IP Library Granted Patent US 6,960,653
Granted Patent B2
US 6,960,653 · App. 10/211,411 · Granted Nov 1, 2005

Method and kit for detecting, or determining the quantity of, beta-lactam penicillins

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Quick Facts
Patent No.
US 6,960,653
App. No.
10/211,411
Granted
Nov 1, 2005
Kind
B2
Abstract

The invention provides a hapten comprising a 6-[D-α-aminoacetamido] penicillin derivative crosslinked at the α-amino group with a substituted or unsubstituted phenyldicarbaldehyde. In addition, the invention provides an immunogen comprising the aforementioned hapten coupled to an antigenicity-conferring carrier material, a conjugate comprising the aforementioned hapten coupled to a labelling agent, as well as, antibodies raised against the aforementioned immunogen and capable of binding with at least one structural epitope of an intact β-lactam ring.

Claims (28)

1. A hapten comprising a 6-[D-α-aminoacetamido] penicillin derivative crosslinked at the α-amino group with a substituted or unsubstituted phenyldicarbaldehyde selected from the group consisting of substituted or unsubstituted phthalaldehyde, substituted or unsubstituted isophthalaldehyde and substituted or unsubstituted terephthalaldehyde.

2. A hapten according to claim 1 , wherein the phenyldicarbaldehyde is a substituted or unsubstituted terephthalaldehyde.

3. A process for preparing a hapten, wherein a substituted or unsubstituted phenyldicarbaldehyde selected from the group consisting of substituted or unsubstituted phthalaldehyde, substituted or unsubstituted isophthalaldehyde, and substituted or unsubstituted terephthalaldehyde, or a mixture thereof, is reacted with a 6-[D-α-aminoacetamido] penicillin derivative in a solvent selected from the group consisting of dimethylformamide and dimethylsulfoxide.

4. An immunogen comprising a hapten, wherein said hapten comprises a 6-[D-α-aminoacetamido] penicillin derivative crosslinked at the α amino group with a substituted or unsubstituted phenyldicarbaldehyde selected from the group consisting of substituted or unsubstituted phthalaldehyde, substituted or unsubstituted isophthalaldehyde, and substituted or unsubstituted terephthalaldehyde, or a mixture thereof, coupled, through a terminal aldehyde on the substituted or unsubstituted phenyldicarbaldehyde, to an antigenicity-conferring carrier material.

5. The immunogen of claim 4 , wherein the carrier material is a protein, a protein fragment, a synthetic polypeptide or a semi-synthetic polypeptide.

6. Antibodies raised against an immunogen, wherein said immunogen comprises a hapten, wherein said hapten comprises a 6-[D-α-aminoacetamido] penicillin derivative crosslinked at the α-amino group with a substituted or unsubstituted phenyldicarbaldehyde selected from the group consisting of substituted or unsubstituted phthalaldehyde, substituted or unsubstituted isophthalaldehyde, and substituted or unsubstituted terephthalaldehyde, or a mixture thereof, coupled, through a terminal aldehyde on the substituted or unsubstituted phenyldicarbaldehyde, to an antigenicity-conferring carrier material.

7. The antibodies of claim 6 , wherein said antibodies are fixed on a backing substrate.

8. A process of preparing antibodies, the process comprising the steps of immunising an animal by repeated administration of an immunogen, wherein said immunogen comprises a hapten, wherein said hapten comprises a 6-[D-α-aminoacetamido] penicillin derivative crosslinked at the α-amino group with a substituted or unsubstituted phenyldicarbaldehyde selected from the group consisting of substituted or unsubstituted phthalaldehyde, substituted or unsubstituted isophthalaldehyde, and substituted or unsubstituted terephthalaldehyde, or a mixture thereof, coupled, through a terminal aldehyde on the substituted or unsubstituted phenyldicarbaldehyde, to an antigenicity-conferring carrier material, and collecting the resulting serum antibodies from the immunised animal.

9. The process of claim 8 , wherein the process further comprises fixing said serum antibodies to a backing substrate.

10. A conjugate comprising a hapten, wherein said hapten comprises a 6-[D-α-aminoacetamido] penicillin derivative crosslinked at the α-amino group with a substituted or unsubstituted phenyldicarbaldehyde selected from the group consisting of substituted or unsubstituted phthalaldehyde, substituted or unsubstituted isophthalaldehyde, and substituted or unsubstituted terephthalaldehyde, or a mixture thereof, covalently bonded, through a terminal aldehyde on the substituted or unsubstituted phenyldicarbaldehyde, to a labelling agent which is detectable.

11. The conjugate of claim 10 , wherein the labelling agent is an enzyme, a luminescent substance, a radioactive substance, or a mixture thereof.

12. A method for detecting, or determining the quantity of, β-lactam penicillins in a sample, the method comprising contacting the sample with a conjugate according to claim 10 , or a mixture thereof, and with antibodies, raised against an immunogen, wherein said immunogen comprises a hapten comprising a 6-[D-α-aminoacetamido] penicillin derivative crosslinked at the α-amino group with a substituted or unsubstituted phenyldicarbaldehyde selected from the group consisting of substituted or unsubstituted phthalaldehyde, substituted or unsubstituted isophthalaldehyde and substituted or unsubstituted terephthalaldehyde, or a mixture thereof, coupled, through a terminal aldehyde on the substituted or unsubstituted phenyldicarbaldehyde, to an antigenicity-conferring carrier material, or a mixture of said antibodies; detecting, or determining the quantity of, bound conjugate; and deducing from a calibration curve the presence, or amount of, β-lactam penicillins in the sample.

13. A kit for detecting, or determining the quantity of, β-lactam penicillins, the kit including a conjugate according to claim 10 , or a mixture thereof, and antibodies raised against an immunogen, wherein said immunogen comprises a hapten comprising a 6-[D-α-aminoacetamido] penicillin derivative crosslinked at the α-amino group with a substituted or unsubstituted phenyldicarbaldehyde selected from the group consisting of substituted or unsubstituted phthalaldehyde, substituted or unsubstituted isophthalaldehyde and substituted or unsubstituted terephthalaldehyde, or a mixture thereof, coupled, through a terminal aldehyde on the substituted or unsubstituted phenyldicarbaldehyde, to an antigenicity-conferring carrier material, or a mixture of said antibodies.

14. The hapten of claim 2 , wherein the phenyldicarbaldehyde is an unsubstituted terephthalaldehyde.

15. The process of claim 3 , wherein the phenyldicarbaldehyde is a substituted or unsubstituted terephthalaldehyde.

16. The process of claim 15 , wherein the phenyldicarbaldehyde is an unsubstituted terephthalaldehyde.

17. The immunogen of claim 4 , wherein the phenyldicarbaldehyde is a substituted or unsubstituted terephthalaldehyde.

18. The immunogen of claim 17 , wherein the phenyldicarbaldehyde is an unsubstituted terephthalaldehyde.

19. The antibodies of claim 6 , wherein the phenyldicarbaldehyde is a substituted or unsubstituted terephthalaldehyde.

20. The antibodies of claim 19 , wherein the phenyldicarbaldehyde is an unsubstituted terephthalaldehyde.

21. The antibodies of claim 6 , wherein said antibodies are capable of binding with at least one structural epitope of an intact β-lactam ring.

22. The process of claim 8 , wherein the phenyldicarbaldehyde is a substituted or unsubstituted terephthalaldehyde.

23. The process of claim 22 , wherein the phenyldicarbaldehyde is an unsubstituted terephthalaldehyde.

24. The conjugate of claim 10 , wherein the phenyldicarbaldehyde is a substituted or unsubstituted terephthalaldehyde.

25. The conjugate of claim 24 , wherein the phenyldicarbaldehyde is an unsubstituted terephthalaldehyde.

26. The conjugate of claim 11 , wherein the enzyme is a peroxidase.

27. The conjugate of claim 26 , wherein the peroxidase is horseradish peroxidase.

28. The conjugate of claim 11 , wherein the luminescent substance is a bioluminescent substance, a chemiluminescent substance or a fluorescent substance.

Assignments (5)
CORRECTIVE ASSIGNMENT TO CORRECT THE NATURE OF CONVENYANCE PREVIOUSLY RECORDED AT REEL: 055950 FRAME: 0471. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Apr 20, 2021
From: RANDOX LABORATORIES LIMITED
To: NORTHERN BANK LIMITED
Reel/Frame 056210/0055 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 15, 2021
From: RANDOX LABORATORIES LIMITED
To: NORTHERN BANK LIMITED
Reel/Frame 055950/0471 →
SECURITY AGREEMENT Recorded Oct 6, 2009
From: RANDOX LABORATORIES LIMITED
To: NORTHERN BANK LIMITED
Reel/Frame 023330/0468 →
SECURITY AGREEMENT Recorded Aug 5, 2004
From: RANDOX LABORATORIES LIMITED
To: ULSTER BANK IRELAND LIMITED (SERVICE ADDRESS: 11-16 DONEGALL SQUARE EAST, BELFAST, IRELAND); ULSTER BANK LIMITED
Reel/Frame 014943/0728 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 22, 2003
From: MCCONNELL, ROBERT IVAN; BENCHIKH, ELOUARD; FITZGERALD, STEPHEN PETER; LAMONT, JOHN VICTOR
To: RANDOX LABORATORIES LIMITED
Reel/Frame 014505/0402 →