Carbonate esters turn camptothecin-unsaturated fatty acid prodrugs into nanomedicines for cancer therapy

We report that carbonate esters could turn hydrophobic camptothecin (CPT)-unsaturated fatty acid prodrugs into nanoaggregates in aqueous solution. The active CPT could be rapidly released once triggered by a reductive stimulus when a carbonate ester was combined with a disulfide bond, resulting in a...

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Veröffentlicht in:Chemical communications (Cambridge, England) England), 2018, Vol.54 (16), p.1996-1999
Hauptverfasser: Li, Yang, Kang, Tianyi, Wu, Yujiao, Chen, Yuwen, Zhu, Jiao, Gou, Maling
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container_end_page 1999
container_issue 16
container_start_page 1996
container_title Chemical communications (Cambridge, England)
container_volume 54
creator Li, Yang
Kang, Tianyi
Wu, Yujiao
Chen, Yuwen
Zhu, Jiao
Gou, Maling
description We report that carbonate esters could turn hydrophobic camptothecin (CPT)-unsaturated fatty acid prodrugs into nanoaggregates in aqueous solution. The active CPT could be rapidly released once triggered by a reductive stimulus when a carbonate ester was combined with a disulfide bond, resulting in a potent in vivo antitumor activity.
doi_str_mv 10.1039/c8cc00639c
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source Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection
subjects Anticancer properties
Chemical compounds
Drugs
Esters
Fatty acids
title Carbonate esters turn camptothecin-unsaturated fatty acid prodrugs into nanomedicines for cancer therapy
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