CN101021506A - Method for measuring low-speed electric interstifial flow in chip capillary cataphoresis - Google Patents

Method for measuring low-speed electric interstifial flow in chip capillary cataphoresis Download PDF

Info

Publication number
CN101021506A
CN101021506A CN200710021018.XA CN200710021018A CN101021506A CN 101021506 A CN101021506 A CN 101021506A CN 200710021018 A CN200710021018 A CN 200710021018A CN 101021506 A CN101021506 A CN 101021506A
Authority
CN
China
Prior art keywords
electroosmotic flow
probe
microchip
mobility
chip
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.)
Granted
Application number
CN200710021018.XA
Other languages
Chinese (zh)
Other versions
CN100473986C (en
Inventor
王伟
赵亮
朱俊杰
张剑荣
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.)
Nanjing University
Yangcheng Institute of Technology
Original Assignee
Nanjing University
Yangcheng Institute of Technology
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 Nanjing University, Yangcheng Institute of Technology filed Critical Nanjing University
Priority to CNB200710021018XA priority Critical patent/CN100473986C/en
Publication of CN101021506A publication Critical patent/CN101021506A/en
Application granted granted Critical
Publication of CN100473986C publication Critical patent/CN100473986C/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Landscapes

  • Investigating Or Analysing Biological Materials (AREA)

Abstract

A method can measure low speed electro-osmotic flow in chip capillary electrophoresis. First of all, measure effective mobility of probe substance by sample zonal method on quick electro-osmotic flow microchip A which being as a reference. The method is simplified as: add a quickly-migrating substance (probe) which can be tested into background electrolyte. Detect electrophoretic pattern when taking hormone background electrolyte with different density from background electrolyte as sample. Based on the peaking time in pattern, effective mobility (Mu eff) of probe substance on reference chip can be calculated. Then, taking same background electrolyte solution without probe as buffer solution and probe substance as sample, detect routine capillary electrophoresis on microchip B with unknown electro-osmotic flow. Apparent mobility (Mu npp) of probe on B can be calculated and curious effective mobility (Mu EOF) can be achieved by the following formula: Mu EOF=Mu npp-Mu eff.

Description

The measuring method of low speed electroosmotic flow in the chip capillary cataphoresis
Technical field
The present invention relates to the measurement of low speed electroosmotic flow.Specifically, be based on an electromigratory material and measure the low speed electroosmotic flow indirectly in the constant principle of the ducted effective mobility of microchip.
Background technology
The micro-fluid control chip electrophoretic technology began to develop rapidly [referring to Manz from nineteen nineties, A., Graber, N., Widmer, H.M., Sens.Actuators B 1990, B1 (1-6), 244-248.], in order to satisfy the application of various aspects, often microchannel is carried out chemistry or physical modification, reduce the interaction of solute and tube wall and suppress electroosmotic flow.Therefore the electroosmotic flow property representation to microchannel just seems extremely important.
Commonly used electroosmotic flow assay method has neutral label method [referring to Jorgenson, J.W., Lukacs, K.D., Anal.Chem.1981,53,1298-1302.] and the current monitoring method [referring to: Huang, X., Gordon, M.J., Zare, R.N., Anal.Chem.1988,60,1837-1838.].The most commonly used is neutral label method, utilizes exactly to move under the effect of a kind of neutral compound in electric field and measures electroosmotic flow; The current monitoring method also is the very high method of a kind of utility ratio, the effect that drives by electric osmose in pipeline is with the solution in the alternative kapillary of a same electrolyte solution (comparing with the solution in the kapillary) that slightly dilutes, by electric current time history plot in the observation circuit, calculate electroosmotic flow according to whole times when replaced of pipeline middle and high concentration solution.
When needs are measured low electroosmotic flow or zero electroosmotic flow, difficulty has just appearred, and in neutral label method and current monitoring method, after through very long transit time, signal can become not obvious or not have signal.Up to the present, also not about hanging down the report of electroosmotic flow or zero electroosmotic flow assay method in the microchip capillary electrophoresis.
Summary of the invention
The purpose of this invention is to provide a kind of method of measuring low electroosmotic flow.
Technical scheme of the present invention is as follows:
The measuring method of low speed electroosmotic flow in a kind of chip capillary cataphoresis, it be at first one as the quick electroosmotic flow microchip A of reference on sample area band method [referring to Wang, W., Zhao, L., Jiang, L.P., Zhang, J.R., Zhu, J.J., Chen, H.Y., Electrophoresis 2006,27,5132-5137.] finish the mensuration of the effective mobility of probe substance, be summarized as follows, in back-ground electolyte, add a fast transferring and material can be determined (probe), after the class background electrolyte that is different from background electrolyte concentration is as sample feeding, obtain electrophoretogram, utilized the appearance time among the figure can calculate the effective mobility (μ of probe substance on the reference chip Eff), then, utilize the identical background electrolyte that does not contain probe as damping fluid, on the microchip B of unknown electroosmotic flow, finish conventional Capillary Electrophoresis with probe substance as sample and detect, can calculate the apparent mobility (μ of probe on microchip B App), can calculate the electroendosmotic mobility (μ that seeks knowledge according to following formula EOF), μ EOFAppEff
The effective mobility of a specific probe substance in the damping fluid of determining is invariable, and just the effective mobility of probe substance on reference chip and electroosmotic flow chip to be measured equates,
Therefore, μ EffA1EffB1
μ wherein EffA1And μ EffB1Be respectively the effective mobility among microchip A and the microchip B.The effective mobility of this probe substance can calculate from its apparent mobility and electroosmotic flow,
μ effA 1 = μ appA 1 - μ EOFA = L A L Aeff t A 1 V A - L A L Aeff t A 2 V A
μ effB 1 = μ appB 1 - μ EOFB = L B L Beff t B 1 V B - L B L Beff t B 2 V B
μ in the above formula AppA1, μ EOFAAnd V ABe respectively apparent mobility, electroendosmotic mobility and the separation voltage of the probe substance among the microchip A, t A1And t A2Be respectively the appearance time of microchip A middle probe material and electroosmotic flow.μ AppB1, μ EOFBAnd V BRepresent the respective amount among the microchip B respectively.L A, L Aeff, L BAnd L BeffBe respectively length and the effective length of microchip A and microchip B.Therefore, μ EOFBCan represent with following formula,
μ EOFB = μ appB 1 - μ appA 1 + μ EOFA = L B L Beff t B 1 V B - L A L Aeff t A 1 V A + L A L Aeff t A 2 V A
If L A=L B=L, L Aeff=L Beff=L EffAnd V A=V B=V, μ EOFBCan be calculated as follows and get.
μ EOFB = LL eff V ( 1 t B 1 - 1 t A 1 + 1 t A 2 )
Four, description of drawings
Fig. 1 is an applied microchip synoptic diagram when measuring electroosmotic flow among the present invention, and wherein: A is a buffer pool, and B is the separating pipe outlet, C is a buffer pool, and D is the sample waste liquid pool, and E is sample channel and separating pipe crossing, F is the damping fluid waste liquid pool, and WE is an electrochemical working electrode.。
The electrophoresis synoptic diagram that Fig. 2 records with indirect method on reference chip A for the present invention, t A1And t A2Be respectively the appearance time of microchip A middle probe material and electroosmotic flow.
The electrophoresis synoptic diagram that Fig. 3 records with direct method on electroosmotic flow chip B to be measured for the present invention, t B1And t B2Be respectively the transit time of microchip B middle probe material and electroosmotic flow.Wherein: the dotted line peak is the signal peak of imaginary electroosmotic flow.
Embodiment
The measurement of the electroosmotic flow of poly dimethyl silica silicon (PDMS) microchip of embodiment 1.Brij 56 modifieds
Electroosmotic flow when being full of phosphate buffer (20mM PBS pH7.00) in the PDMS microchip pipeline of measurement Brij 56 modifieds, with 0.1mM 3,4-dihydroxy benzylamine (DHBA) is as probe substance, 20mM PBS is electrolyte as a setting, not make the PDMS microchip of modification as reference chip A, wherein: AE=0.3cm; EB=3.6cm; CE=ED=0.5cm.In the Capillary Electrophoresis process, separation voltage is set at 800V, detects current potential+1.2V (vs.Ag/AgCl electrode), according to the transit time of measuring gained, t B1=59.2s, t A1=41.2s, t A1=65.0s, the size that calculates electroosmotic flow is (1.40 ± 0.04) * 10 -4Cm 2/ (Vs).Consistent with the document guess value [referring to: Dou, Y.H., Bao, N., Xu, J.J., Meng, F., Chen, H.Y., Electrophoresis 2004,25,3024-3031.].
The measurement of the electroosmotic flow of the PDMS microchip pipeline of embodiment 2. polyvinyl alcohol (PVA) (PVA) modified
Electroosmotic flow when being full of phosphate buffer (20mM PBS pH7.00) in the PDMS microchip pipeline of measurement PVA modified, with 0.1mM 3,4-dihydroxy benzylamine (DHBA) is as probe substance, 20mM PBS is electrolyte as a setting, not make the PDMS microchip of modification as reference chip A, wherein: AE=0.3cm; EB=3.6cm; CE=ED=0.5cm.In the Capillary Electrophoresis process, separation voltage is set at 800V, detects current potential+1.2V (vs.Ag/AgCl electrode), according to the transit time of measuring gained, t B1=98.7s, t A1=41.2s, t A1=65.0s, the size that calculates electroosmotic flow is (0.22 ± 0.02) * 10 -4Cm 2/ (Vs).Consistent with the document guess value [referring to: Wu, D., Luo, Y., Zhou, X., Dai, Z., Lin, B., Electrophoresis 2005,26,211-218.].

Claims (2)

1. the measuring method of low speed electroosmotic flow in the chip capillary cataphoresis is characterized in that: the effective mobility μ that at first records probe substance on a quick electroosmotic flow microchip A as reference Eff, record the apparent mobility μ of probe substance on the microchip B of electroosmotic flow to be measured then App, calculate unknown electroendosmotic mobility μ according to following formula EOF,
μ EOF=μ appeff?。
2. the method for the low electroosmotic flow of fast measuring micro-fluidic chip according to claim 1 is characterized in that: with sample area band method on electroosmotic flow reference chip fast once the property transit time of finishing probe substance and electroosmotic flow measure, directly calculate effective mobility.
CNB200710021018XA 2007-03-22 2007-03-22 Method for measuring low-speed electric interstifial flow in chip capillary cataphoresis Expired - Fee Related CN100473986C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CNB200710021018XA CN100473986C (en) 2007-03-22 2007-03-22 Method for measuring low-speed electric interstifial flow in chip capillary cataphoresis

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CNB200710021018XA CN100473986C (en) 2007-03-22 2007-03-22 Method for measuring low-speed electric interstifial flow in chip capillary cataphoresis

Publications (2)

Publication Number Publication Date
CN101021506A true CN101021506A (en) 2007-08-22
CN100473986C CN100473986C (en) 2009-04-01

Family

ID=38709340

Family Applications (1)

Application Number Title Priority Date Filing Date
CNB200710021018XA Expired - Fee Related CN100473986C (en) 2007-03-22 2007-03-22 Method for measuring low-speed electric interstifial flow in chip capillary cataphoresis

Country Status (1)

Country Link
CN (1) CN100473986C (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104122316A (en) * 2014-06-30 2014-10-29 中国科学院化学研究所 Method for simultaneously measuring mobility and dielectric mobility of particles by use of distributed direct-current electric field
CN108007994A (en) * 2017-06-27 2018-05-08 北京理工大学 A kind of method for measuring Capillary Electrophoresis electroosmotic flow
CN114660283A (en) * 2022-05-24 2022-06-24 佛山微奥云生物技术有限公司 Immunoassay plate type chip based on electrical acceleration and preparation method thereof

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104122316A (en) * 2014-06-30 2014-10-29 中国科学院化学研究所 Method for simultaneously measuring mobility and dielectric mobility of particles by use of distributed direct-current electric field
CN108007994A (en) * 2017-06-27 2018-05-08 北京理工大学 A kind of method for measuring Capillary Electrophoresis electroosmotic flow
CN108007994B (en) * 2017-06-27 2019-12-03 北京理工大学 A method of measurement Capillary Electrophoresis electroosmotic flow
CN114660283A (en) * 2022-05-24 2022-06-24 佛山微奥云生物技术有限公司 Immunoassay plate type chip based on electrical acceleration and preparation method thereof
CN114660283B (en) * 2022-05-24 2022-09-13 佛山微奥云生物技术有限公司 Immunoassay plate type chip based on electrical acceleration and preparation method thereof

Also Published As

Publication number Publication date
CN100473986C (en) 2009-04-01

Similar Documents

Publication Publication Date Title
Wainright et al. Sample pre-concentration by isotachophoresis in microfluidic devices
Wang et al. Measurement of electroosmotic flow in capillary and microchip electrophoresis
Backofen et al. A chip-based electrophoresis system with electrochemical detection and hydrodynamic injection
US8080144B2 (en) Gradient elution electrophoresis
Tomazelli Coltro et al. Electrophoresis microchip fabricated by a direct‐printing process with end‐channel amperometric detection
US20080237044A1 (en) Method and apparatus for concentrating molecules
CN100473986C (en) Method for measuring low-speed electric interstifial flow in chip capillary cataphoresis
LIANG et al. Research and application progress of paper-based microfluidic sample preconcentration
US8366897B2 (en) Gradient elution electrophoresis and detectorless electrophoresis apparatus
Wang et al. Amperometric detection of three purine alkaloids following their separation by micellar electrokinetic capillary chromatography
Müller et al. A conductometric detector for capillary separations
Chen et al. Fabrication and performance of a three‐dimensionally adjustable device for the amperometric detection of microchip capillary electrophoresis
JP2008134199A (en) Microfluid-device electrophoretic method and system
Chen et al. Determination of EOF of PMMA microfluidic chip by indirect laser-induced fluorescence detection
US20120193234A1 (en) Capillary electrophoresis chips
Yu et al. Improved separation efficiency of neurotransmitters on a native printed capillary electrophoresis microchip simply by manipulating electroosmotic flow
Feng et al. On‐chip potential gradient detection with a portable capillary electrophoresis system
Liu et al. Studying drug–plasma protein interactions by two‐injector microchip electrophoresis frontal analysis
Álvarez-Martos et al. Ionic liquids as modifiers for glass and SU-8 electrochemical microfluidic chips
Yao et al. A three-dimensionally adjustable amperometric detector for microchip electrophoretic measurement of nitroaromatic pollutants
Rana et al. Electrophoresis: Basic principle, types, and applications
You et al. Determination of barbituric acid and 2-thiobarbituric acid with end-column electrochemical detection by capillary electrophoresis
Wang et al. Low EOF rate measurement based on constant effective mobility in microchip CE
Wang et al. EOF measurement by detection of a sampling zone with end‐channel amperometry in microchip CE
Jenkins Clinical applications of capillary electrophoresis: Status at the new millennium

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
C17 Cessation of patent right
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20090401

Termination date: 20100322