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Related Concept Videos

Modified-Release Drug Delivery Systems: Stimuli-Activated01:30

Modified-Release Drug Delivery Systems: Stimuli-Activated

32
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...
32
Modified-Release Drug Delivery Systems: Rate-Programmed II01:19

Modified-Release Drug Delivery Systems: Rate-Programmed II

41
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...
41
Modified-Release Drug Delivery Systems: Classification01:23

Modified-Release Drug Delivery Systems: Classification

47
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...
47
Modified-Release Drug Delivery Systems: Rate-Programmed I01:22

Modified-Release Drug Delivery Systems: Rate-Programmed I

35
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,...
35
Site-Targeted Drug Delivery Systems: Polymeric Carriers01:24

Site-Targeted Drug Delivery Systems: Polymeric Carriers

37
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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Modified-Release Drug Delivery Systems: Drug Release Characteristics01:22

Modified-Release Drug Delivery Systems: Drug Release Characteristics

53
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...
53

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Related Experiment Video

Updated: Feb 23, 2026

Microwave-assisted Functionalization of Polyethylene glycol and On-resin Peptides for Use in Chain Polymerizations and Hydrogel Formation
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Modeling drug release through stimuli responsive polymer hydrogels.

Aditya Pareek1, Shantanu Maheshwari1, Sivakumar Cherlo1

  • 1TCS Research, Tata Consultancy Services Ltd., Tata Research Development and Design Centre, 54-B, Hadapsar Industrial Estate, Pune 411013, India.

International Journal of Pharmaceutics
|September 9, 2017
PubMed
Summary

This study introduces a mathematical model for stimuli-responsive hydrogels, enabling controlled drug delivery. The model simulates hydrogel swelling and drug release kinetics, reducing experimental needs.

Keywords:
Controlled drug deliveryDeformationMathematical modelingPolymer hydrogelsRelease kineticspH sensitive

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Area of Science:

  • Biomaterials Science
  • Polymer Chemistry
  • Drug Delivery Systems

Background:

  • Stimuli-responsive hydrogels are gaining interest for controlled and self-regulated drug delivery.
  • Their ability to swell/de-swell under varying pH conditions makes them suitable for drug delivery applications.
  • A mechanistic understanding is crucial for controlling drug release from polymer hydrogels.

Purpose of the Study:

  • To develop a mathematical model for simulating stimuli-responsive hydrogel behavior.
  • To couple Nernst-Planck, Poisson, and force balance equations for predicting swelling and drug release.
  • To validate the model with experimental data and evaluate formulation parameters.

Main Methods:

  • Coupling Nernst-Planck, Poisson, and force balance equations.
  • Incorporating diffusion of ionic species and drug, and hydrogel deformation under osmotic pressure.
  • Simulating swelling behavior and drug release kinetics.

Main Results:

  • The mathematical model successfully simulates hydrogel swelling and drug release kinetics.
  • Model validation was performed using experimental data for poly(hydroxyethyl methacrylate-co-methacrylic acid) (pHEMA-co-MA) gels and Phenylpropanolamine release.
  • The effect of polymer and cross-linker concentrations on hydrogel performance was evaluated.

Conclusions:

  • The developed mathematical model provides a mechanistic understanding of stimuli-responsive hydrogels.
  • This model can optimize drug delivery system design by reducing the number of required experiments.
  • It offers a predictive tool for controlling drug release from hydrogel systems.