Loading…

Endogenous tumor microenvironment-responsive multifunctional nanoplatforms for precision cancer theranostics

[Display omitted] •A discussion on features of pathophysiological barriers for endogenous nanoplatforms.•Strategies for enhancing targeted delivery and controlled release.•Strategies for enhancing multimodal imaging diagnosis with synergistic therapy.•Strategies for real-time monitoring of delivery,...

Full description

Saved in:
Bibliographic Details
Published in:Coordination chemistry reviews 2021-01, Vol.426, p.213529, Article 213529
Main Authors: Wang, Cong, Ding, Shuizi, Wang, Shaoxiong, Shi, Zikuan, Pandey, Nil Kanatha, Chudal, Lalit, Wang, Lingyun, Zhang, Zijian, Wen, Yu, Yao, Hongliang, Lin, Liangwu, Chen, Wei, Xiong, Li
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:[Display omitted] •A discussion on features of pathophysiological barriers for endogenous nanoplatforms.•Strategies for enhancing targeted delivery and controlled release.•Strategies for enhancing multimodal imaging diagnosis with synergistic therapy.•Strategies for real-time monitoring of delivery, release, and therapeutic effects. Multifunctional nanoplatforms (MFNPs) have attracted increasing attention because of their ability to integrate diverse functional diagnostic and therapeutic agents in one system. MFNPs should be biocompatible and smart, have active targeted delivery, exhibit specific target recognition and controlled release properties, exert a high therapeutic effect, and have the excellent visual diagnosing and monitoring abilities for precision cancer theranostics. Numerous strategies have been recently developed to enhance the accuracy of MFNPs for cancer theranostics. The endogenous stimuli-responsive MFNP is one of the most effective strategies and can be classified into six types based on their usage: (1) for enhancing targeted delivery, (2) for improving specific recognition and affinity performance, (3) for enhancing controlled release, (4) for synergistic multimodal diagnosis in vivo, (5) for enhanced synergistic therapy, and (6) for real-time, in situ and visual tracking of delivery, release, and therapeutic effect. Herein, these strategies are reviewed in detail. Furthermore, challenges in enhancing the accuracy of MFNPs and suggestions for further improving the performance of MFNPs are discussed to achieve real precision cancer theranostics with fewer side effects.
ISSN:0010-8545
1873-3840
DOI:10.1016/j.ccr.2020.213529