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Related Concept Videos

Modified-Release Drug Delivery Systems: Rate-Programmed II01:19

Modified-Release Drug Delivery Systems: Rate-Programmed II

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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Polymeric carriers enhance targeted drug delivery by increasing efficacy while minimizing off-target effects. These carriers comprise a biodegradable polymeric backbone integrated with functional elements that enable targeting, improve physicochemical properties, and regulate drug release.Targeting MechanismsThe targeting ability of polymeric carriers is mediated by a homing device, which is a molecular recognition component designed to selectively bind to specific tissues or cells. Monoclonal...
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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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Rate-programmed drug delivery systems (DDS) are designed to release drugs at specific, controlled rates to maintain consistent therapeutic levels. These systems are categorized based on their release mechanisms, including dissolution-controlled DDS, diffusion-controlled DDS, and combined dissolution-diffusion-controlled DDS.In dissolution-controlled DDS, the release rate depends on the slow dissolution of the drug itself or the surrounding matrix. Drugs with inherently slow dissolution rates,...
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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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Drug release from modified-release dosage forms is designed to achieve specific therapeutic effects by controlling the rate and extent of drug release. The classification of these drug release systems is based on key pharmacokinetic assumptions: drug disposition follows first-order kinetics, drug release is the rate-limiting step in absorption, and the released drug is rapidly and completely absorbed.There are four major models of drug release patterns. The first model is the slow zero-order...

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Composite Scaffolds of Interfacial Polyelectrolyte Fibers for Temporally Controlled Release of Biomolecules
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Published on: August 19, 2015

Hollow polypyrrole containers with regulated uptake/release properties.

Bogdan Parakhonskiy1, Daria Andreeva, Helmuth Möhwald

  • 1Max-Planck Institute of Colloids and Interfaces, D14424 Potsdam, Germany.

Langmuir : the ACS Journal of Surfaces and Colloids
|February 26, 2009
PubMed
Summary

Researchers developed polypyrrole microcontainers using electrochemical polymerization. These versatile containers offer tunable sizes and pH-dependent barrier properties for effective encapsulation.

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Area of Science:

  • Materials Science
  • Electrochemistry
  • Nanotechnology

Background:

  • Electrochemical polymerization offers a versatile route for synthesizing conductive polymers.
  • Controlling polymer morphology at the microscale is crucial for advanced applications.

Purpose of the Study:

  • To prepare and characterize polypyrrole microcontainers via electrochemical polymerization.
  • To investigate the influence of electrochemical parameters on microcontainer formation and properties.
  • To evaluate the pH-responsive barrier and permeability characteristics of the synthesized microcontainers.

Main Methods:

  • Electrochemical polymerization of pyrrole on stainless steel electrodes.
  • Varying scan speed and potential range to control size and shell thickness.
  • Detachment of microcontainers using sonication.
  • Assessment of barrier properties and permeability across different pH values.

Main Results:

  • Successfully synthesized polypyrrole microcontainers with tunable sizes (<20 microm).
  • Optimized conditions yielded surfaces with high redox current and microcontainer structures.
  • Microcontainers demonstrated strong barrier properties in acidic media (pH 2-7) and high permeability at pH > 7.
  • Effective encapsulation of low molecular weight species was achieved at low pH.

Conclusions:

  • Electrochemical polymerization provides a controllable method for producing polypyrrole microcontainers.
  • The synthesized microcontainers exhibit pH-switchable barrier and permeability, suitable for encapsulation.
  • These microcontainers hold potential for applications requiring controlled release and protection of active species.