Sankarakumar Niranjani, Tong Yen Wah
Department of Chemical & Biomolecular Engineering, National University of Singapore, Singapore.
J Mater Chem B. 2013 Apr 21;1(15):2031-2037. doi: 10.1039/c3tb00009e. Epub 2013 Mar 8.
Infectious diseases caused by viruses are among the most vexing medical issues that we are yet to solve, even with billions of dollars being spent on drugs and vaccines to combat and prevent such infections. Finding a cure or vaccine for some of the most common or the most deadly viruses such as the influenza or the Ebola virus has been a daunting task due to their constant mutation and adaptation to our attempts. Existing therapeutics that lose their effectiveness with time due to mutations have brought about the need to consider alternative treatment approaches. To cater to the ever-increasing demand for new antiviral strategies, a novel approach of using high affinity polymeric receptors prepared by a molecular imprinting technique to "catch" viruses is presented. After three hours of mixing with the template virus, a very significant reduction in infectivity titers was observed with the virus imprinted particles. The virucidal action of the imprinted particles was rapid, dose dependent on virus and polymer concentration and occurred due to specific adsorption. The fabricated nanoparticles displayed remarkable positive anti-viral results that significantly hindered viral infections as compared to the controls. This work thus successfully demonstrates the application of miniemulsion polymerization to surface imprinting of viruses and the novel application of such imprinted materials in infectious disease treatment. The findings represent a significant breakthrough in the field of molecular imprinting and antiviral therapy and we anticipate this work to be a starting point for path-breaking research in the near future.
由病毒引起的传染病是我们尚未解决的最棘手的医学问题之一,即便已投入数十亿美元用于研发对抗和预防此类感染的药物及疫苗。由于流感病毒或埃博拉病毒等一些最常见或最致命病毒不断变异并适应我们的应对措施,为其找到治愈方法或疫苗一直是一项艰巨任务。因病毒变异致使现有疗法随时间推移失去效力,这就需要考虑采用替代治疗方法。为满足对抗病毒新策略日益增长的需求,本文提出一种利用分子印迹技术制备的高亲和力聚合物受体“捕获”病毒的新方法。与模板病毒混合三小时后,观察到病毒印迹颗粒的感染性滴度显著降低。印迹颗粒的杀病毒作用迅速,取决于病毒和聚合物浓度,且是由特异性吸附引起的。与对照相比,制备的纳米颗粒显示出显著的抗病毒效果,能有效阻碍病毒感染。因此,这项工作成功展示了微乳液聚合在病毒表面印迹中的应用以及此类印迹材料在传染病治疗中的新应用。这些发现代表了分子印迹和抗病毒治疗领域的重大突破,我们预计这项工作将成为在不久的将来开展开创性研究的起点。