Gold nanoparticle aggregation-induced quantitative photothermal biosensing using a thermometer

US11860118B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-11860118-B2
Application numberUS-202017112841-A
CountryUS
Kind codeB2
Filing dateDec 4, 2020
Priority dateDec 5, 2019
Publication dateJan 2, 2024
Grant dateJan 2, 2024

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  5. First independent claim

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Abstract

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A biosensing system configured to detect a target DNA and methods of detecting a target DNS are presented. The biosensing system comprises a biosensor comprising a suspension of a hybridization buffer containing dispersed gold nanoparticles, sodium chloride, and single-stranded DNA probes configured to undergo DNA hybridization with the target DNA.

First claim

Opening claim text (preview).

What is claimed is: 1. A method of detecting a target DNA, the method comprising: adding a DNA sample to a biosensor comprising a suspension of a hybridization buffer containing dispersed gold nanoparticles, sodium chloride, and single-stranded DNA probes configured to undergo DNA hybridization with the target DNA; sending, by a laser, a beam of near-infrared radiation into the biosensor, wherein the beam of near-infrared radiation is configured to induce a photothermal effect in any aggregated gold nanoparticles present in the biosensor; and detecting a temperature of the biosensor after sending the beam of near-infrared radiation into the biosensor; determining whether the target DNA is present in the DNA sample based on the temperature of the biosensor; adding a first solution of the single-stranded DNA probes in the hybridization buffer to a suspension of the dispersed gold nanoparticles to form a protected gold nanoparticle suspension; and adding a second solution of sodium chloride in the hybridization buffer to the protected gold nanoparticle suspension to form the biosensor. 2. The method of claim 1 further comprising: determining, in response to a determination that the target DNA is present in the DNA sample, a concentration of the target DNA in the DNA sample. 3. The method of claim 2 , wherein determining the concentration of the target DNA comprises: determining a temperature change using the temperature of the biosensor and an initial temperature of the biosensor; and determining the concentration of the target DNA using the temperature change. 4. The method of claim 1 , wherein the first solution of the single-stranded DNA probes comprises a minimum concentration of single-stranded DNA probes configured to protect the dispersed gold nanoparticles from the sodium chloride, and wherein the second solution of the sodium chloride comprises a concentration of sodium chloride configured to produce a maximum temperature increase due to gold nanoparticle aggregation. 5. The method of claim 1 further comprising: forming the DNA sample without DNA amplification. 6. A biosensing system configured to detect a target DNA, the biosensing system comprising: a biosensor comprising a suspension of a hybridization buffer containing dispersed gold nanoparticles, sodium chloride, and single-stranded DNA probes configured to undergo DNA hybridization with the target DNA; and a laser configured to direct a beam of near-infrared radiation into the biosensor, wherein the beam of near-infrared radiation is configured to induce a photothermal effect in any aggregated gold nanoparticles present in the biosensor, wherein the dispersed gold nanoparticles have a diameter of at least 20 nanometers. 7. The biosensing system of claim 6 , wherein the biosensor is configured to operate such that the biosensor and a DNA sample to be introduced to the biosensor are label-free and DNA amplification-free. 8. The biosensing system of claim 6 further comprising: a thermometer configured to detect temperature changes of the suspension. 9. The biosensing system of claim 6 , wherein the biosensor comprises a concentration of sodium chloride configured to produce a maximum temperature increase due to gold nanoparticle aggregation without triggering precipitation of aggregated gold nanoparticles. 10. The biosensing system of claim 9 , wherein the biosensor comprises a concentration of single-stranded DNA probes configured to interact with dispersed gold nanoparticles. 11. The biosensing system of claim 9 , wherein the biosensor comprises a concentration of single-stranded DNA probes configured to provide the biosensor with a temperature increase in response to a beam of near-infrared radiation equivalent to a temperature increase in response to a beam of near-infrared radiation of a suspension of dispersed gold nanoparticles. 12. The biosensing system of claim 6 , wherein the laser is a near-infrared (NIR) laser having a wavelength from about 750 nm to about 850 nm. 13. A biosensing system configured to detect a target DNA, the biosensing system comprising: a biosensor comprising a suspension of a hybridization buffer containing dispersed gold nanoparticles, sodium chloride, and single-stranded DNA probes configured to undergo DNA hybridization with the target DNA; a laser configured to direct a beam of near-infrared radiation into the biosensor, wherein the beam of near-infrared radiation is configured to induce a photothermal effect in any aggregated gold nanoparticles present in the biosensor; and a thermometer configured to detect temperature changes of the suspension, wherein the biosensing system has a limit of detection of about 0.28 nM. 14. A biosensing system configured to detect a target DNA, the biosensing system comprising: a biosensor comprising a suspension of a hybridization buffer containing dispersed gold nanoparticles, sodium chloride, and single-stranded DNA probes configured to undergo DNA hybridization with the target DNA; and a laser configured to direct a beam of near-infrared radiation into the biosensor, wherein the beam of near-infrared radiation is configured to induce a photothermal effect in any aggregated gold nanoparticles present in the biosensor, wherein the biosensor comprises a concentration of sodium chloride configured to produce a maximum temperature increase due to gold nanoparticle aggregation without triggering precipitation of aggregated gold nanoparticles, and wherein the biosensor comprises a minimum concentration of single-stranded DNA probes configured to protect the dispersed gold nanoparticles from the sodium chloride. 15. A biosensing system configured to detect a target DNA, the biosensing system comprising: a biosensor comprising a suspension of a hybridization buffer containing dispersed gold nanoparticles, sodium chloride, and single-stranded DNA probes configured to undergo DNA hybridization with the target DNA; and a laser configured to direct a beam of near-infrared radiation into the biosensor, wherein the beam of near-infrared radiation is configured to induce a photothermal effect in any aggregated gold nanoparticles present in the biosensor, wherein the biosensor comprises 40 milliMolar concentration of sodium chloride. 16. An aggregation-induced quantitative photothermal biosensing method of detecting a target, the method comprising: irradiating a biosensor containing a sample with near-infrared radiation for a selected time, wherein the biosensor comprises a suspension of a hybridization buffer containing gold nanoparticles, sodium chloride, and single-stranded DNA probes configured to undergo DNA hybridization with a target, and wherein the near-infrared radiation is configured to induce a photothermal effect in any aggregated gold nanoparticles present in the biosensor; determining a temperature change of the biosensor after irradiating the biosensor with the near-infrared radiation for the selected time; determining a concentration of the target present in the sample using the temperature change of the biosensor; and irradiating the suspension at a power density of 5.2 W/cm 2 for an irradiation time, wherein the irradiation time is from about 5 minutes to about 10 minutes. 17. An aggregation-induced quantitative photothermal biosensing method of detecting a target, the method comprising: irradiating a biosensor containing a sample with near-infrared radiation for a selected time, wherein the biosensor comprises a suspension of a hybridization buffer containing gold nanoparticles, sodium chloride, and single-

Assignees

Inventors

Classifications

  • involving nanosized elements, e.g. nanogaps or nanoparticles (nanopores G01N33/48721; magnetic beads G01N27/745) · CPC title

  • being a hybridisation with immobilised receptors (using a FET type sensor G01N27/4145; concerning the hybridisation C12Q1/68) · CPC title

  • being a redox reaction, e.g. detection by cyclic voltammetry (voltammetry per se G01N27/42, G01N27/48) · CPC title

  • Methods or apparatus for measurement or analysis of nanostructures · CPC title

  • Sensing specific biomolecules, e.g. nucleic acid strands, based on an electrode surface reaction · CPC title

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What does patent US11860118B2 cover?
A biosensing system configured to detect a target DNA and methods of detecting a target DNS are presented. The biosensing system comprises a biosensor comprising a suspension of a hybridization buffer containing dispersed gold nanoparticles, sodium chloride, and single-stranded DNA probes configured to undergo DNA hybridization with the target DNA.
Who is the assignee on this patent?
Univ Texas
What technology area does this patent fall under?
Primary CPC classification G01N27/3278. Mapped technology areas include Physics.
When was this patent published?
Publication date Tue Jan 02 2024 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).