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Cited 2 time in webofscience Cited 2 time in scopus
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Determination of process-related impurities in N-acetylglucosamine prepared by chemical and enzymatic methods: structural elucidation and quantification

Authors
Kim, Yi SooLee, Sung JoongChoi, Jin YoungKim, Yun-HiDesta, Kebede TayePiao, ZheChoi, Su-LimNam, Sang-JipKang, Kyung-YunAbd El-Aty, A. M.Shin, Yong ChulShin, Sung Chul
Issue Date
Jul-2016
Publisher
대한약학회
Keywords
beta-N-acetylglucosamine; Process-related impurity; Tandem mass spectrometry; Chitin; Nuclear magnetic resonance
Citation
Archives of Pharmacal Research, v.39, no.7, pp 937 - 945
Pages
9
Indexed
SCIE
SCOPUS
KCI
Journal Title
Archives of Pharmacal Research
Volume
39
Number
7
Start Page
937
End Page
945
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/15385
DOI
10.1007/s12272-016-0755-3
ISSN
0253-6269
1976-3786
Abstract
beta-N-acetylglucosamine (beta-AG) is a monosaccharide distributed widely in living organisms with various pivotal roles. The presence of particulates and impurities can affect the safety and efficacy of a product for its intended duration of use. Thus, the current study was carried out to identify and quantify the potentially-harmful process related impurities; namely alpha-N,6-diacetylglucosamine (alpha-DAG) and alpha-N-acetylglucosamine (alpha-AG), derived from the chemical and enzymatic synthesis of beta-AG. The impurities were characterized using a high resolution mass spectrometry, a nuclear magnetic resonance spectroscopy, and liquid chromatography-tandem mass spectrometry (LC/MS/MS). The developed method showed a good linearity (R (2) a parts per thousand yen 0.998), satisfactory precision (a parts per thousand currency sign6.1 % relative standard deviation), intra- and inter-day accuracy (88.20-97.50 %), extraction recovery (89.30-110.50 %), matrix effect (89.70-105.20 %), and stability (92.70-101.60 %). The method was successfully applied to determine the level of alpha-DAG that was 3.04 and 0.07 % of the total beta-AG, following chemical and enzymatic methods, respectively. It can be concluded that the enzymatic rather than the chemical method is more efficient for the synthesis of beta-AG. Characterization of impurities heeds the signal for acquiring and evaluating data that establishes biological safety.
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