CN111157733A

CN111157733A - Grating waveguide microfluid detection system

Info

Publication number: CN111157733A
Application number: CN202010055222.9A
Authority: CN
Inventors: 陈昌; 刘博�; 王靖
Original assignee: Shanghai Industrial Utechnology Research Institute
Current assignee: Shanghai Jinguan Technology Co ltd
Priority date: 2020-01-17
Filing date: 2020-01-17
Publication date: 2020-05-15

Abstract

The invention provides a grating waveguide microfluid detection system, which comprises a microfluid chip, a microscope, a measuring device and an analysis device, wherein the microfluid chip is provided with a plurality of micro-channels; the microfluidic chip includes: the grating waveguide comprises an emergent grating which is positioned below the micro-channel and used for guiding light into the micro-channel upwards along the vertical direction; further comprising: the lower cladding, the waveguide layer, the protective layer, the upper cladding and the flow channel cover plate are arranged from bottom to top; the protective layer is used for covering and protecting the emergent grating; the micro-channel penetrates through the upper cladding to expose the protective layer. Has the advantages that: the method comprises the steps of depositing a silicon nitride film with adjustable optical performance on a flexible substrate, expanding the application range and form of SiN optical device materials, realizing the traditional optical system through integrated optics or an on-chip optical device, reducing the size of a chip of the traditional desk-top large-scale optical system, ensuring excellent analysis performance, realizing a high-flux chip-level optical detection and analysis integrated system of biological samples under the micro-nano scale, and greatly reducing the cost.

Description

Grating waveguide microfluid detection system

Technical Field

The invention relates to a grating waveguide microfluid detection system, in particular to a grating waveguide microfluid biological detection system.

Background

In modern biochemical analysis procedures, high-throughput detection devices have been widely used. Most of these devices use biochips based on microfluidic technology or microwell arrays, loaded in high performance optical systems, to perform analysis of biological samples of different sizes, such as nucleic acids, proteins, viruses, bacteria, cells, etc. The design of these optical systems is usually based on complex geometric optics, which is bulky, costly, requires optical alignment, and is costly to maintain.

In the precise medical age, miniaturized, high-performance, low-cost and mobile integrated analysis systems are of great concern. In particular, the lab on chip concept has advanced a lot of progress in manipulating a biological sample based on a microfluidic technology after decades of development, but a real lab on chip system still lacks an integrated system for chip-level on-chip optical detection and analysis of a high-throughput biological sample on a micro-nano scale.

Meanwhile, materials such as optical silicon nitride films and the like are deposited on the high polymer film, the integrated optical device taking SiN as the waveguide is separated from the silicon or glass substrate, and the polymer has certain ductility, so that the application range of the integrated optical device taking SiN and the like as the waveguide is greatly enlarged.

The lower the deposition temperature is, the better the deposition temperature is, in order to not destroy the molecular structure of the polymer, when the film is deposited on the high molecular polymer, the growth temperature of the SiN film which is the mainstream at present is about 400 ℃, and is still too high.

Disclosure of Invention

The device aims to solve a series of new requirements of miniaturization, mobility, integration and the like of the modern biochemical analysis instrument which is large in size and high in cost and meets the requirements of the precise medical era. The chip-level optical detection and analysis system is produced by an integrated circuit mass production process, the function of the traditional optical system is realized by integrating an optical device or an on-chip optical device, the traditional desktop or even large-scale optical system can be reduced to the chip size, the equal or even more excellent analysis performance is ensured, the high-flux chip-level optical detection and analysis integrated system of the biological sample under the micro-nano scale is realized, and the system cost is greatly reduced.

The invention provides a grating waveguide microfluid detection system, comprising: microfluidic chips, microscopes, measurement devices and analysis devices; characterized in that the microfluidic chip comprises: the optical grating waveguide comprises an emergent grating which is positioned below the micro-channel and used for guiding light into the micro-channel upwards along the vertical direction, the microscope is used for collecting optical signals in the micro-channel and transmitting the optical signals to the measuring device, the measuring device is used for processing the optical signals, generating signals to be analyzed and transmitting the signals to be analyzed to the analyzing device, and the analyzing device analyzes the signals to be analyzed to form a spectrum;

the microfluidic chip further comprises: the grating waveguide comprises a lower cladding, a waveguide layer, a protective layer, an upper cladding and a flow channel cover plate which are arranged from bottom to top in sequence, wherein the waveguide layer is made of silicon nitride materials and is used for forming the grating waveguide; the protective layer is made of silicon dioxide materials and is used for covering the grating waveguide and protecting the emergent grating;

the micro-channel penetrates through the upper cladding to expose the protective layer;

the flow channel cover plate covers the upper opening of the micro flow channel, and the micro flow channel cover plate comprises a liquid injection port for injecting a solution containing the biomolecules to be detected into the micro flow channel;

the lower cladding is made of a high polymer material with the thickness of 15-30 mu m, the upper cladding is made of a high polymer material with the thickness of 15-30 mu m, and the width of the micro-channel is 10-100 mu m.

Preferably, a plurality of the grating waveguides are parallel to each other to guide light into the micro channel, and the width of the grating waveguide is 300-600 nm.

Preferably, the refractive index of the waveguide layer is 1.75-2.2.

Preferably, the waveguide layer has a thickness of 150nm to 1000 nm.

Preferably, the micro-channel optical waveguide further comprises an incident grating made of silicon nitride material to form a coupling grating waveguide with the grating waveguide, and the light above the upper cladding layer is guided into the grating waveguide until being guided into the micro-channel upwards along the vertical direction; the protective layer covers and protects the incident grating.

Preferably, a plurality of said coupling grating waveguides are included, parallel to each other.

Preferably, the thickness of the waveguide layer is 150nm-1000nm, and the width of the coupling grating waveguide is 300-600 nm.

Preferably, the optical fiber is optically connected with the grating waveguide.

Preferably, the high molecular polymer material is SU-8 resin, polyimide, polydimethylsilane, polyethylene or benzocyclobutene.

The invention provides a grating waveguide microfluid detection system, which deposits a silicon nitride film with adjustable optical performance at low temperature on a flexible substrate, expands the application range and form of SiN optical device materials, realizes the functions of the traditional optical system through an integrated optical or on-chip optical device, reduces the size of the traditional table type or even large-scale optical system to the size of a chip, ensures the equal or even more excellent analysis performance, realizes a high-flux chip-level optical detection and analysis integrated system of biological samples under the micro-nano scale, and greatly reduces the system cost.

Drawings

FIG. 1 is a side view of a grating waveguide microfluidic detection system according to the present invention;

FIG. 2 is a side view of a coupled grating waveguide microfluidic detection system according to the present invention;

FIG. 3 is a top view of the microfluidic chip of FIG. 1;

FIG. 4 is a side view of the grating waveguide microfluid of FIG. 1;

figure 5 is a side view of the coupled grating waveguide microfluidics of figure 2.

Detailed Description

The following detailed description of embodiments of the invention refers to the accompanying drawings.

In the drawings, the dimensional ratios of layers and regions are not actual ratios for the convenience of description. When a layer (or film) is referred to as being "on" another layer or substrate, it can be directly on the other layer or substrate, or intervening layers may also be present. In addition, when a layer is referred to as being "under" another layer, it can be directly under, and one or more intervening layers may also be present. In addition, when a layer is referred to as being between two layers, it can be the only layer between the two layers, or one or more intervening layers may also be present. Like reference numerals refer to like elements throughout. In addition, when two components are referred to as being "connected," they include physical connections, including, but not limited to, electrical connections, contact connections, and wireless signal connections, unless the specification expressly dictates otherwise.

The invention provides a vertical grating waveguide microfluid detection system, which brings a chip-level on-chip optical detection chip of a high-flux biological sample under a micro-nano scale into a detection and analysis system. The vertical grating waveguide is a grating waveguide for guiding light upward into the microchannel in a vertical direction.

As shown in fig. 1 to 5, a grating waveguide micro-fluid detection system includes: a microfluidic chip (not shown), a microscope 3, a measuring device 4 and an analyzing device 5; the microfluidic chip includes: the grating waveguide 1311, 1312 … 131n and the microchannel 2, the grating waveguide 1311, 1312 … 131n includes an exit grating 1310, the exit grating 1310 is located below the microchannel 2 to guide light into the microchannel 2 upwards along the vertical direction, a new design scheme and idea are provided for different complex integrated structures, exit gratings with different exit directions can be designed, flexibility of detection means is increased, the microscope 3 is used for collecting optical signals in the microchannel 2 and transmitting the optical signals to the measurement device 4, the measurement device 4 is used for processing the optical signals and generating signals to be analyzed and transmitting the signals to be analyzed to the analysis device 5, and the analysis device 5 analyzes the signals to be analyzed to form a spectrum; it should be noted that the above "directing light upward along the vertical direction" may be strictly vertically upward, or may be obliquely upward, and the present invention is not limited thereto.

The microfluidic chip further comprises: the lower cladding layer 141, the waveguide layer 13, the protective layer 12, the upper cladding layer 142 and the flow channel cover plate 15 are sequentially arranged from bottom to top, the waveguide layer 13 is made of silicon nitride, and the waveguide layer 13 is used for forming the grating waveguides 1311, 1312 … 131 n; the protective layer 12 is made of silicon dioxide, has light transmittance, and is used for covering the grating waveguides 1311, 1312 … 131n and protecting the exit grating 1310;

the micro flow channel 2 penetrates through the upper cladding 142 to expose the protective layer 12;

the flow channel cover plate 15 covers the upper opening of the micro flow channel 2, and the micro flow channel cover plate 15 comprises a liquid injection port 151 used for injecting a solution containing biomolecules to be detected into the micro flow channel 2; it should be noted that, a liquid outlet (not shown) is further included to form a circulation system corresponding to the liquid injection port 151 one by one, and the liquid outlet may be an opening on the flow passage cover plate 15; the liquid outlet may also be an opening at both ends of the micro flow channel 2, and the invention is not limited herein.

The lower cladding layer is made of a high polymer material with the thickness of 15-30 mu m, the upper cladding layer is made of a high polymer material with the thickness of 15-30 mu m, the width of the micro-channel is 10-100 mu m, the traditional desktop or even large-scale optical system is reduced to the size of a chip, the same or even more excellent analysis performance is ensured, a high-throughput chip for detecting biological samples in a micro-nano scale is realized, and the system cost is greatly reduced.

Wherein the light source direction is different according to the introduced grating waveguide set 131, such as: fig. 1 is a view of introducing a light source from an optical fiber (not shown) at the left end of the grating waveguide group 131, and fig. 2 is a view of introducing a light source from above the upper cladding 142, which are described separately.

Fig. 1 is described below, i.e., the present grating waveguide microfluidic chip with light source introduced from the optical fiber (not shown) at the left end of the grating waveguide set 131:

as shown in fig. 1 and fig. 3 to 4, the grating waveguide set 131 on one microfluidic includes a plurality of, e.g., n, grating waveguides 1311, 1312 … 131n parallel to each other to guide light vertically upwards into the microchannel 2, in the actual detection, for biomolecules with different labels in the microchannel 2, the grating waveguides 1311, 1312 … 131n can guide light with wavelengths λ 1, λ 2 … λ n vertically upwards into the microchannel 2, respectively, and the labeled biomolecules 21 with different labels excited by light with different wavelengths can simultaneously identify these biomolecules, while the non-excited biomolecules 20 in the excitation light field guided by the grating waveguides 1311, 1312 … 131n will not be identified, and the non-excited biomolecules 20 are normal biomolecules without labels or biomolecules that are labeled but located outside the light field and are not excited; wherein, as shown in FIG. 3, the width of the grating waveguides 1311, 1312 … 131n is 300-600 nm.

As shown in fig. 1 to 3, the waveguide layer 13 has a thickness of 150nm to 1000nm, i.e., the thickness of the horizontal portion of the grating waveguides 1311, 1312 … 131n in fig. 1 to 3 is 150nm to 1000 nm.

The optical fiber is optically connected with the grating waveguide set 131, and further optically connected with the grating waveguides 1311, 1312 … 131n in the grating waveguide set 131.

FIG. 2 is described below, which is the present grating waveguide microfluidic chip with light source introduced from above the upper cladding 142:

as shown in fig. 2, the optical fiber module further includes an incident grating 1310' made of silicon nitride material to form a coupling grating waveguide with the grating waveguides 1311, 1312 … 131n, and guides light above the upper cladding 142 into the grating waveguides 1311, 1312 … 131n until the light is guided upward in the vertical direction into the micro channel 2, and the upper cladding 142 and the channel cover 15 are light-transmissive layers; the protective layer 12 covers and protects the incident grating 1310'.

As shown in fig. 2, 3 and 5, the grating waveguide set 131 on one microfluid includes several, e.g., n, mutually parallel coupled grating waveguides (including grating waveguides 1311, 1312 … 131n), to direct light vertically up the fluidic channel 2, in actual detection, for biomolecules with different labels in the micro flow channel 2, n coupled grating waveguides (including grating waveguides 1311 and 1312 … 131n) can guide light with wavelengths λ 1 and λ 2 … λ n vertically upwards into the micro flow channel 2, and the labeled biomolecules 21 with different labels can be excited by the light with different wavelengths to simultaneously identify the biomolecules, while the non-excited biomolecules 20 that are not in the excited light field introduced by the coupling grating waveguides 1311, 1312 … 131n will not be recognized, the non-excited biomolecules 20 being unlabeled normal biomolecules or biomolecules that are labeled but outside the light field and not excited; wherein, as shown in FIG. 3, the width of the n coupled grating waveguides (each including the grating waveguides 1311, 1312 … 131n) is 300-600nm, and wherein, as shown in FIG. 2, the thickness of the waveguide layer 13 is 150-1000 nm, i.e., the thickness of the horizontal portion of the grating waveguides 1311, 1312 … 131n is 150-1000 nm.

In the invention, the high polymer material is SU-8 resin, polyimide, polydimethylsilane, polyethylene or benzocyclobutene.

In the present invention, the flow path cover 15 is made of PDMS or quartz, and may be made of the above-mentioned polymer material.

In the present invention, the silicon nitride waveguide layer 13 is a silicon nitride thin film layer having a thickness of 150nm to 1000nm formed at a low deposition temperature of 25 to 150 ℃; the refractive index of the silicon nitride film is 1.75-2.2. The silicon nitride film may be a film having a uniform refractive index, or may be a film having a non-uniform refractive index, such as a silicon nitride film having a layered refractive index structure.

Circulating tumor cells are a general term for various tumor cells that leave the tumor tissue and enter the blood circulation system of the human body. By detecting trace circulating tumor cells in peripheral blood and monitoring the trend of the change of the types and the quantity of the circulating tumor cells, the tumor dynamics can be monitored in real time, the treatment effect can be evaluated, and the real-time individual treatment can be realized. The following describes an embodiment of detecting and analyzing circulating tumor cells by using the grating waveguide microfluid detection system of the present invention, and the main steps are as follows:

the first step is as follows: the method comprises the following steps of (1) sorting and enriching various tumor cells possibly existing in collected patient blood samples by adopting an immunomagnetic bead technology (such as immunomagnetic bead positive sorting) or a microfluidic technology to obtain a solution containing circulating tumor cells, or directly adopting the patient blood samples;

the second step is that: adding an antibody group which can be specifically combined with surface antigens of various tumor cells or an aptamer group which can be combined with the surfaces of various tumor cells into the solution or the blood sample containing the circulating tumor cells, wherein the antibody group and the aptamer group modify marks, and the antibody combined with specific tumor cells or the modified marks on the aptamer have uniqueness, so as to obtain the solution or the blood sample containing the marked circulating tumor cells; the labels are n, and can be target probes of fluorescent molecules;

the third step: as shown in fig. 1 and 3, the solution or blood sample obtained in the second step is added into the micro flow channel 2 from the liquid injection port 151, an optical fiber (not shown) guides n different wavelength lights corresponding to the n labels into the grating waveguides 1311, 1312 … 131n in the grating waveguide set 131 and further vertically upwards into the micro flow channel 2, the labeled biomolecules 21 containing different fluorescent molecular labels are circulating tumor cells excited by the different wavelength lights to emit fluorescence with specific wavelength, the microscope 3 is used for collecting fluorescence (optical signal) with specific wavelength and transmitting the fluorescence to the measuring device 4, the measuring device 4 processes and collects fluorescence (optical signal) with specific wavelength and generates a signal to be analyzed and transmits the signal to be analyzed to the analyzing device 5, the analyzing device 5 analyzes the signal to be analyzed to form a spectrum of fluorescence with specific wavelength, the variety of the circulating tumor cells in the solution or the blood sample can be judged by reading the spectrum, various tumor circulating cells can be detected respectively at one time, and the high-flux chip for detecting various tumor cells under the micro-nano scale is realized, so that the tumor dynamics is monitored in real time, the treatment effect is evaluated, and the real-time individual treatment is realized.

The foregoing is only a preferred embodiment of the present invention, and it should be noted that, for those skilled in the art, various modifications and decorations can be made without departing from the principle of the present invention, and these modifications and decorations should also be regarded as the protection scope of the present invention.

Claims

1. A grating waveguide microfluidic detection system, comprising: microfluidic chips, microscopes, measurement devices and analysis devices; characterized in that the microfluidic chip comprises: the optical grating waveguide comprises an emergent grating which is positioned below the micro-channel and used for guiding light into the micro-channel upwards along the vertical direction, the microscope is used for collecting optical signals in the micro-channel and transmitting the optical signals to the measuring device, the measuring device is used for processing the optical signals, generating signals to be analyzed and transmitting the signals to be analyzed to the analyzing device, and the analyzing device analyzes the signals to be analyzed to form a spectrum;

2. The system as claimed in claim 1, wherein a plurality of the grating waveguides are parallel to each other to guide light into the micro flow channel, and the width of the grating waveguides is 300-600 nm.

3. The system of claim 1, wherein the index of refraction of the waveguide layer is 1.75-2.2.

4. A system according to claims 2 to 3, wherein the waveguide layer is of a thickness of

150nm-1000nm。

5. The system of claim 1, further comprising an incident grating of silicon nitride material to form a coupled grating waveguide with the grating waveguide, light above the upper cladding layer being directed into the grating waveguide until directed upward in a vertical direction into the microchannel; the protective layer covers and protects the incident grating.

6. The system of claim 5, comprising a plurality of said coupled grating waveguides parallel to each other.

7. The system as claimed in claim 5, wherein the waveguide layer has a thickness of 150nm-1000nm, and the width of the coupling grating waveguide is 300-600 nm.

8. The system of claim 1, further comprising an optical fiber optically coupled to the grating waveguide.

9. The system of claim 1, wherein the polymeric material is SU-8 resin, polyimide, polydimethylsilane, polyethylene, or benzocyclobutene.