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US4927769A Expired / Lapsed US ⏱️ 0.0 years remaining

Method for enhancement of chemiluminescence

Assignee: Bayer Corp
•
Filing: 1987-07-08
•
Granted: 1990-05-22
•
Expires: 2007-07-08
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Abstract

Abstract A method for enhancing the chemiluminescent signal of an acridinium ester in a chemiluminescent reaction which comprises oxidizing the acridinium ester in the presence of an enhancer selected from the group consisting of: (a) a cationic surfactant; (b) a nonionic surfactant; and (c) a sulfated primary alcohol.

Inventors

  • 👤 Steve C. S. Chang
  • 👤 Thomas E. Miller

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-07 02:40
CPC Classifications
G; G01; G01N; G01N33/00; G01N33/48; G01N33/50; G01N33/58; G01N33/582; G01N33/52; Y; Y10; Y10S; Y10S436/00; Y10S436/805; Y10S436/826; Y10S530/00; Y10S530/802

Claims Analysis

Total Claims: 15
Claim 1
Independent Claim 102 words
A method for enhancing the chemiluminescent signal of an acridinium ester in a chemiluminescent reaction which comprises oxidizing the acridinium ester in the presence of an effective amount of an enhancer to effect enhanced chemiluminescent signal said enhancer selected from the group consisting of: (a) a quarternary amine cationic surfactant of formula: ##STR5## wherein R 1 is C 8 -C 20 alkyl or alkenyl; and R 2 R 3 and R 4 are C 1 -C 4 alkyl or alkenyl. (b) a nonionic surfactant; and (c) a sulfated primary alcohol selected from the group consisting of sodium dodecylsulfate, magnesium dodecylsulfate and tridecylsulfate.
Claim 2
Independent Claim 102 words
A method for enhancing the chemiluminescent signal of an acridinium ester in a chemiluminescent reaction which comprises oxidizing the acridinium ester in the presence of an effective amount of an enhancer to effect enhanced chemiluminescent signal said enhancer selected from the group consisting of: (a) a quarternary amine cationic surfactant of formula: ##STR5## wherein R 1 is C 8 -C 20 alkyl or alkenyl; and R 2 R 3 and R 4 are C 1 -C 4 alkyl or alkenyl. (b) a nonionic surfactant; and (c) a sulfated primary alcohol selected from the group consisting of sodium dodecylsulfate, magnesium dodecylsulfate and tridecylsulfate.
Claim 3
Dependent Claim 144 words
A method as recited in claim 1 wherein the acridinium ester has the formula: ##STR6## where R 1 is alkyl, alkenyl, alkynyl, or aryl; R 2 , R 3 , R 5 , or R 7 are hydrogen, amino, carboxyl, hydroxyl, alkoxyl, nitro, or halide; R 4 or R 8 are hydrogen, alkyl, alkenyl, alkynyl, aryl, alkoxyl, or amino,; R 6 represents the following substituent: R.sub.6 =--R.sub.9 --R.sub.10 where R 9 is omitted or is alkyl, aryl, or aralkyl linking groups, and R 10 is selected from the group consisting of: ##STR7## X is CH 3 SO4, OSO 2 F, halide, OSO 2 CF 3 , OSO 2 C 4 F 9 , or ##STR8## and R is alkyl, aryl, or alralkyl; and finally R 5 , and R 7 substituent positions on the phenoxy ring are interchangeable with the R 6 substituent position.
Claim 4
Dependent Claim 21 words
A method as recited in claim 2 werein R 4 and R 8 are alkyl, alkenyl, alkynyl, aryl, alkoxyl, or amino.
Claim 5
Dependent Claim 56 words
A method as recited in claim 2 wherein R 1 is methyl; R 2 , R 3 , R 5 , and R 7 are hydrogen; R 4 and R 8 are methyl, R 10 is an N-succinimidyloxycarbonyl group attached directly to the para-position of the phenoxy ring, and X is CH 3 SO 4 .
Claim 6
Dependent Claim 24 words
A method as recited in claim 1 wherein the effective amount of enhancer in the chemiluminescent reaction mixture is greater than 0.005% by weight.
Claim 7
Dependent Claim 24 words
A method as recited in claim 5 wherein the effective amount of enhancer in the chemiluminescent reaction mixture is greater than 0.01% by weight.
Claim 8
Dependent Claim 30 words
A method as recited in claim 1 wherein R 1 is C 14 -C 16 alkyl or alkenyl; R 2 , R 3 and R 4 are methyl or ethyl.
Claim 9
Dependent Claim 14 words
A method as recited in claim 7 wherein the cationic surfactant is hexadecyltrimethylammonium chloride.
Claim 10
Dependent Claim 14 words
A method as recited in claim 1 wherein the enhancer is a nonionic surfactant.
Claim 11
Dependent Claim 16 words
A method as recited in claim 9 wherein the nonionic surfactant is a polyoxyethylenated nonionic surfactant.
Claim 12
Dependent Claim 15 words
A method as recited in claim 1 wherein the sulfated primary alcohol is sodium dodecylsulfate.
Claim 13
Dependent Claim 72 words
In a chemiluscent immunoassasy utilizing an acridinium ester as a label wherein the improvement comprises oxidizing the acridinium ester in the presence of an effective amount of an enhancer selected from the group consisting of: (a) a quarternary amine cationic surfactant of formula: ##STR9## wherein R 1 is C 8 -C 20 alkyl or alkenyl; and R 2 , R 3 and R 4 are C 1 -C 4 alkyl or alkenyl.
Claim 14
Dependent Claim 72 words
In a chemiluscent immunoassasy utilizing an acridinium ester as a label wherein the improvement comprises oxidizing the acridinium ester in the presence of an effective amount of an enhancer selected from the group consisting of: (a) a quarternary amine cationic surfactant of formula: ##STR9## wherein R 1 is C 8 -C 20 alkyl or alkenyl; and R 2 , R 3 and R 4 are C 1 -C 4 alkyl or alkenyl.
Claim 15
Dependent Claim 32 words
A chemiluminescent assay as recited in claim 12 wherein R 1 is C 14 -C 16 alkyl or alkenyl; and R 2 , R 3 and R 4 are methyl or ethyl.

References Cited (Backward Citations)

US3714054A Cited
US4462931A Cited
EP0175889A1 Cited
US4745181A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1993-05-21 1993-11-20 1994-05-22 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1997-05-21 1997-11-20 1998-05-22 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 2001-05-21 2001-11-20 2002-05-22 $7700.00 Window Closed / Lapsed

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