Institute for Advanced Biosciences (IAB), University of Grenoble Alpes (UGA)/ INSERM-U1209 / CNRS-UMR 5309, Grenoble, France.
Université de Strasbourg, CNRS, Laboratoire de Bioimagerie et Pathologies UMR 7021, Strasbourg F-67000, France.
Int J Pharm. 2023 Jan 5;630:122439. doi: 10.1016/j.ijpharm.2022.122439. Epub 2022 Nov 26.
Polymeric nanoparticles (NPs) are extremely promising for theranostic applications. However, their interest depends largely on their interactions with immune system, including the capacity to activate inflammation after their capture by macrophages. In the present study, we generated monodisperse poly(ethyl methacrylate) (PEMA) NPs loaded with hydrophobic photoluminescent gold nanoclusters (Au NCs) emitting in the NIR-II optical windows and studied their interaction in vitro with J774.1A macrophages. PEMA NPs showed an efficient time and dose dependent cellular uptake with up to 70 % of macrophages labelled in 24 h without detectable cell death. Interestingly, PEMA and Au-PEMA NPs induced an anti-inflammatory response and a strong down-regulation of nitric oxide level on lipopolysacharides (LPS) activated macrophages, but without influence on the levels of reactive oxygen species (ROS). These polymeric NPs may thus present a potential interest for the treatment of inflammatory diseases.
聚合物纳米颗粒 (NPs) 在治疗应用中极具前景。然而,它们的应用价值在很大程度上取决于其与免疫系统的相互作用,包括被巨噬细胞捕获后引发炎症的能力。在本研究中,我们制备了负载疏水性光致发光金纳米团簇 (Au NCs) 的单分散聚甲基丙烯酸乙酯 (PEMA) NPs,其发射光在近红外二区 (NIR-II) 光学窗口内。我们研究了其与 J774.1A 巨噬细胞的体外相互作用。PEMA NPs 表现出高效的时间和剂量依赖性细胞摄取,在 24 小时内高达 70%的巨噬细胞被标记,且没有可检测的细胞死亡。有趣的是,PEMA 和 Au-PEMA NPs 在脂多糖 (LPS) 激活的巨噬细胞中诱导抗炎反应和一氧化氮 (NO) 水平的强烈下调,但对活性氧 (ROS) 水平没有影响。因此,这些聚合物 NPs 可能在治疗炎症性疾病方面具有潜在的应用价值。
ACS Nano. 2017-6-13
J Biomed Opt. 2015-5
ACS Appl Mater Interfaces. 2021-8-25