Therapeutic Polymer-Based Cannabidiol Formulation: Tackling Neuroinflammation Associated with Ischemic Events in the Brain.
Merari Tumin ChevalierMansoor Al-WaeelAmir M AlsharabasyAna Lúcia RebeloSergio Martin-SaldañaAbhay PanditPublished in: Molecular pharmaceutics (2024)
Cannabidiol (CBD) is the most relevant nonpsychostimulant phytocompound found in Cannabis sativa . 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.
Keyphrases
- induced apoptosis
- inflammatory response
- endothelial cells
- cell cycle arrest
- oxidative stress
- cerebral ischemia
- lipopolysaccharide induced
- traumatic brain injury
- ischemia reperfusion injury
- lps induced
- drug delivery
- endoplasmic reticulum stress
- cognitive impairment
- type diabetes
- cell death
- emergency department
- metabolic syndrome
- cell therapy
- single cell
- blood brain barrier
- spinal cord injury
- multidrug resistant
- blood glucose
- multiple sclerosis
- mesenchymal stem cells
- climate change
- drug induced
- pi k akt
- adverse drug
- human health
- insulin resistance