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Related Concept Videos

Modified-Release Drug Delivery Systems: Site-Targeted01:24

Modified-Release Drug Delivery Systems: Site-Targeted

Site-targeted drug delivery systems enhance therapeutic efficacy while minimizing systemic toxicity and treatment costs. Unlike conventional methods, these systems ensure precise drug delivery, improving bioavailability and reducing side effects. Targeted drug delivery is classified into three levels. First-order targeting directs drugs to the capillary beds of specific organs or tissues. Second-order targets specific cell types, such as tumor cells, using receptor-mediated interactions.
Drug Delivery: Overview01:16

Drug Delivery: Overview

The selection of a drug's delivery route depends upon its physicochemical properties, including lipid or water solubility and ionization, as well as the therapeutic requirement, such as immediate or sustained effect. These routes can be divided into three primary categories: enteral, parenteral, and topical.
Enteral delivery involves administering drugs directly through swallowing, sublingual placement, or buccal application. Orally administered drugs predominantly navigate the gastrointestinal...
Physiological Pharmacokinetic Models: Blood Flow-Limited Versus Diffusion-Limited Models00:57

Physiological Pharmacokinetic Models: Blood Flow-Limited Versus Diffusion-Limited Models

Physiological pharmacokinetic models, often called flow-limited or perfusion models, typically assume a swift drug distribution between tissue and venous blood, creating a rapid drug equilibrium. This premise is based on the idea that drug diffusion is extremely fast, and the cell membrane presents no barrier to drug permeation. In this scenario, where no drug binding occurs, the drug concentration in the tissue equals that of the venous blood leaving the tissue. This greatly simplifies the...
Drug Delivery Systems: Different Types01:27

Drug Delivery Systems: Different Types

Conventional oral drug products, termed immediate-release (IR) formulations, are engineered to promptly release their active pharmaceutical ingredient (API) upon ingestion, typically in tablets or capsules. This rapid release often results in swift drug absorption and consequent pharmacodynamic effects, although the timing and intensity can vary depending on the drug's properties. Prodrugs within these formulations require metabolic conversion to activate their pharmacodynamic effects,...
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...
Passive Diffusion: Overview and Kinetics01:17

Passive Diffusion: Overview and Kinetics

Passive diffusion is a critical process that allows small lipophilic drugs to cross the cell membrane along a concentration gradient. This mechanism's efficiency depends on four primary factors: the membrane's surface area, the drug's lipid-water partition coefficient, the concentration gradient, and the membrane's thickness.
When administered orally, drugs establish a substantial concentration gradient between the gastrointestinal (GI) lumen and the bloodstream, expediting their diffusion into...

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Modeling and Simulations of Olfactory Drug Delivery with Passive and Active Controls of Nasally Inhaled Pharmaceutical Aerosols
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Modeling of diffusion controlled drug delivery.

Juergen Siepmann1, Florence Siepmann

  • 1University of Lille, College of Pharmacy, 3 Rue du Prof. Laguesse, 59006 Lille, France. juergen.siepmann@univ-lille2.fr

Journal of Controlled Release : Official Journal of the Controlled Release Society
|October 25, 2011
PubMed
Summary
This summary is machine-generated.

Mathematical modeling aids drug development by predicting drug release kinetics from delivery systems. This overview guides selecting appropriate diffusion-controlled release models for various devices, accelerating product innovation.

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Area of Science:

  • Pharmacology
  • Chemical Engineering
  • Materials Science

Background:

  • Mathematical modeling accelerates drug development and elucidates release mechanisms from advanced drug delivery systems.
  • In silico simulations offer quantitative prediction of formulation and processing impacts on drug release kinetics.

Purpose of the Study:

  • To provide a comprehensive overview of the current state-of-the-art in modeling drug release from delivery systems.
  • To guide the selection of appropriate mathematical models for diffusion-controlled drug release.

Main Methods:

  • Review of mathematical models for drug release, focusing on diffusion-controlled mass transport.
  • Categorization of models based on device structure, drug concentration-solubility ratio, and geometry (slabs, spheres, cylinders).
  • Inclusion of a "road map" for identifying suitable equations for specific drug delivery systems.

Main Results:

  • Identification of key factors influencing model selection: inner structure, initial drug concentration to solubility ratio, and device geometry.
  • Presentation of relevant equations for reservoir and matrix systems, with or without an initial drug excess.
  • Discussion of model assumptions and limitations for various drug delivery devices.

Conclusions:

  • Mathematical modeling is crucial for understanding and optimizing diffusion-controlled drug release.
  • The provided framework aids in selecting appropriate models, enhancing the efficiency of drug delivery system development.
  • The importance of in silico optimization is expected to grow with advancements in information technology.