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A method for measuring the presence or concentration of an analyte in a sample by spectrophotometry: providing an open top cuvette having a sample with an analyte to be measured; providing a light source and a detector for detecting emitted light; taking at least two measurements that includes: (i)

A method for measuring the presence or concentration of an analyte in a sample by spectrophotometry: providing an open top cuvette having a sample with an analyte to be measured; providing a light source and a detector for detecting emitted light; taking at least two measurements that includes: (i) directing at least two beams of light from the light source to different locations on the cuvette; (ii) passing the at least two beams through the cuvette at their respective locations and through the sample to be measured; and (iii) measuring at least two respective emitted light beams with the detector; and comparing the at least two emitted light beams to determine if: all the emitted light beams should be disregarded; one or more of the emitted light beams should be disregarded; or the sample absorbances should be averaged. In a preferred embodiment, the method includes taking at least three measurements. In another preferred embodiment, the spectrophotometry is absorption spectrophotometry, and the method is performed on a diagnostic analyzer.

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We claim: 1. A method for measuring the presence or concentration of an analyte in a sample by spectrophotometry, comprising: providing an open top cuvette having a sample with an analyte to be measured; providing a light source and a detector for detecting emitted light; taking at least two measur

We claim: 1. A method for measuring the presence or concentration of an analyte in a sample by spectrophotometry, comprising: providing an open top cuvette having a sample with an analyte to be measured; providing a light source and a detector for detecting emitted light; taking at least two measurements that includes: (i) directing at least two beams of light from the light source to different locations on the cuvette; (ii) passing the at least two beams through the cuvette at their respective locations and through the sample to be measured; and (iii) measuring at least two respective emitted light beams with the detector; and comparing the at least two emitted light beams to determine if: all the emitted light beams should be disregarded; one or more of the emitted light beams should be disregarded; or the emitted light beams should be averaged. 2. A method for measuring as claimed in claim 1, further comprising taking at least three measurements and comparing the at least three emitted light beams to determine if: all the emitted light beams should be disregarded; one or more of the emitted light beams should be disregarded; or the emitted light beams should be averaged. 3. A method for measuring as claimed in claim 1, wherein the spectrophotometry is fluorescence spectrophotometry. 4. A method for measuring as claimed in claim 1, wherein the spectrophotometry is absorption spectrophotometry and the step of taking at least two measurements includes: (i) directing at least two beams from the light source to different locations on the cuvette; (ii) passing the at least two beams through the cuvette at their respective locations and through the sample to be measured; and (iii) measuring at least two respective sample absorbances from the emitted light corresponding to the at least two beams with the detector; and comparing the at least two sample absorbances to determine if: all the sample absorbances should be disregarded; one or more of the sample absorbances should be disregarded; or the sample absorbances should be averaged. 5. A method for measuring as claimed in claim 1, wherein a single light source and a single detector are provided and the cuvette is moved relative to the light source and cuvette to produce the at least two beams of light. 6. A method for measuring as claimed in claim 4, wherein prior to the step of directing at least two beams, the method further comprises: (i) directing at least two beams of light from the light source at their respective different locations on the cuvette; (ii) passing the at least two beams through the cuvette alone or the cuvette and sample before the sample has reacted with reagents; and (iii) measuring at least two respective blank absorbances from the emitted light corresponding to the at least two beams with the detector; and selecting at least one blank absorbance; and subtracting at least one blank absorbance from the at least two sample absorbances to result in corrected sample absorbances. 7. A method for measuring as claimed in claim 6, wherein a single light source and a single detector are provided and the cuvette is moved relative to the light source and cuvette to produce the at least two beams of light. 8. A method for measuring as claimed in claim 6, wherein all blank absorbances are selected and each blank absorbance is subtracted from its corresponding sample absorbance at the same location. 9. A method for measuring as claimed in claim 6, wherein the lowest blank absorbance is selected and the lowest blank absorbance is subtracted from each sample absorbance. 10. A method for measuring as claimed in claim 4, wherein after a period of time after the at least two measurements, the method further comprises: taking at least two second measurements at the same location as the at least two measurements to result in at least two second sample absorbances; subtracting the at least two sample absorbances from the second sample absorbances to result in a rate sample absorbance. 11. A method for measuring as claimed in claim 4, wherein the comparison includes comparing the sample absorbances with each other, and if a difference in absorbance between any two absorbances exceeds a predetermined absorbance, then disregarding all sample absorbances. 12. A method for measuring as claimed in claim 4, wherein the comparison includes comparing the sample absorbances with each other: if a difference in absorbance between all absorbances exceeds a predetermined absorbance, then disregarding all sample absorbances; if the difference between a predetermined number of absorbances, which is less than the total number of absorbances, is within the predetermined absorbance, then discarding the remaining absorbances and averaging the absorbances of the predetermined number of absorbances. 13. A method for measuring as claimed in claim 6, wherein the comparison includes comparing the corrected sample absorbances with each other: if a difference in absorbance between all absorbances exceeds a predetermined absorbance, then disregarding all sample absorbances; if the difference between a predetermined number of absorbances, which is less than the total number of absorbances, is within the predetermined absorbance, then discarding the remaining absorbances and averaging the absorbances of the predetermined number of absorbances. 14. A method for measuring as claimed in claim 6, wherein the comparison includes comparing the corrected sample absorbances with each other, and if a difference in absorbance between any two corrected sample absorbances exceeds a predetermined absorbance, then disregarding all corrected sample absorbances. 15. A method for measuring as claimed in claim 1, wherein the comparison detects errors caused by one or more interfering condition(s). 16. A method for measuring as claimed in claim 15, wherein the interfering condition(s) include air bubbles, finger prints, dirt or defects in the cuvette. 17. A method for measuring as claimed in claim 2, wherein the analysis is performed on a diagnostic analyzer. 18. A method for measuring as claimed in claim 1, wherein the light has a wavelength in the range of 300 to 1100 nm. 19. A method for measuring the presence or concentration of an analyte in a sample by absorption spectrophotometry, comprising: providing a cuvette having a sample with an analyte to be measured; providing a source of light and a detector for detecting the light; taking at least three measurements that includes: (i) directing at least three beams of the light to different locations on the cuvette; (ii) passing the at least three beams through the cuvette at their respective locations and through the sample to be measured; and (iii) measuring at least three respective sample absorbances of the transmitted beams with the detector; and comparing the at least three sample absorbances to determine if: all the sample absorbances should be disregarded; one or more of the sample absorbances should be disregarded and the remaining absorbances retained; or all the sample absorbances should be averaged, wherein: if at least two sample absorbances are retained and an average retained absorbance is less than a first selected absorbance then the lowest absorbance is used in determining the presence or concentration of the analyte; or if at least two sample absorbances are retained and an average retained absorbance is greater than or equal to a second selected absorbance then the highest absorbance is used in determining the presence or concentration of the analyte. 20. A method for measuring as claimed in claim 19, wherein a single light source and a single detector are provided and the cuvette is moved relative to the light source and cuvette to produce the at least three beams of light. 21. A method for measuring as claimed in claim 19, wherein the first and second selected absorbances are both one absorbance unit. 22. A method for measuring as claimed in claim 19, wherein the average retained absorbance is based on all sample absorbances. 23. A method for measuring as claimed in claim 19, wherein prior to the step of directing at least three beams, the method further comprises: (i) directing at least three beams of the light at their respective different locations on the cuvette; (ii) passing the at least three beams through the cuvette alone or the cuvette and sample before the sample has reacted with reagents; and (iii) measuring at least three respective blank absorbances of the transmitted beams with the detector; and selecting at least one blank absorbance; and subtracting at least one blank absorbance from the at least three sample absorbances to result in corrected sample absorbances. 24. A method for measuring the presence or concentration of an analyte in a sample by absorption spectrophotometry, comprising: (A) providing a cuvette having a sample with an analyte to be measured; (B) providing a source of light and a detector for detecting the light; (C) taking at least three measurements that includes: (i) directing at least three beams of the light to different locations a, b and c on the cuvette; (ii) passing the at least three beams through the cuvette at their respective locations a, b and c and through the sample to be measured; and (iii) measuring at least three respective sample absorbances Aa, Ab and Ac of the transmitted beams with the detector; (D) determining the absolute value of the difference between each pair of absorbances to arrive at |Aa−Ab|, |Ac−Ab| and |Ac−Aa|; (E) comparing an absolute value of the difference between each pair of absorbances with a predetermined limit; (F) if one or more of each the absolute value of the difference is the predetermined limit, then compare each absorbance to a predetermined absorbance: (i) if one or more absorbances are above the predetermined absorbance, then disregard all readings and proceed to step (K); or (ii) if all absorbances are below the predetermined absorbance, then (G) determine the smallest absolute value of the difference between each pair of absorbances; (H) determine if the smallest absolute value of the difference is <a predetermined fraction of the predetermined limit: (i) if the smallest absolute value of the difference is not less than the predetermined fraction of the limit then disregard all readings and proceed to step (K); or (ii) if the smallest absolute value of the difference is less than the predetermined fraction of the limit, then (I) determine which of the absolute value of the difference between each pair of absorbances is the smallest absolute value of difference; (J) determine which absorbance in the smallest absolute value should be selected or if the results should be disregarded; and (K) either re-evaluating the analysis if the results should be disregarded in steps (F), (H) or (J), or calculating the presence concentration of the analyte in the sample by using the selected absorbance. 25. A method according to claim 24, wherein prior to the step of directing at least three beams, the method further comprises: (i) directing at least three beams of the light at their respective different locations a, b and c on the cuvette; (ii) passing the at least three beams through the cuvette alone or the cuvette and sample before the sample has reacted with reagents; (iii) measuring at least three respective blank absorbances A1a, A1b and A1c of the transmitted beams with the detector; (iv) determining the sample absorbance Aa, Ab, and Ac by subtracting the blank absorbance A1a, A1b and A1c from measured sample absorbance A2a, A2b and A2c respectively; wherein the step (J) of determining which absorbance in the smallest absolute value of the difference between each pair of absorbances should be selected or if the results should be disregarded comprises: (J1) if the smallest absolute value of the difference between each pair of absorbances is |(A2a−A1a)−(A2b−A1b)|, then if A1c+A2c is greater than each of A1a+A2a and A1b+A2b, compare A1a+A2a and A1b+A2b, if A1a+A2a<A1b+A2b then absorbance Aa is the selected absorbance, otherwise absorbance Ab is the selected absorbance, if A1c+A2c is ≦to one of A1a+A2a and A1b+A2b, then disregard all readings and proceed to step (K); (J2) if the smallest absolute value of the difference between each pair of absorbances is |(A2c−A1c) (A2b−A2b)|, then if A1a+A2a is greater than each of A1b+A2b and A1c+A2c, compare A1c+A2c and A1b+A2b, if A1c+A2c<A1b+A2b then absorbance Ac is the selected absorbance, otherwise absorbance Ab is the selected absorbance, if A1a+A2a is ≦to one of A1b+A2b and A1c+A2c, then disregard all readings and proceed to step (K); or (J3) if the smallest absolute value of the difference between each pair of absorbances is |(A2c−A1c) (A2a−A1a)|, then if A1b+A2b is greater than each of A1a+A2a and A1c+A2c, compare A1c+A2c and A1a+A2a, if A1c+A2c<A1a+A2a then absorbance Ac is the selected absorbance, otherwise absorbance Aa is the selected absorbance, if A1b+A2b is ≦to one of A1a+A2a and A1c+A2c, then disregard all readings and proceed to step (K). 26. A method according to claim 24, wherein the predetermined fraction of the limit is 0.75 times the predetermined limit. 27. A method according to claim 24, wherein locations a, b and c, correspond to left L, middle M and right R locations on the cuvette. 28. A method according to claim 24, wherein prior to the step of directing at least three beams, the method further comprises: (i) directing at least three beams of the light at their respective different locations a, b and c on the cuvette; (ii) passing the at least three beams through the cuvette alone or the cuvette and sample before the sample has reacted with reagents; (iii) measuring at least three respective blank absorbances A1a, A1b and A1c of the transmitted beams with the detector; (iv) determining the sample absorbance Aa, Ab, and Ac by subtracting the blank absorbance A1a, A1b and A1c from measured sample absorbance A2a, A2b and A2c, respectively. 29. A method according to claim 25, wherein the predetermined limit is equal to intercept+slope*(minimum of (A2a−A1a), (A2b−A1b) or (A2c−A1c)), wherein the intercept and slope are determined by the analyte being measured. 30. A method according to claim 25, wherein the predetermined absorbance is 1.0. 31. A method according to claim 1 implemented by a computer program interfacing with a computer.