College of Chemistry and Chemical Engineering, Postdoctoral Mobile Station of Basic Medical Science, Hengyang Medical College, University of South China, Hengyang 421001, Hunan, China.
Hunan Province Cooperative Innovation Center for Molecular Target New Drug Study, School of Pharmaceutical Science, University of South China, Hengyang 421001, Hunan, China.
Biomater Sci. 2023 Aug 8;11(16):5576-5589. doi: 10.1039/d3bm00495c.
Silver sulfide (AgS) nanoparticles (NPs) represent one of the most popular inorganic reagents for near-infrared (NIR) photothermal therapy (PTT). However, the extensive biomedical applications of AgS NPs are greatly compromised by the hydrophobicity of the NPs prepared in organic solvents, their low photothermal conversion efficiency, certain surface modification-induced damage to their intrinsic properties and short circulation time. To develop a facile yet efficient green approach to overcome these shortcomings for improved properties and performance of AgS NPs, we report herein the construction of AgS@polydopamine (PDA) nanohybrids a "one-pot" organic-inorganic hybridization strategy, which produces uniform AgS@PDA nanohybrids with well-modulated sizes in the range of 100-300 nm the self-polymerization of dopamine (DA) and subsequent synergistic assembly of PDA with AgS NPs in a three-phase mixed medium containing water, ethanol and trimethylbenzene (TMB). Integration of dual photothermal moieties, , AgS and PDA at a molecular level, endows AgS@PDA nanohybrids with synergistically enhanced NIR photothermal properties that are much better than those of either PDA or AgS NPs due to calculated combination indexes (CIs) of 0.3-0.7 between AgS NPs and PDA based on a modified Chou-Talalay method. Therefore, this study not only developed a facile "one-pot" green approach toward producing uniform AgS@PDA nanohybrids with well-modulated dimensions, but also revealed an unprecedented synergistic mechanism for organic/inorganic nanohybrids that is based on dual photothermal moieties providing enhanced near-infrared photothermal performance.
硫化银(AgS)纳米颗粒(NPs)是最受欢迎的近红外(NIR)光热治疗(PTT)的无机试剂之一。然而,由于在有机溶剂中制备的 NPs 的疏水性、低光热转换效率、某些表面修饰对其固有性质的损害以及短的循环时间,AgS NPs 的广泛生物医学应用受到了极大的限制。为了开发一种简便而有效的绿色方法来克服这些缺点,以改善 AgS NPs 的性能和性能,我们在此报告了 AgS@聚多巴胺(PDA)纳米杂化物的构建,这是一种“一锅法”的有机-无机杂化策略,该策略产生了尺寸均匀的 AgS@PDA 纳米杂化物,尺寸在 100-300nm 范围内可调。该策略利用多巴胺(DA)的自聚合和随后在水、乙醇和均三甲苯(TMB)三相混合介质中 PDA 与 AgS NPs 的协同组装。将双光热基团,AgS 和 PDA 整合到分子水平,赋予 AgS@PDA 纳米杂化物协同增强的 NIR 光热性能,由于基于改良的 Chou-Talalay 方法的计算组合指数(CI)为 0.3-0.7,因此优于 PDA 或 AgS NPs。因此,本研究不仅开发了一种简便的“一锅法”绿色方法来制备尺寸均匀的 AgS@PDA 纳米杂化物,而且还揭示了一种基于双光热基团的有机/无机纳米杂化物的协同机制,这种协同机制基于双光热基团提供增强的近红外光热性能。