Department of Chemistry, Indian Institute of Technology, Kharagpur, W. B, 721302, India.
J Mater Sci Mater Med. 2010 May;21(5):1587-97. doi: 10.1007/s10856-010-3998-4. Epub 2010 Jan 29.
The development of smart targeted nanoparticle that can deliver drugs to direct cancer cells, introduces better efficacy and lower toxicity for treatment. We report the development and characterizations of pH-sensitive carboxymethyl chitosan modified folic acid nanoparticles and manifest their feasibility as an effective targeted drug delivery vehicle. The nanoparticles have been synthesized from carboxymethyl chitosan with covalently bonded bifunctional 2,2'-(ethylenedioxy)-bis-(ethylamine) (EDBE) through the conjugation with folic acid. The conjugation has been analyzed by Fourier transform infrared spectroscopy and nuclear magnetic resonance spectroscopy. The resultant nanoparticles with an average size less then 200 nm measured by dynamic light scattering and transmission electron microscopy. Confocal microscopy and flow cytometric analysis have revealed that folate-mediated targeting significantly enhances the cellular uptake of the nanoparticle and thus facilitates apoptosis of cancer cells (HeLa, B16F1). For the application of the nanoparticles as a drug carrier, Doxorubicin a potent anticancer drug has been loaded into the nanoparticles, with the drug loading amount and the drug release pattern observed.
智能靶向纳米粒子的发展可以将药物直接递送到癌细胞,从而提高治疗效果,降低毒性。我们报告了 pH 敏感的羧甲基壳聚糖修饰的叶酸纳米粒子的开发和特性,并证明了它们作为有效靶向药物传递载体的可行性。纳米粒子是通过羧甲基壳聚糖与双功能 2,2'-(乙二氧基)-双-(乙胺)(EDBE)的共价键合,与叶酸偶联合成的。通过傅里叶变换红外光谱和核磁共振波谱对偶联进行了分析。通过动态光散射和透射电子显微镜测量,得到了平均粒径小于 200nm 的纳米粒子。共焦显微镜和流式细胞术分析表明,叶酸介导的靶向作用显著增强了纳米粒子的细胞摄取,从而促进了癌细胞(HeLa、B16F1)的凋亡。为了将纳米粒子应用于药物载体,将一种有效的抗癌药物阿霉素载入纳米粒子中,观察了药物的载药量和释放模式。