Method and composition useful for determining FK 506
View Patent ↗New derivatives of FK 506 are disclosed. These new derivatives and other derivatives that are useful for determining the levels of FK 506 in a sample are also provided as are assay procedures and kits for use in determining the levels of FK 506 or other macrophilin binding substances in blood, particularly un-extracted blood in the presence of specific binding proteins for FK 506.
1. A method of determining the presence of a macrophilin-binding pharmaceutical in a sample comprising: adding to the sample a binding competitor of the formula:
to displace the macrophilin-binding pharmaceutical from its immunophilin complexes
wherein R is alkyl, aryl, allyl, each having less than 25 carbons or H, and
R′ is alkyl, aryl, allyl, each having less than 25 carbons or H; adding a receptor that binds to the pharmaceutical but not significantly to the binding competitor; detecting the receptor-pharmaceutical complex and correlating the detection with the amount of the pharmaceutical in the sample.
2. The method of claim 1 wherein the pharmaceutical is rapamycin (sirolimus), everolimus or tacrolimus (FK506).
3. A method of determining the presence of a macrophilin-binding pharmaceutical in a sample comprising: adding to the sample a binding competitor of the formula:
to displace the macrophilin-binding pharmaceutical from its immunophilin complexes
wherein R is alkyl, aryl, allyl, each having less than 25 carbons or H, and
R′ is alkyl, aryl, allyl, each having less than 25 carbons or H; adding a receptor that binds to the pharmaceutical but not significantly to the binding competitor; detecting the receptor-pharmaceutical complex and correlating the detection with the amount of the pharmaceutical in the sample.
4. The method of claim 3 wherein the pharmaceutical is rapamycin (sirolimus), everolimus or tacrolimus (FK506).
5. The method of claim 4 wherein R or R′ is ethyl.
6. The method of claim 2 wherein R or R′ is ethyl.
7. The method of claim 1 wherein R or R′ further comprise at least one functional group selected from the group consisting of esters, ethers, amides, phosphates, sulfonates, sulfate, amidines, phosphonates, amine, hydroxyl or carboxylate functional groups.
8. The method of claim 3 wherein R or R′ further comprise at least one functional group selected from the group consisting of esters, ethers, amides, phosphates, sulfonates, sulfate, amidines, phosphonates, amine, hydroxyl or carboxylate functional groups.