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EP3950133A1 - Puce microfluidique et dispositif permettant de déterminer les propriétés physiques et/ou la nature chimique de particules microplastiques solides en suspension dans un échantillon liquide - Google Patents

Puce microfluidique et dispositif permettant de déterminer les propriétés physiques et/ou la nature chimique de particules microplastiques solides en suspension dans un échantillon liquide Download PDF

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Publication number
EP3950133A1
EP3950133A1 EP20305916.7A EP20305916A EP3950133A1 EP 3950133 A1 EP3950133 A1 EP 3950133A1 EP 20305916 A EP20305916 A EP 20305916A EP 3950133 A1 EP3950133 A1 EP 3950133A1
Authority
EP
European Patent Office
Prior art keywords
microfluidic chip
microplastic particles
chip
microfluidic
filter
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
EP20305916.7A
Other languages
German (de)
English (en)
Inventor
Ahmed AMR EWEIS ELSAYED
Mazen ERFAN SAYED AHMED
Frédéric Marty
Tarik Bourouina
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Centre National de la Recherche Scientifique CNRS
Universite Gustave Eiffel
Original Assignee
Chambre De Commerce Et D'industrie De Region Paris Ile De France (esiee Paris)
Centre National de la Recherche Scientifique CNRS
Universite Gustave Eiffel
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Chambre De Commerce Et D'industrie De Region Paris Ile De France (esiee Paris), Centre National de la Recherche Scientifique CNRS, Universite Gustave Eiffel filed Critical Chambre De Commerce Et D'industrie De Region Paris Ile De France (esiee Paris)
Priority to EP20305916.7A priority Critical patent/EP3950133A1/fr
Publication of EP3950133A1 publication Critical patent/EP3950133A1/fr
Pending legal-status Critical Current

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Classifications

    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L3/00—Containers or dishes for laboratory use, e.g. laboratory glassware; Droppers
    • B01L3/50—Containers for the purpose of retaining a material to be analysed, e.g. test tubes
    • B01L3/502—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures
    • B01L3/5027—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip
    • B01L3/502761—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip specially adapted for handling suspended solids or molecules independently from the bulk fluid flow, e.g. for trapping or sorting beads, for physically stretching molecules
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2200/00—Solutions for specific problems relating to chemical or physical laboratory apparatus
    • B01L2200/06—Fluid handling related problems
    • B01L2200/0647—Handling flowable solids, e.g. microscopic beads, cells, particles
    • B01L2200/0652—Sorting or classification of particles or molecules
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2200/00—Solutions for specific problems relating to chemical or physical laboratory apparatus
    • B01L2200/06—Fluid handling related problems
    • B01L2200/0647—Handling flowable solids, e.g. microscopic beads, cells, particles
    • B01L2200/0668—Trapping microscopic beads
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2300/00—Additional constructional details
    • B01L2300/06—Auxiliary integrated devices, integrated components
    • B01L2300/0681—Filter
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2300/00—Additional constructional details
    • B01L2300/08—Geometry, shape and general structure
    • B01L2300/0861—Configuration of multiple channels and/or chambers in a single devices
    • B01L2300/0864—Configuration of multiple channels and/or chambers in a single devices comprising only one inlet and multiple receiving wells, e.g. for separation, splitting
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2300/00—Additional constructional details
    • B01L2300/08—Geometry, shape and general structure
    • B01L2300/0861—Configuration of multiple channels and/or chambers in a single devices
    • B01L2300/0867—Multiple inlets and one sample wells, e.g. mixing, dilution
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2300/00—Additional constructional details
    • B01L2300/08—Geometry, shape and general structure
    • B01L2300/0861—Configuration of multiple channels and/or chambers in a single devices
    • B01L2300/0883—Serpentine channels
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2400/00—Moving or stopping fluids
    • B01L2400/08—Regulating or influencing the flow resistance
    • B01L2400/084—Passive control of flow resistance
    • B01L2400/086—Passive control of flow resistance using baffles or other fixed flow obstructions
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L3/00—Containers or dishes for laboratory use, e.g. laboratory glassware; Droppers
    • B01L3/50—Containers for the purpose of retaining a material to be analysed, e.g. test tubes
    • B01L3/502—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures
    • B01L3/5027—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip
    • B01L3/502769—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip characterised by multiphase flow arrangements
    • B01L3/502776—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip characterised by multiphase flow arrangements specially adapted for focusing or laminating flows

Definitions

  • the invention relates to a device for the determination of the physical properties and chemical nature of the microplastic particles suspended in a liquid sample.
  • microplastics There are still many uncertainties related to the low number of studies on microplastics present in the nature with a size of 10-50 microns or less, representing the detection limit of the most commonly used analytical equipment. Some experimental studies have revealed increasing concentrations of increasingly smaller microplastics. In addition, the toxicity of microplastics and the relative ease with which the number of particles crossing biological barriers is expected to increase as their size decreases. This raises new concerns about microplastics.
  • Detection, identification, and quantification of particulate matter (such as microplastics, in particular) contaminating drinking water is an exhaustive process using the methodologies currently employed in terms of time and cost. Commonly microscopy, or chromatography are used to study microplastics.
  • the integration of several techniques on-chip to achieve high-throughput analysis of drinking water has not been reported.
  • the invention does precise analysis of the particle physical properties, or it determines the chemical nature of the particles.
  • the invention allows automation, thus makes it cheap and its speed is optimized.
  • the invention presents a microfluidic chip used to determine the physical properties and/or the chemical nature of at least the microplastic particles suspended in a liquid sample, so as to distinguish the microplastic particles therein, the microplastic particles having a size smaller than 200 micrometers, the microfluidic chip comprising:
  • the stop area presents a surface inferior to 10 mm 2 , advantageously inferior to 1 mm 2 , advantageously inferior to 0.1 mm 2 [so as to concentrate the microplastic particles on a small surface for their analysis].
  • the stop area presents a surface inferior to 0.5 mm 2 .
  • the microfluidic chip comprises a sorter with:
  • the sorting chamber comprises series of filters to trap the microplastic particles already sorted, with different stop areas, so as to accumulate the sorted microplastic particles in the microfluidic chip according to their size.
  • each filter is spatially shifted with respect to each adjacent filter in the direction of the flow.
  • the filters comprise patterns, these patterns consisting of an array, or a line of elements engraved on-chip.
  • the microfluidic chip comprises the association of the alignment area and an analysis area that makes an analysis on-the-fly (real time or continuously) to determine the chemical nature of the microplastic particles during flow.
  • the alignment area allows the flow of the microplastic particles sequentially one behind another.
  • the alignment can be a cytometer or a serpentine part.
  • the invention relates to a microfluidic chip 1 and a device 2 comprising the microfluidic chip 1, which are used to determine the physical properties and/or the chemical nature of at least the microplastic particles 3 suspended in a liquid sample 4, whatever their shape.
  • the particles 3 may have a size smaller than 200 micrometers each.
  • the liquid sample 4 can be pre-concentrated before its passage in the microfluidic chip 1. It can be extracted from a drinking water bottle and comprises all the microplastic particles 3 contained in the drinking water bottle. For instance, for 1 mL, it can have tens to thousands of microplastic particles. Advantageously, it is thousands of microplastic particles per mL.
  • the microplastic particles 3 can be one of these types of plastics: PMMA, PS, PP, PE, PA, PVC, PTFE, PET, Nylon or others.
  • the device 2 comprises:
  • the pressure means can be for instance a syringe pump, a peristaltic pump or a vacuum pump.
  • Examples of « internal pressure means » can be also, for instance, the capillary suction force, which does not require any apparatus.
  • the spectroscopy means are mini or micro spectrometer.
  • the imaging means 6 can comprise an external digital camera, which can be a high-speed camera, to capture images of the microplastic particles 3 in the water sample 4 during their flow.
  • the device 2 ! a Raman spectroscopy or FTIR spectroscopy analysis on-the-fly (real time or continuously) to determine the chemical nature (plastic composition) of the microplastic particles 3 during flow.
  • spectroscopy means 5 and imaging means 6 can be on-chip or mounted on a separate external system.
  • spectroscopy means 5 and imaging means 6 can give some data and result graphic 7, as illustrated on figure 2d .
  • results can give a chemical or physical property with a spectrum, where the data can be extracted based on further analysis of this kind of graphic.
  • calculating means (not shown) linked to spectroscopy means 5 may be configured to count the number of microplastic particles 3 for each different plastic detected.
  • the present invention relates also to a measurement system comprising an imaging means 6, a spectrometer 10, the measurement system being a bench top or a miniaturized version for portable integration and the device 2, then, the acquired images and spectra will be analysed either using conventional signal processing or using artificial intelligence software based on machine and deep learning to count, classify and identify the measured microplastics with the help of set of data as a database.
  • the microfluidic chip 1 can be fabricated on a silicon-substrate, and top-sealed with a glass-substrate, or a PDMS patch, or any other optically transparent material in the visible or infrared ranges.
  • the microfluidic chip 1 can be replaced by a simpler cartridge designed as a simple reservoir 27 of small surface area for the purpose of facilitating the analysis using the spectroscopy means 5 and imaging means 6.
  • the cartridge can be fabricated either using the microfluidic technologies or using other conventional technologies and corresponding materials used for the fabrication of water filters, which includes plastic materials for instance.
  • the microfluidic chip 1 can be fabricated entirely using PDMS.
  • Microfluidic chip 1 with the alignment area 11 and the analysis area 12
  • the microfluidic chip 1 comprises, in a first microfluidic channel 13, an alignment area 11, and an analysis area 12 downstream the alignment area 11.
  • the alignment area 11 and the analysis area 12 may be configured as follows:
  • the microfluidic chip 1 is implemented in a two-dimensional implementation manner where the focusing fluid 17 only surrounds the water sample 4 from the first microfluidic channel 13 sidewalls.
  • the microfluidic chip 1 is implemented in a three-dimensional implementation manner where the focusing fluid 17 encapsulates the water sample 4 from all sides in the first microfluidic channel 13.
  • Water flow rates can be in the order of microliters per minute (can reach milliliters per minute). Particles can range from a few units to tens of thousands of units per sample. Advantageously, there are thousands of microplastic particles per sample. Each particle can be presented for imaging or spectroscopic analysis during flow for a duration in the order of milliseconds.
  • the water sample comes from one liter of common water, the microplastic particles contained in the liter can be concentrated into a few milliliters to insert it into the chip.
  • the alignment area 11 can be a microflow cytometer.
  • the microfluidic chip 1 is structured to push the focusing fluid 17 with water sample 4 into the first microfluidic channel 13 being configured so that microplastic particles 3 flow at the analysis area 12 until an output 19.
  • the microfluidic chip 1 can be configured so that each microplastic particle 3 is imaged individually as it passes through the analysis area 12 or can be configured so that multiple microplastic particles 3 are imaged simultaneously as they pass through the analysis area 12.
  • the alignment area 11 comprises a serpentine part, to align the flow of single microplastic particle 3, flowing sequentially one behind another.
  • the analysis area 12 can comprise an objective lens for optical spectroscopic analysis, a high-speed camera, or other particle analysis instruments.
  • the microfluidic chip 1 as represented on figure 2a , comprises:
  • Water flow rates can be in the order of microliters per minute (can reach milliliters per minute). Particles can range from a few units to tens of thousands per sample. Sorting of particles is continuous as the water sample flows.
  • the microfluidic chip may comprise a sorter 20 with:
  • the stop area presents a surface inferior to 10 mm 2 , advantageously inferior to 1 mm 2 , advantageously inferior to 0.1 mm 2 , advantageously, inferior to 0.05 mm 2 , advantageously inferior to 0.01 mm 2 [so as to concentrate the microplastic particles on a small surface for their analysis].
  • the evacuation area 32 lets water flow without microplastic particles 3 until the output 19.
  • the sorting chamber comprises series of filters 23 to trap the microplastic particles 3 already sorted, with different stop areas 24, so as to accumulate the sorted microplastic particles 3 in the microfluidic chip 1 according to their size.
  • the sorter 20 comprises a sorting chamber 21 and an evacuation area 32.
  • the sorting chamber 21 comprises a separation area 22 and the filters 23 situated upstream the evacuation area 32.
  • the separation area 22 comprises patterns engraved and stop areas 24 created by the filters 23.
  • the filters 23 can comprise two patterns: first patterns situated downstream the separation area 22, the presentation area 22 having second patterns, second patterns having a gap superior to the gap of the first patterns, which can be in the order of few micrometers or tens of micrometers, for instance.
  • the gap determines the spatial distance between two elements engraved 25 on chip of the same patterns or filters 23.
  • the filters 23 comprise several elements engraved 25 on chip allowing the trapping of the microplastic particles 3 with different sizes according to the distance between two elements engraved 25 on chip.
  • the filters 23 can be on the separation area 22 and reservoirs 27.
  • the separation area 22 is an area for sorting the microplastic particles 3 which enter, the separation area 22 can be formed by an array of elements engraved 25 on chip, the distance between two elements engraved 25 on chip for the separation area 22 being superior to the distance between two elements engraved 25 for the filters 23 on reservoirs 27.
  • the sorting chamber 21 comprises a filter 23, as represented on figure 2a , or a series of filters 23, as illustrated on figure 11 .
  • the filters 23 with the first patterns can stop the microplastic particles 3 thanks to elements engraved 25 on-chip as represented on figure 7b , to let the water sample 4 exit without microplastic particles 3.
  • These patterns can have a period ranging from a fraction of a micron to tens of microns, with one row or more of elements.
  • the density can be in the range of tens to thousands of elements per 1 mm.
  • the filters 23 with the second patterns can stop parts of microplastic particles 3 according to their size and can let small particles 26 pass according to the periodicity/density of elements engraved 25 on chip.
  • the second patterns can create a stop area 24 for particles according to their size. These patterns have a lower density than the elements engraved 25 on-chip, where in this case they will be trapping bigger particles.
  • the gap of the patterns of the sorting section depends on the target particle size. For our application this gap can range from 25 to 250 micrometers.
  • the trapped microplastic particles 3 can be contained in different reservoirs 27 depending on the size of microplastic particles 3, as illustrated on figures 2b and 2c .
  • the first and/or second patterns can consist of an array, a line or elements engraved 25 and disposed according to a pattern of a line or array on-chip, as illustrated on figure 8d .
  • each filter 23 may be spatially shifted with respect to the adjacent filters 23, to enable optical spectroscopic analysis of the trapped microplastic particles 3, without having an interfering optical signal from adjacent filters 23.
  • the first and/or second patterns which trap the microplastic particles 3 can be chosen among the list: pillar-type, weir-type filter or cross-flow filters with obstacles of different shapes like circles, cylinders, squares, or rectangles.
  • Each reservoir 27 can have an output 19 after the filters 23, or each reservoir 27 can be connected to the same output 19.
  • An evacuation area 32 can be situated downstream each filter 23.
  • the first microfluidic channel 13 delivering the water sample 4 can be a single channel, a bifurcated-tree input as shown on figure 9a , or other inputs.
  • the sorting chamber 21 may comprise several reservoirs 27 with walls engraved 27a on the microfluidic chip 1 to guide the microplastic particles 3, each reservoir 27 having a filter 23 enabling the trapping and accumulation of the microplastic particles 3 on-chip, according to their size.
  • a possible structure of the sorter 20 can have only two reservoirs 27, one with a rotation for small particles 26 and the other one for big particles 28, as illustrated on figure 9b .
  • Each reservoir 27 can have a filter 23, which comprises the first patterns (i.e. with a high periodicity of elements engraved 25 on chip) and an output 19 to let the water sample 4 flow without microplastic particles 3.
  • the filters 23 in reservoirs 27 can be arranged differently.
  • a possible architecture has N lines (N being a number chosen by the builder) with walls 27a to form reservoirs 27 in the direction of the flow, a first reservoir 27 having a filter 23 on the first line, a second reservoir 27 has a filter 23 on the second line and so on until N lines, the filter 23 being arranged at different axial positions in regard to the flow in each reservoir 27.
  • a periodicity of several filters 23 at different axial positions can be realized. As shown figure 12a , one periodicity is realized with two different filters 23 which are in two lines and so on each set of two lines. As shown figure 13 , one periodicity is realized with three different filters 23 which are in three lines and so on each set of three lines.
  • a possible architecture for the filters 23 in the sorter 20 can be a succession of steps like a staircase, the filters 23 being offset axially and laterally one after the other, a filter 23 in a first reservoir 27 is lower laterally and further axially than the next filter in a second reservoir and so on, as represented on figure 12b .
  • the microfluidic chip 1 can have a structure such that the separation area 22 sorting the microplastic particles 3 by size, is connected fluidically upstream to several microfluidic channels 13 in parallel, each parallel microfluidic channel 13 being connected upstream to reservoirs 27 which each comprise a filter 23 to trap microplastic particles 3 and let the water sample 4 flow without microplastic particles 3, as illustrated on figure 4 .
  • Each parallel microfluidic channel 13 comprises an alignment area 11 and an analysis area 12.
  • the microfluidic chip 1 can comprise a passive sorter 20 using technique to separate microplastic particles 3 spatially on-chip in the separation area 22, chosen among the list:
  • the microfluidic chip 1 comprises an active sorter 20 using the same techniques mentioned below to separate microplastic particles 3 spatially on-chip in the separation area 22 chosen coupled with electrical / electromagnetic means to separate the microplastic particles 3.
  • the microfluidic chip 1 can be configured to comprise a second microfluidic channel 29 of a pinching fluid 30 which is connected to the first microfluidic channel 13 in front of the sorting chamber 21, the pinching fluid 30 flow F4 being opposite to the water sample 4 flow F3 (which can be F1+F2) in the first microfluidic channel 13 to sort the microplastic particles 3 in the sorting chamber 21.
  • the pinching fluid 30 is delivered by an input pinching fluid 31.
  • the microfluidic chip 1 can comprise an intermediary chamber between the first microfluidic channel 13 and the sorter 20 on-chip to regulate the flow rate of the water sample 4, the focusing fluid 17 and other fluids if needed for sorting the microplastic particles 3.
  • the flow rate of the focusing fluid is higher than the sample fluid.
  • the ratio between the focusing flow rate and sample flow rate is greater than 1. For instance, a typical value for the ratio is 5.
  • the microfluidic chip can comprise a single filter 23 connected fluidically to the first microfluidic channel 13 to trap and accumulate all microplastic particles on a stop area within the microfluidic chip no matter their size, with no need of a sorter 20 neither a sorting chamber 21 nor a separation area 22.
  • Microfluidic chip 1 which combines the sorter 20, the alignment area 11 and the analysis area 12
  • the microfluidic chip 1 comprises the sorter 20 on the one hand, the alignment area 11, and the analysis area 12 on the other hand.
  • the microfluidic chip 1 can have different structures depending on the combination of these three components: the sorter 20, the alignment area 11 and the analysis area 12.
  • the three components can be disposed in any order relative to each other, i.e.:
  • the analysis area 12 comprise spectroscopy means 5 to determinate the chemical nature of the microplastic particles and can allow to measure this chemical nature on-the-fly and in real time.
  • the chip can be used without the analysis area.
  • the reservoirs 27 can be transported with the microplastic particles 3 and then analysed.
  • microfluidic channel 13 Between the sorter 20 and the alignment area 11.
  • the alignment area 11 can comprise a serpentine part or a microflow cytometer.
  • the microfluidic chip 1 can comprise:
  • the microfluidic chip 1 can comprise an intermediary chamber between the first component and the second component to regulate the flow rate of the water sample 4 and other fluid which can be used, between the two first components which are the alignment area 11 and the sorter 20.

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Physics & Mathematics (AREA)
  • Fluid Mechanics (AREA)
  • Dispersion Chemistry (AREA)
  • Analytical Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Hematology (AREA)
  • Clinical Laboratory Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Investigating, Analyzing Materials By Fluorescence Or Luminescence (AREA)
EP20305916.7A 2020-08-07 2020-08-07 Puce microfluidique et dispositif permettant de déterminer les propriétés physiques et/ou la nature chimique de particules microplastiques solides en suspension dans un échantillon liquide Pending EP3950133A1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP20305916.7A EP3950133A1 (fr) 2020-08-07 2020-08-07 Puce microfluidique et dispositif permettant de déterminer les propriétés physiques et/ou la nature chimique de particules microplastiques solides en suspension dans un échantillon liquide

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP20305916.7A EP3950133A1 (fr) 2020-08-07 2020-08-07 Puce microfluidique et dispositif permettant de déterminer les propriétés physiques et/ou la nature chimique de particules microplastiques solides en suspension dans un échantillon liquide

Publications (1)

Publication Number Publication Date
EP3950133A1 true EP3950133A1 (fr) 2022-02-09

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN117554319A (zh) * 2023-10-20 2024-02-13 广东省水利水电科学研究院 一种微塑料丰度的检测方法、系统、装置及存储介质
CN118817658A (zh) * 2024-07-01 2024-10-22 武汉理工大学 一种海洋微塑料智能检测系统及方法

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20130337500A1 (en) * 2009-04-24 2013-12-19 National University Of Singapore System and method for isolation of cells
US20140087456A1 (en) * 2009-04-24 2014-03-27 National University Of Singapore Isolating Target Cells From A Biological Fluid
CN110320250A (zh) 2019-07-30 2019-10-11 大连海事大学 一种电容式海洋微塑料检测装置

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20130337500A1 (en) * 2009-04-24 2013-12-19 National University Of Singapore System and method for isolation of cells
US20140087456A1 (en) * 2009-04-24 2014-03-27 National University Of Singapore Isolating Target Cells From A Biological Fluid
CN110320250A (zh) 2019-07-30 2019-10-11 大连海事大学 一种电容式海洋微塑料检测装置

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN117554319A (zh) * 2023-10-20 2024-02-13 广东省水利水电科学研究院 一种微塑料丰度的检测方法、系统、装置及存储介质
CN117554319B (zh) * 2023-10-20 2024-10-22 广东省水利水电科学研究院 一种微塑料丰度的检测方法、系统、装置及存储介质
CN118817658A (zh) * 2024-07-01 2024-10-22 武汉理工大学 一种海洋微塑料智能检测系统及方法

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