Unlock instant, AI-driven research and patent intelligence for your innovation.

Optical fiber LSPR aptamer biosensor, and preparation method and application thereof

A technology of aptamer sensor and biosensor, applied in the direction of phase influence characteristic measurement, etc., can solve the problems of reducing sensor signal generation, agglomeration, deformation, etc.

Active Publication Date: 2021-09-10
JIANGSU UNIV OF SCI & TECH
View PDF3 Cites 1 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Nanomaterials have extremely high requirements on the environment. In the process of sensor preparation, nanomaterials are prone to agglomeration and deformation due to interference from the external environment (such as dust, static electricity, etc.), which seriously reduces the signal generation of the sensor.

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Optical fiber LSPR aptamer biosensor, and preparation method and application thereof
  • Optical fiber LSPR aptamer biosensor, and preparation method and application thereof
  • Optical fiber LSPR aptamer biosensor, and preparation method and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0037] Example 1 Preparation and Characterization of GO / Au NPs Composite Material

[0038] 1) In this experiment, GO dispersed in the water phase was used as a carrier, and chloroauric acid was reduced in situ on its surface to generate AuNPs, and the GO / AuNPs composite material was obtained.

[0039] 10.0 mg of graphene oxide (GO) was ultrasonicated in 40 mL of water for 1.5 h to fully disperse GO and obtain a 0.25 mg / mL GO aqueous solution. Add 80.0 mg of polyvinylpyrrolidone (polyvinylpyrrolidone, PVP) and 0.2 mL of polydiallyl propylene dimethyl ammonium chloride (Poly dimethyl diallyl ammonium chloride PDDA) into 20 mL of 0.25 mg / mL GO solution, stir for 30 min, and the obtained The solution was centrifuged (rotating speed 10000r / min, time 10min), the supernatant was removed, washed with ethanol and deionized water, centrifuged, and repeated three times to finally obtain 5mL functionalized GO solution. Take 500uL of 1.0% chloroauric acid solution and 2.0mL GO solution, m...

Embodiment 2

[0041] Preparation and Characterization of Embodiment 2 Optical Fiber LSPR Sensor

[0042] Immerse the optical fiber in the piranha solution for 30 minutes, heat it at 70°C to remove the organic matter on the end face of the optical fiber, rinse it with ultrapure water, and dry it. 40 μL of the GO / Au NPs composite material prepared in Example 1 was drop-coated onto the end face of the optical fiber, and dried in a desiccator. The nucleic acid aptamer (5'-SH-(C 2 h 5 ) 6 -GTATAT CAAGCATCG CGT GTT TAC ACATGC GAG AGG TGAA, manufactured by Shanghai Bioengineering Co., Ltd.), configured as a solution with a concentration of 1 μM, immersed the optical fiber in the aptamer solution, and stored at room temperature for 12 hours. Then it was repeatedly washed with Tris-HCl buffer to remove unbound aptamers, and finally dried with nitrogen to complete the construction of the fiber optic LSPR sensor.

[0043] Figure 4 A is the color change before and after dispensing GO / Au NPs compo...

Embodiment 3

[0044] Example 3 Optimization of GO / Au NPs material dispensing amount

[0045] 5 μL, 10 μL, 20 μL, 40 μL, 60 μL, and 80 μL of the GO / Au NPs composite material prepared in Example 2 were used to drop-coat the optical fiber, and the reflected light of the optical fiber sensor was compared. Figure 5 A is the absorbance spectrum of the optical fiber sensor at different dispensing concentrations. It can be seen from the figure that as the dispensing concentration increases, the absorbance of the sensor end face increases continuously; Figure 5 B more intuitively shows the relationship between the amount of GO / AuNPs composite material dispensing and the LSPR peak intensity of the fiber sensor, which is determined by Figure 5 It can be seen that when the dispensing amount is higher than 40 μL, the increase of the absorbance of the end face of the optical fiber sensor tends to be gentle. In summary, the optimal drop-coating volume of the GO / Au NPs composite used in this experiment...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

PropertyMeasurementUnit
Particle sizeaaaaaaaaaa
Login to View More

Abstract

The invention discloses an optical fiber LSPR aptamer biosensor, and a preparation method and application thereof. The optical fiber LSPR aptamer biosensor is obtained by dispensing a GO / Au NPs composite material on an optical fiber sensor and then combining with a T-2 nucleic acid aptamer. The invention also discloses a detection method of T-2 toxin. The prepared optical fiber LSPR sensor is high in T-2 toxin detection sensitivity, the lowest detection limit is 0.249 ng / mL, the specificity for detecting T-2 toxin in food is high, and the detection result is accurate and reliable.

Description

technical field [0001] The invention belongs to the technical field of optical fiber LSPR detection, and specifically relates to an optical fiber LSPR aptamer sensor and a preparation method and application thereof, in particular to a method for detecting T-2 toxin based on the optical fiber LSPR aptamer sensor technology. Background technique [0002] T-2 toxin is a derivative produced by the metabolism of a variety of fungi (mainly Fusarium trilineum) under certain conditions, belonging to the Trichothecenes family (Trichothecenes, TS), and the molecular formula is C 24 h 34 o 9 , is a sesquiterpene compound with stable chemical structure, high temperature resistance and UV resistance. T-2 toxin is widely distributed in nature, mainly produced in barley, wheat, corn and other grains, causing serious harm to the development of agriculture and animal husbandry, and is one of the key toxins to prevent (International journal of food microbiology, 2002, 72 (1-2): 115-123). ...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
IPC IPC(8): G01N21/41
CPCG01N21/41
Inventor 颜辉徐义超方家银熊孟
Owner JIANGSU UNIV OF SCI & TECH