CN104950026B - Electrochemical luminescence bioanalysis flow cell based on magnetic bead - Google Patents

Electrochemical luminescence bioanalysis flow cell based on magnetic bead Download PDF

Info

Publication number
CN104950026B
CN104950026B CN201510345054.6A CN201510345054A CN104950026B CN 104950026 B CN104950026 B CN 104950026B CN 201510345054 A CN201510345054 A CN 201510345054A CN 104950026 B CN104950026 B CN 104950026B
Authority
CN
China
Prior art keywords
funnel
bioanalysis
flow cell
magnetic bead
electrochemical luminescence
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.)
Active
Application number
CN201510345054.6A
Other languages
Chinese (zh)
Other versions
CN104950026A (en
Inventor
谢洪平
魏同洪
葛芝莉
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.)
Suzhou University
Original Assignee
Suzhou University
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 Suzhou University filed Critical Suzhou University
Priority to CN201510345054.6A priority Critical patent/CN104950026B/en
Publication of CN104950026A publication Critical patent/CN104950026A/en
Application granted granted Critical
Publication of CN104950026B publication Critical patent/CN104950026B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Abstract

The present invention relates to a kind of electrochemical luminescence bioanalysis flow cell based on magnetic bead, including with the top opening being oppositely arranged and the funnel of bottom opening, funnel bottom is arranged on the seal of the bottom opening of closing funnel, it is arranged on the working electrode on the upper surface of seal, be embedded on funnel to electrode, the lid of the top opening of closing funnel and the magnet that can be moved relative to working electrode, to axial rings of the electrode along funnel around and be embedded in funnel, funnel includes inwall and the funnel chamber for setting and being formed is enclosed by inwall, the optical channel of lid is provided through on lid, optical channel is connected with funnel chamber, optical mirror slip is provided with optical channel, liquid access way is offered on lid, funnel chamber passes through liquid access way and ft connection, the electrochemical luminescence bioanalysis flow cell based on magnetic bead is integrally miniaturized, ECL reaction reagents for bioanalysis are relatively fewer, the ECL reaction reagents consumed are relatively fewer, and without dead volume, liquid Rapid replacement, realize quick analysis.

Description

Electrochemical luminescence bioanalysis flow cell based on magnetic bead
Technical field
The present invention relates to a kind of electrochemical luminescence bioanalysis flow cell based on magnetic bead, belong to detection device.
Background technology
In in the past few decades, electrochemical luminescence (ECL) bioanalysis research based on magnetic bead achieves huge progress, Corresponding detecting instrument mainly includes electrochemiluminescence cell, electro-optic detector and detector three parts.Electrochemiluminescence cell It is the core of electrochemical luminescence research system.The signal acquisition of ECL analyses and detection all rely on the performance in the pond with setting Meter.But because the electrochemiluminescence cell of current commercialization is still fewer, specialized degree is low and many performances also imperfection, big portion Divide researcher must be according to respective requirement of experiment come designed, designed and making electrochemiluminescence cell.
At present for electrochemiluminescence cell tectonic sieving, compared with frequently be three-electrode system, i.e., working electrode, to electricity Pole and reference electrode.Electrochemiluminescence cell can be divided into flow cell and static pond two types according to input mode.Because with it is quiet State pond is compared, flow cell have the advantages that quickly, reappearance is good, be easy to automate and can monitor on-line, and by extensive Concern, it, which designs and made, also turns into an important directions in electrochemiluminescence cell research.
Although common electrochemiluminescence cell makes and easy to use, but still the part that comes with some shortcomings:
1. three electrodes will be inserted into pond, the space in pond is occupied, development of the detection architecture to miniaturization is limited, this More need to consume substantial amounts of ECL reaction reagents when external actually detected;
2. being loaded manually, pond body is dismantled repeatedly causes the relative position of three electrodes to keep fixed, influence ECL detection knots The reappearance of fruit;
3. the relative area of pair electrode is smaller;
4. pond body is larger dead volume etc..
These will all cause the reduction of electrochemiluminescence cell performance and its analytical precision and sensitivity.In view of above-mentioned Defect, the design people is actively subject to research and innovation, to found a kind of life of the electrochemical luminescence based on magnetic bead of new structure Thing analyzes flow cell, makes it with more the value in industry.
The content of the invention
It is miniaturized it is an object of the invention to provide one kind, and the less electricity based on magnetic bead of ECL reaction reagents consumed Chemiluminescence bioanalysis flow cell.
To achieve these goals, the technical solution adopted in the present invention is as follows:A kind of electrochemical luminescence based on magnetic bead Bioanalysis flow cell, including with the top opening being oppositely arranged and the funnel of bottom opening, be arranged on the funnel bottom to seal Close the seal of the bottom opening of funnel, the working electrode being arranged on the upper surface of the seal, be embedded on the funnel To electrode, the lid of the top opening of the closing funnel and the magnet that can be moved relative to the working electrode, it is described to electrode Along funnel axial rings around and be embedded in funnel, the funnel includes inwall and the funnel chamber for setting and being formed, the lid is enclosed by inwall The optical channel of the lid is provided through on body, the optical channel is connected with funnel chamber, and optics is provided with the optical channel Liquid access way is offered on eyeglass, the lid, the funnel chamber passes through liquid access way and ft connection.
Further, the liquid access way includes feed pathway and liquid outlet channel, and the lid, which has, stretches to institute The plunger portion in funnel chamber is stated, the feed pathway has the feed liquor opening being opened in the plunger portion, the liquid outlet channel Go out liquid opening with being opened in the plunger portion, the feed liquor opening goes out liquid opening less than described in.
Further, the feed liquor opening plaster is leaned on to the inwall, and the plunger portion is in circular platform type, it is described go out liquid opening be Along the spiral slot of the side wall extension of the plunger portion.
Further, the electrochemical luminescence bioanalysis flow cell based on magnetic bead also includes reference electrode, described right Perforate is offered on electrode, one end of the reference electrode is arranged in the perforate.
Further, the electrochemical luminescence bioanalysis flow cell based on magnetic bead includes middle part cylinder, the funnel Formed in the middle part cylinder, the fixing groove of the fixed reference electrode is offered on the middle part cylinder.
Further, the electrochemical luminescence bioanalysis flow cell based on magnetic bead includes being located under the middle part cylinder The bottom cylinder of side, the bottom of the middle part cylinder sets fluted, and the seal is to be protruded out upwards from the bottom cylinder The boss of formation, the seal coordinates with the groove, and the fluting for housing the magnet, institute are offered on the bottom cylinder State fluting and be additionally provided with moving member in the bottom surface of the bottom cylinder, the fluting, the magnet is arranged on the movement On part.
Further, sample holes are offered on the lid, the funnel chamber passes through the sample holes and ft connection, institute State and sealing-plug is provided with sample holes.
Further, the sample holes are formed from bifurcated in the feed pathway.
Further, the electrochemical luminescence flow cell also includes the optical fiber being arranged in the optical channel.
Further, the optical channel is through in the bottom wall of lid, the optical channel from the side wall of the lid and had Reflective mirror is provided with corner, the corner.
By such scheme, the present invention at least has advantages below:The electrochemical luminescence based on magnetic bead of the present invention is biological Then analyze flow cell can pass through work by magnet by the antigen antibody complex absorption with magnetic bead on the working electrode (s Electrode, the detection to electrode and optical channel realization to antigen antibody complex, compared with prior art, should the electrification based on magnetic bead Learn luminous organism analysis flow cell to be integrally miniaturized, funnel is shown in electrochemical luminescence bioanalysis flow cell self structure The effective volume of chamber is smaller, in addition, compared with prior art, the ECL reaction reagents for bioanalysis are relatively fewer, that is, disappeared The ECL reaction reagents of consumption are relatively fewer.
Further:Because the feed liquor opening of feed pathway less than liquid outlet channel goes out liquid opening, to keep unidirectional stream, punching Wash clean, it is to avoid the result of influence detection, what is more, because feed liquor opening plaster is leaned on to inwall, it is along plunger portion to go out liquid opening The spiral slot of side wall extension, and plunger portion design, so as to be more conducive to avoid rinsing dead angle, be more conducive to avoid influence from examining The result of survey.
In addition, by setting sample holes on lid so that detection sample Rapid replacement, and also contribute to improve base In the service life of the electrochemical luminescence bioanalysis flow cell of magnetic bead.Simultaneously as the bottom opening of sample holes is opened for feed liquor Mouthful, and the feed liquor opening plaster is leaned on to inwall, and hopper design is used, so that when inserting sample, sample can be distributed to along inwall On working electrode, detection speed is favorably improved, it helps improve detection sensitivity, realize quick analysis.
Described above is only the general introduction of technical solution of the present invention, in order to better understand the technological means of the present invention, And can be practiced according to the content of specification, below with presently preferred embodiments of the present invention and coordinate accompanying drawing describe in detail as after.
Brief description of the drawings
Fig. 1 is the structural representation of the electrochemical luminescence bioanalysis flow cell based on magnetic bead shown in one embodiment of the invention Figure;
Fig. 2 is the structural representation of lid in Fig. 1;
Fig. 3 is the sectional view of the electrochemical luminescence bioanalysis flow cell based on magnetic bead shown in Fig. 1;
Fig. 4 is the electrochemical luminescence bioanalysis flow cell based on magnetic bead shown in Fig. 1 in the sectional view on another visual angle;
Fig. 5 sample injection times investigate figure;
Fig. 6 washing times investigate figure;
Fig. 7 is the section view of the electrochemical luminescence bioanalysis flow cell based on magnetic bead shown in another embodiment of the present invention Figure.
Embodiment
With reference to the accompanying drawings and examples, the embodiment to the present invention is described in further detail.Implement below Example is used to illustrate the present invention, but is not limited to the scope of the present invention.
Referring to Fig. 1 to Fig. 4, a kind of electrochemical luminescence bioanalysis circulation based on magnetic bead described in the embodiment of the present invention one Pond 100 includes with the top opening (non-label) being oppositely arranged and the funnel 1 of bottom opening (non-label), is arranged on the funnel 1 Bottom with the seal 102 of the bottom opening of closing funnel 1, the working electrode 2 being arranged on the upper surface of the seal 102, Be embedded on the funnel 1 to electrode 3, the lid 40 of the top opening of the closing funnel 1, can relatively described working electrode 2 Mobile magnet 5 and reference electrode 6.The funnel 1 includes inwall 11 and the funnel chamber 12 for setting and being formed is enclosed by inwall 11.In this reality Apply in example, the lid 40 is column structure, the electrochemical luminescence bioanalysis flow cell 100 based on magnetic bead can be divided into Three bulks, bottom cylinder 10, middle part cylinder 20 and the lid 40 set successively including superposition from bottom to up, the bottom cylinder 10, Middle part cylinder 20 and lid 40 are (not shown) fixed by fastener respectively, and the funnel 1 is formed in the middle part cylinder 20, The bottom of the middle part cylinder 20 sets fluted 202, and the seal 102 is to protrude out to be formed convex upwards from bottom cylinder 10 Platform, the seal 102 coordinates to realize the bottom opening of closing funnel 1 with groove 202, in order to realize optimum efficiency, in this implementation In example, the working electrode 2 on the upper surface of seal 102 shelters from the bottom opening of funnel 1, to improve the sensitive of detection Degree, certainly, in other embodiments, the working electrode 2 can not exclusively shelter from the bottom opening of funnel 1, as long as it is located at The underface of the bottom opening of funnel 1, still, the detection sensitivity of such a structure do not have the detection sensitivity in the present embodiment It is high.The magnet 5 is fixed on bottom cylinder 10, and the fluting 103 for housing magnet 5 is offered on the bottom cylinder 10, described Fluting 103, which runs through in the bottom surface 104 of bottom cylinder 10, the fluting 103, is additionally provided with moving member 105, and the magnet 5 is arranged on On moving member 105, when specifically used, after sample is entered in funnel chamber 12, by promote moving member 105 by magnet 5 to The direction of working electrode 2 is moved, so that the antigen antibody complex with magnetic bead is adsorbed on working electrode 2., should in the present embodiment Fluting 103 is screwed hole, and moving member 105 is bolt.In the present embodiment, by the driving of moving member 105, the magnet 5 is with respect to work Make electrode 2 to move up and down, in other embodiments, the moving member 105 can also be other structures, block such as be taken out, in addition, passing through Change the mounting means of moving member 105, to change the moving direction of magnet 5, such as magnet 5 is moved with respect to working electrode or so It is dynamic.The reference electrode 6 is fixed on the cylinder 20 of middle part, and it on middle part cylinder 20 by opening up consolidating for fixed reference electrode 6 Determine groove 61 to realize fixation.
The axial rings to electrode 3 along funnel 1 around and be embedded in funnel 1, in the present embodiment, to electrode 3 by conduction Material, which encloses, to be set to form funnel-shaped structure.It is described that electrode connection is respectively equipped with to electrode 3 and working electrode 2, wherein, on electrode 3 Electrode connection be named as to electrode connection 71, the electrode connection on working electrode 2 is named as working electrode wiring 72, by this It is in the present embodiment, described to the cloth of electrode connection 71 to electrode connection 71 and working electrode wiring 72 to be connected with external power source Put in middle part cylinder 20, and stretched out from the side wall 201 of middle part cylinder 20, the working electrode wiring 72 is arranged in bottom cylinder In 10, working electrode wiring interface 73 is provided with the side wall 101 of the bottom cylinder 10, working electrode wiring 72 enters should Working electrode wiring interface 73.It is described to offering perforate 31 on electrode 3, one end of the reference electrode 6 is arranged on described open On hole 31.
Liquid access way is offered on the lid 40, the funnel chamber 12 is connected by liquid access way and outside Logical, the liquid access way is mainly used in passing in and out the coreaction liquid and cleaning solution of ECL bioanalysis, can be also used for certainly into Sample, in the present embodiment, is connected with pipeline 43 on the liquid access way, and the liquid access way is two, including enters Liquid passage 44 and liquid outlet channel 45, really, the liquid access way may also be only one, or multiple.The lid 40 With the plunger portion 46 stretched in the funnel chamber 12, there is detention space when preventing and rinsing so that rinse more thorough.Institute Stating feed pathway 44 has the feed liquor opening 441 being opened in the plunger portion 46, and the liquid outlet channel 45, which has, is opened in institute State and go out liquid opening 451 in plunger portion 46, the feed liquor opening 441 goes out liquid opening 451, in the present embodiment, institute less than described in Feed liquor opening 441 is stated to recline to formation between the inwall 11 of the funnel 1, and the feed liquor opening 441 and the inwall 11 of funnel 1 The gap flowed through for sample, coreaction liquid, cleaning solution, the plunger portion 46 is in circular platform type, it is described go out liquid opening 451 be along described The spiral slot that the side wall 201 of plunger portion 46 extends.The optical channel 41 of the lid 40, institute are provided through on the lid 40 State optical channel 41 to connect with funnel chamber 12, optical mirror slip 8 is provided with the optical channel 41, can be by the optical mirror slip 8 When flushing, prevent coreaction liquid or cleaning solution from being flowed out out of optical channel 41, so as to rinse more thorough.In the present embodiment, The bottom surface of the lid 40 is arranged with recess 42, and the recess 42 is arranged in the plunger portion 46, and the optical mirror slip 8 is arranged on In the recess 42, to reduce the overall volume of the electrochemical luminescence bioanalysis flow cell 100 based on magnetic bead, in addition, in reality It is specially optics convex lens to apply optical mirror slip 8 used in example, really, can also use planar wave eyeglass.
The electrochemical luminescence bioanalysis flow cell 100 based on magnetic bead (is hereinafter referred to as circulated below by experimental result Pond 100) illustrate
Experiment one:With 125fM Ru (bpy)3 2+/ TPA solution enters as checking matter to the sample injection time of the flow cell 100 Row is investigated.Rinsed first with flushing liquor TPA, then blowing air drains flushing liquor, last sample introduction, in different time points as much as possible Detect the ECL of checking matter.With reference to as shown in figure 5, checking matter ECL intensity is first quick with the increase of sample injection time in preceding 40s Increase, because checking matter progresses into detection architecture, replaces the washing lotion TPA not drained, and its concentration in flow cell 100 is continuous Increase, luminous intensity is continuously increased;Because checking matter replaces most TPA completely after 40s, the content of flow cell 100 is stabilization The 125fM Ru (bpy) of component3 2+/ TPA solution, its ECL intensity tends towards stability and reaches peak.Therefore, it is guarantee checking matter Displacement TPA completely circulates pond 100, so that it is determined that using 45s as optimal sample injection time.
Experiment two:Using TPA as flushing liquor, to above-mentioned 125fM Ru (bpy)3 2+/ TPA detection liquid is rinsed, to investigate The washing time of the flow cell 100.Fig. 6 is the ECL intensity levels of remaining checking matter in flow cell 100 under different washing times.With TPA continuous flushing, ECL intensity levels are constantly reduced, i.e., remaining checking matter concentration is constantly reduced in flow cell 100, after 40s ECL responses are almost reduced to zero.Therefore, to ensure that flow cell 100 is rinsed completely, so that it is determined that using 45s as optimal washing time.
Refer to Fig. 7 and combine Fig. 1 to Fig. 4, the electrochemical luminescence based on magnetic bead described in the embodiment of the present invention two is biological Analyze the basic phase of structure of flow cell and the electrochemical luminescence bioanalysis flow cell 100 based on magnetic bead described in embodiment one Together, difference is:In embodiment one, optical channel 41 is to be through to bottom surface from the top surface of lid 40;And in embodiment two, institute The same bottom surface that lid 40 ' is through to from the side of the lid 40 ' of optical channel 41 ' is stated, but is provided with the optical channel 41 ' Optical fiber 9 ', one end of the optical fiber 9 ' is connected with optics convex lens 8.In addition, in embodiment one, when placing sample every time, needing Lid 40 is removed, or injected by feed pathway 44;And in embodiment two, inserting and moving for the ease of sample Remove, sample holes 47 ' are offered on the lid 40 ', the funnel chamber 12 ' passes through the sample holes 47 ' and ft connection, institute State and rubber stopper 48 ' is provided with sample holes 47 ', the sample holes 47 ' are formed from bifurcated in the feed pathway 44 ', and its is specific Structure is:The sample holes 47 ' have shared major trunk roads with feed pathway 44 ', and sample holes 47 ' and feed pathway 44 ' are also divided The sample introduction point arterial highway of bifurcated formation and feed liquor arterial highway Ju You not be divided from major trunk roads.
Except above-mentioned two is implemented to make an exception, the optical channel can be through to the bottom wall of lid from the side wall of the lid, should Have in optical channel on corner, the corner and be provided with reflective mirror, certainly, optical fiber can also be equally installed in optical channel, this When, then reflective mirror need not be set.
In summary, the above-mentioned electrochemical luminescence bioanalysis flow cell 100 based on magnetic bead will can be carried by magnet 5 The antigen antibody complex of magnetic bead is adsorbed on working electrode 2, is then injected coreaction liquid by liquid access way and is washed Wash, the detection to antigen antibody complex is realized finally by working electrode 2, to electrode 3 and optical channel 41,41 ', with existing skill Art is compared, should the entirety miniaturization of electrochemical luminescence bioanalysis flow cell 100 based on magnetic bead, electrochemical luminescence bioanalysis stream The effective volume that funnel chamber 12,12 ' is shown in the logical self structure of pond 100 is smaller, in addition, compared with prior art, being used for The ECL reaction reagents of bioanalysis are relatively fewer, that is, the ECL reaction reagents consumed are relatively fewer.
Because the feed liquor opening 441 of feed pathway 44 less than liquid outlet channel 45 goes out liquid opening 451, to keep unidirectional stream, Rinse well, it is to avoid the result of influence detection, what is more, because feed liquor opening 441 reclines to the inwall 11, go out liquid opening 451 be along the plunger portion 46 side wall 201 extend spiral slot, and plunger portion 46 design, so as to be more conducive to avoid Dead angle is rinsed, the result for avoiding influence from detecting is more conducive to.
In addition, by setting sample holes 47 ' on lid 40 ' so that detection sample Rapid replacement, and also contribute to Improve the service life of the electrochemical luminescence bioanalysis flow cell based on magnetic bead.Simultaneously as the bottom opening of sample holes 47 ' For feed liquor opening 441 ', and the feed liquor opening 441 ' reclines to the inwall 11 ', and uses hopper design, so as to insert sample During product, sample can be distributed on working electrode 2 ' along inwall 11 ', be favorably improved detection speed, it helps improve detection spirit Sensitivity, realizes quick analysis.
Described above is only the preferred embodiment of the present invention, is not intended to limit the invention, it is noted that for this skill For the those of ordinary skill in art field, without departing from the technical principles of the invention, can also make it is some improvement and Modification, these improvement and modification also should be regarded as protection scope of the present invention.

Claims (10)

1. a kind of electrochemical luminescence bioanalysis flow cell based on magnetic bead, it is characterised in that:Including with the top being oppositely arranged Opening and bottom opening funnel, be arranged on the funnel bottom with the seal of the bottom opening of closing funnel, be arranged on it is described close Working electrode on the upper surface of sealing, be embedded on the funnel to electrode, the lid of the top opening of the closing funnel And the magnet that can be moved relative to the working electrode, the axial rings to electrode along funnel around and be embedded in funnel, the leakage Bucket includes inwall and optical channel that the lid is provided through on the funnel chamber for setting and being formed, the lid is enclosed by inwall, described Optical channel is connected with funnel chamber, is provided with the optical channel on optical mirror slip, the lid and is offered liquid access way, institute State funnel chamber and pass through liquid access way and ft connection.
2. the electrochemical luminescence bioanalysis flow cell according to claim 1 based on magnetic bead, it is characterised in that:The liquid Body access way includes feed pathway and liquid outlet channel, and the lid has the plunger portion stretched in the funnel chamber, described Feed pathway has the feed liquor opening being opened in the plunger portion, and the liquid outlet channel, which has, to be opened in the plunger portion Go out liquid opening, the feed liquor opening goes out liquid opening less than described in.
3. the electrochemical luminescence bioanalysis flow cell according to claim 2 based on magnetic bead, it is characterised in that:It is described enter Liquid opening plaster is leaned on to the inwall, and the plunger portion is in circular platform type, it is described go out liquid opening be to extend along the side wall of the plunger portion Spiral slot.
4. the electrochemical luminescence bioanalysis flow cell according to claim 1 based on magnetic bead, it is characterised in that:The base Also include reference electrode in the electrochemical luminescence bioanalysis flow cell of magnetic bead, it is described to offering perforate, the ginseng on electrode One end than electrode is arranged in the perforate.
5. the electrochemical luminescence bioanalysis flow cell according to claim 4 based on magnetic bead, it is characterised in that:The base Include middle part cylinder in the electrochemical luminescence bioanalysis flow cell of magnetic bead, the funnel formation is in the middle part cylinder, institute State the fixing groove that the fixed reference electrode is offered on the cylinder of middle part.
6. the electrochemical luminescence bioanalysis flow cell according to claim 5 based on magnetic bead, it is characterised in that:The base Include being located at the bottom cylinder below the middle part cylinder, the middle part post in the electrochemical luminescence bioanalysis flow cell of magnetic bead The bottom of body sets fluted, and the seal is to protrude out the boss to be formed upwards from the bottom cylinder, the seal with The groove coordinates, and the fluting for housing the magnet is offered on the bottom cylinder, and the fluting runs through the bottom cylinder Bottom surface, be additionally provided with moving member in the fluting, the magnet is arranged on the moving member.
7. the electrochemical luminescence bioanalysis flow cell based on magnetic bead according to any one in Claims 2 or 3, its It is characterised by:Sample holes are offered on the lid, the funnel chamber passes through the sample holes and ft connection, the sample holes On be provided with sealing-plug.
8. the electrochemical luminescence bioanalysis flow cell according to claim 7 based on magnetic bead, it is characterised in that:It is described enter Sample hole is formed from bifurcated in the feed pathway.
9. the electrochemical luminescence bioanalysis flow cell according to claim 1 based on magnetic bead, it is characterised in that:The electricity Chemiluminescence flow cell also includes the optical fiber being arranged in the optical channel.
10. the electrochemical luminescence bioanalysis flow cell according to claim 1 based on magnetic bead, it is characterised in that:It is described Optical channel, which is through to from the side wall of the lid in the bottom wall of lid, the optical channel, has corner, is provided with the corner Reflective mirror.
CN201510345054.6A 2015-06-19 2015-06-19 Electrochemical luminescence bioanalysis flow cell based on magnetic bead Active CN104950026B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201510345054.6A CN104950026B (en) 2015-06-19 2015-06-19 Electrochemical luminescence bioanalysis flow cell based on magnetic bead

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201510345054.6A CN104950026B (en) 2015-06-19 2015-06-19 Electrochemical luminescence bioanalysis flow cell based on magnetic bead

Publications (2)

Publication Number Publication Date
CN104950026A CN104950026A (en) 2015-09-30
CN104950026B true CN104950026B (en) 2017-07-28

Family

ID=54164840

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201510345054.6A Active CN104950026B (en) 2015-06-19 2015-06-19 Electrochemical luminescence bioanalysis flow cell based on magnetic bead

Country Status (1)

Country Link
CN (1) CN104950026B (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105806828B (en) * 2015-10-29 2019-05-14 北京联众泰克科技有限公司 A kind of Electrogenerated chemiluminescent immunoassay system and its flow cell component
CN106556594A (en) * 2016-12-07 2017-04-05 中国人民解放军第三军医大学第附属医院 Magnetic control electrogenerated chemiluminescence flow detection pond

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1387036A (en) * 2002-07-09 2002-12-25 中国科学院长春应用化学研究所 Capillary electrophoresis and flow injection universal electrochemical light flux detecting pool
CN102066934A (en) * 2008-06-12 2011-05-18 株式会社日立高新技术 Analyzer using magnetic particles
CN203720142U (en) * 2014-03-07 2014-07-16 中国水产科学研究院 Miniaturized electrochemical three-electrode system detection pond
CN104538168A (en) * 2014-12-23 2015-04-22 苏州大学 Magnetic bead preparing method and application

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP6239243B2 (en) * 2013-02-08 2017-11-29 エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft Automatic analyzer

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1387036A (en) * 2002-07-09 2002-12-25 中国科学院长春应用化学研究所 Capillary electrophoresis and flow injection universal electrochemical light flux detecting pool
CN102066934A (en) * 2008-06-12 2011-05-18 株式会社日立高新技术 Analyzer using magnetic particles
CN203720142U (en) * 2014-03-07 2014-07-16 中国水产科学研究院 Miniaturized electrochemical three-electrode system detection pond
CN104538168A (en) * 2014-12-23 2015-04-22 苏州大学 Magnetic bead preparing method and application

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
Polyelectrolyte-based electrochemiluminescence enhancement for Ru(bpy)32+ loaded by SiO2 nanoparticle carrier and its high sensitive immunoassay;Zhi-Li Ge等;《Analytica Chimica Acta》;20150112;第862卷;第24–32页 *

Also Published As

Publication number Publication date
CN104950026A (en) 2015-09-30

Similar Documents

Publication Publication Date Title
Fang et al. Combination of flow injection with capillary electrophoresis. Part I. The basic system
CN101692047B (en) Microfluidic chip for capillary electrophoresis separation and chemiluminescence detection
CN104541162B (en) The electrophoretic separation of analyte
CN104950026B (en) Electrochemical luminescence bioanalysis flow cell based on magnetic bead
Huang et al. Combination of flow injection with capillary electrophoresis: 8. Miniaturized capillary electrophoresis system with flow injection sample introduction and electrogenerated chemiluminescence detection
CN102706836B (en) In-situ preparation method and in-situ detection device of localized surface plasmon resonance (LSPR) chip
Shihabi et al. Felbamate measured in serum by two methods: HPLC and capillary electrophoresis
Zhang et al. Electrokinetic gated injection-based microfluidic system for quantitative analysis of hydrogen peroxide in individual HepG2 cells
Yin et al. Short-capillary electrophoresis with electrochemiluminescence detection using porous etched joint for fast analysis of lidocaine and ofloxacin
Bergström et al. Development of a poly (dimethylsiloxane) interface for on-line capillary column liquid chromatography− capillary electrophoresis coupled to sheathless electrospray ionization time-of-flight mass spectrometry
CN112639456A (en) Electrical separation syringe and analysis method using the same
CN105264370B (en) The measuring method of the sample injection device of flow cytometer showed equipment, flow cytometer showed equipment and hemoglobin components
Hatta et al. The performance of a new linear light path flow cell is compared with a liquid core waveguide and the linear cell is used for spectrophotometric determination of nitrite in sea water at nanomolar concentrations
CN105987887B (en) Differential refractive index detector and liquid chromatograph
CN103869021B (en) Based on high-efficiency liquid chromatography method for detecting and the device of Surface enhanced raman spectroscopy
JP2012063159A (en) Analyzer, analytical method, and storage member
US11913904B2 (en) Reusable cartridge for capillary electrophoresis
CN102661948B (en) Capillary electrophoresis-chemiluminescence detection interface device and preparation method thereof
Liu et al. Sequential capillary electrophoresis analysis using optically gated sample injection and UV/vis detection
CN203881685U (en) Flow injection double-constant-potential excited electrochemiluminescence detection device
CN110108673A (en) For detecting the detection system of Lipoproteins subfractions cholesterol and hdl particle concentration simultaneously
CN207096260U (en) A kind of multi-joint test paper of fluorescence with shade function
Chen et al. Combination of flow injection with electrophoresis using capillaries and chips
Priego‐Capote et al. Dual‐opposite injection capillary electrophoresis for the determination of anionic and cationic homologous surfactants in a single run
Bodor et al. Capillary Isotachophoresis determination of trace oxidized glutathione in blood

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
GR01 Patent grant
GR01 Patent grant