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Isolation and characterization of enantioselective DNA aptamers for ibuprofen

Authors
Kim, Yeon SeokHyun, Chang JunKim, In AeGu, Man Bock
Issue Date
15-5월-2010
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Keywords
Ibuprofen; Enantioselective aptamer; SELEX
Citation
BIOORGANIC & MEDICINAL CHEMISTRY, v.18, no.10, pp.3467 - 3473
Indexed
SCIE
SCOPUS
Journal Title
BIOORGANIC & MEDICINAL CHEMISTRY
Volume
18
Number
10
Start Page
3467
End Page
3473
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/116447
DOI
10.1016/j.bmc.2010.03.074
ISSN
0968-0896
Abstract
Single stranded DNA aptamers that can bind to ibuprofen, a widely used anti-inflammation drug, were selected from random DNA library of 10(15) nucleotides by FluMag-SELEX process. Five different sequences were selected and their enantioselectivity and affinity were characterized. Three out of five aptamer candidates did not show any affinity to (S)-ibuprofen, but only to racemic form of ibuprofen, suggesting that they are (R)-ibuprofen specific aptamers. Another two aptamer candidates showed affinity to both racemic form and (S)-ibuprofen, which were considered as (S)-ibuprofen specific aptamers. The affinity of five ssDNA aptamers isolated was in a range of 1.5-5.2 mu M. In addition, all of these five aptamers did not show any affinity to analogues of ibuprofen in its profen's group (fenoprofen, flubiprofen, and naproxen) and the antibiotics of oxytetracycline, another control. (C) 2010 Elsevier Ltd. All rights reserved.
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