JP2004256519A - Chlorobutanol-containing artificial tear liquid - Google Patents
Chlorobutanol-containing artificial tear liquid Download PDFInfo
- Publication number
- JP2004256519A JP2004256519A JP2004012058A JP2004012058A JP2004256519A JP 2004256519 A JP2004256519 A JP 2004256519A JP 2004012058 A JP2004012058 A JP 2004012058A JP 2004012058 A JP2004012058 A JP 2004012058A JP 2004256519 A JP2004256519 A JP 2004256519A
- Authority
- JP
- Japan
- Prior art keywords
- fragrance
- artificial tear
- flavor
- salt
- chlorobutanol
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- OSASVXMJTNOKOY-UHFFFAOYSA-N chlorobutanol Chemical compound CC(C)(O)C(Cl)(Cl)Cl OSASVXMJTNOKOY-UHFFFAOYSA-N 0.000 title claims abstract description 110
- 239000000607 artificial tear Substances 0.000 title claims abstract description 103
- 229960004926 chlorobutanol Drugs 0.000 title claims abstract description 55
- 239000007788 liquid Substances 0.000 title abstract description 5
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims abstract description 84
- 150000003839 salts Chemical class 0.000 claims abstract description 31
- 238000000034 method Methods 0.000 claims abstract description 27
- 239000000796 flavoring agent Substances 0.000 claims description 78
- 235000019634 flavors Nutrition 0.000 claims description 78
- 239000003205 fragrance Substances 0.000 claims description 52
- 239000002826 coolant Substances 0.000 claims description 28
- -1 alkali metal salt Chemical class 0.000 claims description 24
- 235000005979 Citrus limon Nutrition 0.000 claims description 14
- 244000131522 Citrus pyriformis Species 0.000 claims description 14
- 244000004281 Eucalyptus maculata Species 0.000 claims description 14
- 244000223014 Syzygium aromaticum Species 0.000 claims description 14
- 235000016639 Syzygium aromaticum Nutrition 0.000 claims description 14
- 239000007967 peppermint flavor Substances 0.000 claims description 12
- 240000002943 Elettaria cardamomum Species 0.000 claims description 10
- ISAOCJYIOMOJEB-UHFFFAOYSA-N benzoin Chemical compound C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 claims description 10
- 235000005300 cardamomo Nutrition 0.000 claims description 10
- XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 claims description 10
- 150000003505 terpenes Chemical class 0.000 claims description 10
- NOOLISFMXDJSKH-UHFFFAOYSA-N DL-menthol Natural products CC(C)C1CCC(C)CC1O NOOLISFMXDJSKH-UHFFFAOYSA-N 0.000 claims description 9
- 229910052783 alkali metal Inorganic materials 0.000 claims description 9
- GLZPCOQZEFWAFX-UHFFFAOYSA-N Geraniol Chemical compound CC(C)=CCCC(C)=CCO GLZPCOQZEFWAFX-UHFFFAOYSA-N 0.000 claims description 8
- 159000000000 sodium salts Chemical group 0.000 claims description 8
- DTGKSKDOIYIVQL-WEDXCCLWSA-N (+)-borneol Chemical compound C1C[C@@]2(C)[C@@H](O)C[C@@H]1C2(C)C DTGKSKDOIYIVQL-WEDXCCLWSA-N 0.000 claims description 5
- REPVLJRCJUVQFA-UHFFFAOYSA-N (-)-isopinocampheol Natural products C1C(O)C(C)C2C(C)(C)C1C2 REPVLJRCJUVQFA-UHFFFAOYSA-N 0.000 claims description 5
- DSSYKIVIOFKYAU-XCBNKYQSSA-N (R)-camphor Chemical compound C1C[C@@]2(C)C(=O)C[C@@H]1C2(C)C DSSYKIVIOFKYAU-XCBNKYQSSA-N 0.000 claims description 5
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- 244000165082 Lavanda vera Species 0.000 claims description 5
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- 235000006886 Zingiber officinale Nutrition 0.000 claims description 5
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims description 5
- 150000003863 ammonium salts Chemical class 0.000 claims description 5
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- DTGKSKDOIYIVQL-UHFFFAOYSA-N dl-isoborneol Natural products C1CC2(C)C(O)CC1C2(C)C DTGKSKDOIYIVQL-UHFFFAOYSA-N 0.000 claims description 5
- 235000008397 ginger Nutrition 0.000 claims description 5
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- 239000001102 lavandula vera Substances 0.000 claims description 5
- 235000018219 lavender Nutrition 0.000 claims description 5
- 229940041616 menthol Drugs 0.000 claims description 5
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 claims description 5
- 239000008371 vanilla flavor Substances 0.000 claims description 5
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- 239000005792 Geraniol Substances 0.000 claims description 4
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- 235000001050 hortel pimenta Nutrition 0.000 claims 2
- NOOLISFMXDJSKH-UTLUCORTSA-N (+)-Neomenthol Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@@H]1O NOOLISFMXDJSKH-UTLUCORTSA-N 0.000 claims 1
- 239000000243 solution Substances 0.000 abstract description 6
- 235000002639 sodium chloride Nutrition 0.000 description 40
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 18
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 18
- 239000004480 active ingredient Substances 0.000 description 16
- 239000001509 sodium citrate Substances 0.000 description 13
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 13
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 12
- NOOLISFMXDJSKH-KXUCPTDWSA-N (-)-Menthol Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@H]1O NOOLISFMXDJSKH-KXUCPTDWSA-N 0.000 description 10
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 9
- 239000001103 potassium chloride Substances 0.000 description 9
- 235000011164 potassium chloride Nutrition 0.000 description 9
- 239000011780 sodium chloride Substances 0.000 description 9
- 238000003860 storage Methods 0.000 description 9
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 8
- 238000002360 preparation method Methods 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 6
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 230000007774 longterm Effects 0.000 description 6
- OVBJJZOQPCKUOR-UHFFFAOYSA-L EDTA disodium salt dihydrate Chemical compound O.O.[Na+].[Na+].[O-]C(=O)C[NH+](CC([O-])=O)CC[NH+](CC([O-])=O)CC([O-])=O OVBJJZOQPCKUOR-UHFFFAOYSA-L 0.000 description 5
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- 239000008103 glucose Substances 0.000 description 5
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- 229940037001 sodium edetate Drugs 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 4
- 239000004372 Polyvinyl alcohol Substances 0.000 description 4
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 4
- 229960000686 benzalkonium chloride Drugs 0.000 description 4
- CADWTSSKOVRVJC-UHFFFAOYSA-N benzyl(dimethyl)azanium;chloride Chemical compound [Cl-].C[NH+](C)CC1=CC=CC=C1 CADWTSSKOVRVJC-UHFFFAOYSA-N 0.000 description 4
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- 229960003333 chlorhexidine gluconate Drugs 0.000 description 4
- YZIYKJHYYHPJIB-UUPCJSQJSA-N chlorhexidine gluconate Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O.OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O.C1=CC(Cl)=CC=C1NC(=N)NC(=N)NCCCCCCNC(=N)NC(=N)NC1=CC=C(Cl)C=C1 YZIYKJHYYHPJIB-UUPCJSQJSA-N 0.000 description 4
- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 description 4
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- XONPDZSGENTBNJ-UHFFFAOYSA-N molecular hydrogen;sodium Chemical compound [Na].[H][H] XONPDZSGENTBNJ-UHFFFAOYSA-N 0.000 description 1
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Abstract
Description
本発明は、クロロブタノール及びクエン酸又はその塩を配合した人工涙液、及び、クロロブタノールを配合した人工涙液においてクエン酸又はその塩を更に配合する、クロロブタノール含有人工涙液のｐＨ低下抑制方法に関する。 The present invention relates to an artificial tear containing chlorobutanol and citric acid or a salt thereof, and an artificial tear containing chlorobutanol and further containing citric acid or a salt thereof, which suppresses a decrease in pH of a chlorobutanol-containing artificial tear. About the method.
人工涙液は、現行の基準においては、配合できる有効成分は、無機塩類の塩化カリウム、塩化カルシウム、塩化ナトリウム、炭酸水素ナトリウム、炭酸ナトリウム、乾燥炭酸ナトリウム、硫酸マグネシウム、リン酸水素ナトリウム、リン酸二水素ナトリウム及びリン酸二水素カリウム、アミノ酸類のアミノエチルスルホン酸、コンドロイチン硫酸ナトリウム、Ｌ−アスパラギン酸カリウム、Ｌ−アスパラギン酸マグネシウム及びＬ−アスパラギン酸マグネシウム・カリウム（等量混合物）、粘稠剤のポリビニルアルコール、ポリビニルピロリドン、ヒドロキシエチルセルロース、ヒドロキシプロピルメチルセルロース、ブドウ糖及びメチルセルロースであり、ｐＨが５．５〜８．０、浸透圧比が０．８５〜１．５５（対生理食塩水浸透圧比）、効能又は効果が、目の疲れ、涙液の補助（目のかわき）、ハードコンタクトレンズ又はソフトコンタクトレンズを装着しているときの不快感及び目のかすみ（めやにの多いときなど）である眼科用薬である（一般用医薬品製造（輸入）承認基準、２０００年版）。従来、人工涙液は単に涙液の代用として使用されることが多く、組成的にも涙液に近づけた処方とされることが多かった。近年、ユーザーの好みの多様化やソフトコンタクトレンズユーザーの増加から、人工涙液についても清涼化剤を配合したものが上市されるようになった。しかし、その清涼感については清涼化剤の配合量が少ない場合は期待される程の清涼感が得られず、かといって清涼化剤の配合量が多くなると点眼直後の刺激感が強くなってしまい、満足すべきものはなかった。 Under the current standards, artificial tears can be combined with the following active ingredients: inorganic salts such as potassium chloride, calcium chloride, sodium chloride, sodium bicarbonate, sodium carbonate, dried sodium carbonate, magnesium sulfate, sodium hydrogen phosphate, and phosphoric acid Sodium dihydrogen and potassium dihydrogen phosphate, amino acids such as aminoethylsulfonic acid, sodium chondroitin sulfate, potassium L-aspartate, magnesium L-aspartate and potassium magnesium L-aspartate (mixture of equal amounts), thickener Of polyvinyl alcohol, polyvinylpyrrolidone, hydroxyethylcellulose, hydroxypropylmethylcellulose, glucose and methylcellulose, having a pH of 5.5 to 8.0 and an osmotic pressure ratio of 0.85 to 1.55 (to osmotic pressure ratio of physiological saline). Ophthalmology whose effects or effects are tiredness of the eyes, assisting tears (drying eyes), discomfort when wearing hard or soft contact lenses and blurring of the eyes (such as when there are many eyes) It is a drug (over-the-counter drug manufacturing (import) approval standard, 2000 version). Conventionally, artificial tears have often been used merely as substitutes for tears, and in many cases, the formulations have been formulated to be close to tears. In recent years, with the diversification of user preferences and the increase of soft contact lens users, artificial tears containing a cooling agent have come to market. However, as for the cooling sensation, when the amount of the cooling agent is small, the expected cooling sensation cannot be obtained, and when the amount of the cooling agent is large, the stimulating feeling immediately after instillation becomes strong. At last, nothing was satisfactory.
上記背景において、本発明者らは、清涼化剤を高い濃度で配合した人工涙液であっても局所麻酔作用を有するクロロブタノールを配合することによって、清涼感を維持したままで点眼直後の刺激感を和らげることができることを見出した。しかしながら、クロロブタノールは、中性付近の水溶液中では保存中に分解しやすく、分解すると水溶液のｐＨを低下させる方向に強力に作用するため、ｐＨが中性付近（５．５〜８．０）になければならない人工涙液には、十分な量のクロロブタノールを配合することができなかった。このような状況において、本発明は、クロロブタノール含有人工涙液のｐＨの低下を抑制する方法及び、これによりｐＨの低下を抑制したクロロブタノール含有人工涙液を提供することを目的とする。 In the above-mentioned background, the present inventors have found that even if artificial tears containing a high concentration of a cooling agent, chlorobutanol having a local anesthetic action is blended, so that stimulation immediately after instillation is maintained while maintaining a refreshing feeling. I found that the feeling can be softened. However, chlorobutanol is easily decomposed during storage in an aqueous solution near neutral, and when decomposed, acts strongly in the direction of lowering the pH of the aqueous solution, so that the pH is around neutral (5.5 to 8.0). A sufficient amount of chlorobutanol could not be incorporated into the artificial tears that had to be present. In such a situation, an object of the present invention is to provide a method for suppressing a decrease in pH of chlorobutanol-containing artificial tears and a chlorobutanol-containing artificial tear in which the decrease in pH is suppressed.
本発明者らは、ｐＨの低下を抑制するためにクロロブタノール含有人工涙液に配合し得る物質を求めて検討を重ねた結果、クロロブタノール含有人工涙液にクエン酸又はその塩を所定の配合比条件を満たす量で配合することにより、中性付近でｐＨの低下が極めて少ない製剤が得られることを見出し、本発明を完成するに至った。 The present inventors have repeatedly studied a substance that can be added to chlorobutanol-containing artificial tears in order to suppress a decrease in pH. As a result, citric acid or a salt thereof is added to chlorobutanol-containing artificial tears in a predetermined manner. It has been found that by blending in an amount that satisfies the specific conditions, a formulation with a very small decrease in pH near neutrality can be obtained, and the present invention has been completed.
すなわち本発明は、
（１）クロロブタノール及びクエン酸又はその塩を含有する人工涙液、
（２）クエン酸又はその塩の含有量が、クロロブタノールの含有量に対してモル比で２以上である、上記（１）に記載の人工涙液、
（３）クロロブタノールを０．００１〜０．３％（Ｗ／Ｖ）含有するものである、上記（１）又は（２）に記載の人工涙液、
（４）クエン酸又はその塩の濃度が０．００２〜３％（Ｗ／Ｖ）である、上記（１）ないし（３）の何れかに記載の人工涙液、
（５）クエン酸のアルカリ金属塩、アルカリ土類金属塩又はアンモニウム塩を含有する、上記（１）ないし（４）の何れかに記載の人工涙液、
（６）アルカリ金属塩がナトリウム塩又はカリウム塩である、上記（５）に記載の人工涙液、
（７）さらに清涼化剤を含有する上記（１）ないし（６）の何れかに記載の人工涙液、
（８）清涼化剤が、テルペノイド、クローブ香料、ペパーミント香料、ユーカリ香料、レモン香料、ローレル香料、ラベンダー香料、タラゴン香料、カルダモン香料、シダー香料、グレープフルーツ香料、オレンジ香料、ショウガ香料、ベルガモット香料、コリアンダー香料、シナモン香料、ジャスミン香料、ローズマリー香料、ローズ香料、パイン香料、カルダモン香料、ベンゾイン香料、ゼラニウム香料、カモミール香料、マージョラム香料、スペアミント香料、フェンネル香料及びバニラフレーバーよりなる群から選ばれる少なくとも１種である、上記（７）に記載の人工涙液、
（９）清涼化剤が、テルペノイドである、上記（７）に記載の人工涙液、
（１０）テルペノイドが、メントール、カンフル、ボルネオール、ゲラニオール、メントン、シネオール及びリモネンよりなる群から選ばれる少なくとも１種である、上記（９）に記載の人工涙液、
（１１）清涼化剤が、クローブ香料及びペパーミント香料を含むものである、上記（７）に記載の人工涙液、
（１２）清涼化剤が、さらにユーカリ香料及びレモン香料よりなる群から選ばれる少なくとも１種を含むものである、上記（１１）に記載の人工涙液、
（１３）清涼化剤が、クローブ香料、ペパーミント香料、ユーカリ香料及びレモン香料を含むものである、上記（７）、（８）、（１１）及び（１２）の何れかに記載の人工涙液、
（１４）清涼化剤の濃度が０．０００１〜０．２％（Ｗ／Ｖ）である、上記（７）ないし（１３）の何れかに記載の人工涙液、
（１５）ｐＨが５．５〜８．０である、上記（１）ないし（１４）の何れかに記載の人工涙液、
（１６）該人工涙液がコンタクトレンズ装用時の人工涙液である、上記（１）ないし（１５）の何れかに記載の人工涙液、
（１７）該コンタクトレンズがソフトコンタクトレンズである、上記（１６）に記載の人工涙液、
（１８）クエン酸又はその塩を配合するクロロブタノール含有人工涙液のｐＨ低下抑制方法、
（１９）クエン酸又はその塩の含有量が、クロロブタノールの含有量に対してモル比で２以上である、上記（１８）に記載のｐＨ低下抑制方法、
（２０）該人工涙液中のクロロブタノール濃度が０．００１〜０．３％（Ｗ／Ｖ）である、上記（１８）又は（１９）に記載のｐＨ低下抑制方法、
（２１）該人工涙液中のクエン酸又はその塩の濃度が０．００２〜３％（Ｗ／Ｖ）である、上記（１８）ないし（２０）の何れかに記載のｐＨ低下抑制方法、
（２２）クエン酸のアルカリ金属塩、アルカリ土類金属塩又はアンモニウム塩を含有する、上記（１８）ないし（２１）の何れかに記載のｐＨ低下抑制方法、
（２３）アルカリ金属塩がナトリウム塩又はカリウム塩である、上記（２２）に記載のｐＨ低下抑制方法、
（２４）該人工涙液がさらに清涼化剤を含有するものである、上記（１８）ないし（２３）の何れかに記載のｐＨ低下抑制方法、
（２５）清涼化剤が、テルペノイド、クローブ香料、ペパーミント香料、ユーカリ香料、レモン香料、ローレル香料、ラベンダー香料、タラゴン香料、カルダモン香料、シダー香料、グレープフルーツ香料、オレンジ香料、ショウガ香料、ベルガモット香料、コリアンダー香料、シナモン香料、ジャスミン香料、ローズマリー香料、ローズ香料、パイン香料、カルダモン香料、ベンゾイン香料、ゼラニウム香料、カモミール香料、マージョラム香料、スペアミント香料、フェンネル香料及びバニラフレーバーよりなる群から選ばれる少なくとも１種である、上記（２４）に記載のｐＨ低下抑制方法、
（２６）該人工涙液中の清涼化剤の濃度が０．０００１〜０．２％（Ｗ／Ｖ）である、上記（２４）又は（２５）に記載のｐＨ低下抑制方法、
（２７）該人工涙液のｐＨが５．５〜８．０である、上記（１８）ないし（２６）の何れかに記載のｐＨ低下抑制方法、
（２８）該人工涙液がコンタクトレンズ装用時の人工涙液である、上記（１８）ないし（２７）の何れかに記載のｐＨ低下抑制方法、及び
（２９）該コンタクトレンズがソフトコンタクトレンズである、上記（２８）に記載のｐＨ低下抑制方法、を提供する。
That is, the present invention
(1) artificial tears containing chlorobutanol and citric acid or a salt thereof,
(2) The artificial tear according to (1), wherein the content of citric acid or a salt thereof is 2 or more in molar ratio with respect to the content of chlorobutanol.
(3) The artificial tear according to the above (1) or (2), which contains 0.001 to 0.3% (W / V) of chlorobutanol.
(4) The artificial tear according to any one of the above (1) to (3), wherein the concentration of citric acid or a salt thereof is 0.002 to 3% (W / V).
(5) The artificial tear according to any one of the above (1) to (4), which comprises an alkali metal salt, an alkaline earth metal salt or an ammonium salt of citric acid.
(6) The artificial tear according to (5), wherein the alkali metal salt is a sodium salt or a potassium salt.
(7) The artificial tear according to any one of the above (1) to (6), further comprising a cooling agent.
(8) The refreshing agent is terpenoid, clove flavor, peppermint flavor, eucalyptus flavor, lemon flavor, laurel flavor, lavender flavor, tarragon flavor, cardamom flavor, cedar flavor, grapefruit flavor, orange flavor, ginger flavor, bergamot flavor, coriander At least one selected from the group consisting of fragrance, cinnamon fragrance, jasmine fragrance, rosemary fragrance, rose fragrance, pine fragrance, cardamom fragrance, benzoin fragrance, geranium fragrance, chamomile fragrance, marjoram fragrance, spearmint fragrance, fennel fragrance and vanilla flavor The artificial tear according to the above (7),
(9) The artificial tear according to the above (7), wherein the cooling agent is a terpenoid.
(10) The artificial tear according to the above (9), wherein the terpenoid is at least one selected from the group consisting of menthol, camphor, borneol, geraniol, menthone, cineol, and limonene.
(11) The artificial tear according to the above (7), wherein the refreshing agent contains a clove flavor and a peppermint flavor.
(12) The artificial tear according to the above (11), wherein the cooling agent further comprises at least one selected from the group consisting of a eucalyptus flavor and a lemon flavor.
(13) The artificial tear according to any one of the above (7), (8), (11) and (12), wherein the cooling agent comprises a clove flavor, a peppermint flavor, a eucalyptus flavor, and a lemon flavor.
(14) The artificial tear according to any one of the above (7) to (13), wherein the concentration of the cooling agent is 0.0001 to 0.2% (W / V).
(15) The artificial tear according to any one of the above (1) to (14), wherein the pH is 5.5 to 8.0.
(16) The artificial tear according to any one of the above (1) to (15), wherein the artificial tear is an artificial tear when a contact lens is worn.
(17) The artificial tear according to (16), wherein the contact lens is a soft contact lens.
(18) a method for suppressing a decrease in pH of chlorobutanol-containing artificial tears containing citric acid or a salt thereof,
(19) The method for suppressing pH decrease according to (18), wherein the content of citric acid or a salt thereof is 2 or more in molar ratio with respect to the content of chlorobutanol.
(20) The method for suppressing a decrease in pH according to (18) or (19), wherein the chlorobutanol concentration in the artificial tear is 0.001 to 0.3% (W / V).
(21) The method of any one of the above (18) to (20), wherein the concentration of citric acid or a salt thereof in the artificial tear is 0.002 to 3% (W / V),
(22) The method for suppressing a decrease in pH according to any one of the above (18) to (21), comprising an alkali metal salt, an alkaline earth metal salt or an ammonium salt of citric acid,
(23) the method for suppressing a decrease in pH according to (22), wherein the alkali metal salt is a sodium salt or a potassium salt;
(24) The method for suppressing a decrease in pH according to any one of the above (18) to (23), wherein the artificial tear fluid further contains a cooling agent.
(25) The refreshing agent is a terpenoid, clove flavor, peppermint flavor, eucalyptus flavor, lemon flavor, laurel flavor, lavender flavor, tarragon flavor, cardamom flavor, cedar flavor, grapefruit flavor, orange flavor, ginger flavor, bergamot flavor, coriander At least one selected from the group consisting of fragrance, cinnamon fragrance, jasmine fragrance, rosemary fragrance, rose fragrance, pine fragrance, cardamom fragrance, benzoin fragrance, geranium fragrance, chamomile fragrance, marjoram fragrance, spearmint fragrance, fennel fragrance and vanilla flavor The method for suppressing a decrease in pH according to the above (24),
(26) The method for suppressing a decrease in pH according to (24) or (25), wherein the concentration of the cooling agent in the artificial tear is 0.0001 to 0.2% (W / V).
(27) the method of any one of (18) to (26), wherein the artificial tear has a pH of 5.5 to 8.0;
(28) The method for suppressing pH decrease according to any of (18) to (27) above, wherein the artificial tear is artificial tear when a contact lens is worn, and (29) the contact lens is a soft contact lens. A method for suppressing a decrease in pH according to the above (28).
本発明により、長期保存中のクロロブタノール含有人工涙液におけるｐＨ低下を効果的に抑制することができる。その結果、クロロブタノール含有人工涙液のｐＨの保存安定性を高め、長期保存後であって中性付近に維持することができるのみならず、より多くの量のクロロブタノールを配合することができるようになるため、清涼化剤の配合濃度を高めた人工涙液を提供することが可能となる。 ADVANTAGE OF THE INVENTION According to this invention, pH fall in chlorobutanol containing artificial tear during long-term storage can be suppressed effectively. As a result, the storage stability of the pH of the chlorobutanol-containing artificial tear can be increased, and not only can the pH be maintained near neutral after long-term storage, but also a larger amount of chlorobutanol can be blended. Therefore, it is possible to provide an artificial tear with an increased concentration of a cooling agent.
以下、本発明についてさらに詳細に説明する。
本発明の人工涙液中におけるクエン酸又はその塩の含有量は、クロロブタノールの含有量に対してモル比で２以上あることが好ましい。これは、クロロブタノールの含有量に対してクエン酸又はその塩の含有量をモル比で２未満しか配合しないとクロロブタノールによる製剤のｐＨ低下傾向に十分対処できないことによる。ｐＨ低下の抑制を一層確実にするためには、クエン酸又はその塩の含有量は、クロロブタノールの含有量に対してモル比で２．５以上あることが、より好ましい。
Hereinafter, the present invention will be described in more detail.
The content of citric acid or a salt thereof in the artificial tear of the present invention is preferably 2 or more in molar ratio to the content of chlorobutanol. This is because if the content of citric acid or a salt thereof is less than 2 in a molar ratio with respect to the content of chlorobutanol, the tendency of the chlorobutanol to lower the pH of the preparation cannot be sufficiently coped with. In order to further suppress the decrease in pH, the content of citric acid or a salt thereof is more preferably 2.5 or more in molar ratio to the content of chlorobutanol.
本発明の人工涙液中におけるクロロブタノールの配合量は、０．００１〜０．３（Ｗ／Ｖ）％が好ましいが、これは、製剤、特に清涼化剤配合の製剤の点眼直後の刺激の緩和には０．００１（Ｗ／Ｖ）％以上の濃度のクロロブタノールが必要である一方、０．３（Ｗ／Ｖ）％で十分な刺激緩和効果が得られそれ以上濃度を高める必要がなく、また高めてもそれ以上の効果増強はないからである。本発明の人工涙液中におけるクロロブタノールの配合量は、より好ましくは０．０１〜０．２（Ｗ／Ｖ）％、さらに好ましくは０．０２〜０．１（Ｗ／Ｖ）％である。 The compounding amount of chlorobutanol in the artificial tears of the present invention is preferably 0.001 to 0.3 (W / V)%, but this is a factor of irritation immediately after instillation of a preparation, particularly a preparation containing a cooling agent. For relaxation, chlorobutanol at a concentration of 0.001 (W / V)% or more is required, while a sufficient stimulation-relieving effect is obtained at 0.3 (W / V)%, and there is no need to increase the concentration further. This is because, even if it is increased, there is no further effect enhancement. The blending amount of chlorobutanol in the artificial tears of the present invention is more preferably 0.01 to 0.2 (W / V)%, further preferably 0.02 to 0.1 (W / V)%. .
本発明の人工涙液中におけるクエン酸又はその塩の濃度は０．００２〜３％（Ｗ／Ｖ）であることが好ましい。これは、クエン酸又はその塩の濃度が０．００２％（Ｗ／Ｖ）未満では、製剤のｐＨ低下抑制には不十分であり、３％（Ｗ／Ｖ）を超えるとクエン酸又はその塩自体が刺激性を生じる虞があるからである。クエン酸又はその塩の濃度は、特に好ましくは０．０１〜１（ｗ／ｖ）％である。 The concentration of citric acid or a salt thereof in the artificial tear of the present invention is preferably 0.002 to 3% (W / V). This is because when the concentration of citric acid or its salt is less than 0.002% (W / V), it is insufficient to suppress the pH of the preparation, and when it exceeds 3% (W / V), citric acid or its salt This is because it may cause irritation. The concentration of citric acid or a salt thereof is particularly preferably 0.01 to 1 (w / v)%.
クエン酸塩としては、例えば、アルカリ金属塩（ナトリウム塩、カリウム塩等）、アルカリ土類金属塩、アンモニウム塩等の無機塩基との塩のうち、薬剤学的に許容される塩を適宜用いることができる。 As the citrate, for example, a pharmaceutically acceptable salt among salts with an inorganic base such as an alkali metal salt (sodium salt, potassium salt, etc.), an alkaline earth metal salt, and an ammonium salt may be appropriately used. Can be.
本発明の人工涙液に用いることのできる清涼化剤としては、テルペノイド、クローブ香料、ペパーミント香料、ユーカリ香料、レモン香料、ローレル香料、ラベンダー香料、タラゴン香料、カルダモン香料、シダー香料、グレープフルーツ香料、オレンジ香料、ショウガ香料、ベルガモット香料、コリアンダー香料、シナモン香料、ジャスミン香料、ローズマリー香料、ローズ香料、パイン香料、カルダモン香料、ベンゾイン香料、ゼラニウム香料、カモミール香料、マージョラム香料、スペアミント香料、フェンネル香料及びバニラフレーバー等を挙げることができる。テルペノイドとしては、例えば、メントール、メントン、カンフル、ボルネオール、ゲラニオール、シネオール、リモネン、オイゲノール、シトラール、ピネン、リナロール、フェンチルアルコール、ヨノン、サフラナール、テルピネン等のモノテルペンを挙げることができるが、その中でも特にメントール、カンフル、ボルネオ−ル、ゲラニオール、メントン、シネオール及びリモネンを用いるのが好ましい。これらの清涼化剤は１種単独で、又は２種以上を適宜組み合わせて、使用することができる。
なお本出願人は、特願２００１−３９０１５２号において、クローブ香料をペパーミント香料と併用することにより、使用感の良い点眼剤を得ることができ、また当該点眼剤には更にユーカリ香料及びレモン香料よりなる群から選ばれる少なくとも１種の香料を含有してもよく、クローブ香料、ペパーミント香料、ユーカリ香料及びレモン香料の４種の香料を組み合わせることにより、更に使用感の良い点眼剤を得ることができることを見出している。
そこで、この知見に着目して、本発明の人工涙液に用いる清涼化剤として、クローブ香料とペパーミント香料を併用してもよい。また、本発明の人工涙液には更にユーカリ香料及びレモン香料よりなる群から選ばれる少なくとも１種の香料を含有してもよく、クローブ香料、ペパーミント香料、ユーカリ香料及びレモン香料の４種の香料を組み合わせることにより、更に使用感の良い人工涙液を得ることができる。
As a cooling agent that can be used in the artificial tears of the present invention, terpenoids, clove flavor, peppermint flavor, eucalyptus flavor, lemon flavor, laurel flavor, lavender flavor, tarragon flavor, cardamom flavor, cedar flavor, grapefruit flavor, orange Fragrance, ginger flavor, bergamot flavor, coriander flavor, cinnamon flavor, jasmine flavor, rosemary flavor, rose flavor, pine flavor, cardamom flavor, benzoin flavor, geranium flavor, chamomile flavor, marjoram flavor, spearmint flavor, fennel flavor and vanilla flavor And the like. Examples of terpenoids include monoterpenes such as menthol, menthol, camphor, borneol, geraniol, cineol, limonene, eugenol, citral, pinene, linalool, fentyl alcohol, yonone, safranal, and terpinene. In particular, it is preferable to use menthol, camphor, borneol, geraniol, menthon, cineol and limonene. These cooling agents can be used alone or in an appropriate combination of two or more.
In addition, the present applicant, in Japanese Patent Application No. 2001-390152, by using a clove flavor together with a peppermint flavor, it is possible to obtain an eye drop having a good feeling in use, and the eye drops further include a eucalyptus flavor and a lemon flavor. It may contain at least one flavor selected from the group consisting of: a combination of four flavors of clove flavor, peppermint flavor, eucalyptus flavor, and lemon flavor, whereby an eyedrop having a better feeling in use can be obtained. Heading.
Then, paying attention to this finding, a clove flavor and a peppermint flavor may be used in combination as a cooling agent used in the artificial tears of the present invention. The artificial tears of the present invention may further contain at least one flavor selected from the group consisting of eucalyptus flavor and lemon flavor, and four flavors of clove flavor, peppermint flavor, eucalyptus flavor and lemon flavor. By combining these, artificial tears with a better feeling of use can be obtained.
本発明の人工涙液は、含有されるクロロブタノールが局所麻酔作用を発揮して清涼化剤による投与直後の刺激を和らげるため、清涼化剤の配合濃度を従来よりも高め、高清涼感の人工涙液とすることが可能である。したがって、本発明の人工涙液には清涼化剤を０．２（Ｗ／Ｖ）％まで配合することができる。清涼化剤の配合濃度は、好ましくは０．０００１〜０．１（Ｗ／Ｖ）％、特に好ましくは０．００１〜０．０５（Ｗ／Ｖ）％である。 The artificial tears of the present invention, the contained chlorobutanol exerts a local anesthetic action to relieve the irritation immediately after administration with the cooling agent, so that the concentration of the cooling agent is higher than before, and artificial tears with high refreshing feeling It can be liquid. Therefore, the artificial tear of the present invention can contain a cooling agent up to 0.2 (W / V)%. The concentration of the cooling agent is preferably 0.0001 to 0.1 (W / V)%, particularly preferably 0.001 to 0.05 (W / V)%.
本発明の人工涙液は、非酸素透過性ハードコンタクトレンズ、酸素透過性ハードコンタクトレンズ、ソフトコンタクトレンズ等の各種コンタクトレンズの装用時においても投与することができ、とりわけソフトコンタクトレンズ装用時において有利に投与される。 The artificial tear of the present invention can be administered even when wearing various contact lenses such as non-oxygen-permeable hard contact lenses, oxygen-permeable hard contact lenses, and soft contact lenses, and is particularly advantageous when wearing soft contact lenses. To be administered.
本発明の人工涙液は、ｐＨ５．５〜８．０、浸透圧比０．８５〜１．５５（対生理食塩水浸透圧比）に調整される。 The artificial tear of the present invention is adjusted to a pH of 5.5 to 8.0 and an osmotic pressure ratio of 0.85 to 1.55 (to a physiological saline osmotic pressure ratio).
本発明の人工涙液には、薬剤学的に許容され、本発明の人工涙液の長期保存によるｐＨ変化を惹起せず、かつ人工涙液として配合が許されている有効成分以外の有効成分を含有しないという条件で、各種成分を添加することができる。ここに現行の基準においては、人工涙液に配合できる有効成分は、アミノエチルスルホン酸、コンドロイチン硫酸ナトリウム、Ｌ−アスパラギン酸カリウム、Ｌ−アスパラギン酸マグネシウム、Ｌ−アスパラギン酸カリウム・マグネシウム（等量混合物）、炭酸水素ナトリウム、炭酸ナトリウム、塩化カリウム、塩化カルシウム、塩化ナトリウム、リン酸水素ナトリウム、リン酸二水素ナトリム、リン酸二水素カリウム、乾燥炭酸ナトリウム、硫酸マグネシウム、ポリビニルアルコール、ポリビニルピロリドン、ヒドロキシエチルセルロース、ヒドロキシプロピルメチルセルロース、ブドウ糖、メチルセルロースである（一般用医薬品製造（輸入）承認基準、２０００年版）。 The artificial tears of the present invention are pharmaceutically acceptable, do not cause a pH change due to long-term storage of the artificial tears of the present invention, and are active ingredients other than the active ingredients that are allowed to be blended as artificial tears Various components can be added on condition that they do not contain. According to the current standards, the active ingredients that can be incorporated into artificial tears include aminoethylsulfonic acid, sodium chondroitin sulfate, potassium L-aspartate, magnesium L-aspartate, and potassium-magnesium L-aspartate (equivalent mixture. ), Sodium hydrogen carbonate, sodium carbonate, potassium chloride, calcium chloride, sodium chloride, sodium hydrogen phosphate, sodium dihydrogen phosphate, potassium dihydrogen phosphate, dried sodium carbonate, magnesium sulfate, polyvinyl alcohol, polyvinyl pyrrolidone, hydroxyethyl cellulose , Hydroxypropyl methylcellulose, glucose and methylcellulose (Standards for OTC drug manufacture (import) approval, 2000 version).
本発明の人工涙液には、通常点眼剤に用いられている添加剤を配合してよい。そのような添加剤の例としては、緩衝剤、等張化剤、保存剤、溶解補助剤、安定化剤、懸濁化剤、界面活性剤、キレート剤、粘稠剤、ｐＨ調整剤等を挙げることができ、これらは本発明の効果を損なわない範囲で常用量配合することができる。 The artificial tears of the present invention may contain additives commonly used in eye drops. Examples of such additives include buffers, isotonic agents, preservatives, solubilizers, stabilizers, suspending agents, surfactants, chelating agents, thickeners, pH adjusters, and the like. These can be added at ordinary doses within a range that does not impair the effects of the present invention.
緩衝剤としては、例えば、ホウ酸又はその塩であるホウ砂等、酒石酸又はそのナトリウム塩等、グルコン酸又はそのナトリウム塩等、酢酸又はそのナトリウム塩等、リン酸又はリン酸水素二ナトリウム、リン酸二水素ナトリウム（有効成分でもある）等、各種アミノ酸等を配合することができる。 As the buffer, for example, boric acid or a salt thereof such as borax, tartaric acid or a sodium salt thereof, gluconic acid or a sodium salt thereof, acetic acid or a sodium salt thereof, phosphoric acid or disodium hydrogen phosphate, phosphorus Various amino acids such as sodium dihydrogen acid (which is also an active ingredient) can be blended.
等張化剤としては、水溶性で眼刺激性などの悪影響を示さないものであれば、特に制限はなく、例えば、ソルビトール、グルコース、マンニトール、グリセリン、プロピレングリコール、塩化ナトリウム、塩化カリウム等を挙げることができる（塩化ナトリウム、塩化カリウムは、有効成分でもある）。 The tonicity agent is not particularly limited as long as it is water-soluble and does not show adverse effects such as eye irritation. Examples thereof include sorbitol, glucose, mannitol, glycerin, propylene glycol, sodium chloride, potassium chloride and the like. (Sodium chloride and potassium chloride are also active ingredients).
保存剤としては、例えば、パラオキシ安息香酸エステル類、塩化ベンザルコニウム、塩化ベンゼトニウム、ベンジルアルコール、ソルビン酸又はその塩、グルコン酸クロルヘキシジン、デヒドロ酢酸ナトリウム、塩化セチルピリジニウム、塩酸アルキルジアミノエチルグリシン等を挙げることができる。 Examples of the preservative include paraoxybenzoate esters, benzalkonium chloride, benzethonium chloride, benzyl alcohol, sorbic acid or a salt thereof, chlorhexidine gluconate, sodium dehydroacetate, cetylpyridinium chloride, alkyldiaminoethylglycine hydrochloride, and the like. be able to.
溶解補助剤としては、例えば、ポリソルベート８０、ポリビニルピロリドン（有効成分でもある）、ポリエチレングリコール、プロピレングリコール、ポリオキシエチレン硬化ヒマシ油６０、ステアリン酸ポリオキシル４０等を挙げることができる。 Examples of the solubilizer include polysorbate 80, polyvinylpyrrolidone (also an active ingredient), polyethylene glycol, propylene glycol, polyoxyethylene hydrogenated castor oil 60, and polyoxyl stearate 40.
安定化剤としては、例えばエデト酸ナトリウム、シクロデキストリン、縮合リン酸又はその塩、亜硫酸塩等を挙げることができる。 Examples of the stabilizer include sodium edetate, cyclodextrin, condensed phosphoric acid or a salt thereof, and a sulfite.
懸濁化剤としては、例えば、メチルセルロース、ヒドロキシプロピルセルロース、ポリビニルピロリドン（有効成分でもある）、ポリオキシエチレン硬化ヒマシ油６０、ステアリン酸ポリオキシル４０、ポリエチレングリコール、カルボキシメチルセルロースナトリウム、ポリビニルアルコール（有効成分でもある）等を挙げることができる。 Examples of the suspending agent include methylcellulose, hydroxypropylcellulose, polyvinylpyrrolidone (also an active ingredient), polyoxyethylene hydrogenated castor oil 60, polyoxyl stearate 40, polyethylene glycol, sodium carboxymethylcellulose, and polyvinyl alcohol (even an active ingredient). Yes) and the like.
界面活性剤としては、非イオン界面活性剤、陰イオン界面活性剤、両性界面活性剤、陽イオン界面活性剤のいずれもが使用可能である。 As the surfactant, any of a nonionic surfactant, an anionic surfactant, an amphoteric surfactant, and a cationic surfactant can be used.
陰イオン界面活性剤としては、例えばラウロイルサルコシンナトリウム、ラウロイル−Ｌ−グルタミン酸トリエタノールアミン、ミリスチルサルコシンナトリウム等が挙げられ、両性界面活性剤としては、例えばラウリルジメチルアミノ酢酸ベタイン、２−アルキル−Ｎ−カルボキシメチル−Ｎ−ヒドロキシエチルイミダゾリニウムベタイン、塩酸アルキルジアミノグリシン等が挙げられ、非イオン界面活性剤としては、例えばポリソルベート８０、ポリオキシエチレン硬化ヒマシ油６０、ステアリン酸ポリオキシル４０、ポリオキシエチレンラウリルエーテル等が挙げられ、陽イオン界面活性剤としては、例えば塩化ベンゼトニウム、塩化ベンザルコニウム、塩化セチルピリジニウム等を挙げることができる。 Examples of the anionic surfactant include sodium lauroyl sarcosine, triethanolamine lauroyl-L-glutamate, and sodium myristyl sarcosine. Examples of the amphoteric surfactant include lauryl dimethylamino acetate betaine and 2-alkyl-N-. Carboxymethyl-N-hydroxyethylimidazolinium betaine, alkyldiaminoglycine hydrochloride, and the like. Examples of the nonionic surfactant include polysorbate 80, polyoxyethylene hydrogenated castor oil 60, polyoxyl stearate 40, and polyoxyethylene lauryl. Examples of the cationic surfactant include benzethonium chloride, benzalkonium chloride, and cetylpyridinium chloride.
キレート剤としては、例えばエデト酸ナトリウム、縮合リン酸又はその塩（縮合リン酸ナトリウム等）等を挙げることができる。 Examples of the chelating agent include sodium edetate, condensed phosphoric acid or a salt thereof (eg, condensed sodium phosphate).
粘稠剤としては、例えばメチルセルロース（有効成分でもある）、ヒドロキシエチルセルロース（有効成分でもある）、ヒドロキシプロピルセルロース、ヒドロキシプロピルメチルセルロース（有効成分でもある）、コンドロイチン硫酸ナトリウム（有効成分でもある）、カルボキシメチルセルロースナトリウム、ポリビニルピロリドン（有効成分でもある）、ポリビニルアルコール（有効成分でもある）、ポリエチレングリコール等を挙げることができる。 Examples of the thickener include methylcellulose (also an active ingredient), hydroxyethylcellulose (also an active ingredient), hydroxypropyl cellulose, hydroxypropylmethylcellulose (also an active ingredient), sodium chondroitin sulfate (also an active ingredient), carboxymethylcellulose Examples thereof include sodium, polyvinylpyrrolidone (also an active ingredient), polyvinyl alcohol (also an active ingredient), and polyethylene glycol.
ｐＨ調整剤としては、例えば、水酸化ナトリウム、水酸化カリウム、炭酸ナトリウム（有効成分でもある）、塩酸、リン酸、酢酸等を挙げることができる。 Examples of the pH adjuster include sodium hydroxide, potassium hydroxide, sodium carbonate (which is also an active ingredient), hydrochloric acid, phosphoric acid, and acetic acid.
以下に、試験例及び実施例を挙げて本発明をさらに具体的に説明するが、これらは単なる例示であり、本発明がこれらにより限定されることは意図しない。
［試験例］
〔試験方法〕
下記の試験液を調製し、ろ過滅菌後、無色ガラスアンプル（容量５ml）に充填し、４０℃、７５％（相対湿度）の加速試験の条件下で保存した。用いたクエン酸ナトリウムは２水塩（ＭＷ＝２９４．１０）、クロロブタノール（ＭＷ＝１７７．４６）は水分含量４．９％のものであった。
Hereinafter, the present invention will be described more specifically with reference to Test Examples and Examples, but these are merely examples, and it is not intended that the present invention be limited by these.
[Test example]
〔Test method〕
The following test solution was prepared, sterilized by filtration, filled in a colorless glass ampoule (volume: 5 ml), and stored under the conditions of an accelerated test at 40 ° C. and 75% (relative humidity). The sodium citrate used was dihydrate (MW = 294.10), and chlorobutanol (MW = 177.46) had a water content of 4.9%.
〔試験結果〕
各試験例につき、試験液の６ケ月保存後のｐＨを測定した。また、クロロブタノール残存率、ｌ−メントール残存率及び外観を測定した。試験結果は次のとおりであった。
〔Test results〕
For each test example, the pH of the test solution after storage for 6 months was measured. Further, the residual ratio of chlorobutanol, the residual ratio of 1-menthol, and the appearance were measured. The test results were as follows.
以上の加速試験結果から、クロロブタノールを含有する人工涙液にクエン酸ナトリウムを共存させないか（試験例３及び５）、クロロブタノールの含有量に対してクエン酸ナトリウムをモル比で２未満しか共存させないと（試験例１）、長期保存で人工涙液のｐＨの低下を十分に抑制できない製剤となるが、より多いモル比でクエン酸ナトリウムを共存させると（試験例２及び４）、長期保存後であってもクロロブタノール含有人工涙液のｐＨ低下を十分に抑制できる製剤が得られることが判る。 From the above accelerated test results, whether sodium citrate was allowed to coexist in artificial tears containing chlorobutanol (Test Examples 3 and 5), or sodium citrate coexisted in a molar ratio of less than 2 with respect to the content of chlorobutanol If not performed (Test Example 1), the preparation will not be able to sufficiently suppress the decrease in pH of artificial tears during long-term storage, but if sodium citrate is used in a larger molar ratio (Test Examples 2 and 4), long-term storage will occur. It can be seen that even after the preparation, a preparation which can sufficiently suppress the decrease in pH of the artificial tears containing chlorobutanol can be obtained.
次に、常法により以下の処方により本発明の人工涙液を製造した。なお、用いたクエン酸ナトリウムは２水塩、クロロブタノールは、水分含量４．９％のものであった。
［実施例１］ 人工涙液
塩化ナトリウム・・・・・・・・・・・・・・０．５５ｇ
塩化カリウム・・・・・・・・・・・・・・・０．１５ｇ
ブドウ糖・・・・・・・・・・・・・・・・・０．００５ｇ
ホウ酸・・・・・・・・・・・・・・・・・・０．５ｇ
クエン酸ナトリウム・・・・・・・・・・・・０．２ｇ
ヒドロキシエチルセルロース・・・・・・・・０．１ｇ
エデト酸ナトリウム・・・・・・・・・・・・０．０１ｇ
塩酸・・・・・・・・・・・・・・・・・・・適量
ポリソルベート８０・・・・・・・・・・・・０．３ｇ
ｌ−メントール・・・・・・・・・・・・・・０．１ｇ
グルコン酸クロルヘキシジン液 (20 w/v%)・・０．０２５ｍＬ
クロロブタノール・・・・・・・・・・・・・０．０５ｇ
精製水・・・・・・・・・・・・・・・・・・適量
全量 １００ｍＬ（ｐＨ５．８）
モル比（クエン酸ナトリウム／クロロブタノール）＝２．５
Next, the artificial tear of the present invention was produced by the following formulation according to a conventional method. The sodium citrate used was dihydrate and chlorobutanol had a water content of 4.9%.
[Example 1] Artificial tear sodium chloride ··· 0.55 g
Potassium chloride 0.15g
Dextrose 0.005g
Boric acid 0.5 g
Sodium citrate 0.2 g
Hydroxyethyl cellulose 0.1 g
Sodium edetate 0.01g
Hydrochloric acid ・ ・ ・ ・ ・ ・ ・ ・ ・ Suitable amount of polysorbate 80 ・ ・ ・ ・ 0.3g
l-menthol 0.1g
Chlorhexidine gluconate solution (20 w / v%) 0.025 mL
Chlorobutanol ... 0.05g
Purified water ...
Total volume 100mL (pH 5.8)
Molar ratio (sodium citrate / chlorobutanol) = 2.5
［実施例２］ 人工涙液
塩化ナトリウム・・・・・・・・・・・・・・・０．５ｇ
塩化カリウム・・・・・・・・・・・・・・・・０．１５ｇ
塩化カルシウム・・・・・・・・・・・・・・・０．０１５ｇ
ホウ酸・・・・・・・・・・・・・・・・・・・０．７ｇ
クエン酸ナトリウム・・・・・・・・・・・・・０．１ｇ
ヒドロキシプロピルメチルセルロース2910・・・０．２ｇ
水酸化ナトリウム・・・・・・・・・・・・・・適量
ｌ−メントール・・・・・・・・・・・・・・・０．０１ｇ
ボルネオール・・・・・・・・・・・・・・・・０．００２ｇ
マクロゴール４０００・・・・・・・・・・・・０．３ｇ
塩化ベンザルコニウム液 (10 w/v%)・・・・・・０．０５ｍＬ
クロロブタノール・・・・・・・・・・・・・・０．０１ｇ
精製水・・・・・・・・・・・・・・・・・・・適量
全量 １００ｍＬ（ｐＨ６．５）
モル比（クエン酸ナトリウム／クロロブタノール）＝６．３
[Example 2] Artificial tear sodium chloride 0.5 g
Potassium chloride 0.15g
Calcium chloride: 0.015g
Boric acid 0.7g
Sodium citrate 0.1g
Hydroxypropyl methylcellulose 2910 ・ ・ ・ 0.2g
Sodium hydroxide ・ ・ ・ Appropriate amount l-menthol ・ ・ ・ ・ ・ ・ 0.01g
Borneol ... 0.002g
Macrogol 4000 0.3g
Benzalkonium chloride solution (10 w / v%) ・ ・ ・ ・ ・ ・ 0.05mL
Chlorobutanol 0.01 g
Purified water ...
Total volume 100mL (pH 6.5)
Molar ratio (sodium citrate / chlorobutanol) = 6.3
［実施例３］ 人工涙液
塩化ナトリウム・・・・・・・・・・・・・・・０．５５ｇ
塩化カリウム・・・・・・・・・・・・・・・・０．１６ｇ
ホウ酸・・・・・・・・・・・・・・・・・・・１．２ｇ
乾燥炭酸ナトリウム・・・・・・・・・・・・・０．０６ｇ
リン酸水素ナトリウム・・・・・・・・・・・・０．１８ｇ
クエン酸ナトリウム・・・・・・・・・・・・・０．２ｇ
ヒドロキシエチルセルロース・・・・・・・・・０．１ｇ
塩酸・・・・・・・・・・・・・・・・・・・・適量
ｌ−メントール・・・・・・・・・・・・・・・０．０２ｇ
カンフル・・・・・・・・・・・・・・・・・・０．０１ｇ
ポリオキシエチレン硬化ヒマシ油６０・・・・・０．２ｇ
塩化ベンザルコニウム液 (10 w/v%)・・・・・・０．０５ｍＬ
クロロブタノール・・・・・・・・・・・・・・０．０２５ｇ
精製水・・・・・・・・・・・・・・・・・・・適量
全量 １００ｍＬ（ｐＨ７．２）
モル比（クエン酸ナトリウム／クロロブタノール）＝５．１
[Example 3] Artificial tear sodium chloride 0.55 g
Potassium chloride: 0.16 g
1.2 g of boric acid
Dry sodium carbonate 0.06g
Sodium hydrogen phosphate 0.18g
Sodium citrate ... 0.2g
Hydroxyethyl cellulose 0.1 g
Hydrochloric acid ... appropriate amount 1-menthol ... 0.02g
Camphor 0.01g
Polyoxyethylene hydrogenated castor oil 60 ... 0.2g
Benzalkonium chloride solution (10 w / v%) ・ ・ ・ ・ ・ ・ 0.05mL
Chlorobutanol 0.025 g
Purified water ...
Total volume 100mL (pH 7.2)
Molar ratio (sodium citrate / chlorobutanol) = 5.1
［実施例４］ 人工涙液
塩化ナトリウム・・・・・・・・・・・・・・・０．５５ｇ
塩化カリウム・・・・・・・・・・・・・・・・０．１５ｇ
ブドウ糖・・・・・・・・・・・・・・・・・・０．２ｇ
ホウ酸・・・・・・・・・・・・・・・・・・・０．５ｇ
クエン酸ナトリウム・・・・・・・・・・・・・０．４ｇ
エデト酸ナトリウム・・・・・・・・・・・・・０．０１ｇ
クロロブタノール・・・・・・・・・・・・・・０．１ｇ
塩酸・・・・・・・・・・・・・・・・・・・・適量
ポリソルベート８０・・・・・・・・・・・・・０．１６２ｇ
ｌ−メントール・・・・・・・・・・・・・・・０．０２ｇ
グルコン酸クロルヘキシジン液 (20 w/v%)・・・０．０２５ｍＬ
精製水・・・・・・・・・・・・・・・・・・・適量
全量 １００ｍＬ（ｐＨ６．０）
モル比（クエン酸ナトリウム／クロロブタノール）＝２．５
[Example 4] Artificial tear sodium chloride ··· 0.55 g
Potassium chloride 0.15g
Glucose 0.2 g
0.5 g of boric acid
Sodium citrate 0.4g
Sodium edetate 0.01g
Chlorobutanol 0.1 g
Hydrochloric acid ..... appropriate amount polysorbate 80 ..... 162g
l-menthol ... 0.02g
Chlorhexidine gluconate solution (20 w / v%) ・ ・ ・ 0.025mL
Purified water ...
Total volume 100mL (pH 6.0)
Molar ratio (sodium citrate / chlorobutanol) = 2.5
［実施例５］ 人工涙液
塩化ナトリウム・・・・・・・・・・・・・・・０．５５ｇ
塩化カリウム・・・・・・・・・・・・・・・・０．１５ｇ
ブドウ糖・・・・・・・・・・・・・・・・・・０．２ｇ
ホウ酸・・・・・・・・・・・・・・・・・・・０．５ｇ
クエン酸ナトリウム・・・・・・・・・・・・・０．４ｇ
エデト酸ナトリウム・・・・・・・・・・・・・０．０１ｇ
クロロブタノール・・・・・・・・・・・・・・０．１ｇ
塩酸・・・・・・・・・・・・・・・・・・・・適量
ポリソルベート８０・・・・・・・・・・・・・０．１６２ｇ
ｌ−メントール・・・・・・・・・・・・・・・０．０１ｇ
ネオフレーバー AL07531* ・・・・・・・・・・０．１ｇ
グルコン酸クロルヘキシジン液 (20 w/v%)・・・０．０２５ｍＬ
精製水・・・・・・・・・・・・・・・・・・・適量
全量 １００ｍＬ（ｐＨ６．０）
モル比（クエン酸ナトリウム／クロロブタノール）＝２．５
＊ ネオフレーバー AL07531
表示成分： エタノール ４０．１％
香料 ５９．９％
（クローブ香料、ペパーミント香料、ユーカリ香料及びレモン香料を含有。
更に、エステル類、フェノールエーテル類、ケトン類、ラクトン類、芳香族アルデヒド類を含有。）
[Example 5] Artificial tear sodium chloride ····· 0.55 g
Potassium chloride 0.15g
Glucose 0.2 g
0.5 g of boric acid
Sodium citrate 0.4g
Sodium edetate 0.01g
Chlorobutanol 0.1 g
Hydrochloric acid ..... appropriate amount polysorbate 80 ..... 162g
l-menthol 0.01g
NEO Flavor AL07531 *・ ・ ・ ・ ・ ・ ・ ・ ・ ・ 0.1g
Chlorhexidine gluconate solution (20 w / v%) ・ ・ ・ 0.025mL
Purified water ...
Total volume 100mL (pH 6.0)
Molar ratio (sodium citrate / chlorobutanol) = 2.5
* Neoflavor AL07531
Ingredients: Ethanol 40.1%
Fragrance 59.9%
(Contains clove flavor, peppermint flavor, eucalyptus flavor and lemon flavor.
In addition, it contains esters, phenol ethers, ketones, lactones, and aromatic aldehydes. )
本発明の人工涙液においては、クロロブタノールの分解によるｐＨの低下が有意に抑制され、それにより、長期保存後であっても製造時のｐＨに近いｐＨの人工涙液であって、かつ、清涼化剤の配合濃度を高めた人工涙液を提供することができる。 In the artificial tears of the present invention, the decrease in pH due to the decomposition of chlorobutanol is significantly suppressed, whereby artificial tears having a pH close to the pH at the time of production even after long-term storage, and An artificial tear having an increased concentration of a cooling agent can be provided.
Claims (29)
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| EP2014333A1 (en) * | 2007-07-12 | 2009-01-14 | Hakiman Shargh Research Company | Use of cooling agents for treatment or prevention of lacrimation or eye burning |
| JP2014108960A (en) * | 2012-12-04 | 2014-06-12 | Rohto Pharmaceut Co Ltd | Composition for mucosal application |
| JP2016210773A (en) * | 2015-04-30 | 2016-12-15 | 國家衛生研究院 | Artificial-tear composition |
| JP6050454B1 (en) * | 2015-09-28 | 2016-12-21 | 参天製薬株式会社 | Aqueous pharmaceutical composition |
| JP2019142979A (en) * | 2012-09-27 | 2019-08-29 | 千寿製薬株式会社 | Aqueous liquid formulation |
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| WO2017057434A1 (en) * | 2015-09-28 | 2017-04-06 | 参天製薬株式会社 | Aqueous pharmaceutical composition |
| WO2019235456A1 (en) * | 2018-06-05 | 2019-12-12 | 千寿製薬株式会社 | Aqueous liquid agent |
| JP2019210288A (en) * | 2018-06-05 | 2019-12-12 | 千寿製薬株式会社 | Liquid chemical |
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