Your browser doesn't support javascript.
loading
NQO1-activated multifunctional theranostic probe for imaging-guided mitochondria-targeted photodynamic therapy and boosting immunogenic cell death.
Cao, Chen; Li, Jiansen; Zhang, Xinlu; Zhang, Xu; Gong, Xiaoqun; Wang, Sheng.
Afiliação
  • Cao C; School of Life Sciences, Tianjin University, Tianjin 300072, China.
  • Li J; School of Life Sciences, Tianjin University, Tianjin 300072, China.
  • Zhang X; School of Life Sciences, Tianjin University, Tianjin 300072, China.
  • Zhang X; School of Life Sciences, Tianjin University, Tianjin 300072, China.
  • Gong X; School of Life Sciences, Tianjin University, Tianjin 300072, China. Electronic address: gongxiaoqun@tju.edu.cn.
  • Wang S; School of Life Sciences, Tianjin University, Tianjin 300072, China. Electronic address: shengwang@tju.edu.cn.
Talanta ; 272: 125786, 2024 May 15.
Article em En | MEDLINE | ID: mdl-38382303
ABSTRACT
NAD(P)H quinine oxidoreductase (NQO1) is overexpressed in many types of cancer cells, and have been used as a biomarker for cancer diagnosis and targeted therapy. The development of activatable theranostic agents is highly desirable for precise cancer diagnosis and therapy. Herein, a NQO1-activated near-infrared multifunctional theranostic probe I-HCy-Q is successfully developed for imaging guided photodynamic therapy. The NIR fluorescence (λex/em = 685/703 nm) and capacity of reactive oxygen species generation are sensitive controllable by the level of NQO1, the linear detection range of NQO1 and limit of detection are 0.05-1.5 µg/mL and 5.66 ng/mL, respectively. On the one hand, I-HCy-Q can monitor the activity of NQO1 and distinguish the NQO1 positive cancer cells; on the other hand, the capacity of mitochondria-targeted photodynamic therapy makes I-HCy-Q an effective inducer of apoptosis and immunogenic cell death. Attribute to its complementary advantages, I-HCy-Q holds potential for the imaging and treatment of tumors in complex organisms.
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article