X-ray Activated Nanoprodrug for Visualization of Cortical Microvascular Alterations and NIR-II Image-Guided Chemo-Radiotherapy of Glioblastoma.
Lichao SuKang ZhuXiaoguang GeYing WuJieping ZhangGuoyu WangDaojia LiuLing ChenQingqing LiJunqiang ChenJibin SongPublished in: Nano letters (2024)
The permeability of the highly selective blood-brain barrier (BBB) to anticancer drugs and the difficulties in defining deep tumor boundaries often reduce the effectiveness of glioma treatment. Thus, exploring the combination of multiple treatment modalities under the guidance of second-generation near-infrared (NIR-II) window fluorescence (FL) imaging is considered a strategic approach in glioma theranostics. Herein, a hybrid X-ray-activated nanoprodrug was developed to precisely visualize the structural features of glioma microvasculature and delineate the boundary of glioma for synergistic chemo-radiotherapy. The nanoprodrug comprised down-converted nanoparticle (DCNP) coated with X-ray sensitive poly(Se-Se/DOX- co -acrylic acid) and targeted Angiopep-2 peptide (DCNP@P(Se-DOX)@ANG). Because of its ultrasmall size and the presence of DOX, the nanoprodrug could easily cross BBB to precisely monitor and localize glioblastoma via intracranial NIR-II FL imaging and synergistically administer antiglioblastoma chemo-radiotherapy through specific X-ray-induced DOX release and radiosensitization. This study provides a novel and effective strategy for glioblastoma imaging and chemo-radiotherapy.
Keyphrases
- high resolution
- blood brain barrier
- locally advanced
- photodynamic therapy
- cancer therapy
- early stage
- fluorescence imaging
- combination therapy
- rectal cancer
- radiation therapy
- dual energy
- radiation induced
- squamous cell carcinoma
- randomized controlled trial
- systematic review
- electron microscopy
- mass spectrometry
- drug delivery
- endothelial cells
- high glucose
- optic nerve
- iron oxide
- single molecule
- smoking cessation