Pre-activated nanoparticles with persistent luminescence for deep tumor photodynamic therapy in gallbladder cancer.
Sarun JuengpanichShijie LiTaorui YangTianao XieJiadong ChenYukai ShanJiyoung LeeZiyi LuTianen ChenBin ZhangJiasheng CaoJiahao HuJicheng YuYanfang WangWin TopatanaZhen GuXiujun CaiMing-Yu ChenPublished in: Nature communications (2023)
Phototherapy of deep tumors still suffers from many obstacles, such as limited near-infrared (NIR) tissue penetration depth and low accumulation efficiency within the target sites. Herein, stimuli-sensitive tumor-targeted photodynamic nanoparticles (STPNs) with persistent luminescence for the treatment of deep tumors are reported. Purpurin 18 (Pu18), a porphyrin derivative, is utilized as a photosensitizer to produce persistent luminescence in STPNs, while lanthanide-doped upconversion nanoparticles (UCNPs) exhibit bioimaging properties and possess high photostability that can enhance photosensitizer efficacy. STPNs are initially stimulated by NIR irradiation before intravenous administration and accumulate at the tumor site to enter the cells through the HER2 receptor. Due to Pu18 afterglow luminescence properties, STPNs can continuously generate ROS to inhibit NFκB nuclear translocation, leading to tumor cell apoptosis. Moreover, STPNs can be used for diagnostic purposes through MRI and intraoperative NIR navigation. STPNs exceptional antitumor properties combined the advantages of UCNPs and persistent luminescence, representing a promising phototherapeutic strategy for deep tumors.
Keyphrases
- photodynamic therapy
- quantum dots
- energy transfer
- fluorescence imaging
- signaling pathway
- induced apoptosis
- magnetic resonance imaging
- cell proliferation
- cancer therapy
- low dose
- papillary thyroid
- immune response
- light emitting
- radiation therapy
- squamous cell carcinoma
- single molecule
- computed tomography
- dna damage
- pi k akt
- drug release
- contrast enhanced
- binding protein
- diffusion weighted imaging
- drug delivery