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US4782017A Expired / Lapsed US ⏱️ 0.0 years remaining

Analytical element and method for determination of theophylline by enzyme inhibition

Assignee: Clinical Diagnostic Systems Inc
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Filing: 1986-08-25
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Granted: 1988-11-01
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Expires: 2006-08-25
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Abstract

Abstract Theophylline can be determined with an analytical element and method which utilize the inhibition, by theophylline, of alkaline phosphatase activity on an appropriate substrate. The assay is carried out at a pH of 9 or less. The element comprises a porous spreading zone and at least one other zone in fluid contact with the spreading zone. The isoenzyme of alkaline phosphatase and a suitable substrate for the isoenzyme are located in different zones of the element. The element also contains a buffer for maintaining the pH at 9 or less, substantially all of which is located in the spreading zone.

Inventors

  • 👤 Paul H. Frickey
  • 👤 Gary E. Norton

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-30 00:28
CPC Classifications
G; G01; G01N; G01N33/00; G01N33/48; G01N33/50; G01N33/52; G01N33/525; G01N33/526; C; C12; C12Q; C12Q1/00; C12Q1/34; C12Q1/42; C12Q2334/00; C12Q2334/10; Y; Y10; Y10S; Y10S435/00; Y10S435/805; Y10S436/00; Y10S436/822

Claims Analysis

Total Claims: 22
Claim 1
Independent Claim 100 words
A dry analytical element for the determination of theophylline comprising, in fluid contact, a porous spreading zone and at least one additional zone, said element containing an isoenzyme of alkaline phosphatase which is capable of acting on a substrate for said isoenzyme at a pH of 9 or less, and a substrate for said isoenzyme, provided said phosphatase and substrate are in different zones of said element, said element further containing a buffer which is capable of maintaining the pH at 9 or less during said determination, provided that substantially all of said buffer is in said porous spreading zone.
Claim 2
Dependent Claim 100 words
A dry analytical element for the determination of theophylline comprising, in fluid contact, a porous spreading zone and at least one additional zone, said element containing an isoenzyme of alkaline phosphatase which is capable of acting on a substrate for said isoenzyme at a pH of 9 or less, and a substrate for said isoenzyme, provided said phosphatase and substrate are in different zones of said element, said element further containing a buffer which is capable of maintaining the pH at 9 or less during said determination, provided that substantially all of said buffer is in said porous spreading zone.
Claim 3
Dependent Claim 13 words
The element of claim 1 wherein said buffer is a nitrogen-containing organic buffer.
Claim 4
Dependent Claim 22 words
The element of claim 2 wherein said buffer is selected from the group consisting of tris(hydroxymethyl)aminomethane.HCl, glycylglycine, N-tris(hydroxymethyl)-methyl-2-aminoethanesulfonic acid and N-2-hydroxyethylpiperazine-N'-2-ethanesulfonic acid.
Claim 5
Dependent Claim 25 words
The element of claim 1 wherein said buffer is capable of maintaining the pH during said theophylline determination at from about 7 to about 9.
Claim 6
Dependent Claim 14 words
The element of claim 1 wherein said phosphatase substrate is in said spreading zone.
Claim 7
Dependent Claim 26 words
The element of claim 1 wherein said substrate is an organic mono- or diester of phosphoric acid and said phosphatase isoenzyme is bovine liver alkaline phosphatase.
Claim 8
Dependent Claim 93 words
An analytical element for the determination of theophylline comprising: a support having thereon, in order and in fluid contact: a first layer containing an isoenzyme of alkaline phosphatase which is capable of acting on a substrate for said isoenzyme at a pH of 9 or less, a radiation-blocking layer, and a porous spreading layer containing a substrate for said isoenzyme, said element further containing a buffer which is capable of maintaining the pH at 9 or less during said determination, provided that substantially all of said buffer is in said porous spreading layer.
Claim 9
Dependent Claim 93 words
An analytical element for the determination of theophylline comprising: a support having thereon, in order and in fluid contact: a first layer containing an isoenzyme of alkaline phosphatase which is capable of acting on a substrate for said isoenzyme at a pH of 9 or less, a radiation-blocking layer, and a porous spreading layer containing a substrate for said isoenzyme, said element further containing a buffer which is capable of maintaining the pH at 9 or less during said determination, provided that substantially all of said buffer is in said porous spreading layer.
Claim 10
Dependent Claim 17 words
The element of claim 7 further comprising a subbing layer between said radiation-blocking and porous spreading layers.
Claim 11
Dependent Claim 16 words
The element of claim 7 wherein said porous spreading layer is a blush polymer spreading layer.
Claim 12
Dependent Claim 13 words
The element of claim 9 wherein said porous spreading layer comprises titanium dioxide.
Claim 13
Dependent Claim 45 words
The element of claim 7 wherein said substrate is selected from the group consisting of p-nitrophenyl phosphate and 4-(4-nitro-2-methlsulfonyl phenylazo)naphthol-1-phosphate, said alkaline phosphatase is bovine liver alkaline phosphatase, and said buffer is selected from the group consisting of tris(hydroxymethyl)aminomethane.HCl, glycylglycine, N-tris(hydroxymethyl)-methyl-2-aminoethanesulfonic acid and N-2-hydroxyethylpiperazine-N'-2-ethanesulfonic acid.
Claim 14
Dependent Claim 16 words
The element of claim 11 wherein said substrate is p-nitrophenyl phosphate and said buffer is tris(hydroxymethyl)aminomethane.HCl.
Claim 15
Independent Claim 148 words
A method for the determination of theophylline comprising the steps of: A. at a pH of 9 or less, contacting a sample of a biological fluid suspected of containing theophylline with a dry analytical element comprising, in fluid contact, a porous spreading zone and at least one additional zone, said element containing an isoenzyme of alkaline phosphatase which is capable of acting on a substrate for said isoenzyme at a pH of 9 or less, and a substrate for said isoenzyme, provided said phosphatase and substrate are in different zones of said element, said element further containing a buffer which is capable of maintaining the pH at 9 or less during said determination, provided that substantially all of said buffer is in said porous spreading zone, and B. determining a detectable change resulting from said contact as an indication of the amount of theophylline in said biological fluids.
Claim 16
Independent Claim 148 words
A method for the determination of theophylline comprising the steps of: A. at a pH of 9 or less, contacting a sample of a biological fluid suspected of containing theophylline with a dry analytical element comprising, in fluid contact, a porous spreading zone and at least one additional zone, said element containing an isoenzyme of alkaline phosphatase which is capable of acting on a substrate for said isoenzyme at a pH of 9 or less, and a substrate for said isoenzyme, provided said phosphatase and substrate are in different zones of said element, said element further containing a buffer which is capable of maintaining the pH at 9 or less during said determination, provided that substantially all of said buffer is in said porous spreading zone, and B. determining a detectable change resulting from said contact as an indication of the amount of theophylline in said biological fluids.
Claim 17
Dependent Claim 17 words
The method of claim 13 carried out at a pH of from about 7 to about 9.
Claim 18
Dependent Claim 16 words
The method of claim 13 wherein said biological fluid is human blood serum or whole blood.
Claim 19
Independent Claim 144 words
A method for the determination of theophylline comprising the steps of: A. at a pH of 9 or less, contacting a sample of a human biological fluid suspected of containing theophylline with a dry analytical element comprising: a support having thereon, in order and in fluid contact: a first layer containing an isoenzyme of alkaline phosphatase which is capable of acting on a substrate for said isoenzyme at a pH of 9 or less, a radiation-blocking layer, and a porous spreading layer containing a substrate for said isoenzyme, said element further containing a buffer which is capable of maintaining the pH at 9 or less during said determination, provided that substantially all of said buffer is in said porous spreading layer, and B. determining a detectable change resulting from said contact as an indication of the amount of theophylline in said human biological fluid.
Claim 20
Independent Claim 144 words
A method for the determination of theophylline comprising the steps of: A. at a pH of 9 or less, contacting a sample of a human biological fluid suspected of containing theophylline with a dry analytical element comprising: a support having thereon, in order and in fluid contact: a first layer containing an isoenzyme of alkaline phosphatase which is capable of acting on a substrate for said isoenzyme at a pH of 9 or less, a radiation-blocking layer, and a porous spreading layer containing a substrate for said isoenzyme, said element further containing a buffer which is capable of maintaining the pH at 9 or less during said determination, provided that substantially all of said buffer is in said porous spreading layer, and B. determining a detectable change resulting from said contact as an indication of the amount of theophylline in said human biological fluid.
Claim 21
Dependent Claim 17 words
The method of claim 16 carried out at a pH of from about 7 to about 9.
Claim 22
Dependent Claim 16 words
The method of claim 16 wherein said human biological fluid is blood serum or whole blood.

References Cited (Backward Citations)

US4042335A Cited
US4264727A Cited
US4555484A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1991-11-01 1992-05-02 1992-11-01 $2000.00 Window Closed / Lapsed
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