CÚRAM, SFI Research Centre for Medical Devices, University of Galway, Galway H92 W2TY, Ireland.
Mol Pharm. 2024 Apr 1;21(4):1609-1624. doi: 10.1021/acs.molpharmaceut.3c00244. Epub 2024 Feb 27.
Cannabidiol (CBD) is the most relevant nonpsychostimulant phytocompound found in . CBD has been extensively studied and has been proposed as a therapeutic candidate for neuroinflammation-related conditions. However, being a highly lipophilic drug, it has several drawbacks for pharmaceutical use, including low solubility and high permeability. Synthetic polymers can be used as drug delivery systems to improve CBD's stability, half-life, and biodistribution. Here, we propose using a synthetic polymer as a nanoparticulate vehicle for CBD (NPCBD) to overcome the pharmacological drawbacks of free drugs. We tested the NPCBD-engineered system in the context of ischemic events in a relevant oxygen and glucose deprivation (OGD) model in primary cortical cells (PCC). Moreover, we have characterized the inflammatory response of relevant cell types, such as THP-1 (human monocytes), HMC3 (human microglia), and PCC, to NPCBD and observed a shift in the inflammatory state of the treated cells after the ischemic event. In addition, NPCBD exhibited a promising ability to restore mitochondrial function after OGD insult in both HMC3 and PCC cells at low doses of 1 and 0.2 μM CBD. Taken together, these results suggest the potential for preclinical use.
大麻二酚(CBD)是在 中发现的最相关的非精神类植物化合物。CBD 已经被广泛研究,并被提议作为与神经炎症相关疾病的治疗候选物。然而,由于它是一种高度亲脂性药物,对于药物用途有几个缺点,包括低溶解度和高通透性。合成聚合物可用作药物递送系统,以提高 CBD 的稳定性、半衰期和生物分布。在这里,我们提出使用合成聚合物作为 CBD 的纳米颗粒载体(NPCBD),以克服游离药物的药理学缺点。我们在原代皮质细胞(PCC)中的相关氧葡萄糖剥夺(OGD)模型中测试了 NPCBD 工程系统在缺血事件中的情况。此外,我们还对相关细胞类型(如 THP-1(人单核细胞)、HMC3(人小胶质细胞)和 PCC)对 NPCBD 的炎症反应进行了表征,并观察到缺血事件后处理细胞的炎症状态发生了转变。此外,NPCBD 在低剂量 1 和 0.2 μM CBD 下,在 HMC3 和 PCC 细胞中均显示出在 OGD 损伤后恢复线粒体功能的有希望的能力。综上所述,这些结果表明 NPCBD 具有潜在的临床前应用前景。