Biosensor based on a tethered particle
US-2017362645-A1 · Dec 21, 2017 · US
US9638693B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9638693-B2 |
| Application number | US-201314436301-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 4, 2013 |
| Priority date | Oct 27, 2012 |
| Publication date | May 2, 2017 |
| Grant date | May 2, 2017 |
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The invention relates to a method for producing a nanoporous layer on a substrate.
Opening claim text (preview).
The invention claimed is: 1. A method for producing a nanoporous layer on a substrate, comprising the following steps in order: a) selecting two types of particles, particles A and particles B, having different melting points; b) suspending both particles A and particles B in a solvent, thereby forming a suspension containing particles A and particles B; c) applying the suspension containing particles A and particles B to the substrate; d) melting, in a controlled manner, particles B having a lower melting point S mB , without reaching a melting point S mA of particles A which is higher than S mB , thereby forming a nanoporous layer on the substrate; and e) checking a surface of the nanoporous layer formed on the substrate. 2. The method according to claim 1 , comprising selecting particles A and B such that difference in the melting points S mA and S mB is caused by a different chemical composition of particles A and B. 3. The method according to claim 1 , comprising selecting particles A and B such that difference in the melting points S mA and S mB is caused by a different size of particles A and B. 4. The method according to claim 1 , comprising selecting particles o A and B such that difference in the melting points S mA and S mB is caused by a different shape of particles A and B. 5. The method according to claim 1 , wherein particles A and B are established at a weight ratio, with respect to each other, of A:B of 5:1 to 1000000:1 wt/wt. 6. The method according to claim 1 , wherein particles A and B are selected such that the melting points S mA and S mB differ by at least 1 K. 7. The method according to claim 1 , wherein steps a) to e) are carried out again after step e). 8. The method according to claim 1 , wherein during or after production of the nanoporous layer, functionalization of the nanoporous layer is carried out using immunologically active antibodies or antigens. 9. The method according to claim 8 , wherein the nanoporous layer after having been functionalized is contacted with a conductor, so as to conduct and detect electrical signals after immunologically active antigens or antibodies have bound to an analyte. 10. The method according to claim 1 , wherein average diameters of particles A and B are each 1 nm to 10 μm. 11. The method according to claim 1 , wherein particles A and B each comprise materials which conduct electricity. 12. The method according to claim 1 , wherein particles A and B each comprise semiconductor materials. 13. The method according to claim 1 , wherein particles A and B each comprise materials selected from the group consisting of gold, silver, platinum, aluminum oxide, silicon, copper, chromium, carbon, silver chloride, titanium, titanium oxide, iron oxide, magnesium oxide, zinc oxide, silicon oxide, silicon nitride and polyaniline.
Nanosized particles · CPC title
with ligand physically entrapped within the solid phase (liposomes G01N33/5432; immunological test elements G01N33/54386) · CPC title
comprising at least one non-porous part · CPC title
by application of heat or pressure and heat (C23C24/04 takes precedence) · CPC title
After-treatment · CPC title
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