Author
Listed:
- Hong-Wei An
(National Center for Nanoscience and Technology (NCNST)
Chinese Academy of Sciences (CAS))
- Li-Li Li
(National Center for Nanoscience and Technology (NCNST))
- Yi Wang
(National Center for Nanoscience and Technology (NCNST)
University of Chinese Academy of Sciences)
- Ziqi Wang
(Heilongjiang Key Laboratory of Scientific Research in Urology)
- Dayong Hou
(Heilongjiang Key Laboratory of Scientific Research in Urology)
- Yao-Xin Lin
(National Center for Nanoscience and Technology (NCNST)
University of Chinese Academy of Sciences)
- Sheng-Lin Qiao
(National Center for Nanoscience and Technology (NCNST)
University of Chinese Academy of Sciences)
- Man-Di Wang
(National Center for Nanoscience and Technology (NCNST)
University of Chinese Academy of Sciences)
- Chao Yang
(National Center for Nanoscience and Technology (NCNST))
- Yong Cong
(National Center for Nanoscience and Technology (NCNST)
University of Chinese Academy of Sciences)
- Yang Ma
(National Center for Nanoscience and Technology (NCNST)
University of Chinese Academy of Sciences)
- Xiao-Xiao Zhao
(National Center for Nanoscience and Technology (NCNST)
University of Chinese Academy of Sciences)
- Qian Cai
(National Center for Nanoscience and Technology (NCNST))
- Wen-Ting Chen
(National Center for Nanoscience and Technology (NCNST))
- Chu-Qi Lu
(National Center for Nanoscience and Technology (NCNST))
- Wanhai Xu
(Heilongjiang Key Laboratory of Scientific Research in Urology)
- Hao Wang
(National Center for Nanoscience and Technology (NCNST)
University of Chinese Academy of Sciences)
- Yuliang Zhao
(National Center for Nanoscience and Technology (NCNST)
Chinese Academy of Sciences (CAS)
University of Chinese Academy of Sciences)
Abstract
Achieving the activation of drugs within cellular systems may provide targeted therapies. Here we construct a tumour-selective cascade activatable self-detained system (TCASS) and incorporate imaging probes and therapeutics. We show in different mouse models that the TCASS system accumulates in solid tumours. The molecules show enhanced accumulation in tumour regions via the effect of recognition induced self-assembly. Analysis of the molecular penetration in tumour tissue shows that in vivo self-assembly increases the penetration capability compared to typical soft or hard nanomaterials. Importantly, the in vivo self-assembled molecules exhibit a comparable clearance pathway to that of small molecules, which are excreted from organs of the reticuloendothelial system (liver and kidney), while are relatively slowly eliminated from tumour tissues. Finally, this system, combined with the NIR probe, shows high specificity and sensitivity for detecting bladder cancer in isolated intact patient bladders.
Suggested Citation
Hong-Wei An & Li-Li Li & Yi Wang & Ziqi Wang & Dayong Hou & Yao-Xin Lin & Sheng-Lin Qiao & Man-Di Wang & Chao Yang & Yong Cong & Yang Ma & Xiao-Xiao Zhao & Qian Cai & Wen-Ting Chen & Chu-Qi Lu & Wanha, 2019.
"A tumour-selective cascade activatable self-detained system for drug delivery and cancer imaging,"
Nature Communications, Nature, vol. 10(1), pages 1-15, December.
Handle:
RePEc:nat:natcom:v:10:y:2019:i:1:d:10.1038_s41467-019-12848-5
DOI: 10.1038/s41467-019-12848-5
Download full text from publisher
Corrections
All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:10:y:2019:i:1:d:10.1038_s41467-019-12848-5. See general information about how to correct material in RePEc.
If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.
We have no bibliographic references for this item. You can help adding them by using this form .
If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.
For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .
Please note that corrections may take a couple of weeks to filter through
the various RePEc services.