![]() DROP RECOVERY METHOD AND ASSOCIATED DROUGHT RECOVERY SYSTEM
专利摘要:
The invention relates to a drop recovery method (4), comprising the following steps: - supply of a chip (20) comprising a fluid circulation duct (46), - injection of an emulsion (6) of drops injecting a carrier fluid (26) to form a working fluid (28) comprising emulsion drops spaced apart from one another along the conduit, - conveying the working fluid in the conduit, - injection of a separating fluid (33) for separating the working fluid into a plurality of successive pockets (35), each pocket being isolated from the next pocket by a separator (80), - conveying the pockets and separators, to an outlet ( 66) of the chip, - recovery in a compartment (82) of a recovery medium (34) of at least one bag comprising a drop recovered after the conveying. 公开号:FR3038530A1 申请号:FR1556424 申请日:2015-07-07 公开日:2017-01-13 发明作者:Laurent Boitard;Nicolas Bremond;Rodriguez Jairo Garnica;Jerome Bibette 申请人:Centre National de la Recherche Scientifique CNRS;Ecole Superieure de Physique et Chimie Industrielles de Ville Paris ; IPC主号:
专利说明:
Drop recovery method and associated drop recovery system The present invention relates to a method for recovering drops comprising the following steps: - providing a chip comprising a fluid circulation conduit defining successively in a fluid flow direction, an inlet zone, a spacing zone, an injection zone and a separation zone, - injection of an emulsion of drops of an internal fluid dispersed in an external fluid, in the inlet zone, - injection of at least one carrier fluid miscible with the fluid external in the spacing zone, to form in the flow conduit a working fluid comprising carrier fluid and drops of the emulsion spaced from each other along the conduit, - conveying the working fluid in the conduit of circulation. The method according to the invention makes it possible, for example, to form an emulsion drop by drop with a determined content or to reinject an emulsion, then to space the drops of the emulsion before isolating them one by one on a solid support. The solid support is, for example, a 96, 386 or 1536-well plate, or a petri dish or a MALDI plate. Drop microfluidics are used in a large number of laboratories to miniaturize biological and biochemical reactions in bioreactors from a few picoliters to a few nanoliters. Sampling speeds, more than 1000 drops per second and reduced sample volume make this technology very attractive for the screening of molecules and cells. Over the last 10 years, a large number of modules have been developed to manipulate these micrometric drops: mixing and adding compounds, drop melting, detection of fluorescent markers, incubation and selections of drops of interest. The publication "Fluorescence-activated droplet sorting (FADS): Efficient microfluidic cell sorting based on enzymatic activity", by Baret et al. published online April 23, 2009 in the journal Lab on a Chip illustrates this principle. An emulsion of drops is injected into a sorting device, the drops of the emulsion are spaced with an injection of fluorinated oil without surfactant. The drops are then sent to a sort interface. A measurement is made, all the drops having a signal greater than a detection threshold are collected in the same tube. Such a system allows the separation of the emulsion into two droplet populations and the recovery of each population. However, this method does not recover the drops individually. However, it is important in some applications to be able to recover isolated drops in a macroscopic support. For example, in the field of high-throughput screening of cells, it is desired to test numerous isolated cells at a time, then select and recover the most interesting cells. Isolation of the cells in separate drops facilitates the tests, then the re-culturing of the selected cells makes it possible to obtain clones generating monoclonal antibodies or industrial enzymes. With the method previously described, about a thousand mixed drops are recovered together at the exit of the system, so it is necessary to perform many subsequent steps to isolate cells with the best arrangements to synthesize the compound of interest. Alternatively, the method described above can be used to recover only one drop but this is difficult to implement because of the small volume of the drop to handle and, in addition, in this case, the rest of the drops is lost or eliminated . The publication "Interfacing picoliter droplet microfluidics with addressable microliter compartments using fluorescence activated cell sorting" by Bai et al., Published online December 28, 2013 in the journal Sensors and Actuators B: Chemical, provides a method for isolating drops one by one. This method consists of gelling the drops containing the molecules or cells of interest before placing them in a fluorescence activated cell sort flow cytometer (called FACS for Fluorescence Activated Cell Sorter) which will then distribute them in a plate. However, many drops are lost. In addition, a major disadvantage of this method is the gelling step of the drop which imposes temperature conditions that are not necessarily compatible with all biochemical or biological reactions. Indeed, the authors place their samples in an ice bath, which will stop any reaction. The patent application WO2012042060 describes a system for producing and recovering drops. The drops are generated at a compatible frequency synchronized with the speed of movement of the drop recovery element. However, this system does not allow to reinject an emulsion. In addition, the separation of the drops requires a large amount of oil which makes it difficult to handle them. Finally, this system does not allow to add a reagent (lysis liquid for example) once the drop formed. An object of the invention is to provide a more reliable and accurate drop recovery method than existing methods, allowing individual monitoring of each drop and effective recovery of its contents. For this purpose, the subject of the invention is a process of the aforementioned type, characterized in that the process comprises the following steps: injection of an immiscible separating fluid with the carrier fluid into the injection zone, to separate the working fluid in a plurality of successive pockets comprising carrier fluid, each pocket being isolated from the next bag by a separator consisting of separator fluid, - conveying pockets and separators, in the separation zone, to an output of the chip - Recovery in a compartment of a recovery medium of at least one bag comprising a drop recovered after conveying. The method according to the invention may comprise one or more of the following characteristics, taken separately or in any technically possible combination: the circulation duct is wider in the separation zone than in the separation zone; each pocket comprises carrier fluid and strictly less than two drops, the output of the chip opens into an evacuation tube having an outlet, the support comprises several compartments separated from each other, and the method comprises, after each recovery step, a step of relative movement of the support relative to the chip, the outlet of the discharge tube being placed opposite a different compartment after each movement of the support, - the method comprises a step of detecting the passage of successive drops or a detection of the passage of the successive pockets, the displacement of the support is controlled according to each detection of drops or each pocket detection, so that a single pocket comprising a drop detected in the detection step is recovered in each compartment of the support, - the detection of a drop controls the injection of a volume of fluid separator and pocket formation; the method comprises a pocket detection step in a detection zone downstream of the separation zone; the method comprises a step of adding a complementary solution in at least one pocket, the pocket in which the complementary solution is added comprises a drop of emulsion and the method comprises a step of melting said drop of emulsion with the added solution added. the formation of the bags is carried out at a frequency of between 1 bag per second and 1000 bags per second; the diameter of each drop is less than or equal to that of the circulation duct 46; the diameter of each pocket is greater than or equal to that of the circulation duct 46; - The diameter of each separator is greater than or equal to that of the flow conduit 46, the separating fluid is preferably a gas. The subject of the invention is also a drop recovery system comprising: a chip comprising a fluid circulation duct defining successively in the direction of circulation of the fluids, an inlet zone, a spacing zone, a zone of injection and a separation zone, - a device for injecting an emulsion of drops of an internal fluid dispersed in an external fluid, in the inlet zone, - a device for injecting at least one fluid carrier miscible with the external fluid in the spacing zone, for forming in the circulation conduit a working fluid comprising carrier fluid and drops of emulsion spaced from each other along the conduit; injecting an immiscible separator fluid with the carrier fluid into the injection zone, to separate the working fluid into a plurality of successive pockets comprising carrier fluid, each pocket t isolated from the next bag by a separator consisting of separating fluid, and - a control unit adapted to circulate the working fluid in the flow conduit, and to convey the pockets and separators, in the separation zone, to an output of the chip, - a recovery medium, the support comprising at least one compartment, for the recovery of at least one pocket comprising a drop in the compartment. The drop recovery system according to the invention may comprise one or more of the following characteristics, taken separately or in any technically possible combination: the output of the chip opens into a discharge tube having an outlet, the support comprising several compartments separated from each other, and the system comprises a device for relative movement of the support relative to the chip, after each recovery, the displacement device being adapted to place the outlet of the discharge tube facing the a different compartment after each movement of the support relative to the chip, the system comprises a sensor adapted to detect the passage of successive drops in the spacing zone, the displacement device being controlled according to each drop detection, for a single pocket comprising a drop detected at the detection step to be recovered from in each compartment of the support, the output of the chip opens into an evacuation tube, the evacuation tube defines an internal lumen opening on an open mouth, the evacuation tube comprising an outer wall and the system comprises a mouthpiece having a through passage, the discharge tube being placed in the through passage and the system includes a blowing unit capable of injecting a flow of air into the through passage so that a portion of the air runs along the outer wall of the evacuation tube, up to the mouth of the evacuation tube. The invention also relates to a bag distribution device comprising: - an evacuation tube, defining an inner lumen opening on an open mouth, the evacuation tube comprising an outer wall; a circulation device in the internal lumen of the evacuation tube of a plurality of successive pockets comprising a carrier fluid, each pouch being isolated from the next bag by a separator constituted by a separating fluid, the separating fluid being immiscible with the carrier fluid; - A nozzle having a through passage, the discharge tube being placed in the through passage of the nozzle; a blowing unit capable of injecting a stream of air into the through passage so that a portion of the air runs along the outer wall of the discharge tube, up to the mouth of the evacuation tube; . The invention also relates to a bag distribution method comprising the following steps: - providing a dispensing device as previously described; - Circulation of the successive pockets in the inner lumen, - air injection into the through passage of the nozzle, the air flow and the flow of the pockets being adjusted so that each pocket is detached successively from the mouth of the evacuation tube. The invention will be better understood on reading the description which follows, given solely by way of example, and with reference to the appended drawings, in which: FIG. 1 is a diagrammatic representation of a first system of Figure 2 is a schematic representation of an emulsion prior to injection into the drop recovery system; recovery of drops according to the invention; - Figure 4 is a detailed representation of part of a third drop recovery system; FIG. 5 is a detailed representation of part of a fourth recovery system; FIG. 6 is a detailed representation of a pocket dispensing device of a fifth recovery system; FIG. 7 is a detailed representation of the pocket dispensing device of FIG. 6, in a subsequent step of a bag dispensing method; Fig. 8 is a pocket distribution result obtained after pocket distribution by the pocket delivery device of Fig. 6; Fig. 9 is another pocket distribution result obtained after pocket distribution by the pocket delivery device of Fig. 6. In the following description, the terms "upstream" and "downstream" and the terms "input" and "output" are used with reference to the normal flow direction of the system fluids. The term "longitudinal" is defined with respect to the direction of the flow path in the chip. The planes that are perpendicular to the longitudinal direction are called "transverse plane". The term "diameter" of an element refers to the maximum extent of the element considered in a transverse plane. We call "drop frequency", the number of drops per second passing in front of a fixed point of the circulation duct. A first drop recovery system 1 is shown in FIG. The first collection system 1 of drops is provided to isolate and recover separately the drops 4 of an emulsion 6. An emulsion 6 of drops 4 is shown in FIG. 2. The emulsion 6 consists of a plurality of drops 4 of an internal fluid 8 dispersed in an external fluid 10. The emulsion 6 is substantially stable, which means that for a fixed volume of the emulsion 6, the number and the volume of the drops 4 vary by less than 5% when the fixed volume of the emulsion 6 is stored between -80 ° C. and 80 ° C., at 1 bar for 48 hours. h. Emulsion 6 is concentrated. This means that the volume fraction of drops 4 in the emulsion 6 is between 30% and 40%. Each drop 4 constitutes a closed compartment filled with internal fluid 8. The drops 4 of the emulsion 6 are preferably substantially monodisperse. The drops 4 have, for example, a volume of between 2 μl and 2 μl. At least some drops 4 of the emulsion 6 are different from other drops 4 of the emulsion 6. Each drop 4 comprises an internal fluid 8 potentially different from a drop 4 to another. Advantageously, the internal fluid 8 of all the drops 4 comprises at least one common base 12. For example, the common base 12 is a buffer solution adapted to the survival of cells such as a phosphate buffered saline solution or a culture medium. The internal fluid 8 of each drop 4 consists of clean elements 14 to the drop 4 and the common base 12. The proportions of the clean elements 14 and the common base 12 and / or the natures of the clean elements 14 vary from a drop 4 to another. For example, the clean elements 14 of a drop 4 are a cell and elements secreted by the cell, such as proteins. Advantageously, more than 10% of the volume of the drop 4 consists of the common base 12. The internal fluid 8 of each drop 4 is immiscible with the external fluid 10. It is understood by immiscible that the partition coefficient between the two fluids is less than 10 "3. The drops 4 are well defined in the emulsion 6 and the exchanges between two adjacent drops 4 in the emulsion 6 are limited to soluble or slightly soluble compounds in the external fluid 10, that is to say with a partition coefficient greater than or equal to 103 and in cases where the compositions are different between drops 4 neighbors. Advantageously, the common base 12 is immiscible with the external fluid 8. In the example, the internal fluid 8 is an aqueous phase and the external fluid 10 is an organic phase including an oily phase. The external fluid 10 comprises for example hydrofluoroethers such as FC-40 or HFE-7500, forming a fluorinated oil. The external fluid 10 further comprises, advantageously, a surfactant. The surfactant is suitable for stabilizing the emulsion 6. The surfactant is, for example, a block copolymer of polyethylene glycol and perfluoropolyether (PEG-PFPE). For example, the concentration of surfactant in the external fluid 10 is between 2% and 5%. The emulsion 6 is, for example, prepared by means of a preparation device and stored before being used in the first recovery system 1. The first recovery system 1 is intended to separately recover the drops 4 of the emulsion 6. The first drop recovery system 1, shown in FIG. 1, comprises a separation chip 20, a control unit 21 and a device 22 for injecting the emulsion 6 into the chip 20. In addition, the first system recovery device 1 comprises a device 24 for injecting carrier fluid 26 into the chip 20 to form a working fluid 28, a device 32 for injecting a separating fluid 33 into the chip 20 and a recovery medium 34. As will be described later, the control unit 21 is able to control the injection into the chip 20 of the separating fluid 33 by the device 32 for injecting the separating fluid 33 to separate the working fluid 28 into a plurality successive pockets 35, likely to contain a drop 4, as shown in Figure 1. In addition, the first drop recovery system 1 comprises a sensor 36 capable of detecting the passage of successive drops 4 of the emulsion 6 into the working fluid 28. The first drop recovery system 1 further comprises a discharge tube 38, an output detector 40 and a relative displacement device 42 of the support 34 with respect to the chip 20. The chip 20 comprises a fluid flow conduit 46 defining successively in the flow direction of the fluids, an inlet zone 48, a spacer zone 50 of the drops advantageously having a measuring region 52, an injection zone 54 separating fluid 33 and a separation zone 56. The circulation duct 46 extends along a longitudinal axis X. The chip 20 is, in the example, a rectangular block extended along the longitudinal axis X and a transverse axis Y perpendicular to the longitudinal axis X. In addition, the chip has a thickness along an axis of elevation Z perpendicular to the longitudinal axis X and the transverse axis Y. In the following, the terms "lower" and "higher" refer to the axis of elevation Z, perpendicular to the longitudinal axis X. The direction of the elevation axis Z is for example substantially vertical . For example, the cross section, that is to say along a plane comprising the transverse axis Y and the elevation axis Z, of the circulation duct 46 is rectangular. The circulation duct 46 is delimited by four side walls. Alternatively, the cross section has other shapes. The maximum area of the cross section of the duct 46 is less than 1 mm 2. The chip 20 is transparent at least in the measurement region 52. Advantageously, the chip 20 is made of transparent material, for example polydimethylsiloxane (PDMS). The material of the chip 20 is impermeable to the carrier fluid 26. In a variant, the material of the chip 20 is, moreover, impermeable to the separating fluid 33, for example when the separating fluid 33 is a liquid. The chip 20 has a first inlet 60 opening into the inlet zone 48 of the circulation duct 46, at least a second inlet 62 opening into the spacing zone 50 of the circulation duct 46 and at least a third inlet 64 opening into the injection zone 54 of the circulation duct 46. The chip 20 has an outlet 66 through which the flow duct 46 opens into the evacuation tube 38. The first inlet 60 is in fluid communication upstream with the injection device 22 of the emulsion, as illustrated in FIG. The inlet zone 48 of the circulation duct 46 extends from the first inlet 60 to the spacer zone 50. The shape of the circulation duct 46 in the inlet zone 48 is adapted to allow the injection of the emulsion 6 into the entry zone 48 and the passage of a drop 4 at a time to the spacing zone 48. In the example shown in FIG. 1, the circulation duct 46 in the inlet zone 48 has a first portion 68 and a second portion forming a convergent tip 70. The first portion 68 has a constant diameter along the longitudinal axis X. The second portion 70 opens into the spacing zone of the circulation duct. It allows the passage of a drop 4 at a time to the spacing zone 48. The second portion 70 has a convergent tip shape in the direction of flow of the fluids along a plane comprising the longitudinal axis X and the transverse axis Y. The angle of the convergent tip 70 is adapted to prevent the drops 4 coalescing . For example, the opposite side walls of the circulation duct 46 at the convergent point 70 form between them an angle of between 45 ° and 70 °. The diameter of the first portion 68 is the maximum diameter of the convergent tip 70. For example, the minimum diameter of the convergent tip 70 is substantially equal to the average diameter of the drops 4. The second inlet 62 is in fluid communication upstream with the injection device of the carrier fluid 26 as illustrated in FIG. The shape of the circulation duct 46 in the spacer zone 50 is adapted to allow the injection of the carrier fluid 26 between the drops 4 of the emulsion 6. Thus, the circulation duct 46 comprises in the spacer zone 50, a junction 72 with the second inlet 62. Advantageously, the junction 72 comprises at least one secondary channel 74 with an angle of between 45 ° and 90 ° with respect to the longitudinal ae X and opening into the circulation duct 46. In the example shown in FIG. 1, the junction 72 comprises two secondary channels 74 opening on either side of the circulation duct 46. The circulation duct 46 has, in the spacer zone 50 away from the junction 72, a cross-section of diameter smaller than that of the first portion of the vicinity of the inlet 60, for example, substantially equal to 400% Preferably, this diameter is equal to the minimum diameter of the convergent tip 70. The spacer zone 50 extends from the inlet zone 48 to the injection zone 54. The spacer zone 50 further has a measurement region 52 in which the drops 4 are detected by the sensor 36, as will be described later. The dimension of this measurement region 52 is for example equal to the diameter of a drop 4. Alternatively, the measurement region 52 extends in a transverse plane on a surface equal to the section of the circulation duct 46. The length of the spacer zone 50 is preferably greater than 3 times the diameter of the circulation conduit 46. The third inlet 64 is in fluid communication upstream with the separator fluid injection device 32 as illustrated in FIG. The shape of the circulation duct 46 in the injection zone 54 is adapted to allow the injection of the separating fluid 33 between the drops 4 of the working fluid 28. Thus, the circulation duct 46 comprises in the injection zone 54, a junction 76 with the third inlet 64. The circulation duct 46 in the separation zone 56 has a flared shape so that the dimension of the circulation duct reaches the internal diameter of the evacuation tube 38. The diameter of the circulation duct 46 is greater at the outlet of the separation zone 56 than in the spacing zone 50. The circulation duct 46 has a maximum diameter in the separation zone of between 10 μm and 2 mm, advantageously greater than the diameter of the drop 4. The control unit 21 is capable of controlling the flow rates of the various fluids 6, 26, 28 , 33, to receive the signals of the sensor 36 and the output detector 40 and to record the characteristics of the drops 4. The control unit 21 is able to control the injection device 22 of an emulsion, the device of injection 24 of the carrier fluid, the injection device 32 of the separating fluid. The injection device 22 of an emulsion is suitable for injecting an emulsion 6 of drops 4 of an internal fluid 8 dispersed in an external fluid 10 in the entry zone 48 by the first inlet 60. The control unit 21 is capable of controlling the injection device 22 of the emulsion 6 so that it injects the emulsion 6 into the inlet zone 48 at a flow rate of between 1 μl / h and 500 μl / h and advantageously at a speed of flow rate of 80 pL / h. The injection device 22 of an emulsion comprises for example a container in which is placed a volume of the emulsion 6 between 1 nL and 2 mL. The injection device 22 of an emulsion further comprises a connecting pipe for placing the container in fluid communication with the first inlet 60 and a means for circulating the emulsion, as illustrated in FIG. . For example, the injection device 22 of the emulsion comprises a syringe pump, a syringe filled with emulsion 6 and a connecting pipe. The injection device 24 of the carrier fluid is adapted to inject the carrier fluid 26 into the spacer zone 50 by the second inlet 62 in order to form a working fluid 28 in the circulation conduit 46. The control unit 21 is adapted to control the injection device 24 of the carrier fluid 26 so that it injects carrier fluid 26 into the spacer zone 50 by the second inlet 62 at a flow rate of between 5 μl / h and 5 mL / h and advantageously at a flow rate of 1mL / h. The injection flow rate of the carrier fluid 26 is, for example, adjusted so that the frequency of the drops 4 in the spacing zone 50 is, for example, between 0.5 drops per second and 500 drops per second and advantageously 30 drops per seconds. The injection device 24 of the carrier fluid 26 comprises for example a container in which is placed a volume of the carrier fluid 26 of between 10 μL and 10 mL. The injection device 24 further comprises a connection pipe for putting in fluid communication the container and the second inlet 62 and a means for circulating the carrier fluid 26. Similarly, the injection device 24 comprises for example a syringe pump, a syringe filled with carrier fluid 26 and a connecting pipe. The carrier fluid 26 is miscible with the external fluid 10. For example, the carrier fluid 26 used is the same as the external fluid 10 that is to say the fluorinated oil HFE with the same surfactant with a concentration between 0% and 0.5%. The working fluid 28 comprises carrier fluid 26, external fluid 10 and drops 4 of emulsion 6 spaced from each other along the flow conduit 48. The control unit 21 is adapted to circulate the fluid 28 in the circulation duct 46 downstream of the spacer zone 50. The control unit 21 imposes a fixed flow rate for the working fluid 28 by controlling the flow rates of the injection device 22 of the emulsion 6 and the injection device 24 of the carrier fluid 26. The control unit 21 also controls the flow rate of the injection device 32 of the separating fluid 33. For example, the control unit 21 is adapted to vary the flow rate of the injection device 32 of the separating fluid 33 according to the presence or not of a drop 6 detected by the sensor 36 in the spacing zone. The sensor 36 is able to detect the passage of successive drops 4 of the emulsion 6 in the spacing zone 50. In addition, the sensor 36 is capable of making a measurement within the drop 4. For example, the measurement is an optical measurement, such as a fluorescence measurement. The control unit 21 is able to store the information measured by the drop sensor 4 by drop 4. The measurement depends on the internal fluid 8 present in the drop 4. Advantageously, the measurement makes it possible to determine the nature or the concentration of the clean element 14 at each drop 4. The control unit 21 is able to trigger the injection of fluid separator according to the measurement of the sensor 36. The injection device 32 of the separating fluid 33 is able to inject the immiscible separating fluid 33 with the carrier fluid 26 into the injection zone 54 to separate the working fluid 28 into a plurality of successive pockets 35 comprising carrier fluid 26. Each pocket 35 is isolated from the next pocket 35 by a separator 80 consisting of separator fluid 33. The separating fluid 33 is immiscible with the carrier fluid 26. The separating fluid 33 is preferably a gas. In the example, the separating fluid 33 is air. The separator 80 is an air bubble. The diameter of each pocket 35 is greater than or equal to that of the circulation duct 46. The volume of each separator 80 is greater than twice the volume of a drop 4. The diameter of each separator 80 is greater than or equal to that of the circulation conduit 46. The diameter of each separator 80 is for example equal to the inside diameter The control unit 21 is able to circulate the pockets 35 and the separators 80, in the separation zone, towards the outlet 66 of the chip 20. The support 34 comprises at least one compartment 82 adapted to receive a pocket 35. For example, the support 34 is a petri dish. Advantageously, the support 34 has several compartments 82 separated from each other. For example, the support 34 is a 96-well plate, each well being a separate recovery compartment 82. Alternatively, the carrier 34 is a 24-well or 384-well plate or the like. The discharge tube 38 has an inlet 84 and an outlet 86 and an internal lumen 87 opening through the inlet 84 and the outlet 86. The internal lumen 87 extends in the extension of the circulation duct 46. The inlet 84 of the evacuation tube 38 is sealingly connected to the outlet 66 of the chip 20. The outlet 86 of the evacuation tube 38 is adapted to be placed facing the compartment 82, for the recovery of at least one pocket 35 comprising a drop 4 in the compartment 82. The discharge tube 38 is for example a teflon capillary having an internal diameter advantageously greater than 0.1 mm. The size of the evacuation tube 38 is adapted to the desired pocket size. The volume of the pockets 35 is greater than the volume of a drop of diameter equal to the inside diameter of the discharge tube 38, so as to facilitate their visualization by the output detector 40 and their deposit in the support 34. The output detector 40 is located downstream of the separation zone 56. Advantageously, the output detector 40 is able to successively detect each pocket 35 in the evacuation tube 38. Depending on the size of the drops, the output detector 40 is also advantageously able to detect the drops 4 in the discharge tube 38. The control unit 21 is able to control the displacement of the support 34. In the example, the displacement device 42 is a robotic stage. The displacement device 42 is able to move the support 34 relative to the discharge tube 38 and to the chip 20. For example, the plate is able to move the support 34 horizontally at a speed of between 0.5 mm. 1 and 45 mm. Advantageously, the control unit 21 is able to control the displacement device 42 as a function of each drop detection 4 by the sensor 36, so that a single pocket 35 comprising a drop 4 detected at the detection step is recovered. in each compartment 82 of the support 34. Alternatively or in addition, the control unit 21 controls the displacement device 42 according to the signals detected by the output detector 40. For example, the detection of the drops 4 or pockets 35 by the output detector 40 makes it possible to trigger the movement of the displacement device 42 in order to put a drop 4 by compartments 82. After each recovery, the displacement device 42 is adapted to place the outlet 86 of the discharge tube 38 facing a different compartment 82 after each movement of the support 34 relative to the chip 20. A drop recovery method 4 according to the invention will now be described. The first drop recovery system 1 is provided. The injection device 22 of the emulsion 6 is supplied with an emulsion 6 as previously described. The emulsion 6 of drops 4 is injected into the inlet zone 48 of the chip 20 by means of the injection device 22 of the emulsion 6. The emulsion 6 is circulated for example at a flow rate of 80 μL / h. The drops 4 of the emulsion 6 arrive one by one in the spacing zone 50 because of the convergent tip 70 of the inlet zone 48. The carrier fluid 26 is injected into the spacer zone 50 by means of the injection device 24 of the carrier fluid 26 to form a working fluid in the circulation duct. The carrier fluid 26 is circulated for example at a flow rate of 1 mL / h. Each drop 4 is spaced from the other drops 4 by carrier fluid 26. The distance between each drop 4 is, for example, greater than the internal diameter of the discharge tube 38. The distance between each drop 4 in the spacer zone 50 is sufficient to be able to inject separating fluid 33 between the drops 4 without disturbing the working fluid 28. The working fluid 28 is conveyed in the circulation duct 46. The drops 6 in the working fluid 28 are spaced and arranged along the circulation duct 46. The drops 6 of the working fluid 28 pass one by one in the measurement region 52. A step of detecting the passage of successive drops 6 in the measurement region 52 is implemented by the sensor 36. The sensor 36 measures information relating to the drop 6. For example, the measurement is a fluorescence measurement representative of the clean element 14 of the drop 6. The collected information is for example an enzymatic activity, a number of cells, a biomass or quantity of protein produced in the drop. The control unit 21 stores the number of the drop 6 and the measured information in order. The drops 6 of the working fluid 28 pass one by one into the injection zone 54. The control unit 21 triggers the injection of the separating fluid 33 as a function of the measurement of the sensor 36, so that there is a separator 80 between each drop 4. The separating fluid 33 is injected into the injection zone 54 by means of the separating fluid injection device 32. The separating fluid 33 separates the working fluid 28 into a plurality of successive pockets 35. The separating fluid 33 is injected between two successive drops 4 of the working fluid 28. The injection of separating fluid 33 allows the formation of pockets 35 and separators 80. Each separator 80 separates two successive pockets 35 of working fluid 28. It is immiscible with the pocket 35. The pockets 35 are working fluid cavities 28 separated by the separator 80. The pockets 35 comprise mainly carrier fluid 26. At least one pocket 35 preferably, more than 100% of the pockets 35 additionally contain one drop 4 of the emulsion 6. The volume of the pockets 35 is greater than the volume of a drop of diameter equal to the inside diameter of the evacuation tube 38. The injection rate of the separating fluid 33 by the separating fluid injection device 32 is adjusted by the control unit 21 so that each pocket 35 contains strictly less than two drops 4. For example, the adjustment is passive , the injection rate of the separating fluid 33 is constant. Some pockets 35 are empty of drops 4 of other pockets 35 comprise a drop 4 only. Advantageously, the injection flow rate of the separating fluid 33 by the separator fluid injection device 32 is adjusted in real time by the control unit 21 so that each pocket 35 contains exactly one drop 4 of the emulsion 6. For example, the detection of a drop 4 by the sensor 36, causes the control unit 21 to control the injection of a determined volume of separator fluid 33 enabling the formation of a pocket 35. This active mechanism ensures that each pocket formed is not empty and contains only one drop 4. The frequency of formation of the pockets 35 depends on the size of the drops 4. The greater the volume of the drops 4, the more the frequency of formation of the pockets 35 is slow. The formation of the pockets 35 is, for example, carried out at a frequency of between 0.5 pockets per second and 500 pockets per second. The pockets 35 are then conveyed into the evacuation tube 38. The pockets 35 and the separators 80 are conveyed in the separation zone 56, to the output 66 of the chip by the control unit 21, the circulation duct 46 having a larger and larger diameter. The flow rate of the fluids is preserved during this change of scale but the frequency of the drops 4 is changed. Thus, the frequency of circulation of the pockets 35 in the evacuation tube 38 is less than the flow frequency of the drops 4 at the outlet 66 of the spacing zone 50. This frequency decrease is proportional to the square of the ratio of the internal diameter of the discharge tube 38 on the diameter of the circulation duct 46. The pockets 35 and the separators 80 enter successively into the evacuation tube 38. The change of scale makes it possible to modify the frequency of circulation of the drops 4. For example, when there is a drop 4 per bag 35, the drops 4 in the evacuation tube 38 circulate at the circulation frequency of the bags 35. . For example, the dimensions are adapted so that if the drops 4 circulate at 100 drops per second in front of a point of the measurement region 52, they flow at 6 drops per second into the evacuation tube 38. Advantageously, the speed of circulation of the pockets 35 in the evacuation tube 38 is less than the maximum speed of displacement of the displacement device 42. Advantageously, each pocket 35 is detected by the output detector 40. In a variant, the drops 4 in the pockets are detected by the output detector 40. Then at least one pocket 35 comprising a drop 4 is recovered in a compartment 82 of the support 34. The pocket 35 is recovered in the compartment 82 placed under the outlet 86 of the discharge tube 38. The control unit 21 triggers the movement of the displacement device 42 as a function of the measurement of the output detector 40 so that each pocket 35 or drop 4 is recovered in a compartment 82 different from the support 34. Each drop 4 is drawn by the control unit 21. For example the drops 4 are detected at the sensor 36 and are numbered. Each drop 4 of the emulsion 6 is thus associated with both a measurement and the compartment 82 in which it has been recovered. In addition, the method comprises, after each recovery step, a step of relative displacement of the support 34 with respect to the chip 20, the outlet 86 of the discharge tube 38 being placed opposite a different compartment 82 after each displacement. of support 34. The displacement of the support 34 is controlled by the control unit 21 as a function of each drop detection 4, so that a single pocket 35 comprising a drop 4 detected in the detection step is recovered in each compartment 82 of the support 34 . A second recovery system 100 will be presented with reference to FIG. 3. The second recovery system differs from the first recovery system 1 in that it comprises an injection device 102 of a complementary solution 104 in at least one pocket 35. The complementary solution 104 is immiscible with the separating fluid 33. Moreover, the complementary solution 104 is advantageously miscible with the internal fluid 18 and immiscible with the carrier fluid 26. For example, the additional solution 104 added makes it possible to dilute the drop 4 of the emulsion 6. In a variant, the complementary solution 104 added comprises a marker facilitating the detection of the drop 4 within the bag 35 by the output detector 40 Alternatively, the added solution 104 added is a cell lysis reagent or a reagent for facilitating the cryopreservation of the internal fluid drop 4. The control unit 21 is able to control the injection device 102 of the complementary solution. 104. The method for recovering drops with the second recovery system 100 differs from the method previously described in that the method comprises a step of adding a complementary solution 104 in at least one pocket 35. For example, the same volume of solution complementary 104 is added in each pocket 35 by the injection device 102 of a complementary solution 104. Advantageously, the pocket 35 in which the complementary solution is added comprises a drop of emulsion 6 and the method additionally comprises a step of melting said drop of emulsion 6 with the added solution 104 added. The fusion is called passive. The low concentration of surfactant present in the carrier fluid 26 no longer makes it possible to stabilize the drops 6 of the coalescence. The drop of emulsion and the drop of complementary fluid being confined in the pocket 35 between two separators 80 have a high probability of contact. The invention which has just been described provides a more reliable and more accurate method of recovering drops 4 than existing methods, allowing individual follow-up of each drop 4. In effect, each drop 4 is recovered individually in a compartment 82 of FIG. support 34. Once the drops 4 recovered in the macroscopic support 34, it is possible to carry out analysis steps, chemical reactions or conventional biological reactions on the content of the drops 4. For example, if the drops 4 contain cells, the recovery system 1, 100 makes it possible to recover the drops 4 individually before culturing the cells separately. The recovery system 1, 100 makes it possible to recover individual drops 4 from a small quantity of drops 4 of an emulsion 6. For example, starting from 0.1 μl of emulsion 6 containing 10,000 drops per μl. , the recovery system 1, 100 can individually recover 1000 drops. In addition, each drop 4 is associated with a measurement signal. The recovery system 1, 100 makes it possible to have a link between the individual information of the drop 4 and the isolated drop 4. Each drop 4 analyzed is recoverable. The measurement made in the measurement region 52 is precise because the surface of the measurement region 52 is adapted to the volume of the drop 4. The passage in a macroscopic scale makes it possible to recover the contents of the drop 4 in a support 34 more easily manipulable. Finally the system 1, 100 is automatable. Indeed, the size of the pockets 35 facilitates the handling of the drops 4 and allows the use of various instruments for recovery and after recovery. The placement of a drop 4 in each pocket 35 allows in particular to manipulate a macroscopic object of significantly greater volume than that of an individual drop 4, which facilitates handling and guarantees the integrity of the drop 4. In a variant, the output 66 of the chip opens directly opposite a compartment 82 of the support 34 and the displacement device 42 is able to place the output 66 of the chip 20 opposite a different compartment 82 after each movement. of the support 34 with respect to the chip 20. In a variant, the drop recovery system comprises a device for preparing the emulsion 6 placed upstream of the inlet zone 48 of the chip 20. The flow rates are advantageously adjusted by the control unit 21 as a function of the maximum speed of displacement of the displacement device 42. In one example, the recovery system 1, 100 further comprises an incubation zone. Emulsion 6 comprises drops 4 comprising a cell or no cell. The method comprises culturing each recovered cell. The analysis of drops 4 before selection makes it possible, for example, to cultivate only those cells that can generate an interesting clone. In addition, it is not necessary to carry out several subcultures of clones before obtaining a monoclonal culture since the cell is already isolated before culturing. This avoids having to perform multiple limit dilutions. For example, in the case of the screening of bacteria synthesizing a compound of interest, the system makes it possible to associate the signal measured for each drop 4 containing a bacterium or a colony derived from a single cell to the compartment 84 in which the drop 4 has been recovered. Thus, the bacterium is cultured in a culture medium adapted according to the measured information. A third recovery system 110 will be presented with reference to FIG. 4. The third recovery system 110 differs from the recovery systems 1, 100 previously described in that the injection of the emulsion 6 into the chip 20 is provided by a lower part of the chip 20. As shown in Figure 4, the chip 20 comprises an upper block 112 and a lower block 114 defining between them the flow conduit 46. The chip 20 further comprises, in the input zone 48, a connection block of In the input area 48, the lower block 114 is sandwiched between the upper block 112 and the input connection block 116 in the elevation direction Z. For example, the upper block 112 and the connection block 116 is made of PDMS and the lower block 114 is made of glass. The input connection block 116 defines an input conduit 118 extending in the elevation direction Z. In the entry zone 48, the lower block 114 is pierced with an inlet orifice 120. The inlet orifice 120 passes through the entire thickness of the lower block 114 and opens out through the upper face of the lower block 114 into the circulation duct 46 and the lower face of the lower block 114 in the inlet duct 118. The inlet duct 118 is aligned with the inlet port 120. For example, the inlet duct 118 is centered with respect to the inlet port 120. The diameter of the inlet orifice 120 is greater than the diameter of the inlet duct 118. For example, the diameter of the inlet duct 118 is 750 micrometers (μm) and the diameter of the inlet orifice 120 is 1.4 mm. The inlet duct 118 opens downstream into the inlet orifice 120 and upstream through the first inlet 60 into an injection tube 122 connected to the injection device 22 of the emulsion. The method of recovering the drops 4 with the third recovery system 110 differs from the recovery methods previously described in that the injection of the emulsion 6 is facilitated. Indeed, the flow of drops 4 passes directly from the injection tube 122 to the inlet conduit 118, then through the inlet port 120 before arriving in the flow conduit 46 without encountering obstacles. The apparent light is continuous and of increasing diameter in the direction of circulation of the emulsion 6, the injection tube 122 to the inlet duct 118 and the inlet duct 118 to the inlet orifice 120. prevents blockages of drops 4 in connection blind spots. In this third recovery system 110, during the transfer of the emulsion 6 into the chip 20, drop losses 4 are limited. The injection provided in the third recovery system 110 is particularly advantageous for the emulsions 6 comprising an internal fluid 8 less dense than the external fluid 10. Indeed, if the elevation direction Z is vertical, the buoyancy of Archimedes favors the rising drops 4 in the direction of elevation Z in the inlet duct 118. A fourth recovery system 130 will be presented with reference to FIG. 5. The fourth recovery system 130 differs from the recovery systems 1, 100, 110 previously described in that the outlet of the pockets 35 and the separators 80 of the chip 20 is provided on an upper part of the chip 20. As shown in FIG. 5, the chip 20 comprises an upper block 132 and a lower block 134 defining between them the circulation conduit 46. The chip 20 further comprises, at the output 66 of the chip, a block of output connection 136. At the output 66, the upper block 132 is sandwiched between the lower block 134 and the input connection block 136 in the elevation direction Z. The upper block 132 defines an outlet duct 138. The outlet duct 138 extends in the elevation direction Z, perpendicularly to the circulation duct 46. The outlet duct 138 opens out through the outlet 66 into the internal lumen 87 of the discharge tube 38. The diameter of the outlet duct 138 is smaller than the internal diameter of the discharge tube 38. The connection block 136 defines an orifice 140 of greater diameter than the diameter of the outlet duct 138. The diameter of the orifice 140 is substantially equal to the external diameter of the evacuation tube 38. In one example, the discharge tube 38 has an inner diameter of 750 micrometers and an outer diameter of 1.6 mm, the outlet conduit 138 has a diameter of 500 micrometers and the orifice 140 has a diameter of 1.6 mm. The evacuation tube 38 is introduced into the orifice 140 of the connection block 136 so that the lumen of the outlet duct 138 and the internal lumen 87 of the evacuation tube 38 are continuous. The upstream end 142 of the evacuation tube 38 is in contact with the upper face of the upper block 132. The method of recovering the drops 4 with the fourth recovery system 130 differs from the methods previously described in that the transfer of the pockets and separators 80 from the chip 20 to the discharge tube 38 is facilitated. Indeed, the flow of pockets 35 and separator 80 passes directly from the flow conduit 46 to the outlet conduit 138, then into the lumen 87 of the discharge tube 38 without encountering obstacles. The pockets 35 circulate in conduits 138, 87 whose diameter increases from the chip 20 to the discharge tube 38 in the direction of flow of the drops 4 contained in the pockets 35 and separator 80. In addition, because of the direction of the outlet duct 138, the drops 4 are not stuck in a blind spot at the time of the change of scale. This makes it possible to prevent blockages of drops or separator in blind angles of connection. The output of the chip 20 provided in this fourth recovery system 130 is particularly advantageous when the carrier fluid 26 is less dense than the separator fluid 33. In fact, if the elevation direction Z is vertical, the buoyancy pushes the mounting drops 4 in the direction of elevation Z in the outlet duct 138 and in the inner lumen 87. A fifth recovery system 150 will be presented with reference to FIGS. 6 to 9. The fifth recovery system 150 differs from the recovery systems 1, 100, 110, 130, previously described in that the system 150 comprises a distribution device 152 pockets 35. The bag dispensing device 152 comprises the discharge tube 38, a circulation device 154 of a plurality of successive pockets 35, each pocket 35 being isolated from the next pocket 35 by a separator 80 consisting of separating fluid 33 in the internal lumen 87 of the evacuation tube 38. The pocket dispensing device 152 further comprises a nozzle 156 adapted to receive the discharge tube 38 and a blowing unit 158. The circulation device 154 is able to control the flow rate of the pockets 35 in the internal lumen 87 of the evacuation tube 38. For example, the circulation device 154 is controlled by the control unit 121. The dispensing device put into circulation 154 controls the injection device 22 of the emulsion 6, the device 24 for injecting carrier fluid 26 and / or the device 32 for injecting the separating fluid 33 into the chip 20 so that the pockets 35 circulate in the internal lumen 87 at a flow rate of between 100 μl / h and 5 ml / h and advantageously at a flow rate of 2 ml / h. The discharge tube 38 has a main portion 160 and an outlet portion 162 connected by a narrowing zone 164. The internal lumen 87 of the evacuation tube 38 opens onto an open mouth 166 in the outlet portion 162. The main portion 160 extends from the upstream end 142 of the discharge tube 38, for example disposed at the outlet of the chip 66 to the narrowing zone 164. The outlet portion 162 extends from the narrowing zone 64 at the open mouth 166 located at the downstream end of the evacuation tube 38. The outer diameter of the outlet portion 162 of the evacuation tube 38 is smaller than the outside diameter of the main portion 160 of the evacuation tube 38. For example, the outer diameter of the outlet portion 162 is substantially equal to the inside diameter of the main portion 160. For example, the main portion 160 has an outer diameter of 1.6 mm and an internal diameter of 0.75 mm, and the outlet portion 162 has an outer diameter of 0.75 mm and an internal diameter of 0.3 mm. . In addition, the recovery device 152 advantageously comprises an additional injection fluid injection device 168. The additional separator fluid injection device 168 is adapted to add separating fluid 33 in at least one separator 80 circulating in the main portion 160 of the evacuation tube 38. The additional separator fluid injection device 168 is suitable for add more than 2 cm of separating fluid between the pockets 35. The tip 156 is for example a glass tube. The end piece 156 is extended in the elevation direction Z. The end piece 156 has a through passage 170 in which the outlet portion 162 of the discharge tube 38 is disposed. The end piece 156 comprises a cylindrical upper portion 172 and a hollow lower portion 174 having a frustoconical or curved section. The through passage 170 is extended in the direction of elevation Z and opens into the lower portion 174 through an orifice delimited by a collar 176. The diameter of the orifice delimited by the collar 176 of the nozzle 156 is slightly greater than the external diameter of the outlet portion 162 of the tube 38. The internal diameter of the upper portion 172 is greater than the external diameter of the outlet portion 162 of the evacuation tube 38. The lower portion 174 of the nozzle 156 advantageously has a beveled shape at 45 °. The discharge tube 38 is placed in the through passage 170 of the nozzle 156 so that the discharge tube 38 protrudes out of the nozzle 156. The mouth 166 is out of the nozzle 156. By For example, the mouth 166 of the evacuation tube 38 is at a distance from the neck 176 of the nozzle 156 of between 1 mm and 10 mm. The outer wall 164 of the evacuation tube 38 bears on the collar 176 of the nozzle 156 at the outlet of the through passage 170. The blowing unit 158 is able to inject a stream of air into the through passage 170 so that a portion of the air runs along the outer wall 164 of the evacuation tube 38, to the mouth 166 of the evacuation tube 38. For example, the blowing unit 158 comprises a tube Injection injection 3 m long and 150 μm internal diameter and the injection pressure at the inlet of the injection tube is between 500 mbar and 1600 mbar. The bag distribution device 152 comprises a control unit 180 able to control the blowing unit 158 so that it injects air into the through passage 170 at a flow rate of between 1 pL / h and 2. mL / h and advantageously at a flow rate of 500 μl / h. In addition, the control unit 180 controls the bag circulation device 154. A pouch distribution method will now be described. A dispensing device 152 as previously described is provided. Pockets 35 and separators 80 are circulated in the inner lumen 87 by the circulation device 154. In one example, additional separating fluid is injected into the separators 80 by the injection device 168. Air is injected into the through passage 170 of the nozzle 156 by the blowing unit 158. The air flow rate and the flow rate of the pockets 35 are adjusted by the control unit 180 so that each pocket 35 detaches successively from the mouth 166 of the evacuation tube 38. This device improves the distribution of drops. FIG. 7 shows the ejection of a pocket 35. Part of the carrier fluid 26 of the pocket 26 adheres to the outer wall 164 of the evacuation tube 138 by capillarity. The flow of air along the outer wall 164 of the discharge tube 38 makes it possible to unhook the bag 35. The injection of air by the blowing unit 158 through the nozzle 156 makes it possible to eject the bag 35 discharge tube 38 before the arrival of the next bag 35 while preventing the pocket 35 remains attached to the mouth 166 Figures 8 and 9 show distribution results obtained for different experimental conditions. The recovery medium 34 is a sheet of paper. These results were obtained with a flow of pockets in the evacuation tube 38 maintained at three pockets per second by the control unit 180. In the example of FIG. 8, the pockets 35 were recovered on the support 34 under fragmentation conditions. The pockets 35 are recovered one by one on the support 34. Each pocket is ejected from the outlet before the arrival of the next pocket 35. However, some pockets 35 fragment upon ejection. An airflow greater than 1.6 bar results in fragmentation of the individual pockets recovered. Each task 182 formed on the support 34 comes only from a pocket 35. The same pocket 35 which has fragmented during the ejection forms a group 186 of small visible spots on the support 34. Some pockets 35 do not fragment and form a wider spot 184. In a second example of distribution shown in FIG. 9, the flow rates are adjusted so that the pockets 35 retain their integral volume during the ejection. The individual pockets are dispensed without fragmentation. The spots 184 obtained on the support 34 have substantially the same diameter. The adjustment of the parameters makes it easier to extract and locate the pockets 35 on the support 34.
权利要求:
Claims (15) [1" id="c-fr-0001] 1Drop recovery method (4), comprising the following steps: - supplying a chip (20) comprising a fluid circulation conduit (46) defining successively in a fluid flow direction, an inlet zone ( 48), a spacer zone (50), an injection zone (54) and a separation zone (56), - an injection of an emulsion (6) of drops (4) of an internal fluid (8). ) dispersed in an external fluid (10), in the inlet zone (48), - injecting at least one carrier fluid (26) miscible with the external fluid (10) in the spacing zone (50), for forming in the circulation conduit (46) a working fluid (28) comprising carrier fluid (26) and drops (4) of the emulsion (6) spaced from each other along the conduit (46), conveying the working fluid (28) in the circulation duct (46), characterized in that the method comprises the following steps: injection of a fluid a separator (33) immiscible with the carrier fluid (26) in the injection zone, for separating the working fluid (28) into a plurality of successive pockets (35) comprising carrier fluid (26), each pocket ( 35) being isolated from the next pocket (35) by a separator (80) consisting of separating fluid (33), - conveying the pockets (35) and separators (80), in the separation zone (56), to a output (66) of the chip (20), - recovery in a compartment (82) of a recovery medium (34) of at least one bag (35) comprising a drop (4) recovered after the conveying. [2" id="c-fr-0002] The method of claim 1, wherein the circulation conduit (46) is wider in the separation zone (56) than in the spacer zone (50). [3" id="c-fr-0003] 3. - Method according to any one of claims 1 or 2, wherein each pocket (35) comprises carrier fluid (26) and strictly less than two drops (4). [4" id="c-fr-0004] 4, - Method according to any one of the preceding claims, wherein the outlet (66) of the chip (20) opens into a discharge tube (38) having an outlet (86). [5" id="c-fr-0005] 5. - Method according to claim 4, wherein the support (34) comprises several compartments (82) separated from each other, and the method comprises, after each recovery step, a step of relative movement of the support (34) by relative to the chip (20), the outlet (86) of the discharge tube (38) being placed opposite a different compartment (82) after each movement of the support (34). [6" id="c-fr-0006] 6. - Method according to any one of the preceding claims, comprising a step of detecting the passage of successive drops (4) or a detection of the passage of successive pockets (35). [7" id="c-fr-0007] 7. - Method according to claims 5 and 6, taken together wherein, the displacement of the support (34) is controlled according to each detection of drops (4) or each pocket detection (35), for a single pocket (35) comprising a drop (4) detected at the detection step is recovered in each compartment (82) of the support (34). [8" id="c-fr-0008] 8. - Method according to any one of claims 6 or 7, wherein the detection of a drop (4) controls the injection of a separating fluid volume (33) and the formation of a pocket (35) . [9" id="c-fr-0009] 9. - Method according to any one of the preceding claims, comprising a pocket detection step (35) in a detection zone downstream of the separation zone (56). [10" id="c-fr-0010] 10. - Method according to any one of the preceding claims, comprising a step of adding a complementary solution (104) in at least one bag (35). [11" id="c-fr-0011] 11. - The method of claim 10, wherein the bag (35) in which the complementary solution (104) is added comprises a drop (4) of emulsion (6) and the method comprises a step of melting said drop ( 4) emulsion (6) with the added solution (104) added. [12" id="c-fr-0012] 12. A system for recovering drops (1, 100, 110, 130, 150), comprising: a chip (20) comprising a fluid circulation duct (46) defining successively in the direction of flow of the fluids, a zone of inlet (48), a spacer zone (50), an injection zone (54) and a separation zone (56), - a device (22) for injecting an emulsion (6) with drops ( 4) an internal fluid (8) dispersed in an external fluid (10), in the inlet zone (48), - a device (24) for injecting at least one carrier fluid (26) miscible with the external fluid (10) in the spacer zone (50) to form a working fluid (28) in the circulation conduit (46) comprising carrier fluid (26) and drops of the emulsion (6) spaced from each other along the conduit (46), - a device (32) for injecting a separating fluid (33) immiscible with the carrier fluid (26) in the injection zone (54), for to separate the working fluid (28) in a plurality of successive pockets (35) comprising carrier fluid (26), each pocket (35) being isolated from the next pocket (35) by a separator (80) consisting of separating fluid (33). ), and - a control unit (21) adapted to circulate the working fluid (28) in the circulation duct (46), and to convey the pockets (35) and the separators (80), in the zone of separation (56), to an output (66) of the chip (20), - a recovery medium (34), the support (34) comprising at least one compartment (82), for the recovery of at least one pocket (35) comprising a drop (4) in the compartment (82). [13" id="c-fr-0013] 13. - A drop recovery system (1, 100, 110, 130, 150) according to claim 12, wherein the outlet (66) of the chip (20) opens into a discharge tube (38) having an outlet (86), the carrier (34) having a plurality of compartments (82) separated from each other, and the system comprises a relative displacement device (42) of the carrier (34) relative to the chip (20), after each recovery , the displacement device (42) being adapted to place the outlet (86) of the evacuation tube (38) facing a different compartment (82) after each movement of the support (34) relative to the chip (20). ). [14" id="c-fr-0014] 14. - A drop recovery system (1, 100, 110, 130, 150) according to claim 13, comprising a sensor (36) adapted to detect the passage of successive drops (4) in the spacing zone (50). , the displacement device (42) being controlled according to each detection of drops (4), so that a single pocket (35) comprising a drop (4) detected in the detection step is recovered in each compartment (82). ) of the support (34). [15" id="c-fr-0015] 15. - A drop recovery system (1, 100, 110, 130, 150) according to claim 12 to 14, wherein the outlet (66) of the chip (20) opens into an evacuation tube (38), the discharge tube (38) defines an internal lumen (87) opening into an open mouth (166), the discharge tube (38) comprising an outer wall (164) and the system (1, 100, 110, 130 , 150) comprises a tip (156) having a through passage (170), the discharge tube (38) being located in the through passage (170) and the system (1, 100, 110, 130, 150) includes a blowing unit (158) for injecting a flow of air into the through passage (170) so that a portion of the air runs along the outer wall (164) of the discharge tube (38), until at the mouth (166) of the discharge tube (38).
类似技术:
公开号 | 公开日 | 专利标题 EP3319728B1|2020-03-18|Droplet recuperation method and associated droplet recuperation system JP2021041402A|2021-03-18|Systems and methods US9926521B2|2018-03-27|Microfluidic particle-analysis systems US7312085B2|2007-12-25|Microfluidic particle-analysis systems WO2005071097A1|2005-08-04|Device for dispensing microfluidic droplets, particularly for cytometry CN103718041A|2014-04-09|Microchip-based apparatus for examining platelet composite functions JP2008005749A|2008-01-17|Chip for cell separation and method for culturing cell using the same CN102395889B|2014-02-26|Sample solution introduction kit and sample solution injector CN106660042A|2017-05-10|Microfluidic device CA2791565A1|2011-09-09|Multi-reactor unit for dynamic cell culture EP3519092A1|2019-08-07|Microfluidic method for handling microdrops EP3565668A1|2019-11-13|Drop recovery system and associated method EP3728556A1|2020-10-28|Microfluidic chip, microfluidic lab-on-a-chip, method for producing such a chip and analysis method EP3077500A1|2016-10-12|Facility for coupling a bioreactor with a device for physicochemically analysing or collecting samples FR3075817A1|2019-06-28|MICRO-FLUIDIC CHIP AND LABORATORY ON MICRO-FLUIDIC CHIP EP3443322B1|2020-01-01|Method and system for the recovery of products from an emulsion EP3766581B1|2021-12-22|Micro-fluidic system including an amplification reaction chamber EP3698871A1|2020-08-26|Laser based sorting of droplets in microfluidic streams CN112236218A|2021-01-15|System and method for continuous flow emulsion processing FR3075823A1|2019-06-28|METHOD OF ANALYZING A CELLULAR SAMPLE USING A MICRO-FLUIDIC CHIP LABORATORY
同族专利:
公开号 | 公开日 EP3319728A1|2018-05-16| EP3319728B1|2020-03-18| FR3038530B1|2017-08-18| US20180193829A1|2018-07-12| WO2017005872A1|2017-01-12|
引用文献:
公开号 | 申请日 | 公开日 | 申请人 | 专利标题 US20110053798A1|2009-09-02|2011-03-03|Quantalife, Inc.|System for mixing fluids by coalescence of multiple emulsions| EP2436444A1|2010-10-01|2012-04-04|Centre National de la Recherche Scientifique |Microfluidic device for production and collection of droplets of a fluid| US7138254B2|1999-08-02|2006-11-21|Ge Healthcare Corp.|Methods and apparatus for performing submicroliter reactions with nucleic acids or proteins| US10222391B2|2011-12-07|2019-03-05|The Johns Hopkins University|System and method for screening a library of samples|US10544413B2|2017-05-18|2020-01-28|10X Genomics, Inc.|Methods and systems for sorting droplets and beads| US10357771B2|2017-08-22|2019-07-23|10X Genomics, Inc.|Method of producing emulsions| EP3953035A1|2019-04-08|2022-02-16|Withings|System and apparatus for injecting droplets in a microfluidic system|
法律状态:
2016-05-23| PLFP| Fee payment|Year of fee payment: 2 | 2017-01-13| PLSC| Search report ready|Effective date: 20170113 | 2017-07-28| PLFP| Fee payment|Year of fee payment: 3 | 2018-05-02| PLFP| Fee payment|Year of fee payment: 4 | 2020-07-27| PLFP| Fee payment|Year of fee payment: 6 |
优先权:
[返回顶部]
申请号 | 申请日 | 专利标题 FR1556424A|FR3038530B1|2015-07-07|2015-07-07|DROP RECOVERY METHOD AND ASSOCIATED DROUGHT RECOVERY SYSTEM|FR1556424A| FR3038530B1|2015-07-07|2015-07-07|DROP RECOVERY METHOD AND ASSOCIATED DROUGHT RECOVERY SYSTEM| US15/741,885| US20180193829A1|2015-07-07|2016-07-07|Droplet recuperation method and associated droplet recuperation system| EP16741562.9A| EP3319728B1|2015-07-07|2016-07-07|Droplet recuperation method and associated droplet recuperation system| PCT/EP2016/066180| WO2017005872A1|2015-07-07|2016-07-07|Droplet recuperation method and associated droplet recuperation system| 相关专利
Sulfonates, polymers, resist compositions and patterning process
Washing machine
Washing machine
Device for fixture finishing and tension adjusting of membrane
Structure for Equipping Band in a Plane Cathode Ray Tube
Process for preparation of 7 alpha-carboxyl 9, 11-epoxy steroids and intermediates useful therein an
国家/地区
|