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Cyclodextrin-based supramolecular nanogels decorated with mannose for short peptide encapsulation
Archana Sumohan Pillai1, Mohamed Achraf Ben Njima2, Yasmine Ayadi3
1Département de Chimie, École Normale Supérieure-PSL University Paris, France; Chimie ParisTech, PSL University, CNRS, Institut de Recherche de Chimie Paris, 75005 Paris, France.
International Journal of Pharmaceutics
|June 26, 2024
Summary
Researchers developed new physically cross-linked nanogels using self-assembly. These novel nanogels, formed from α-cyclodextrin and modified mannose, show potential for drug delivery applications.
Area of Science:
- Supramolecular Chemistry
- Materials Science
- Nanotechnology
Background:
- Nanogels are nanoscale hydrogel particles used in various applications.
- Developing novel, physically cross-linked nanogels is crucial for advanced materials.
- Self-assembly offers a straightforward route to nanogel fabrication.
Purpose of the Study:
- To devise a simple method for creating physically cross-linked nanogels.
- To investigate the self-assembly mechanism of novel nanogels.
- To evaluate the potential of these nanogels for drug delivery.
Main Methods:
- Synthesis of alkyl chain-modified mannose.
- Self-assembly of modified mannose and α-cyclodextrin in water via magnetic stirring.
- Physicochemical and structural analyses (¹H NMR, X-ray diffraction).
- Drug encapsulation studies using a model peptide.
Main Results:
- Successfully fabricated physically cross-linked nanogels with diameters of 100-150 nm.
- Elucidated a supramolecular, hierarchical formation mechanism involving inclusion complexes and subsequent interactions.
- Demonstrated successful encapsulation of a model peptide, indicating drug delivery potential.
Conclusions:
- A novel, straightforward method for creating physically cross-linked nanogels via self-assembly was established.
- The nanogels exhibit a unique supramolecular formation pathway.
- These nanogels show promise as a platform for water-soluble drug delivery.

