Method for producing improved sensor

• US 5,783,054 A
• Filed: 04/09/1997
• Issued: 07/21/1998
• Est. Priority Date: 10/01/1992
• Status: Expired due to Term

• Current Assignee: Biosensor Enterprises, LLC
• Original Assignee: Australian Membrane and Biotechnology Research Institute, University of Sydney
• Inventors: Raguse, Burkhard, Cornell, Bruce A., Pace, Ronald J., Braach-Maksvytis, Vijoleta L.
• Primary Examiner(s): Bell, Bruce F.
• Application Number:
  US08/826,903
• Time in Patent Office: 468 Days
• Field of Search: 204/296, 204/418, 204/403, 521/27, 435/4, 436/501, 436/71
• US Class Current: 204/403.08
• CPC Class Codes: B01D 69/122 Separate manufacturing of ultra-thin membranes
• CPC Class Codes: B01D 69/141 Heterogeneous membranes, e.g. containing dispersed material; Mixed matrix membranes
• CPC Class Codes: C07F 9/10 Phosphatides, e.g. lecithin
• CPC Class Codes: C12Q 1/002 Electrode membranes
• CPC Class Codes: C12Q 1/003 Functionalisation
• CPC Class Codes: G01N 2410/10 Valinomycins and derivatives thereof
• CPC Class Codes: G01N 27/327 Biochemical electrodes , e.g. electrical or mechanical details for in vitro measurements
• CPC Class Codes: G01N 31/22 using chemical indicators G01N31/02 takes precedence
• CPC Class Codes: G01N 31/221 for investigating pH value
• CPC Class Codes: G01N 33/54373 involving physiochemical end-point determination, e.g. wave-guides, FETS, gratings
• CPC Class Codes: G01N 33/5438 Electrodes
• CPC Class Codes: Y10S 435/817 Enzyme or microbe electrode

Abstract

The present invention relates to a novel method for producing an electrode membrane combination. This novel method employs compound including a linker lipid for use in attaching a membrane including a plurality of ionophores to an electrode and providing a space between the membrane and the electrode, the electrode being either in part or totally made up of the linker lipid. The linker lipid comprises within the same molecule a hydrophobic region capable of spanning the membrane, an attachment group used to attach the molecule to an electrode surface, and a hydrophilic region intermediate said hydrophobic region and the attachment group.

Claims

1. A method of producing an electrode membrane combination comprising the steps of:

(1) Forming a solution containing reservoir lipids comprising within a same molecule an attachment region, hydrophobic regions, and an hydrophilic region positioned between the attachment region and the hydrophobic region, and optionally a head group attached to the hydrophobic region made from the hydrophilic region; and

spacer compounds comprising within the same molecule a hydrophilic group and an attachment group;

(2) contacting the electrode with the solution from step (1), the composition of the electrode and the attachment regions being selected such that the attachment regions chemisorbed to the electrode;

(3) rinsing the electrode;

(4) contacting the coated electrode from step (3) with a solution of lipid and ionophore in a carrier solvent containing less than 2% of an alkane; and

(5) adding an aqueous solution to the electrode from step (4).

2. A method as claimed in claim 1 in which the reservoir lipid is 23-(20'"'"'-oxo-19'"'"'-oxaeicosa-(Z)-9'"'"'-ene)-70-phenyl-20,25,28,42,45-pentaoxo-24aza-19,29,32,35,38,41,46,47,52,55-decaoxa-58,59-dithioahexaconta-(Z)-9-ene or reservoir phytanyl lipid (B)of the structural formula:

##STR1## or reservoir phytanyl lipid (C) of the structural formula;

##STR2##

3. A method as claimed in claim 1 in which the spacer molecule is a low molecular weight molecule containing within the same structure a thio or disulfide group and one or more hydroxyl or carboxylic acid groups.

4. A method as claimed in claim 1 in which the spacer molecule is bis(2-hydroxyethyl) disulfide or 2-mercaptoethanol.

5. A method as claimed in claim 1 in which the solution of step 1 contains a mixture of reservoir lipid A, membrane spanning linker lipids and bis-(2-hydroxyethyl)disulfide.

6. A method as claimed in claim 5 in which the hydrophobic region of a proportion of the linker lipids have covalently attached thereto an ionophore via a hydrophobic spacer.

7. A method as claimed in claim 1 in which the solution of step 1 contains a mixture of reservoir lipid A, membrane spanning linker lipids and bis-(2-hydroxyethyl) disulfide in a ratio of 2:

1;

3.

8. A method as claimed in claim 1 in which the spacer molecule is mercaptoacetic acid, the disulfide of mercapto acetic acid, mercaptopropionic acid or the disulfide of mercaptopropionic acid, 3-mercapto-1,2-propanedio or the disulfide of 3-mercapto-1,2-propanediol.

9. A method as claimed in claim 1 in which the lipid and ionophore solution in step (4) contains no alkane.

10. A method as claimed in claim 1 in which the lipid in step (4) is glycerol monophytanyl ether.

11. A method as claimed in claim 1 in which the lipid in step (4) is a mixture of glycerol monophytanyl ether and a lipid having a polyethylene glycol group of between 600-6000 g/mol as ahead group.

12. A method as claimed in claim 1 in which the lipid is a mixture of glycerol monophytanyl ether and 1-3% of a lipid having a polyethylene glycol head group.

13. A method as claimed in claim 12 in which the polyethylene glycol has a molecular weight in the range of 600-3000 g/mol.

14. A method as claimed in claim 1 in which the polyethylene glycol containing lipid comprises in the same molecule a phytanyl group attached to a succinate group at one end and a polyethylene glycol 2000 attached to the other end of the succinate.

15. A method as claimed in claim 1 in which the lipid is a mixture of glycerol monophytanyl ether and a lipid having a phosphatidyl choline head group.

16. A method as claimed in claim 1 in which the lipid is a mixture of glycerol monophytanyl ether and up to 20% of a lipid having a phosphatidyl choline head group.

17. A method as claimed in claim 1 in which the lipid is a mixture of glycerol monophytanyl ether and up to 20% of a lipid having a phosphatidyl choline head group and up to 3% of a lipid having as a head group a polyethylene glycol of molecular weight between 600-3000 g/mol.

18. A method as claimed in claim 1 in which the lipid is a mixture of glycerol monophytanyl ether and a lipid having a head group in which the head group is a Galβ

1-3-GalNAcβ

1-4Gal(3-2α

-NeuAc)β

1-4Glc-1-1 ceramide carbohydrate head group.

19. A method as claimed in claim 1 in which a plurality of ionophores are functionalised with a derivative of a low molecular weight analyte whose presence is to be detected.

20. A membrane electrode combination produced by the method as claimed in any one of claims 1 to 19.