State Key Laboratory of Medicinal Chemical Biology, Tianjin Key Laboratory of Biosensing and Molecular Recognition, Research Centre for Analytical Sciences, College of Chemistry, Nankai University, Tianjin 300071, People's Republic of China.
J Med Chem. 2023 Nov 23;66(22):15370-15379. doi: 10.1021/acs.jmedchem.3c01479. Epub 2023 Nov 14.
A DNA-functionalized porphyrinic MOF (porMOF) drug delivery system was successfully constructed. porMOF as a photosensitizer and drug delivery carrier can integrate photodynamic therapy (PDT) and chemotherapy. Via the strong coordination interaction between the zirconium cluster of porMOF and the terminal phosphate group of DNA, the stable modification of the DNA layer on the porMOF surface is achieved. Meanwhile, the introduction of C/G-rich base pairs into the DNA double-stranded structure provides more binding sites of chemotherapeutic drug doxorubicin (DOX). AS1411, an aptamer of nucleolin proteins that are overexpressed by cancer cells, is introduced in the double-stranded terminal, which can endow the nanosystem with the ability to selectively recognize cancer cells. C-rich sequences in DNA double strands form an i-motif structure under acidic conditions to promote the highly efficient release of DOX in cancer cells. and experiments demonstrate that the synergistic PDT/chemotherapy modality achieves highly efficient cancer cell killing and tumor ablation without undesirable side effects.
成功构建了一种 DNA 功能化卟啉 MOF(porMOF)药物传递系统。porMOF 作为光敏剂和药物载体,可将光动力疗法(PDT)和化学疗法相结合。通过 porMOF 中的锆簇与 DNA 末端磷酸基团之间的强配位相互作用,实现了 DNA 层在 porMOF 表面的稳定修饰。同时,将富含 C/G 的碱基对引入 DNA 双链结构中,为化疗药物阿霉素(DOX)提供了更多的结合位点。双链末端引入了核仁蛋白的适体 AS1411,使纳米系统具有选择性识别癌细胞的能力。在酸性条件下,DNA 双链中的 C-丰富序列形成 i-motif 结构,促进 DOX 在癌细胞中的高效释放。体外和体内实验证明,协同 PDT/化疗方式可高效杀死癌细胞并消融肿瘤,而无不良副作用。