Facile Transformation from Rofecoxib to a New Near-Infrared Lipid Droplet Fluorescent Probe and Its Investigations on AIE Property, Solvatochromism and Mechanochromism.
Yongbo WeiWei LiuZexin WangNannan ChenJingming ZhouTong WuYuqiu YeYanbing KeHong JiangXin ZhaiLijun XiePublished in: Molecules (Basel, Switzerland) (2023)
Lipid-related cancers cause a large number of deaths worldwide. Therefore, development of highly efficient Lipid droplets (LDs) fluorescent imaging probes will be beneficial to our understanding of lipid-related cancers by allowing us to track the metabolic process of LDs. In this work, a LDs-specific NIR ( λ max = 698 nm) probe, namely BY1, was rationally designed and synthesized via a one-step reaction by integrating triphenylamine (electron-donor group) unit into the structure of rofecoxib. This integration strategy enabled the target BY1 to form a strong Donor-Acceptor (D-A) system and endowed BY1 with obvious aggregation-induced emission (AIE) effect. Meanwhile, BY1 also showed observable solvent effect and reversible mechanochromatic luminescent property, which could be interpreted clearly via density functional theory (DFT) calculations, differential scanning calorimetry (DSC), powder X-ray diffraction (XPRD), and single crystal X-ray data analysis. More importantly, BY1 exhibited highly specific fluorescent imaging ability (Pearson's correlation = 0.97) towards lipid droplets in living HeLa cells with low cytotoxicity. These results demonstrated that BY1 is a new promising fluorescent probe for lipid droplets imaging, and it might be beneficial to facilitate biological research of lipid-related cancers.
Keyphrases
- living cells
- fluorescent probe
- high resolution
- density functional theory
- highly efficient
- fatty acid
- quantum dots
- molecular dynamics
- fluorescence imaging
- induced apoptosis
- computed tomography
- single cell
- magnetic resonance imaging
- electron microscopy
- molecular docking
- cell proliferation
- mass spectrometry
- molecular dynamics simulations
- solar cells
- drug release
- solid state