Publication:

Nanosized Glutathione- and Enzyme-Sensitive Carriers Based on Hyaluronic Acid for Hydrophilic Payload Delivery

 
dc.contributor.authorAjmeera, Suresh
dc.contributor.authorTejeda Gabriela Ines
dc.contributor.authorPancaro, Alessia
dc.contributor.authorDerveaux, Elien
dc.contributor.authorBronckaers, Annelies
dc.contributor.authorAdriaensens, Peter
dc.contributor.authorNelissen, Inge
dc.contributor.authorSmeets, Karen
dc.contributor.authorEthirajan, Anitha
dc.contributor.imecauthorAjmeera, Suresh
dc.contributor.imecauthorPancaro, Alessia
dc.contributor.imecauthorEthirajan, Anitha
dc.contributor.orcidimecEthirajan, Anitha::0000-0002-2264-2536
dc.date.accessioned2025-07-24T03:58:53Z
dc.date.available2025-07-24T03:58:53Z
dc.date.issued2025
dc.description.abstractRedox-responsive nanocarriers (NCs) for drug delivery have gained continuous interest in precision medicine. However, the complexity of the redox balance between different oxidative (e.g., reactive oxygen species) and antioxidative (e.g., glutathione, GSH) species in various pathological conditions (e.g., tumors, inflammation) makes site-specific payload release challenging. Moreover, hydrophilic bioactive substances undergo rapid clearance by the reticuloendothelial system. These obstacles underscore the necessity for novel strategies to enhance the precision and safety of redox-responsive NCs for hydrophilic payload delivery. Herein, we present a simple and efficient approach to fabricate hydrophilic cargo-loaded dual-responsive hyaluronic acid (HA)-based NCs using inverse miniemulsion interfacial cross-linking chemistry. By simply combining HA and bis(4-hydroxyphenyl) disulfide (HPD) as separate precursors in the formulation (i.e., without the need for prior chemical conjugation of HA and HPD), biopolymer-based NCs sensitive to hyaluronidase and GSH are achieved. A fluorescent dye, sulforhodamine B, and an anticancer drug, doxorubicin (DOX), were used as payloads. The characterization of NCs using dynamic light scattering and transmission electron microscopy exhibited <200 nm size with a narrow distribution and a core–shell nanocapsule morphology. We successfully obtained NCs with an encapsulation efficiency >90%, and the release studies showed that the encapsulated payloads were liberated in a sustained and controlled manner upon exposure to both GSH and enzymatic triggers at varying concentrations. In in vitro studies, no noticeable cytotoxicity was observed when human-derived dental pulp stem cells and lung cancer cells (A549) were exposed to NCs (up to 100 μg/mL), and a decrease in cell viability of A549 cells was observed with increasing concentrations of DOX-loaded NCs. Moreover, the NCs were internalized in the cells after 24 h of exposure. These dual-responsive, biocompatible, and biodegradable NCs have enormous scope in the delivery of hydrophilic therapeutics to treat various life-threatening ailments.
dc.description.wosFundingTextThe authors acknowledge financial support from the Special Research Fund (BOF) program of Hasselt University (B20KP07, BOF21GP08). Alessia Pancaro is a Research Foundation Flanders (FWO) postdoctoral fellow (12AR624N). The FWO and Hasselt University are acknowledged for the NMR support provided for this research (AUHL/15/2-GOH3816N). The authors also acknowledge the Advanced Optical Microscopy Center at Hasselt University for their support with the microscopy experiments, which were made possible by FWO project I001222N. This work is further supported by Hasselt University (IMO-IMOMEC) and VITO. Dr. S. Smeets (Applied and Analytical Chemistry, NMR facility, IMO-IMOMEC, Hasselt University) and S. Duwe (Advanced Optical Microscopy Center, Hasselt University) are thanked for their contributions to the NMR and confocal microscopy measurements, respectively. Prof. J. D'Haen (Analytical & Microscopical Services, IMO-IMOMEC, Hasselt University) and Mrs. H. Penxten (Materials Chemistry Research Group, IMO-IMOMEC, Hasselt University) are thanked for providing access to the TEM and ATR-FTIR instruments, respectively.
dc.identifier.doi10.1021/acsanm.5c01242
dc.identifier.issn2574-0970
dc.identifier.urihttps://imec-publications.be/handle/20.500.12860/45929
dc.publisherAMER CHEMICAL SOC
dc.source.beginpage14481
dc.source.endpage14496
dc.source.issue29
dc.source.journalACS APPLIED NANO MATERIALS
dc.source.numberofpages16
dc.source.volume8
dc.subject.keywordsCELLS IN-VITRO
dc.subject.keywordsRESPONSIVE NANOCAPSULES
dc.subject.keywordsSPATIOTEMPORAL RELEASE
dc.subject.keywordsDRUG
dc.subject.keywordsPOLYMERIZATION
dc.subject.keywordsNANOPARTICLES
dc.subject.keywordsNANOCARRIERS
dc.subject.keywordsPROTECTION
dc.subject.keywordsNANOGELS
dc.subject.keywordsHYBRID
dc.title

Nanosized Glutathione- and Enzyme-Sensitive Carriers Based on Hyaluronic Acid for Hydrophilic Payload Delivery

dc.typeJournal article
dspace.entity.typePublication
Files

Original bundle

Name:
Nanosized Glutathione.pdf
Size:
1.53 MB
Format:
Adobe Portable Document Format
Description:
Accepted
Publication available in collections: