Rungnim Chompoonut, Rungrotmongkol Thanyada, Poo-Arporn Rungtiva P
National Nanotechnology Center (NANOTEC), National Science and Technology Development Agency (NSTDA), Pathum Thani 12120, Thailand.
Structural and Computational Biology Research Group, Department of Biochemistry, Faculty of Science, Chulalongkorn University, Bangkok 10330, Thailand; Ph.D. Program in Bioinformatics and Computational Biology, Faculty of Science, Chulalongkorn University, Bangkok 10330, Thailand.
J Mol Graph Model. 2016 Nov;70:70-76. doi: 10.1016/j.jmgm.2016.09.011. Epub 2016 Sep 21.
In the present study, we describe here the pH condition activating doxorubicin (DOX) anticancer drugs loading and release over single-wall carbon nanotube (SWNT) non-covalently wrapped with chitosan (CS). The possibility of drug displacement on DOX/CS/SWNT nanocarrier was investigated using molecular dynamics simulations. The drug loading and release were monitored via displacement analysis and binding energy calculations. The simulated results clearly showed that the drugs well interacted with the CS/SWNT at physiological pH (pH 7.4), where CS was in the deprotonated form. Contrastingly, in weakly acidic environments (pH 5.0-6.5) which is a pH characteristics of certain cancer environments, the protonated CS became loosen wrapped around the SWNT and triggered drugs release as a result of charge-charge repulsion between CS and drug molecules. The obtained data fulfil the understanding at atomic level of drug loading and release controlled by pH-sensitive polymer, which might be useful for further cancer therapy researches.
在本研究中,我们在此描述了激活阿霉素(DOX)抗癌药物在壳聚糖(CS)非共价包裹的单壁碳纳米管(SWNT)上负载和释放的pH条件。使用分子动力学模拟研究了DOX/CS/SWNT纳米载体上药物置换的可能性。通过置换分析和结合能计算监测药物的负载和释放。模拟结果清楚地表明,在生理pH(pH 7.4)下,药物与CS/SWNT良好相互作用,此时CS呈去质子化形式。相反,在某些癌症环境的pH特征的弱酸性环境(pH 5.0 - 6.5)中,质子化的CS围绕SWNT的包裹变得松散,并由于CS与药物分子之间的电荷 - 电荷排斥而触发药物释放。所获得的数据实现了对由pH敏感聚合物控制的药物负载和释放的原子水平的理解,这可能对进一步的癌症治疗研究有用。