In Vitro Anti-Inflammatory and Antioxidant Activities of pH-Responsive Resveratrol-Urocanic Acid Nano-Assemblies.
Heegyeong SongSeok KangYing YuSung Yun JungKyeongsoon ParkSang-Min KimHaK-Jun KimJae Gyoon KimSung-Eun KimPublished in: International journal of molecular sciences (2023)
Inflammatory environments provide vital biochemical stimuli (i.e., oxidative stress, pH, and enzymes) for triggered drug delivery in a controlled manner. Inflammation alters the local pH within the affected tissues. As a result, pH-sensitive nanomaterials can be used to effectively target drugs to the site of inflammation. Herein, we designed pH-sensitive nanoparticles in which resveratrol (an anti-inflammatory and antioxidant compound (RES)) and urocanic acid (UA) were complexed with a pH-sensitive moiety using an emulsion method. These RES-UA NPs were characterized by transmission electron microscopy, dynamic light scattering, zeta potential, and FT-IR spectroscopy. The anti-inflammatory and antioxidant activities of the RES-UA NPs were assessed in RAW 264.7 macrophages. The NPs were circular in shape and ranged in size from 106 to 180 nm. The RES-UA NPs suppressed the mRNA expression of the pro-inflammatory molecules inducible nitric oxide synthase (iNOS), cyclooxygenase-2 (COX-2), interleukin-1β (IL-1β), and tumor necrosis factor-α (TNF-α) in lipopolysaccharide (LPS)-stimulated RAW 264.7 macrophages in a concentration-dependent manner. Incubation of LPS-stimulated macrophages with RES-UA NPs reduced the generation of reactive oxygen species (ROS) in a concentration-dependent manner. These results suggest that pH-responsive RES-UA NPs can be used to decrease ROS generation and inflammation.
Keyphrases
- anti inflammatory
- oxidative stress
- nitric oxide synthase
- reactive oxygen species
- dna damage
- oxide nanoparticles
- drug delivery
- nitric oxide
- rheumatoid arthritis
- electron microscopy
- ischemia reperfusion injury
- diabetic rats
- induced apoptosis
- inflammatory response
- cell death
- high resolution
- photodynamic therapy
- risk assessment
- toll like receptor
- signaling pathway
- mass spectrometry
- heat shock
- drug induced
- heat stress
- drug release