Doxorubicin prodrug-based nanomedicines for the treatment of cancer.
Antitumor
Cancer therapy
Doxorubicin
Nanomedicine
Prodrug
Stimuli responsive
Journal
European journal of medicinal chemistry
ISSN: 1768-3254
Titre abrégé: Eur J Med Chem
Pays: France
ID NLM: 0420510
Informations de publication
Date de publication:
05 Oct 2023
05 Oct 2023
Historique:
received:
11
05
2023
revised:
27
06
2023
accepted:
27
06
2023
medline:
19
7
2023
pubmed:
14
7
2023
entrez:
13
7
2023
Statut:
ppublish
Résumé
The chemotherapeutic drug of doxorubicin (DOX) has witnessed widespread applications for treating various cancers. DOX-treated dying cells bear cellular modifications which allow enhanced presentation of tumor antigen and neighboring dendritic cell activation. Furthermore, DOX also facilitate the immune-mediated clearance of tumor cells. However, disadvantages such as severe off-target toxicity, and prominent hydrophobicity have resulted in unsatisfactory clinical therapeutic outcomes. The effective delivery of DOX drug molecules is still challenging despite the rapid advances in nanotechnology and biomaterials. Huge progress has been witnessed in DOX nanoprodrugs owing to their brilliant benefits such as tumor stimuli-responsive drug release capacity, high drug loading efficiency and so on. This review summarized recent progresses of DOX prodrug-based nanomedicines to provide deep insights into future development and inspire researchers to explore DOX nanoprodrugs with real clinical applications.
Identifiants
pubmed: 37441851
pii: S0223-5234(23)00578-0
doi: 10.1016/j.ejmech.2023.115612
pii:
doi:
Substances chimiques
Prodrugs
0
Doxorubicin
80168379AG
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
115612Informations de copyright
Copyright © 2023 Elsevier Masson SAS. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of competing interest The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.