Приказ основних података о документу

dc.creatorPolović, Natalija
dc.creatorĆirković-Veličković, Tanja
dc.date.accessioned2018-11-22T00:12:09Z
dc.date.available2018-11-22T00:12:09Z
dc.date.issued2008
dc.identifier.issn1872-213X
dc.identifier.urihttps://cherry.chem.bg.ac.rs/handle/123456789/101
dc.description.abstractAllergen specific immunotherapy, comprised of subcutanoues injections of increasing doses of allergen extracts, has been shown to be the only treatment able to influence the natural progression of allergic disease. Different forms of local immunotherapies, involving oral, sublingual and nasal routes of allergen adminstration, have also been considered in clinical practice. The inability of the protein to survive gastrointestinal physiological barriers is a generally encountered problem in oral administration of protein drugs. In order to overcome the problems of low allergen bioavailability and absorptivity, during oral immunotherapy, several stabilization strategies have been outlined in the recent years. This review focuses on interventions including: hexose monosaccharide, ethyl alcohol and water vehicles, oxygen-containing metal salt based preparations, particles with enteric coating, and poly (lactic-co-glycolic) acid microspheres. Regarding the enormous potential of oral responsiveness and/or oral tolerance, research that focuses on new and improved carriers or vehicles for safe allergen oral delivery has great potential in treating allergic diseases. This article also review some of the recent patent related to the field. © 2008 Bentham Science Publishers Ltd.en
dc.rightsrestrictedAccess
dc.sourceRecent Patents on Inflammation and Allergy Drug Discovery
dc.subjectAllergyen
dc.subjectOral allergen deliveryen
dc.subjectOral immunotherapyen
dc.titleNovel formulations for oral allergen vaccinationen
dc.typearticle
dc.rights.licenseARR
dc.citation.volume2
dc.citation.issue3
dc.citation.spage215
dc.citation.epage221
dc.identifier.doi10.2174/187221308786241956
dc.citation.other2(3): 215-221
dc.type.versionpublishedVersionen
dc.identifier.scopus2-s2.0-61449517858


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