Kim Kibeom, Chejara Mamta Ramgopal, Yoon Been, Park Myoung-Hwan
Department of Chemistry and Life Science, Sahmyook University Seoul 01795 South Korea
Department of Convergence Science, Sahmyook University Seoul 01795 South Korea.
RSC Adv. 2024 Aug 28;14(37):27385-27393. doi: 10.1039/d4ra06051b. eCollection 2024 Aug 22.
Gold nanorods (GNRs) have received much attention as potential drug-delivery vehicles because of their various advantages such as good biocompatibility, passive targeting, responsiveness to stimuli, and easy post-functionalization by surface modification. However, the drug structure might be changed for loading into GNRs, making it difficult to load various drugs, and the space to contain drugs is small, making it difficult to deliver sufficient drugs required for treatment compared with other porous materials. Herein, we report an amphiphilic polymer-coated GNR platform for chemo- and photothermal combination therapy. Amphiphilic polymers comprise hydrophobic alkyl chains for drug encapsulation, polyethylene glycol for biocompatibility, and folic acid for cancer targeting. GNRs generate heat energy under near-infrared light irradiation, promoting controlled drug release, and inducing cellular uptake by deforming the cell membrane. On-demand release behavior was traced with Nile red, and targeting and delivery efficiency were confirmed with paclitaxel through cellular experiments. This GNR-based platform enables combination therapy with passive and active targeting to enhance the efficacy of cancer treatment.
金纳米棒(GNRs)作为潜在的药物递送载体受到了广泛关注,因为它们具有多种优势,如良好的生物相容性、被动靶向性、对刺激的响应性以及通过表面修饰易于进行后功能化。然而,为了装载到GNRs中,药物结构可能会发生变化,这使得难以装载各种药物,并且容纳药物的空间较小,与其他多孔材料相比,难以递送治疗所需的足够药物。在此,我们报道了一种用于化疗和光热联合治疗的两亲性聚合物包覆的GNR平台。两亲性聚合物包括用于药物包封的疏水烷基链、用于生物相容性的聚乙二醇以及用于癌症靶向的叶酸。GNRs在近红外光照射下产生热能,促进药物的可控释放,并通过使细胞膜变形诱导细胞摄取。用尼罗红追踪按需释放行为,并通过细胞实验用紫杉醇确认靶向和递送效率。这种基于GNR的平台能够实现被动和主动靶向的联合治疗,以提高癌症治疗的疗效。