcium (30 mM) mixtures was observed in HT-29 cell lines, compared to approximately 55% decrease by the same combination in SW-480 cell lines. With combinations of aspirin (5 mM) and folic acid (1.5 mM), HT-29 cells demonstrated a 30% decrease in cell viability compared to approximately 38% decrease in the SW-480 cell line. Overall, all drug combinations demonstrated significant synergistic responses in the cell lines tested with the SW-480 cell line being more significantly affected by the drug regimens than the HT-29 cell line. Drug encapsulated nanoparticles demonstrated a spherical morphology, <125 nm average particle size (aspirin and folic acid) of nanoparticles and encapsulation efficiencies in the range of 80-91%. Drug release from nanoparticles was controlled with approximately 60% of the original amount released over a 96 h period. Conventional formulations exhibited faster kinetics of drug release when compared to the PLGA nanoparticles. Overall, the cell line studies demonstrate, for the first time, the ability of novel chemopreventive combinations to inhibit the growth of colon cancer cells whereas the nanotechnology-based drug delivery system provides valuable evidence for targeted therapy towards colon cancer chemoprevention.
这项工作的目的是评估一种新的化学预防联合用药方案的协同抑制反应,该方案由阿司匹林与钙和叶酸联合组成,针对两种人结肠癌细胞系 HT-29 和 SW-480。随后,基于阳性反应,开发了基于纳米技术的制剂,用于将这些组合方案靶向递送到结肠,以预防结肠癌。此外,还测试了使用控释聚合物壳聚糖、果胶和羟丙基甲基纤维素 (HPMC) 的常规药物制剂,以比较药物的释放情况。化学预防联合方案在 XTT 测定研究中与单个药物相比,在两种细胞系中均显示出显著的协同疗效。在 HT-29 细胞系中,阿司匹林(15mM)和钙(30mM)混合物的细胞活力降低了约 45%,而在 SW-480 细胞系中,相同组合的细胞活力降低了约 55%。在阿司匹林(5mM)和叶酸(1.5mM)的组合中,HT-29 细胞的细胞活力降低了 30%,而 SW-480 细胞系的细胞活力降低了约 38%。总体而言,所有药物组合在测试的细胞系中均表现出显著的协同反应,SW-480 细胞系受药物方案的影响比 HT-29 细胞系更为显著。药物包封的纳米粒子表现出球形形态,<125nm 的平均粒径(阿司匹林和叶酸)和 80-91%的包封效率。纳米粒子的药物释放受到控制,在 96 小时内释放约 60%的原始药物量。与 PLGA 纳米粒子相比,常规制剂表现出更快的药物释放动力学。总体而言,细胞系研究首次证明了新型化学预防联合用药方案抑制结肠癌细胞生长的能力,而基于纳米技术的药物传递系统为结肠癌化学预防的靶向治疗提供了有价值的证据。