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Related Concept Videos

Nitric Oxide Signaling Pathway01:28

Nitric Oxide Signaling Pathway

Nitric oxide (NO), an inorganic gas, acts as a potent second messenger in most animal and plant tissues. NO diffuses out of the cells that produce it and enters the neighboring cells to generate a downstream response. NO synthase (NOS) catalyzes NO production by the deamination of the amino acid arginine. There are three isoforms of NOS. Endothelial cells have endothelial NOS (eNOS), nerve and muscle cells have neuronal NOS (nNOS), and macrophages produce inducible NOS (iNOS) upon exposure to...
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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 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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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: 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...
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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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Synthesis of Stimuli-responsive Nanogels using Aqueous One-step Crosslinking and Co-nanopolymerization
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Published on: January 24, 2025

Compartmentalized nanocomposite for dynamic nitric oxide release.

John J Koehler1, Jianxiu Zhao, Sabrina S Jedlicka

  • 1Department of Agricultural and Biological Engineering, Purdue University, West Lafayette, IN, USA.

The Journal of Physical Chemistry. B
|November 4, 2008
PubMed
Summary

This study introduces a novel light-activated nitric oxide (NO) releasing nanocomposite. This material precisely controls NO flux for biological applications, mimicking cellular strategies.

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Area of Science:

  • Biomaterials Science
  • Nanotechnology
  • Cellular Signaling

Background:

  • Nitric oxide (NO) is a crucial cell-signaling molecule with concentration-dependent roles in differentiation and apoptosis.
  • Precisely controlling NO levels is vital for understanding and manipulating cellular processes.
  • Existing methods for NO delivery often lack dynamic control and biological mimicry.

Purpose of the Study:

  • To develop and characterize a novel nitric oxide releasing nanocomposite.
  • To achieve photostimulated and dynamically modulated NO flux within biological ranges.
  • To mimic cellular compartmentalization strategies for enhanced NO delivery.

Main Methods:

  • Encapsulation of a photosensitive NO donor within 150 nm lipid vesicles.
  • Doping of these vesicles into a biocompatible porous silica matrix.
  • Characterization of NO release using a NO-selective amperometric microsensor and light stimulation.

Main Results:

  • The nanocomposite demonstrated photostimulated NO release with a surface flux of 14 pmol-cm(-2) sec(-1).
  • NO concentration profiles showed expected diffusion behavior in an aqueous environment.
  • Light pulsing generated uniform, duration-matched NO concentration pulses.
  • A linear relationship between NO surface concentration and photon flux was established.

Conclusions:

  • The developed nanocomposite offers a novel platform for controlled nitric oxide delivery.
  • Photostimulation allows for precise, dynamic modulation of NO flux at the material surface.
  • This technology has potential applications in areas requiring controlled NO signaling, mimicking biological systems.