3B's Research Group, I3Bs-Research Institute on Biomaterials, Biodegradables and Biomimetics, University of Minho, Headquarters of the European Institute of Excellence on Tissue Engineering and Regenerative Medicine, AvePark, Parque de Ciência e Tecnologia, Zona Industrial da Gandra, 4805-017 Barco, Guimarães, Portugal.
ICVS/3B's-PT Government Associate Laboratory, 4710-057 Braga, Guimarães, Portugal.
Int J Mol Sci. 2024 Oct 4;25(19):10693. doi: 10.3390/ijms251910693.
There is growing evidence on the significant role of prolonged inflammation in triggering and progressing of numerous diseases with substantial health and socioeconomic impacts, such as musculoskeletal, cardiovascular and autoimmune disorders, and cancer. Therefore, there is an urgent need to develop therapies that can overcome the main challenges of currently used approaches, such as non-target action, partial modulation of the complex inflammatory pathways, and short-term effects, to effectively manage and resolve chronic inflammatory states. This work investigates the therapeutic synergy of clinically relevant anti-inflammatory agents approaching naïve and classically activated macrophages owing to their central role in inflammation. Aiming at human therapies, a dual-loading nanoplatform reunites molecules with different physico-chemical properties in a single system, seeking to more effectively and comprehensively regulate macrophage functions for precision cell guidance and greater versatility in disease managing. To build this platform, palmitic acid chitosan, superparamagnetic iron oxide nanoparticles, the clinically approved NSAID celecoxib (also known as Celebrex), and RNA technologies were combined into superparamagnetic polymeric micelles (SPMs). Our findings demonstrated that traditional anti-inflammatory drugs such as celecoxib and microRNA molecules were efficiently delivered by the SPMs, altering the inflammatory profile of naïve (M0φ) and M1-primed macrophages (M1φ) assessed by gene and protein expression. The impact of the dual-loaded SPMs in naïve Mφ is an interesting finding towards the modulation of the initial immune response, reducing the potential for chronic inflammation and promoting tissue healing. Collectively, these encouraging results demonstrate the promise of multi-nanomedicine strategies to enhance the efficacy of therapeutic interventions by offering a fresh approach to more precisely and carefully regulated nanotherapeutics delivery.
越来越多的证据表明,长期炎症在引发和进展许多疾病方面起着重要作用,这些疾病对健康和社会经济都有重大影响,如肌肉骨骼、心血管和自身免疫性疾病以及癌症。因此,迫切需要开发能够克服当前应用方法的主要挑战的治疗方法,例如非靶向作用、对复杂炎症途径的部分调节以及短期效果,以有效管理和解决慢性炎症状态。这项工作研究了临床相关抗炎剂对幼稚和经典激活的巨噬细胞的治疗协同作用,因为它们在炎症中起着核心作用。鉴于人类治疗,双重负载纳米平台将具有不同物理化学性质的分子结合在单个系统中,旨在更有效地和全面地调节巨噬细胞功能,实现精确的细胞导向和更大的疾病管理多功能性。为了构建这个平台,将棕榈酸壳聚糖、超顺磁性氧化铁纳米粒子、临床批准的 NSAID 塞来昔布(也称为 Celebrex)和 RNA 技术结合到超顺磁性聚合物胶束(SPM)中。我们的研究结果表明,传统的抗炎药物,如塞来昔布和 microRNA 分子,通过 SPM 有效地递送到幼稚(M0φ)和 M1 诱导的巨噬细胞(M1φ)中,通过基因和蛋白质表达评估改变了它们的炎症特征。双重负载的 SPM 在幼稚 Mφ 中的影响是一个有趣的发现,它可以调节初始免疫反应,降低慢性炎症的潜力,并促进组织愈合。总的来说,这些令人鼓舞的结果表明,多纳米医学策略有希望通过提供一种更精确和谨慎的纳米治疗药物传递方法来增强治疗干预的效果。