Diamine acid fluorescent chelates

Claim 2

A metal chelate for use in the fluorometric quantification of a biologically active organic species comprising an essentially 1:1 molar chelate complex of a rare earth metal ion capable of forming a fluorescent complex with a species-linked diamine triacetic acid having the structural formula: ##STR11## wherein R is a two to eight atom long covalent bridge selected from carbon-oxygen ether bridges, carbon-nitrogen secondary and tertiary amide bridges and carbon-carbon alkylene, cycloalkylene and arylene bridges, T is the biologically active organic species to be fluorometrically quantified, T being other than an aliphatic mono- or polyamine, or aliphatic mono- or polyol, but comprising at least one originally present or added primary amine, secondary amine, thiol or hydroxyl functional group, and L is said at least one functional group in deprotonated form covalently bonding T to the indicated carbonyl carbon of the diamine triacetic acid.

Claim 3

The metal chelate of claim 1 wherein the rare earth metal ion is selected from among ions of terbium, dysprosium, europium, samarium and neodimium.

Claim 4

The metal chelate of claim 1 wherein R is selected from two to eight atom long carbon-oxygen ether bridges and two to four carbon atom long alkylene bridges.

Claim 5

The metal chelate of claim 3 wherein the rare earth metal ion is selected from among ions of terbium, dysprosium, europium, samarium and neodimium.

Claim 6

The metal chelate of claim 1 wherein T is a therapeutic drug.

Claim 7

The metal chelate of claim 1 wherein T is an enzyme.

Claim 8

The metal chelate of claim 1 wherein T is a hormone.

Claim 9

The metal chelate of claim 1 wherein T is a macromolecular species.

Claim 10

The metal chelate of claim 1 wherein T is an antibody.

Claim 11

The metal chelate of claim 1 wherein T is a lipid.

Claim 12

The metal chelate of claim 1 wherein T is an antigen.

Claim 13

The metal chelate of claim 1 wherein T is a hapten.

Claim 14

The metal chelate of claim 1 wherein R is selected from the group consisting of ethylene, n-propylene, isopropylene, n-butylene, 1- and 2-methylpropylene, 1-propylethylene, 1-cyclohexylethylene, 1-phenylethylene, alkyl substituted 1-phenylethylenes and propylenes, 1-benzylethylene, 2-amidopropylene, cyclohexyl-1,2-ene, phenyl-1,3-ene, --CH 2 --CH 2 --O--CH 2 --CH 2 --, and --CH 2 --CH 2 --O--CH 2 --CH 2 --O--CH 2 --CH 2 --.

Claim 15

The metal chelate of claim 3 wherein the metal ion is selected from among the ions of europium and terbium.

Claim 16

The metal chelate of claim 14 wherein R is a two carbon atom long alkylene bridge.

Claim 17

The metal chelate of claim 15 wherein the metal ion is terbium ion.

Claim 18

An activated fluorescent rare earth metal ion chelate combination for use in the fluorometric quantification of a biologically active organic species comprising an essentially 1:1 molar chelate complex of a rare earth metal ion capable of forming a fluorescent complex with a species-linked diamine triacetic acid having the structural formula: ##STR12## wherein R is a two to eight atom long covalent bridge selected from carbon-oxygen ether bridges, carbon-nitrogen secondary and tertiary amide bridges and carbon-carbon alkylene, cycloalkylene and arylene bridges, T is the biologically active organic species to be fluorometrically quantified, T being other than an aliphatic mono- or polyamine, or aliphatic mono- or polyol, but comprising at least one originally present or added primary amine, secondary amine, thiol or hydroxyl functional group, and L is said at least one functional group in deprotonated form covalently bonding T to the indicated carbonyl carbon of the diamine triacetic acid in combination with a fluorescent excitation efficiency promoter.

Claim 19

An activated fluorescent rare earth metal ion chelate combination for use in the fluorometric quantification of a biologically active organic species comprising an essentially 1:1 molar chelate complex of a rare earth metal ion capable of forming a fluorescent complex with a species-linked diamine triacetic acid having the structural formula: ##STR12## wherein R is a two to eight atom long covalent bridge selected from carbon-oxygen ether bridges, carbon-nitrogen secondary and tertiary amide bridges and carbon-carbon alkylene, cycloalkylene and arylene bridges, T is the biologically active organic species to be fluorometrically quantified, T being other than an aliphatic mono- or polyamine, or aliphatic mono- or polyol, but comprising at least one originally present or added primary amine, secondary amine, thiol or hydroxyl functional group, and L is said at least one functional group in deprotonated form covalently bonding T to the indicated carbonyl carbon of the diamine triacetic acid in combination with a fluorescent excitation efficiency promoter.

Claim 20

The activated fluorescent chelate combination of claim 17 wherein the rare earth metal ion is selected from among ions of terbium, dysprosium, europium, samarium and neodimium.

Claim 21

The activated fluorescent chelate combination of claim 17 wherein R is selected from two to eight atom long carbon-oxygen ether bridges and two to four carbon long alkylene bridges.

Claim 22

The activated fluorescent chelate complex of claim 19 wherein the rare earth metal ion is selected from among ions of terbium, dysprosium, europium, samarium and neodimium.

Claim 23

The activated fluorescent chelate complex of claim 17 wherein T is a therapeutic drug.

Claim 24

The activated fluorescent chelate complex of claim 17 wherein T is an enzyme.

Claim 25

The activated fluorescent chelate complex of claim 17 wherein T is a macromolecular species.

Claim 26

The activated fluorescent chelate complex of claim 17 wherein T is an antibody.

Claim 27

The activated fluorescent chelate complex of claim 17 wherein T is an antigen.

Claim 28

The activated fluorescent chelate complex of claim 17 wherein T is a lipid.

Claim 29

The activated fluorescent chelate complex of claim 17 wherein T is a hapten.

Claim 30

The activated fluorescent chelate complex of claim 17 wherein the fluorescent excitation efficiency promoter is a salicylate.

Claim 31

The activated fluorescent chelate complex of claim 27 wherein the metal ion is terbium ion, R is a two carbon atom long alkylene bridge and the fluorescent excitation efficiency promoter is 5-sulfosalicylic acid.

Claim 32

The process for preparing a fluorescent species-linked diamine triacetic acid which comprises the steps of a. contacting in liquid phase a biologically active organic species molecule having a functional group selected from ##STR13## but being other than an aliphatic mono- or polyamine, or an aliphatic mono- or polyol with a molar excess of a diaminedianhydride of the formula ##STR14## wherein R is a two to eight atom long covalent bridge selected from carbon-oxygen ether bridges, carbon-nitrogen secondary and tertiary amide bridges and carbon-carbon alkylene, cycloalkylene and arylene bridges, per mole of species molecule at a temperature of from about 5° C. to about 100° C. for from about 0.5 hours to about two days, b. hydrolyzing the remaining anhydride groups, c. recovering the species-linked diamine triacetic acid which is formed in step b, d. contacting the recovered species-linked diamine triacetic acid with a solution of a rare earth metal ion capable of forming a fluorescent complex with said triacetic acid and e. contacting said fluorescent complex with a substantial molar excess of a fluorescent excitation efficiency promoter.

Claim 33

The process for preparing a fluorescent species-linked diamine triacetic acid which comprises the steps of a. contacting in liquid phase a biologically active organic species molecule having a functional group selected from ##STR13## but being other than an aliphatic mono- or polyamine, or an aliphatic mono- or polyol with a molar excess of a diaminedianhydride of the formula ##STR14## wherein R is a two to eight atom long covalent bridge selected from carbon-oxygen ether bridges, carbon-nitrogen secondary and tertiary amide bridges and carbon-carbon alkylene, cycloalkylene and arylene bridges, per mole of species molecule at a temperature of from about 5° C. to about 100° C. for from about 0.5 hours to about two days, b. hydrolyzing the remaining anhydride groups, c. recovering the species-linked diamine triacetic acid which is formed in step b, d. contacting the recovered species-linked diamine triacetic acid with a solution of a rare earth metal ion capable of forming a fluorescent complex with said triacetic acid and e. contacting said fluorescent complex with a substantial molar excess of a fluorescent excitation efficiency promoter.