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
  • B01L3/02—Burettes; Pipettes
  • B01L3/0241—Drop counters; Drop formers
• • 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
  • B01L3/502784—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 droplet or plug flow, e.g. digital microfluidics
  • B01L3/502792—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 droplet or plug flow, e.g. digital microfluidics for moving individual droplets on a plate, e.g. by locally altering surface tension
• • 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
  • B01L2300/089—Virtual walls for guiding liquids
• • 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 method and a device for moving and dosing amounts of liquid on a microscopic scale with a
• Liquid drop is moved along a conventional surface, because even on very smooth surfaces, part of the liquid drop adheres to the surface.
• the object is achieved according to the invention by providing a method for microdosing liquid drops, in which the liquid drops are moved loss-free with an inhomogeneous electric field on a carrier with an ultraphobic surface.
• the invention relates to a method for moving or dosing liquid drops on a microscopic scale, characterized in that the
• An electrically charged tip or a wire is preferably used as the manipulator.
• a voltage of 100 to 1000 volts, preferably 400 to 600 volts, is applied between the manipulator and the carrier to generate the electric field.
• the tension can vary widely depending on the geometry of the arrangement.
• the invention also relates to a device for microdosing liquid drops which have at least one carrier with an ultraphobic surface, optionally at least one liquid reservoir, an electrically chargeable manipulator and a means for generating an inhomogeneous electric field.
• This manipulator can optionally also be an ultraphobic tip / wire or the like.
• a drop of liquid in the sense of the invention consists of any liquid and preferably has a volume of 10 "12 to 10 " 6 liters, particularly preferably 10 "9 to 10 " 6 liters. According to the invention, such a drop is moved losslessly with a displaceable electric field on an ultraphobic surface.
• a drop of liquid is preferably separated from a liquid reservoir by means of the electric field.
• Several drops of liquid can be combined and mixed on an ultraphobic surface using the electric field. All of these process steps can also be carried out in any combination with one another.
• the electric field is any between a tip, which preferably has a diameter of 0.01 to 1 mm Has length, has an ultraphobic surface, and a preferably metallic carrier. This tip is used to move liquid drops on the ultraphobic surface. Because the tip has an ultraphobic surface, no liquid components stick to the tip.
• the liquid reservoir has the
• Ultraphobic surfaces in the sense of the invention are characterized in that the contact angle of a drop of water lying on the surface is more than 150 ° and the roll angle does not exceed 10 °.
• the roll angle here is understood to be the angle of inclination of a fundamentally planar but structured surface against the horizontal, at which a standing water drop of volume 10 ⁇ l is moved due to gravity when the surface is inclined.
• Such an ultraphobic surface is described in international patent application WO 99/10322.
• a hydrophobic material in the sense of the invention is a material that has a contact angle, based on water, of greater than 90 ° on a flat, non-structured surface.
• An oleophobic material in the sense of the invention is a material which, on a flat, non-structured surface, has a contact angle of greater than 90 °, based on long-chain n-alkanes, such as n-decane.
• the ultraphobic surface is preferably an aluminum surface which is provided with microstructures, anodized, optionally sealed, calcined, optionally coated with an adhesion promoter layer and then provided with a hydrophobic and / or oleophobic coating, as is the case in the international market
• Patent application WO 99/10323 is described.
• the manipulator and / or the carrier can be made entirely of aluminum or preferably has an aluminum coating, the aluminum being treated as indicated above.
• the ultraphobic surface is also preferably an aluminum surface, which is optionally anodized, sealed with hot water or steam, optionally coated with an adhesion promoter layer and then provided with a hydrophobic and / or oleophobic coating, as described in international patent application WO 99 / 10324.
• the dosing tip can be made entirely of aluminum or preferably has an aluminum coating, the aluminum being treated as indicated above.
• the ultraphobic surface is furthermore preferably a surface which is coated with Ni (OH) 2 particles, optionally coated with an adhesion promoter and is finally provided with a hydrophobic and / or oleophobic coating, as described in international patent application WO 99/10111.
• the Ni (OH) particles preferably have a diameter ds 0 of 0.5 to 20 ⁇ m.
• the ultraphobic surface is made of
• Tungsten carbide which is structured with a laser, optionally coated with an adhesion promoter and then provided with a hydrophobic and / or oleophobic coating, as described in international patent application WO 99/10113.
• the dosing tip is preferably only coated with tungsten carbide, which is then treated as indicated above.
• the tungsten carbide preferably has a layer thickness of 10 to 500 ⁇ m.
• the surface is preferably sandblasted with an abrasive, optionally coated with an adhesion promoter layer and then provided with a hydrophobic and / or oleophobic coating, as is the case in the international
• Patent application WO 99/10112 is described.
• Suitable as hydrophobic and / or oleophobic coating of the surfaces mentioned are all surface-active phobicization aids with any molecular weight. These compounds are cationic, anionic, amophotere and / or non-ionic surface-active compounds, e.g. in the directory “Surfactants Europa, A Dictionary of Surface Active Agents available in Europe, Edited by Gordon L. Hollis, Royal Socity of Chemistry, Cambridge, 1995.
• anionic phobicization aids alkyl sulfates, ether sulfates, ether carboxylates, phosphate esters, sulfosucinates, sulfosuccinatamides, paraffin sulfonates, olefin sulfonates, sarcosinates, isothionates, taurates and Linginian compounds.
• Quaternary alkylammonium compounds and imidazoles may be mentioned as cationic phobicization aids.
• Amphoteric phobicization aids are, for example, betaines, glycinates, propionates and imidazoles.
• nonionic phobicization aids are: alkoxylates, alkylamides, esters, amine oxides and alkylpolyglycosides. Also suitable are: reaction products of alkylene oxides with alkylatable compounds, such as. B. fatty alcohols, fatty amines, fatty acids, phenols, alkylphenols, arylalkylphenols, such as styrene-phenol condensates, carboxamides and resin acids.
• Phobicizing aids are particularly preferred in which 1 to 100%, particularly preferably 60 to 95%, of the hydrogen atoms are substituted by fluorine atoms.
• Examples include perfluorinated alkyl sulfate, perfluorinated alkyl sulfonates, perfluorinated alkyl phosphonates, perfluorinated alkyl phosphinates and perfluorinated carboxylic acids.
• polymeric phobicization aids for hydrophobic coating or as polymeric hydrophobic material for the surface.
• These polymeric phobicization aids can be nonionic, anionic, cationic or amphoteric compounds.
• polymeric phobicization auxiliaries can be homopolymers and copolymers, graft and graft copolymers and statistical block polymers.
• Particularly preferred polymeric auxiliaries are those of the AB-,
• the A segment is a hydrophilic homopolymer or copolymer and the B block is a hydrophobic homopolymer or copolymer or a salt thereof.
• Anionic, polymeric phobing aids are also particularly preferred, in particular condensation products of aromatic sulfonic acids with formaldehyde and alkylnaphthalene sulfonic acids or from formaldehyde, naphthalene sulfonic acids and / or benzenesulfonic acids, condensation products of optionally substituted phenol with formaldehyde and sodium bisulfite.
• condensation products which can be obtained by reacting naphthols with alkanols, additions of alkylene oxide and at least partial conversion of the terminal hydroxyl groups into sulfo groups or half esters of maleic acid and phthalic acid or succinic acid.
• the phobicization aid is from the group of the sulfosuccinic acid esters and alkylbenzenesulfonates.
• Sulfated, alkoxylated fatty acids or their salts are also preferred.
• Alkoxylated fatty acid alcohols are understood in particular to be those with 5 to 120, with 6 to 60, very particularly preferably with 7 to 30 ethylene oxide units, C 6 -C 22 fatty acid alcohols which are saturated or unsaturated, in particular stearyl alcohol.
• the sulfated alkoxylated fatty acid alcohols are preferably present as a salt, in particular as an alkali or amine salt, preferably as a diethylamine salt.
• Preferred areas of application for the method according to the invention and the device according to the invention are biochemical or chemical methods in which microscopic volumes of liquid have to be moved, mixed or metered. Examples include:
• the polymerase chain reaction PCR polymerase chain reaction
• ELISA enzyme linked immunosorbent assay
• the method according to the invention is easier to carry out than the conventional one
• Another object of the invention is the use of the device according to the invention for metering liquids on a microscopic scale, in particular in the range from 10 "6 to 10 " 12 liters.
• 1 shows a plastic plate 2 for moving liquid drops 4, 5 with a plurality of electrodes 3
• Fig. 2 shows an aluminum plate 7 with an electrically charged tip 10 as
• FIG. 3 shows a round tip 12 with a ring electrode 13 for removing small volumes of liquid 15 from a supply 14
• FIG. 4 shows an arrangement of three tips 16 to form an almost triangular gap M, which can be used instead of the ring electrode 13 in FIG. 3 for removing small amounts of liquid from a supply.
• FIG. 1 shows a device 1 according to the invention for the residue-free movement of liquid drops (here aqueous solutions) on solid surfaces.
• the device consists of a substrate 2 (here plexiglass), on the surface of which round, electrically conductive electrodes 3 (diameter 1 mm, spacing 5 mm) are inserted, which are flush with the surface of the substrate.
• a substrate 2 here plexiglass
• electrically conductive electrodes 3 diameter 1 mm, spacing 5 mm
• Electrodes 3 can have different voltages applied to each other.
• the surface of the substrate 2 is provided with an approximately 5 ⁇ m thick electrically insulating ultraphobic coating.
• an approx. 5 ⁇ m thick layer of aluminum is evaporated onto the substrate.
• the Al layer is anodized, treated with hot steam and provided with a hydrophobic coating.
• the substrate is immersed in a 1% strength by weight solution of Fluowet PL80 from Clariant for 5 hours at pH 7, rinsed with water and dried at 60.degree.
• the anodic oxidation of the aluminum surface was carried out in in sulfuric acid with continuous electrolyte movement under laminar flow conditions.
• the electrolyte temperature of 20 ° C was controlled by a thermostat.
• the distance between the substrate material and the counter electrode made of AlMg3 was half hard 5 cm.
• the current density during the anodic oxidation was kept constant at 10 mA / cm 2 .
• the oxidation was continued until an approximately 2-3 ⁇ m thick oxide layer was formed.
• the sample was 5 min. in distilled water and then 1 min. rinsed in methanol. After drying (air, room temperature), the sample was treated in a beaker, which had previously been boiled several times with distilled water, in distilled water at 100 ° C. for 15 minutes. After this treatment, it was rinsed in methanol (1 min) at 80 ° C. in a drying cabinet 1
• the Al layer has been completely transformed into an aluminum oxide layer by this treatment.
• a drop 5 can be moved on the surface in the direction of a directly adjacent electrode by switching this electrode to a potential of 800 V with respect to the other electrodes. The drop then lies over the relevant electrode.
• the movement of the drop 5 on the surface can be controlled as desired within the electrode grid.
• the droplets 4, 5 are moved on the ultraphobic surface without leaving any residue, ie without any liquid residues adhering along the movement track.
• a drop 4 (diameter approx. 1 mm) of a solution of 4- (6-diethylamino-3-diethylimino-3H-xanthe-9-yl) - 1, 3-benzodisulfonic acid (Kiton Red, concentration 1 x 10 "2 mol / 1 in water) is on the ultraphobic surface.
• the drop 4 is displaced along a closed path over 8 electrodes (length of the path 40 mm). This process is repeated 10 times, so that the total path is 400 mm, then the drop is removed and a drop of pure water is also moved 10 times along the previously used closed path.
• the example shown here can also be used in a corresponding manner for liquid drops which are surrounded on all sides by solid walls, e.g. in columns or tubes. These designs thus allow the loss-free conveyance of liquids solely by changing electrical fields, i.e. without mechanically moving parts.
• FIG. 2 shows a device 6 according to the invention for the complete transfer of liquid drops (here aqueous solutions) with the aid of a movable tip 10.
• the device has a support plate 7 made of aluminum with an ultraphobic
• the tip also has an ultraphobic surface.
• the ultraphobic coating is produced in accordance with Example 1.
• a drop 8 of a solution of 4- (6-diethylamino-3-diethylimino-2H-xanthe-9-yl) - 1,3-benzodisulfonic acid (Kiton Red, concentration 1 x 10 "2 mol / 1 in water) is located itself on the ultraphobic surface.
• the drop 8 can be picked up with the aid of the tip 10.
• the tip is approached up to a distance of approximately 5 mm, a voltage of 800 V being present between the tip 10 and the substrate plate 7.
• the radius of the tip is approximately 0.5 mm.
• the drop hanging on the tip is transferred to a vessel with 65 ⁇ l water by switching off the voltage.
• Another example shows the dosing and complete transfer of liquid drops using the device in FIG. 2.
• Example 2 With the help of the tip 10, the drop 8 is picked up as in Example 2.
• the drop hanging on the tip is inserted into a recess 11 of the device by switch the voltage filed.
• the other drop 9 is picked up with the tip and combined with the drop 8 in the depression. Then both drops are taken up with the tip and transferred into a vessel with 65 ⁇ l of water according to Example 2.
• the dye concentrations in the water were then determined spectrophotometrically.
• the transfer was carried out 5 times in the same way, with no loss of the transferred volumes V 3 and V 4 within the relative dosing errors of 1.5%.
• the arrangement consists of an electrode 12 with a round tip (diameter 1 mm) and an annular one
• Electrode 13 (inner diameter 0.5 mm). Both electrodes are provided with an ultrahydrophobic coating, the production of which is described in Example 1.
• the assembly is immersed in an aqueous solution of 4- (6-diethylamino-3-diethylimino-3H-xanthe-9-yl) -l, 3-benzodisulfonic acid (Kiton red, concentration 10 "2 mol / 1 in water) (as in 3)
• a voltage of 900 V is applied between the ring 13 and the electrode 12
• a drop of liquid 15 is removed from the supply 14 and remains adhering to the electrode 12.
• the drop By tilting and depositing the electrical field to the side, the drop can drop in The volume of the drop 15 was determined by measuring the fluorescence intensity of the dye in a known volume of water
• Fig. 4 Arrangement as used in Fig. 4.
• three round electrodes 16 (diameter 1 mm) are provided with an ultrahydrophobic coating, the manufacture of which Position in example 1 is described.
• the electrodes 16 are arranged as described in FIG. 4 to form an almost triangular spade M, which has the same function as the ring electrode 13 in FIG. 3.
• a drop of liquid is removed from a supply. If the dosage is repeated 30 times, a volume of (50.0 ⁇ 0.3) ⁇ 10 "12 liters is obtained.
• structures round, square or arbitrarily shaped gaps in cross section or in plan view
• structures are particularly suitable for this purpose, which can be generated by known microscructure techniques (e.g. light, X-ray or electron lithographic techniques), since small volumes to be metered require correspondingly small structures.

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• Chemical & Material Sciences (AREA)
• Health & Medical Sciences (AREA)
• Dispersion Chemistry (AREA)
• Clinical Laboratory Science (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Analytical Chemistry (AREA)
• General Health & Medical Sciences (AREA)
• Hematology (AREA)
• Apparatus Associated With Microorganisms And Enzymes (AREA)
• Vibration Prevention Devices (AREA)
• Sampling And Sample Adjustment (AREA)
• Application Of Or Painting With Fluid Materials (AREA)
• Feeding, Discharge, Calcimining, Fusing, And Gas-Generation Devices (AREA)
• Extraction Or Liquid Replacement (AREA)
• Micromachines (AREA)
• Manipulator (AREA)
• Devices For Use In Laboratory Experiments (AREA)
• Physical Or Chemical Processes And Apparatus (AREA)

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• 1999
  • 1999-10-05 DE DE19947788A patent/DE19947788A1/de not_active Withdrawn
• 2000
  • 2000-09-22 JP JP2001527923A patent/JP2003511247A/ja active Pending
  • 2000-09-22 CA CA002387581A patent/CA2387581C/fr not_active Expired - Fee Related
  • 2000-09-22 DE DE50003758T patent/DE50003758D1/de not_active Expired - Lifetime
  • 2000-09-22 WO PCT/EP2000/009272 patent/WO2001024934A1/fr active IP Right Grant
  • 2000-09-22 AU AU76589/00A patent/AU779566B2/en not_active Ceased
  • 2000-09-22 AT AT00966067T patent/ATE249886T1/de not_active IP Right Cessation
  • 2000-09-22 US US10/089,933 patent/US7214302B1/en not_active Expired - Fee Related
  • 2000-09-22 EP EP00966067A patent/EP1222031B1/fr not_active Expired - Lifetime

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