Carriers coated with polysaccharides, their preparation and use

• US 7,179,660 B1
• Filed: 03/06/2000
• Issued: 02/20/2007
• Est. Priority Date: 03/06/2000
• Status: Expired due to Term

• Current Assignee: Siemens Healthcare Diagnostics Products GmbH (Siemens AG)
• Original Assignee: DADE Behring Beteiligungs GmbH (Siemens AG)
• Inventors: Schelp, Carsten, Kirakossian, Hrair, Pease, John S., Stohr, Uwe, Wiegand, Andreas, Pirio, Marcel R.
• Primary Examiner(s): Chin; Christopher L.
• Application Number:
  US10/220,623
• Time in Patent Office: 2,542 Days
• Field of Search: None
• US Class Current: 436/529
• CPC Class Codes: G01N 33/548 Carbohydrates, e.g. dextran
• CPC Class Codes: Y10S 435/969 Multiple layering of reactants
• CPC Class Codes: Y10S 436/827 Lectins
• CPC Class Codes: Y10T 428/2991 Coated

Abstract

A polysaccharide coated carrier having a coating of at least two successive layers of polysaccharide. The first polysaccharide layer spontaneously associates with a second polysaccharide layer and, optionally, the carrier. Each successive layer of polysaccharide spontaneously associates with a preceding layer. Spontaneous association occurs due to the presence of oppositely charged functional groups on each layer of polysaccharide or due to a spontaneous reaction between the functional groups the layers. The carrier may be any surface such as a tube, microtitration plate, bead, particle or the like and is suitable for use in diagnostic or therapeutic methods.

Claims

1. A polysaccharide coated carrier comprising a carrier having a coating of at least two successive layers of polysaccharides, wherein a first polysaccharide layer is associated with a second polysaccharide layer and wherein the first polysaccharide is an aminodextran and the second polysaccharide is an amine-reactive dextran.

2. The carrier of claim 1 wherein each of said successive polysaccharide layers alternate between an aminodextran and an amine reactive dextran.

3. The carrier of claim 1 wherein said polysaccharides have pendent functional groups and said functional groups of said successive polysaccharide layers are charged oppositely of said functional groups of said preceding polysaccharide layers.

4. The carrier of claim 1 wherein said polysaccharides have pendant functional groups and said successive layers of polysaccharide are covalently coupled to said preceding polysaccharide layers by reaction between said functional groups of said successive layers with said functional groups of said preceding layers.

5. The carrier of claim 4 wherein the reaction between said functional groups is a spontaneous reaction.

6. The carrier according to claim 1 wherein the amine reactive functional group of the amine reactive dextran is an aldehyde group or a carboxyl group.

7. The carrier of claim 1 wherein said first polysaccharide layer is associated with said carrier through oppositely charged functional groups.

8. The carrier of claim 7 wherein said carrier and said polysaccharides have pendent functional groups.

9. The carrier of claim 8 wherein said carrier is a carboxylated carrier.

10. The carrier according to claim 1 wherein said carrier material is selected from the group consisting of natural, synthetic or modified naturally occurring polymers;

silicones;

glasses;

ceramics;

inorganic powders;

magnetic materials; and

metals;

or a combination thereof.

11. The carrier according to claim 1 wherein said carrier is selected from the group consisting of strips, sheets, rods, tubes, wells, microtitration plates, beads and particles.

12. The carrier according to claim 1 wherein said carrier is a magnetic or non-magnetic particle.

13. The carrier according to claim 1 wherein said carrier is a carboxylated latex particle.

14. The carrier according to claim 13 wherein said particle is in the size range of 0.1 to 10 μ

m.

15. The carrier according to claim 1 of wherein said carrier is associated with at least one reporter molecule.

16. The carrier according to claim 15 wherein said reporter molecule is selected from the group consisting of dyes, radiolabels, sensitizers, fluorescers and chemiluminescers.

17. The carrier according to claim 1 wherein said aminodextran has a molecular weight of 10,000 to 2,000,000 daltons.

18. The carrier according to claim 1 wherein the outermost layer of polysaccharide has at least one pendent functional group.

19. The carrier according to claim 18 wherein said pendent functional group is selected from the group consisting of aldehydes, carboxyl groups, maleimido groups, and sulfhydryl groups.

20. The carrier according to claim 18 wherein said pendent functional group is bound to a specific binding partner.

21. The carrier according to claim 20 wherein said specific binding partner is selected from the group consisting of antibodies, antibody fragments, receptors, ligands, oligonucleotides, oligonucleotide-binding proteins, lectins, haptens, antigens, immunoglobulin binding proteins, avidin, streptavidin, and biotin.

22. A method for preparing the polysaccharide coated carrier of claim 1 wherein the carrier comprises amine reactive functional groups, said method comprising:

(a) covalently coupling the first polysaccharide layer to said carrier by reaction between the amine reactive functional groups of the carrier and the amine functional groups of the polysaccharide of the first coating layer; and

(b) covalently coupling the second polysaccharide layer to the first polysaccharide layer by reaction between the amine functional groups of the first polysaccharide layer and the amine reactive functional groups of the second polysaccharide layer.

23. The method according to claim 22 wherein carbodiimide conjugation chemistry is used for the coupling of the polysaccharides of the first coating layer to said carrier.

24. The method according to claim 22 wherein the coupling of the polysaccharides of the second coating layer to the first coating layer is done in the presence of a mild reducing agent.

25. The method according to claim 22 wherein carbodiimide conjugation chemistry is used for the coupling of the polysaccharides of the second coating layer to the first coating layer.

26. The method according to claim 22 wherein the specific binding partners are covalently bound to the coating layer by reaction between the pendent functional groups of the coating layer and functional groups of the specific binding partners.

27. The carrier according to claim 1 for use in in-vitro and/or in-vivo diagnostic methods.

28. The carrier according to claim 1 for use in a method for the quantitative and/or qualitative determination of an analyte.

29. Composition comprising the carrier according to claim 1 in a pharmaceutically acceptable medium.

30. The carrier according to claim 1 for use in a therapeutic method.

31. A method for quantitative or qualitative determination of an analyte in a sample, said method comprising:

(a) combining in an assay medium a sample suspected of containing the analyte and a carrier according to claim 1 wherein the carrier comprises a specific binding partner for the analyte and

(b) determining the extent of binding of the analyte to the specific binding partner for the analyte, the extent thereof being related to the presence or amount of the analyte in the sample.

32. A method for quantitative or qualitative determination of an analyte in a sample, said method comprising:

(a) combining in an assay medium a sample suspected of containing the analyte and a carrier according to claim 1 wherein the carrier comprises an analyte analog and the medium further comprises a specific binding partner for the analyte and

(b) determining the extent of binding of the analyte to the specific binding partner for the analyte, the extent thereof being related to the presence or amount of the analyte in the sample.