Biomedical Department, Engineering Facility, Baskent UniversityAnkara, Turkey; Department of Electrical and Computer Engineering, Duke University, Pratt School of Engineering, Durham, NC, USA.
Department of Dermatology, Duke University, School of Medicine, Durham, NC, USA.
Int J Biol Macromol. 2023 Aug 1;245:125215. doi: 10.1016/j.ijbiomac.2023.125215. Epub 2023 Jun 5.
Incidence of various cancers including melanoma continues to rise worldwide. While treatment options have expanded in the recent years, the benefit of these treatments suffer from short period of duration for many patients. Hence, new treatment options are highly desired. Here, we propose a method combining a Dextran/reactive-copolymer/AgNPs nanocomposite and a harmless visible light approach to obtain a plasma substitute carbohydrate-based nanoproduct (D@AgNP) that shows strong antitumor activity. Light-driven polysaccharide-based nanocomposite provided essential conditions for extra small (8-12nm) AgNPs capping with subsequent specific self-assembly into spherical-like cloud nanostructures. Obtained biocompatible D@AgNP are stable over six months at room temperature and demonstrated absorbance peak at 406 nm. New formulated nanoproduct revealed efficient anticancer properties against A375 with IC50 0.0035 mg/mL following 24-h incubation; complete cell death is achieved at 0.001 mg/mL and 0.0005 mg/mL by 24- and 48-h time points, respectively. SEM examination shows that D@AgNP altered the shape of the cell structure and damaged the cell membrane. TEM finding shows that D@AgNP are mostly localized at vesicles such as the endosomes, lysosomes and mitochondria. It is anticipated that the introduced new method serves as the cornerstone for improving the generation of biocompatible hydrophilic carbohydrate-based anticancer drugs.
包括黑色素瘤在内的各种癌症的发病率在全球范围内持续上升。虽然近年来治疗选择有所扩大,但许多患者的治疗效果都受益于治疗持续时间短。因此,非常需要新的治疗选择。在这里,我们提出了一种方法,将葡聚糖/反应性共聚物/AgNPs 纳米复合材料与无害的可见光方法结合起来,获得一种等离子体替代物碳水化合物纳米产品(D@AgNP),它具有很强的抗肿瘤活性。光驱动的多糖基纳米复合材料为后续的特异性自组装成球状云纳米结构提供了超小(8-12nm)AgNPs 封端的必要条件。获得的生物相容性 D@AgNP 在室温下稳定六个月以上,并且在 406nm 处显示出吸收峰。新配方的纳米产品在 24 小时孵育后对 A375 具有有效的抗癌特性,IC50 为 0.0035mg/mL;在 24 和 48 小时时,分别达到 0.001mg/mL 和 0.0005mg/mL 的完全细胞死亡。SEM 检查显示,D@AgNP 改变了细胞结构的形状并破坏了细胞膜。TEM 发现表明,D@AgNP 主要定位于内体、溶酶体和线粒体等囊泡中。预计所提出的新方法将成为改善生物相容性亲水性碳水化合物抗癌药物生成的基石。