Automatic differentiation of a sample solution and a control solution

• US 7,670,846 B2
• Filed: 06/24/2003
• Issued: 03/02/2010
• Est. Priority Date: 06/29/2002
• Status: Expired due to Fees

• Current Assignee: Roche Diabetes Care Inc. (Roche Holding AG)
• Original Assignee: Roche Diagnostics Operations Incorporated (Roche Holding AG)
• Inventors: Horn, Carina, Frey, Guenter, Gaa, Otto, Murawski, Hans-Ruediger, Kintzig, Hans
• Primary Examiner(s): WALLENHORST, MAUREEN
• Application Number:
  US10/518,968
• Publication Number:
  US 20050244981A1
• Time in Patent Office: 2,443 Days
• Field of Search: 436/8, 436/13, 436/14, 436/16, 436/164, 436/166, 436/171, 436/174, 422/82.05, 422/82.09, 356/51, 356/300, 356/317, 356/318, 356/319, 356/432, 356/436, 356/441, 356/442
• US Class Current: 436/164
• CPC Class Codes: G01N 33/96 involving blood or serum control standard
• CPC Class Codes: Y10T 436/10 Composition for standardization, calibration, simulation, stabilization, preparation or preservation; processes of use in preparation for chemical testing
• CPC Class Codes: Y10T 436/104165 Lipid, cholesterol, or triglyceride standard or control
• CPC Class Codes: Y10T 436/104998 Glucose, ketone, nitrate standard or control
• CPC Class Codes: Y10T 436/106664 Blood serum or blood plasma standard or control
• CPC Class Codes: Y10T 436/25 including sample preparation

Abstract

The invention concerns a method for automatically differentiating between a sample liquid and a control liquid especially within the context of analytical measuring systems, wherein the presence of a special property of the control liquid and/or at least two criteria are used for the differentiation. In addition the invention concerns appropriate control liquids that are suitable for the new method.

Claims

1. A method for automatically determining whether a sample liquid to be tested in an optical measuring instrument is a test sample or a control sample;

comprising;

(a) providing an optical measuring instrument effective for measuring sample liquids for an analyte of interest, wherein each of said sample liquids may be a test sample or a control sample;

(b) providing one or more control samples containing a known concentration of said analyte of interest, wherein each of said control samples has been provided with a special optical property that is not present in any of said test samples;

(c) using said optical measuring instrument to measure one of said sample liquids for the analyte of interest, wherein the optical measurement additionally evaluates said special optical property; and

(d) automatically determining whether the measured sample liquid is a control sample or a test sample by causing the optical measuring instrument to identify the results of the evaluation of said special optical property as being consistent with either a control sample or a test sample;

wherein said using said optical measuring instrument comprises using a photometer to measure absorption or remission in the IR range;

wherein said special optical property is provided by providing a dye in the control sample; and

wherein the dye is an IR dye which does not have a substantial absorption in the wavelength range in which the measurement signal for the analyte of interest is detected.

2. A method according to claim 1 wherein the dye is a member selected from the group consisting of metal complexes of quinolinequinones, nickel dithiolene dyes, nickel tetramine dyes, quinone dyes, phthalocyanine dyes, naphthocyanine dyes, and azo dyes.

3. A method according to claim 1 wherein the dye is (2-[2- [2-chloro-3-[[1,3-dihydro-1,1-dimethyl-3-(4-sulfobutyl)-2H-benz[e]indol-2ylidene[-1- cyclopentene-1yl[ethenyl]-1,1-dimethyl-3-(4-sulfobutyl)-1H-benz[e]indolium, internal salt, sodium salt.

4. A method according to claim 1 wherein said special optical property is a higher decrease in remission in comparison to the decrease in remission typically observed in a test sample.

5. A method according to claim 1 wherein said optical measuring instrument evaluates two or more properties in the measured sample liquid, wherein said two or more properties, in combination, have been identified as being indicative of either a control sample or a test sample;

and further wherein said automatically determining step includes causing the measuring instrument to identify the results of the evaluation of said two or more properties as being consistent with either a control sample or a test sample.

6. A method according to claim 5 wherein one of said two or more properties is an optical property.

7. A method for automatically determining whether a sample liquid to be tested in an optical measuring instrument is a test sample or a control sample;

comprising;

(a) providing a photometer effective for measuring sample liquids for an analyte of interest, wherein each of said sample liquids may be a test sample or a control sample;

(b) providing one or more control samples containing a known concentration of said analyte of interest, wherein each of said control samples has been provided with an IR dye that is not present in any of said test samples, wherein the IR dye does not have a substantial absorption in the wavelength range in which a measurement signal for the analyte of interest is detected;

(c) using said photometer to measure one of said sample liquids for the analyte of interest, and additionally using said photometer to measure absorption or remission in the IR range; and

(d) automatically determining whether the measured sample liquid is a control sample or a test sample by causing the photometer to identify the results of the measurement of absorption or remission in the IR range as being consistent with either a control sample or a test sample.