Vichare Riddhi, Kulahci Yalcin, McCallin Rebecca, Zor Fatih, Selek Fatma Nurefsan, Liu Lu, Crelli Caitlin, Troidle Anneliese, Herneisey Michele, Nichols James M, Shepherd Andrew J, Gorantla Vijay S, Janjic Jelena M
School of Pharmacy and Graduate School of Pharmaceutical Sciences, Duquesne University, Pittsburgh, PA, USA.
Department of Surgery, Wake Forest University School of Medicine, Winston-Salem, NC, USA.
J Nanobiotechnology. 2025 Feb 4;23(1):80. doi: 10.1186/s12951-025-03164-w.
In inflammatory diseases or following an injury, dysregulated inflammation is a common driver of pain and tissue damage. Macrophages are immune cells that contribute to the initiation, maintenance, and resolution of inflammation due to their phenotypic plasticity in response to signals from inflammatory microenvironments. Macrophages infiltrate and polarize toward a pro-inflammatory phenotype (M-like), thereby increasing the severity of inflammation. Therefore, we aimed to suppress the pro-inflammatory activity of M-like macrophages and decrease their infiltration at the site of inflammatory insult to resolve tissue inflammation. To achieve this, we developed a theranostic curcumin-loaded nanoemulsion platform that delivers a low dose of curcumin, a known anti-inflammatory phytochemical, to macrophages and allows in vivo tracking of macrophages by near-infrared fluorescence (NIRF) imaging technique. In vitro, we showed that curcumin-loaded nanoemulsion suppressed polarization of macrophages towards M-like phenotype, consequently decreasing the release of pro-inflammatory cytokines and mediators like IL-6, IL-[Formula: see text] TNF-[Formula: see text], and nitric oxide (NO). Furthermore, curcumin-loaded nanoemulsion increased the level of IL-10, an anti-inflammatory cytokine, and protected macrophages against ferroptosis compared to drug-free nanoemulsion. In a rodent model of Complete Freund's adjuvant (CFA)-induced inflammation, we demonstrated that infiltrating macrophages sequestered curcumin-loaded nanoemulsion droplets and acted as cellular drug depots at the site of inflammation. This consequently decreased macrophage infiltration at the CFA-induced inflammation site in both sexes compared to drug-free nanoemulsion, as demonstrated by NIRF imaging, H&E staining, and immunofluorescence. Taken together, our results indicated that the anti-inflammatory efficacy of curcumin was significantly improved when directly delivered to pro-inflammatory macrophages via theranostic nanoemulsion. This work opens an avenue for exploring theranostic nanoemulsions as a platform for delivering natural anti-inflammatory products for immune modulation.
在炎症性疾病或受伤后,炎症调节失调是疼痛和组织损伤的常见驱动因素。巨噬细胞是免疫细胞,由于其对炎症微环境信号的表型可塑性,有助于炎症的启动、维持和消退。巨噬细胞浸润并向促炎表型(M样)极化,从而增加炎症的严重程度。因此,我们旨在抑制M样巨噬细胞的促炎活性,并减少其在炎症损伤部位的浸润,以解决组织炎症。为了实现这一目标,我们开发了一种治疗诊断型载姜黄素纳米乳剂平台,该平台将低剂量的姜黄素(一种已知的抗炎植物化学物质)递送至巨噬细胞,并允许通过近红外荧光(NIRF)成像技术在体内追踪巨噬细胞。在体外,我们表明载姜黄素纳米乳剂抑制巨噬细胞向M样表型的极化,从而减少促炎细胞因子和介质如IL-6、IL-[公式:见原文]、TNF-[公式:见原文]和一氧化氮(NO)的释放。此外,与无药纳米乳剂相比,载姜黄素纳米乳剂增加了抗炎细胞因子IL-10的水平,并保护巨噬细胞免受铁死亡。在完全弗氏佐剂(CFA)诱导的炎症的啮齿动物模型中,我们证明浸润的巨噬细胞隔离了载姜黄素纳米乳剂液滴,并在炎症部位充当细胞药物储存库。如NIRF成像、苏木精和伊红(H&E)染色以及免疫荧光所示,与无药纳米乳剂相比,这在两性中均减少了CFA诱导的炎症部位的巨噬细胞浸润。综上所述,我们的结果表明,当通过治疗诊断型纳米乳剂直接递送至促炎巨噬细胞时,姜黄素的抗炎功效显著提高。这项工作为探索治疗诊断型纳米乳剂作为递送天然抗炎产品以进行免疫调节的平台开辟了一条途径。