Polymeric bile acid sequestrants: Review of design, in vitro binding activities, and hypocholesterolemic effects
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11110%2F18%3A10373186" target="_blank" >RIV/00216208:11110/18:10373186 - isvavai.cz</a>
Alternative codes found
RIV/61389013:_____/18:00483932
Result on the web
<a href="https://doi.org/10.1016/j.ejmech.2017.12.015" target="_blank" >https://doi.org/10.1016/j.ejmech.2017.12.015</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.ejmech.2017.12.015" target="_blank" >10.1016/j.ejmech.2017.12.015</a>
Alternative languages
Result language
angličtina
Original language name
Polymeric bile acid sequestrants: Review of design, in vitro binding activities, and hypocholesterolemic effects
Original language description
Polymeric bile acid sequestrants (BAS) have recently attracted much attention as lipid-lowering agents. These non-absorbable materials specifically bind bile acids (BAs) in the intestine, preventing bile acid (BA) reabsorption into the blood through enterohepatic circulation. Therefore, it is important to understand the structure-property relationships between the polymer sequestrant and its ability to bind specific BAs molecules. In this review, we describe pleiotropic effects of bile acids, and we focus on BAS with various molecular architectures that result in different mechanisms of BA sequestration. Here, we present 1) amphiphilic polymers based on poly(meth)acrylates, poly(meth)acrylamides, polyalkylamines and polyallylamines containing quaternary ammonium groups, 2) cyclodextrins, and 3) BAS prepared via molecular imprinting methods. The synthetic approaches leading to individual BAS preparation, as well as results of their in vitro BA binding activities and in vivo lipid-lowering activities, are discussed.
Czech name
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
10608 - Biochemistry and molecular biology
Result continuities
Project
Result was created during the realization of more than one project. More information in the Projects tab.
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Others
Publication year
2018
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
European Journal of Medicinal Chemistry
ISSN
0223-5234
e-ISSN
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Volume of the periodical
144
Issue of the periodical within the volume
January
Country of publishing house
FR - FRANCE
Number of pages
18
Pages from-to
300-317
UT code for WoS article
000425198100024
EID of the result in the Scopus database
2-s2.0-85038845951