Nitric oxide (NO) is a short-lived, bioactive gas that has been found to have affinitive effects on cardiovascular diseases as well as cancer biology, while NO deficiency may cause serious pathological responses. The existing chemically-synthesized NO donors have inevitable systemic toxicity and cannot be released adaptively. Hence, L-arginine, an endogenous NO precursor, merits investigation as a natural efficient NO donor. Herein, we designed amino acid-doped L-arginine CDs-based bioenzyme-responsive NO donors, which could adaptively replenish NO/ONOO- in response to different microenvironments. Our results indicated the mechanism of the NO/ONOO- supplementation of L-arginine-based CDs and their potential for nonpharmaceutical gas-involving theranostics for the first time.
Keyphrases
- nitric oxide
- quantum dots
- nitric oxide synthase
- amino acid
- hydrogen peroxide
- cardiovascular disease
- cancer therapy
- room temperature
- oxidative stress
- papillary thyroid
- visible light
- type diabetes
- kidney transplantation
- stem cells
- drug delivery
- risk assessment
- climate change
- bone marrow
- highly efficient
- cell therapy
- oxide nanoparticles
- childhood cancer
- ionic liquid
- carbon dioxide
- coronary artery disease
- smoking cessation