2022
DOI: 10.1016/j.jconrel.2022.06.004
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Taxanes prodrug-based nanomedicines for cancer therapy

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Cited by 16 publications
(9 citation statements)
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“…24 In the past twenty years, prodrug nanomedicines have been extensively explored for cancer therapy. [25][26][27] These delivery platforms effectively protect the encapsulated agents from degradative processes, such as metabolism and hydrolysis. 28 More importantly, nanomedicines could considerably improve the tumor-targeting ability of the drugs via the enhanced permeability and retention (EPR) effect.…”
Section: Chao Wangmentioning
confidence: 99%
“…24 In the past twenty years, prodrug nanomedicines have been extensively explored for cancer therapy. [25][26][27] These delivery platforms effectively protect the encapsulated agents from degradative processes, such as metabolism and hydrolysis. 28 More importantly, nanomedicines could considerably improve the tumor-targeting ability of the drugs via the enhanced permeability and retention (EPR) effect.…”
Section: Chao Wangmentioning
confidence: 99%
“…The self-assembled polymeric prodrug micelles are very stable in a physiological environment and can reduce unwanted drug leakage of drugs before reaching tumor tissue, thereby effectively inhibiting side effects of chemotherapeutic drugs on normal cells ( Sun et al, 2018 ; Shukla et al, 2022 ; Sun et al, 2022 ). The polymeric prodrug micelles not only have the advantages of improved chemical stability, high DLC and low side effects, but they can also be used as drug carriers, thereby constituting a multidrug codelivery system that can be used for combination therapy and for improving therapeutic efficacy ( Li S. et al, 2020 ; Ma et al, 2021 ).…”
Section: Introductionmentioning
confidence: 99%
“…Cancer and bacillosis remain major threats to human health, and the exploitation of efficient chemotherapy for restraining or killing them has become a global focus. [1][2][3] Although many drugs with promising antitumor or antiviral activities, such as curcumin, vincristine, paclitaxel and quinolones, have been reported, [4][5][6] the low solubility is still a major obstacle limiting their clinical application. 7 The common means of intravenous administration will cause either aggregation, which may create safety problems, or inadequate drug doses at the target site with low bioavailability due to low solubility.…”
Section: Introductionmentioning
confidence: 99%