Compound biochip based on photon crystal

A photonic crystal and biochip technology, which is applied in the field of preparation methods of composite biochips, can solve problems such as hindering the extension of biomolecules and steric hindrance, and achieve the effects of improving performance, promoting development and application.

Inactive Publication Date: 2009-02-04
SOUTHEAST UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

The technical effect of this patented innovation lies with introducing colloidoscopic photosensitive crystal (CPC) films into flexible or rigid surfaces that improve their ability to detect various types of molecules such as DNA, proteins, cells, bacteria, etc., which has potential applications in fields like genetic testing and medical diagnoses.

Problems solved by technology

Technologies described in this patents involve creation of tiny patterns called quantum dots made up of atoms arranged periodically along one direction through interaction between electric field lines. These minute patternings allow for precise control over how electrical charges move within these systems. Quantum Dot Colours (QCs) represent unique optoeletransistence (OPT)-effective semiconductor material that allows for efficient coupling of incident lights onto surfaces containing nanoplasmonium cations. They exhibit very weak absorption at visible frequencies but they absorb strongly infrared waves when excited by near-infrared rays. By combining multiple types of QCDs together, researchers may study both polarizable and nonpolarized states simultaneously without having to label each individual particle separately. Additionally, composites consisted of specialty resin films attached to transparent conductors could improve sensor performance while reducing costs compared to traditional methods like liquid phase epithography.

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0023] 1. First wash the ordinary glass slide with washing solution, then ultrasonically wash it with deionized water for 3 times, and dry it in a dust-free place for later use.

[0024] 2. Preparation method of silicon dioxide photonic crystal: control the particle size of silicon dioxide nanoparticles by temperature control method. For example, if the signal to be measured is cy3 and its emission wavelength is 570nm, adjust the temperature of the oil bath to 40 degrees, and select a fast gap Formula feeding method, first 88ml of absolute ethanol and 3.2ml of tetraethyl orthosilicate mixed solution and 20ml of ammonia water and 88ml of absolute ethanol mixed solution are added to the flask, and at the same time start stirring at a speed of 350 rpm; then add 16ml of ammonia water; after 5-10 minutes, add 176ml of absolute ethanol and 4ml of ethyl orthosilicate mixture. After reacting for 3 hours, silica nanoparticles with good monodispersity can be obtained. After centrifugal pu

Embodiment 2

[0028] 1. Preparation of the plastic sheet: firstly make a PS plastic sheet with a size of 76.2mm*25.4mm*1mm, and then cool it to room temperature. The plastic sheet was ultrasonically cleaned with deionized water, and its surface was oxidized with oxygen plasma.

[0029] 2. Preparation method of polystyrene photonic crystal: under the protection of nitrogen, add 10ml of styrene, 225ml of ultrapure water and 1ml of methacrylic acid into a three-necked flask, and stir at a speed of 350r / min. Raise the temperature to 70°C, add 0.32g of potassium persulfate as an initiator after stabilization, and react for at least 10 hours to obtain polystyrene microspheres with a particle size of about 245nm. After centrifugal purification, adjust the concentration of the microspheres to 2-2.5% with deionized water, and disperse them by ultrasonic. Fix the plastic sheet prepared in step 1 on the puller, and pull it up at a speed of 1.6um / s, and the microspheres will self-assemble into photon

Embodiment 3

[0032] 1. Preparation of silicon wafers: Clean the ordinary silicon wafers purchased, and oxidize the surface with oxygen plasma.

[0033] 2. Preparation of polymethyl methacrylate (PMMA) photonic crystal: The preparation of PMMA adopts a soap-free suspension polymerization method at boiling temperature. First put 40ml of methyl methacrylate into a narrow-necked bottle, add 0.1ml of methacrylic acid and 150ml of ultrapure water, heat to boiling under stirring, add initiator potassium peroxodisulfate 5 minutes after boiling, and react for 1.5 h. After centrifugal purification, adjust the concentration of microspheres to 2-2.5% with deionized water, and disperse them by ultrasonic. Fix the silicon wafer prepared in step 1 on the puller, and pull it up at a speed of 1.6um / s, and the microspheres will self-assemble into photonic crystals on the surface of the silicon wafer.

[0034] 3. The method of tiling the agarose membrane: as described in Example 1.

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PUM

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Abstract

A making method of a composite type biological chip based on a photonic crystal comprises four steps which are preparation of hard substrates, preparation of photonic crystal thin membranes, connection of membranous substrates and surface treatment of the substrates. (1) the preparation of hard substrates: common hard substrates are cleaned by soapy water, washed by de-ionized water and dried, and amino-group or hydroxyl is decorated on the surfaces of the substrates; (2) the preparation of photonic crystal: the nano-microspheres such as specific monodisperse silicon dioxide or polystyrene and the like, which are different in size according to the positions of testing signals, are assembled on the surfaces of the treated substrates to form the photonic crystal thin membrane with the thickness of 20 to 30 microns (3) the connection of membranous substrates: the surface of the photonic crystal thin membrane is laid with a layer of the membranous substrate and the connection is fixed by utilizing the chemisorption or the mutual function between positive and negative charges; (4) the surface treatment of the substrates: by using the methods such chemisorption and the like, chemical groups which can be fixedly connected with biomolecules to be tested are decorated on the membranous layer parts of the surfaces of the composite substrates which are formed in the step (3).

Description

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Claims

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Application Information

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Owner SOUTHEAST UNIV
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