IP Library Granted Patent US 10,351,897
Granted Patent B2
US 10,351,897 · App. 15/118,297 · Granted Jul 16, 2019

Acetaminophen adducts and methods of use thereof

Inventors: Laura P. James (Little Rock, AR); Jack Hinson (Little Rock, AR); Dean Roberts (Little Rock, AR); Pritmohinder S. Gill (Little Rock, AR)
Assignee: BioVentures, LLC
C12Q1/48C07K14/4708C12N9/1007C12N9/107C12N9/1014C12N9/1096C12Q1/527C12Y201/01005G01N33/53
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Quick Facts
Patent No.
US 10,351,897
App. No.
15/118,297
Granted
Jul 16, 2019
Kind
B2
Abstract

The present disclosure relates to acetaminophen protein adducts and methods of diagnosing acetaminophen toxicity using the acetaminophen protein adducts. The present disclosure provides acetaminophen (APAP)-protein adducts and methods of detecting acetaminophen-induced toxicity in a subject using APAP-protein adducts. One aspect of the present disclosure provides an APAP-protein adduct for diagnosing acetaminophen-induced toxicity. According to the present disclosure, the inventors have identified proteins that are modified by N-acetyl-pbenzoquinoneimine (NAPQI) in subjects with acetaminophen-induced toxicity. Non-limiting examples of proteins modified by NAPQI include betaine-homocysteine S-methyltransferase 1, cytoplasmic aspartate aminotransferase, 1,4-alpha-glucan branching enzyme, formimidoyltransferase-cyclodeaminase, and dystrophin.

Claims (16)

1. A method of treating acetaminophen-induced toxicity in a subject in need thereof, the method comprising:

a) obtaining a biological sample from the subject;

b) measuring the amount of acetaminophen (APAP)-protein adduct in the sample by detecting one or more APAP-protein adducts, wherein each APAP-protein adduct comprises a protein covalently modified with N-acetyl-p-benzoquinone (NAPQI), and wherein the protein is selected from the group consisting of betaine-homocysteine S-methyltransferase 1, cytoplasmic aspartate aminotransferase, 1,4-alpha-glucan-branching enzyme, formimidoyltransferase-cyclodeaminase, and dystrophin;

c) comparing the measured amount of the acetaminophen-protein adduct in the sample to a reference value, wherein a greater amount of acetaminophen-protein adduct in the sample compared to the reference value indicates acetaminophen-induced toxicity in the subject; and

d) administering treatment for acetaminophen-induced toxicity after step c) to the subject.

2. The method of claim 1 , wherein the acetaminophen-induced toxicity is directly or indirectly associated with acetaminophen overdose.

3. The method of claim 1 , wherein the acetaminophen-induced toxicity is hepatotoxicity.

4. The method of claim 1 , wherein the biological sample is a biological fluid selected from the group consisting of blood, plasma, serum, urine, saliva and hair.

5. The method of claim 1 , wherein the biological sample is from a subject with hepatotoxicity of unknown etiology.

6. A method of treating acetaminophen-induced toxicity in a subject in need thereof, the method comprising:

a) obtaining a sample from the subject;

b) measuring the amount of acetaminophen (APAP)-protein adduct in the sample to determine a profile of APAP-protein adducts in the subject, the profile comprising the identity and concentration in the sample from the subject of one or more APAP-protein adducts, wherein each APAP-protein adduct comprises a protein covalently modified with N-acetyl-p-benzoquinone (NAPQI), and wherein the protein is selected from the group consisting of betaine-homocysteine S-methyltransferase 1, cytoplasmic aspartate aminotransferase, 1,4-alpha-glucan-branching enzyme, formimidoyltransferase-cyclodeaminase, and dystrophin;

c) comparing the profile determined in (b) to a database comprising the presence and concentration of one or more APAP-protein adducts correlated with acetaminophen toxicity;

d) identifying a matching entry of the database in which the identity and concentration of the one or more APAP-protein adducts matches the identity and concentration of the one or more APAP-protein adducts in the sample;

e) determining the acetaminophen toxicity comprising the particular acetaminophen toxicity of the matching entry; and

f) administering treatment for acetaminophen-induced toxicity after step e) to the subject.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 31, 2017
From: BOARD OF TRUSTEES OF THE UNIVERSITY OF ARKANSAS
To: BIOVENTURES, LLC
Reel/Frame 041137/0734 →
CORRECTIVE ASSIGNMENT TO CORRECT THE MISSING ASSIGNEE NAME PREVIOUSLY RECORDED ON REEL 039760 FRAME 0163. ASSIGNOR(S) HEREBY CONFIRMS THE MISSING ASSIGNEE ARKANSAS CHILDREN'S HOSPITAL RESEARCH INSTITUTE, INC. SHOULD BE ADDED TO THE RECORDATION.. Recorded Sep 20, 2016
From: JAMES, LAURA P.; HINSON, JACK; ROBERTS, DEAN; GILL, PRITMOHINDER S.
To: BOARD OF TRUSTEES OF THE UNIVERSITY OF ARKANSAS; ARKANSAS CHILDREN'S HOSPITAL RESEARCH INSTITUTE, INC.
Reel/Frame 040086/0137 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 15, 2016
From: JAMES, LAURA P.; HINSON, JACK; ROBERTS, DEAN; GILL, PRITMOHINDER S.
To: BOARD OF TRUSTEES OF THE UNIVERSITY OF ARKANSAS
Reel/Frame 039760/0163 →
Continuity (2)
Provisional Application 61940023 · Feb 14, 2014
Related Publication 20170175166A1 · Jun 22, 2017