| Literature DB >> 30195803 |
Wenli Zhang1, Xiaofeng Zhang2, Yingli Shen3, Feng Shi3, Chaojun Song4, Tianshuai Liu2, Peng Gao2, Bin Lan2, Miao Liu3, Sicheng Wang5, Li Fan6, Hongbing Lu7.
Abstract
The limitation of light penetration depth invalidates the application of photodynamic therapy in deep-seated tumors. X-ray excited photodynamic therapy (X-PDT), which is based on X-rays excited luminescent nanoparticles (XLNP), provides a new strategy for PDT in deep tissues. However, the high X-ray dosage used and non-specific cytotoxicity of the nanoparticle-photosensitizer nanocomposite (NPs-PS) hamper in-vivo X-PDT applications. To address these problems, a simple and efficient NPs-PS nanocomposite using β-NaGdF4: Tb3+ nanoparticles and widely used PS called Rose Bengal (RB) was designed. With perfectly matched spectrum of NPs emission and RB absorption upon X-ray excitation and covalent conjugation of a large amount of RB on NP surfaces to minimize the energy transfer distance, the system demonstrated ultra-high FRET efficiency up to 99.739%, which leads to maximum production of singlet oxygen for PDT with significantly increased anti-tumor efficacy. By 2-aminoethylphosphonic acid surface modification of NPs, excellent biocompatibility was achieved even at a high concentration of 1 mg/mL. The in-vivo X-PDT efficacy was found around 90% of HepG2 tumor growth inhibition with X-ray dose of only 1.5 Gy, which shows the best anti-tumor efficacy at same X-ray dose level reported so far. The present work provides a promising platform for in-vivo X-PDT in deep tumors.Entities:
Keywords: Antitumor nanocomposite; Deep-seated tumor therapy; FRET; Rear-earth nanoparticles; X-ray excited photodynamic therapy
Mesh:
Substances:
Year: 2018 PMID: 30195803 DOI: 10.1016/j.biomaterials.2018.09.001
Source DB: PubMed Journal: Biomaterials ISSN: 0142-9612 Impact factor: 12.479