School of Biological and Medical Engineering and ‡School of Chemistry and Chemical Engineering, Hefei University of Technology , Hefei, Anhui 230009, P.R. China.
ACS Appl Mater Interfaces. 2017 Dec 6;9(48):41782-41793. doi: 10.1021/acsami.7b15780. Epub 2017 Nov 22.
Large-size-induced long-term retention in the body has hampered the translational applications of many reported nanomedicines. Herein, we reported a multifunctional theranostic agent composed of ultrasmall poly(acrylic acid)-functionalized NiSe nanoparticles (PAA-NiSe NPs), which were successfully obtained through a facile ambient aqueous precipitation strategy. Without exhibiting any noticeable toxicity, the as-prepared PAA-NiSe NPs (average diameter of 6.40 ± 1.89 nm) showed considerable absorption in near-infrared (NIR) region and high photothermal conversion efficiency of 54.06%, which could induce remarkable photoacoustic signals for tumor imaging and heat for localized ablation of cancerous cells upon exposure to NIR light. Notably, the ultrasmall PAA-NiSe NPs, unlike conventional nanomaterials with larger sizes, showed reasonable body clearance within 8 h after intravenous injection. Furthermore, ascribed to protonation process of amino groups in DOX molecules and carboxyl groups in PAA molecules in an acidic microenvironment, the drug-loaded (doxorubicin hydrochloride, DOX·HCl) PAA-NiSe NPs (PAA-NiSe-DOX NPs) revealed promoted drug release at acidic pH, which could be useful for acidic tumor microenvironment responsive drug delivery. Evident from the results of cell-killing assay in vitro and tumor treatment study in vivo, PAA-NiSe-DOX NPs exhibited evident synergistic effects on killing 4T1 breast cancer cells. Thus, this study presents a multifunctional theranostic agent composed of ultrasmall PAA-NiSe NPs for potential cancer treatment without long-term toxicity concerns.
大尺寸导致的长期体内滞留阻碍了许多已报道的纳米医学的转化应用。在此,我们报道了一种多功能治疗剂,由超小的聚(丙烯酸)功能化 NiSe 纳米粒子(PAA-NiSe NPs)组成,该纳米粒子是通过简便的环境水相沉淀策略成功获得的。所制备的 PAA-NiSe NPs(平均直径为 6.40 ± 1.89nm)在近红外(NIR)区域具有相当的吸收能力和 54.06%的高光热转换效率,在暴露于 NIR 光时可产生显著的光声信号,用于肿瘤成像和局部消融癌细胞的热量。值得注意的是,与传统的大尺寸纳米材料不同,超小的 PAA-NiSe NPs 在静脉注射后 8 小时内表现出合理的体内清除率。此外,由于 DOX 分子中的氨基和 PAA 分子中的羧基在酸性微环境中的质子化过程,载药(盐酸多柔比星,DOX·HCl)的 PAA-NiSe NPs(PAA-NiSe-DOX NPs)在酸性 pH 下显示出促进的药物释放,这对于酸性肿瘤微环境响应性药物输送可能是有用的。从体外细胞杀伤实验和体内肿瘤治疗研究的结果来看,PAA-NiSe-DOX NPs 对杀死 4T1 乳腺癌细胞表现出明显的协同作用。因此,本研究提出了一种由超小 PAA-NiSe NPs 组成的多功能治疗剂,用于潜在的癌症治疗,而不会引起长期毒性问题。