Carboxylesterase Activatable Molecular Probe for Personalized Treatment Guidance by Analyte-Induced Molecular Transformation.
Benhao LiHengke LiuMengyao ZhaoXinming ZhangPeng HuangXiaoyuan Shawn ChenJing LinPublished in: Angewandte Chemie (International ed. in English) (2024)
Accurate visualization of tumor microenvironment is of great significance for personalized medicine. Here, we develop a near-infrared (NIR) fluorescence/photoacoustic (FL/PA) dual-mode molecular probe (denoted as NIR-CE) for distinguishing tumors based on carboxylesterase (CE) level by an analyte-induced molecular transformation (AIMT) strategy. The recognition moiety for CE activity is the acetyl unit of NIR-CE, generating the pre-product, NIR-CE-OH, which undergoes spontaneous hydrogen atom exchange between the nitrogen atoms in the indole group and the phenol hydroxyl group, eventually transforming into NIR-CE-H. In cellular experiments and in vivo blind studies, the human hepatoma cells and tumors with high level of CE were successfully distinguished by both NIR FL and PA imaging. Our findings provide a new molecular imaging strategy for personalized treatment guidance.
Keyphrases
- fluorescence imaging
- energy transfer
- fluorescent probe
- photodynamic therapy
- drug release
- living cells
- single molecule
- high glucose
- quantum dots
- endothelial cells
- high resolution
- induced apoptosis
- diabetic rats
- drug delivery
- molecular dynamics
- oxidative stress
- combination therapy
- electron transfer
- pluripotent stem cells