Tumor microenvironment responsive drug delivery systems

Conventional tumor-targeted drug delivery systems (DDSs) face challenges, such as unsatisfied systemic circulation, low targeting efficiency, poor tumoral penetration, and uncontrolled drug release. Recently, tumor cellular molecules-triggered DDSs have aroused great interests in addressing such dil...

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Published inAsian journal of pharmceutical sciences Vol. 15; no. 4; pp. 416 - 448
Main Authors He, Qunye, Chen, Jun, Yan, Jianhua, Cai, Shundong, Xiong, Hongjie, Liu, Yanfei, Peng, Dongming, Mo, Miao, Liu, Zhenbao
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 01.07.2020
Shenyang Pharmaceutical University
Elsevier
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Summary:Conventional tumor-targeted drug delivery systems (DDSs) face challenges, such as unsatisfied systemic circulation, low targeting efficiency, poor tumoral penetration, and uncontrolled drug release. Recently, tumor cellular molecules-triggered DDSs have aroused great interests in addressing such dilemmas. With the introduction of several additional functionalities, the properties of these smart DDSs including size, surface charge and ligand exposure can response to different tumor microenvironments for a more efficient tumor targeting, and eventually achieve desired drug release for an optimized therapeutic efficiency. This review highlights the recent research progresses on smart tumor environment responsive drug delivery systems for targeted drug delivery. Dynamic targeting strategies and functional moieties sensitive to a variety of tumor cellular stimuli, including pH, glutathione, adenosine-triphosphate, reactive oxygen species, enzyme and inflammatory factors are summarized. Special emphasis of this review is placed on their responsive mechanisms, drug loading models, drawbacks and merits. Several typical multi-stimuli responsive DDSs are listed. And the main challenges and potential future development are discussed. [Display omitted]
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These authors contributed equally to this work.
ISSN:1818-0876
2221-285X
2221-285X
DOI:10.1016/j.ajps.2019.08.003