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  5. Application of polymeric nanoparticles and micelles in insulin oral delivery
 
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Application of polymeric nanoparticles and micelles in insulin oral delivery

Journal
Journal of Food and Drug Analysis
Journal Volume
23
Journal Issue
3
Pages
351-358
Date Issued
2015
Author(s)
Alai M.S.
WEN-JEN LIN  
Pingale S.S.
DOI
10.1016/j.jfda.2015.01.007
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84955292281&doi=10.1016%2fj.jfda.2015.01.007&partnerID=40&md5=e588fdd5561c6a0aa4e13bf9f704bbf2
https://scholars.lib.ntu.edu.tw/handle/123456789/539747
Abstract
Diabetes mellitus is an endocrine disease in which the pancreas does not produce sufficient insulin or the body cannot effectively use the insulin it produces. Insulin therapy has been the best choice for the clinical management of diabetes mellitus. The current insulin therapy is via subcutaneous injection, which often fails to mimic the glucose homeostasis that occurs in normal individuals. This provokes numerous attempts to develop a safe and effective noninvasive route for insulin delivery. Oral delivery is the most convenient administration route. However, insulin cannot be well absorbed orally because of its rapid enzymatic degradation in the gastrointestinal tract. Therefore, nanoparticulate carriers such as polymeric nanoparticles and micelles are employed for the oral delivery of insulin. These nanocarriers protect insulin from degradation and facilitate insulin uptake via a transcellular and/or paracellular pathway. This review article focuses on the application of nanoparticles and micelles in insulin oral delivery. The recent advances in this topic are also reviewed. ? 2015, Food and Drug Administration, Taiwan. Published by Elsevier Taiwan LLC. All rights reserved.
Subjects
diabetes mellitus; insulin; micelles; nanoparticles; oral delivery
SDGs

[SDGs]SDG3

Other Subjects
enzyme inhibitor; glucose; insulin; nanocarrier; nanoparticle; penetration enhancing agent; polymeric nanoparticle; unclassified drug; conjugation; diabetes mellitus; drug absorption; drug bioavailability; drug delivery system; enteric coated tablet; enzymatic degradation; gastrointestinal tract; glucose homeostasis; human; insulin treatment; micelle; nonhuman; particle size; physical chemistry; Review; surface charge
Type
review

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