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
  • B01L3/502707—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 the manufacture of the container or its components
• • G—PHYSICS
  • G01—MEASURING; TESTING
  • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
  • G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
  • G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
  • G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
  • G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
  • G01N33/543—Immunoassay; Biospecific binding assay; Materials therefor with an insoluble carrier for immobilising immunochemicals
  • G01N33/544—Immunoassay; Biospecific binding assay; Materials therefor with an insoluble carrier for immobilising immunochemicals the carrier being organic
  • G01N33/545—Synthetic resin
• • G—PHYSICS
  • G01—MEASURING; TESTING
  • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
  • G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
  • G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
  • G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
  • G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
  • G01N33/543—Immunoassay; Biospecific binding assay; Materials therefor with an insoluble carrier for immobilising immunochemicals
  • G01N33/551—Immunoassay; Biospecific binding assay; Materials therefor with an insoluble carrier for immobilising immunochemicals the carrier being inorganic
  • G01N33/552—Glass or silica
• • 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
  • B01L2300/12—Specific details about materials
• • 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
  • B01L2300/16—Surface properties and coatings
• • 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
  • B01L2400/04—Moving fluids with specific forces or mechanical means
  • B01L2400/0403—Moving fluids with specific forces or mechanical means specific forces
  • B01L2400/0415—Moving fluids with specific forces or mechanical means specific forces electrical forces, e.g. electrokinetic

Definitions

• the present invention relates to a component for microsystem for biological or biochemical analysis, this component using a composite material. It also relates to a method for producing such a component.
• a microsystem for biological or biochemical analysis is produced from a support or substrate chosen so that a surface (which may consist of several zones) of this support or substrate provides one or more functions. It can be a chemical functionality or an electrical functionality.
• the supports are made of glass or silica, which allows the attachment of biological or biochemical elements by a well controlled coupling chemistry, for example by silanization.
• Fluid circulation microsystems generally use electrokinetic pumps, such as electro-osmosis, to circulate fluids in micro-channels and micro-reservoirs made in the supports. These pumping modes impose the existence of electrically active surfaces. It is the use of high electric fields, combined with the presence of electrically active surfaces, which allows fluid flow.
• electrokinetic pumps such as electro-osmosis
• Glass or silicon supports are therefore very suitable for obtaining chemical and electrical functionalities.
• inert materials such as polymers, plastics, glues
• the chemistry for attaching biological or biochemical elements to these inert materials depends on their chemical formulation and remains difficult to implement.
• Materials such as molded plastics for making micro-channels, polymers or photosensitive resins for making microstructures would be very widely used since it would be possible to easily attach biological or biochemical elements to them. Indeed, these materials are low cost and can be used in large series.
• electrokinetic flows are problematic in materials such as conventional polymers and require the use of heavy techniques such as plasma activation in order to generate surfaces. electrically charged. However, it has been shown that this does not permanently activate the treated surface. The system therefore evolves over time.
• the present invention provides a solution to the problems set out above. It allows the use of chemically inert materials (polymers, resins, plastics, adhesives, etc.) to make supports for components for microsystems of biological or biochemical analysis, these inert materials being used in combination with a material functionalizable to allow the attachment of biological or biochemical elements.
• the biological or biochemical elements can then be grafted by conventional techniques, for example by a silanization technique.
• the biologically or biochemically functionalizable material is incorporated directly into the inert material (plastic, glue) to obtain a composite material.
• the inert material plastic, glue
• Several solutions can be envisaged to obtain this composite material.
• One solution is to make a mixture of two liquid phases which, after several technological steps, are frozen in the form of a composite material.
• One of the phases (for example synthetic silica) makes it possible to ensure functionalization by a bonding chemistry identical to that carried out on a glass substrate (for example silanization).
• Another solution consists in mixing, either directly with a plastic constituting the inert material, or with a photosensitive polymer or not, elements (preferably beads) made of silica, glass, metal or functionalizable polymer.
• elements preferably beads
• the beads ensure the attachment of biological or biochemical elements and also have the advantage of increasing the attachment surface for biological or biochemical elements.
• the composite material obtained makes it possible to produce components structured by methods used in microtechnology. Functionalization also takes place either on the phase dispersed in the photosensitive material, or on elements included in this material.
• the deposited material can also be a material providing electrical functionality to the component, which allows the circulation of fluids by electrokinetic pumping.
• the subject of the invention is therefore a component for a biological or biochemical analysis microsystem formed from a support and having at least one surface area chemically functionalized, to allow the formation of a chemistry for the attachment of elements.
• biological or biochemical, and / or electrically to allow the formation of electric charges therein
• the support comprises at least one part made of composite material, the composite material being a mixture of at least one inert material and at least one chemically and / or electrically functionalizable material for providing said functionalized surface area.
• the inert material of the composite material is a material chosen from a polymer, a plastic, a resin and an adhesive.
• the polymer can be a polyimide, a poly (dimethylsiloxane) or a photosensitive resin of the epoxy type.
• Said part can form the support in its entirety.
• the support may comprise a substrate supporting said part.
• the substrate can be made of a material chosen from glass, silica, silicon, a polymer and a metal.
• the functionalizable material is chosen from silica, synthesized silica, silicon nitride, a metal and a functionalizable polymer.
• the composite material can be a mixture comprising a phase of inert material and a phase of functionalizable material.
• the functionalizable material can be in the form of beads.
• Said surface area can support chemical functions capable of ensuring the attachment of biological elements or other chemical functions to said surface area.
• Said surface area can support chemical functions capable of ensuring the presence of electrical charges on said surface area.
• the subject of the invention is also a method of producing a component for a microsystem for biological or biochemical analysis from a support, the support having to present at least one surface area chemically functionalized to allow the formation of a chemistry for attaching biological or biochemical elements, and / or electrically, to allow the formation of electrical charges therein, characterized in that it comprises the production of a support comprising at least one part made of composite material, the composite material being a mixture of at least one inert material and at least one chemically and / or electrically functionalizable material to provide said functionalized surface area.
• the composite material can be obtained by mixing in liquid phases the inert material and the functionalizable material, the mixture then being solidified to provide said part in composite material.
• the composite material can be obtained by dispersing elements of functionalizable material in the inert material in the liquid phase, the mixture then being solidified to provide said part in composite material.
• said elements made of functionalizable material are in the form of balls.
• the inert liquid phase material in which said elements are dispersed can be poured onto a support with imprint (s) before being solidified.
• the impression support (s) can be removed after the mixture has solidified.
• the inert liquid phase material in which said elements are dispersed can be deposited on a support before being solidified. If the inert material is a photosensitive material, said part made of composite material can be, after solidification, structured by photo-lithography. If the deposit is made on a surface of the support having at least one imprint, the composite material can be, after solidification, removed from the imprint. If the inert material is a photosensitive material, the removal of the composite material from the imprint can be done by photo-lithography.
• the support having a face with at least one imprint
• elements of functionalizable material are deposited at the bottom of the imprint, then the inert material in liquid phase is poured onto said face of the support, then the inert material is solidified to provide the composite material at the bottom of the imprint, the support being finally removed.
• said elements made of functionalizable material are in the form of balls. Whatever the mode of implementation, solidification can be obtained by heat treatment.
• FIGS. 1A and 1B are sectional views illustrating the production of a first component for a biological or biochemical analysis microsystem according to the invention
• FIGS. 2A and 2B are sectional views illustrating the production of a second component for a biological or biochemical analysis microsystem according to the invention
• FIG. 3A and 3B are sectional views illustrating the production of a third component for a biological or biochemical analysis microsystem according to the invention
• FIG. 4A to 4C are sectional views illustrating the production of a fourth component for microsystem for biological or biochemical analysis according to the invention.
• FIGS. 1A and 1B illustrate the production of a component for a biological or biochemical analysis microsystem using an imprint support.
• FIG. 1A shows a support 10, for example made of silicon, the upper face of which has been machined or engraved to form an imprint consisting of a depression 11 extended by trenches 12.
• liquid composite material e.g. poly (dimethylsiloxane)
• microbeads for example silica beads 1 ⁇ m in diameter
• the medium and its content are. then placed in an oven maintained at 60 ° C for 4 hours.
• the component 16 obtained is shown in FIG. 1B. It comprises a base 14 complementary to the depression 11 and walls 15 perpendicular to the base and complementary to the trenches 12. Two consecutive walls define a channel. The component obtained is ready to undergo chemical and / or electrical protocols allowing it to be functionalized.
• FIGS. 2A and 2B illustrate the production of a component for a microsystem for biological or biochemical analysis from a photosensitive composite material.
• Polymer or photosensitive resin patterns can be produced on flat substrates, which avoids the use of complex engraving machines. For example, the production of studs or channels in a glass or silicon slide is replaced by a simple photo-1ithography.
• the deep etching of the glass is delicate. It cannot be produced by plasma because of the blocking of the etching by the ionic and metallic impurities contained in the glass.
• the glass is therefore etched by isotropic chemistry, which prevents the production of fine patterns with low steps.
• the invention allows to realize such structures using a photosensitive composite material.
• FIG. 2A shows a silicon support 20 with a diameter of 100 mm, the upper face of which is covered with a layer of composite material 21.
• the composite material consists of a photosensitive polyimide sold under the name "Probimide 7510" in which microbeads are dispersed, for example silica beads 1 ⁇ m in diameter.
• the mixture is deposited with the spinner on the support 20 at a speed of 3000 revolutions / minute then annealed at 110 ° C. on a hot plate.
• the composite material is exposed by ultraviolet rays through a mask and then developed in order to obtain the desired component, for example that shown in FIG. 2B where trenches 22 are visible in the composite material 21.
• the composite material is annealed at 150 ° C on a hot plate, then at 300 ° C in a heat treatment oven.
• FIGS. 3A and 3B illustrate the production of a component for a biological or biochemical analysis microsystem for which the composite material is located in a channel.
• FIG. 3A shows a polymer support 30, one face of which has an imprint 31 produced by a conventional technique such as stamping, molding or laser ablation.
• a layer 32 of composite material is deposited on the face having an imprint by covering the walls of the imprint.
• the composite material consists of a photosensitive polyimide sold under the name "Probimide 7510" in which microbeads are dispersed, for example silica beads of 1 ⁇ m in diameter.
• the composite material is deposited by soaking and then annealed at 110 ° C on a heating plate.
• FIGS. 4A to 4C illustrate the production of a component for a biological or biochemical analysis microsystem where the composite material is obtained by depositing inert material on a bed of beads.
• FIG. 4A shows a support 40, for example a silicon support 100 mm in diameter, the upper face of which has been machined or engraved to form an imprint consisting of a series of parallel trenches 41. Trenches 41 are deposited at the bottom 42 silica beads 100 ⁇ m in diameter.
• an inert material 43 for example a poly (dimethylsiloxane)
• the inert material fills the trenches 41 and mixes with the balls 42 at the bottom of the trenches.
• the whole is placed in an oven at 60 ° C for 4 hours. After evacuation of the solvents contained in the polymer, the mold is removed.
• the component shown in Figure 4C consisting of a base 44 and walls 45, the top 46 of the walls being of composite material. The component is ready to undergo chemical protocols allowing it to be functionalized.
• a silanization treatment makes it possible to fix chemical functions on the surface of these materials which will subsequently ensure the attachment of biological elements or chemical functions.
• silanes can be used. Each has its own fixing protocol on the surface of the material to be functionalized. The choice of silane to use depends on the chemical function that you want to use either directly or for the subsequent carrying out of a chemical reaction or the fixation of a biological element. Among the most commonly used silanes, mention may be made of aminopropyltriethoxysilane, aminopropyldimethylethoxysilane, epoxy silane, 2- (hydroxyethyl) -3- aminopropyltriethoxysilane.
• silanization protocol used for aminopropyltriethoxysilane is as follows: treatment of the surface concerned with an oxygen plasma (Nextral 310) at 150 watts for 30 seconds to create silanol functions on the surface;
• Oligonucleotides synthesized with an aldehyde function can be fixed directly or via a glutaraldehyde if the oligonucleotides are synthesized with an NH 2 function.
• This silanization technique makes it possible to fix oligonucleotides, proteins or any biological or chemical element compatible with the functions present on the silane attached to the functionalized material (amino functions, aldehyde acid, activated ester, etc.).
• the material to be functionalized is a layer of gold, the fixing of thiols or of disulfurized compounds on the surface of this metallic layer.
• different thiols make it possible to obtain on the surface of the layer to functionalize the chemical functions necessary for the desired chemical reactions.
• electrical charges can be obtained on the surface of synthetic silica, silicon, silicon nitride and silicon oxide by grafting an aminopropyltriethoxysilane onto the layer to be functionalized according to the protocol presented above.
• a treatment in an acid medium (for example 0.2M HCl) makes it possible to protect the amino group of the silane and to obtain electrical charges on the surface of the functionalized material.

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• 2002
  • 2002-02-21 FR FR0202206A patent/FR2836072B1/fr not_active Expired - Fee Related
• 2003
  • 2003-02-20 WO PCT/FR2003/000567 patent/WO2003071277A1/fr active Application Filing
  • 2003-02-20 US US10/475,634 patent/US7214478B2/en not_active Expired - Fee Related
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