Richard N. Zare - Stanford CA, US Maria T. Dulay - Sunnyvale CA, US Joselito P. Quirino - Stanford CA, US Bryson Bennett - Murray UT, US
Assignee:
The Board of Trustees of the Leland Stanford Junior University - Stanford CA
International Classification:
B01D015/08
US Classification:
210656, 210635, 2101982, 210658, 2101983
Abstract:
A separation column and a method of making the separation column are provided. The separation column includes a separation channel and fritless separation medium in the channel. The separation medium includes a porous matrix, and the porous matrix includes a metal organic polymer, such as a photopolymer. The separation medium can be used to separate a sample of analytes.
Separation Column Having A Photopolymerized Sol-Gel Component And Associated Methods
Richard N. Zare - Stanford CA, US Maria T. Dulay - Sunnyvale CA, US Joselito P. Quirino - Sunnyvale CA, US Bryson D. Bennett - Murray UT, US
Assignee:
The Board of Trustees of the Leland Stanford Junior University - Stanford CA
International Classification:
B01D015/08
US Classification:
2101982, 2101983, 210635, 210656, 210658
Abstract:
A separation column and a method of preparing the separation column are provided. The separation column includes a separation channel and a porous matrix in the channel. The porous matrix includes a metal organic polymer, such as a photopolymer. The porous matrix can be a separation medium adapted to separate a sample of analytes or a frit adapted to retain a separation medium in the channel.
Bonded Phase Photopolymerized Sol-Gel Column And Associated Methods
Richard N. Zare - Stanford CA, US Maria T. Dulay - Sunnyvale CA, US Joselito P. Quirino - Stanford CA, US Bryson Bennett - Murray UT, US
Assignee:
The Board of Trustees of the Leland Stanford Junior University - Stanford CA
International Classification:
B01D015/08
US Classification:
2101982, 2101983, 210635, 210656, 210658
Abstract:
A separation column and a method of making the separation column are provided. The separation column includes a separation channel and a separation medium in the channel. The separation medium includes a porous matrix, and the porous matrix includes a support and a stationary phase. The support includes a metal organic polymer, such as a photopolymer, and the stationary phase includes a bonded phase. The separation medium can be used to separate a sample of analytes.
Fused-Silica Capillaries With Photopolymer Components
Richard N. Zare - Stanford CA, US Maria T. Dulay - Sunnyvale CA, US Jing-Ran Chen - Shaumburg IL, US
International Classification:
B01D 15/08
US Classification:
2101982, 210635, 210656, 96101
Abstract:
A separation column is provided with a photopolymer component which, when irradiated, causes controlled porosity polymerization. A particularly preferred embodiment is wherein the separation medium is retained by a photopolymer frit, which can be reliably and reproducibly generated with controlled porosity.
Fused-Silica Capillaries With Photopolymer Components
Richard Zare - Stanford CA, US Maria Dulay - Sunnyvale CA, US Jing-Ran Chen - Shaumburg IL, US
International Classification:
B01D015/08
US Classification:
210/198200, 210/656000
Abstract:
A separation column is provided with a photopolymer component which, when irradiated, causes controlled porosity polymerization. A particularly preferred embodiment is wherein the separation medium is retained by a photopolymer frit, which can be reliably and reproducibly generated with controlled porosity.
Immobilized-Enzyme Microreactor Devices For Characterization Of Biomolecular Analytes And Associated Methods
Richard Zare - Stanford CA, US Maria Dulay - Sunnyvale CA, US Quentin Baca - Albuquerque NM, US Gabriele Trapp - Goeppingen, DE
International Classification:
B01D015/08
US Classification:
210656000, 210635000, 435004000, 435007100
Abstract:
A method that comprises providing a polymerized sol-gel material (PSG) and linking an enzyme to a surface of the PSG via covalent linkage is provided. The surface of the PSG is derivatized with a linker that comprises a functional group for linking itself to the surface of the PSG and a functional group for linking itself with then enzyme. The linked-enzyme PSG, or microreactor, is an effective means of at least partially digesting a substrate, such as a biological substrate. The activity of the enzyme of the microreactor may be significantly enhanced, up to 200-fold for example, relative to the activity of the enzyme free of the microreactor. The microreactor is thus an effective vehicle for digesting a substrate such as a biomolecule, a protein, an oligonucleotide, a peptide, a steroid, and/or an organic acid, after which, any remaining substrate and one or more digestion product(s) may be separated and detected. Microreactors and integrated devices that incorporate microreactors, such as columns, pipet tips, wells, and well-plates, are also provided.
Immobilized-Enzyme Microreactor Devices For Characterization Of Biomolecular Analytes And Associated Methods
A method that comprises providing a polymerized sol-gel material (PSG) and linking an enzyme to a surface of the PSG via covalent linkage is provided. The surface of the PSG is derivatized with a linker that comprises a functional group for linking itself to the surface of the PSG and a functional group for linking itself with the enzyme. The linked-enzyme PSG, or microreactor, is an effective means of at least partially digesting a substrate, such as a biological substrate. The activity of the enzyme of the microreactor may be significantly enhanced, up to 200-fold for example, relative to the activity of the enzyme free of the microreactor. The microreactor is thus an effective vehicle for digesting a substrate such as a biomolecule, a protein, an oligonucleotide, a peptide, a steroid, and/or an organic acid, after which, any remaining substrate and one or more digestion product(s) may be separated and detected. Microreactors and integrated devices that incorporate microreactors, such as columns, pipet tips, wells, and well-plates, are also provided.
Immobilized-Enzyme Microreactor Devices For Characterization Of Biomolecular Analytes And Associated Methods
Richard N. Zare - Stanford CA, US Maria T. Dulay - Sunnyvale CA, US
International Classification:
B01D 15/08
US Classification:
210656, 204456, 435 4
Abstract:
A method that comprises providing a polymerized sol-gel material (PSG) and linking an enzyme to a surface of the PSG via covalent linkage is provided. The surface of the PSG is derivatized with a linker that comprises a functional group for linking itself to the surface of the PSG and a functional group for linking itself with the enzyme. The linked-enzyme PSG, or microreactor, is an effective means of at least partially digesting a substrate, such as a biological substrate. The activity of the enzyme of the microreactor may be significantly enhanced, up to 200-fold to over 2000-fold, for example, relative to the activity of the enzyme free of the microreactor. The microreactor is thus an effective vehicle for digesting a substrate such as a biomolecule, a protein, an oligonucleotide, a peptide, a steroid, and/or an organic acid, after which, any remaining substrate and one or more digestion product(s) may be separated and detected. Microreactors and integrated devices that incorporate microreactors, such as chips, columns, pipet tips, wells, and well-plates, are also provided.