Microneedle arrays for biosensing and drug delivery
US-2016095541-A1 · Apr 7, 2016 · US
US11685113B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11685113-B2 |
| Application number | US-201816491478-A |
| Country | US |
| Kind code | B2 |
| Filing date | Mar 6, 2018 |
| Priority date | Mar 6, 2017 |
| Publication date | Jun 27, 2023 |
| Grant date | Jun 27, 2023 |
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The present invention relates to a method for three dimensional printing of a porous object enabling the capillary transport of hydrophilic fluids, for use as liquid handling device, for example as a point of care diagnostic device. The invention also provides the porous object obtainable or obtained by such methods, and its use in liquid handling or as a point of care diagnostic device.
Opening claim text (preview).
The invention claimed is: 1. A method for three-dimensional printing of a porous device for liquid handling, the porous device comprising hydrophobic sections delineating one or more interconnected chambers and/or channels enabling the capillary transport of hydrophilic fluids, the method being a method without sintering and comprising: (a) providing a printing device comprising: means for spreading a dry powder of a particulate material on a powder bed surface, one or more depositing outlets for depositing at least one printing liquid on the powder bed surface, a computing unit that controls movement of the depositing outlets relative to the powder bed surface, wherein the printing device allows for selectively depositing one or more printing liquids on the powder bed and, a printing liquid comprising a hydrophobizing agent and a binder agent suitable for binding powder material; (b) spreading a layer of dry powder of a particulate material over a powder plate in order to create a powder bed; (c) depositing the printing liquid at predetermined positions on the powder bed, thereby binding the powder particles and providing hydrophobic sections on the powder particles; (d) lowering the powder bed and spreading an additional layer of dry powder of the particulate material, wherein the dry powder is applied on the underlying layer obtained in (c); and (e) repeating (c) and (d) until the porous device is formed, whereby at each repetition of (c) an additional layer of the porous device is formed and wherein at least part of the powder of the particulate material of the powder bed is bound to bound material of the layer formed in (c); wherein the binding of layers results from the directed depositing of the binder agent, and the depositing of the hydrophobizing agent results in delineating one or more interconnected chambers and/or channels within the hydrophobic sections, whereby the chambers and/or channels are filled with a hydrophilic particulate material enabling capillary transport of hydrophilic fluids in between the hydrophilic particulate material. 2. The method according to claim 1 , further comprising selectively depositing an additional printing liquid comprising a compound for capturing and/or detecting an analyte in a dedicated zone of the channels and/or chambers. 3. The method according to claim 2 , wherein the compound for capturing and/or detecting an analyte is selected from the group consisting of an antibody, a DNA molecule, a RNA molecule, an enzyme, an enzyme substrate, a color indicator, an enzyme cofactor, an enzyme inhibitor, an antibody-enzyme conjugate, a labeled antibody, and a chemical reactant. 4. The method of claim 1 , wherein the printing liquid further comprises a solvent, and the method further comprises drying the porous device to remove the solvent at a temperature of at most 40° C. 5. The method according to claim 1 , wherein the hydrophobizing agent is selected from the group consisting of waxes, silanes, alkyl and alkenyl ketene dimers, acid anhydrides, hydrophobic polymers, hydrophobic particles, fluorinated molecules, molecules containing apolar hydrocarbon moieties, and combinations thereof. 6. The method according to claim 1 , wherein the binder agent is selected from the group consisting of acetophenone, butanone, hexanone, propanone, methylethylketone, pentanone, toluene, chloroform, ethyl acetate, and combinations thereof. 7. The method according to claim 1 , wherein the printing device further comprises at least one additional printing liquid, and wherein different printing liquids are deposited on the powder bed from different depositing outlets. 8. The method according to claim 1 , wherein the dry powder material comprises an organic and/or an inorganic particulate material having a particle size varying between 1 μm and 250 μm. 9. The method according to claim 1 , wherein the dry powder material comprises a polymer and wherein the binder agent is a solvent for the polymer. 10. The method according to claim 9 , wherein the polymer is polymethyl methacrylate, and wherein the binder agent is selected from the group consisting of acetophenone, butanone, propanone, hexanone, and combinations thereof. 11. The method according to claim 1 , wherein the channels and/or chambers have a height of about 100 μm to about 10000 μm. 12. The method according to claim 1 , wherein the channels and/or chambers have a width of about 100 μm to about 10000 μm.
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