pH-Responsive supramolecular vesicles for imaging-guided drug delivery: Harnessing aggregation-induced emission

Bibliographic Details
Title: pH-Responsive supramolecular vesicles for imaging-guided drug delivery: Harnessing aggregation-induced emission
Authors: Xin-Rui Wang, Wei-Xiu Lin, Yi-Long Lu, Dietmar Kuck, Wen-Rong Xu
Source: Royal Society Open Science, Vol 11, Iss 9 (2024)
Publisher Information: The Royal Society, 2024.
Publication Year: 2024
Collection: LCC:Science
Subject Terms: supramolecular vesicles, pH-responsive, drug delivery, aggregation-induced emission, imaging-guided, Science
More Details: The water-soluble tribenzotriquinacene-based hexacarboxylic acid ammonium salt, TBTQ-C 6 , acts as the host component (H) forming host–guest complexes with tetraphenylethylene (TPE)-functionalized monotopic and tetratopic quaternary ammonium derivatives, G1 and G2, to yield supra-amphiphiles. These supra-amphiphiles self-assemble to form pH-responsive fluorescent vesicles, which have allowed us to capitalize on the aggregation-induced emission (AIE) effect for imaging-guided drug delivery systems. These systems exhibit efficient drug loading and pH-responsive delivery capabilities. Upon encapsulation of the anticancer drug doxorubicin (DOX), both the TPE and DOX chromophores undergo dual-fluorescence deactivation due to the energy transfer relay (ETR) effect. Under acidic conditions, the release of DOX interrupts the ETR effect, resulting in the fluorescence recovery of TPE fluorogens and DOX, allowing for real-time visual monitoring of the drug release process. Cytotoxicity experiments confirmed the low toxicity of the unloaded vectors to normal cells, while the DOX-loaded vectors were found to significantly enhance the anticancer activity of DOX against cancer cells in vitro. The AIE-featured supramolecular vesicles presented in this research hold great potential for imaging-guided drug delivery systems.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 2054-5703
Relation: https://doaj.org/toc/2054-5703
DOI: 10.1098/rsos.240664
Access URL: https://doaj.org/article/aee6f3bc553748a58cbb956289d164a4
Accession Number: edsdoj.6f3bc553748a58cbb956289d164a4
Database: Directory of Open Access Journals
More Details
ISSN:20545703
DOI:10.1098/rsos.240664
Published in:Royal Society Open Science
Language:English