| Literature DB >> 30035840 |
Hongmin Chen1, Yuwei Qiu1, Dandan Ding1, Huirong Lin1, Wenjing Sun1, Geoffrey D Wang2, Weicheng Huang3, Weizhong Zhang2, Daye Lee2, Gang Liu1, Jin Xie2, Xiaoyuan Chen4.
Abstract
Photosensitizers (PS) are an essential component of photodynamic therapy (PDT). Conventional PSs are often porphyrin derivatives, which are associated with high hydrophobicity, low quantum yield in aqueous solutions, and suboptimal tumor-to-normal-tissue (T/N) selectivity. There have been extensive efforts to load PSs into nanoparticle carriers to improve pharmacokinetics. The approach, however, is often limited by PS self-quenching, pre-mature release, and nanoparticle accumulation in the reticuloendothelial system organs. Herein, a novel, nanoparticle-based PS made of gadolinium-encapsulated graphene carbon nanoparticles (Gd@GCNs), which feature a high 1 O2 quantum yield, is reported. Meanwhile, Gd@GCNs afford strong fluorescence and high T1 relaxivity (16.0 × 10-3 m-1 s-1 , 7 T), making them an intrinsically dual-modal imaging probe. Having a size of approximately 5 nm, Gd@GCNs can accumulate in tumors through the enhanced permeability and retention effect. The unbound Gd@GCNs cause little toxicity because Gd is safely encapsulated within an inert carbon shell and because the particles are efficiently excreted from the host through renal clearance. Studies with rodent tumor models demonstrate the potential of the Gd@GCNs to mediate image-guided PDT for cancer treatment. Overall, the present study shows that Gd@GCNs possess unique physical, pharmaceutical, and toxicological properties and are an all-in-one nanotheranostic tool with substantial clinical translation potential.Entities:
Keywords: gadolinium-encapsulated graphene carbon dots (Gd@GCNs); imaging agent; photodynamic therapy; renal clearance; singlet oxygen
Year: 2018 PMID: 30035840 PMCID: PMC6435436 DOI: 10.1002/adma.201802748
Source DB: PubMed Journal: Adv Mater ISSN: 0935-9648 Impact factor: 30.849