CD-functionalized chitosan hydrogels for pH-responsive drug delivery
Traditional chitosan hydrogels are highly biocompatible but too hydrophilic to effectively load and sustain release of hydrophobic drugs. In a
A forum for researchers, students and applicants in the field of cyclodextrin technology
Traditional chitosan hydrogels are highly biocompatible but too hydrophilic to effectively load and sustain release of hydrophobic drugs. In a
The study investigates the effectiveness of a cationic cyclodextrin polymer-based delivery system for intracellular transport of RNA molecules. Efficient delivery
The authors hypothesized that integrating tumor-targeted topoisomerase I inhibitor delivery with optimized PARP inhibitor scheduling could enable effective combination therapy
Traditional chitosan hydrogels are highly biocompatible but too hydrophilic to effectively load and sustain release of hydrophobic drugs. In a
The study investigates the effectiveness of a cationic cyclodextrin polymer-based delivery system for intracellular transport of RNA molecules. Efficient delivery
The authors hypothesized that integrating tumor-targeted topoisomerase I inhibitor delivery with optimized PARP inhibitor scheduling could enable effective combination therapy
A recent study demonstrated how alkali metal adduct formation can significantly improve the analysis of O-methylated cyclodextrin isomers using cyclic
Researchers at Case Western Reserve University incorporated γ-cyclodextrin oligomers into native collagen gels during fibril formation and studied loading/release of
Cyclodextrins (CDs) have undergone a remarkable evolution over the past three decades, transitioning from classical solubilizing agents to multifunctional platforms