WO2011040572A1

WO2011040572A1 - Ophthalmic composition

Info

Publication number: WO2011040572A1
Application number: PCT/JP2010/067153
Authority: WO
Inventors: 江利松本; 一宏福嶋; 千夏古宮; 健一春名; 雅美東田; 元気飯塚
Original assignee: ロート製薬株式会社
Priority date: 2009-09-30
Filing date: 2010-09-30
Publication date: 2011-04-07
Also published as: JP6359586B2; HK1171380A1; JP2011093898A; JP2019043970A; CN102548562B; JP5700994B2; JP2015025011A; CN102548562A; JP2016145249A; JP2017160274A

Abstract

Disclosed are: an ophthalmic composition according to a non-conventional novel preparation, which has histamine release inhibitory action; and an ophthalmic composition for a silicone hydrogel contact lens, which is capable of suppressing adsorption of terpenoid to a silicone hydrogel contact lens. Specifically, the ophthalmic composition is prepared using (A) 0.001-2 w/v% of a polymer that has a phosphorylcholine analogous group in a side chain in combination with (B-1) 0.001-0.02 w/v% of menthol. Meanwhile, the ophthalmic composition for a silicone hydrogel contact lens is prepared using (A) a polymer that has a phosphorylcholine analogous group in a side chain in combination with (B-2) terpenoid.

Description

Ophthalmic composition

The present invention relates to an ophthalmic composition exhibiting a histamine release inhibitory action. Moreover, this invention relates to the ophthalmic composition for silicone hydrogel contact lenses which can suppress adsorption | suction to the silicone hydrogel contact lens of a terpenoid.

In recent years, the increase in allergic patients and the severity of allergic symptoms have become problems. Many symptoms of allergic patients are known to be type I allergic symptoms, that is, allergic symptoms caused by the release of chemical mediators such as histamine from mast cells and basophils upon contact with allergens . In order to prevent or ameliorate this type I allergic symptom, it is effective to suppress histamine release itself, and the development of an ophthalmic composition exhibiting histamine release inhibitory action is desired. In particular, if an ophthalmic composition exhibiting a histamine release inhibitory activity can be developed using a component that has not been clarified so far, the preparation having a new added value can be provided.

In recent years, the number of wearers of contact lenses has increased, and among them, the wearers of silicone hydrogel lenses with high oxygen permeability have increased. Silicone hydrogel contact lenses achieve oxygen permeability several times that of conventional hydrogel contact lenses by adding silicone to the hydrogel. Therefore, it is highly anticipated that oxygen deficiency, which is a weak point of conventional soft contact lenses, can be improved and adverse effects on the cornea due to oxygen deficiency can be greatly suppressed. In general, it is indispensable to design eye drops applied to the eye of a contact lens wearer with sufficient consideration of safety and the like according to the type and characteristics of the contact lens.

On the other hand, a polymer having a phosphorylcholine-like group in the side chain is known as a compound having high biocompatibility. In addition, the polymer is known to be effective for skin care because it has functions such as keratin protection and moisture retention (see Patent Document 1). Furthermore, it has been found that the polymer is effective in prevention or treatment of dry eye (see Patent Document 2) and improvement in retention of active ingredients (see Patent Document 3) in the ophthalmic field. Thus, the polymer has not only biocompatibility but also various actions, and has attracted attention as a functional material. In particular, in recent years, the use of the polymer in the ophthalmic field has been actively attempted, and a prescription of an ophthalmic composition containing the polymer has also been reported (see Patent Documents 4-5).

In addition, terpenoids such as menthol are used as a refreshing agent in the ophthalmic field. Furthermore, the refreshing action of terpenoids is expected to have an effect of improving eye discomfort and imparting a sense of relaxation and refreshment.

However, regarding the polymers and terpenoids having a phosphorylcholine-like group in the side chain as described above, little is known about the effect on histamine release. The current situation is that nobody can see. In addition, the present situation is that no study has been made on the influence of these in combination on the silicone hydrogel lens.

JP-A-9-52848 Japanese Patent Laid-Open No. 10-324634 JP 11-335301 A JP 2008-273959 A JP 7-166154 A

With the background of the above-mentioned conventional technology, it is desired to develop an ophthalmic composition that exhibits a histamine release inhibitory action with a novel formulation that has not been used conventionally.

In addition, the present inventors have surprisingly found that a silicone hydrogel contact lens (hereinafter also referred to as “SHCL”) has a property of easily adsorbing terpenoids. Thus, when the compounding component of eyedrops adsorb | sucks to a contact lens, there exists a possibility of causing a deformation | transformation and a quality change of a contact lens, and also anxious about the influence by the adsorbed component staying on a lens. In particular, since SHCL is harder than soft contact lenses that do not contain silicone as a raw material, it tends to cause a deterioration in the feeling of use due to lens deformation and wettability reduction. In addition, considering that CLCL is often used continuously over a relatively long period of time compared to soft contact lenses that do not contain silicone as a raw material, it can be said that when the lens is deformed, it is used continuously over a long period of time. , Can cause serious eye disease or ocular mucosal disease. Against this background, development of means for suppressing adsorption of terpenoids to SHCL is also required.

Therefore, an object of the present invention is to provide an ophthalmic composition exhibiting a histamine release-inhibiting action with a novel formulation that has not been conventionally used.

Another object of the present invention is to provide an ophthalmic composition for SHCL that can suppress adsorption of terpenoids to SHCL.

The inventors of the present invention tried to create an ophthalmic composition exhibiting a histamine release-inhibiting action and conducted extensive studies. Surprisingly, in the polymer and menthol having a phosphorylcholine-like group in the side chain, each histamine alone was used. It has been found that when these are used in combination at a specific blending ratio, a particularly excellent histamine release inhibitory effect is exhibited by a synergistic action, although the release inhibitory action is weak or absent.

In addition, the present inventors have found that SHCL has a property of easily adsorbing terpenoids, and as a means for solving this, a combination of a polymer having a phosphorylcholine-like group in the side chain and a terpenoid is used for SHCL. It was also found that it is effective in suppressing adsorption of terpenoids. Furthermore, the present inventors have found that, among SHCLs, nonionic silicone hydrogel contact lenses (hereinafter sometimes referred to as “nonionic SHCL”) have extremely high adhesion of corneal epithelial cells, Surprisingly, as a means for solving this problem, the inventors have also found that a combination of a polymer having a phosphorylcholine-like group in the side chain and a terpenoid can effectively suppress the adhesion of corneal cells to the nonionic SHCL surface. . The present invention has been completed by further studies based on this finding.

That is, the present invention provides the following ophthalmic compositions.
Item 1-1. (A) 0.001 to 2 w / v% of a polymer obtained by polymerizing the monomer represented by the general formula (I) alone or with another monomer capable of copolymerization;

[Wherein n1 is an integer of 2 to 4, R ₁ is a hydrogen atom or a methyl group, R ₂ is a group represented by — (R ₆ O) _n2 —R ₆ — (R ₆ has 1 to 4 carbon atoms] And n2 represents an integer of 0 to 5), and R ₃ to R ₅ are the same or different and each represents a hydrogen atom or an alkyl group having 1 to 4 carbon atoms. ]
(B-1) An ophthalmic composition comprising 0.001 to 0.02 w / v% menthol.
Item 1-2. The component (A) is a polymer of a monomer represented by the general formula (I), or a copolymer of a monomer represented by the general formula (I) and a monomer represented by the following general formula (II). The ophthalmic composition according to Item 1-1.

[Wherein R ₇ represents a hydrogen atom or a methyl group, and R ₈ represents a hydrogen atom or an alkyl group having 1 to 6 carbon atoms. ]
Item 1-3. Item 1. The ophthalmic composition according to Item 1-1 or 1-2, wherein the component (A) is a copolymer of 2-methacryloyloxyethyl phosphorylcholine and butyl methacrylate.
Item 1-4. Item 4. The ophthalmic composition according to any one of Items 1-1 to 1-3, comprising 0.02 to 20000 parts by weight of the total amount of component (B-1) per 100 parts by weight of component (A).
Item 1-5. Item 5. The ophthalmic composition according to any one of Items 1-1 to 1-4, which is an eye drop.
Item 1-6. Item 5. The ophthalmic composition according to any one of Items 1-1 to 1-4, which is an eye wash.
Item 1-7. Item 5. The ophthalmic composition according to any one of Items 1-1 to 1-4, which is a contact lens mounting solution.
Item 1-8. Item 5. The ophthalmic composition according to any one of Items 1-1 to 1-4, which is an eye drop for contact lenses.
Item 1-9. Item 5. The ophthalmic composition according to any one of Items 1-1 to 1-4, which is an eye drop for a soft contact lens.
Item 1-10. Item 5. The ophthalmic composition according to any one of Items 1-1 to 1-4, which is an eye drop for a silicone hydrogel contact lens.
Item 1-11. Item 5. The ophthalmic composition according to any one of Items 1-1 to 1-4, which is an eye drop for an ionic silicone hydrogel contact lens.
Item 1-12. Item 5. The ophthalmic composition according to any one of Items 1-1 to 1-4, which is an eye drop for a nonionic silicone hydrogel contact lens.

Moreover, this invention provides the ophthalmic composition for silicone hydrogel contact lenses hung up below.
Item 2-1. (A) a polymer obtained by polymerizing the monomer represented by the general formula (I) alone or with another monomer capable of copolymerization;

[Wherein n1 is an integer of 2 to 4, R ₁ is a hydrogen atom or a methyl group, R ₂ is a group represented by — (R ₆ O) _n2 —R ₆ — (R ₆ has 1 to 4 carbon atoms] And n2 represents an integer of 0 to 5), and R ₃ to R ₅ are the same or different and each represents a hydrogen atom or an alkyl group having 1 to 4 carbon atoms. ]
(B-2) An ophthalmic composition for a silicone hydrogel contact lens, comprising a terpenoid.
Item 2-2. The component (A) is a polymer of a monomer represented by the general formula (I), or a copolymer of a monomer represented by the general formula (I) and a monomer represented by the following general formula (II). The ophthalmic composition for silicone hydrogel contact lenses according to Item 2-1.

[Wherein R ₇ represents a hydrogen atom or a methyl group, and R ₈ represents a hydrogen atom or an alkyl group having 1 to 6 carbon atoms. ]
Item 2-3. Item 3. The ophthalmic composition for a silicone hydrogel contact lens according to Item 2-1 or 2-2, wherein the component (A) is a copolymer of 2-methacryloyloxyethyl phosphorylcholine and butyl methacrylate.
Item 2-4. Item (B-2) The ophthalmic composition for silicone hydrogel contact lenses according to any one of Items 2-1 to 2-3, containing menthol as a component.
Item 2-5. Item 5. The ophthalmic composition for silicone hydrogel contact lenses according to any one of Items 2-1 to 2-4, wherein the blending ratio of the component (A) is 0.0001 to 5 w / v%.
Item 2-6. Item (B-2) The ophthalmic composition for silicone hydrogel contact lenses according to any one of Items 2-1 to 2-5, wherein the blending ratio of the component is 0.0001 to 1 w / v%.
Item 2-7. The ophthalmic composition for a silicone hydrogel contact lens according to any one of Items 2-1 to 2-6, wherein the total amount of the component (B-2) is 0.0002 to 50000 parts by weight per 100 parts by weight of the component (A) .
Item 2-8. The ophthalmic composition for silicone hydrogel contact lenses according to any one of Items 2-1 to 2-7, which is an eye drop for silicone hydrogel contact lenses.
Item 2-9. The ophthalmic composition for silicone hydrogel contact lenses according to any one of Items 2-1 to 2-7, which is an eye wash for silicone hydrogel contact lenses.
Item 2-10. The ophthalmic composition for silicone hydrogel contact lenses according to any one of Items 2-1 to 2-7, which is a contact lens mounting liquid for silicone hydrogel contact lenses.
Item 2-11. The ophthalmic composition for silicone hydrogel contact lenses according to any one of Items 2-1 to 2-8, which is an eye drop for an ionic silicone hydrogel contact lens.
Item 2-12. Item 9. The ophthalmic composition for silicone hydrogel contact lenses according to any one of Items 2-1 to 2-8, which is an eye drop for a nonionic silicone hydrogel contact lens.

Furthermore, the present invention provides the following methods.
Item 3. In the ophthalmic composition, (A) 0.001 to 2 w / v% of a polymer obtained by polymerizing the monomer represented by the general formula (I) alone or with another copolymerizable monomer, and (B-1) menthol 0.001 to 0.02 A method for imparting histamine release inhibitory action to an ophthalmic composition, characterized by using w / v% in combination.
Item 4. (A) a polymer obtained by polymerizing a monomer represented by the general formula (I) alone or with another monomer capable of copolymerization and (B-2) an ophthalmic composition containing a terpenoid, and a silicone hydrogel contact lens. A method for suppressing adsorption of a terpenoid to a silicone hydrogel contact lens, which is characterized in that it is contacted.
Item 5. The ophthalmic composition is characterized in that (B) a terpenoid is blended with a polymer obtained by polymerizing the monomer represented by the general formula (I) alone or with another monomer capable of copolymerization, A method of imparting to the ophthalmic composition an action of suppressing adsorption of terpenoids to a silicone hydrogel contact lens.
Item 6. (A) a polymer obtained by polymerizing the monomer represented by the general formula (I) alone or with another monomer capable of copolymerization, and (B-2) an ophthalmic composition containing a terpenoid, and a nonionic silicone hydrogel contact A method for suppressing adhesion of corneal epithelial cells to a nonionic silicone hydrogel contact lens, comprising contacting the lens.
Item 7. The ophthalmic composition is characterized in that (B) a terpenoid is blended with a polymer obtained by polymerizing the monomer represented by the general formula (I) alone or with another monomer capable of copolymerization, A method of imparting to the ophthalmic composition an action of suppressing adhesion of corneal epithelial cells to a nonionic silicone hydrogel contact lens.

Furthermore, the present invention provides the uses listed below.
Item 8-1. A polymer obtained by polymerizing 0.001 to 2 w / v% of the monomer represented by (A) the general formula (I) alone or with another monomer capable of copolymerization,

[Wherein n1 is an integer of 2 to 4, R ₁ is a hydrogen atom or a methyl group, R ₂ is a group represented by — (R ₆ O) _n2 —R ₆ — (R ₆ has 1 to 4 carbon atoms] And n2 represents an integer of 0 to 5), and R ₃ to R ₅ are the same or different and each represents a hydrogen atom or an alkyl group having 1 to 4 carbon atoms. ]
With 0.001 to 0.02w / v% (B-1) menthol,
Use for the manufacture of an ophthalmic composition.
Item 8-2. Item 8. The use according to Item 8-1, wherein the ophthalmic composition is an eye drop.
Item 8-3. Item 9. The use according to Item 8-1, wherein the ophthalmic composition is an eye wash.
Item 8-4. Item 9. The use according to Item 8-1, wherein the ophthalmic composition is a contact lens mounting solution.
Item 8-5. Item 9. The use according to Item 8-1, wherein the ophthalmic composition is an eye drop for contact lenses.
Item 8-6. Item 9. The use according to Item 8-1, wherein the ophthalmic composition is an eye drop for soft contact lenses.
Item 8-7. Item 9. The use according to Item 8-1, wherein the ophthalmic composition is an eye drop for a silicone hydrogel contact lens.
Item 8-8. Item 8. The use according to Item 8-1, wherein the ophthalmic composition is an eye drop for an ionic silicone hydrogel contact lens.
Item 8-9. Item 9. The use according to Item 8-1, wherein the ophthalmic composition is an eye drop for a nonionic silicone hydrogel contact lens.
Item 8-10. Item 9. The use according to Item 8-1, wherein the ophthalmic composition is a histamine release inhibitor.
Item 8-11. Item 8. The use according to Item 8-1, wherein the ophthalmic composition is an antiallergic agent, an eye itch suppressor, or an agent that suppresses discomfort when wearing a contact lens.
Item 9-1. (A) a polymer obtained by polymerizing the monomer represented by the general formula (I) alone or with another monomer capable of copolymerization;

[Wherein n1 is an integer of 2 to 4, R ₁ is a hydrogen atom or a methyl group, R ₂ is a group represented by — (R ₆ O) _n2 —R ₆ — (R ₆ has 1 to 4 carbon atoms] And n2 represents an integer of 0 to 5), and R ₃ to R ₅ are the same or different and each represents a hydrogen atom or an alkyl group having 1 to 4 carbon atoms. ]
(B-2) with a terpenoid
Use for the manufacture of an ophthalmic composition for silicone hydrogel contact lenses.
Item 9-2. Item 9. The use according to Item 9-1, wherein the ophthalmic composition for a silicone hydrogel contact lens is an eye drop for a silicone hydrogel contact lens.
Item 9-3. Item 9. The use according to Item 9-1, wherein the ophthalmic composition for a silicone hydrogel contact lens is an eyewash for a silicone hydrogel contact lens.
Item 9-4. Item 9. The use according to Item 9-1, wherein the ophthalmic composition for a silicone hydrogel contact lens is a contact lens mounting liquid for a silicone hydrogel contact lens.
Item 9-5. The use according to Item 9-1, wherein the ophthalmic composition is a histamine release inhibitor.
Item 9-6. Item 9. The use according to Item 9-1, wherein the ophthalmic composition is an antiallergic agent, an eye itching inhibitor, or a discomfort inhibitor when wearing a contact lens.

Since the ophthalmic composition of the present invention exhibits an excellent histamine release inhibitory action, it is useful for ophthalmic preparations for uses such as antiallergy, itching, and discomfort when wearing contact lenses.

In addition, the present inventors have clarified that SHCL has a property of easily adsorbing terpenoids, but according to the ophthalmic composition for SHCL of the present invention, it suppresses the adsorption of terpenoids to SHCL. It is possible to secure sufficient safety in using SHCL.

Furthermore, the present inventors have clarified that nonionic SHCL has a unique property that corneal cells easily adhere, but according to the ophthalmic composition for SHCL of the present invention, non-ionic SHCL Corneal cell adhesion to ionic SHCL can be effectively suppressed. Therefore, according to the ophthalmic composition for SHCL of the present invention, it is possible to reduce damage to the corneal surface even when the lens is removed from the eye, and it is possible to wear nonionic SHCL with high safety. To do.

In Test Example 1, it is a figure which shows the result of having evaluated the histamine release inhibitory effect of the test substance (Examples 1-1 to 1-6 and Comparative Examples 1-1 to 1-9) of various density | concentrations. In Test Example 1, the results of evaluating the histamine release inhibitory effect of various concentrations of test substances (Examples 1-7 to 1-10 and Comparative Examples 1-3 to 1-5, 1-8 and 1-10) FIG. In Test Example 1, the results of evaluating the histamine release inhibitory effect of various concentrations of test substances (Examples 1-11 to 1-14 and Comparative Examples 1-4 to 1-6, 1-8 and 1-11) FIG. In Test Example 1, it is a figure which shows the result of having evaluated the histamine release inhibitory effect of the test substance (Comparative Examples 1-4-1-5 and 1-12-1-14) of various density | concentrations. In the reference test example 1, it is a figure which shows the result of having evaluated the histamine release inhibitory effect about the pyridoxine hydrochloride single (reference example 1) and the combination (reference example 2) of the pyridoxine hydrochloride and MPC polymer. In Experiment 2, it is a figure which shows the result of having measured the adsorption amount of the menthol to SHCL using each prescription liquid (Example 2-1 and Comparative Example 2-1). In Experiment 2, it is a figure which shows the result of having measured the adsorption amount of the camphor to SHCL using each prescription liquid (Example 2-1 and Comparative Example 2-1). In the reference test example 2, it is a figure which shows the result of having evaluated the adhesiveness of the corneal epithelial cell to various soft contact lenses. In Experiment 3, it is a figure which shows the result of having evaluated the corneal epithelial cell adhesion inhibitory effect with respect to nonionic SHCL of each prescription liquid (Example 3-1 and Comparative Examples 3-1 and 3-3). In Test Example 3, it is a figure which shows the result of having evaluated the corneal epithelial cell adhesion inhibitory effect with respect to nonionic SHCL of each prescription liquid (Example 3-2, Comparative Examples 3-2, 3-4). In Experiment 3, it is a figure which shows the result of having evaluated the corneal epithelial cell adhesion inhibitory effect with respect to nonionic SHCL of each prescription liquid (Example 3-3, Comparative Examples 3-5, 3-6). In Experiment 3, it is a figure which shows the result of having evaluated the corneal epithelial cell adhesion inhibitory effect with respect to nonionic SHCL of each prescription liquid (Example 3-4, Comparative Examples 3-1 and 3-7). In the reference test example 3, it is a figure which shows the result of having evaluated the corneal epithelial cell adhesion inhibitory effect with respect to nonionic SHCL about the tetrahydrozoline hydrochloride independent (reference example 3) and the combination of tetrahydrozoline hydrochloride and MPC polymer (reference example 4).

The present invention relates to an ophthalmic composition that exhibits an excellent inhibitory effect on histamine release (hereinafter sometimes referred to as ophthalmic composition-1), and an ophthalmic composition for SHCL that can suppress adsorption of terpenoids to SHCL (hereinafter referred to as ophthalmic composition). In some cases) and various methods. Hereinafter, specific embodiments will be described in detail for each of these inventions. In this specification, the unit “w / v%” of the blending ratio is synonymous with “g / 100 mL”.

1. Ophthalmic composition-1
The ophthalmic composition-1 of the present invention is a polymer obtained by polymerizing a monomer represented by the following general formula (I) with another monomer that can be copolymerized alone or copolymerized (hereinafter, simply referred to as “component (A)”) May be included) at a rate of 0.001 to 2 w / v%.

In general formula (I), n1 represents an integer of 2 to 4, preferably 2 or 3, and more preferably 2.

In general formula (I), R ₁ represents a hydrogen atom or a methyl group, preferably a methyl group.

In the general formula (I), R ₂ represents a group represented by — (R ₆ O) _n2 —R ₆ —. Here, R ₆ represents an alkylene group having 1 to 4 carbon atoms. Specific examples of such an alkylene group include a methylene group, an ethylene group, a propylene group, and a butylene group. R ₆ is preferably an alkylene group having 1 to 3 carbon atoms, more preferably an alkylene group having 2 carbon atoms (ethylene group). N2 represents an integer of 0 to 5, preferably an integer of 0 to 2, and more preferably 0.

In general formula (I), R ₃ to R ₅ are the same or different and each represents a hydrogen atom or an alkyl group having 1 to 4 carbon atoms. Examples of such an alkyl group include a methyl group, an ethyl group, an n-propyl group, and an n-butyl group. R ₃ to R ₅ are preferably a hydrogen atom or an alkyl group having 1 to 2 carbon atoms, more preferably an alkyl group having 1 carbon atom (methyl group).

Formula Preferable examples of the monomer represented by (I), 2-methacryloyloxyethyl phosphorylcholine (MPC; n1 is 2, R ₁ is methyl, R ₂ is an ethylene group, R 3 _~ R ₅ is a methyl group) 2-methacryloyloxyethyl phosphorylethanolamine (MPE; n1 is 2, R ₁ is methyl group, R ₂ is ethylene group, R ₃ to R ₅ are hydrogen atoms), particularly preferably 2-methacryloyloxyethyl phosphorylcholine The

In the ophthalmic composition-1 of the present invention, the component (A) is a polymer of a monomer represented by the general formula (I) (hereinafter sometimes simply referred to as “monomer (I)”). It may also be a copolymer of monomer (I) and another monomer, or a mixture of a polymer of monomer (I) and a copolymer of monomer (I) and another monomer. There may be.

When a copolymer is used as the component (A), as a monomer other than the monomer (I), the finally obtained copolymer is pharmaceutically, pharmacologically (pharmaceutically) or physiologically. Although it does not restrict | limit as long as it is accept | permitted, As a suitable example, the monomer (henceforth only described as "monomer (II)") represented by the following general formula (II) is illustrated.

In the general formula (II), R ₇ represents a hydrogen atom or a methyl group, preferably a methyl group.

In the general formula (II), R ₈ represents a hydrogen atom or an alkyl group having 1 to 6 carbon atoms. Examples of such an alkyl group include a methyl group, an ethyl group, an n-propyl group, an n-butyl group, an n-pentyl group, and an n-hexyl group. R ₈ is preferably an alkyl group having 1 to 5 carbon atoms, more preferably an alkyl group having 1 to 4 carbon atoms, and particularly preferably an alkyl group having 4 carbon atoms (n-butyl group).

Preferred examples of the monomer (II) include butyl methacrylate (BMA; R ₇ is methyl group, R ₈ is n-butyl group), methyl methacrylate (MMA; R ₇ is methyl group, R ₈ is methyl group), 2- Examples thereof include hydroxyethyl methacrylate (HEMA; R ₇ is methyl group, R ₈ is hydroxyethyl group); more preferably, 2-hydroxyethyl methacrylate, butyl methacrylate; and particularly preferably butyl methacrylate.

When monomer (II) can take the form of a salt (for example, when R ₇ is a hydrogen atom), monomer (II) may be a salt. Examples of the salt form of monomer (II) include alkali metal salts such as sodium and potassium.

When using a copolymer as the component (A), the composition ratio of the monomer (I) and other monomers varies depending on the structure of the monomer used, etc., but effectively exerts a preventive or therapeutic effect on dry eye. From the viewpoint, the monomer (I) is usually 50 to 95 mol%, preferably 60 to 90 mol%, more preferably 75 to 85 mol%, based on the total amount of the copolymer.

In addition, the molecular weight of the polymer used as the component (A) varies depending on the type of monomer, etc., and is limited as long as it is pharmaceutically, pharmacologically (pharmaceutically) or physiologically acceptable. However, for example, the weight average molecular weight is 5,000 to 2,000,000, preferably 40,000 to 1,200,000, more preferably 100,000 to 1,000,000, and particularly preferably 400,000 to 800,000. The weight average molecular weight is measured by GPC analysis.

Monomer (I) and monomer (II) are known compounds or known methods from known compounds (for example, JP-A-58-154591, JP-A-60-184093, polymer articles) Vol.35, 423-427, 1978, published by the Society of Polymer Science, Japan).

The polymer used as the component (A) can be obtained by polymerizing the monomer (I) and, if necessary, other monomers according to a known method in the field of polymer chemistry. Specifically, the polymerization reaction is carried out in the presence of a polymerization initiator in an appropriate solvent such as water, methanol, ethanol, propanol, t-butanol, benzene, toluene, dimethylformamide, tetrahydrofuran, chloroform, or a mixed solvent thereof. The polymerization may be performed for a certain period of time under appropriate temperature conditions.

In the ophthalmic composition-1 of the present invention, among the components (A), the polymer of the monomer (I), the copolymer of the monomer (I) and the monomer (II); more preferably MPC or MPE Polymer, copolymer of MPC or MPE and HEMA or BMA; even more preferably, homopolymer of MPC, copolymer of MPC and HEMA, copolymer of MPC and BMA; particularly preferably copolymer of MPC and BMA Examples are polymers. In the present specification, the MPC homopolymer or the copolymer of MPC and monomer (II) may be referred to as MPC polymer.

The polymer used as the component (A) can be a commercially available product, and as the commercially available component (A), the Lipidure series (trade name: “LIPIDURE-PMB (BG ) ”,“ LIPIDURE-PMB (Ph10) ”,“ LIPIDURE-PMB ”,“ LIPIDURE-HM ”,“ LIPIDURE-HM-500 ”).

In the ophthalmic composition-1 of the present invention, the blending ratio of the component (A) is set within the range of 0.001 to 2 w / v% of the total amount of the component (A) with respect to the total amount of the ophthalmic composition-1. However, from the viewpoint of further enhancing the histamine release inhibitory action, it is more preferably 0.005 to 2 w / v%, still more preferably 0.01 to 2 w / v%, still more preferably 0.01 to 1 w / v%, particularly preferably. Examples are 0.01 to 0.5 w / v%. The blending ratio of the component (A) exemplified here is also suitable from the viewpoint of suppressing menthol adsorption to SHCL or suppressing adhesion of corneal epithelial cells to nonionic SHCL.

In addition to the component (A), the ophthalmic composition-1 of the present invention contains menthol (hereinafter sometimes simply referred to as the component (B-1)) at a rate of 0.001 to 0.02 w / v%. . In this way, by using the components (A) and (B-1) in combination at a specific ratio, it is possible to synergistically enhance and exhibit the histamine release inhibitory action. Further, the combined use of the component (A) and the component (B-1) is also effective in obtaining an effect of inhibiting menthol adsorption on SHCL and an effect of inhibiting cell adhesion on nonionic SHCL.

The menthol used as the component (B-1) is not particularly limited as long as it is pharmaceutically, pharmacologically (pharmaceutically) or physiologically acceptable, and may be any of d-form, l-form or dl-form. Good. In the present invention, an essential oil containing menthol may be used as the component (B-1). Examples of such essential oils include cool mint oil, peppermint oil, and peppermint oil.

Of these (B-1) components, l-menthol and the like are preferable from the viewpoint of further enhancing the histamine release inhibitory action.

In the ophthalmic composition-1 of the present invention, the blending ratio of the component (B-1) is in the range of 0.001 to 0.02 w / v% of the total amount of the component (B-1) with respect to the total amount of the ophthalmic composition-1. However, it is preferably 0.001 to 0.015 w / v%, more preferably 0.001 to 0.01 w / v% from the viewpoint of further enhancing the histamine release inhibitory action. The blending ratio of the component (B-1) exemplified here is also effective for suppressing adsorption of menthol to SHCL or suppressing adhesion of corneal epithelial cells to nonionic SHCL. In addition, when using the essential oil containing menthol as said (B-1) component, it sets so that the menthol content in the essential oil mix | blended may satisfy | fill the said mixture ratio.

In the ophthalmic composition-1 of the present invention, the ratio of the component (B-1) to the component (A) is not particularly limited as long as the blending ratio described above is satisfied, but it further enhances the histamine release inhibitory action. From the viewpoint, the ratio that the total amount of component (B-1) is 0.02 to 20000 parts by weight, preferably 0.2 to 2000 parts by weight, more preferably 0.2 to 200 parts by weight per 100 parts by weight of the total amount of component (A) is satisfied. It is desirable to do. The blending ratio of the component (B-1) exemplified here is effective in suppressing adsorption of menthol to SHCL or suppressing adhesion of corneal epithelial cells to nonionic SHCL, but nonionic SHCL From the standpoint of further enhancing the adhesion-suppressing action of corneal epithelial cells, the total amount of component (B-1) is preferably 0.4 to 100 parts by weight per 100 parts by weight of component (A). In addition, when using the essential oil containing menthol as said (B-1) component, the menthol content in the essential oil mix | blended is set so that the said ratio may be satisfy | filled.

The ophthalmic composition-1 of the present invention preferably further contains a buffering agent in addition to the components (A) and (B-1). The buffering agent that can be incorporated into the ophthalmic composition-1 of the present invention is not particularly limited as long as it is pharmaceutically, pharmacologically (pharmaceutically) or physiologically acceptable. Examples of such buffers include borate buffer, phosphate buffer, carbonate buffer, citrate buffer, acetate buffer, tris buffer, epsilon-aminocaproic acid, aspartic acid, aspartate and the like. These buffering agents may be used in combination. Preferred buffering agents are borate buffer, phosphate buffer, carbonate buffer, and citrate buffer, and particularly preferred buffers are borate buffer and phosphate buffer. Examples of the boric acid buffer include borates such as alkali metal borate and alkaline earth metal borate. Examples of the phosphate buffer include phosphates such as alkali metal phosphates and alkaline earth metal phosphates. Examples of the carbonate buffer include carbonates such as alkali metal carbonates and alkaline earth metal carbonates. Examples of the citrate buffer include alkali metal citrate and alkaline earth metal citrate. Moreover, you may use the borate or the hydrate of a phosphate as a borate buffer or a phosphate buffer. As more specific examples, boric acid or a salt thereof (sodium borate, potassium tetraborate, potassium metaborate, ammonium borate, borax, etc.), phosphoric acid or a salt thereof (disodium hydrogen phosphate, dihydrogen phosphate) Sodium, potassium dihydrogen phosphate, trisodium phosphate, dipotassium phosphate, calcium monohydrogen phosphate, calcium dihydrogen phosphate), carbonic acid or a salt thereof (sodium hydrogen carbonate, sodium carbonate, ammonium carbonate, potassium carbonate, Calcium carbonate, potassium hydrogen carbonate, magnesium carbonate, etc.), citric acid or a salt thereof (sodium citrate, potassium citrate, calcium citrate, sodium dihydrogen citrate, disodium citrate, etc.), acetic acid or a salt thereof (ammonium acetate) , Potassium acetate, calcium acetate, sodium acetate, etc.), asparagus Examples thereof include formic acid or a salt thereof (sodium aspartate, magnesium aspartate, potassium aspartate, etc.). These buffering agents may be used alone or in any combination of two or more. Among these buffering agents, boric acid buffering agents are preferably used from the viewpoint of further enhancing the effects of the present invention. Among boric acid buffering agents, boric acid and / or borax are particularly preferable, and an embodiment in which boric acid and borax are used in combination is most preferable.

When a buffering agent is blended in the ophthalmic composition-1 of the present invention, the blending ratio of the buffering agent varies depending on the type of buffering agent used, the type and amount of other blending components, and should be specified uniformly. However, for example, the total amount of the buffer is 0.01 to 10 w / v%, preferably 0.1 to 5 w / v%, more preferably 0.5 to 2 w with respect to the total amount of ophthalmic composition-1. A ratio of / v% is exemplified. In particular, when the buffer is a borate buffer, for example, the total amount of borate buffer is 0.1 to 5 w / v%, preferably 0.1 to 3 w / v with respect to the total amount of ophthalmic composition-1. Examples are v%, more preferably 0.2 to 2 w / v%, particularly preferably 0.5 to 2 w / v%.

The ophthalmic composition-1 of the present invention preferably further contains a surfactant. The surfactant that can be blended in the ophthalmic composition-1 of the present invention is not particularly limited as long as it is pharmaceutically, pharmacologically (pharmaceutically) or physiologically acceptable, and is nonionic surfactant. Any of an agent, an amphoteric surfactant, an anionic surfactant, and a cationic surfactant may be used.

Specific examples of the nonionic surfactant that can be blended in the ophthalmic composition-1 of the present invention include monolauric acid POE (20) sorbitan (polysorbate 20), monopalmitic acid POE (20) sorbitan (polysorbate 40). POE sorbitan fatty acid esters such as monostearic acid POE (20) sorbitan (polysorbate 60), tristearic acid POE (20) sorbitan (polysorbate 65), monooleic acid POE (20) sorbitan (polysorbate 80); POE / POP block copolymers such as poloxamer 235, poloxamer 188, poloxamer 403, poloxamer 237 and poloxamer 124; POE cured castor oil such as POE (60) hydrogenated castor oil (polyoxyethylene hydrogenated castor oil 60); POE ( 9) POE alkyl ethers such as lauryl ether; POE-POP alkyl ethers such as POE (20) POP (4) cetyl ether POE (10) POE alkylphenyl ethers such as nonylphenyl ether. In the compounds exemplified above, POE is polyoxyethylene, POP is polyoxypropylene, and the numbers in parentheses indicate the number of moles added. Specific examples of amphoteric surfactants that can be incorporated into the ophthalmic composition-1 of the present invention include alkyldiaminoethylglycine. Specific examples of the cationic surfactant that can be blended in the ophthalmic composition-1 of the present invention include benzalkonium chloride and benzethonium chloride. Specific examples of the anionic surfactant that can be incorporated into the ophthalmic composition-1 of the present invention include alkylbenzene sulfonate, alkyl sulfate, polyoxyethylene alkyl sulfate, and aliphatic α-sulfomethyl. Examples include esters and α-olefin sulfonic acids. In the ophthalmic composition-1 of the present invention, these surfactants may be used alone or in combination of two or more. Among these surfactants, nonionic surfactants are preferred, and particularly preferred surfactants include POE (60) hydrogenated castor oil (polyoxyethylene hydrogenated castor oil 60), poloxamer 407, monooleic acid. POE (20) sorbitan (polysorbate 80).

When the surfactant is blended with the ophthalmic composition-1 of the present invention, the blending ratio of the surfactant can be appropriately set according to the kind of surfactant, the kind and amount of other blending components, and the like. As an example of the blending ratio of the surfactant, the total amount of the surfactant is 0.001 to 1.0 w / v%, preferably 0.005 to 0.5 w / v with respect to the total amount of the ophthalmic composition-1. %, More preferably 0.01 to 0.3 w / v%.

The ophthalmic composition-1 of the present invention preferably further contains an isotonic agent. The isotonic agent that can be incorporated into the ophthalmic composition-1 of the present invention is not particularly limited as long as it is pharmaceutically, pharmacologically (pharmaceutically) or physiologically acceptable. Specific examples of such isotonic agents include, for example, sodium bisulfite, sodium sulfite, potassium chloride, calcium chloride, sodium chloride, magnesium chloride, potassium acetate, sodium acetate, sodium bicarbonate, sodium carbonate, sodium thiosulfate, magnesium sulfate , Glycerin, propylene glycol and the like. These isotonic agents may be used alone or in any combination of two or more.

When an isotonic agent is blended in the ophthalmic composition-1 of the present invention, the blending ratio of the isotonic agent varies depending on the type of tonicity agent used and cannot be uniformly defined. For example, the total amount of tonicity agent is 0.01 to 10 w / v%, preferably 0.05 to 5 w / v%, more preferably 0.1 to 2 w /% with respect to the total amount of ophthalmic composition-1. The ratio of v% is exemplified.

The pH of the ophthalmic composition-1 of the present invention is not particularly limited as long as it is within a pharmaceutically, pharmacologically (pharmaceutically) or physiologically acceptable range. An example of the pH of the ophthalmic composition-1 of the present invention is in the range of 4.0 to 9.5, preferably 5.0 to 8.5, and more preferably 5.5 to 8.0.

In addition, the osmotic pressure of the ophthalmic composition-1 of the present invention is not particularly limited as long as it is within a range acceptable for a living body. An example of the osmotic pressure ratio of the ophthalmic composition-1 of the present invention is preferably in the range of 0.7 to 5.0, more preferably 0.9 to 3.0, particularly preferably 1.0 to 2.0. Can be mentioned. The osmotic pressure can be adjusted by a method known in the art using inorganic salts, polyhydric alcohols, sugar alcohols, saccharides and the like. The osmotic pressure ratio is the ratio of the osmotic pressure of the sample to the osmotic pressure of 0.9w / v% sodium chloride aqueous solution based on the 15th revised Japanese Pharmacopoeia. Measure with reference to. The standard solution for osmotic pressure ratio measurement is sodium chloride (Japanese Pharmacopoeia standard reagent) dried at 500-650 ° C for 40-50 minutes, then allowed to cool in a desiccator (silica gel), accurately weigh 0.900 g and purify. Dissolve in water to prepare exactly 100 mL, or use a commercially available standard solution for osmotic pressure ratio measurement (0.9 w / v% sodium chloride aqueous solution).

The ophthalmic composition-1 of the present invention can contain a proper amount of various active ingredients (pharmacologically active ingredients, physiologically active ingredients, etc.) in combination with the above ingredients.

Further, in the ophthalmic composition-1 of the present invention, various components and additives are appropriately selected in accordance with conventional methods depending on the use and form as long as they do not impair the effects of the invention. The above can be used in combination.

The ophthalmic composition-1 of the present invention is prepared by adding a desired amount of the above-mentioned components (A) and (B-1) and, if necessary, other blending components to a desired concentration. For example, in the case of eye drops, contact lens mounting solution, eye wash or contact lens care agent, the above components are dissolved or suspended in purified water, adjusted to a predetermined pH and osmotic pressure, and sterilized by filtration sterilization or the like. Can be prepared. For the dissolution of highly hydrophobic components such as menthol (terpenoids), after stirring together with components that have a solubilizing action such as surfactants in advance, it may be dissolved or suspended by adding purified water. Good.

The ophthalmic composition-1 of the present invention is not particularly limited as long as it can be used in the ophthalmic field, and examples thereof include a liquid form and an ointment form. Among these, liquid is preferable. When the ophthalmic composition-1 of the present invention is liquefied, water that is pharmaceutically, pharmacologically (pharmaceutically) or physiologically acceptable may be used as an aqueous carrier. Examples include distilled water, normal water, purified water, sterilized purified water, water for injection, distilled water for injection, and the like. These definitions are based on the 15th revision Japanese Pharmacopoeia.

In addition, the ophthalmic composition-1 of the present invention comprises eye drops (however, eye drops include eye drops that can be applied while wearing contact lenses), eye ointments, eye wash (however, eye lenses are contact lenses) Including eye wash that can be washed while wearing), contact lens mounting fluid, contact lens care agent (contact lens disinfectant, contact lens preservative, contact lens cleaner, contact lens cleaner, etc.) ) Etc. Among these, eye drops, eye washes, and contact lens mounting liquids, in particular eye drops, are suitable formulation forms of the ophthalmic composition-1 of the present invention. In the present specification, the term “contact lens” includes all contact lenses including hard contact lenses, oxygen-permeable hard contact lenses, soft contact lenses, and silicone hydrogel lenses.

In addition, as shown in Test Example 2 to be described later, the inventors' research has revealed that menthol is significantly more easily adsorbed by SHCL than conventional soft contact lenses not containing a silicone material. On the other hand, according to the ophthalmic composition-1 of the present invention, by using the components (A) and (B-1) together, adsorption of menthol to SHCL can be suppressed, and SHCL is used with high safety. It is possible to do. In view of the adsorption inhibitory effect of menthol, an example of a suitable formulation form of the ophthalmic composition-1 of the present invention is an eye drop that can be instilled during SHCL wearing (SHCL eye drop). In particular, among SHCL, ionic SHCL is more easily adsorbed by menthol than nonionic SHCL, and a higher menthol adsorption suppression effect is required. According to this, the adsorption of menthol to ionic SHCL can also be effectively suppressed. In view of such characteristics, an example of a suitable formulation form of the ophthalmic composition-1 of the present invention is an eye drop that can be instilled during ionic SHCL wearing (an eye drop for ionic SHCL). In addition, in this specification, when it only displays as SHCL, both ionic and nonionic SHCL are included. Here, ionic SHCL refers to SHCL with an ionic component content of 1 mol% or more in the SHCL material in accordance with US FDA (US Food and Drug Administration) standards, and nonionic SHCL refers to US FDA (US According to Food and Drug Administration), this refers to SHCL whose ionic component content in contact lens materials is less than 1 mol%.

In addition, as shown in Reference Test Example 2 to be described later, the study by the present inventors has revealed that ionic epithelial cells are remarkably easily adhered to nonionic SHCL among soft contact lenses. Furthermore, when the component (A) is present alone, adhesion of corneal epithelial cells to nonionic SHCL can hardly be suppressed, and even when the component (B-1) is present alone, It has also been clarified by the present inventor that adhesion of corneal epithelial cells to ionic SHCL cannot be sufficiently suppressed. Such a contact lens having high adhesion of corneal cells is obtained from the eye tissue when the contact lens is worn, when the corneal cell adheres to the lens on the cornea and the lens moves or when the lens is removed. May cause damage to the surface of the cornea and pain associated therewith, which may significantly reduce the quality of life (QOL) of the contact lens user. In contrast, according to the ophthalmic composition-1 of the present invention, the combined use of the above components (A) and (B-1) can synergistically suppress corneal cell adhesion with high nonionic SHCL. Thus, it is possible to wear nonionic SHCL with high safety, and the above-mentioned problems peculiar to nonionic SHCL can be solved. That is, when the ophthalmic composition-1 of the present invention is supplied as an eye drop that can be instilled while wearing nonionic SHCL (an eye drop for nonionic SHCL), the histamine release inhibitory effect and the terpenoid to SHCL In addition to the effect of suppressing adsorption of corneal cells, it can also have an effect of suppressing adhesion of corneal cells to nonionic SHCL. In view of such effects, an example of a suitable formulation form of the ophthalmic composition-1 of the present invention is an eye drop that can be instilled while wearing a non-ionic SHCL (non-ionic SHCL eye drop). . As an example of a suitable application target for exhibiting the corneal epithelial cell adhesion inhibitory effect using the ophthalmic composition-1 of the present invention, among nonionic SHCL, mention may be made of nonionic SHCL having a water content of 35% or less. it can. Since SHCL contains a hydrogel material, it contains at least more than 0% moisture.

Here, the moisture content of SHCL indicates the ratio of water in SHCL, and is specifically determined by the following formula.

Moisture content (%) = (weight of hydrated water / weight of hydrated SHCL) x 100
Such moisture content can be measured by a gravimetric method according to the description of ISO18369-4: 2006.

The ophthalmic composition-1 of the present invention is an eye drop that can be instilled while wearing a contact lens (eye drop for contact lens), an eye wash that can be washed while wearing a contact lens (eye wash for contact lens), and an eye drop for SHCL , Ionic SHCL eye drops, or non-ionic SHCL eye drops, it may be applied directly to the eye wearing each lens, or applied to the eye before each lens is attached. May be.

Since the ophthalmic composition-1 of the present invention can exert a histamine release inhibitory action by the synergistic action of the components (A) and (B-1), it is antiallergic (for pollen, etc.), itching is suppressed, and contact lenses are not used. Can be used for purposes such as pleasure suppression. The ophthalmic composition-1 of the present invention is effective for preventing or treating dry eye and dry eyes based on the component (A), and is also useful for improving dry eye and dry eyes.

The container for storing the ophthalmic composition-1 of the present invention may be made of glass or plastic. When the plastic container is used as the container for storing the ophthalmic composition-1 of the present invention, the constituent material of the plastic container is not particularly limited. For example, polyethylene naphthalate, polyarylate, polyethylene terephthalate, polypropylene, polyethylene , Any one of polyimide, a copolymer thereof, or a mixture of two or more. The copolymer is mainly composed of any one of ethylene-2,6-naphthalate units, arylate units, ethylene terephthalate units, propylene units, ethylene units, and imide units, and other polyester units and imide units. Examples of the copolymer include.

2. Ophthalmic composition-2
The ophthalmic composition-2 of the present invention is an ophthalmic composition used for SHCL.

The ophthalmic composition-2 of the present invention is a polymer in which the monomer represented by the general formula (I) is polymerized with another monomer that can be copolymerized alone or copolymerized (hereinafter simply referred to as “component (A)”) Is also included. The types of component (A) used in ophthalmic composition-2 of the present invention and preferred examples of component (A) are the same as component (A) used in ophthalmic composition-1. .

In the ophthalmic composition-2 of the present invention, the content of the component (A) is not particularly limited, but from the viewpoint of further enhancing the action of inhibiting the adsorption of terpenoids to SHCL, the total amount of the ophthalmic composition-2 The total amount of component (A) is 0.0001 to 5 w / v%, preferably 0.001 to 2 w / v%, more preferably 0.01 to 1 w / v%, still more preferably 0.01 to 0.5 w / v%, and particularly preferably 0.02 to 0.5% w / v. When the content ratio of component (A) satisfies the above range, it is effective to more effectively suppress the adhesion of corneal epithelial cells to nonionic SHCL, but particularly when it is 0.05 to 0.25 w / v%. It becomes possible to remarkably enhance the adhesion-suppressing effect of corneal epithelial cells on nonionic SHCL.

The ophthalmic composition-2 of the present invention contains a terpenoid (hereinafter sometimes referred to as the component (B-2)) in addition to the component (A). Thus, by using the components (A) and (B-2) in combination, it becomes possible to effectively suppress the adsorption of terpenoids to SHCL. Such combined use of component (A) and component (B-2) is also effective in obtaining an effect of inhibiting cell adhesion to nonionic SHCL.

The terpenoid used as the component (B-2) is not particularly limited as long as it is pharmaceutically, pharmacologically (pharmaceutically) or physiologically acceptable. Specific examples of such terpenoids include menthol, menthone, camphor, borneol, geraniol, cineol, citronellol, carvone, anethole, eugenol, limonene, linalool, linalyl acetate, and derivatives thereof. These compounds may be d-form, l-form or dl-form. In the present invention, an essential oil containing the above compound may be used as a terpenoid. Examples of such essential oils include eucalyptus oil, bergamot oil, peppermint oil, cool mint oil, spearmint oil, peppermint oil, fennel oil, cinnamon oil, and rose oil. These terpenoids may be used alone or in any combination of two or more.

Among these (B-2) components, from the viewpoint of further enhancing the terpenoid adsorption inhibitory action on SHCL or the cell adhesion inhibitory action on nonionic SHCL, preferably, menthol, camphor, borneol and the like, Preferred essential oils containing these include cool mint oil, peppermint oil, peppermint oil, camphor oil and the like. More preferably, menthol and camphor (d-camphor, dl-camphor, etc.) are mentioned, and more preferably, menthols such as l-menthol, d-menthol and dl-menthol or derivatives thereof are included, and these are contained. Examples of essential oils include cool mint oil, peppermint oil, and peppermint oil. Particularly preferred is l-menthol.

In the ophthalmic composition-2 of the present invention, the content ratio of the component (B-2) is not particularly limited, but from the viewpoint of further enhancing the action of inhibiting the adsorption of terpenoids to SHCL, the total amount of the ophthalmic composition-2 is used. On the other hand, the total amount of component (B-2) is 0.0001 to 1 w / v%, preferably 0.001 to 0.08 w / v%, more preferably 0.001 to 0.05 w / v%, and particularly preferably 0.001 to 0.02 w / v%. Is mentioned. When the content ratio of the component (B-2) satisfies the above range, it is effective in further effectively suppressing adhesion of corneal epithelial cells to nonionic SHCL. In addition, when using the essential oil containing a terpenoid as said (B-2) component, it sets so that the total amount of terpenoid content in the essential oil mix | blended may satisfy | fill the said content rate.

In the ophthalmic composition-2 of the present invention, the ratio of the component (B-2) to the component (A) is not particularly limited as long as the content ratio described above is satisfied, but the action of inhibiting adsorption of terpenoids to SHCL From the viewpoint of further increasing the total amount of component (A), the total amount of component (B-2) is 0.0002 to 50,000 parts by weight, preferably 0.02 to 500 parts by weight, more preferably 0.2 to 500 parts by weight, per 100 parts by weight of component (A). It is desirable to satisfy this ratio. In addition, from the viewpoint of further enhancing the cell adhesion inhibitory action to nonionic SHCL while having the adsorption inhibitory action of terpenoids on SHCL, the total amount of (A) ingredient per 100 parts by weight of (B-2) ingredient It is desirable that the ratio is such that the total amount is 0.2 to 5000 parts by weight, preferably 0.2 to 2000 parts by weight, and more preferably 0.4 to 100 parts by weight.

In addition, in the ophthalmic composition-2, from the viewpoint of having an excellent inhibitory action on histamine release while having an inhibitory action on adsorption of terpenoids to SHCL or an inhibitory action on cell adhesion to nonionic SHCL, (B -2) Menthol is used as the component, and the content of component (A) is 0.001 to 2 w / v%, preferably 0.005 to 2 w / v%, more preferably 0.01 to the total amount of ophthalmic composition-2. To 2 w / v%, particularly preferably 0.01 to 1 w / v%, most preferably 0.01 to 0.5 w / v%, and the content of component (B-2) is 0.001 to 0.02 w / v%, preferably 0.001 It is desirable to satisfy ˜0.015 w / v%, more preferably 0.001 to 0.01 w / v%. Furthermore, from the viewpoint of having an excellent inhibitory action on histamine release while having an action to suppress adsorption of terpenoids to SHCL or a cell adhesion inhibitory action to nonionic SHCL, the above (A) and (B- 2) The ratio of the component (A) to the component (B-2) is 100% by weight of the total amount of the component (A), and the total amount of the component (B-2) is 0.02 to 20000 wt. Part, preferably 0.2 to 2000 parts by weight, more preferably 0.2 to 200 parts by weight.

The ophthalmic composition-2 of the present invention preferably further contains a buffer in addition to the components (A) and (B-2). The kind of the buffer used in the ophthalmic composition-2 of the present invention, a suitable example of the buffer, and the content of the buffer are the same as those of the buffer used in the ophthalmic composition-1. It is.

Moreover, it is preferable that the ophthalmic composition-2 of the present invention further contains a surfactant. About the kind of surfactant used in the ophthalmic composition-2 of the present invention, a preferable example of the surfactant, and the content ratio of the surfactant, the surfactant used in the ophthalmic composition-1 It is the same as the case of.

Furthermore, the ophthalmic composition-2 of the present invention preferably further contains an isotonic agent. The type of tonicity agent used in the ophthalmic composition-2 of the present invention, a suitable example of the tonicity agent, and the content ratio of the tonicity agent are used in the ophthalmic composition-1. The same as in the case of the tonicity agent.

The pH and osmotic pressure of the ophthalmic composition-2 of the present invention are the same as those of the ophthalmic composition-1.

In addition to the above-described components, the ophthalmic composition-2 of the present invention can contain active ingredients (pharmacologically active ingredients, physiologically active ingredients, etc.) and other various ingredients and additives.

The ophthalmic composition-2 of the present invention is prepared by adding a desired amount of the above-mentioned components (A) and (B-2), and other components as necessary to a desired concentration.

The dosage form of the ophthalmic composition-2 of the present invention is the same as that of the ophthalmic composition-1.

The ophthalmic composition-2 of the present invention is used as an ophthalmic composition for SHCL, and specific examples of the formulation include eye drops that can be instilled while wearing SHCL (eye drops for SHCL), eyewash while wearing SHCL. Possible eyewashes (SHCL eyewashes), SHCL mounting solutions, SHCL care agents (including SHCL disinfectants, SHCL preservatives, SHCL cleaners, SHCL cleaners, etc.) and the like. In addition, in the case of the eye drops for SHCL and the eye wash for SHCL, it may be directly applied to the eye wearing SHCL, or may be applied to the eye before wearing SHCL.

Among these, the eye drops for SHCL, the eye wash for SHCL, the detergent for SHCL, and the SHCL mounting solution are preferable, and the eye drops for SHCL are particularly suitable for the ophthalmic composition-2 of the present invention.

Among SHCLs, ionic SHCL is more easily adsorbed by terpenoids than nonionic SHCL, and a higher level of terpenoid adsorption suppression effect is required, but according to the ophthalmic composition-2 of the present invention. Moreover, adsorption of terpenoids to ionic SHCL can also be effectively suppressed. In view of such characteristics, as an example of a suitable formulation form of the ophthalmic composition-2 of the present invention, preferably an ophthalmic composition for ionic SHCL, more preferably an eye drop for ionic SHCL, an eye wash for ionic SHCL, An ionic SHCL cleaning agent, an ionic SHCL mounting solution, particularly preferably an ionic SHCL eye drop.

In addition, as shown in Reference Test Example 1 to be described later, the study by the present inventors has revealed that nonionic SHCL, among soft contact lenses, easily adheres to corneal epithelial cells. Therefore, an ophthalmic composition applied to nonionic SHCL is required to have an action of suppressing adhesion of corneal epithelial cells to nonionic SHCL. On the other hand, according to the ophthalmic composition-2 of the present invention, the combined use of the components (A) and (B-2) can synergistically suppress corneal cell adhesion with high nonionic SHCL. It is possible to wear nonionic SHCL with high safety. In view of such characteristics, as an example of a suitable formulation form of the ophthalmic composition-2 of the present invention, an ophthalmic composition for nonionic SHCL, more preferably an eye drop for nonionic SHCL, an eyewash for nonionic SHCL Nonionic SHCL cleaning agents, nonionic SHCL mounting solutions, particularly preferably nonionic SHCL eye drops.

When the ophthalmic composition-2 of the present invention is used as an ophthalmic composition for nonionic SHCL, the water content of the nonionic SHCL to be applied is not particularly limited, but at least more than 0% And 35% or less. Here, as the method for measuring the water content of the nonionic SHCL to be used, the method described in the column of the “ophthalmic composition-1” is used.

The ophthalmic composition-2 of the present invention is effective for the prevention or treatment of dry eye based on the above component (A), and is also useful for improving dry eye. When the ophthalmic composition-2 of the present invention is in an aspect capable of exhibiting an excellent histamine release inhibitory action, it is used for applications such as antiallergy (for pollen, etc.), itching, and discomfort when wearing contact lenses. it can.

The container for storing the ophthalmic composition-2 of the present invention is the same as the case of the ophthalmic composition-1.

3. Method for imparting histamine release inhibitory action As described above, the ophthalmic composition has a histamine release inhibitory action that is synergistically enhanced by combining the components (A) and (B-1) at a specific content ratio. Can be made.

Accordingly, the present invention, from yet another point of view, in an ophthalmic composition, (A) a polymer obtained by polymerizing a monomer represented by the general formula (I), either alone or with another copolymerizable monomer, 0.001 to 2 w / v % And (B-1) menthol 0.001 to 0.02 w / v% in combination, a method for imparting a histamine inhibitory action to an ophthalmic composition is provided.

In this method, the types and content ratios and ratios of the components (A) and (B-1) to be used, the types and content ratios of other components, the formulation form of the ophthalmic composition, and the container for storing the ophthalmic composition The type and the like are the same as in “1. Ophthalmic composition-1”.

4). Method for inhibiting adsorption of terpenoids on SHCL, method for imparting terpenoid adsorption inhibition on SHCL to ophthalmic compositions As described above, by using a combination of components (A) and (B-2), terpenoids on SHCL Adsorption can be suppressed.

Therefore, the present invention, from yet another point of view, (A) a polymer obtained by polymerizing the monomer represented by the general formula (I) alone or with another monomer capable of copolymerization, and (B-2) a terpenoid. Provided is a method for suppressing adsorption of terpenoids to SHCL, which comprises contacting an ophthalmic composition containing SHCL with SHCL. The present invention also includes (B-2) a terpenoid in an ophthalmic composition, together with a polymer obtained by polymerizing the monomer represented by the general formula (I) alone or with another monomer capable of copolymerization. There is also provided a method for imparting an action of inhibiting terpenoid adsorption to SHCL to the ophthalmic composition.

In these methods, the types and content ratios of the components (A) and (B-2) to be used, the types and content ratios of other components to be blended, the types of SHCL to be applied, etc. are described in “2. Same as “Ophthalmic Composition-2”.

5. Method for inhibiting adhesion of corneal epithelial cells to nonionic SHCL, method for imparting corneal epithelial cell adhesion inhibiting action to nonionic SHCL to ophthalmic composition As described above, combining components (A) and (B-2) Can be used to synergistically suppress adhesion of corneal epithelial cells to nonionic SHCL.

Therefore, the present invention, from yet another point of view, (A) a polymer obtained by polymerizing the monomer represented by the general formula (I) alone or with another monomer capable of copolymerization, and (B-2) a terpenoid. Provided is a method for suppressing adhesion of corneal epithelial cells to nonionic SHCL, which comprises bringing the ophthalmic composition contained therein into contact with nonionic SHCL. The present invention also includes (B-2) a terpenoid in an ophthalmic composition, together with a polymer obtained by polymerizing the monomer represented by the general formula (I) alone or with another monomer capable of copolymerization. There is also provided a method for imparting to the ophthalmic composition an action for suppressing adhesion of corneal epithelial cells to nonionic SHCL.

In these methods, the types and content ratios of the components (A) and (B-2) to be used, the types and content ratios of other components to be blended, the types of nonionic SHCL to be applied, etc. This is the same as “2. Ophthalmic composition-2”.

EXAMPLES The present invention will be described in detail below based on examples, but the present invention is not limited to these examples.
Test Example 1: Histamine release inhibitory effect test 1 × 10 ^{5 of} a rat basophil cell line (RBL-2H3) suspended in DMEM medium (Invitrogen) supplemented with 10% by volume fetal calf serum (Invitrogen) A 96-well microtiter plate (Corning) was seeded at a density of cells / cm ² and cultured at 37 ° C. under 5% CO ₂ for 24 hours. Thereafter, the culture supernatant is removed by aspiration, and 0.2 ml of PIPES buffer in which the test substance is dissolved so as to have the concentration shown in Tables 1 to 4 is added per well, for 1 hour at 37 ° C. under 5% CO ₂ . Incubated. PIPES buffer is Hanks balanced salt (manufactured by Invitrogen) supplemented with 20 mM PIPES (Piperazine-1,4-bis (2-ethanesulfonic acid; manufactured by Sigma)) and 0.1 w / v bovine serum albumin (manufactured by Sigma). , Composition: CaCl ₂ 1.26 mM, MgCl ₂ · 6H ₂ O 0.493 mM, MgSO ₄ · 7H ₂ O 0.407 mM, KCl 5.33 mM, KH ₂ PO ₄ 0.441 mM, NaHCO ₃ 4.17 mM, NaCl 137.93 mM, Na ₂ HPO ₄ 0.338 mM) was used. Thereafter, 2 μl of 1 mM A23187 (reagent: Sigma) was added to each well and further incubated for 20 minutes at 37 ° C. under 5% CO ₂ . The supernatant of each well was collected, and the histamine concentration was quantified using an ELISA kit (Oxford Biochemical Research). In addition, as a control, a PIPES buffer solution that does not dissolve the test substance was added in an amount of 0.2 ml per well and tested in the same manner as above, and a blank was tested in the same manner as the control except that A23187 was not added. Similarly, the histamine concentration was quantified. Using the histamine concentration of each obtained sample, the histamine release inhibition rate (%) was calculated according to the following calculation formula.

[Equation 1]
Histamine release inhibition rate (%)
= {1-(histamine concentration of each sample-blank histamine concentration) / (control histamine concentration-blank histamine concentration)} x 100

The obtained results are shown in FIGS. In the case of MPC polymer (0.0001 to 2.0 w / v%) alone (Comparative Examples 1-2 to 1-8), no histamine release inhibitory effect was observed. In addition, when menthol alone was 0.01 ヒ w / v%, 0.001 w / v%, or 0.02 w / v% (Comparative Examples 1-1, 1-10, and 1-11), an inhibitory effect on histamine release was observed. . On the other hand, when MPC polymer 0.001 to 2.0 w / v% and menthol 0.001 to 0.02 w / v% are used in combination (Examples 1-1 to 1-14), histamine release is synergistically suppressed. Was confirmed. When the menthol concentration was 0.05 w / v%, normal measurement of histamine concentration was impossible due to cytotoxicity (impossible to measure).

Reference Test Example 1: Histamine release inhibitory effect test In order to evaluate the histamine release inhibitory effect of the combined use of pyridoxine hydrochloride and MPC polymer, which are known to have a histamine release inhibitory action, pyridoxine hydrochloride at concentrations shown in Table 5 as test substances and Using MPC polymer, the histamine release inhibition rate was determined in the same manner as in Test Example 1 above.

The obtained results are shown in FIG. As shown in FIG. 5, even when pyridoxine hydrochloride and MPC polymer were used in combination, a synergistic improvement in the histamine release inhibitory effect was not observed. That is, it has been clarified that the synergistic improvement in the histamine release inhibitory effect observed in Test Example 1 is a unique effect observed when the MPC polymer and menthol are used in combination at a specific content ratio.

Test Example 2: Inhibition test of adsorption of terpenoid to SHCL The following experiment was conducted using two types of SHCL shown in Table 6 to evaluate the adsorption property of terpenoid to SHCL. In addition, all SHCL used for this test is a commercial item.

Two types of SHCL shown in Table 6 were immersed in 5 mL of physiological saline solution for 72 hours (lens pretreatment). Moreover, the prescription liquid was created according to Table 7, and each prescription liquid was filled into 6 mL capacity | capacitance headspace vials 5mL at a time. Pretreated SHCL was immersed in this formulation solution, and shaken at 34 ° C. at 120 times / min for 24 hours. Pull up the SHCL and lightly rinse with 100 mL of saline to remove excess solution attached to the lens surface, then transfer to 5 mL of saline filled in headspace vials, and 24 times at 34 ° C at 120 times / min. The mixture was shaken over time to elute the terpenoid adsorbed on SHCL. Next, SHCL was transferred to physiological saline filled in another headspace vial, and the remaining liquid was recovered as an eluate. Menthol and camphor contained in the eluate were quantified by gas chromatography (elution first sample).

The same operation was repeated, and the elution operation was repeated until menthol and camphor were no longer detected. The elution amount was totaled for each component, and this was calculated as the adsorption amount of menthol and camphor on SHCL.

The obtained results are shown in FIGS. In the formulation solution containing terpenoids (menthol, camphor) and no MPC polymer (Comparative Example 2-1), adsorption of menthol and camphor was confirmed in both SHCLs. In addition, when ionic SHCL and nonionic SHCL were compared, it was shown that both menthol and camphor had a higher adsorption amount in ionic SHCL, and ionic SHCL had a larger problem of terpenoid adsorption.

On the other hand, in the prescription liquid (Example 2-1) containing MPC polymer together with menthol and camphor, the adsorption of menthol and camphor on SHCL was remarkably suppressed. In particular, almost no adsorption of camphor was observed in nonionic SHCL.

Reference Test Example 2: Evaluation of Adhesion of Corneal Epithelial Cells of Various Soft Contact Lenses The following experiment was conducted using five types of soft contact lenses shown in Table 8 to evaluate the adhesion of corneal epithelial cells on the surface of the soft contact lens. . The soft contact lenses used in this test are all commercially available products.

Specifically, it was evaluated by the following method. Each soft contact lens was immersed one by one in a 24-well microplate containing 900 μL of growth medium (DMEM medium containing 10% fetal bovine serum) so that the convex surface was on the top. Each well was seeded with 100 μL each of a cell suspension (1 × 10 ⁵ cell / ml) of a rabbit corneal epithelial cell line SIRC (ATCC number: CCL-60) prepared using a growth medium, and incubated at 37 ° C., 5 ° C. After culturing for 48 hours under% CO ₂ conditions, the number of viable cells adhered to the soft contact lens was counted. As a control, cells were cultured on the bottom of the microplate without immersing any lens, and the number of viable cells in the wells was counted (control group). Note that Cell Counting Kit (manufactured by Dojindo Laboratories) was used for the measurement of the number of viable cells. The ratio of the number of viable cells adhering to the surface of each soft contact lens (ratio of the number of viable cells to the control group;%) was calculated with respect to the total number of viable cells contained in the wells of the control group.

The obtained results are shown in FIG. As is clear from FIG. 8, the lenses A and B, which are nonionic SHCL, are compared with the lens C, which is an ionic silicone hydrogel contact lens, and the lens D or E, which is a nonsilicone hydrogel contact lens. It was confirmed that there was remarkable corneal epithelial cell adhesion. In addition, when the adhesion state of the cells to the soft contact lens was observed with a microscope, cell adhesion was hardly confirmed in the lenses C, D, and E, but corneal epithelial cells were present on the entire surfaces of the lenses A and B. It was confirmed that they were adhered. From the above results, it was confirmed that nonionic SHCL has significantly higher adhesion of corneal epithelial cells than other types of lenses, and wearing nonionic SHCL has adverse effects such as damage to the corneal surface. It became clear that it could be given.

Test Example 3: Adhesion Inhibition Test of Corneal Epithelial Cells to Nonionic SHCL The following experiment was performed using the lens B shown in Table 8 above, and the corneal epithelial cell adhesion to the nonionic SHCL surface was evaluated. Specifically, it was evaluated by the following method. Using the growth medium (DMEM medium containing 10% fetal bovine serum), the formulation solutions (Examples 3-1 to 3-4 and Comparative Examples 3-1 to 3-7) having the compositions shown in Tables 9 and 10 were aseptically prepared. It was prepared. 1000 μL of each formulation solution was placed in a 24-well microplate, and SHCL was immersed therein with the convex surface up. Further, 100 μL each of cell suspension (1 × 10 ⁵ cell / ml) of a rabbit corneal epithelial cell line SIRC (ATCC number: CCL-60) prepared using a growth medium was seeded at 37 ° C., 5% CO 2. After culturing for 48 hours under _two conditions, the number of viable cells adhered to nonionic SHCL was counted. As a control, only the DMEM medium was used instead of the formulation solution, and the number of viable cells adhered to the nonionic SHCL was similarly counted. Compare the number of viable cells adhered to the SHCL surface in the wells of the control group and the number of viable cells adhered to the SHCL surface in each test solution, and calculate the corneal cell adhesion inhibition rate of each test solution according to the following formula. (N = 3). Note that Cell Counting Kit (manufactured by Dojindo Laboratories) was used for the measurement of the number of viable cells.

The blank used was treated in the same manner as above except that SHCL and cells were not added.

[Equation 2]
Cell adhesion inhibition rate (%) = {1- (A450 in the sample group−A450 in the blank group) / (A450 in the control group−A450 in the blank group)} × 100
* In the formula, A450 indicates the absorbance at a wavelength of 450 nm measured using Cell Counting Kit (Dojindo Laboratories).

The obtained results are shown in FIGS. When observed under a microscope, it was confirmed that corneal cells adhered to the surface of the nonionic SHCL in the well in the control group.

Further, as is apparent from FIGS. 9 to 12, the formulation liquids of Examples 3-1 to 3-4 containing both the MPC polymer and the terpenoid contained Comparative Example 3-1 containing only one of the MPC polymer and the terpenoid. It was confirmed that a higher inhibition rate of corneal epithelial cell adhesion was obtained compared to the case of the prescription liquids of ˜3-7. This demonstrates that by using an ophthalmic composition containing an MPC polymer and a terpenoid, adverse effects such as damage to the corneal surface caused by nonionic SHCL can be suppressed.

Reference test example 3: Adhesion inhibition test of corneal epithelial cells to nonionic SHCL In order to evaluate the adhesion inhibitory effect of corneal epithelial cells to nonionic SHCL by the combined use of tetrahydrozoline hydrochloride and MPC polymer, Using the test solution having the composition shown in Table 11, the cell adhesion inhibition rate was determined in the same manner as in Test Example 3 above.

The obtained results are shown in FIG. As shown in FIG. 13, when tetrahydrozoline hydrochloride and MPC polymer were used in combination, the result was that corneal cells were promoted to adhere to the surface of nonionic SHCL as compared with tetrahydrozoline hydrochloride alone. That is, it has been clarified that the effect of suppressing the adhesion of corneal epithelial cells to nonionic SHCL observed in Test Example 3 above is a unique effect observed when MPC polymer and terpenoid are used in combination.

Formulation Example 1
Content ratio (w / v%)
MPC polymer ^{# 1} 0.5
L-Menthol 0.01
Sodium chloride 0.5
Potassium chloride 0.1
Boric acid 0.8
Borax 0.2
Hydrochloric acid appropriate amount Sodium hydroxide appropriate amount
Purified water appropriate amount <br/> 100mL
pH 7.0
# 1 MPC polymer is the same as used in Table 1.

The ophthalmic composition formulation of Formulation Example 1 above was prepared according to a conventional method, and 15 mL of a 15 mL capacity PET container was filled to prepare eye drops and SHCL eye drops.

Formulation Example 2
Content ratio (w / v%)
MPC polymer ^{# 1} 0.05
L-Menthol 0.002
D-Camphor 0.001
Sodium chloride 0.8
Boric acid 0.4
Borax 0.1
Hydrochloric acid Appropriate amount Sodium hydroxide Appropriate amount
Purified water Appropriate amount <br/> Total amount 100mL
pH 7.5
# 1 MPC polymer is the same as used in Table 1.

The ophthalmic composition formulation of Formulation Example 2 above was prepared according to a conventional method, and 10 mL of a 10 mL PET container was filled with 10 mL of eye drops, contact lens mounting solution, SHCL eye drop, and SHCL contact lens mounting solution. did. Moreover, it replaced with said container and 500 mL capacity | capacitance PET containers were filled with 500 mL, and the eyewash and the SHCL eyewash were each manufactured.

Claims

(A) 0.001 to 2 w / v% of a polymer obtained by polymerizing the monomer represented by the general formula (I) alone or with another monomer capable of copolymerization;

[Wherein n1 is an integer of 2 to 4, R 1 is a hydrogen atom or a methyl group, R 2 is a group represented by — (R 6 O) n2 —R 6 — (R 6 has 1 to 4 carbon atoms] And n2 represents an integer of 0 to 5), and R 3 to R 5 are the same or different and each represents a hydrogen atom or an alkyl group having 1 to 4 carbon atoms. ]
(B-1) An ophthalmic composition comprising 0.001 to 0.02 w / v% menthol.
The ophthalmic composition according to claim 1, which is an eye drop for contact lenses.
The ophthalmic composition according to claim 1 or 2, which is used for suppressing itching.
The ophthalmic composition according to any one of claims 1 to 3, which is used for suppressing discomfort when wearing a contact lens.
(A) a polymer obtained by polymerizing the monomer represented by the general formula (I) alone or with another monomer capable of copolymerization;

[Wherein n1 is an integer of 2 to 4, R 1 is a hydrogen atom or a methyl group, R 2 is a group represented by — (R 6 O) n2 —R 6 — (R 6 has 1 to 4 carbon atoms] And n2 represents an integer of 0 to 5), and R 3 to R 5 are the same or different and each represents a hydrogen atom or an alkyl group having 1 to 4 carbon atoms. ]
(B-2) An ophthalmic composition for a silicone hydrogel contact lens, comprising a terpenoid.
The ophthalmic composition for silicone hydrogel contact lenses according to claim 5, which is an eye drop for silicone hydrogel contact lenses.
0.001 to 2 w / v% (A) a polymer obtained by polymerizing the monomer represented by the general formula (I) alone or with another monomer capable of copolymerization;

[Wherein n1 is an integer of 2 to 4, R 1 is a hydrogen atom or a methyl group, R 2 is a group represented by — (R 6 O) n2 —R 6 — (R 6 has 1 to 4 carbon atoms] And n2 represents an integer of 0 to 5), and R 3 to R 5 are the same or different and each represents a hydrogen atom or an alkyl group having 1 to 4 carbon atoms. ]
With 0.001 to 0.02w / v% (B-1) menthol,
Use for the manufacture of an ophthalmic composition.
The use according to claim 7, wherein the ophthalmic composition is an eye drop for contact lenses.
The use according to claim 7 or 8, wherein the ophthalmic composition is a histamine release inhibitor.
(A) a polymer obtained by polymerizing the monomer represented by the general formula (I) alone or with another monomer capable of copolymerization;

[Wherein n1 is an integer of 2 to 4, R 1 is a hydrogen atom or a methyl group, R 2 is a group represented by — (R 6 O) n2 —R 6 — (R 6 has 1 to 4 carbon atoms] And n2 represents an integer of 0 to 5), and R 3 to R 5 are the same or different and each represents a hydrogen atom or an alkyl group having 1 to 4 carbon atoms. ]
(B-2) with a terpenoid
Use for the manufacture of an ophthalmic composition for silicone hydrogel contact lenses.