CN110736780A - biological sample analysis system - Google Patents

biological sample analysis system Download PDF

Info

Publication number
CN110736780A
CN110736780A CN201911159949.5A CN201911159949A CN110736780A CN 110736780 A CN110736780 A CN 110736780A CN 201911159949 A CN201911159949 A CN 201911159949A CN 110736780 A CN110736780 A CN 110736780A
Authority
CN
China
Prior art keywords
sample
electrode pair
current
electrochemically active
correlation
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
CN201911159949.5A
Other languages
Chinese (zh)
Inventor
庞莹莹
赵东旭
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Beijing Yi Zhi Lian Technology Co Ltd
Original Assignee
Beijing Yi Zhi Lian Technology Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Beijing Yi Zhi Lian Technology Co Ltd filed Critical Beijing Yi Zhi Lian Technology Co Ltd
Priority to CN201911159949.5A priority Critical patent/CN110736780A/en
Publication of CN110736780A publication Critical patent/CN110736780A/en
Withdrawn legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N27/00Investigating or analysing materials by the use of electric, electrochemical, or magnetic means
    • G01N27/26Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating electrochemical variables; by using electrolysis or electrophoresis
    • G01N27/416Systems
    • G01N27/4166Systems measuring a particular property of an electrolyte
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01BMEASURING LENGTH, THICKNESS OR SIMILAR LINEAR DIMENSIONS; MEASURING ANGLES; MEASURING AREAS; MEASURING IRREGULARITIES OF SURFACES OR CONTOURS
    • G01B7/00Measuring arrangements characterised by the use of electric or magnetic techniques
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01RMEASURING ELECTRIC VARIABLES; MEASURING MAGNETIC VARIABLES
    • G01R29/00Arrangements for measuring or indicating electric quantities not covered by groups G01R19/00 - G01R27/00
    • G01R29/24Arrangements for measuring quantities of charge

Abstract

A biological sample analysis system, wherein a electrode pair and a second electrode pair are provided in a sample flow path, electrochemically active molecules having opposite polarities are provided between a electrode pair and the second electrode pair, respectively, and sample parameters are determined based on a current variation of the electrode pair when the sample passes through the electrode pair and/or a second current variation of the second electrode pair when the sample passes through the second electrode pair.

Description

biological sample analysis system
Technical Field
The present invention relates to an analysis system for measuring a test electrochemical variable, and more particularly, to a biological sample analysis system for analyzing a biological sample by measuring an electrochemical variable.
Background
The electrochemical analysis method is a -class analysis method established based on the relationship between the composition and content of the analyzed solution and its electrochemical properties in an electrolytic cell by using the basic principle and experimental technique of electrochemistry, and is generally to make the sample solution to be analyzed form an electrolytic cell, and then convert the concentration of the sample to be measured into electrical parameters for measurement according to the relationship between some measured electrical parameters (such as current, potential difference, resistance, etc.) of the formed cell and the physical or chemical properties of the substance to be measured.
In order to solve the above problems, the invention of CN104583767B provides improved techniques, which can amplify the signal of the sample when passing through the electrode pair by disposing a solution of electrochemically active molecules that undergo redox reaction on the electrode pair between the electrode pair, thereby increasing the baseline current between the electrode pair, and thus amplifying the signal of the sample when passing through the electrode pair, thereby increasing the sensitivity of detection.
However, the resulting change in the specimen across the pair of electrodes includes a specimen volume-induced current change and a specimen charge-induced current change, which for a neutral specimen can be determined by a standard volume of specimen to current change curve or table, from which the specimen volume can be determined; however, for the charged sample whose volume and charge are unknown, the current change due to the volume and the current change due to the sample charge cannot be determined in the prior art, and in the CN104583767B, when the volume and charge of the charged sample are calculated, the volume of the charged sample can be determined only by using the total current change value of the charged sample as the current change value due to the volume, and the charge of the charged sample can be determined by using the total current change value of the charged sample as the current change value due to the sample charge, which results in inaccurate calculation.
Disclosure of Invention
The present invention provides, as an improvement of CN104583767B, biological sample analysis systems, which can determine the charge-induced tunnel current variation and the volume-induced tunnel current variation when a charged sample with unknown volume and charge passes through parallel electrodes, thereby more accurately determining the parameters of the biological sample.
according to the present invention, there are provided biological sample analysis systems including a sample channel in which a first 0 electrode pair and a second electrode pair are provided, wherein a current direction of the first electrode pair is perpendicular to a sample flow direction, a current direction of the second electrode pair is perpendicular to the sample flow direction, a th solution containing a th electrochemically active molecule is disposed in a movement path between the first electrode pair, a second solution containing a second electrochemically active molecule is disposed in a movement path between the second electrode pair, the first th and second electrochemically active molecules are electrochemically active particles having different kinds of charges, and a signal analyzer determining a volume and a charge amount of the sample based on a current change amount of the sample at a th electrode pair of a electrode pair and electrode pair and/or a current change amount of the sample at the second electrode pair.
, the th electrochemically active molecule is an electrochemically active molecule capable of undergoing a redox reaction on the th electrode pair, and the second electrochemically active molecule is an electrochemically active molecule capable of undergoing a redox reaction on the second electrode pair.
, the biological sample analysis system is used for analyzing biological samples such as cells, viruses, proteins, etc.
, the test sample of the biological sample analysis system is the same attribute sample.
Further , the electrode pair and the second electrode pair are disposed along the same sample flow path.
, the concentration of the th electrochemically active molecule in the solution is the same as the concentration of the second electrochemically active molecule in the second solution.
, the length of the electrode pair is equal to the length of the second electrode pair, and the distance between the electrode pair is equal to the distance between the second electrode pair.
Further , the current variation and the second current variation are generated when the same sample passes through the electrode pair and the second electrode pair, respectively.
, the th current variation is an average value of current variation values generated by the plurality of samples passing through the th electrode pair in a specific time, and the second current variation is an average value of current variation values generated by the plurality of samples passing through the second electrode pair.
Further , setting the voltage between the electrode pair to be th voltage, the voltage between the second electrode pair to be second voltage, the th voltage and the second voltage making the reference current when no sample passes between the th electrode pair equal to the reference current when no sample passes between the second electrode pair.
The step further includes a correlation storage unit that stores a correlation between the standard sample and the current change value.
, the correlation relationships stored in the correlation relationship storage unit include a correlation between a current change amount of the standard neutral sample when the standard neutral sample passes through the th solution and a volume of the standard neutral sample, a correlation between a current change amount of the standard neutral sample when the standard neutral sample passes through the second solution and a volume of the standard neutral sample, a correlation between a current change amount of the sample having an identical electrical property to the th electrochemically active molecule, a correlation between a current change amount of the sample having a different standard volume and a different standard charge amount when the sample having an identical electrical property to the th solution, a correlation between a current change amount of the sample having an identical electrical property to the second electrochemically active molecule, a correlation between a current change amount of the sample having a different standard volume and a different standard
, the signal analysis unit determines the volume and the charge amount of the sample according to the correlation stored in the correlation storage unit and the th current variation of the sample passing through the th electrode pair, the th electrode pair and the second current variation of the sample passing through the second electrode pair.
Step , the signal analysis portion determines the volume V and the charge Q of the sample according to the following steps, 1, judging whether the sample is charged or not, if the sample is not charged, the step 2 is performed, if the sample is charged, the step 3 is performed, 2, calculating the volume V of the sample according to the th current variation and the correlation between the current variation and the volume of the standard neutral sample passing through the th solution stored in the storage portion, and ending the analysis, 3, calculating X = (A-B)/2, Y = (A + B)/2, wherein X represents the amount of current variation caused by the charge of the sample in the solution electrically identical to the sample, X represents the amount of current variation caused by the charge of the sample in the solution electrically different from the sample, Y represents the amount of current variation caused by the volume of the sample, A is the amount of current variation with the larger absolute value of the current variation of the th sample and the second current variation, B is the amount of current variation of the second sample 539, and the amount of current variation caused by the sample, and the volume of the sample is calculated based on the correlation between the current variation and the volume of the standard neutral sample, and the volume of the sample, and the correlation between the stored in the sample, and the volume of the stored values of the sample, and the stored values of the standard neutral sample, and the correlation of the stored values of the stored in the stored volume of the stored in the stored solution, and the stored values of the stored in the stored volume.
And , calculating the absolute value of the difference between the th current variation and the second current variation, if the absolute value is less than the threshold, judging that the sample is not charged, and if the absolute value is greater than the threshold, judging that the sample is charged.
In the step (5), in the step , the column closest to the V value is selected from the correlation table of the solutions corresponding to the a values, and the Q value corresponding to the X value in the column is determined by fitting, and is the Q value of the charge of the sample.
Optionally, in the step (5), from the correlation table of the solution corresponding to the value a, a V1 value column and a V2 value column which are closest to the value V are selected, and a corresponding value Q1 of the value X in the V1 value column and a corresponding value Q2 in the V2 value column are determined by fitting; the sample charge Q value was calculated from (Q-Q1)/(V-V1) = (Q2-Q1)/(V2-V1).
Detailed Description
In order to more clearly illustrate the technical solutions of the present invention, the present invention will be briefly described below by using embodiments, and it is obvious that the following description is only embodiments of the present invention, and it is obvious for those skilled in the art to obtain other technical solutions according to these embodiments without inventive labor, and also fall into the disclosure of the present invention.
The biological sample analysis system according to an embodiment of the present invention is a biological sample analysis system for detecting a biological sample, and a detection target of the biological sample may be a conventional sample including nucleic acid (DNA or RNA), amino acid, protein, pollen, virus, cells, organic particles, inorganic particles, or the like.
A th electrode pair and the second electrode pair are provided along the same sample flow path, the length of the th electrode pair is equal to the length of the second electrode pair, the distance between the th electrode pair is equal to the distance between the second electrode pair, the current direction of the th electrode pair is perpendicular to the sample flow direction, the current direction of the second electrode pair is perpendicular to the sample flow direction, a 5 th solution containing a th electrochemically active molecule is disposed in a moving path between the th electrode pair, a second solution containing a second electrochemically active molecule is disposed in a moving path between the second electrode pair, a th electrochemically active molecule and the second electrochemically active molecule are electrochemically active particles having different kinds of charges, for example, a th electrochemically active molecule is an electrochemically active molecule having a positive charge that is capable of undergoing a redox reaction on the second electrode pair, a second electrochemically active molecule having a negative charge that is capable of undergoing a redox reaction on the second electrode pair, a second electrode pair is disposed between a positive charge concentration of the electrochemically active molecule in the second electrochemically active molecule that is capable of undergoing a redox reaction on the second electrode pair, a voltage of no current is equal to the second reference voltage , and a reference voltage is not applied between the second electrode pair when a reference voltage is equal to the second electrode pair, no current is applied between the second electrode pair, no reference voltage, no reference.
, the correlation relationship stored in the correlation relationship storage unit includes the correlation relationship between the current change when the standard neutral sample passes through the th solution and the volume of the standard neutral sample, the correlation relationship between the current change when the standard neutral sample passes through the second solution and the volume of the standard neutral sample, the correlation relationship between the current change when the standard neutral sample passes through the th solution and the charge amount and the volume of the sample with the same electric property as the th electrochemically active molecule, the correlation relationship between the current change when the different standard volumes and the different standard charge amount samples pass through the second solution and the correlation relationship between the charge amount and the volume of the sample with the same electric property as the second electrochemically active molecule and the current change when the different standard volumes and the different standard charge amount samples pass through the second solution.
The sample is a -identical attribute sample, the th and second current changes may be generated between th and second electrode pairs respectively from a sample, or may be an average of current changes generated between th electrode pairs from a plurality of samples, when the latter is used, the average of current changes between th electrode pairs within a specific time period is selected as a th current change, the time for the sample to pass through the second electrode pair within the specific time period is determined according to the flow speed of the sample in the sample flow path, and the average of current changes between the second electrode pairs within the time period is selected as the second current change.
The signal analysis section determines the volume and the charge amount of the sample based on the correlation stored in the correlation storage section and the th current variation of the th electrode pair when the sample passes through the th electrode pair and the second current variation of the second electrode pair when the sample passes through the second electrode pair;
(1) calculating the absolute value of the difference between the th current variation and the second current variation, if the absolute value is less than the threshold, judging that the sample does not have the sample, entering the step (2), if the absolute value is more than the threshold, judging that the sample has the charge, and carrying out the step (3), wherein the threshold can be determined according to the precision of the current sensor;
(2) calculating a sample volume V through the current variation and the correlation between the current variation and the volume of the standard neutral sample passing through the solution stored in the storage unit, or calculating the volume V of the sample through the second current variation and the correlation between the current variation and the volume of the standard neutral sample passing through the second solution stored in the storage unit;
(3) calculating X = (A-B)/2, Y = (A + B)/2, wherein X represents the current change caused by the sample charge in the solution with the same electrical property as the sample charge, X represents the current change caused by the sample charge in the solution with the different electrical property as the sample charge, Y represents the current change caused by the sample volume, A is the current change with the large absolute value in the th current change and the second current change, and B is the current change with the small absolute value in the th current change and the second current change;
(4) calculating a sample volume V based on the correlation between the Y value and the volume and the current change value of the standard neutral sample passing through the solution corresponding to the A value stored in the storage unit;
(5) in step (5), from the correlation table of the solution corresponding to the value A, a column closest to the value V is selected, and the value Q corresponding to the column X is determined by interpolation, and the value Q of the sample charge is obtained, and from the correlation table of the solution corresponding to the value A, a column V1 and a column V2 closest to the value V are selected, and the corresponding value Q1 of the value X in the column V1 and the corresponding value Q2 in the column V2 are determined by fitting, and the value Q of the sample is obtained from (Q-Q1)/(V-V1) = (Q2-Q1)/(V2-V1).
Further, it is to be understood that after reading the above disclosure of the present invention, the scope of the present invention is not limited to the above embodiments, and that various changes or modifications may be made by those skilled in the art without departing from the principle of the present invention, which is also defined in the scope of the appended claims.

Claims (10)

  1. A biological sample analysis system of the type 1 and , comprising a sample flow path in which a th electrode pair and a second electrode pair are provided, wherein the current direction of the th electrode pair is perpendicular to the sample flow direction, the current direction of the second electrode pair is perpendicular to the sample flow direction, a th solution containing th electrochemically active molecules is disposed in a moving path between the th electrode pair, a second solution containing second electrochemically active molecules is disposed in a moving path between the second electrode pair, the th electrochemically active molecules and the second electrochemically active molecules are electrochemically active particles having different types of charges, and a signal analyzer for determining the volume and the charge amount of the sample based on the th current variation of the th electrode pair when the sample passes through the th electrode pair and/or the second current variation of the second electrode pair when the sample passes through the second electrode pair.
  2. 2. The biological sample analysis system according to claim 1, wherein the th electrochemically active molecule is an electrochemically active molecule capable of undergoing a redox reaction on the th electrode pair, and the second electrochemically active molecule is an electrochemically active molecule capable of undergoing a redox reaction on the second electrode pair.
  3. 3. The biological sample analysis system of claim 2, wherein: the biological sample analysis system is used for analyzing biological samples such as cells, viruses, proteins and the like.
  4. 4. The biological sample analysis system according to claim 3, wherein the th electrode pair and the second electrode pair are arranged along the same sample flow path.
  5. 5. The system for analyzing a biological sample according to claim 4, wherein the concentration of electrochemically active molecules in the th solution is the same as the concentration of second electrochemically active molecules in the second solution.
  6. 6. The system according to claim 5, wherein the th electrode pair has a length equal to that of the second electrode pair, and the th electrode pair has a distance equal to that of the second electrode pair.
  7. 7. The system according to claim 6, wherein the th and second current variations are generated when the same sample passes between the th and second electrode pairs, respectively.
  8. 8. The system for analyzing a biological sample according to claim 7, wherein the th current variation is an average value of current variation values generated by the sample between the th electrode pair in a specific time, and the second current variation is an average value of current variation values generated by the sample between the second electrode pair in a specific time.
  9. 9. The biological sample analysis system of claim 8, wherein: the device further comprises a correlation storage unit for storing the correlation between the standard sample and the current variation value.
  10. 10. The biological sample analysis system according to claim 9, wherein the correlation stored in the correlation storage unit includes a correlation between a change in current when the standard neutral sample passes through the th solution and a volume of the standard neutral sample, a correlation between a change in current when the standard neutral sample passes through the second solution and a volume of the standard neutral sample, a correlation between a change in current when the sample having an electrical property identical to that of the th electrochemically active molecule, a change in current when the sample having a different standard volume and a different standard charge amount passes through the th solution, and a correlation between a change in current when the sample having an electrical property identical to that of the second electrochemically active molecule, a change in current when the sample having a different standard volume and a different standard charge amount passes through the second solution, and a charge amount and a volume.
CN201911159949.5A 2019-11-23 2019-11-23 biological sample analysis system Withdrawn CN110736780A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201911159949.5A CN110736780A (en) 2019-11-23 2019-11-23 biological sample analysis system

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201911159949.5A CN110736780A (en) 2019-11-23 2019-11-23 biological sample analysis system

Publications (1)

Publication Number Publication Date
CN110736780A true CN110736780A (en) 2020-01-31

Family

ID=69273625

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201911159949.5A Withdrawn CN110736780A (en) 2019-11-23 2019-11-23 biological sample analysis system

Country Status (1)

Country Link
CN (1) CN110736780A (en)

Similar Documents

Publication Publication Date Title
KR101256133B1 (en) Method and apparatus for detection of abnormal traces during electrochemical analyte detection
Lewenstam et al. Application of ion‐selective electrodes in clinical analysis
US9535033B2 (en) Sample analysis method
JP5309024B2 (en) Electrochemical detection of magnetic particle migration
Čížková et al. Verification of applicability of mercury meniscus modified silver solid amalgam electrode for determination of heavy metals in plant matrices
CN105784814A (en) Sensor based on concentration cell principle
US10520460B2 (en) Method for determining diffusion
Jin et al. Assay of glutathione in individual mouse peritoneal macrophages by capillary zone electrophoresis with electrochemical detection
JP4918237B2 (en) Biological quantification method
RU2564516C2 (en) Capacitance measurement method and its application
RU2013119959A (en) SYSTEMS AND METHODS OF DIFFERENCE BETWEEN THE CONTROL SAMPLE AND THE TESTED FLUID MEDIA USING CAPACITY RESISTANCE
CN110736780A (en) biological sample analysis system
SU1333244A3 (en) Device for potentiometric determination of concentration of ions in solutions
CN110736781A (en) biological sample analysis method
CN111077204A (en) Biomolecule analysis test system
Kahlert et al. Application of a New pH‐Sensitive Electrode as a Detector in Flow Injection Potentiometry
KR101736651B1 (en) Methods of using information from recovery pulses in electrochemical analyte measurements as well as devices, apparatuses and systems incorporating the same
Liu et al. Adsorptive voltammetric behaviors of resveratrol at graphite electrode and its determination in tablet dosage form
Kikas et al. Potentiometric measurements in sequential injection analysis lab-on-valve (SIA-LOV) flow-system
US6736958B1 (en) Ion sensing method
EP3155425B1 (en) Transformed response potentiometric titrations
RU2262098C2 (en) Method of monitoring water hardness in water heater
TW201202692A (en) Measurement device and measurement method utilizing the same
RU39204U1 (en) ELECTROCHEMICAL CELL
Ab Rahim et al. Performance Analysis of Optimized Screen-Printed Electrodes for Electrochemical Sensing

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
WW01 Invention patent application withdrawn after publication

Application publication date: 20200131

WW01 Invention patent application withdrawn after publication