| Literature DB >> 33819814 |
Yanhong Duo1, Daoming Zhu2, Xiurong Sun3, Meng Suo2, Zheng Zheng4, Wei Jiang5, Ben Zhong Tang6.
Abstract
Sonodynamic therapy (SDT), as an efficient way of tumor treatment, has the advantages of deep tumor penetration and high therapeutic efficacy. However, developing efficient sonosensitizers are still challenging. AIEgen-based SDT is rarely reported and it is urgent to develop novel AIEgen-active sonosensitizers. Furthermore, the AIEgen-based theranostic system is promisingly needed to be proved on PDX models to be closer to the clinic. Herein, we constructed a novel AIEgen based SDT system and found that DCPy has advantages over traditional sonosensitizers in SDT. Then, a patient-derived MVs/AIEgen hybrid system (AMVs) prepared by electroporation was used for personalized SDT in bladder cancer patient-derived xenograft (PDX) models. Impressively, AMVs displayed the superior tumor targeting ability and efficient personalized SDT therapy on PDX models, both of which were much more improved compared with PLGA/AIEgens nanoparticles and cell line-derived micro vesicles. This work provides new ideas for both the design of AIE-active sonosensitizers and the SDT treatment of cancers, further expanding the potential clinical application of AIEgens in the future.Entities:
Keywords: Aggregation-induced emission; Patient-derived microvesicles; Patient-derived xenograft models; Personalized sonodynamic cancer therapy; Sonosensitizers
Year: 2021 PMID: 33819814 DOI: 10.1016/j.biomaterials.2021.120755
Source DB: PubMed Journal: Biomaterials ISSN: 0142-9612 Impact factor: 12.479