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Rate-programmed drug delivery systems release drugs in a controlled manner to maintain therapeutic levels. Three main designs include reservoir, matrix, and hybrid systems.Reservoir systems consist of a drug core enclosed within a membrane that controls drug release. In non-swelling reservoir systems, polymers like ethyl cellulose or polymethacrylates are used. These do not hydrate in aqueous media and control release through membrane thickness, porosity, or insolubility. This type includes...
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Stimuli-activated drug delivery systems are designed to release drugs in response to specific physical, chemical, or biological stimuli. These systems often utilize hydrogels—three-dimensional, hydrophilic polymer networks capable of swelling in aqueous environments and retaining significant fluid volumes. Upon exposure to particular stimuli, these hydrogels undergo structural transitions that allow the embedded drug to be released. Due to this adaptive behavior, such systems are also called...

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Programmable Control of Active Ingredient Release in Pickering Emulsions Using Light.

Jie Liu1, Zichun Song1, Jing Luo1

  • 1Key Laboratory of Synthetic and Biological Colloids, Ministry of Education, School of Chemical and Material Engineering, Jiangnan University, Wuxi, Jiangsu, 214122, China.

Small (Weinheim an Der Bergstrasse, Germany)
|March 4, 2025
PubMed
Summary

This study introduces light-responsive nanogates in Pickering emulsions for controlled release. UV light triggers the opening of these nanogates, enabling programmable delivery of active substances without disrupting the emulsion.

Keywords:
azo‐benzeneoil‐water interfacepickering emulsionprogramable release

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Area of Science:

  • Colloid and Surface Science
  • Materials Science
  • Nanotechnology

Background:

  • Pickering emulsions are vital for delivering active ingredients in diverse fields like pharmaceuticals and cosmetics.
  • Current methods for releasing encapsulated substances often require emulsion disruption, posing a challenge for programmable release.
  • A need exists for non-invasive, controlled release mechanisms for active ingredients within stable emulsion systems.

Purpose of the Study:

  • To develop a Pickering emulsion system with a light-responsive colloidal layer acting as nanogates.
  • To demonstrate programmable release of encapsulated active substances using UV light as a remote stimulus.
  • To investigate the control over release kinetics by adjusting system parameters.

Main Methods:

  • Fabrication of a colloidal layer with azobenzene-functionalized silica particles at the oil-water interface.
  • Utilizing UV and visible light to induce cis-trans isomerization of azobenzene, controlling inter-particle gaps (nanogates).
  • Monitoring the release of a model active substance (perylene) under controlled light irradiation cycles.

Main Results:

  • Demonstrated a 'nanogate' effect where UV irradiation opened gaps between colloidal particles.
  • Achieved programmable release of perylene from Pickering emulsion droplets triggered by UV light.
  • Showcased precise control over perylene release amount by tuning particle size and light exposure duration, maintaining emulsion stability.

Conclusions:

  • Developed a novel Pickering emulsion system with light-activated nanogates for programmable release.
  • The system offers non-invasive, remote control over active substance release using UV-visible light.
  • Presents a versatile platform for applications in food, cosmetics, and pharmaceuticals requiring controlled delivery.