Self‐Boosting Programmable Release of Multiple Therapeutic Agents by Activatable Heterodimeric Prodrug‐Enzyme Assembly for Antitumor Therapy

Abstract: Endogenous stimuli‐responsive prodrugs, due to their disease lesion specificity and reduced systemic toxicity, have been widely explored for antitumor therapy. However, reactive oxygen species (ROS) as classical endogenous stimuli in the tumor microenvironment (TME) are not enough to achieve the expected drug release. Herein, a ROS‐activatable heterodimeric prodrug‐loaded enzyme assembly is developed for self‐boosting programmable release of multiple therapeutic agents. The heterodimeric prodrug NBS‐TK‐PTX (namely NTP) is composed of 5‐(ethylamino)‐9‐diethylaminobenzo[a]phenothiazinium chloride analog (NBS), paclitaxel (PTX) and ROS‐responsive thioketal (TK) linker, which shows a strong binding affinity with glucose oxidase (GOx), thus obtaining NTP@GOx assembly. Notably, the enzymatic activity of GOx in NTP@GOx is inhibited by NTP. The programmable release is achieved by following steps: i) NTP@GOx is partially dissociated in acidic TME, thus releasing a small segment of NTP and GOx. Thereupon, the enzymatic activity of GOx is recovered; ii) GOx‐triggered pH reduction further facilitates the dissociation of NTP@GOx, thus accelerating a large amount of NTP and GOx release; iii) The TK linker of prodrug NTP is cleaved by hydrogen peroxide generated by GOx catalysis, thus expediting the release of NBS for Type‐I photodynamic therapy and PTX for chemotherapy, respectively. The NTP@GOx shows great potential for multimodal synergistic cancer therapy.

Location
Deutsche Nationalbibliothek Frankfurt am Main
Extent
Online-Ressource
Language
Englisch

Bibliographic citation
Self‐Boosting Programmable Release of Multiple Therapeutic Agents by Activatable Heterodimeric Prodrug‐Enzyme Assembly for Antitumor Therapy ; day:21 ; month:11 ; year:2024 ; extent:12
Advanced science ; (21.11.2024) (gesamt 12)

Creator
Jiang, Shanshan
Gurram, Bhaskar
Zhu, Junfei
Lei, Shan
Zhang, Yifan
He, Ting
Tagit, Oya
Fang, Hui
Huang, Peng
Lin, Jing

DOI
10.1002/advs.202409960
URN
urn:nbn:de:101:1-2411211406307.421345182737
Rights
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Last update
15.08.2025, 7:33 AM CEST

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Associated

  • Jiang, Shanshan
  • Gurram, Bhaskar
  • Zhu, Junfei
  • Lei, Shan
  • Zhang, Yifan
  • He, Ting
  • Tagit, Oya
  • Fang, Hui
  • Huang, Peng
  • Lin, Jing

Other Objects (12)