Determination of unsaturated thyroxine binding protein sites using fluorescence polarization techniques

• US 4,476,228 A
• Filed: 11/08/1982
• Issued: 10/09/1984
• Est. Priority Date: 11/08/1982
• Status: Expired due to Term

• Current Assignee: Abbott Laboratories
• Original Assignee: Abbott Laboratories
• Inventors: Spring, Thomas G., Huchzermeier, Roy F.
• Primary Examiner(s): Nucker, Christine M.
• Application Number:
  US06/440,068
• Time in Patent Office: 701 Days
• Field of Search: 936/500, 936/537, 936/546, 549/800, 549/223
• US Class Current: 436/500
• CPC Class Codes: C07D 311/82 Xanthenes
• CPC Class Codes: C07D 493/10 Spiro-condensed systems
• CPC Class Codes: G01N 33/78 Thyroid gland hormones , e.g. T3, T4, TBH, TBG or their receptors
• CPC Class Codes: Y10S 436/80 Fluorescent dyes, e.g. rhodamine

Abstract

This invention encompasses a method for measuring unsaturated thyroxine binding protein sites in a sample comprising intermixing with the sample an effective amount of fluorescent labeled tracer having binding affinity for thyroxine binding proteins and then measuring the amount of tracer bound to the thyroxine binding protein using fluorescence polarization techniques.

Claims

1. A method for determining unsaturated thyroxine binding protein sites in a sample containing thyroxine binding proteins, comprising:

(a) treating the sample with a composition comprising a nonfluorescent surfactant in a buffered medium having a pH greater than 7.0;

(b) contacting the treated sample with a fluorescent labeled tracer wherein said fluorescent labeled tracer has a preferential binding affinity for thyroxine binding globulin, thereby forming a complex between the thyroxine binding proteins and fluorescent labeled tracer; and

(c) determining the amount of complex formed utilizing fluorescence polarization techniques, as a measure of the unsaturated thyroxine binding protein sites in the sample.

2. A method according to claim 1 wherein the nonfluorescent surfactant is sodium dodecyl sulfate.

3. A method according to claim 2 wherein the pH of the buffered media is in the range of 8.0-9.0.

4. A method according to claim 3 wherein the buffer is sodium bicarbonate.

5. A method according to claim 2 wherein the buffered media comprises triethylenediamine in a phosphate buffer.

6. A method according to claim 1 wherein the fluorescent labeled tracer comprises a thyroxine-fluorescein conjugate.

7. A method according to claim 6 wherein the thyroxine-fluorescein conjugate is a compound of the formula:

##STR11## wherein m is an integer of from 2 to 8.

8. A method according to claim 7 wherein m is an integer of from 2 to 4.

9. A method according to claim 8 wherein m is 3.

10. A method as in any of claims 1-9 wherein steps (a) and (b) are conducted simultaneously.