ACS Appl Bio Mater. 2024 Jun 17;7(6):3796-3809. doi: 10.1021/acsabm.4c00171. Epub 2024 May 22.
Drug resistance and off-target toxicity are two of the greatest challenges to chemotherapeutic melanoma treatments. Nitric oxide (NO) represents an attractive alternative to conventional therapeutics due to its numerous anticancer properties and low probability of engendering resistance. As NO is highly reactive, macromolecular NO donors are needed for the controlled and targeted delivery of NO for therapeutic applications. Herein, mesoporous silica nanoparticles (MSNs) coated with hyaluronic acid (HA) were developed as a NO delivery system to facilitate controlled delivery to cancer cells through both passive and active targeting via the enhanced permeation and retention effect and directed binding of HA with CD44 receptors, respectively. The aminosilane modification, HA concentration, and HA molecular weight were systematically evaluated to facilitate the MSN coating and NO loading. The hydrodynamic diameter and dispersity of the nanoparticles increased after HA coating due to the hydrophilic nature of HA, with greater increases observed at higher HA molecular weight. Lower starting concentrations of HA and aminosilanes with longer alkyl chains favored more efficient HA coating. Faster NO-release kinetics and lower NO payloads were observed for the HA-coated MSNs relative to uncoated MSNs. However, the localized delivery of NO to cancer cells through the active targeting conferred by HA increased levels of oxidative stress and induced mitochondria-mediated apoptosis in melanoma cells. Cytotoxicity was also evaluated against human dermal fibroblasts, with the use of 6 kDa HA-coated MSNs resulting in the greatest therapeutic indices. Enhanced internalization of HA-coated nanoparticles into melanoma cells versus uncoated nanoparticles was visualized with confocal microscopy and quantified by fluorescence spectroscopy. In total, HA-coated MSNs represent a promising NO delivery system for potential use as a chemotherapeutic for skin melanomas.
耐药性和脱靶毒性是化疗治疗黑色素瘤的两大挑战。由于一氧化氮 (NO) 具有多种抗癌特性,且产生耐药性的可能性较低,因此它代表了一种有吸引力的传统治疗方法替代物。由于 NO 具有很高的反应性,因此需要使用大分子 NO 供体来控制和靶向输送 NO,以实现治疗应用。在此,开发了涂有透明质酸 (HA) 的介孔硅纳米粒子 (MSNs) 作为 NO 递送系统,通过增强的渗透和保留效应以及 HA 与 CD44 受体的定向结合,分别通过被动和主动靶向来促进向癌细胞的控制释放。对氨基硅烷改性、HA 浓度和 HA 分子量进行了系统评估,以促进 MSN 的涂层和 NO 的加载。由于 HA 的亲水性,涂覆 HA 后纳米粒子的水动力直径和分散性增加,并且在更高的 HA 分子量下观察到更大的增加。较低的起始 HA 浓度和具有较长烷基链的氨基硅烷有利于更有效地进行 HA 涂层。与未涂覆的 MSNs 相比,涂覆有 HA 的 MSNs 表现出更快的 NO 释放动力学和更低的 NO 有效负载。然而,通过 HA 赋予的主动靶向将 NO 局部递送至癌细胞增加了氧化应激水平,并诱导黑色素瘤细胞中线粒体介导的细胞凋亡。还针对人真皮成纤维细胞评估了细胞毒性,使用 6 kDa 的 HA 涂覆的 MSNs 导致最大的治疗指数。通过共聚焦显微镜观察到 HA 涂覆的纳米粒子比未涂覆的纳米粒子更有效地进入黑色素瘤细胞内化,并通过荧光光谱法进行定量。总的来说,HA 涂覆的 MSNs 代表了一种有前途的 NO 递送系统,可作为皮肤黑色素瘤的化疗药物。