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Tumor microenvironment responsive drug delivery systems.
He, Qunye; Chen, Jun; Yan, Jianhua; Cai, Shundong; Xiong, Hongjie; Liu, Yanfei; Peng, Dongming; Mo, Miao; Liu, Zhenbao.
Afiliação
  • He Q; Xiangya School of Pharmaceutical Sciences, Central South University, Changsha 410013, China.
  • Chen J; Xiangya School of Pharmaceutical Sciences, Central South University, Changsha 410013, China.
  • Yan J; Xiangya School of Pharmaceutical Sciences, Central South University, Changsha 410013, China.
  • Cai S; Xiangya School of Pharmaceutical Sciences, Central South University, Changsha 410013, China.
  • Xiong H; Xiangya School of Pharmaceutical Sciences, Central South University, Changsha 410013, China.
  • Liu Y; School of Chemistry and Chemical Engineering, Central South University, Changsha 410083, China.
  • Peng D; School of Pharmacy, Hunan University of Chinese Medicine, Changsha 410208, China.
  • Mo M; Department of Urology, Xiangya Hospital, Central South University, Changsha 410008, China.
  • Liu Z; Xiangya School of Pharmaceutical Sciences, Central South University, Changsha 410013, China.
Asian J Pharm Sci ; 15(4): 416-448, 2020 Jul.
Article em En | MEDLINE | ID: mdl-32952667
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Asian J Pharm Sci Ano de publicação: 2020 Tipo de documento: Article País de afiliação: China País de publicação: Holanda

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Asian J Pharm Sci Ano de publicação: 2020 Tipo de documento: Article País de afiliação: China País de publicação: Holanda