Publication: Simple and fast analysis of iohexol in human serums using micro-hydrophilic interaction liquid chromatography with monolithic column
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0
Issued Date
2016
Resource Type
File Type
application/pdf
ISSN
16159306
Other identifier(s)
2-s2.0-84988380509
Rights Holder(s)
มหาวิทยาลัยศรีนครินทรวิโรฒ
Bibliographic Citation
Journal of Separation Science. Vol 39, No.18 (2016), p.3521-3527
Suggested Citation
Chaloemsuwiwattanakan T., Sangcakul A., Kitiyakara C., Nacapricha D., Wilairat P., Chaisuwan P. Simple and fast analysis of iohexol in human serums using micro-hydrophilic interaction liquid chromatography with monolithic column. Journal of Separation Science. Vol 39, No.18 (2016), p.3521-3527. doi:10.1002/jssc.201600475 Retrieved from: https://hdl.handle.net/20.500.14740/5253
Abstract
A simple and rapid method based on micro-liquid chromatography using a synthetic monolithic capillary column was developed for determination of iohexol in human serums, a marker to evaluate the glomerular filtration rate. A hydrophilic methacrylic acid-ethylene dimethacrylate monolith provided excellent selectivity and efficiency for iohexol with separation time of 3 min using a mobile phase of 40:60 v/v 50 mM phosphate buffer pH 5/methanol. Four serum protein removal, methods using perchloric acid, 50% acetonitrile, 0.1 M zinc sulfate, and centrifuge membrane filter were examined. The method of zinc sulfate was chosen due to its simplicity, compatibility with the mobile phase system, nontoxicity, and low cost. Interday calibration curves were conducted over iohexol concentrations range of 2–500 mg/L (R2 = 0.9997 ± 0.0001) with detection limit of 0.44 mg/L. Intra- and interday precisions for peak area and retention time were less than 2.8 and 1.4%, respectively. The method was successfully applied to serum samples with percent recoveries from 102 to 104. The method was applied to monitor released iohexol from healthy subject. Compared with the commercially available reversed-phase high-performance liquid chromatography method, the presented method provided simpler chromatogram, faster separation with higher separation efficiency and much lower sample and solvent consumption. © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Subject(s)
Body fluids
Chromatographic analysis
Chromatography
Column chromatography
Efficiency
Ethylene
Filtration
High performance liquid chromatography
Hydrophilicity
Liquids
Separation
Zinc
Ethylene dimethacrylate
Glomerular filtration rate
Hydrophilic interaction liquid chromatographies
Iohexol
Micro-liquid chromatography
Monolithic capillary column
Reversed phase high performance liquid chromatography
Separation efficiency
Liquid chromatography
Acetonitrile
Ethylene glycol dimethacrylate
Iohexol
Methacrylic acid
Methanol
Perchloric acid
Zinc sulfate
Article
Calibration
Controlled study
Drug blood level
Drug determination
Drug structure
Glomerulus filtration rate
Human
Hydrophilic interaction chromatography
Limit of detection
Membrane filter
Normal human
PH
Priority journal
Retention time
Reversed phase high performance liquid chromatography
Serum
Chromatographic analysis
Chromatography
Column chromatography
Efficiency
Ethylene
Filtration
High performance liquid chromatography
Hydrophilicity
Liquids
Separation
Zinc
Ethylene dimethacrylate
Glomerular filtration rate
Hydrophilic interaction liquid chromatographies
Iohexol
Micro-liquid chromatography
Monolithic capillary column
Reversed phase high performance liquid chromatography
Separation efficiency
Liquid chromatography
Acetonitrile
Ethylene glycol dimethacrylate
Iohexol
Methacrylic acid
Methanol
Perchloric acid
Zinc sulfate
Article
Calibration
Controlled study
Drug blood level
Drug determination
Drug structure
Glomerulus filtration rate
Human
Hydrophilic interaction chromatography
Limit of detection
Membrane filter
Normal human
PH
Priority journal
Retention time
Reversed phase high performance liquid chromatography
Serum
