Shano Leon Bernet, Karthikeyan Subramani, Kennedy Lourdusamy John, Chinnathambi Shanmugavel, Pandian Ganesh N
Department of Physics, School of Advanced Sciences, Vellore Institute of Technology (VIT), Chennai, Tamil Nadu, India.
Centre for Healthcare Advancement, Innovation and Research, Vellore Institute of Technology (VIT), Chennai, Tamil Nadu, India.
Front Bioeng Biotechnol. 2024 Jun 13;12:1397804. doi: 10.3389/fbioe.2024.1397804. eCollection 2024.
Metal-organic frameworks (MOFs) have emerged as promising nanocarriers for cancer treatment due to their unique properties. Featuring high porosity, extensive surface area, chemical stability, and good biocompatibility, MOFs are ideal for efficient drug delivery, targeted therapy, and controlled release. They can be designed to target specific cellular organelles to disrupt metabolic processes in cancer cells. Additionally, functionalization with enzymes mimics their catalytic activity, enhancing photodynamic therapy and overcoming apoptosis resistance in cancer cells. The controllable and regular structure of MOFs, along with their tumor microenvironment responsiveness, make them promising nanocarriers for anticancer drugs. These carriers can effectively deliver a wide range of drugs with improved bioavailability, controlled release rate, and targeted delivery efficiency compared to alternatives. In this article, we review both experimental and computational studies focusing on the interaction between MOFs and drug, explicating the release mechanisms and stability in physiological conditions. Notably, we explore the relationship between MOF structure and its ability to damage cancer cells, elucidating why MOFs are excellent candidates for bio-applicability. By understanding the problem and exploring potential solutions, this review provides insights into the future directions for harnessing the full potential of MOFs, ultimately leading to improved therapeutic outcomes in cancer treatment.
金属有机框架材料(MOFs)因其独特的性质已成为癌症治疗中颇具前景的纳米载体。MOFs具有高孔隙率、大比表面积、化学稳定性和良好的生物相容性,是高效药物递送、靶向治疗和控释的理想选择。它们可以被设计成靶向特定的细胞器,以破坏癌细胞中的代谢过程。此外,用酶进行功能化可模拟其催化活性,增强光动力疗法并克服癌细胞的凋亡抗性。MOFs可控且规则的结构以及它们对肿瘤微环境的响应性,使其成为抗癌药物颇具前景的纳米载体。与其他载体相比,这些载体能够有效递送多种药物,提高生物利用度、控制释放速率并提高靶向递送效率。在本文中,我们综述了聚焦于MOFs与药物相互作用的实验研究和计算研究,阐明了其在生理条件下的释放机制和稳定性。值得注意的是,我们探讨了MOF结构与其损伤癌细胞能力之间的关系,阐明了为什么MOFs是生物适用性的优秀候选者。通过了解问题并探索潜在解决方案,本综述为充分发挥MOFs的全部潜力提供了未来方向的见解,最终改善癌症治疗的疗效。