γ-Glutamyl Transferase/Glutathione Cascade-Responsive Unimolecular Nanoprodrug for Precise Cancer Chemotherapy

Nanoprodrug, utilizing precisely engineered nanomaterial as both a carrier and a caging agent, enables targeted delivery and precise release of toxic antitumor drugs into tumor tissues. To further promote the stability and tumor selectivity, a series of hyperbranched polymer-based unimolecular nanoprodrugs were prepared and analyzed. The toxic drug camptothecin was covalently conjugated to the nanostructures through glutathione cleavable linkers to allow for potent release in tumors. A γ-glutamyl transferase responsive moiety was decorated on the nanoprodrugs to tune the surface charges and promote cancer cell uptake. By combining the advantages of stimuli-responsiveness and the stable polymeric nanostructure, the optimized nanoprodrug showed satisfactory cancer/normal cell selectivity, safety, and anticancer efficacy both in vitro and in vivo.

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Publication Details

Journal
Biomacromolecules
Published
2026-05-02
DOI
https://doi.org/10.1021/acs.biomac.6c00054
Primary Topic
Nanoplatforms for cancer theranostics
Type
article
Field-Weighted Citation Impact
0.00

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article

γ-Glutamyl Transferase/Glutathione Cascade-Responsive Unimolecular Nanoprodrug for Precise Cancer Chemotherapy

Jianing Yu, Huanfang Liu, Yichuan Zhang, Mingyue Luo et al.
Biomacromolecules
Nanoplatforms for cancer theranostics
article

γ-Glutamyl Transferase/Glutathione Cascade-Responsive Unimolecular Nanoprodrug for Precise Cancer Chemotherapy

Jianing Yu, Huanfang Liu, Yichuan Zhang, Mingyue Luo, L Zhang, Jie Chen, Wenyu Han, Lida Du, Hao Liu, Wenjing Li, Min Wang, Jiawen Guo, Hebin Xu
article en

Abstract

Nanoprodrug, utilizing precisely engineered nanomaterial as both a carrier and a caging agent, enables targeted delivery and precise release of toxic antitumor drugs into tumor tissues. To further promote the stability and tumor selectivity, a series of hyperbranched polymer-based unimolecular nanoprodrugs were prepared and analyzed. The toxic drug camptothecin was covalently conjugated to the nanostructures through glutathione cleavable linkers to allow for potent release in tumors. A γ-glutamyl transferase responsive moiety was decorated on the nanoprodrugs to tune the surface charges and promote cancer cell uptake. By combining the advantages of stimuli-responsiveness and the stable polymeric nanostructure, the optimized nanoprodrug showed satisfactory cancer/normal cell selectivity, safety, and anticancer efficacy both in vitro and in vivo.

Biomacromolecules
Qingdao University (CN), Henan University (CN), Innovative Clinical Research (US), Sarepta Therapeutics (United States) (US)
National Natural Science Foundation of China, Education Department of Henan Province
Good health and well-being
Openalex Percentile: Top 14%
Nanoplatforms for cancer theranostics
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