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CN101403742A - Method for dielectric characterization of micro-nano biological particle by optoelectronic forceps - Google Patents

Method for dielectric characterization of micro-nano biological particle by optoelectronic forceps Download PDF

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CN101403742A
CN101403742A CNA2008101950862A CN200810195086A CN101403742A CN 101403742 A CN101403742 A CN 101403742A CN A2008101950862 A CNA2008101950862 A CN A2008101950862A CN 200810195086 A CN200810195086 A CN 200810195086A CN 101403742 A CN101403742 A CN 101403742A
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dielectric characterization
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CN101403742B (en
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易红
朱晓璐
倪中华
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Southeast University
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Abstract

利用光电镊对微纳米生物粒子进行介电表征的方法是通过逐步改变光图案的移动速度使粒子达到失步前的最大同步速度,并结合激励信号的频率调节,测出生物粒子在激励信号的一定频率范围内的最大同步速度曲线,进而完成粒子的介电表征。本发明提供的这种介电表征方法充分利用了光电镊的灵活性优势,同时避免了在芯片上制作复杂的物理实体电极阵列,在成本、功能、性能方面均优于目前的微纳米粒子的介电表征方法,为生物医学检测领域的跨越式发展提供了十分重要的手段。

Figure 200810195086

The method of using photoelectric tweezers to carry out dielectric characterization of micro-nano biological particles is to gradually change the moving speed of the light pattern to make the particles reach the maximum synchronous speed before out of synchronization, and combine the frequency adjustment of the excitation signal to measure the biological particle in the excitation signal. The maximum synchronous velocity curve in a certain frequency range, and then complete the dielectric characterization of the particles. The dielectric characterization method provided by the present invention makes full use of the flexibility advantages of photoelectric tweezers, and avoids making complex physical entity electrode arrays on the chip, and is superior to current micro-nanoparticles in terms of cost, function and performance. The dielectric characterization method provides a very important means for the leapfrog development in the field of biomedical detection.

Figure 200810195086

Description

Utilize the photoelectricity tweezer micro-nano biomone to be carried out the method for dielectric characterization
Technical field
The present invention be a kind of photoelectricity micro-fluidic device that uses to the method that micro-nano biomone characterizes and differentiates, relate to micro-fluidic field, particularly micro-fluidic biological medical science chip field.
Background technology
The dielectric property of micro-nano biomone and its structure and chemical composition are closely related, can be used as " fingerprint " of demarcating micro-nano biomone particular type.The process of obtaining the particle dielectric property is called dielectric characterization.Electricity rotation dielectrophoresis (electrorotation dielectrophoresis, ROT-DEP) be exactly technology that is used for the biomone dielectric characterization wherein, it utilizes the alternating voltage signal of several outs of phase to form rotating electric field on electrorotation chip, and fine particle just can rotate under the effect of rotating electric field.Biomone is because of the difference of its dielectric properties, and the rotation that is produced response is also different.Therefore, utilize these characteristics just can realize dielectric characterization to biomone, this feasible micro-sick cell is identified from a large amount of normal cells becomes possibility.Obtain the dielectric property method of biological particle based on electricity rotation dielectrophoresis technology, owing to have non-destructive, implement simply, satisfy the Touchless manipulation demand, and characterize chip and have the little integrated level advantages of higher of volume, become the important technology that enables that present realization biological particle characterizes diagnosis, just become a kind of important method of major disease diagnosis.In addition, conventional dielectrophoresis (conventional dielectrophoresis, cDEP) and row ripple dielectrophoresis (travelling-wave dielectrophoresis, twDEP) the dielectrophoresis phenomenon of these two kinds of biological particles also is used to judge qualitatively the dielectric property of biomone once in a while, but need to make complicated microelectrode, the extensive degree of application is not as good as electricity rotation dielectrophoresis.On the whole, there is following point in research field at the dielectric characterization chip at present: one, aspect the economy of making the dielectric characterization chip: present electricity rotation dielectrophoresis test chip, major part has only the simple electrode structure that produces electricity rotation dielectrophoresis, ignored the sample pre-treatments function, and some integrated sample feedings, the chip of pretreatment function such as separation, owing to need the complex manipulation of realization to biomone, thereby need design and make corresponding complicated electrode structure, the manufacturing process complexity, cost of manufacture is very high, is not suitable for making the disposable detection chip of a large amount of jettisonables that are used for medical diagnosis.Two, aspect the function implementation of the dielectric characterization of biomone: present chip realizes that dielectric characterization depends on the microelectrode array with given shape more, and these electrod-arrays lack flexibility, cause under different situations, needing to make different microelectrode arrays, increased the difficulty and the loaded down with trivial details Cheng Du that make and operate greatly, be difficult to promote the use of.
In recent years, utilization photoelectricity micro-fluidic device is handled micro-nano biomone and is become a kind of new microscopic particle manipulation technology.This principle based on photoelectric flexible operated tool is as follows: this photoelectricity micro-fluidic device is three layers of hamburger structure, the liquid that contains sample particles is positioned between the glass (upper strata) and photoconductive layer (lower floor) that is coated with ITO (indium-tin oxide) film, and wherein photoconductive layer is deposited on the ito glass of lower floor.Conducting material has high electrical resistance unglazed according under the situation, and when accepting illumination, the area pellucida photoproduction carrier concentration improves rapidly and makes its local conductivity improve several magnitude rapidly, cause the difference of light and shade district fluid layer dividing potential drop, form inhomogeneous field in the space and produced " light-induction dielectrophoresis " phenomenon.So if with an aperture particle circle is lived, particle is trapped within the aperture by the effect of light-induction dielectrophoresis power so, particle will be with the moving of aperture, and this method of light pattern manipulation of particles of utilizing is called photoelectricity tweezer method.But this method can only be used for handling, and can't different particles be characterized, and moves with identical speed because different types of particle can both be followed the aperture of same speed, on the motion phenomenon without any difference.This just can't characterize different particles.
Therefore, if a kind of new method can be provided, make it possible to utilize this manipulate tools of photoelectricity tweezer to realize the sign of biomone, so just can solve the high and flexible poor problem of general dielectric characterization chip cost, also can excavate the new using value of photoelectricity tweezer simultaneously.
Given this, the present invention proposes a kind of method of utilizing the photoelectricity tweezer that biological particle is characterized: utilize the photoelectricity tweezer to the step-out phenomenon in the biomone driving process (being that the too fast particle that causes of light pattern translational speed can't be caught up with), measure the maximum synchronous speed of biomone in certain exciting signal frequency scope, can realize the dielectric characterization of particle.
Summary of the invention
Technical matters: the purpose of this invention is to provide a kind of method of utilizing the photoelectricity tweezer micro-nano biomone to be carried out dielectric characterization, to solve general biomone dielectric characterization chip manufacturing cost height, the baroque defective of microelectrode, also can expand the application of photoelectricity tweezer simultaneously greatly.
Technical scheme: the present invention proposes to use particle (promptly being driven in the process of particle movement at light pattern by the step-out phenomenon in the photoelectricity tweezer driving process, the too fast particle that causes of light pattern translational speed can't be caught up with), measure biomone in certain exciting signal frequency scope maximum synchronous speed, can realize the dielectric characterization of particle.
At present mostly the dielectric characterization of biomone is to compose by imaginary part that Clausius-Mosso of measuring particle is put forward (Clausius-Mossotti) complex factor and realizes that this mainly is in order to utilize electrorotation chip.And in fact, under considerable situation, measure Clausius-Mosso to put forward the real part spectrum of complex factor and also can reach particle is characterized, and then reach the purpose of differentiating and distinguishing.The present invention just is being based on this, utilizes the correlativity of the real part that driving force that the photoelectricity tweezer produced and Clausius-Mosso put forward complex factor, carries the real part of complex factor by Clausius-Mosso of measuring particle and composes the dielectric characterization of realizing biomone.
The step-out phenomenon of micro-nano biomone under photoelectricity tweezer manipulation effect will definitely be avoided in little manipulation process, but exactly the feasible dielectric characterization to particle of this phenomenon becomes possibility.Specifically, when particle to be measured during by photoelectricity tweezer driven, particle will be followed by the track of light pattern; But after the translational speed of light pattern increases to a certain degree, particle will not catch up with the motion of light pattern.In other words, there is a maximum synchronous speed in particle when following the light pattern motion.The suffered dielectrophoretic force of particle that is in maximum synchronous speed is maximum, again because dielectrophoretic force is proportional to the gradient of electric field intensity square, so be in the gradient maximum of electric field intensity square of the residing position of particle of maximum synchronous speed, in other words, particle will reach maximum synchronous speed in the position of the gradient maximum of electric field intensity square.In addition, the maximum synchronous speed of particle and the Clausius-Mossotti factor of particle or effective polarizability (dielectric property that has reflected particle) are closely related, and the frequency dependence of the Clausius-Mossotti factor of particle has determined the maximum synchronous speed of particle to have frequencydependence characteristic.Therefore, the frequency characteristic of the maximum synchronous speed by measuring particle, and in conjunction with the quantitative relationship between the Clausius-Mossotti factor three of the maximal value of the gradient of the maximum synchronous speed of particle, electric field intensity square and particle, can draw the frequency characteristic of the Clausius-Mossotti factor of particle, and then can parse the dielectric parameter of particle, realize the dielectric characterization of biomone.This new method does not relate to the making of any physical entity microelectrode, and has made full use of the flexibility advantage of photoelectricity tweezer, and therefore this method not only greatly reduces the cost of biomone dielectric characterization, and performance is very superior.
Specifically utilize the photoelectricity tweezer to be: when utilizing light pattern to drive micro-nano biomone to the method that micro-nano biomone carries out dielectric characterization, make particle reach the maximal rate synchronous by the translational speed that progressively changes light pattern with light pattern, be that particle is about to not catch up with the critical velocity that light pattern moves, and in conjunction with the frequency adjustment of pumping signal, measure the maximum synchronous speed curve of biomone in the certain frequency scope of pumping signal, and then finish the dielectric characterization of particle.
The concrete steps of this dielectric characterization method are:
Step 1: the sample solution that will contain intended particle is expelled in each miniflow body cavity of dielectric characterization chip by each injection port;
Step 2: projection dummy electrodes pattern in each the miniflow body cavity on chip;
Step 3: the voltage of sinusoidal excitation signal is added between the upper strata conducting film and lower floor's conductive layer of the chip that uses, makes electric field pass the miniflow body cavity, and set original frequency;
Step 4: in each the miniflow body cavity on chip, constantly change the translational speed of dummy electrodes pattern, particle is being pushed away by the dummy electrodes pattern or, reach maximum synchronous speed, and note the maximum synchronous speed in the particle movement process up to particle in tow along straightaway;
Step 5: change the frequency of pumping signal, make frequency hopping to a new Frequency point of pumping signal, repeating step 4 then;
Step 6: draw out the variation spectral line of the maximum synchronous speed of intended particle in the survey frequency scope with exciting signal frequency.
Shifting gears of the translational speed of described dummy electrodes pattern is to start from scratch progressively to increase, or dichotomy changes speed; Even particle is out-of-step free under initial velocity, the mean value of then choosing initial velocity value and most probable velocity value is as next test speed value, otherwise if particle step-out under initial velocity, then choose mean value between initial velocity value and zero as next test speed value, and the like, constantly increase or reduce the translational speed of light pattern, until the maximum synchronous speed that finds particle to move with light pattern with dichotomy.
Beneficial effect: provided by the inventionly utilize the photoelectricity tweezer carries out dielectric characterization to micro-nano biomone method to make maximum synchronous speed before particle reaches step-out by the translational speed that progressively increases light pattern, and regulate in conjunction with the frequency body of pumping signal, measure the maximum synchronous speed of biomone in the certain frequency scope of pumping signal, and then finish the dielectric characterization of particle.This method has made full use of the flexibility advantage of photoelectricity tweezer, avoided on chip, making complicated physical entity electrod-array simultaneously, and particle handled and test is integrated in one, and only need one road sinusoidal excitation signal (present electric rotary test chip needs the sinusoidal signal more than 3 tunnel).Therefore, dielectric characterization method provided by the invention all is better than the dielectric characterization method of current micro-and nano-particles at cost, function, aspect of performance, for the great-leap-forward development of biomedical detection range provides very necessary means, will be widely used in fields such as medical diagnosis on disease and treatment, molecular biology, public health quarantine, judicial expertise, Food Hygiene Surveillances.
Description of drawings
Fig. 1 is the employed dielectric characterization chip structure of an embodiment of the invention synoptic diagram;
Fig. 2 is the light pattern that utilizes in the embodiment of the invention photoelectricity tweezer that biomone the is carried out dielectric characterization synoptic diagram (chip is thrown off the vertical view behind the upper substrate) of arranging.
Have among the above figure:
First injection port 1101, second injection port 1102, the 3rd injection port 1103, transparent insulation cover plate 120, the indium and tin oxide film 130 that the upper strata is transparent, the first miniflow body cavity 1401, the second miniflow body cavity 1402, the 3rd miniflow body cavity 1403, middle ware interlayer 150, transparent insulation substrate 160, the dummy electrodes cambium layer of forming by silicon nitride layer 171, photoconductive layer 172 and transparency conducting layer 173 170, rectangle dummy electrodes 1801, circular dummy electrodes 1802, aperture dummy electrodes 190, rectangle frame dummy electrodes 200.
Embodiment
The embodiment of the photoelectricity tweezer carries out dielectric characterization to biomone method that utilizes provided by the invention is referring to Fig. 1 and Fig. 2.This method the pattern of chip structure, material and the light pattern that can use be not limited to present embodiment.
Employed dielectric characterization chip comprises first injection port 1101, second injection port 1102, the 3rd injection port 1103 in the present embodiment, transparent insulation cover plate 120, the indium and tin oxide film 130 that the upper strata is transparent, the first miniflow body cavity 1401, the second miniflow body cavity 1402, the 3rd miniflow body cavity 1403, middle ware interlayer 150, transparent insulation substrate 160, the dummy electrodes cambium layer of forming by silicon nitride layer 171, photoconductive layer 172 and transparency conducting layer 173 170.Silicon nitride layer 171 can prevent hydrolysis, photoconductive layer 172 has photoconductive characteristic, promptly when by illumination when bright its inner charge carrier quantity increase severely, and not by illumination when bright its inner charge carrier quantity seldom, the ratio that its bright electricity is led with dark conductance can reach more than 10000 at least; The material of photoconductive layer 172 can be selected the cadmium sulfide (CdS) of amorphous silicon hydride or doping or the cadmium selenide (CdSe) that mixes or the combination of cadmium sulfide and cadmium selenide.The purpose of three miniflow body cavitys is arranged is simultaneously three kinds of different sample particle to be characterized to employed chip in the present embodiment, and three miniflow body cavitys separate three kinds of samples to prevent mutual pollution.In addition, can respectively in three miniflow body cavitys the form characteristics according to corresponding particle throw difform light pattern, be beneficial to the dielectric characterization of various different particles.
In the present embodiment, it is as follows to utilize the photoelectricity tweezer biomone to be carried out the concrete steps of method of dielectric characterization:
Step 1: be expelled to the sample solution of three kinds of intended particles in the first miniflow body cavity 1401, the second miniflow body cavity 1402, the 3rd miniflow body cavity 1403 of dielectric characterization chip respectively by three injection ports;
Step 2: as shown in Figure 2, projection rectangle dummy electrodes 1801 and circular dummy electrodes 1802 in miniflow body cavity 1401; Projection aperture dummy electrodes 190 in miniflow body cavity 1402; Projection rectangle frame dummy electrodes 200 in miniflow body cavity 1403;
Step 3: the voltage of sinusoidal excitation signal is added between upper strata indium and tin oxide film 130 and the transparency conducting layer 173, and sets original frequency;
Step 4: in miniflow body cavity 1401, rectangle dummy electrodes 1801 is maintained static, move circular dummy electrodes 1802 according to the direction of arrow among Fig. 2, and start from scratch and increase translational speed gradually, particle between two rectangle dummy electrodes 1801 is being pushed away by circular dummy electrodes 1802 or in tow along straightaway, is noting the maximum synchronous speed in the particle movement process; In miniflow body cavity 1402, move aperture dummy electrodes 190 according to the direction of arrow among Fig. 2, and start from scratch and increase translational speed gradually, the particle that is positioned at aperture is by 190 tractions of aperture dummy electrodes and move, and notes the maximum synchronous speed in the particle movement process; In miniflow body cavity 1403, move rectangle frame dummy electrodes 200 according to the direction of arrow among Fig. 2, and start from scratch and increase translational speed gradually, the particle that is positioned at rectangle frame is by 200 tractions of rectangle frame dummy electrodes and move, and notes the maximum synchronous speed in the particle movement process;
Step 5: change the frequency of pumping signal, make frequency hopping to a new Frequency point of pumping signal, repeating step 4 then;
Step 6: draw out the variation spectral line of the maximum synchronous speed of target organism particle in the survey frequency scope with exciting signal frequency.

Claims (3)

1.一种利用光电镊对微纳米生物粒子进行介电表征的方法,其特征在于:在利用光图案驱动微纳米生物粒子的同时,通过逐步改变光图案的移动速度使粒子达到与光图案同步的最大速度,即粒子即将跟不上光图案移动的临界速度,并结合激励信号的频率调节,测出生物粒子在激励信号的一定频率范围内的最大同步速度曲线,进而完成粒子的介电表征。1. A method for dielectric characterization of micro-nano biological particles using photoelectric tweezers, characterized in that: while using light patterns to drive micro-nano biological particles, the particles are synchronized with the light patterns by gradually changing the moving speed of the light patterns The maximum velocity of the biological particles, that is, the critical velocity at which the particles will not be able to keep up with the movement of the light pattern, combined with the frequency adjustment of the excitation signal, measures the maximum synchronous velocity curve of the biological particles within a certain frequency range of the excitation signal, and then completes the dielectric characterization of the particles . 2.如权利要求1所述的利用光电镊对微纳米生物粒子进行介电表征的方法,其特征在于该介电表征方法的具体步骤为:2. utilize photoelectric tweezers as claimed in claim 1 to carry out the method for dielectric characterization of micro-nano biological particle, it is characterized in that the concrete steps of this dielectric characterization method are: 步骤1:将含有目标粒子的样品溶液通过各个进样口(110)注射到介电表征芯片的各个微流体腔(140)中;Step 1: Inject the sample solution containing target particles into each microfluidic cavity (140) of the dielectric characterization chip through each injection port (110); 步骤2:在芯片上的每个微流体腔(140)中投射虚拟电极图案(180);Step 2: Projecting dummy electrode patterns (180) in each microfluidic chamber (140) on the chip; 步骤3:将正弦激励信号的电压加于所使用芯片的上层导电膜(130)和下层导电层(173)之间,使电场穿过微流体腔(140),并设定初始频率;Step 3: Apply the voltage of the sinusoidal excitation signal between the upper conductive film (130) and the lower conductive layer (173) of the chip used, so that the electric field passes through the microfluidic cavity (140), and set the initial frequency; 步骤4:在芯片上的每个微流体腔(140)中,不断改变虚拟电极图案(180)的移动速度,使粒子被虚拟电极图案(180)推着或拖着沿直线行进,直到粒子达到最大同步速度,并记录下粒子运动过程中的最大同步速度;Step 4: In each microfluidic chamber (140) on the chip, constantly change the moving speed of the virtual electrode pattern (180), so that the particles are pushed or dragged along a straight line by the virtual electrode pattern (180), until the particle reaches The maximum synchronous speed, and record the maximum synchronous speed during the particle movement; 步骤5:改变激励信号的频率,使激励信号的频率跳变到一个新的频率点,然后重复步骤4;Step 5: Change the frequency of the excitation signal, so that the frequency of the excitation signal jumps to a new frequency point, and then repeat step 4; 步骤6:绘制出目标粒子在测量频率范围内的最大同步速度随激励信号频率的变化谱线。Step 6: Draw the variation spectrum of the maximum synchronous velocity of the target particle with the frequency of the excitation signal within the measurement frequency range. 3.如权利要求2所述的利用光电镊对微纳米生物粒子进行介电表征的方法,其特征在于,所述的虚拟电极图案(180)的移动速度的改变方式是从零开始逐步增大,或是二分法改变速度;即若粒子在初始速度下不失步,则选取初始速度值和最大可能速度值的平均值作为下一个试验速度值,反之若粒子在初始速度下失步,则选取初始速度值和零之间的平均值作为下一个试验速度值,依次类推,不断以二分法增大或减小光图案的移动速度,直至找到粒子随光图案移动的最大同步速度。3. the method utilizing photoelectric tweezers to carry out dielectric characterization to micro-nano biological particles as claimed in claim 2, is characterized in that, the change mode of the moving speed of described virtual electrode pattern (180) is to increase gradually from zero , or change the velocity by dichotomy; that is, if the particle does not lose synchronization at the initial velocity, the average value of the initial velocity value and the maximum possible velocity value is selected as the next test velocity value, otherwise, if the particle loses synchronization at the initial velocity, then The average value between the initial velocity value and zero is selected as the next experimental velocity value, and so on, and the moving velocity of the light pattern is continuously increased or decreased by dichotomy until the maximum synchronous velocity of the particles moving with the light pattern is found.
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