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Prodrug strategies for targeted therapy triggered by reactive oxygen species
Jorge Peiró Cadahía1, Viola Previtali2, Nikolaj S Troelsen2
1Nuevolution A/S , Rønnegade 8 , 2100 Copenhagen , Denmark.
Abstract:
Increased levels of reactive oxygen species (ROS) have been associated with numerous pathophysiological conditions including cancer and inflammation and the ROS stimulus constitutes a potential trigger for drug delivery strategies. Over the past decade, a number of ROS-sensitive functionalities have been identified with the purpose of introducing disease-targeting properties into small molecule drugs - a prodrug strategy that offers a promising approach for increasing the selectivity and efficacy of treatments. This review will provide an overview of the ROS-responsive prodrugs developed to date. A discussion on the current progress and limitations is provided along with a reflection on the unanswered questions that need to be addressed in order to advance this novel approach to the clinic.
Insights
Reactive oxygen species (ROS) trigger innovative prodrug strategies for targeted cancer and inflammation treatments. This review explores ROS-responsive prodrugs, highlighting progress and future clinical directions.
Area of Science:
- Biomedical Engineering
- Drug Delivery Systems
- Oncology
Background:
- Elevated reactive oxygen species (ROS) levels are linked to diseases like cancer and inflammation.
- ROS can be leveraged as a stimulus for advanced drug delivery systems.
- Prodrug strategies utilizing ROS-sensitivity offer enhanced treatment selectivity and efficacy.
Purpose of the Study:
- To provide a comprehensive overview of ROS-responsive prodrugs developed over the last decade.
- To analyze the current advancements and inherent limitations in ROS-sensitive prodrug technology.
- To identify key unanswered questions for the clinical translation of this approach.
Main Methods:
- Literature review of ROS-responsive prodrugs.
- Analysis of identified ROS-sensitive functionalities.
- Discussion of disease-targeting properties in small molecule drugs.
Main Results:
- Numerous ROS-sensitive functionalities have been identified for prodrug design.
- ROS-responsive prodrugs demonstrate potential for improved therapeutic outcomes.
- The development of these prodrugs is an active area of research.
Conclusions:
- ROS-responsive prodrugs represent a promising strategy for targeted therapy.
- Further research is needed to overcome current limitations and advance clinical application.
- Addressing specific unanswered questions is crucial for the successful translation of ROS-sensitive prodrugs to the clinic.
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