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US4212939A Expired / Lapsed US ⏱️ 0.0 years remaining

Substrate solution for carboxylic ester hydrolase determination

Assignee: UAB RESEARCH FOUNDATION NON-PROFIT CORP
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Filing: 1977-11-22
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Granted: 1980-07-15
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Expires: 1997-11-22
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Abstract

Abstract A clear, stable aqueous reagent solution comprising a mixture of a water insoluble vinyl ester of an alkyl, alkenyl, or alkyl-aryl carboxylic acid, nonionic detergents, inorganic salts, enzyme activators, and a buffer, which when combined with a suitable acetaldehyde detection system is useful for the analysis of the action of certain carboxylic ester hydrolases.

Inventors

  • 👤 James E. Myrick
  • 👤 Leo M. Hall

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-27 14:40
CPC Classifications
C; C12; C12Q; C12Q1/00; C12Q1/34; C12Q2334/00; G; G01; G01N; G01N2333/00; G01N2333/90; G01N2333/902; G01N2333/904; G01N2333/914; G01N2333/916; G01N2333/918; Y; Y10; Y10T; Y10T436/00; Y10T436/10; Y10T436/107497

Claims Analysis

Total Claims: 14
Claim 1
Independent Claim 129 words
A stable, clear reagent solution for the analysis of carboxylic acid ester hydrolases which comprises a water insoluble vinyl ester of carboxylic acid, a nonionic detergent, a buffer, and neutral salts, wherein the value of the HLB of said detergent is from 13 to 18, said HLB value being chosen to obtain the highest specific activity for said ester hydrolase; wherein the ionic strength of said solution is adjusted by inclusion of said neutral salts to obtain the highest specific activity for said ester hydrolase; wherein the amounts of said ester, detergent and buffer, said HLB value and said ionic strength are chosen so that when said hydrolase is mixed with said reagent, the mixture is clear and has a stable spectrophotometric absorbance, and wherein said buffer is N,N-bis(2-hydroxy-ethyl)glycine.
Claim 2
Dependent Claim 129 words
A stable, clear reagent solution for the analysis of carboxylic acid ester hydrolases which comprises a water insoluble vinyl ester of carboxylic acid, a nonionic detergent, a buffer, and neutral salts, wherein the value of the HLB of said detergent is from 13 to 18, said HLB value being chosen to obtain the highest specific activity for said ester hydrolase; wherein the ionic strength of said solution is adjusted by inclusion of said neutral salts to obtain the highest specific activity for said ester hydrolase; wherein the amounts of said ester, detergent and buffer, said HLB value and said ionic strength are chosen so that when said hydrolase is mixed with said reagent, the mixture is clear and has a stable spectrophotometric absorbance, and wherein said buffer is N,N-bis(2-hydroxy-ethyl)glycine.
Claim 3
Dependent Claim 39 words
The reagent solution of claim 1, wherein enzyme activators are added thereto and wherein said enzyme activators are selected from the group consisting of bile salts, bile acids, alkyl quaternary ammonium compounds, alkyl-aryl quaternary ammonium compounds and mixtures thereof.
Claim 4
Dependent Claim 33 words
The reagent solution of claim 2, wherein said enzyme activators are selected from the group consisting of deoxycholate acid, a salt of deoxycholate acid, cetyltrimethyl ammonium bromide, cetyldimethylbenzyl ammonium chloride and mixtures thereof.
Claim 5
Dependent Claim 60 words
The reagent solution of claim 2, wherein said vinyl ester of a carboxylic acid is selected from the group consisting of vinyl acetate, vinyl proprionate, vinyl butyrate, vinyl crotonate, vinyl valerate, vinyl hexanoate, vinyl octanoate, vinyl nonamoate, vinyl decanoate, vinyl neodecanoate, vinyl laurate, vinyl myristate, vinyl palmitate, vinyl oleate, vinyl stearate, divinyl suberate, vinyl omega-phenyl nonanoate and vinyl omega-phenyl octanoate.
Claim 6
Dependent Claim 26 words
The reagent solution of claim 2, wherein said non-ionic detergent is selected from the group consisting of polyoxyethylenated alcohols, polyoxyethylenated alkylphenols, their ethers and mixtures thereof.
Claim 7
Dependent Claim 26 words
The reagent solution of claim 2, wherein said nonionic detergent is selected from the group consisting of polyoxyethylene (23) lauryl ether, polyoxyethylenated tert-octyl-phenol and mixtures thereof.
Claim 8
Dependent Claim 24 words
The reagent solution of claim 2, wherein said neutral salts are selected from the group consisting of potassium chloride, sodium chloride, and mixtures thereof.
Claim 9
Dependent Claim 58 words
The reagent solution of claim 2, wherein the concentration of said ester is from 5 to 15 mM; the concentration of said detergent is from 5 to 150 mM; the concentration of said buffer is from 0.05 up to the limit of solubility; and wherein the concentration of said neutral salt is from 0 to about 3 M.
Claim 10
Dependent Claim 14 words
The reagent solution of claim 2, wherein an acetaldehyde detection system is added thereto.
Claim 11
Dependent Claim 44 words
The reagent solution of claim 9, wherein said acetaldehyde detection system is enzymatic and is based upon the oxidation or reduction of said acetaldehyde with simultaneous reduction or oxidation, respectively, of a suitable electron donor or acceptor which can be measured spectrophotometrically or flurometrically.
Claim 12
Dependent Claim 63 words
The reagent solution of claim 10, wherein said enzymatic acetaldehyde detection system consists of alcohol dehydrogenase and β-dihydronicotinamide adenine dinucleotide (NADH), which are added in sufficient quantity to reduce said acetaldehyde to ethanol and oxidize said NADH to β-nicotinamide adenine dinucleotide (NAD + ), whereby the rate of hydrolysis of said vinyl ester may be quantitated by the rate of disappearance of NADH.
Claim 13
Dependent Claim 38 words
The reagent solution of claim 9, wherein said acetaldehyde detection system is chemical and is based upon the combination of said acetaldehyde which an amine dye forming a colored Schiff base which can be determined spectrophotometrically or fluorometrically.
Claim 14
Dependent Claim 22 words
The reagent solution of claim 2, wherein said reagent solution is made to undergo lyophilization and results in a dry powdery agent.

References Cited (Backward Citations)

US4022667A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1983-07-15 1984-01-14 1984-07-15 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1987-07-15 1988-01-14 1988-07-15 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1991-07-15 1992-01-14 1992-07-15 $7700.00 Window Closed / Lapsed

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