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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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Modified-release drug delivery systems improve drug efficacy and minimize side effects by controlling the rate and location of drug release. These systems fall into three categories: rate-programmed, stimuli-activated, and site-targeted.Rate-programmed systems release drugs at a predetermined rate, maintaining consistent therapeutic levels and reducing fluctuations that could lead to toxicity or subtherapeutic effects. These systems use polymeric matrices, reservoir-based designs, or osmotic...
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Micro-patterned drug delivery device for light-activated drug release.

Raiyan T Zaman1, Ashwini Gopal, Kathryn Starr

  • 1Stanford University School of Medicine, Stanford, California 94305, USA. rtzaman@stanford.edu

Lasers in Surgery and Medicine
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Summary

This study demonstrates a novel micro-patterned drug delivery device for ocular applications. The device showed excellent stability and controlled dye release via mechanical or laser methods, with a 13-day half-life and minimal inflammation.

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Area of Science:

  • Biomaterials Science
  • Ophthalmology
  • Drug Delivery Systems

Background:

  • Development of micro-patterned drug delivery devices for sustained ocular drug release.
  • Evaluation of long-term stability and controlled release mechanisms.

Purpose of the Study:

  • Fabricate and assess a micro-patterned drug delivery device for ocular use.
  • Investigate dye release using mechanical puncture and laser photodisruption.
  • Determine the long-term stability and retention of the released marker dye.

Main Methods:

  • Fabrication of a transparent, biocompatible polymer device with two reservoirs containing sodium fluorescein dye.
  • Implantation in rabbit eyes, followed by topical glycerol application to reduce light scattering.
  • Dye release induced by a 28-gauge needle or an ophthalmic Nd:YAG laser.
  • Fluorescence spectrophotometry for dye half-life measurement and histological analysis of surrounding tissues.

Main Results:

  • No leakage of sodium fluorescein dye observed post-implantation.
  • Ablation threshold for device perforation determined to be 6-10 mJ, creating 100-500 µm holes.
  • Measured dye half-life in the vitreous chamber was 13 days.
  • Histology revealed minimal immune and foreign body responses, including mild inflammation.

Conclusions:

  • The micro-patterned drug delivery device exhibits minimal inflammatory response and retains its contents effectively.
  • Controlled release of marker dye was achieved through mechanical or laser-induced disruption.
  • The device demonstrates potential for controlled drug delivery in treating ocular diseases with a long retention time.