IP Library Granted Patent US 10,197,566
Granted Patent B2
US 10,197,566 · App. 14/417,006 · Granted Feb 5, 2019

Biosensor comprising metal nanoparticles

Inventors: Pablo Del Pino González De La Higuera (Zaragoza, ES); Beatriz Pelaz Garcia (Zaragoza, ES); Ester Polo Tobajas (Zaragoza, ES); Valeria Grazú Bonavía (Zaragoza, ES); Jesús Martínez De La Fuente (Zaragoza, ES); Victor Parro Garcia (Zaragoza, ES)
Assignees: UNIVERSIDAD DE ZARAGOZA; FUNDACIÓN AGENCIA ARAGONESA PARA LA INVESTIGACIÓN Y EL DESARROLLO; CONSEJO SUPERIOR DE INVESTIGACIONES CIENTÍFICAS
G01N33/54386G01N21/29G01N21/554G01N21/78G01N33/54326G01N33/54346B82Y15/00G01N2021/786G01N2201/02G01N2201/06113Y10S977/954
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Quick Facts
Patent No.
US 10,197,566
App. No.
14/417,006
Granted
Feb 5, 2019
Kind
B2
Abstract

The present invention discloses a biosensor for visual detection of an analyte, based on the light to heat conversion properties of metal nanoparticles: the analyte is visually detected by the color change in the support areas (where the analyte is present), produced as a result of the heat generated by the metal nanoparticles where they are irradiated with an external light source. Use of said biosensor in a method for the detection of analytes is also claimed.

Claims (37)

1. A method for detecting an analyte in a sample, comprising the steps of:

(a1) adding the sample comprising the analyte to a support with a first analyte recognition molecule immobilized thereon, wherein the support comprises a heat sensitive surface;

(b1) incubating the support of step (a1) with metal nanoparticles functionalized with a second analyte recognition molecule; and

(c1) irradiating the support of step (b1) with an external light source; or

(a2) adding the sample comprising the analyte to a support with a first analyte recognition molecule immobilized thereon, wherein the support does not comprises a heat sensitive surface;

(b2) incubating the support of step (a2) with metal nanoparticles functionalized with a second analyte recognition molecule;

(c2) placing the support of step (b2) on a heat sensitive surface; and

(d2) irradiating the support of step (c2) with an external light source.

2. The method of claim 1 , wherein the analyte is an additive, a drug, a pathogenic microorganism, a food component, a pesticide, a toxic compound or oxygen.

3. The method of claim 1 , wherein the analyte is visually detected by a color change in the support area where the analyte is present; and wherein the color change is produced as a result of heat generated by the metal nanoparticles when they are irradiated with the external light source.

4. The method of claim 1 , wherein the heat sensitive surface comprises any surface capable of experiencing a structural change when heated, resulting in image development.

5. The method of claim 1 , wherein the external light source is capable of causing excitation of surface plasmon absorption band of the metal nanoparticles.

6. The method of claim 4 , wherein the external light source produces radiation of wavelength of between 750 nm and 110 nm.

7. The method of claim 4 , wherein the external light source is a monochromatic or a polychromatic light source.

8. The method of claim 1 , wherein the metal nanoparticles comprise gold, silver or copper.

9. The method of claim 1 , wherein the heat sensitive surface is a thermal paper or a temperature sensitive polymer.

10. The method of claim 9 , wherein the temperature sensitive polymer comprises poly(N-isopropylacrylamide), poly(N-vinylpiperidine) or poly(N-inylcaprolactam).

11. A method for detecting an analyte in a sample, comprising the steps of:

(a3) adding the sample comprising the analyte to a support with a first analyte recognition molecule immobilized thereon, wherein the support comprises a heat sensitive surface;

(b3) incubating the support of step (a3) with a second analyte recognition molecule bound to at least one label molecule;

(c3) incubating the support of step (b3) with metal nanoparticles functionalized with at least one molecule capable of specifically binding to the label molecule; and

(d3) irradiating the support of step (c3) with an external light source; or

(a4) adding the sample comprising the analyte to a support with a first analyte recognition molecule immobilized thereon, wherein the support does not comprise a heat sensitive surface;

(b4) incubating the support of step (a4) with a second analyte recognition molecule bound to at least one label molecule;

(c4) incubating the support of step (b4) with metal nanoparticles functionalized with at least one molecule capable of specifically binding to the label molecule;

(d4) placing the support of step (c4) on a heat sensitive surface; and

(d4). irradiating the support of step (d4) with an external light source.

12. The method of step 11 , wherein the analyte is visually detected by a color change in the support area where the analyte is present; and wherein the color change is produced as a result of heat generated by the metal nanoparticles when they are irradiated with the external light source.

13. The method of claim 11 , wherein the label molecule is biotin and wherein the at least one molecule capable of specifically binding the label molecule is avidin or streptavidin; or wherein the label molecule is avidin or streptavidin and the at least one molecule capable of specifically binding the label molecule is biotin.

14. The method of claim 11 , wherein the heat sensitive surface comprises any surface capable of experiencing a structural change when heated, resulting in image development.

15. The method of claim 11 , wherein the external light source is capable of causing excitation of surface plasmon absorption band of the metal nanoparticles.

16. The method of claim 14 , wherein the external light source produces radiation of wavelength of between 750 nm and 110 nm.

17. The method of claim 14 , wherein the external light source is a monochromatic or a polychromatic light source.

18. The method of claim 11 , wherein the metal nanoparticles comprise gold, silver or copper.

19. The method of claim 11 , wherein the heat sensitive surface is a thermal paper or a temperature sensitive polymer.

20. The method of claim 19 , wherein the temperature sensitive polymer comprises poly(N-isopropylacrylamide), poly(N-vinylpiperidine) or poly(N-vinylcaprolactam).

21. The method of claim 11 , wherein the analyte is an additive, a drug, a pathogenic microorganism, a food component, a pesticide, a toxic compound or oxygen.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 18, 2025
From: UNIVERSIDAD DE ZARAGOZA; FUNDACIÓN AGENCIA ARAGONESA PARA LA INVESTIGACIÓN Y EL DESARROLLO (ARAID)
To: CONSEJO SUPERIOR DE INVESTIGACIONES CIENTÍFICAS (CSIC)
Reel/Frame 070884/0720 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 13, 2017
From: DE LA FUENTE, JESUS MARTINEZ
To: FUNDACION AGENCIA ARAGONESA PARA LA INVESTIGACION Y EL DESARROLLO
Reel/Frame 042700/0819 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 13, 2017
From: GARCIA, VICTOR PARRO
To: CONSEJO SUPERIOR DE INVESTIGACIONES CIENTIFICAS
Reel/Frame 042700/0823 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 13, 2017
From: DE LA HIGUERA, PABLO DEL PINO GONZALEZ; GARCIA, BEATRIZ PELAZ; TOBAJAS, ESTER POLO; BONAVIA, VALERIA GRAZU
To: UNIVERSIDAD DE ZARAGOZA
Reel/Frame 042805/0816 →
Priority Claims (1)
ES 201231209 · Jul 26, 2012 · national
Continuity (1)
Related Publication 20150293084A1 · Oct 15, 2015