Methods, compositions, devices, and kits for performing phospholipid separation

Patent metadata

Field	Value
Publication number	US-9951092-B2
Application number	US-201113580884-A
Country	US
Kind code	B2
Filing date	May 20, 2011
Priority date	May 20, 2010
Publication date	Apr 24, 2018
Grant date	Apr 24, 2018

Abstract

Methods, kits and devices for separating phospholipids and proteins from small molecules in biochemical samples can feature an apparatus having a wetting barrier, at least one fit and a separation media. For example, an apparatus can include at least one wall defining a chamber having an exit and an entrance; a wetting barrier disposed between the exit and entrance, so as to define a separation media space located between the wetting barrier and the exit and a sample receiving area located between the wetting barrier and the entrance; and a separation media disposed adjacent to the wetting barrier and having a specific affinity for phospholipids. The wetting barrier is adapted to (i) retain the liquid sample and a protein precipitating agent in the sample receiving area under a first force, thereby facilitating the formation of a protein precipitate and a processed sample, and (ii) flow the processed sample through the wetting barrier and separation media under a second force, wherein the second force is greater than the first force, thereby retaining the protein precipitate in the sample receiving area, retaining phospholipids in the separation media, and eluting small molecules.

First claim

The invention claimed is:

1. An apparatus for separating a liquid sample potentially comprising one or more proteins, phospholipids, and small molecules, the apparatus comprising:
a housing having at least one wall defining one or more chambers, each chamber having (i) an exit opening and an entrance opening;
(ii) a wetting barrier having a first plurality of openings and disposed between the exit opening and entrance opening, so as to define a separation media space located between the wetting barrier and the exit opening and a sample receiving area located between the wetting barrier and the entrance opening;
(iii) a separation media disposed between the wetting barrier and the exit opening and having a specific affinity for phospholipids; and
at least one frit disposed between the wetting barrier and the entrance opening, the at least one frit having a second plurality of openings, the second plurality of openings larger than the first plurality of openings of the wetting barrier; and
wherein the wetting barrier is adapted to (i) retain the liquid sample and a protein precipitating agent in the sample receiving area under a first force, thereby facilitating the formation of a protein precipitate and a processed sample, and (ii) flow the processed sample through the wetting barrier and separation media under a second force, wherein the second force is greater than the first force, thereby retaining the protein precipitate in the sample receiving area, retaining phospholipids in the separation media, and eluting small molecules;
wherein the separation media has a core composition and a surface composition represented by formula 1:
W—[X]-Q  (Formula 1)

wherein
X represents the core composition;
W and Q occupy free valences of the core or surface composition that are not X;
W is a hydroxyl group;
Q is an aliphatic silane group wherein the aliphatic group comprises 6 to 30 carbons,

wherein W and Q form said surface composition; and
the ratio W to Q is between 3.5 and 13.6.

2. An apparatus for separating a liquid sample potentially comprising one or more proteins, phospholipids, and small molecules, the apparatus comprising:
a housing having at least one wall defining one or more chambers, each chamber having (i) an exit opening and an entrance opening;
(ii) a wetting barrier having a first plurality of openings and disposed between the exit opening and entrance opening, so as to define a separation media space located between the wetting barrier and the exit opening and a sample receiving area located between the wetting barrier and the entrance opening;
(iii) a separation media disposed between the wetting barrier and the exit opening and having a specific affinity for phospholipids; and
at least one frit disposed between the wetting barrier and the entrance opening, the at least one frit having a second plurality of openings, the second plurality of openings larger than the first plurality of openings of the wetting barrier; and
wherein the wetting barrier is adapted to (i) retain the liquid sample and a protein precipitating agent in the sample receiving area under a first force, thereby facilitating the formation of a protein precipitate and a processed sample, and (ii) flow the processed sample through the wetting barrier and separation media under a second force, wherein the second force is greater than the first force, thereby retaining the protein precipitate in the sample receiving area, retaining phospholipids in the separation media, and eluting small molecules;
wherein the separation media has a core composition and a surface composition represented by formula 1 below:
W—[X]-Q  (Formula 1)

wherein,
X represents the core composition;
W and Q occupy free valences of the core or surface composition that are not X;
W is hydrogen or a hydroxyl group,

wherein at least a fraction of W is hydroxyl;
Q is Si—R 1 ; and
R 1 is a higher alkyl; wherein the ratio of concentration of hydroxyl to Si—R 1 is 3.5-13.6.

3. A method for separating a liquid sample potentially comprising one or more proteins, phospholipids, and small molecules, the method comprising:
providing a housing having at least one wall defining one or more chambers, each chamber having (i) an exit opening and an entrance opening, (ii) a wetting barrier having a first plurality of openings and disposed between the exit opening and entrance opening, so as to define a separation media space located between the wetting barrier and the exit opening and a sample receiving area located between the wetting barrier and the entrance opening, (iii) a separation media disposed between the wetting barrier and the exit opening and having a specific affinity for phospholipids, and at least one frit disposed between the wetting barrier and the entrance opening, the at least one frit having a second plurality of openings larger than the first plurality of openings of the wetting barrier;
contacting the liquid sample and a protein precipitating agent in the sample receiving area under a first force, thereby forming a protein precipitate and a processed sample; and
flowing the processed sample through the wetting barrier and separation media under a second force, wherein the second force is greater than the first force, thereby retaining at least a fraction of the protein precipitate in the sample receiving area, retaining phospholipids in the separation media, and eluting small molecules; and
wherein the separation media has a core composition and a surface composition represented by formula 1 below:
W—[X]-Q  (Formula 1)

wherein,
X represents the core composition;
W and Q occupy free valences of the core or surface composition that are not X;
W is a hydroxyl group;
Q is an aliphatic silane group wherein the aliphatic group comprises 6 to 30 carbons,

wherein W and Q form said surface composition; and
the ratio W to Q is between 3.5 and 13.6.

4. A method for separating a liquid sample potentially comprising one or more proteins, phospholipids, and small molecules, the method comprising:
providing a housing having at least one wall defining one or more chambers, each chamber having (i) an exit opening and an entrance opening, (ii) a wetting barrier having a first plurality of openings and disposed between the exit opening and entrance opening, so as to define a separation media space located between the wetting barrier and the exit opening and a sample receiving area located between the wetting barrier and the entrance opening, (iii) a separation media disposed between the wetting barrier and the exit opening and having a specific affinity for phospholipids, and at least one frit disposed between the wetting barrier and the entrance opening, the at least one frit having a second plurality of openings larger than the first plurality of openings of the wetting barrier;
contacting the liquid sample and a protein precipitating agent in the sample receiving area under a first force, thereby forming a protein precipitate and a processed sample; and
flowing the processed sample through the wetting barrier and separation media under a second force, wherein the second force is greater than the first force, thereby retaining at least a fraction of the protein precipitate in the sample receiving area, retaining phospholipids in the separation media, and eluting small molecules; and
wherein the separation media has a core composition and a surface composition represented by formula 1 below:
W—[X]-Q  (Formula 1)

wherein,
X represents the core composition;
W and Q occupy free valences of the core or surface composition that are not X;
W is hydrogen or a hydroxyl group, wherein at least a fraction of W is hydroxyl;
Q is Si—R 1 ; and
R 1 is a higher alkyl; wherein the rat

Assignees

• Iraneta Pamela C
• Walter Thomas H
• Zhang Xin
• Walsh Daniel P
• Wyndham Kevin D
• Fisk Raymond P
• Waters Technologies Corp

Inventors

• Iraneta Pamela C
• Walter Thomas H
• Zhang Xin
• Walsh Daniel P
• Wyndham Kevin D
• Fisk Raymond P

Classifications

• B01J20/287

  Non-polar phases; Reversed phases · CPC title

• B01D15/327

  with hydrophobic interaction · CPC title

• C07F9/103 Primary

  Extraction or purification by physical or chemical treatment of natural phosphatides; Preparation of compositions containing phosphatides of unknown structure · CPC title

• B01J2220/64

  In a syringe, pipette, e.g. tip or in a tube, e.g. test-tube or u-shape tube · CPC title

• G01N2030/8813

  biological materials · CPC title