Biosensor calibration coding systems and methods

US10488395B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10488395-B2
Application numberUS-201916420990-A
CountryUS
Kind codeB2
Filing dateMay 23, 2019
Priority dateMar 7, 2014
Publication dateNov 26, 2019
Grant dateNov 26, 2019

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  2. Abstract

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Abstract

Official abstract text for this publication.

A test sensor ( 100 ) for determining an analyte concentration in a biological fluid comprises a strip including a fluid receiving area ( 128 ) and a port-insertion region ( 126 ). A first row of optically transparent ( 132 ) and non-transparent positions forms a calibration code pattern ( 130 ) disposed within a first area of the port-insertion region ( 126 ). A second row of optically transparent ( 142 ) and non-transparent positions forms a synchronization code pattern ( 140 ) disposed within a second area of the port-insertion region ( 126 ). The second area is different from the first area. The synchronization code pattern ( 140 ) corresponds to the calibration code pattern ( 130 ) such that the synchronization code pattern ( 140 ) provides synchronization of the serial calibration code pattern ( 130 ) during insertion of the port-insertion region ( 126 ) into the receiving port of the analyte meter.

First claim

Opening claim text (preview).

The invention claimed is: 1. A method for determining an analyte concentration in a biological fluid using a calibrated correlation equation, the method comprising the following acts: (a) transmitting light waves through first optically transparent openings in a test sensor including a first row of sequential optically transparent and non-transparent positions forming calibration coding patterns; (b) near simultaneous to act (a), transmitting light waves through second optically transparent openings in the test sensor including a second row of sequential optically transparent and non-transparent positions forming synchronization coding patterns that correspond to the calibration coding patterns; (c) receiving the light waves transmitted through the first optically transparent openings in a first light sensor; (d) receiving the light waves transmitted through the second optically transparent openings in a second light sensor; (e) generating a series of calibration code signals in response to light waves being received and not received by the first light sensor due to the optically transparent and non-transparent positions passing the first light sensor during the insertion of the test sensor into an analyte measuring device; (f) near simultaneous to act (e), generating a series of synchronization code signals in response to light waves being received and not received by the second light sensor due to the optically transparent and non-transparent positions passing the second light sensor during the insertion of the test sensor into the analyte measuring device, the series of synchronization code signals corresponding to the series of calibration code signals; (g) calibrating at least one correlation equation in response to the generating the series of calibration code signals; and (h) determining an analyte concentration based on the at least one calibrated correlation equation, wherein the analyte concentration is determined by reacting the analyte in a reaction that produces an output signal, the analyte concentration being determined using the at least one calibrated correlation equation and the produced output signal. 2. The method of claim 1 , further comprising detecting the insertion of the test sensor into an insertion port of an analyte meter, the detecting occurring immediately prior to the transmitting of light waves in steps (a) and (b). 3. The method of claim 1 , wherein the second row of sequential optically transparent and non-transparent positions are evenly spaced. 4. The method of claim 1 , wherein the test sensor is for determining blood glucose concentration. 5. The method of claim 1 , wherein at least a portion of the sequential optically transparent and non-transparent positions are staggered. 6. The method of claim 1 , wherein the reaction is an electrochemical reaction and the output signal is an electric signal.

Assignees

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Classifications

  • producing a change of colour · CPC title

  • Fluorescence · CPC title

  • Investigating reagent band (test-element handling not specific to a test method G01N33/4875; analytical elements specific to chemical analysis of biological material G01N33/52; autometer with reagent band G01N35/04) · CPC title

  • Corrective measures, e.g. error detection, compensation for temperature or hematocrit, calibration (coding of calibration information G01N33/48771) · CPC title

  • Calibration; base line adjustment; drift compensation · CPC title

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What does patent US10488395B2 cover?
A test sensor ( 100 ) for determining an analyte concentration in a biological fluid comprises a strip including a fluid receiving area ( 128 ) and a port-insertion region ( 126 ). A first row of optically transparent ( 132 ) and non-transparent positions forms a calibration code pattern ( 130 ) disposed within a first area of the port-insertion region ( 126 ). A second row of optically transpa…
Who is the assignee on this patent?
Ascensia Diabetes Care Holdings Ag
What technology area does this patent fall under?
Primary CPC classification G01N33/48771. Mapped technology areas include Physics.
When was this patent published?
Publication date Tue Nov 26 2019 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).