Redox-responsive nano-carriers as tumor-targeted drug delivery systems
- PMID: 30138802
- DOI: 10.1016/j.ejmech.2018.08.034
Redox-responsive nano-carriers as tumor-targeted drug delivery systems
Abstract
With ever increasing scientific knowledge and awareness, research is underway around the globe to design new types of stimuli (external/internal) responsive nano-carriers for biotechnological applications at large and biomedical/pharmaceutical in particular. Based on literature evidence, stimuli-responsive carriers have been classified into four major categories, i.e. (1) physical, (2) chemical, (3) biological, and (4) dual (combination of any of the first three classes). Among various types, redox-responsive nano-carriers are of supreme interests and discussed here in this review. The difference in redox potential in tumor and normal tissue is considered as a potential target for tumor targeting leading to the development of redox-responsive drug delivery systems (DDS). In this regard, a high concentration of glutathione in tumor/intracellular environment has extensively been exploited. Disulfide bonds were found as a promising tool for designing redox-responsive which tend to cleave in a reductive environment forming sulfhydryl groups. Many nano-carriers have been explored widely to control tumor growth. These systems were used against the tumor xenograft animal model and showed improved tumor targeting with tumor growth inhibition. Herein, an effort has been made to summarize various aspects from design to development of numerous types of redox-responsive DDS including liposomes, micelles, nanoparticles, nanogel and prodrug based nanomedicines. An emphasis is also given on various types of nano-carriers with special reference to the tumor-targeted drug delivery applications. Also, dual responsive nano-carriers (in addition to redox-responsive) have also been briefly discussed. Towards the end of the chapter, the information is also given on their future perspectives.
Keywords: Biomedical applications; Nano-carriers; Nanoparticles; Redox responsive drug delivery systems; Stimuli-responsive; Tumor targeting.
Copyright © 2018 Elsevier Masson SAS. All rights reserved.
Similar articles
-
Endogenous and Exogenous Stimuli-Responsive Drug Delivery Systems for Programmed Site-Specific Release.Molecules. 2019 Mar 21;24(6):1117. doi: 10.3390/molecules24061117. Molecules. 2019. PMID: 30901827 Free PMC article. Review.
-
Nanomedicines for advanced cancer treatments: Transitioning towards responsive systems.Int J Pharm. 2016 Dec 30;515(1-2):132-164. doi: 10.1016/j.ijpharm.2016.10.013. Epub 2016 Oct 7. Int J Pharm. 2016. PMID: 27725268 Review.
-
Dual thermoresponsive and pH-responsive self-assembled micellar nanogel for anticancer drug delivery.Drug Deliv. 2014 Jun;21(4):258-64. doi: 10.3109/10717544.2013.838717. Epub 2013 Oct 9. Drug Deliv. 2014. PMID: 24102086
-
A Comprehensive Outlook of Synthetic Strategies and Applications of Redox-Responsive Nanogels in Drug Delivery.Macromol Biosci. 2019 Aug;19(8):e1900071. doi: 10.1002/mabi.201900071. Epub 2019 Jul 12. Macromol Biosci. 2019. PMID: 31298803 Review.
-
Redox-responsive nanoparticles based on Chondroitin Sulfate and Docetaxel prodrug for tumor targeted delivery of Docetaxel.Carbohydr Polym. 2021 Mar 1;255:117393. doi: 10.1016/j.carbpol.2020.117393. Epub 2020 Nov 10. Carbohydr Polym. 2021. PMID: 33436222
Cited by
-
Nano-drug delivery system for pancreatic cancer: A visualization and bibliometric analysis.Front Pharmacol. 2022 Oct 18;13:1025618. doi: 10.3389/fphar.2022.1025618. eCollection 2022. Front Pharmacol. 2022. PMID: 36330100 Free PMC article.
-
Dual Receptor-Targeted and Redox-Sensitive Polymeric Micelles Self-Assembled from a Folic Acid-Hyaluronic Acid-SS-Vitamin E Succinate Polymer for Precise Cancer Therapy.Int J Nanomedicine. 2020 Apr 24;15:2885-2902. doi: 10.2147/IJN.S249205. eCollection 2020. Int J Nanomedicine. 2020. PMID: 32425522 Free PMC article.
-
Novel CD44-targeting and pH/redox-dual-stimuli-responsive core-shell nanoparticles loading triptolide combats breast cancer growth and lung metastasis.J Nanobiotechnology. 2021 Jun 23;19(1):188. doi: 10.1186/s12951-021-00934-0. J Nanobiotechnology. 2021. PMID: 34162396 Free PMC article.
-
Glutathione Depletion and Stalwart Anticancer Activity of Metallotherapeutics Inducing Programmed Cell Death: Opening a New Window for Cancer Therapy.ACS Omega. 2024 Apr 16;9(19):20670-20701. doi: 10.1021/acsomega.3c08890. eCollection 2024 May 14. ACS Omega. 2024. PMID: 38764686 Free PMC article. Review.
-
Smart and Multi-Functional Magnetic Nanoparticles for Cancer Treatment Applications: Clinical Challenges and Future Prospects.Nanomaterials (Basel). 2022 Oct 12;12(20):3567. doi: 10.3390/nano12203567. Nanomaterials (Basel). 2022. PMID: 36296756 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources