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Related Concept Videos

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

Modified-Release Drug Delivery Systems: Stimuli-Activated

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

Site-Targeted Drug Delivery Systems: Polymeric Carriers

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

Modified-Release Drug Delivery Systems: Classification

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...
Ion Exchange01:17

Ion Exchange

Ion exchange chromatography separates charged molecules from a solution by reversibly exchanging them with mobile, or 'active', ions associated with the oppositely charged stationary phase. This method can be used to separate ions, soften and deionize water, and purify solutions. The polymers comprising the ion-exchange column are high-molecular-weight and chemically stable polymers, crosslinked to be porous and essentially insoluble. They are also functionalized with either acidic or basic...

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Related Experiment Video

Updated: Jun 5, 2026

An Injectable and Drug-loaded Supramolecular Hydrogel for Local Catheter Injection into the Pig Heart
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Stable environmentally sensitive cationic hydrogels for controlled delivery applications.

Namita Deo1, S Ruetsch, K R Ramaprasad

  • 1TRI/Princeton, 601 Prospect Avenue, P. O. Box 625, Princeton, NJ 08542, USA. ndeo@triprinceton.com

Journal of Cosmetic Science
|January 19, 2011
PubMed
Summary

New cationic hydrogels synthesized from N-isopropylacrylamide (NIPAM) and (3-acrylamidopropyl)trimethylammonium chloride (AAPTAC) show enhanced stability and tunable properties. These thermosensitive materials offer potential in drug delivery and environmental remediation.

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Area of Science:

  • Materials Science
  • Polymer Chemistry
  • Biomaterials

Background:

  • Thermosensitive hydrogels are crucial for controlled release applications.
  • Cationic hydrogels often suffer from limited pH stability.
  • Developing stable, responsive hydrogels is an ongoing challenge.

Purpose of the Study:

  • To synthesize novel thermosensitive, cationic hydrogels with enhanced colloidal stability.
  • To investigate the influence of a new cationic comonomer on hydrogel properties.
  • To explore the potential applications of these hydrogels in drug delivery and environmental remediation.

Main Methods:

  • Dispersion copolymerization of N-isopropylacrylamide (NIPAM) and (3-acrylamidopropyl)trimethylammonium chloride (AAPTAC).
  • Characterization of hydrogel particle size, colloidal stability, and hydrophobicity/hydrophilicity.
  • Utilized pyrene fluorescence spectroscopy for hydrophobicity analysis.

Main Results:

  • Synthesized stable poly(NIPAM-co-AAPTAC) hydrogels with a broad pH stability range (1.5-11.0).
  • Demonstrated significant sensitivity to temperature, pH, and salt concentration, with particle size decreasing with increased temperature and salt.
  • Hydrophobicity/hydrophilicity was effectively controlled by pH and temperature.

Conclusions:

  • The novel cationic comonomer significantly enhances hydrogel stability across a wide pH range.
  • These thermosensitive hydrogels exhibit tunable properties suitable for controlled active delivery in cosmetic and medical fields.
  • Potential applications include scavenging environmental toxins and developing advanced drug delivery systems.