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Determination of Thiamine in Pharmaceutical Preparations by Reverse Phase Liquid Chromatography Without Use of Organic Solvent

Authors
Suh, Joon HyukKim, JunghyunJung, JuheeKim, KyunghyunLee, Seul GiCho, Hyun-DeokJung, YuraHan, Sang Beom
Issue Date
20-Jun-2013
Publisher
KOREAN CHEMICAL SOC
Keywords
Very polar compound; Thiamine; Room temperature ionic liquids (RTILs); Reverse phase high performance liquid chromatography (RP-HPLC)
Citation
BULLETIN OF THE KOREAN CHEMICAL SOCIETY, v.34, no.6, pp 1745 - 1750
Pages
6
Journal Title
BULLETIN OF THE KOREAN CHEMICAL SOCIETY
Volume
34
Number
6
Start Page
1745
End Page
1750
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/14539
DOI
10.5012/bkcs.2013.34.6.1745
ISSN
0253-2964
1229-5949
Abstract
A novel green aqueous mobile phase modified with room temperature ionic liquids (RTILs) was employed in the absence of volatile organic solvents or ion-pairing reagents to analyze thiamine, a very polar compound, by reverse phase high performance liquid chromatography (RP-HPLC). Due to its strongly hydrophilic nature, thiamine was eluted near the column dead time (to) using a mobile phase without adding RTILs or ion-pairing reagents, even if a 100% aqueous mobile phase, which has weak elution power under reverse phase conditions, was used. Thus, 1-ethyl-3-methyl-imidazolium hexafluorophosphate ([EMIM][PF6]), which has the strongest chaotropic effect, was selected as a mobile phase additive to improve retention and avoid baseline disturbances at to. Various mobile phase parameters such as cation moiety, chaotropic anion moiety, pH and concentration of RTILs were optimized to determine thiamine at the proper retention time. Method validation was performed to assess linearity, intra- and inter-day accuracy and precision, recovery and repeatability; all results were found to be satisfactory. The developed method was also compared to the current official United States Pharmacopoeia (USP) and Korean Pharmacopoeia (KP) methods using an organic mobile phase containing an ion-pairing reagent by means of evaluating various chromatographic parameters such as the capacity factor, theoretical plate number, peak asymmetry and tailing factor. The results indicated that the proposed method exhibited better efficiency of thiamine analysis than the official methods, and it was successfully applied to quantify thiamine in pharmaceutical preparations.
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