Molecular Imaging Innovations Institute, Department of Radioloy, Weill Cornell Medicine, 413 East 69th Street Box 290, New York, NY, 10021, USA.
Macromol Rapid Commun. 2017 Oct;38(20). doi: 10.1002/marc.201700366. Epub 2017 Sep 12.
DNA nanostructures largely rely on pairing DNA bases; thus, sequence designing is required. Here, this study demonstrates a sequence-independent strategy to fabricate DNA nanogel (NG) inspired by cisplatin, a chemotherapeutic drug that acts as a DNA crosslinker. A simple heating and cooling of the genomic DNA extracts and cisplatin produces DNA NG with a size controlled by the heating time. Furthermore, the drug-loaded NG is formulated by spontaneously mixing DNA segments, cisplatin, and doxorubicin. The in vitro cell studies demonstrate that the doxorubicin-loaded NG alters the drug distribution in cells while its cytotoxic potential is well-maintained. This chemotherapeutic-inspired method provides a facile one-pot and cost-effective strategy to fabricate size-controllable DNA NG that potentially acts as drug carrier.
DNA 纳米结构在很大程度上依赖于 DNA 碱基的配对;因此,需要进行序列设计。在本研究中,我们展示了一种序列无关的策略,受顺铂(一种作为 DNA 交联剂的化疗药物)的启发来制备 DNA 纳米凝胶 (NG)。通过简单地加热和冷却基因组 DNA 提取物和顺铂,可以在加热时间控制下生成具有特定尺寸的 DNA NG。此外,通过自发混合 DNA 片段、顺铂和阿霉素,可以制备载药的 NG。体外细胞研究表明,载阿霉素的 NG 改变了药物在细胞内的分布,同时保持了其细胞毒性潜力。这种受化疗启发的方法提供了一种简便的一锅法和具有成本效益的策略,可以制备尺寸可控的 DNA NG,有望作为药物载体。