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Highly Sensitive System and Methods for Analysis of Troponin

Inactive Publication Date: 2018-04-12
RGT UNIV OF CALIFORNIA +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

The patent describes a method for detecting the presence or absence of a single molecule of troponin in a sample. The method involves labeling the molecule with a fluorescent moiety and detecting the presence or absence of the label. The detection is done by using a single molecule detector that can detect the fluorescent moiety. The method has a high sensitivity and can be used to detect even small amounts of troponin in a sample. The technical effect of the invention is to provide a reliable and sensitive method for detecting troponin in samples.

Problems solved by technology

In some embodiments, the condition is cardiac toxicity.

Method used

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  • Highly Sensitive System and Methods for Analysis of Troponin
  • Highly Sensitive System and Methods for Analysis of Troponin
  • Highly Sensitive System and Methods for Analysis of Troponin

Examples

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Effect test

example 1

Assays for Biomarkers: Cardiac Troponin I (cTnI)

[0274]The assay: The purpose of this assay was to detect the presence of cardiac Troponin I (cTnI) in human serum. The assay format was a two-step sandwich immunoassay based on a mouse monoclonal capture antibody and a goat polyclonal detection antibody. Ten microliters of sample were required. The working range of the assay is 0-900 pg / ml with a typical analytical limit of detection of 1-3 pg / ml. The assay required about four hours of bench time to complete.

[0275]Materials: the following materials were used in the procedure described below: Assay plate: Nunc Maxisorp, product 464718, 384 well, clear, passively coated with monoclonal antibody, BiosPacific A34440228P Lot # A0316 (5 μg / ml in 0.05 M sodium carbonate pH 9.6, overnight at room temperature); blocked with 5% sucrose, 1% BSA in PBS, and stored at 4° C. For the standard curve, Human cardiac Troponin I (BiosPacific Cat # J34000352) was used. The diluent for the standard concentr...

example 2

Bead-Based Assays for TnI

[0289]The assays described above use the same microtiter plate format where the plastic surface is used to immobilize target molecules. The single particle analyzer system also is compatible with assays done in solution using microparticles or beads to achieve separation of bound from unbound entities.

[0290]Materials: MyOne Streptavidin C1 microparticles (MPs) are obtained from Dynal (650.01-03, 10 mg / ml stock). Buffers use in the assay include: 10× borate buffer saline Triton Buffer (BBST) (1.0 M borate, 15.0 M sodium chloride, 10% Triton X-100, pH 8.3); assay buffer (2 mg / ml normal goat IgG, 2 mg / ml normal mouse IgG, and 0.2 mg / ml MAB-33-IgG-Polymer in 0.1 M Tris (pH 8.1), 0.025 M EDTA, 0.15 M NaCl, 0.1% BSA, 0.1% Triton X-100, and 0.1% NaN3, stored at 4 C); and elution buffer (BBS with 4 M urea, 0.02% Triton X-100, and 0.001% BSA, stored at 2-8 C). Antibodies used in the sandwich bead-based assay include: Bio-Ab (A34650228P (BiosPacific) with 1-2 biotins ...

example 3

tion Range for cTnI in a Population of Normal Non-Diseased Subjects

[0298]A reference range or normal range for cTnI concentrations in human serum was established using serum samples from 88 apparently healthy subjects (non-diseased). A sandwich immunoassay as described in Example 1 was performed and the number of signals or events as described above were counted using the single particle analyzer system of the invention. The concentration of serum troponin I was determined by correlating the signals detected by the analyzer with the standard curve as described above. All assays were perfumed in quadruplicate.

[0299]In accordance with recommendations by the current European and American Cardiology Societies (ESC / ACC) troponin assays should quantify accurately the 99th percentile of the normal range with an assay imprecision (CV) of less than 10% in order to distinguish reliably between patients with ACS and patients without ischemic heart disease, and risk stratification for adverse c...

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Abstract

The invention provides methods, compositions, kits, and systems for the sensitive detection of cardiac troponin. Such methods, compositions, kits, and systems are useful in diagnosis, prognosis, and determination of methods of treatment in conditions that involve release of cardiac troponin.

Description

CROSS REFERENCE[0001]This application is a continuation of U.S. patent application Ser. No. 14 / 921,553 filed on Oct. 23, 2015, which is a continuation of U.S. patent application Ser. No. 13 / 798,547 filed on Mar. 13, 2013, now U.S. Pat. No. 9,182,405, which is a continuation of U.S. patent application Ser. No. 13 / 667,372, filed on Nov. 2, 2012, now U.S. Pat. No. 8,535,895, which is a continuation of U.S. patent application Ser. No. 12 / 902,182, filed on Oct. 12, 2010, now U.S. Pat. No. 8,343,728, which is a continuation of U.S. patent application Ser. No. 12 / 062,412, filed Apr. 3, 2008, now U.S. Pat. No. 7,838,250, which claims priority under 35 U.S.C. § 119 to U.S. Provisional Application 60 / 914,995, filed Apr. 30, 2007, and U.S. Provisional Application 60 / 925,402, filed Apr. 19, 2007. This application is a continuation in part of U.S. patent application Ser. No. 11 / 784,213 filed on Apr. 4, 2007 which claims priority under 35 U.S.C. § 119 to U.S. Provisional Application No. 60 / 789,30...

Claims

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Application Information

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IPC IPC(8): G01N33/68G01N21/64G01N33/58
CPCG01N2800/50G01N2800/325G01N33/68G01N21/6428G01N21/6486G01N33/582G01N33/6887G01N33/6893G01N2333/47G01N2800/32G01N2800/324
Inventor GOIX, PHILIPPE J.PUSKAS, ROBERTTODD, JOHNLIVINGSTON, RICHARDHELD, DOUGLASWU, ALLAN H.B.
Owner RGT UNIV OF CALIFORNIA
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