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Glutathione-depleting polyprodrug nanoparticle for enhanced photodynamic therapy and cascaded locoregional chemotherapy.
Zhang, Xinlu; Zhang, Xu; Chen, Shutong; Liu, Yongxin; Cao, Chen; Cheng, Guohui; Wang, Sheng.
Affiliation
  • Zhang X; Tianjin Key Laboratory of Function and Application of Biological Macromolecular Structures, School of Life Sciences, Faculty of Medicine, Tianjin University, Tianjin 300072, China.
  • Zhang X; Tianjin Key Laboratory of Function and Application of Biological Macromolecular Structures, School of Life Sciences, Faculty of Medicine, Tianjin University, Tianjin 300072, China.
  • Chen S; Tianjin Key Laboratory of Function and Application of Biological Macromolecular Structures, School of Life Sciences, Faculty of Medicine, Tianjin University, Tianjin 300072, China.
  • Liu Y; Tianjin Key Laboratory of Function and Application of Biological Macromolecular Structures, School of Life Sciences, Faculty of Medicine, Tianjin University, Tianjin 300072, China.
  • Cao C; Tianjin Key Laboratory of Function and Application of Biological Macromolecular Structures, School of Life Sciences, Faculty of Medicine, Tianjin University, Tianjin 300072, China.
  • Cheng G; School of Pharmacy, Xuzhou Medical University, Xuzhou 221004, China. Electronic address: chengguohui@xzhmu.edu.cn.
  • Wang S; Tianjin Key Laboratory of Function and Application of Biological Macromolecular Structures, School of Life Sciences, Faculty of Medicine, Tianjin University, Tianjin 300072, China. Electronic address: shengwang@tju.edu.cn.
J Colloid Interface Sci ; 670: 279-287, 2024 Sep 15.
Article in En | MEDLINE | ID: mdl-38763024
ABSTRACT
Nanomedicines that combine reactive oxygen species (ROS)-responsive polyprodrug and photodynamic therapy have shown great potential for improving treatment efficacy. However, the consumption of ROS by overexpressed glutathione in tumor cells is a major obstacle for achieving effective ROS amplification and prodrug activation. Herein, we report a polyprodrug-based nanoparticle that can realize ROS amplification and cascaded drug release. The nanoparticle can respond to the high level of hydrogen peroxide in tumor microenvironment, achieving self-destruction and release of quinone methide. The quinone methide depletes intracellular glutathione and thus decreases the antioxidant capacity of cancer cells. Under laser irradiation, a large amount of ROS will be generated to induce cell damage and prodrug activation. Therefore, the glutathione-depleting polyprodrug nanoparticles can efficiently inhibit tumor growth by enhanced photodynamic therapy and cascaded locoregional chemotherapy.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Photochemotherapy / Prodrugs / Reactive Oxygen Species / Nanoparticles / Glutathione / Antineoplastic Agents Limits: Animals / Humans Language: En Journal: J Colloid Interface Sci Year: 2024 Document type: Article Affiliation country: China Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Photochemotherapy / Prodrugs / Reactive Oxygen Species / Nanoparticles / Glutathione / Antineoplastic Agents Limits: Animals / Humans Language: En Journal: J Colloid Interface Sci Year: 2024 Document type: Article Affiliation country: China Country of publication: United States