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Cited by 675

The DOI matches its Crossref record; 5 of the 5 references it cites were found in a registry or an index.

Reactive‐Oxygen‐Species‐Responsive Drug Delivery Systems: Promises and Challenges

Open access
Saravanakumar, Gurusamy, Kim, Jihoon, Kim, Won Jong·2017·Advanced Science

Abstract

Given the increasing evidence indicates that many pathological conditions are associated with elevated reactive oxygen species (ROS) levels, there have been growing research efforts focused on the development of ROS‐responsive carrier systems because of their promising potential to realize more specific diagnosis and effective therapy. By judicious utilization of ROS‐responsive functional moieties, a wide range of carrier systems has been designed for ROS‐mediated drug delivery. In this review article, insights into design principle and recent advances on the development of ROS‐responsive carrier systems for drug delivery applications are provided alongside discussion of their in vitro and in vivo evaluation. In particular, the discussions in this article will mainly focus on polymeric nanoparticles, hydrogels, inorganic nanoparticles, and activatable prodrugs that have been integrated with diverse ROS‐responsive moieties for spatiotemporally controlled release of drugs for effective therapy.

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Metadata

Authors
Saravanakumar, G., Kim, J., & Kim, W. J.
Venue
Advanced Science
Publisher
Wiley
Published
2016-06-08
Volume
4
Issue
1
Pages
1600124-1600124
ISSN
2198-3844 (ISSN-L)
OpenAlex
W2410933689
Cited by
675
References
5
FWCI
18.42
Type
journal article
Language
en
Open access
gold

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CoChat. (2026). Citation check: Reactive‐Oxygen‐Species‐Responsive Drug Delivery Systems: Promises and Challenges. https://app.cochat.ai/papers/10.1002/advs.201600124
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Saravanakumar, G., Kim, J., & Kim, W. J. (2017). Reactive‐Oxygen‐Species‐Responsive Drug Delivery Systems: Promises and Challenges. Advanced Science. https://doi.org/10.1002/advs.201600124

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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