98%
921
2 minutes
20
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.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1016/j.jconrel.2022.08.008 | DOI Listing |
[This corrects the article DOI: 10.1039/D4RA03171G.].
View Article and Find Full Text PDFInt J Pharm
August 2025
Department of Pharmaceutical Engineering and Technology, Indian Institute of Technology (IIT) BHU, Varanasi 221005 UP, India. Electronic address:
The present research aims to develop cetuximab-conjugated paclitaxel-loaded redox-sensitive TPGS/HSPC mixed micelles for EGFR-targeted lung cancer treatment. The dialysis bag diffusion method was utilized to formulate the mixed micelles. Further, various physicochemical characterization parameters have been performed.
View Article and Find Full Text PDFColloids Surf B Biointerfaces
October 2025
Department of Organ transplantation and Hepatobiliary surgery, First Affiliated Hospital, China Medical University, Nanjingbei Street 155, Shenyang, Liaoning Province 110001, China. Electronic address:
Inspired by the strong permeability, sensitive response, accurate biological recognition and efficient biotransformation of viruses, we designed virus-mimic nanoparticles for cancer therapy. We first prepared virus-like mesoporous silica nanoparticles (VSN) with a spiky tubular rough surface via a single-micelle epitaxial growth procedure, grafted glutathione (GSH) sensitive disulfide bonds and chiral dipeptide cysteine-arginine (Cys-Arg) onto VSN (VSCA) to enable easier engulfment and stimuli response release in the reductive tumor microenvironment, and modified hyaluronic acid (HA) acting both as a tumor-targeting ligand to CD44 receptors and a natural biodegradable polysaccharide to construct VSCA-HA. Studies demonstrated the virus-like morphology, mesoscopic structure, highly stability and redox responsiveness of VSCA-HA.
View Article and Find Full Text PDFInt J Pharm
June 2025
Biomedical Engineering Division, Faculty of Chemical Engineering, Tarbiat Modares University, Tehran, Iran. Electronic address:
Systemic drug administration usually results in low drug accumulation in bone tissue and causes toxicity and side effects. A promising method is the synthesis of bone tissue-targeting nanocarriers that are smart in response to the cancer environment. To achieve this goal, polymeric nanomicelles composed of hyaluronic acid (HA), alendronate (ALN), dithiodipropionic acid (DPA, containing disulfide bond -SS-), and hexadecanol (C) were prepared for curcumin (CUR) delivery.
View Article and Find Full Text PDFACS Macro Lett
January 2025
Department of Chemistry, Indian Institute of Technology Kharagpur, Kharagpur, West Bengal 721302, India.
Despite having several advantages, bicontinuously structured polymeric nanoparticles (BSPNPs) are far less explored in the field of controlled drug delivery owing to the requirement of complex precursor copolymers and the associated multistep synthetic procedures. In this work, we report the synthesis of a redox-sensitive diblock copolymer (P1), which was subsequently utilized to prepare doxorubicin (DOX) containing a pH-labile prodrug (P2). P1 and P2 spontaneously self-assembled in aqueous media above their critical aggregation concentration, forming micellar nanoparticles with rare bicontinuous morphology that promotes loading of both hydrophobic and hydrophilic cargoes in different compartments.
View Article and Find Full Text PDF