Packing material for liquid chromatography
US-2018104669-A1 · Apr 19, 2018 · US
US11247192B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11247192-B2 |
| Application number | US-201716327437-A |
| Country | US |
| Kind code | B2 |
| Filing date | Aug 10, 2017 |
| Priority date | Aug 26, 2016 |
| Publication date | Feb 15, 2022 |
| Grant date | Feb 15, 2022 |
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Provided is a packing material for HILIC columns for more accurately and more easily performing oligosaccharide analysis by liquid chromatography; an HILIC column which is filled with the packing material for HILIC columns; and a method for analyzing an oligosaccharide with use of this packing material for HILIC columns A packing material for HILIC columns according to the present invention is composed of particles, each of which is obtained by reacting glycidol to a hydroxyl group of a porous cross-linked polymer base material having the hydroxyl group, and which have a hydrophilicity index of 2.30 or more and a surface-pH index of from 0.95 to 1.05.
Opening claim text (preview).
The invention claimed is: 1. A packing material for HILIC columns, comprising a cross-linked polymer base material having a hydroxyl group, wherein the cross-linked polymer base material is porous particles; a glycidol is reacted with the hydroxyl group of the cross-linked polymer base material; the packing material has a hydrophilicity index of 2.30 or more; and the packing material has a surface-pH index of from 0.95 to 1.05, wherein the hydrophilicity index is defined by a separation coefficient of α1 (U/2dU), when performing a liquid chromatography measurement of a uridine (U) and a 2′-deoxyuridine (2dU) in a HILIC separation mode condition; the surface-pH index is a separation coefficient of α2 (Tb/Tp), when performing a liquid chromatography measurement of a theobromine (Tb) and a theophylline (Tp) in a HILIC separation mode condition; the separation coefficient α1 (U/2dU) and the separation coefficient α2 (Tb/Tp) are ratios of retention factors k of the materials, respectively; each retention factor k is defined by k=(t−t 0 )/t 0 , wherein t 0 is an elution time of toluene and, t is an elution time of each substance; and a condition of the liquid chromatography measurement in the HILIC separation mode is shown as below: a column temperature is 30° C.; and a mobile phase is a mixed liquid of acetonitrile and an aqueous solution in a ratio (acetonitrile/aqueous solution) of 90/10 (volume before mixing) wherein the aqueous solution contains 10 mM acetic acid and 10 mM ammonium acetate. 2. The packing material for HILIC columns according to claim 1 , wherein the porous cross-linked polymer base material having a hydroxyl group is a copolymer of vinyl alcohol and triallyl isocyanurate. 3. A HILIC column, comprising the packing material for HILIC columns according to claim 1 , and a liquid chromatography casing in which the packing material for HILIC columns is filled. 4. A method for analyzing oligosaccharides, comprising analyzing oligosaccharides in a HILIC mode using the HILIC column according to claim 3 . 5. The method for analyzing oligosaccharides according to claim 4 , wherein a composition of a mobile phase is constant during the measurement (in an isocratic elution condition) and a column temperature is constant during the measurement method for analyzing oligosaccharides. 6. The method for analyzing oligosaccharides according to claim 4 , wherein a molecular size of the oligosaccharides to be analyzed is 17 mer or more. 7. The packing material for HILIC columns according to claim 1 , wherein a particle size of the porous particles is 1 to 30 μm as a volume average particle diameter, and an average pore diameter of pores forming the porous particles is from 3 to 30 nm.
Polar phases · CPC title
Sorbents applied to inner surfaces of columns or capillaries · CPC title
Integrated analysis systems specially adapted therefor, not covered by a single one of the groups G01N30/04 - G01N30/86 · CPC title
Use in a single column · CPC title
involving saccharides · CPC title
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