Compositions and methods for solid phase extraction of lipids

US10434492B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10434492-B2
Application numberUS-78516010-A
CountryUS
Kind codeB2
Filing dateMay 21, 2010
Priority dateJan 26, 2007
Publication dateOct 8, 2019
Grant dateOct 8, 2019

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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Abstract

Official abstract text for this publication.

A composition, method and device for the preparation of biological samples for subsequent instrumental analyses, such as GC, GC-MS, LC and LC-MS analysis, using a solid phase extraction (SPE) process is described. Through SPE process alone or an integrated combination of protein precipitation, filtration, and SPE using a hydrophobic zirconia-coated chromatographic media, interfering compounds, such as proteins, glycerides and phosphate-containing compounds, are eliminated from the biological, food, environmental and biotechnology samples, affording an enhanced analyte response during the instrumental analysis.

First claim

Opening claim text (preview).

What is claimed is: 1. A solid phase extraction (SPE) media for selective removal of lipids from a sample comprising: a. a porous silica substrate with any one or more of a particle size ranging from about 10 nm to about 1000 μm, a pore size ranging from about 30 Å to about 1000 Å, and a surface area ranging from about 5 m 2 /g to about 1000 m 2 /g; b. a hydrophobic alkyl linker having an attached end and a free end opposite the attached end, the attached end covalently bonded to the substrate, wherein the alkyl ranges from C 3 to C 18 ; and, c. zirconia bonded to the porous silica substrate through a bridging bond. 2. The SPE media of claim 1 , wherein the sample comprises a biological sample, a food matrix, an environmental sample, a sample from a biotechnology process, or any combination thereof. 3. The SPE media of claim 1 , wherein the sample further comprises an acidic analyte, a non-acidic analyte, or a mixture of an acidic analyte and a non-acidic analyte. 4. A solid phase extraction (SPE) media for selective removal of lipids from a sample comprising: a. a porous silica substrate with any one or more of a particle size ranging from about 10 nm to about 1000 μm, a pore size ranging from about 30 Å to about 1000 Å, and a surface area ranging from about 5 m 2 /g to about 1000 m 2 /g; b. a hydrophobic alkyl linker comprising an attached end covalently bonded to the substrate and a free end opposite the attached end, wherein the alkyl ranges from C 3 to C 18 ; and, c. zirconia covalently bonded through a bridging bond coupled to the free end of the hydrophobic alkyl linker. 5. The SPE media of claim 4 , wherein the sample comprises a biological sample, a food matrix, an environmental sample, a sample from a biotechnology process, or any combination thereof. 6. The SPE media of claim 4 , wherein the sample further comprises an acidic analyte, a non-acidic analyte, or a mixture of an acidic analyte and a non-acidic analyte. 7. A solid phase extraction (SPE) media for selective removal of lipids from a sample, the SPE comprising a mixture of: a. a first particle comprising zirconia bonded through a bridging bond to a porous silica substrate having any one or more of a particle size ranging from about 10 nm to about 1000 μm, a pore size ranging from about 30 Å to about 1000 Å, and a surface area ranging from about 5 m 2 /g to about 1000 m 2 /g, b. a second particle comprising a hydrophobic alkyl linker ranging from C 3 to C 18 having an attached end and a free end opposite the attached end, the attached end covalently bonded to a second porous silica substrate, the second porous silica substrate having any one or more of a particle size ranging from about 10 nm to about 1000 μm, a pore size ranging from about 30 Å to about 1000 Å, and a surface area ranging from about 5 m 2 /g to about 1000 m 2 /g. 8. The SPE media of claim 7 , wherein the sample comprises a biological sample, a food matrix, an environmental sample, a sample from a biotechnology process, or any combination thereof. 9. The SPE media of claim 7 , wherein the sample further comprises an acidic analyte, a non-acidic analyte, or a mixture of an acidic analyte and a non-acidic analyte.

Assignees

Inventors

Classifications

  • comprising silica · CPC title

  • B01J20/06Primary

    comprising oxides or hydroxides of metals not provided for in group B01J20/04 · CPC title

  • with separation columns in parallel · CPC title

  • Cartridges · CPC title

  • Compounds of Ti, Zr, Hf · CPC title

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What does patent US10434492B2 cover?
A composition, method and device for the preparation of biological samples for subsequent instrumental analyses, such as GC, GC-MS, LC and LC-MS analysis, using a solid phase extraction (SPE) process is described. Through SPE process alone or an integrated combination of protein precipitation, filtration, and SPE using a hydrophobic zirconia-coated chromatographic media, interfering compounds, …
Who is the assignee on this patent?
Lu Xiaoning, Shimelis Olga I, Ye Maochun M, and 1 more
What technology area does this patent fall under?
Primary CPC classification B01J20/06. Mapped technology areas include Operations & Transport.
When was this patent published?
Publication date Tue Oct 08 2019 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).