Sensitivity and the dynamic range of photometric assays by generating multiple calibration

Patent metadata

Field	Value
Publication number	US-10288609-B2
Application number	US-201815951536-A
Country	US
Kind code	B2
Filing date	Apr 12, 2018
Priority date	Apr 26, 2012
Publication date	May 14, 2019
Grant date	May 14, 2019

Abstract

A method for determining the amount of a specific analyte by photometric assays, wherein the specific analyte in a sample reacts with an analyte specific reaction partner in a reaction mixture. At least two calibration curves are generated, the first calibration curve recorded at a first wavelength is optimized for low concentrations of the specific analyte thereby maximizing the lower detection limit and, the second calibration curve recorded at a second wavelength is optimized for high concentrations of the specific analyte thereby maximizing the upper detection limit. The optimized lower detection limit and the optimized upper detection limit results in an extended dynamic range.

First claim

What is claimed is:

1. A method for determining the amount of a specific analyte by photometric assays across a wide range using a spectrophotometer, wherein the specific analyte in a sample reacts with an analyte specific reaction partner in a reaction mixture, comprising the steps of:
a) generating at least two calibration curves, wherein
the first calibration curve recorded at a first wavelength is optimized for low concentrations of the specific analyte thereby maximizing the lower detection limit, and
the second calibration curve recorded at a second wavelength is optimized for high concentrations of the specific analyte thereby maximizing the upper detection limit;

b) irradiating the reaction mixture using the spectrophotometer with light concentrated at at least the first and second wavelengths and measuring simultaneously the optical signal for the specific analyte of a sample to be determined in the reaction mixture at least at the first and second wavelengths using the spectrophotometer;
c) selecting either the first or the second calibration curve for quantification of the specific analyte, by the following criteria:
for increasing calibration curves:
if the optical signal of the first and/or the second wavelength is lower than a corresponding predetermined threshold value, the concentration of the analyte is determined by the use of the first calibration curve recorded at the first wavelength;
if the optical signal of the first and/or the second wavelength exceeds a corresponding predetermined threshold value, the concentration of the analyte is determined by the use of the second calibration curve recorded at the second wavelength;

for decreasing calibration curves:
if the optical signal of the first and/or the second wavelength is lower than a corresponding predetermined threshold value, the concentration of the analyte is determined by the use of the second calibration curve recorded at the second wavelength;
if the optical signal of the first and/or the second wavelength exceeds a corresponding predetermined threshold value, the concentration of the analyte is determined by the use of the first calibration curve recorded at the first wavelength, and

d) quantifying the amount of the specific analyte by comparison with the selected calibration curve.

2. The method according to claim 1 , wherein in turbidimetric and nephelometric immunoassays the specific analyte is quantified from the change in the turbidity of the reaction mixture based on the agglutination of the specific analyte and an analyte specific binding partner.

3. The method according to claim 1 , wherein in colorimetric assays the specific analyte is quantified with the aid of a color reagent.

4. The method according to claim 1 , wherein the first calibration curve is recorded at a first wavelength and at a first reaction time.

5. The method according to claim 1 , wherein the second calibration curve is recorded at a second wavelength and of a second reaction time.

6. The method according to claim 1 , wherein the simultaneous measurement of the optical signal for the specific analyte of a sample to be determined in the reaction mixture is performed at least at the first and second wavelengths over the complete reaction time.

7. The method according to claim 1 , wherein the measurement results are stored in a data management system of the instrument platform.

8. The method according to claim 1 , wherein further wavelengths are determined as a blank value for the correction of interferences and compensation of photometric noise.

9. The method according to claim 1 , wherein at least two calibration curves are generated that are recorded at the same wavelengths and at different reaction times.

10. The method according to claim 1 , wherein the analyte specific reaction partner further comprises binding proteins, antigens, antigen fragments, antibodies, antibody fragments, nucleic acids, receptors and particle enhanced binding partners, enzymes, substrates or specific chemical reagents leading to a color change or to a turbidity change in the presence of an analyte.

11. A computer-implemented method of determining the optimal wavelength, reaction time and threshold according to claim 1 , comprising the steps of:
a) receiving a dataset representing the absorbance values of the samples recorded at multiple wavelengths over the complete reaction time simultaneously available on an analyzer, wherein said dataset includes a plurality of data points for:
standards for the calibration,
a blank sample for determination of lower detection limit,
at least 2 samples for the determination of the precision, and/or
dilution series;

b) setting the threshold values at a concentration where the calibration curves change from the first to the second calibration curve, by using for lower concentrations the first calibration curve for the analyte quantification and by using for higher concentrations the second calibration curve for the analyte quantification; and
c) determining the first and second wavelength as well as the first and the second reaction time, analyzing the kinetic curves and selecting the optimal set up for the first calibration curve and the second calibration curve.

12. The method of claim 1 in which the first wavelength is different from the second wavelength.

13. A method for increasing the sensitivity and/or dynamic range of photometric assays using a spectrophotometer, wherein the specific analyte in a sample reacts with an analyte specific reaction partner in a reaction mixture, comprising the steps of:
a) generating at least two calibration curves, wherein
the first calibration curve recorded at a first wavelength is optimized for low concentrations of the specific analyte thereby maximizing the lower detection limit, and
the second calibration curve recorded at a second wavelength is optimized for high concentrations of the specific analyte thereby maximizing the upper detection limit;

b) irradiating the reaction mixture using the spectrophotometer with light concentrated at at least the first and second wavelengths and measuring simultaneously the optical signal for the specific analyte of a sample to be determined in the reaction mixture at least at the first and second wavelengths using the spectrophotometer;
c) selecting either the first or the second calibration curve for quantification of the specific analyte, by the following criteria:
for increasing calibration curves:
if the optical signal of the first and/or the second wavelength is lower than a corresponding predetermined threshold value, the concentration of the analyte is determined by the use of the first calibration curve recorded at the first wavelength,
if the optical signal of the first and/or the second wavelength exceeds a corresponding predetermined threshold value, the concentration of the analyte is determined by the use of the second calibration curve recorded at the second wavelength;

for decreasing calibration curves:
if the optical signal of the first and/or the second wavelength is lower than a corresponding predetermined threshold value, the concentration of the analyte is determined by the use of the second calibration curve recorded at the second wavelength,
if the optical signal of the first and/or the second wavelength exceeds a corresponding predetermined threshold value, the concentration of the analyte is determined by the use of the first calibration curve recorded at the first wavelength; and

d) quantifying the amount of the specific analyte by comparison with the selected calibration curve.

14. A computer readable medium including

Assignees

• Roche Diagnostics Operations Inc

Inventors

• Brueckner Thorsten
• Lopez-Calle Eloisa
• Oranth Norbert
• Roedl Josef

Classifications

• G01N21/78

  producing a change of colour · CPC title

• G16B20/00

  ICT specially adapted for functional genomics or proteomics, e.g. genotype-phenotype associations · CPC title

• G01N33/6827

  Total protein determination, e.g. albumin in urine · CPC title

• G01N33/54393 Primary

  Improving reaction conditions or stability, e.g. by coating or irradiation of surface, by reduction of non-specific binding, by promotion of specific binding · CPC title

• G01N33/573

  for enzymes or isoenzymes · CPC title