IP Library Granted Patent US 9,827,552
Granted Patent B2
US 9,827,552 · App. 14/333,561 · Granted Nov 28, 2017

Functionalized lipid modification of solid phase surfaces for use in chromatography

Inventors: R. Kenneth Marcus (Clemson, SC); Kenneth A. Christensen (Clemson, SC)
Assignee: Clemson University
B01J20/281B01D15/206B01D15/3823B01J20/285B01J20/28023B01J20/28052B01J20/321B01J20/3272B01J20/3274B01J20/3293C07K1/20G01N30/50G01N33/54353G01N33/54393B01J2220/56G01N2030/8813Y10T436/255
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Quick Facts
Patent No.
US 9,827,552
App. No.
14/333,561
Granted
Nov 28, 2017
Kind
B2
Abstract

A solid phase for use in separation has been modified using an aqueous phase adsorption of a headgroup-modified lipid to generate analyte specific surfaces for use as a stationary phase in separations such as high performance liquid chromatography (HPLC) or solid phase extraction (SPE). The aliphatic moiety of the lipid adsorbs strongly to a hydrophobic solid surface, with the hydrophilic and active headgroups orienting themselves toward the more polar mobile phase, thus allowing for interactions with the desired solutes. The surface modification approach is generally applicable to a diversity of selective immobilization applications such as protein immobilization clinical diagnostics and preparative scale HPLC as demonstrated on capillary-channeled fibers, though the general methodology could be implemented on any hydrophobic solid support material.

Claims (12)

1. A surface modified solid phase for a chromatography separation protocol comprising:

a polymeric solid phase comprising a hydrophobic surface;

a lipid, the lipid including a hydrophobic end and a headgroup opposite the hydrophobic end, the hydrophobic end having the structure of:

wherein m is from 6 to 30, the hydrophobic end being adsorbed to the hydrophobic surface of the polymeric solid phase such that the hydrophobic end of the lipid lays along or intercollates into the hydrophobic surface, the headgroup comprising a functional group that is configured for binding a targeted analyte, the functional group including a coenzyme, a nucleotide, or a polypeptide.

2. The surface modified solid phase of claim 1 , wherein the lipid is a phospholipid, a glycerolipid, a glycerophospholipid, or a fatty acid.

3. The surface modified solid phase of claim 1 , further comprising a hydrophilic spacer between the hydrophobic end and the headgroup.

4. The surface modified solid phase of claim 3 , wherein the hydrophilic spacer comprises a polyethylene glycol spacer.

5. The surface modified solid phase of claim 1 , wherein the polymeric solid phase comprises a fiber.

6. The surface modified solid phase of claim 5 , wherein the fiber is a capillary-channeled fiber.

7. The surface modified solid phase of claim 1 , wherein the polymeric solid phase comprises a polyolefin, a polyester, a polyaniline, a polylactic acid, a polyamide, a poly(styrene-divinyl benzene), a methacrylate, a polymer blend and/or a copolymer thereof.

8. A chromatography separation device comprising the surface modified solid phase of claim 1 held in a casing.

9. The chromatography separation device of claim 8 , wherein the casing comprises an interior that is surface modified with the lipid adsorbed thereto.

Assignments (3)
CONFIRMATORY LICENSE Recorded Feb 22, 2017
From: CLEMSON UNIVERSITY
To: NATIONAL SCIENCE FOUNDATION
Reel/Frame 041773/0350 →
CONFIRMATORY LICENSE Recorded Jan 5, 2015
From: CLEMSON UNIVERSITY
To: NATIONAL SCIENCE FOUNDATION
Reel/Frame 034719/0614 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 15, 2014
From: MARCUS, R. KENNETH; CHRISTENSEN, KENNETH A.
To: CLEMSON UNIVERSITY
Reel/Frame 033542/0527 →
Continuity (2)
Provisional Application 61847135 · Jul 17, 2013
Related Publication 20150024511A1 · Jan 22, 2015