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

Modified-Release Drug Delivery Systems: Drug Release Characteristics

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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Modified-release (MR) dosage forms are designed to extend drug release over time, thereby maintaining stable plasma concentrations and reducing dosing frequency. However, their bioavailability is typically below 100% due to incomplete drug release and presystemic metabolism, and limitations in drug permeability across the gastrointestinal epithelium, all of which can restrict the fraction of the drug reaching systemic circulation. Consequently, studying the in vivo bioavailability of MR...
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Modified-Release Drug Delivery Systems: Influencing Factors

Modified-release drug delivery systems are designed to optimize the therapeutic effect of drugs by minimizing side effects, reducing the dosage required, and controlling drug release to align with pharmacokinetic and pharmacodynamic needs. The system depends on two key factors: the drug's release from the formulation and its movement through the body to the target site. Unlike conventional dosage forms, where absorption is the limiting step, the rate of drug release is the key determinant in...
Bioavailability Enhancement: Drug Stability Enhancement and GI Retention01:05

Bioavailability Enhancement: Drug Stability Enhancement and GI Retention

Improving a drug's stability in the gastrointestinal (GI) tract is paramount for enhancing its bioavailability and therapeutic effectiveness. Various strategies are employed to protect the drug from the harsh gastric milieu and to ensure its release and absorption at the desired site within the GI tract.Polymer coatings are one such method used to shield drugs from the stomach's acidic environment. By preventing premature drug release, these coatings improve the bioavailability of unstable...
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Oral Drug Delivery Systems: Delayed-Release Systems

Delayed-release drug delivery systems are specialized pharmaceutical formulations designed to postpone the release of active compounds until the drug reaches a specific region of the gastrointestinal (GI) tract, typically the intestine. These systems are essential for drugs that may cause gastric irritation, are unstable in acidic environments, or need to exert therapeutic effects locally in the intestinal or colonic regions.The core feature of delayed-release systems is the use of enteric...

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Alternating Magnetic Field-Responsive Hybrid Gelatin Microgels for Controlled Drug Release
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Structured drug-eluting bioresorbable films: microstructure and release profile.

M Zilberman1, Y Shifrovitch, M Aviv

  • 1Department of Biomedical Engineering, Faculty of Engineering Tel Aviv University, Tel Aviv 69978, Israel. meitalz@eng.tau.ac.il

Journal of Biomaterials Applications
|July 18, 2008
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Summary

Researchers developed bioresorbable drug-eluting films with controlled drug release. Film structure, determined by solvent evaporation, influences drug dispersion and release profiles for biomedical applications.

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Area of Science:

  • Biomaterials Science
  • Polymer Chemistry
  • Drug Delivery Systems

Background:

  • Bioresorbable drug-eluting films offer versatile biomedical applications, including biodegradable medical devices and antibiotic coatings for implants.
  • These films combine mechanical support with controlled drug release, crucial for preventing infections and promoting healing.

Purpose of the Study:

  • To investigate the preparation and characterization of bioresorbable drug-loaded polymer films.
  • To analyze how film structure (drug location/dispersion) and processing parameters affect drug release profiles.
  • To explore the potential for engineering films with tailored drug release behaviors for specific applications.

Main Methods:

  • Preparation of two distinct film structures (A-type: surface crystals, B-type: bulk dispersion) via solution processing.
  • Analysis of the influence of solvent evaporation rate and drug hydrophilicity on film structuring.
  • Characterization of drug release profiles, including burst effect and release rate, in relation to film type and composition.

Main Results:

  • Film structure (A-type vs. B-type) is primarily dictated by solvent evaporation rate during film formation.
  • A-type films generally show a ~30% burst release followed by a constant rate, influenced by polymer weight loss.
  • B-type films exhibit low burst release, with drug release governed by the polymer degradation profile.

Conclusions:

  • The location and dispersion of drugs within bioresorbable films significantly impact their release kinetics.
  • Tailoring processing parameters and selecting appropriate polymer and drug components allow for the engineering of desired drug release profiles.
  • These findings enable the development of advanced bioresorbable drug-eluting film-based implants for diverse biomedical needs.