Advancements in redox-sensitive micelles as nanotheranostics: A new horizon in cancer management

World Health Organisation (WHO) delineated cancer as one of the foremost reasons for mortality with 10 million deaths in the year 2020. Early diagnosis and effective drug delivery are of utmost importance in cancer management. The entrapment of both bio-imaging dyes and drugs will open novel avenues...

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Published inJournal of controlled release Vol. 349; pp. 1009 - 1030
Main Authors Sikder, Anupama, Vambhurkar, Ganesh, Amulya, Etikala, Bagasariya, Deepkumar, Famta, Paras, Shah, Saurabh, Khatri, Dharmendra Kumar, Singh, Shashi Bala, Sinha, V.R., Srivastava, Saurabh
Format Journal Article
LanguageEnglish
Published Elsevier B.V 01.09.2022
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Summary:World Health Organisation (WHO) delineated cancer as one of the foremost reasons for mortality with 10 million deaths in the year 2020. Early diagnosis and effective drug delivery are of utmost importance in cancer management. The entrapment of both bio-imaging dyes and drugs will open novel avenues in the area of tumor theranostics. Elevated levels of reactive oxygen species (ROS) and glutathione (GSH) are the characteristic features of the tumor microenvironment (TME). Researchers have taken advantage of these specific TME features in recent years to develop micelle-based theranostic nanosystems. This review focuses on the advantages of redox-sensitive micelles (RSMs) and supramolecular self-assemblies for tumor theranostics. Key chemical linkers employed for the tumor-specific release of the cargo have been discussed. In vitro characterisation techniques used for the characterization of RSMs have been deliberated. Potential bottlenecks that may present themselves in the bench-to-bedside translation of this technology and the regulatory considerations have been deliberated. [Display omitted] •Utilization of redox-sensitive micelles (RSMs) and supramolecular assemblies for redox-triggered cancer theranostics has been conveyed.•Various linkers for imparting the redox-responsive behaviour of RSMs have been discussed.•The preparation methods for fabricating RSMs along with the pros and cons of each method have been deliberated.•In vitro characterisation and in vivo efficacy of RSMs has been illustrated.•Challenges associated with the clinical translation of RSMs and their way forwards have been conveyed.
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ISSN:0168-3659
1873-4995
DOI:10.1016/j.jconrel.2022.08.008