Ultrasensitive rapid antigen detection kit and detection method thereof
US-2024345078-A1 · Oct 17, 2024 · US
US10598575B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10598575-B2 |
| Application number | US-201615213128-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 18, 2016 |
| Priority date | Jul 17, 2015 |
| Publication date | Mar 24, 2020 |
| Grant date | Mar 24, 2020 |
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The invention provides enrichment platform devices for size-based capture of particles in solution. The enrichment platform device is useful for label-free capture of any particle. The invention relates to enrichment platform devices using nanowires and vertically aligned carbon nanotubes. The invention provides methods for making the enrichment platform devices. The invention provides methods for using the enrichment platform devices for filtering particles, capturing particles, concentrating particles, and releasing viable particles.
Opening claim text (preview).
What is claimed is: 1. A method of making an enrichment platform device comprising vertically-aligned carbon nanotubes (VACNT), the method comprising: depositing a single layer of metal catalyst thin film on a continuous substrate by ebeam evaporation and lift-off process; patterning the metal catalyst thin film using lithography; depositing carbon nanotube (CNT) precursor material on the metal catalyst thin film using chemical vapor deposition (CVD) to create VACNT such that the device comprises VACNT attached to the single layer of metal catalyst thin film that is directly attached to the continuous substrate, each VACNT being separated by a VACNT gap having a VACNT gap size, wherein at least one VACNT gap size is different from another VACNT gap size, wherein each VACNT gap size is selected to capture a particle having a particle size commensurate with the VACNT gap size so that different sized particles are releasably captured in an appropriate sized VACNT gap, the capture mechanism consisting essentially of the particles fitting in the VACNT gaps via mechanical interference; and bonding a cover to the substrate to encase the VACNT. 2. The method of claim 1 , wherein the metal catalyst thin film is an iron-catalyst thin film, a nickel-catalyst thin film, or a cobalt-catalyst thin film. 3. The method of claim 1 , wherein the metal catalyst thin film has a thickness that is adjustable to tune gap size, diameter, and density of the VACNT. 4. The method of claim 3 , wherein increasing the metal catalyst thin film thickness increases the VACNT gap size. 5. The method of claim 3 , wherein the gap size is tuned between 1 nm and 500 nm. 6. The method of claim 3 , wherein increasing the metal catalyst thin film thickness increases the VACNT diameter. 7. The method of claim 3 , wherein increasing the metal catalyst thin film thickness decreases the VACNT density. 8. The method of claim 3 , wherein the metal catalyst thin film thickness is less than 20 nm. 9. The method of claim 1 , wherein the precursor comprises doping material. 10. The method of claim 9 , wherein the doping material is selected from the group consisting of: nitrogen, boron, silicon, aluminum, phosphorus, and lithium. 11. The method of claim 1 , wherein the precursor material comprises benzylamine. 12. The method of claim 1 , wherein the particles being releasably captured are viable virus particles.
Specific details about materials · CPC title
by adsorption or absorption · CPC title
Orthomyxoviridae, e.g. influenza virus · CPC title
Connecting closures to device or container · CPC title
filtration · CPC title
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