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Method for measuring free hemoglobin by double-optical-path multiposition intra-frequency-domain fluorescence light intensity

A technology of hemoglobin and fluorescent light, which is applied in the field of measuring free hemoglobin with fluorescent light intensity, can solve the problems of non-linear light intensity and inability to completely eliminate fluorescent background noise, achieve suppression and blood scattering, solve non-destructive testing problems, and have strong measurement pertinence Effect

Inactive Publication Date: 2017-12-01
TIANJIN UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

[0004] However, due to the influence of incident light intensity, optical path length and measured target concentration, the fluorescence has a serious self-absorption problem, as well as the scattering property of blood, which will lead to nonlinearity of light intensity, and cannot completely eliminate the influence of fluorescence background noise , Aiming at the above problems, this method proposes a method for measuring free hemoglobin by fluorescence light intensity in the frequency domain with dual optical paths and multiple positions

Method used

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  • Method for measuring free hemoglobin by double-optical-path multiposition intra-frequency-domain fluorescence light intensity
  • Method for measuring free hemoglobin by double-optical-path multiposition intra-frequency-domain fluorescence light intensity
  • Method for measuring free hemoglobin by double-optical-path multiposition intra-frequency-domain fluorescence light intensity

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Embodiment 1

[0059] The embodiment of the present invention provides a method for measuring free hemoglobin with fluorescence light intensity in the frequency domain with dual optical paths and multiple positions, and the devices used are such as figure 2 As shown, it includes: a fluorescent excitation light source 3 , a blood bag 5 , a displacement platform 6 and a light intensity receiving device 7 .

[0060] Wherein, ensure that the light output port of the fluorescence excitation light source 3 and the incident slit of the light intensity receiving device 7 are close to the blood bag 5, drive the fluorescence excitation light source 3 with a square wave signal to make it emit a square wave light signal, and the fluorescence excitation light source 3 is at position a Under the two optical paths at position a (corresponding to the first optical path 1) and position a' (corresponding to the second optical path 2), the blood sample in the blood bag 5 is excited, and the fluorescence is rec...

Embodiment 2

[0067] The difference between the embodiment of the present invention and the embodiment 1 is only that the fluorescence excitation light source 3 and the movement mode of the light intensity receiving device 7 are different, see the following description for details:

[0068] see image 3 , ensure that the light exit port of the fluorescence excitation light source 3 and the incident slit of the light intensity receiving device 7 are close to the blood bag 5, drive the fluorescence excitation light source 1 with a square wave signal to make it emit a square wave light signal, and the fluorescence excitation light source 3 matches the blood bag 5 The blood sample inside is excited, and the light intensity receiving device 7 receives the fluorescence light intensity at the position a under the double optical path: position a and position a'. Control the light intensity receiving device 7 to move to position b through the displacement platform 6, and receive the fluorescent ligh...

Embodiment 3

[0073] During specific implementation, due to the limitation of the space structure, it may occur that the fluorescence excitation light source 3 and the light intensity receiving device 7 cannot be close to the blood bag 5. An optical fiber is used as an incident optical fiber 4 and an outgoing optical fiber 8 .

[0074] see Figure 4 The fluorescence excitation light source 1 is driven by a square wave signal to emit a square wave light signal, the fluorescence excitation light source 3 excites the blood sample in the blood bag 5 through the incident optical fiber 4, and the fluorescence light intensity is received by the light intensity receiving device 7 through the exit optical fiber 8 , the incident optical fiber 4 and the outgoing optical fiber 8 are respectively close to the blood bag 5, the incident optical fiber 4 is at position a, and the fluorescence excitation light source 3 passes through the incident optical fiber 4 at this position. Excitation is carried out, ...

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Abstract

The invention discloses a method for measuring free hemoglobin by double-optical-path multiposition intra-frequency-domain fluorescence light intensity. The method includes driving a fluorescence excitation light source by square wave signals, clinging a light outlet of a fluorescence excitation light source and an entrance slit of a light intensity receiving device to a blood bag, exciting a blood sample by the fluorescence excitation light source, and receiving fluorescence light intensity by the light intensity receiving device; controlling the fluorescence excitation light source to move to different positions and changing optical path measurement by a displacement platform, transforming the fluorescence light intensities collected at multiple positions under the two optical paths into a frequency domain, creating intra-frequency-domain fluorescence light intensities, combining with chemical testing data after normalization, and creating a mathematical model; collecting fluorescence light intensities of an unknown blood sample at multiple positions under the two optical paths, transforming the fluorescence light intensities into a frequency domain, creating intra-frequency-domain fluorescence light intensities, and inputting the fluorescence light intensities into the mathematical model after normalization to acquire the content of the free hemoglobin. The method has the advantages that influences of fluorescence background noise are eliminated, and light intensity nonlinearity caused by fluorescence self-absorption, blood scattering and the like is inhibited.

Description

technical field [0001] The invention relates to the field of stoichiometry for concentration analysis of light-intensity complex solutions, in particular to a method for measuring free hemoglobin with fluorescent light intensity in a dual optical path and multi-position frequency domain. Background technique [0002] In the existing technology, the more mature technology is to detect the content of free hemoglobin in the blood bag through chemical testing, which has the outstanding advantage of high accuracy, but the chemical testing method needs to open the blood bag to take out the sample for testing, which cannot meet the needs of fast, fast and efficient testing. Non-contact and pollution-free requirements. [0003] The study found that fluorescence light intensity measurement is also possible to detect the content of free hemoglobin in blood bags due to its non-contact, non-polluting, and highly targeted characteristics. [0004] However, due to the influence of incide...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): G01N21/64
CPCG01N21/64G01N21/6402G01N2021/6417
Inventor 李刚倪静罗永顺万兴华林凌
Owner TIANJIN UNIV
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