Nano Self-Assemblies of Caffeic Acid-Fibronectin Mimic a Peptide Conjugate for the Treatment of Corneal Epithelial Injury.
Yiping WuLulu DuXiaoning XuYuhan HuJia LiuJingwei ZhangLei LeiWenfang HeZihao ShengYuanao NiJia QuXingyi LiJun JiangPublished in: Molecular pharmaceutics (2023)
Rapid corneal re-epithelialization is important for corneal wound healing. Corneal epithelial cell motility and oxidative stress are important targets for therapeutic intervention. In this study, we covalently conjugated the antioxidant caffeic acid (CA) with a bioactive peptide sequence (PHSRN) to generate a CA-PHSRN amphiphile, which was formulated into nanoparticular eye drops with an average size of 43.21 ± 16 nm. CA-PHSRN caused minimal cytotoxicity against human corneal epithelial cells (HCECs) and RAW264.7 cells, exhibited an excellent free radical scavenging ability, and remarkably attenuated reactive oxygen species (ROS) levels in H 2 O 2 -stimulated HCECs. The antioxidant and anti-inflammatory activities of CA-PHSRN were assessed in lipopolysaccharide (LPS)-stimulated RAW264.7 cells. The results show that CA-PHSRN treatment effectively prevented LPS-induced DNA damage and significantly reduced the levels of LPS-induced pro-inflammatory cytochemokines (i.e., iNOS, NO, TNF-α, IL-6, and COX-2) in a dose-dependent manner. Moreover, using a rabbit corneal epithelial ex vivo migration assay, we demonstrated that the proposed CA-PHSRN accelerated corneal epithelial cell migration and exhibited high ocular tolerance and ocular bioavailability after topical instillation. Taken together, the proposed CA-PHSRN nanoparticular eye drops are a promising therapeutic formulation for the treatment of corneal epithelial injury.
Keyphrases
- wound healing
- lps induced
- oxidative stress
- inflammatory response
- optical coherence tomography
- dna damage
- anti inflammatory
- induced apoptosis
- reactive oxygen species
- protein kinase
- cataract surgery
- cell migration
- randomized controlled trial
- endothelial cells
- cell death
- photodynamic therapy
- drug delivery
- cell cycle arrest
- nitric oxide
- combination therapy
- endoplasmic reticulum stress
- induced pluripotent stem cells
- nitric oxide synthase
- sensitive detection
- pi k akt
- loop mediated isothermal amplification