2009
DOI: 10.1016/j.jconrel.2008.12.003
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Prediction of drug release from ethylcellulose coated pellets

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Cited by 86 publications
(37 citation statements)
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“…Nevertheless, the release of the active agent from delivery systems can be classified based on other mechanisms, such as, erosion (the product gradually dissolves in membrane shell), diffusion (the oil diffuses out of delivery system), extraction (mechanical forces during chewing or processing enlarge area of oil) and burst (a reservoir system ruptures under influence of mechanical or osmotic forces) [115]. Several diffusion models have been proposed in the literature to describe the release of an active agent from microcapsules [86,[116][117][118][119][120][121][122][123]. Table 5 presents a summary of the model release related to the diffusion of active agents through the polymeric membranes of microcapsules.…”
Section: Microcapsules Morphology and Release Mechanismsmentioning
confidence: 99%
“…Nevertheless, the release of the active agent from delivery systems can be classified based on other mechanisms, such as, erosion (the product gradually dissolves in membrane shell), diffusion (the oil diffuses out of delivery system), extraction (mechanical forces during chewing or processing enlarge area of oil) and burst (a reservoir system ruptures under influence of mechanical or osmotic forces) [115]. Several diffusion models have been proposed in the literature to describe the release of an active agent from microcapsules [86,[116][117][118][119][120][121][122][123]. Table 5 presents a summary of the model release related to the diffusion of active agents through the polymeric membranes of microcapsules.…”
Section: Microcapsules Morphology and Release Mechanismsmentioning
confidence: 99%
“…The osmolality of the gastrointestinal tract varies between 100 and 400 mOsm/kg (19). Muschert et al investigated different pellets containing various drugs under physiological (0.28-0.62 osmol/kg) conditions and concluded that the variation in the drug release rates from ethyl cellulose-coated pellets were only minor, irrespective of the type of the drug and pellet starter core (20,21).…”
Section: Introductionmentioning
confidence: 99%
“…In the second step alkali cellulose is further treated with ethyl chloride to yield raw EC. Similar to many cellulose derivatives, EC is a nontoxic, nonallergic, and nonirritant polymer characterized by an excellent film-forming ability (Muschert et al 2009). Among its many applications, EC can be used to encapsulate various drugs and/or chemicals through different techniques (Dow Chemical Company 1998).…”
Section: Introductionmentioning
confidence: 99%