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Osmotic Drug Delivery System as a Part of Modified Release Dosage Form
Author(s) -
Rajesh A. Keraliya,
Chirag Patel,
Pranav Patel,
Vipul Keraliya,
Tejal Soni,
Rajnikant C. Patel,
M. M. Patel
Publication year - 2012
Publication title -
isrn pharmaceutics
Language(s) - English
Resource type - Journals
eISSN - 2090-6153
pISSN - 2090-6145
DOI - 10.5402/2012/528079
Subject(s) - drug delivery , osmosis , drug , semipermeable membrane , delivery system , chemistry , dissolution testing , membrane , dosage form , controlled release , osmotic pressure , nanotechnology , biomedical engineering , chromatography , pharmacology , materials science , engineering , medicine , biochemistry , biopharmaceutics classification system
Conventional drug delivery systems are known to provide an immediate release of drug, in which one can not control the release of the drug and can not maintain effective concentration at the target site for longer time. Controlled drug delivery systems offer spatial control over the drug release. Osmotic pumps are most promising systems for controlled drug delivery. These systems are used for both oral administration and implantation. Osmotic pumps consist of an inner core containing drug and osmogens, coated with a semipermeable membrane. As the core absorbs water, it expands in volume, which pushes the drug solution out through the delivery ports. Osmotic pumps release drug at a rate that is independent of the pH and hydrodynamics of the dissolution medium. The historical development of osmotic systems includes development of the Rose-Nelson pump, the Higuchi-Leeper pumps, the Alzet and Osmet systems, the elementary osmotic pump, and the push-pull system. Recent advances include development of the controlled porosity osmotic pump, and systems based on asymmetric membranes. This paper highlights the principle of osmosis, materials used for fabrication of pumps, types of pumps, advantages, disadvantages, and marketed products of this system.

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