2017
DOI: 10.1007/978-981-10-4361-1_85
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Development of a Zein-Based System for Colon Specific Delivery

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Cited by 7 publications
(4 citation statements)
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“…Its biodegradability, biocompatibility, availability, low cost as well as safety (classified as GRAS by the FDA) made it a suitable candidate for drug delivery applications [77]. Among those applications, zein was utilized for the fabrication of scaffolds for tissue engineering [78][79][80][81][82], vaccine delivery [83], DNA transfection [84], oral delivery of peptides and proteins [85], and colon-specific drug delivery [86]. The rising potential of the specific use of zein in bone tissue engineering refers to its perfect membrane forming ability (osteoconductivity), optimum biodegradability, suitable mechanical properties (toughness, flexibility, and compressibility), resistance to degradation by microbial enzymes, and intrinsic anti-oxidant activity [87,88].…”
Section: Zeinmentioning
confidence: 99%
“…Its biodegradability, biocompatibility, availability, low cost as well as safety (classified as GRAS by the FDA) made it a suitable candidate for drug delivery applications [77]. Among those applications, zein was utilized for the fabrication of scaffolds for tissue engineering [78][79][80][81][82], vaccine delivery [83], DNA transfection [84], oral delivery of peptides and proteins [85], and colon-specific drug delivery [86]. The rising potential of the specific use of zein in bone tissue engineering refers to its perfect membrane forming ability (osteoconductivity), optimum biodegradability, suitable mechanical properties (toughness, flexibility, and compressibility), resistance to degradation by microbial enzymes, and intrinsic anti-oxidant activity [87,88].…”
Section: Zeinmentioning
confidence: 99%
“…[13][14][15][16] However, to the best of our knowledge, there has been few reports on the application of Zein-based formulation as a colon-targeted delivery system so far. 17,18 The reason could be derived from at least two aspects: (1) the issues of premature drug release or incomplete disintegration of drug carriers are likely to be encountered, and (2) the designed trigger-release mechanism may fail to work due to possible aggregation of Zein colloidal particles. To address these problems, further suface functionlization of zein-based vehicles is necessary to achieve desirable outcomes.…”
Section: Introductionmentioning
confidence: 99%
“…When orally administered, Zein is relatively resistant to digestive enzymes, which is associated with the fact that Zein particles display a long residence time within the gastrointestinal (GI) tract before being degraded . Because of these advantages, Zein-based particulate systems have received extensive attention as promising delivery vehicles specifically for hydrophobic active molecules. However, to the best of our knowledge, there have been few reports on the application of Zein-based formulation as a colon-targeted delivery system so far. , The reason could be derived from at least two aspects: (1) the issues of premature drug release or incomplete disintegration of drug carriers are likely to be encountered, and (2) the designed trigger-release mechanism may fail to work due to possible aggregation of Zein colloidal particles. To address these problems, further suface functionlization of zein-based vehicles is necessary to achieve desirable outcomes.…”
Section: Introductionmentioning
confidence: 99%
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