Patent US891568A successfully refreshed from Google Patents.
Patent US4729950A successfully refreshed from Google Patents.
US4729950A
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Enhanced luminescent or luminometric assay
Assignee: BTG International Ltd
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Filing: 1985-07-29
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Granted: 1988-03-08
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Expires: 2005-07-29
Abstract
Abstract It has been a problem that the chemiluminescent emission produced by the peroxidase-catalyzed oxidation of a 2,3-dihydro-1,4-phthalazinedione is often weak or gives a poor signal-background ratio and therefore does not give the high degree of sensitivity required for assay purposes, particularly for assay of peroxidase used to label a reagent for example in ELISA. The present invention solves the problem by the finding the certain narrowly defined aromatic amines are enhancers of the reaction and accordingly provides for their use in an assay and kit. The amines are of general formula (I) <IMAGE> (1) wherein the R symbols (that is, R, R1, R2, R3, R4, R5 and R6) have any of the meanings (a) to (j) given below, all other R symbols in each meaning are hydrogen atoms and the fused rings are to be read in the same configurational sense as formula I: (a) R=R1=CH3; R4= <IMAGE> (b) R4= <IMAGE> cyclohexyl, or alkyl or alkoxy having 1 to 4 carbon atoms (c) R2, R3 and R4 together represent the polycyclic fused ring system: <IMAGE> (d) R3 and R4 together represent the fused ring or ring system <IMAGE> (e) R3 and R4 together represent the fused ring system <IMAGE> and R5 and R6 together represent the fused ring <IMAGE> (f) R2=NH2 and R4= <IMAGE> (g) R2=R6=CH3 and R4= <IMAGE> (h) R3=C2H5 (i) R2=R4=CH3 and (j) R3=R4=CH3.
Inventors
- 👤 Larry J. Kricka
- 👤 Angela M. O'Toole
- 👤 Gary H. G. H. Thorpe
- 👤 Thomas P. Whitehead
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-10-25 13:04
CPC Classifications
G; G01; G01N; G01N33/00; G01N33/48; G01N33/50; G01N33/53; G01N33/531; G01N33/532; G01N33/535; C; C12; C12Q; C12Q1/00; C12Q1/26; C12Q1/28; Y; Y10; Y10S; Y10S435/00; Y10S435/81; Y10S435/968; Y10S435/975; Y10S436/00; Y10S436/80
Claims Analysis
Total Claims: 12
Claim 1
Independent Claim
260 words
In a luminescent or luminometric assay which comprises carrying out a chemiluminescent reaction between a peroxidase, an oxidant, and a chemiluminescent 2,3-dihydro-1,4-phthalazinedione and measuring or detecting the chemiluminescence thereby produced, the improvement wherein the reaction is carried out in the presence of an aromatic amine of the general formula ##STR20## wherein the R symbols, namely R, R 1 , R 2 , R 3 , R 4 , R 5 and R 6 , have any of the meanings (a) to (j) given below, all other R symbols in each meaning are hydrogen atoms and the fused rings are to be read in the same configurational sense as formula 1, whereby sides "a", "b" and "d" in formula (1) are fused to sides "a", "b" and "d" respectively in the formulae below: (a) R=R 1 =CH 3 ; R 4 = ##STR21## (b) R 4 = ##STR22## cyclohexyl, or alkyl or alkoxy having 1 to 4 carbon atoms (c) R 2 , R 3 and R 4 together represent the polycyclic fused ring system: ##STR23## (d) R 3 and R 4 together represent the fused ring or ring system ##STR24## (e) R 3 and R 4 together represent the fused ring system ##STR25## and R 5 and R 6 together represent the fused ring ##STR26## (f) R 2 =NH 2 and R 4 = ##STR27## (g) R 2 =R 6 =CH 3 and R 4 = ##STR28## (h) R 3 =C 2 H 5 (i) R 2 =R 4 =CH 3 and (j) R 3 =R 4 =CH 3 .
Claim 2
Dependent Claim
260 words
In a luminescent or luminometric assay which comprises carrying out a chemiluminescent reaction between a peroxidase, an oxidant, and a chemiluminescent 2,3-dihydro-1,4-phthalazinedione and measuring or detecting the chemiluminescence thereby produced, the improvement wherein the reaction is carried out in the presence of an aromatic amine of the general formula ##STR20## wherein the R symbols, namely R, R 1 , R 2 , R 3 , R 4 , R 5 and R 6 , have any of the meanings (a) to (j) given below, all other R symbols in each meaning are hydrogen atoms and the fused rings are to be read in the same configurational sense as formula 1, whereby sides "a", "b" and "d" in formula (1) are fused to sides "a", "b" and "d" respectively in the formulae below: (a) R=R 1 =CH 3 ; R 4 = ##STR21## (b) R 4 = ##STR22## cyclohexyl, or alkyl or alkoxy having 1 to 4 carbon atoms (c) R 2 , R 3 and R 4 together represent the polycyclic fused ring system: ##STR23## (d) R 3 and R 4 together represent the fused ring or ring system ##STR24## (e) R 3 and R 4 together represent the fused ring system ##STR25## and R 5 and R 6 together represent the fused ring ##STR26## (f) R 2 =NH 2 and R 4 = ##STR27## (g) R 2 =R 6 =CH 3 and R 4 = ##STR28## (h) R 3 =C 2 H 5 (i) R 2 =R 4 =CH 3 and (j) R 3 =R 4 =CH 3 .
Claim 3
Dependent Claim
164 words
An assay according to claim 1 wherein the chemiluminescent 2,3-dihydro-1,4-phthalazinedione is of general formula (2) ##STR29## wherein Z 1 is amino or substituted amino, and each of Z 2 , Z 3 and Z 4 is H, optionally substituted C 1 -C 6 alkyl, optionally substituted C 1 -C 6 alkenyl, hydroxyl, C 1 -C 6 alkoxyl, carboxyl, amino or substituted amino, or Z 2 is amino or substituted amino and each of Z 1 , Z 3 and Z 4 is H, optionally substituted C 1 -C 6 alkyl, optionally substituted C 1 -C 6 alkenyl, hydroxyl, C 1 -C 6 alkoxyl, carboxyl, amino or substituted amino, or Z 1 and Z 2 are taken together and are an amino or substituted amino derivative of a benzo group and each of Z 3 and Z 4 is H, optionally substituted C 1 -C 6 alkyl, optionally substituted C 1 -C 6 alkenyl, hydroxyl, C 1 -C 6 alkoxyl, carboxyl, amino or substituted amino.
Claim 4
Dependent Claim
14 words
An assay according to claim 2 wherein the chemiluminescent 2,3-dihydro-1,4-phthalazinedione is luminol or isoluminol.
Claim 5
Dependent Claim
12 words
An assay according to claim 1, wherein the peroxidase is horseradish peroxidase.
Claim 6
Dependent Claim
38 words
An assay according to claim 1, wherein the peroxidase is present in an analyte in a free or conjugated form and its presence or the amount thereof is deduced from the detection or measurement, respectively, of the chemiluminescence.
Claim 7
Dependent Claim
16 words
An assay according to claim 1 wherein the aromatic amine is N,N,N',N'-tetramethylbenzidine, 4-benzyloxyaniline, 3-aminofluoranthrene or 4-methoxyaniline.
Claim 8
Dependent Claim
241 words
A kit for use in a luminescent or luminometric assay comprising the following components in separate containers: a chemiluminescent 2,3-dihydro-1,4-phthalazinedione, a peroxidase, and an aromatic amine of the general formula ##STR30## wherein the R symbols, namely R, R 1 , R 2 , R 3 , R 4 , R 5 and R 6 , have any of the meanings (a) to (j) given below, all other R symbols in each meaning are hydrogen atoms and the fused rings are to be read in the same configurational sense as formula 1, whereby sides "a", "b" and "d" in formula 1 are fused to sides "a", "b" and "d" respectively in the formulae below: (a) R=R 1 =CH 3 ; R 4 = ##STR31## (b) R 4 = ##STR32## cyclohexyl, or alkyl or alkoxy having 1 to 4 carbon atoms (c) R 2 , R 3 and R 4 together represent the polycyclic fused ring system: ##STR33## (d) R 3 and R 4 together represent the fused ring or ring system ##STR34## (e) R 3 and R 4 together represent the fused ring system ##STR35## and R 5 and R 6 together represent the fused ring ##STR36## (f) R 2 =NH 2 and R 4 = ##STR37## (g) R 2 =R 6 =CH 3 and R 4 = ##STR38## (h) R 3 =C 2 H 5 (i) R 2 =R 4 =CH 3 and (j) R 3 =R 4 =CH 3 .
Claim 9
Dependent Claim
241 words
A kit for use in a luminescent or luminometric assay comprising the following components in separate containers: a chemiluminescent 2,3-dihydro-1,4-phthalazinedione, a peroxidase, and an aromatic amine of the general formula ##STR30## wherein the R symbols, namely R, R 1 , R 2 , R 3 , R 4 , R 5 and R 6 , have any of the meanings (a) to (j) given below, all other R symbols in each meaning are hydrogen atoms and the fused rings are to be read in the same configurational sense as formula 1, whereby sides "a", "b" and "d" in formula 1 are fused to sides "a", "b" and "d" respectively in the formulae below: (a) R=R 1 =CH 3 ; R 4 = ##STR31## (b) R 4 = ##STR32## cyclohexyl, or alkyl or alkoxy having 1 to 4 carbon atoms (c) R 2 , R 3 and R 4 together represent the polycyclic fused ring system: ##STR33## (d) R 3 and R 4 together represent the fused ring or ring system ##STR34## (e) R 3 and R 4 together represent the fused ring system ##STR35## and R 5 and R 6 together represent the fused ring ##STR36## (f) R 2 =NH 2 and R 4 = ##STR37## (g) R 2 =R 6 =CH 3 and R 4 = ##STR38## (h) R 3 =C 2 H 5 (i) R 2 =R 4 =CH 3 and (j) R 3 =R 4 =CH 3 .
Claim 10
Dependent Claim
164 words
A kit according to claim 7 wherein the chemiluminescent 2,3-dihydro-1,4-phthalazinedione is of general formula (2): ##STR39## wherein Z 1 is amino or substituted amino, and each of Z 2 , Z 3 and Z 4 is H, optionally substituted C 1 -C 6 alkyl, optionally substituted C 1 -C 6 alkenyl, hydroxyl, C 1 -C 6 alkoxyl, carboxyl, amino or substituted amino, or Z 2 is amino or substituted amino and each of Z 1 , Z 3 and Z 4 is H, optionally substituted C 1 -C 6 alkyl, optionally substituted C 1 -C 6 alkenyl, hydroxyl, C 1 -C 6 alkoxyl, carboxyl, amino or substituted amino, or Z 1 and Z 2 are taken together and are an amino or substituted amino derivative of a benzo group and each of Z 3 and Z 4 is H, optionally substituted C 1 -C 6 alkyl, optionally substituted C 1 -C 6 alkenyl, hydroxyl, C 1 -C 6 alkoxyl, carboxyl, amino or substituted amino.
Claim 11
Dependent Claim
16 words
A kit according to claim 7 wherein the aromatic amine is N,N,N',N'-tetramethylbenzidine, 4-benzyloxyaniline, 3-aminofluoranthrene or 4-methoxyaniline.
Claim 12
Dependent Claim
37 words
A kit according to claim 7, wherein the peroxidase is present in an analyte in free or conjugated form and its presence or the amount thereof is deduced from the detection or measurement, respectively, of the chemiluminescence.
References Cited (Backward Citations)
US4290773A
Cited
US4598044A
Cited
USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1991-03-08 | 1991-09-07 | 1992-03-08 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1995-03-08 | 1995-09-07 | 1996-03-08 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1999-03-08 | 1999-09-07 | 2000-03-08 | $7700.00 | Window Closed / Lapsed |