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Published on: August 23, 2018
Cyclodextrin-based host-guest supramolecular nanoparticles for delivery: from design to applications.
Qi-Da Hu1, Gu-Ping Tang, Paul K Chu
1Institute of Chemical Biology and Pharmaceutical Chemistry, Zhejiang University , Hangzhou 310028, China.
Cyclodextrins (CDs) are key to supramolecular nanotechnology, enabling advanced drug delivery systems. Host-guest interactions with CDs create functional nanoparticles for targeted therapies and improved biocompatibility.
Area of Science:
- Supramolecular Chemistry
- Nanotechnology
- Materials Science
Background:
- Host-guest interactions are fundamental to supramolecular nanotechnology.
- Cyclodextrins (CDs) offer biocompatibility and tunable properties for nanodelivery systems.
- Polymer modification of CDs enhances their functionality and application potential.
Purpose of the Study:
- To describe design strategies for employing CDs in host-guest delivery systems.
- To highlight the development of multifunctional CD-based supramolecular nanoparticles.
- To explore the potential of these nanoparticles in clinical applications, particularly for targeted drug and gene delivery.
Main Methods:
- Utilizing host-guest interactions between cyclodextrins and guest moieties (e.g., adamantyl groups).
- Designing nanoparticles with specific functionalities like coating protection, conformational flexibility, and drug delivery.
- Incorporating features for controlled particle size, biodegradability, controlled release, and targeted delivery through self-assembly.
Main Results:
- CD-based host-guest systems demonstrate improved biocompatibility and enhanced delivery efficacy, especially to tumors.
- Core-shell nanoparticles with hydrophobic cores and hydrophilic shells effectively carry insoluble drugs.
- Multifunctional nanoparticles exhibit controlled release triggered by tumor microenvironments or external stimuli.
Conclusions:
- CD-based host-guest supramolecular nanoparticles offer versatile platforms for advanced drug and gene co-delivery.
- These systems show significant potential for synergistic inhibition of malignant tissue growth.
- Optimized nanoparticle designs are expected to expedite in vivo applications and clinical acceptance.
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