Sample preservation method and sample application substrate

Patent metadata

Field	Value
Publication number	US-9989446-B2
Application number	US-201213985360-A
Country	US
Kind code	B2
Filing date	Feb 27, 2012
Priority date	Feb 28, 2011
Publication date	Jun 5, 2018
Grant date	Jun 5, 2018

Abstract

The invention discloses a sample preservation method which comprises the following steps: a) providing a paper substrate comprising ligands, where the ligands comprise charged groups, b) applying a sample comprising at least one analyte and at least one contaminant on the paper substrate, c) drying the sample on the paper substrate and, d) extracting at least part of the paper substrate to provide a solution of the analyte.

First claim

The invention claimed is:

1. A sample preservation method comprising the steps of:
a) providing a paper substrate comprising ligands, wherein each said ligand is covalently bound to cellulose, wherein each said ligand comprises negatively charged groups and groups capable of hydrophobic interactions, and wherein said ligands are selected from N-benzyl-N-methylethanolamine, N,N-dimethylbenzylamine, N-benzoyl homocysteine, or any combination thereof;
b) applying a sample comprising at least one analyte and at least one contaminant on said paper substrate, wherein said at least one analyte comprises a protein;
c) drying said sample on said paper substrate;
d) storing said paper substrate with said sample for at least 24 hours in order to preserve the sample for later analysis; and
e) extracting at least part of said paper substrate to provide a solution of said analyte.

2. The sample preservation method of claim 1 , further comprising after step c) a step c′) of punching or cutting out a piece of predetermined area from said paper substrate with said sample and in step e) extracting said piece of predetermined area.

3. The sample preservation method of claim 1 , further comprising a step c″) of washing said paper substrate.

4. The sample preservation method of claim 1 , wherein said sample comprises a biological fluid.

5. The sample preservation method of claim 1 , wherein said at least one analyte is charged, with a net charge opposite the charged groups comprised in the ligands.

6. The sample preservation method of claim 1 , wherein at least one contaminant comprises charged groups, with a net charge opposite to the charged groups comprised in the ligands.

7. The sample preservation method of claim 1 , wherein step a) further comprises reacting a base paper with a ligand precursor reagent to provide said paper substrate comprising ligands.

8. The sample preservation method of claim 1 , wherein step a) further comprises:
a′) reacting a fibre pulp with a ligand precursor reagent to obtain intact fibres comprising covalently bound ligands; and
a″) on a continuous-web paper machine forming a paper web comprising at least 90 weight (wt) % of said intact fibres with covalently bound ligands.

9. The sample preservation method of claim 1 , wherein said paper substrate comprises at least 50 micromol/gram ligands.

10. The sample preservation method of claim 1 , wherein said charged groups are negatively charged over at least part of a pH 5 to pH 9 interval.

11. The sample preservation method of claim 1 , wherein said at least one analyte comprises a biopharmaceutical.

12. The sample preservation method of claim 1 , wherein said ligands comprise N-benzoyl homocysteine.

13. The sample preservation method of claim 1 , wherein said cellulose is activated by reaction with allylglycidyl ether.

14. The sample preservation method of claim 1 , further comprising a step f) of analyzing said solution with respect to one or more of the concentration, structural integrity or biological activity of said analyte.

15. The sample preservation method of claim 14 , wherein step f) comprises analyzing said solution by mass spectrometry, an immunoassay or a biological assay.

16. The sample preservation method of claim 14 , wherein in the solution provided in step e), the ratio of said analyte concentration to the total concentration of contaminants is at least about twice as high as in said sample.

17. The sample preservation method of claim 1 , wherein said contaminants comprise phospholipids.

18. The sample preservation method of claim 17 , wherein in the solution provided in step e), the ratio of said analyte concentration to the total concentration of phospholipids is at least about twice as high as in said sample.

19. The sample preservation method of claim 1 , wherein said paper substrate further comprises groups capable of non charge-charge interactions with at least one analyte.

20. The sample preservation method of claim 19 , wherein said non charge-charge interactions comprise hydrophobic interactions, hydrogen bonding, thiophilic interactions, van der Waals interactions or cation-pi interactions.

Assignees

• Mallender Philip Robert
• Green Douglas Mark
• Clegg Sarah Janet
• Johnson Barry Edmund
• Hedin Dahlstrom Jimmy
• Algotsson Mattias
• Palmgren Ronnie
• Ge Healthcare Uk Ltd

Inventors

• Mallender Philip Robert
• Green Douglas Mark
• Clegg Sarah Janet
• Johnson Barry Edmund
• Hedin Dahlstrom Jimmy
• Algotsson Mattias
• Palmgren Ronnie

Classifications

• D21H11/20 Primary

  Chemically or biochemically modified fibres · CPC title

• D21H17/18

  forming new compounds in situ, e.g. within the pulp or paper, by chemical reaction with itself, or other added substances, e.g. by grafting on the fibres · CPC title

• G01N1/28 Primary

  Preparing specimens for investigation {including physical details of (bio-)chemical methods covered elsewhere, e.g. G01N33/50, C12Q}(mounting specimens on microscopic slides G02B21/34; means for supporting the objects or the materials to be analysed in electron microscopes H01J37/20 {; laboratory gas handling apparatus B01L5/00}) · CPC title

• D21H27/08

  Filter paper (self-supporting filtering material B01D39/14; making on paper-making machines D21F11/14) · CPC title