Method for manufacturing hydrophilic glass substrate

By treating glass substrates with alcohol and forming a hydrophilic polymer layer, the method addresses the challenge of achieving controlled surface roughness, enhancing cell capture efficiency and enabling effective drug testing.

JP7735713B2Active Publication Date: 2025-09-09SUMITOMO RUBBER INDUSTRIES LTD
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Patent Information

Application Number
JP2021130685
Authority / Receiving Office
JP · JP
Patent Type
Patents
Current Assignee / Owner
Filing Date
2021-08-10
Publication Date
2025-09-09
Estimated Expiration
2041-08-10

AI Technical Summary

Technical Problem

Existing methods for creating a hydrophilic substrate surface with controlled roughness for capturing specific cells, such as cancer cells, face challenges in achieving smoothness and uniformity, affecting the efficiency of cell capture.

Method used

A method involving alcohol treatment of glass substrates followed by the formation of a hydrophilic polymer layer controls the surface roughness, resulting in a hydrophilic glass substrate with low surface roughness and high smoothness, enhancing the ability to capture specific cells.

Benefits of technology

The method improves the capture efficiency of cells like cancer cells, enabling accurate determination of their numbers in bodily fluids and facilitating drug efficacy testing outside the body.

✦ Generated by Eureka AI based on patent content.

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Abstract

To provide a method for producing a hydrophilic glass substrate provided with a hydrophilic polymer layer whose surface irregularities are controlled.SOLUTION: A method for producing a hydrophilic glass substrate includes the step of forming a hydrophilic polymer layer on a glass substrate subjected to alcohol treatment.SELECTED DRAWING: None
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Description

[Technical Field]

[0001] The present disclosure relates to a method for manufacturing a hydrophilic glass substrate. [Background technology]

[0002] A technology has been proposed to coat the surface of a substrate with a special polymer in order to create devices for capturing specific cells in blood and body fluids (blood cells, cancer cells present in blood and body fluids, etc.).

[0003] However, it is difficult to create a smooth surface by coating some special polymers, and the roughness of the surface affects the ability to capture specific cells. Therefore, there is a need to provide a substrate with a surface with controlled roughness that is excellent in the ability to capture specific cells such as cancer cells (see Patent Document 1, etc.). [Prior art documents] [Patent documents]

[0004] [Patent Document 1] Special Publication No. 2005-523981 Summary of the Invention [Problem to be solved by the invention]

[0005] The present disclosure has an object to solve the above-mentioned problems and to provide a method for producing a hydrophilic glass substrate having a hydrophilic polymer layer with controlled surface roughness formed thereon. [Means for solving the problem]

[0006] The present disclosure relates to a method for producing a hydrophilic glass substrate, which includes a step of forming a hydrophilic polymer layer on a glass substrate that has been subjected to an alcohol treatment. [Effects of the Invention]

[0007] According to the present disclosure, a method for manufacturing a hydrophilic glass substrate includes a step of forming a hydrophilic polymer layer on a glass substrate that has been subjected to alcohol treatment, and therefore it is possible to provide a hydrophilic glass substrate on which a hydrophilic polymer layer having a surface with controlled roughness has been formed, which is expected to improve the ability to capture specific cells such as cancer cells. [Brief explanation of the drawings]

[0008] [Figure 1] 1 is a photograph of an example of the hydrophilic glass substrates produced in Example 3 and Comparative Example 1. FIG. DETAILED DESCRIPTION OF THE INVENTION

[0009] The present disclosure provides a method for producing a hydrophilic glass substrate, which includes a step of forming a hydrophilic polymer layer on a glass substrate that has been subjected to alcohol cleaning. By forming a hydrophilic polymer layer on the surface of a glass substrate that has been previously subjected to alcohol treatment, it is possible to control the unevenness of the substrate surface, and to provide a hydrophilic glass substrate coated with a hydrophilic polymer layer that has low surface roughness and high smoothness.

[0010] Tumor cells (e.g., cancer cells) present in bodily fluids, such as circulating tumor cells (several to several hundred per mL of blood), are very rare. Therefore, capturing as many tumor cells as possible in collected bodily fluids is considered important for testing. The method disclosed herein involves coating a hydrophilic polymer on the surface of a glass substrate previously treated with alcohol, thereby controlling the surface roughness and forming a hydrophilic polymer layer with low surface roughness and high smoothness. The roughness of the hydrophilic polymer layer influences the ability to capture specific cells, such as cancer cells. Controlling the surface roughness and increasing the smoothness is expected to achieve excellent specific cell capture performance. Therefore, measuring the number of tumor cells captured in the hydrophilic polymer layer formed on the surface of an alcohol-treated glass substrate can determine the number of tumor cells in bodily fluids, potentially enabling confirmation of the effectiveness of cancer treatment. Furthermore, culturing the captured tumor cells and confirming the efficacy of anticancer drugs, etc., using the cultured cells allows for confirmation of the efficacy of anticancer drugs, etc., outside the body prior to administration, and is also useful for selecting anticancer drugs, etc.

[0011] (Method of manufacturing hydrophilic glass substrate) The method for producing the hydrophilic glass substrate includes a step of forming a hydrophilic polymer layer on a glass substrate that has been subjected to an alcohol treatment (hereinafter also referred to as an "alcohol-treated glass substrate").

[0012] The type of glass constituting the glass substrate is not particularly limited, and examples thereof include soda-lime glass, alkali-free glass, borosilicate glass (SiO-B-ZnO-based glass, SiO-B-Bi-O-based glass, etc.), potash glass, crystal glass (glass containing PbO, such as SiO-PbO-based glass, SiO-PbO-B-O-based glass, SiO-B-PbO-based glass, etc.), titanium crystal glass, barium glass, boron glass (B-ZnO-PbO-based glass, B-ZnO-Bi-O-based glass, B-Bi-O-based glass, B-ZnO-based glass, etc.), strontium glass, aluminosilicate glass, soda-zinc glass, soda-barium glass (BaO-SiO-based glass, etc.), etc. These glasses may be used alone or in combination of two or more.

[0013] The thickness of the glass substrate is not particularly limited, but the average thickness is preferably 100 μm or more and 3000 μm or less, and more preferably 100 μm or more and 1000 μm or less. The average thickness is determined by measuring the thickness at any 10 points using a micrometer and averaging the measured values.

[0014] As the alcohol treatment agent used for the alcohol treatment, for example, a treatment agent containing various alcohols can be used. Examples of various alcohols include monohydric alcohols and polyhydric alcohols, with monohydric alcohols being preferred. The alcohol may be either an acyclic alcohol (straight-chain or branched alcohol) or a cyclic alcohol, with acyclic alcohols being preferred. The alcohol may be either saturated or unsaturated, with saturated alcohols being preferred. The alcohol may contain an ether bond in the hydrocarbon chain or various substituents other than a hydroxyl group. The alcohol is preferably in a liquid state at room temperature (25°C). One or more types of alcohol may be used in combination.

[0015] The number of carbon atoms in the monohydric alcohol is preferably 1 to 8, more preferably 1 to 4, and still more preferably 1 or 2. Specific examples of the monohydric alcohol include aliphatic alcohols such as methanol, ethanol, (n-, iso-)propanol, (n-, sec-, tert-)butanol, pentanol, hexanol, heptanol, octanol, nonanol, and decanol. Among these, from the viewpoint of controlling the unevenness of the hydrophilic polymer layer, methanol treatment, ethanol treatment, and propanol treatment using methanol, ethanol, and propanol are preferred.

[0016] The number of carbon atoms in the polyhydric alcohol is preferably 2 to 8, and more preferably 2 to 4. Specific examples of the polyhydric alcohol include dihydric aliphatic alcohols such as ethylene glycol, diethylene glycol, triethylene glycol, tetraethylene glycol, propylene glycol, 1,3-propanediol, and dipropylene glycol; and trihydric aliphatic alcohols such as glycerin.

[0017] The alcohol treatment may be either a treatment using a treatment agent containing only one or more alcohols, or a treatment using a mixed treatment agent containing one or more alcohols and water and / or an organic solvent other than the alcohols (mixed solvent treatment). The organic solvent other than the alcohol is preferably one that has good compatibility with alcohol, such as the aforementioned organic solvents other than alcohol that have good compatibility. In a mixed treatment agent containing alcohol and water and / or an organic solvent other than the alcohols, the alcohol content may be appropriately selected, but is preferably 50% by mass or more, and more preferably 80% by mass or more.

[0018] The treatment method with the alcohol treatment agent can be any method that allows contact between the alcohol treatment agent and the glass substrate, such as immersing the glass substrate in the alcohol treatment agent, applying the alcohol treatment agent to the glass substrate (with a brush or the like) or spraying it, or pouring the alcohol treatment agent into a container (glass substrate) such as a slide chamber.

[0019] From the viewpoint of controllability of the surface irregularities, it is preferable to perform the alcohol treatment two or more times. The number of alcohol treatments is defined as one period from contacting (treating) the alcohol treatment agent with the glass substrate (under conditions where the alcohol treatment agent is oscillated in approximately horizontal and vertical directions as necessary) to stopping the contact (treatment) between the alcohol treatment agent and the glass substrate. For example, a series of processes, including injecting the alcohol treatment agent into a container (glass substrate) and leaving it (contact), sucking or pushing out the alcohol treatment agent using a discharge device such as a pipette as necessary (oscillation in approximately horizontal and vertical directions), and then discharging the alcohol treatment agent from the container (release of contact), corresponds to one alcohol treatment, and the number of alcohol treatments is two if such a series of processes is performed twice.

[0020] The treatment temperature of the alcohol treatment agent may be appropriately set in consideration of the treatment efficiency, the unevenness of the hydrophilic polymer layer, etc., and can be, for example, 5 to 80°C.

[0021] The treatment time of the alcohol treatment agent (contact time between the alcohol treatment agent and the glass substrate) may also be selected appropriately from the same perspective, but is preferably 1 minute or more, more preferably 3 minutes or more, and even more preferably 5 minutes or more. The upper limit of the treatment time is not particularly limited, but from the viewpoint of production efficiency, it is preferably 5 hours or less, more preferably 1 hour or less, and even more preferably 30 minutes or less. The treatment time is the treatment time per alcohol treatment (the time the alcohol treatment agent is in contact with the glass substrate). For example, when alcohol treatment is performed two or more times, it is desirable that the treatment time for each alcohol treatment be within the above range.

[0022] An alcohol-treated glass substrate can be produced by contacting the alcohol treating agent with a glass substrate by various methods and then drying (natural drying, etc.) as necessary.

[0023] At least a portion (part or all) of the surface of the alcohol-treated glass substrate (where the hydrophilic polymer layer is not formed) preferably has a water contact angle of 65 degrees or less, more preferably 62 degrees or less. There is no particular lower limit, and the smaller the limit, the better. In this specification, the contact angle of water can be measured by the method described in the examples below.

[0024] After preparing an alcohol-treated glass substrate by the above-mentioned method or the like, a hydrophilic polymer layer is formed on the surface of the alcohol-treated glass substrate, thereby obtaining a hydrophilic glass substrate having a hydrophilic polymer layer formed on the surface of the alcohol-treated glass substrate.

[0025] The hydrophilic polymer constituting the hydrophilic polymer layer can be appropriately selected from those having hydrophilicity. For example, homopolymers and copolymers of one or more hydrophilic monomers, copolymers of one or more hydrophilic monomers with other monomers, etc. The hydrophilic polymers may be used alone or in combination of two or more.

[0026] Examples of the homopolymers and copolymers of the hydrophilic monomers include polyacrylic acid, polyacrylic acid esters, polymethacrylic acid, polymethacrylic acid esters, polyacryloylmorpholine, polymethacryloylmorpholine, polyacrylamide, polymethacrylamide, polyalkoxyalkyl acrylates, and polyalkoxyalkyl methacrylates.

[0027] The hydrophilic monomer in the copolymer of the hydrophilic monomer and another monomer may be any of various monomers having a hydrophilic group, such as known hydrophilic groups such as an amide group, a sulfate group, a sulfonic acid group, a carboxylic acid group, a hydroxyl group, an amino group, an amide group, and an oxyethylene group.

[0028] Specific examples of hydrophilic monomers include (meth)acrylic acid, (meth)acrylic acid esters, (alkoxyalkyl (meth)acrylates such as methoxyethyl (meth)acrylate, and hydroxyalkyl (meth)acrylates such as hydroxyethyl (meth)acrylate), (meth)acrylamide, and (meth)acrylamide derivatives having a cyclic group ((meth)acryloylmorpholine, etc.). Among these, (meth)acrylic acid, (meth)acrylic acid esters, alkoxyalkyl (meth)acrylates, and (meth)acryloylmorpholine are preferred, alkoxyalkyl (meth)acrylates are more preferred, and 2-methoxyethyl acrylate is particularly preferred.

[0029] The other monomer in the copolymer of the hydrophilic monomer and the other monomer may be appropriately selected within a range that does not inhibit the effects of the hydrophilic polymer, such as an aromatic monomer such as styrene, vinyl acetate, or N-isopropylacrylamide that can impart temperature responsiveness.

[0030] Among them, the hydrophilic polymer is preferably at least one selected from the group consisting of a polymer represented by the following formula (I) and poly(meth)acryloylmorpholine. [ka] (In the formula, R 1 is a hydrogen atom or a methyl group, R 2 represents an alkyl group, m is 1 to 5, and n is the number of repetitions.

[0031] R 2 The number of carbon atoms in the alkyl group is preferably 1 to 10, and more preferably 1 to 5. 2 is particularly preferably a methyl group or an ethyl group. m is preferably 1 to 3. n (the number of repeating units) is preferably 70 to 2,500, more preferably 90 to 1,500.

[0032] Furthermore, as the hydrophilic polymer, a copolymer of at least one hydrophilic monomer selected from the group consisting of a compound represented by the following formula (I-1) and (meth)acryloylmorpholine and the other monomers described above can also be suitably used. [ka] (In the formula, R 1 , R 2 , m is the same as above.)

[0033] Among the above-mentioned hydrophilic polymers, the hydrophilic polymer represented by the formula (I) is particularly suitable from the viewpoint of the roughness of the hydrophilic polymer layer.

[0034] The thickness (film thickness) of the hydrophilic polymer layer (layer formed of a hydrophilic polymer) is preferably 10 to 1000 nm, more preferably 30 to 700 nm, and even more preferably 50 to 350 nm. By adjusting the thickness within the above range, good low adsorption to proteins and cells and selective capture of cancer cells can be expected.

[0035] At least a part (part or all) of the surface of the hydrophilic polymer layer (the surface of the hydrophilic polymer layer in the hydrophilic glass substrate) preferably has a water contact angle of 60 degrees or less, more preferably 50 degrees or less. There is no particular lower limit, and the smaller the lower limit, the better.

[0036] The surface roughness Ra of the hydrophilic polymer layer (the surface of the hydrophilic polymer layer in the hydrophilic glass substrate) is preferably 0.30 μm or less, more preferably 0.20 μm or less, even more preferably 0.10 μm or less, and particularly preferably 0.06 μm or less. There is no particular lower limit, and the smaller the limit, the better. In this specification, the surface roughness Ra is the centerline surface roughness Ra defined by JIS B0601-2001.

[0037] A hydrophilic polymer layer can be produced by coating all or part of the surface of an alcohol-treated glass substrate with a hydrophilic polymer solution or dispersion by known techniques, such as (1) injecting a hydrophilic polymer solution or dispersion, prepared by dissolving or dispersing a hydrophilic polymer in various solvents, onto the surface (concave portions of the substrate), holding the solution for a predetermined period of time, and then drying, or (2) spraying the hydrophilic polymer solution or dispersion onto the surface of the alcohol-treated glass substrate. This produces a hydrophilic glass substrate having a polymer layer formed thereon (a hydrophilic glass substrate having a hydrophilic polymer layer formed thereon). Furthermore, by adding other components as necessary to the hydrophilic glass substrate having a hydrophilic polymer layer formed on the surface of the alcohol-treated glass substrate, a device capable of capturing, culturing, testing, etc., specific cells can be produced.

[0038] As for the solvent, injection method, coating (spraying) method, and the like, conventionally known materials and methods can be applied. The holding and drying times for (1) and (2) may be set appropriately depending on the size of the substrate, the type of liquid introduced, etc. The holding time is preferably 10 seconds to 10 hours, more preferably 1 minute to 5 hours, and even more preferably 5 minutes to 2 hours. Drying is preferably carried out at room temperature (about 23°C) to 80°C, and more preferably room temperature to 40°C. Drying may also be carried out under reduced pressure. Furthermore, after a certain period of holding, excess hydrophilic polymer solution / dispersion may be appropriately discharged and dried.

[0039] The solvent is not particularly limited as long as it can dissolve the hydrophilic polymer, and may be appropriately selected depending on the hydrophilic polymer to be used. Examples of the solvent include water, organic solvents, and mixed solvents thereof. Examples of the organic solvent include alcohols such as methanol, ethanol, n-propanol, i-propanol, and methoxypropanol; ketones such as acetone and methyl ethyl ketone; tetrahydrofuran, acetonitrile, ethyl acetate, and toluene.

[0040] The method for producing the hydrophilic glass substrate includes first treating the surface of the glass substrate with alcohol, and then forming a hydrophilic polymer layer on the surface of the alcohol-treated glass substrate thus produced. This controls the surface irregularities, allowing the formation of a hydrophilic polymer layer with small surface roughness and high smoothness.

[0041] For example, specific cells can be captured by contacting a sample (blood or body fluid) with a hydrophilic glass substrate in which a hydrophilic polymer layer is formed on the surface of an alcohol-treated glass substrate. Then, by measuring the number of captured specific cells, the number of specific cells in the collected blood or body fluid can be determined, and the effectiveness of cancer treatment can be confirmed. [Example]

[0042] The present disclosure will be specifically described below based on examples, but the present disclosure is not limited to these examples.

[0043] (Preparation of hydrophilic polymers) Poly(2-methoxyethyl acrylate) (PMEA) was prepared by thermally polymerizing 2-methoxyethyl acrylate (25 wt % toluene) at 60°C for 7 hours using a 12.5 mg / ml toluene solution of AIBN (azobisisobutyronitrile).

[0044] Example 1 Methanol was added to slide chamber A (non-coated, Matsunami Glass Industry Co., Ltd., bottom: soda-lime glass, water contact angle: 69.7°) and left for 5 minutes. After that, the bottom was treated by sucking up and pushing out methanol twice with a pipette. After that, the methanol was sucked out and the slide was air-dried (alcohol treatment: 1 time). The resulting alcohol-treated slide chamber was filled with a 0.16% methanol solution of PMEA, and then immediately dried in a vacuum oven at 40°C for 5 minutes to prepare a hydrophilic glass substrate.

[0045] Example 2 Methanol was added to slide chamber A (bottom: soda-lime glass, water contact angle: 69.7°) and left for 5 minutes. After that, the bottom was treated by sucking up and pushing out the methanol twice with a pipette. Then, the methanol was sucked out. Methanol was added again and the mixture was left for 5 minutes. After that, the bottom surface was treated by sucking up and pushing out the methanol twice with a pipette. Then, the methanol was sucked out and the mixture was allowed to dry naturally (alcohol treatment: 2 times). The resulting alcohol-treated slide chamber was filled with a 0.16% methanol solution of PMEA, and then immediately dried in a vacuum oven at 40°C for 5 minutes to prepare a hydrophilic glass substrate.

[0046] Example 3 Methanol was added to slide chamber A (bottom: soda-lime glass, water contact angle: 69.7°) and left for 5 minutes. After that, the bottom was treated by sucking up and pushing out the methanol twice with a pipette. Then, the methanol was sucked out. Methanol was added again and left for 5 minutes. After that, the bottom of the tube was treated by sucking up and pushing out the methanol twice with a pipette. Then, the methanol was sucked out. Methanol was added once more and the mixture was left for 5 minutes. After that, the mixture was washed twice by sucking up and pushing out the methanol with a pipette. After that, the mixture was sucked up and air-dried (alcohol treatment: 3 times). The resulting alcohol-treated slide chamber (alcohol-treated glass substrate) was poured with the prepared 0.16% methanol solution of PMEA, and then immediately vacuum-dried in an oven at 40°C for 5 minutes to prepare a hydrophilic glass substrate.

[0047] Example 4 A hydrophilic glass substrate was prepared in the same manner as in Example 3, except that the time for adding methanol and leaving it to stand was changed to 1 minute.

[0048] Example 5 A hydrophilic glass substrate was prepared in the same manner as in Example 3, except that the time for adding methanol and leaving it to stand was changed to 3 minutes.

[0049] Example 6 A hydrophilic glass substrate was prepared in the same manner as in Example 1, except that slide chamber A was replaced with slide chamber B (manufactured by AGC Technoglass, bottom surface made of soda-lime glass, water contact angle: 60.4 degrees).

[0050] Example 7 A hydrophilic glass substrate was prepared in the same manner as in Example 3, except that methanol was changed to ethanol.

[0051] Example 8 A hydrophilic glass substrate was prepared in the same manner as in Example 3, except that propanol was used instead of methanol.

[0052] (Comparative Example 1) A hydrophilic glass substrate was prepared in the same manner as in Example 1, except that the slide chamber A was not subjected to the methanol treatment.

[0053] (Comparative Example 2) A hydrophilic glass substrate was prepared in the same manner as in Example 6, except that the slide chamber B was not subjected to the methanol treatment.

[0054] (Comparative Example 3) The prepared 0.25% methanol solution of PMEA was poured into the untreated slide chamber B. Then, it was immediately vacuum-dried in an oven at 40°C for 5 minutes. Thereafter, methanol was poured into the glass (treatment temperature: room temperature) and the glass was naturally dried to prepare a hydrophilic glass substrate.

[0055] [Water contact angle (alcohol-treated glass substrate and untreated glass substrate)] 2 μl of distilled water was dropped onto the surface of the alcohol-treated or untreated glass substrate, and the contact angle after 30 seconds was measured by the θ / 2 method (room temperature).

[0056] [Water contact angle (hydrophilic glass substrate)] 2 μl of distilled water was dropped onto the surface of the prepared hydrophilic glass substrate (surface of the hydrophilic polymer layer), and the contact angle after 30 seconds was measured by the θ / 2 method (room temperature).

[0057] [Thickness of hydrophilic polymer layer (coating layer)] The thickness (film thickness) of the hydrophilic polymer layer on the hydrophilic glass substrate was measured (photographed) by using a TEM to measure (photograph) a cross section of the hydrophilic polymer layer at an acceleration voltage of 15 kV and 1000x magnification.

[0058] [Surface roughness Ra] Using a laser microscope, the surface roughness was measured non-contact at four points (first peak) on one hydrophilic glass substrate (hydrophilic polymer layer), and the average of the Ra values ​​at the four points was taken as the surface roughness Ra (μm) (average of the centerline surface roughness Ra specified in JIS B 0601-2001).

[0059] [Surface condition] The condition of the surface of the prepared hydrophilic glass substrate (surface of the hydrophilic polymer layer) was visually observed.

[0060] [Table 1]

[0061] In Comparative Examples 1 and 2, the entire surface was slightly cloudy. This cloudiness is thought to be due to the surface irregularities that were formed due to the surface roughness of the polymer layer, which caused diffuse reflection of light from the irregularities. In Comparative Example 3, in which methanol treatment was performed after the formation of the polymer layer, the surface roughness was large and the surface was slightly cloudy.

[0062] In contrast, in Examples 1 to 8, which used alcohol-treated glass substrates, the substrates were transparent with no visible cloudiness. Furthermore, the surface roughness was also reduced. It is easy to imagine that a surface with cloudiness and high surface roughness would exhibit different specific cell capture performance than a transparent substrate with low surface roughness, which would cause variations in capture performance. Therefore, it was expected that a surface with controlled roughness and no cloudiness (small Ra) would exhibit capture performance with less variation.

[0063] The present disclosure (1) is a method for producing a hydrophilic glass substrate, which includes a step of forming a hydrophilic polymer layer on a glass substrate that has been subjected to an alcohol treatment.

[0064] The present disclosure (2) is the method for producing a hydrophilic glass substrate according to the present disclosure (1), wherein the alcohol used in the alcohol treatment is at least one selected from the group consisting of methanol, ethanol, and propanol.

[0065] The present disclosure (3) is a method for producing a hydrophilic glass substrate according to the present disclosure (1) or (2), in which the alcohol treatment is carried out two or more times.

[0066] The present disclosure (4) is a method for producing a hydrophilic glass substrate according to any one of the present disclosures (1) to (3), wherein the treatment time for the alcohol treatment is 1 minute or longer.

[0067] The present disclosure (5) is a method for producing a hydrophilic glass substrate according to any one of the present disclosures (1) to (3), wherein the treatment time for the alcohol treatment is 3 minutes or more.

[0068] The present disclosure (6) is a method for producing a hydrophilic glass substrate according to any one of the present disclosures (1) to (3), wherein the treatment time for the alcohol treatment is 5 minutes or more.

[0069] The present disclosure (7) is a method for producing a hydrophilic glass substrate according to any one of the present disclosures (1) to (6), wherein the hydrophilic polymer layer is formed using a hydrophilic polymer solution.

[0070] The present disclosure (8) is a method for producing a hydrophilic glass substrate according to any one of the present disclosures (1) to (7), wherein the hydrophilic polymer layer is formed from a hydrophilic polymer represented by the following formula (I): [ka] (In the formula, R 1 is a hydrogen atom or a methyl group, R 2represents an alkyl group, m is 1 to 5, and n is the number of repetitions.

[0071] The present disclosure (9) is a method for producing a hydrophilic glass substrate according to any one of the present disclosures (1) to (8), wherein the thickness of the hydrophilic polymer layer is 10 to 1000 nm.

Claims

1. The method includes forming a hydrophilic polymer layer on an alcohol-treated glass substrate, The hydrophilic polymer layer is formed from a hydrophilic polymer represented by the following formula (I): the thickness of the hydrophilic polymer layer is 10 to 1000 nm; The method for producing a hydrophilic glass substrate, wherein the hydrophilic polymer layer has a surface roughness Ra of 0.10 μm or less. 【Chemical 1】 (In the formula, R 1 represents a hydrogen atom or a methyl group, R 2 represents an alkyl group, m represents 1 to 5, and n represents the number of repetitions.)

2. 2. The method for producing a hydrophilic glass substrate according to claim 1, wherein the alcohol used in the alcohol treatment is at least one selected from the group consisting of methanol, ethanol, and propanol.

3. 3. The method for producing a hydrophilic glass substrate according to claim 1, wherein the alcohol treatment is carried out two or more times.

4. 4. The method for producing a hydrophilic glass substrate according to claim 1, wherein the treatment time for the alcohol treatment is 1 minute or more.

5. The method for producing a hydrophilic glass substrate according to any one of claims 1 to 3, wherein the treatment time for the alcohol treatment is 3 minutes or more.

6. 4. The method for producing a hydrophilic glass substrate according to claim 1, wherein the treatment time for the alcohol treatment is 5 minutes or more.

7. 7. The method for producing a hydrophilic glass substrate according to claim 1, wherein the hydrophilic polymer layer is formed using a hydrophilic polymer solution.

8. The method for producing a hydrophilic glass substrate according to any one of claims 1 to 7, wherein the thickness of the hydrophilic polymer layer is 30 to 700 nm.

Citation Information

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