In Situ Hybridization of Polymeric Curcumin to Arginine-Derived Carbon Quantum Dots for Synergistic Treatment of Bacterial Infections.
Hong-Jyuan JianAnisha AnandJui-Yang LaiBinesh UnnikrishnanHuan-Tsung ChangScott G HarrounChih-Ching HuangPublished in: ACS applied materials & interfaces (2023)
Effective infectious keratitis treatment must eliminate the pathogen, reduce the inflammatory response, and prevent persistent damage to the cornea. Infectious keratitis is generally treated with broad-spectrum antibiotics; however, they have the risk of causing corneal epithelial cell damage and drug resistance. In this study, we prepared a nanocomposite (Arg-CQDs/pCur) from arginine (Arg)-derived carbon quantum dots (Arg-CQDs) and polymeric curcumin (pCur). Partial carbonization of arginine hydrochloride in the solid state by mild pyrolysis resulted in the formation of CQDs, which exhibited enhanced antibacterial activity. pCur was formed by the polymerization of curcumin, and further crosslinking reduced its cytotoxicity and improved antioxidative, anti-inflammatory, and pro-proliferative activities. The pCur in situ conjugated with Arg-CQDs to form the Arg-CQDs/pCur nanocomposite, which showed a minimum inhibitory concentration of ca. 10 μg mL -1 , which was >100-fold and >15-fold lower than that of the precursor arginine and curcumin, respectively, against Staphylococcus aureus , Escherichia coli , and Pseudomonas aeruginosa . The Arg-CQDs/pCur nanocomposite with combined antibacterial, antioxidative, anti-inflammatory, pro-proliferative properties, and long-term retention on cornea enabled synergistic treatment of bacterial keratitis. In a rat model, it can effectively treat P. aeruginosa -induced bacterial keratitis at a concentration 4000-fold lower than the commercially used drug, Sulmezole eye drops. Arg-CQDs/pCur nanocomposites have great potential for application in antibacterial and anti-inflammatory nanoformulations for clinical use to treat infectious diseases.
Keyphrases
- anti inflammatory
- quantum dots
- escherichia coli
- inflammatory response
- nitric oxide
- pseudomonas aeruginosa
- staphylococcus aureus
- cancer therapy
- drug delivery
- oxidative stress
- emergency department
- reduced graphene oxide
- infectious diseases
- solid state
- drug induced
- multidrug resistant
- lipopolysaccharide induced
- drug resistant
- cystic fibrosis
- amino acid
- drug release
- lps induced
- replacement therapy
- solid phase extraction
- endothelial cells
- carbon nanotubes
- high resolution