Abstract:
Provided is a separating agent comprising a carrier and a ligand fixed on a surface of a carrier by chemical bonding, in which the carrier is a core-shell particle formed of a non-porous core and a porous shell, the shell having a pore diameter of 9 nm or more and formed of a hydrolysate of polyalkoxysiloxane, and the ligand is an optically active polymer, optically inactive polyester, protein, nucleic acid, or optically active organic compound with a molecular weight of 50 to 1000.
Abstract:
The invention relates to poly-amide bonded hydrophilic interaction chromatography (HILIC) stationary phases and novel HILIC methods for use in the characterization of large biological molecules modified with polar groups, known to those skilled in the art as glycans. The invention particularly provides novel, poly-amide bonded materials designed for efficient separation of large biomolecules, e.g. materials having a large percentage of larger pores (i.e. wide pores). Furthermore, the invention advantageously provides novel HILIC methods that can be used in combination with the stationary phase materials described herein to effectively separate protein and peptide glycoforms by eliminating previously unsolved problems, such as on-column aggregation of protein samples, low sensitivity of chromatographic detection of the glycan moieties, and low resolution of peaks due to restricted pore diffusion and long intra/inter-particle diffusion distances.
Abstract:
The present invention relates to novel carbohydrate polyether compositions that are soluble in aqueous media and particularly to carbohydrate polyether compositions exhibiting reverse thermogelation properties in aqueous media. Also, since the carbohydrate polyethers of the present invention can be conveniently controlled with respect to functionality, molecular weight, polydispersity index, microstructure and tertiary structure, they can be customized for use in a variety of applications.
Abstract:
Described is an affinity microcolumn comprising a high surface area material, which has high flow properties and a low dead volume, contained within a housing and having affinity reagents bound to the surface of the high surface area material that are either activated or activatable. The affinity reagents bound to the surface of the affinity microcolumn further comprise affinity receptors for the integration into high throughput analysis of biomolecules.
Abstract:
Gas chromatography column comprising a substrate, a channel formed in said substrate, a cover closing said substrate and a stationary phase covering the walls of said channel, wherein said stationary phase is made of SiOxCyHz with x between 1.6 and 1.8, y between 1 and 2.2 and z between 3 and 4, wherein said stationary phase is porous with a porosity of between 10% and 40%.
Abstract translation:气相色谱柱,包括基底,在所述基底中形成的通道,封闭所述基底的盖和覆盖所述通道壁的固定相,其中所述固定相由SiO x CyHz制成,x在1.6和1.8之间,y在1和2.2之间 和z在3和4之间,其中所述固定相是多孔的,孔隙率在10%和40%之间。
Abstract:
Provided are graft copolymer particles enabling introduction of adsorptive functional groups adsorbing metals and others, a method for producing same, and an adsorbent using same. (1) Porous graft copolymer particles containing graft chains introduced into porous particles (particle surface having an average pore diameter of 0.01-50 μm) including at least one resin selected from olefin resins, water-insoluble modified polyvinyl alcohol resins, amide resins, cellulosic resins, chitosan resins and (meth)acrylate resins. (2) A method for producing porous graft copolymer particles including (I) melt-kneading a polymer A and a polymer B other than the polymer A to obtain a compound material, (II) extracting and removing the polymer B from the compound material to obtain a porous material of the polymer A, (III) granulating the porous material, and (IV) introducing graft chains into the porous particles. (3) An adsorbent of porous graft copolymer particles.
Abstract:
The invention relates to poly-amide bonded hydrophilic interaction chromatography (HILIC) stationary phases and novel HILIC methods for use in the characterization of large biological molecules modified with polar groups, known to those skilled in the art as glycans. The invention particularly provides novel, poly-amide bonded materials designed for efficient separation of large biomolecules, e.g. materials having a large percentage of larger pores (i.e. wide pores). Furthermore, the invention advantageously provides novel HILIC methods that can be used in combination with the stationary phase materials described herein to effectively separate protein and peptide glycoforms by eliminating previously unsolved problems, such as on-column aggregation of protein samples, low sensitivity of chromatographic detection of the glycan moieties, and low resolution of peaks due to restricted pore diffusion and long intra/inter-particle diffusion distances.
Abstract:
An object of the present invention is to provide a stationary phase that increases the number of column stages and that exhibits an excellent molecular discrimination ability. It was discovered that the number of column stages can be increased and an excellent molecular discrimination ability can be realized by a stationary phase that contains a polymer having, in main chain repeat units, an aromatic ring that forms a portion of the main chain and a bipolar atomic group that forms a portion of the main chain, wherein the stationary phase has a specific surface area of 5 to 1000 m2/g.
Abstract:
Storage stable polyhydroxylated aromatic ether adducts of polyalkylene oxide are described. Reactive compositions are formed by combining an ether adduct with an aldehyde, optionally further adding a phenolic-aldehyde prepolymer. The reactive compositions are cured by removing water, by acidification, or both. The cured compositions sorb solvated compounds from environments containing water. The cured compositions are also useful for pre-loading with compounds that are subsequently released at a controlled rate into environments containing water.