JP2017065717A - NSAIDs-CONTAINING SPRAY AGENT - Google Patents
NSAIDs-CONTAINING SPRAY AGENT Download PDFInfo
- Publication number
- JP2017065717A JP2017065717A JP2015192400A JP2015192400A JP2017065717A JP 2017065717 A JP2017065717 A JP 2017065717A JP 2015192400 A JP2015192400 A JP 2015192400A JP 2015192400 A JP2015192400 A JP 2015192400A JP 2017065717 A JP2017065717 A JP 2017065717A
- Authority
- JP
- Japan
- Prior art keywords
- nsaids
- container
- spray
- bottle body
- content liquid
- 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.)
- Pending
Links
- 239000007921 spray Substances 0.000 title claims abstract description 53
- 239000003795 chemical substances by application Substances 0.000 title claims abstract description 33
- 239000007788 liquid Substances 0.000 claims abstract description 51
- 229940021182 non-steroidal anti-inflammatory drug Drugs 0.000 claims abstract description 48
- 230000007797 corrosion Effects 0.000 claims abstract description 12
- 238000005260 corrosion Methods 0.000 claims abstract description 12
- 229920003002 synthetic resin Polymers 0.000 claims abstract description 10
- 239000000057 synthetic resin Substances 0.000 claims abstract description 10
- 239000000041 non-steroidal anti-inflammatory agent Substances 0.000 claims abstract description 9
- -1 polyethylene Polymers 0.000 claims description 34
- 239000003595 mist Substances 0.000 claims description 20
- 230000005484 gravity Effects 0.000 claims description 7
- 239000004743 Polypropylene Substances 0.000 claims description 5
- 229920001155 polypropylene Polymers 0.000 claims description 5
- 238000011049 filling Methods 0.000 claims description 4
- 238000005507 spraying Methods 0.000 claims description 4
- 239000004698 Polyethylene Substances 0.000 claims description 3
- 239000004793 Polystyrene Substances 0.000 claims description 3
- 229920000728 polyester Polymers 0.000 claims description 3
- 229920000573 polyethylene Polymers 0.000 claims description 3
- 229920002223 polystyrene Polymers 0.000 claims description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 16
- 235000014113 dietary fatty acids Nutrition 0.000 description 11
- 239000000194 fatty acid Substances 0.000 description 11
- 229930195729 fatty acid Natural products 0.000 description 11
- 239000003921 oil Substances 0.000 description 11
- 235000019198 oils Nutrition 0.000 description 11
- 238000000034 method Methods 0.000 description 10
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- 239000000443 aerosol Substances 0.000 description 8
- 238000005096 rolling process Methods 0.000 description 7
- 239000002253 acid Substances 0.000 description 6
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- 239000002184 metal Substances 0.000 description 5
- 238000002360 preparation method Methods 0.000 description 5
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- 238000000071 blow moulding Methods 0.000 description 4
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- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
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- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
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- 239000002738 chelating agent Substances 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 239000002826 coolant Substances 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 235000011187 glycerol Nutrition 0.000 description 3
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- 229920001223 polyethylene glycol Polymers 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- PRAKJMSDJKAYCZ-UHFFFAOYSA-N squalane Chemical compound CC(C)CCCC(C)CCCC(C)CCCCC(C)CCCC(C)CCCC(C)C PRAKJMSDJKAYCZ-UHFFFAOYSA-N 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- 239000002562 thickening agent Substances 0.000 description 3
- XMGQYMWWDOXHJM-JTQLQIEISA-N (+)-α-limonene Chemical compound CC(=C)[C@@H]1CCC(C)=CC1 XMGQYMWWDOXHJM-JTQLQIEISA-N 0.000 description 2
- NOOLISFMXDJSKH-KXUCPTDWSA-N (-)-Menthol Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@H]1O NOOLISFMXDJSKH-KXUCPTDWSA-N 0.000 description 2
- YWWVWXASSLXJHU-AATRIKPKSA-N (9E)-tetradecenoic acid Chemical compound CCCC\C=C\CCCCCCCC(O)=O YWWVWXASSLXJHU-AATRIKPKSA-N 0.000 description 2
- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 2
- MPDGHEJMBKOTSU-YKLVYJNSSA-N 18beta-glycyrrhetic acid Chemical compound C([C@H]1C2=CC(=O)[C@H]34)[C@@](C)(C(O)=O)CC[C@]1(C)CC[C@@]2(C)[C@]4(C)CC[C@@H]1[C@]3(C)CC[C@H](O)C1(C)C MPDGHEJMBKOTSU-YKLVYJNSSA-N 0.000 description 2
- GECRRQVLQHRVNH-MRCUWXFGSA-N 2-octyldodecyl (z)-octadec-9-enoate Chemical compound CCCCCCCCCCC(CCCCCCCC)COC(=O)CCCCCCC\C=C/CCCCCCCC GECRRQVLQHRVNH-MRCUWXFGSA-N 0.000 description 2
- HIQIXEFWDLTDED-UHFFFAOYSA-N 4-hydroxy-1-piperidin-4-ylpyrrolidin-2-one Chemical compound O=C1CC(O)CN1C1CCNCC1 HIQIXEFWDLTDED-UHFFFAOYSA-N 0.000 description 2
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- 208000034656 Contusions Diseases 0.000 description 2
- RGHNJXZEOKUKBD-SQOUGZDYSA-N D-gluconic acid Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O RGHNJXZEOKUKBD-SQOUGZDYSA-N 0.000 description 2
- NOOLISFMXDJSKH-UHFFFAOYSA-N DL-menthol Natural products CC(C)C1CCC(C)CC1O NOOLISFMXDJSKH-UHFFFAOYSA-N 0.000 description 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- 235000006679 Mentha X verticillata Nutrition 0.000 description 2
- 235000002899 Mentha suaveolens Nutrition 0.000 description 2
- 235000001636 Mentha x rotundifolia Nutrition 0.000 description 2
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 2
- 229920000881 Modified starch Polymers 0.000 description 2
- 239000004909 Moisturizer Substances 0.000 description 2
- 208000000112 Myalgia Diseases 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- ZTHYODDOHIVTJV-UHFFFAOYSA-N Propyl gallate Chemical compound CCCOC(=O)C1=CC(O)=C(O)C(O)=C1 ZTHYODDOHIVTJV-UHFFFAOYSA-N 0.000 description 2
- 208000010040 Sprains and Strains Diseases 0.000 description 2
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- 229940124532 absorption promoter Drugs 0.000 description 2
- VJHCJDRQFCCTHL-UHFFFAOYSA-N acetic acid 2,3,4,5,6-pentahydroxyhexanal Chemical compound CC(O)=O.OCC(O)C(O)C(O)C(O)C=O VJHCJDRQFCCTHL-UHFFFAOYSA-N 0.000 description 2
- 150000005215 alkyl ethers Chemical class 0.000 description 2
- 230000000202 analgesic effect Effects 0.000 description 2
- 230000003110 anti-inflammatory effect Effects 0.000 description 2
- 230000003078 antioxidant effect Effects 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
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- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 description 2
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Images
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Abstract
Description
本発明は非ステロイド性消炎鎮痛薬(Non−Steroidal Anti−Inflammatory Drugs:NSAIDs)を含有する内容液を、液化ガスや圧縮ガスを使用せず、容器の腐食が防止でき、容器が転がりにくく、内容液をミスト状に投与可能な、外用のNSAIDs含有スプレー剤に関する。さらに詳しくは、本発明は、NSAIDsを含有する内容液を、合成樹脂製のボトル本体と液化ガスや圧縮ガスを使用せずにミスト状に噴霧可能なディスペンサーからなるスプレー容器に充填することにより、液化ガスや圧縮ガスを使用せず、容器の腐食が防止でき、容器が転がりにくく、内容液をミスト状に投与可能な、NSAIDs含有スプレー剤に関するものである。 The present invention is a content liquid containing non-steroidal anti-inflammatory drugs (NSAIDs), which does not use liquefied gas or compressed gas, can prevent corrosion of the container, and the container is difficult to roll. The present invention relates to an NSAIDs-containing spray for external use, which can administer the liquid in a mist form. More specifically, the present invention fills a liquid container containing NSAIDs into a spray container composed of a synthetic resin bottle body and a dispenser that can be sprayed in a mist form without using liquefied gas or compressed gas. The present invention relates to an NSAIDs-containing spray agent that does not use liquefied gas or compressed gas, can prevent corrosion of the container, is difficult to roll, and can administer the content liquid in a mist form.
従来、スポーツ時における打撲や捻挫、筋肉痛、肩こりに伴う肩の痛み、腰痛、関節痛、肘の痛みなどの局所の炎症症状を緩解することを目的として、非ステロイド性消炎鎮痛薬(Non−Steroidal Anti−Inflammatory Drugs:NSAIDs)を皮膚から吸収させる製品が多く販売されている。これらの製品には、パップ剤やテープ剤などの貼付剤や、軟膏剤、クリーム剤、液剤などの塗布剤があり、剤形の特長から目的に応じて使い分けられている。 Conventionally, non-steroidal anti-inflammatory analgesics (Non−) have been used to relieve local inflammatory symptoms such as bruises and sprains during sports, muscle pain, shoulder pain associated with stiff shoulders, back pain, joint pain, and elbow pain. There are many products on the market that absorb Steroidal Anti-Inflammatory Drugs (NSAIDs) from the skin. These products include patches such as poultices and tapes, and coating agents such as ointments, creams, and liquids, and are used properly according to the purpose of the dosage form.
貼付剤は、患部に長時間貼付できるため、薬効の持続性に優れた製剤としてよく用いられている。塗布剤は、展延性に優れ、投与する部位の形状にかかわらず投与できる利点がある。その中でも、液剤は、軟膏剤やクリーム剤よりも粘性が低いためべとつき感が抑制された剤形である。また、液剤は、アルコールや水が主成分であることから、液剤の使用時には、気化熱により少なからず清涼感が得られるため夏季に好まれ、かつ炎症部位を冷やす効果が期待できる。さらに、液剤は、内容液を手にとらずに吐出部を介して患部に投与できるよう製品形態を工夫することで、手を汚すことなく投与できる利点がある。しかし、吐出部が円形などの固有の形状を有するため、液剤を関節のような凹凸部へ投与する際は、内容液を塗り広げにくい課題がある。また、このような液剤は、吐出部と皮膚が接触するため、皮膚の常在細菌などにより吐出部が汚染されるだけでなく、炎症部位への投与時に圧痛を伴う課題がある。 Since patches can be applied to affected areas for a long time, they are often used as preparations having excellent drug efficacy. The coating agent is excellent in spreadability and has an advantage that it can be administered regardless of the shape of the administration site. Among them, the liquid is a dosage form in which the stickiness is suppressed because the viscosity is lower than that of an ointment or cream. In addition, since the liquid agent is mainly composed of alcohol or water, the liquid agent is preferred in summer because it can provide a refreshing feeling due to the heat of vaporization, and an effect of cooling the inflamed site can be expected. Furthermore, a liquid agent has the advantage that it can administer without making a hand dirty by devising a product form so that a content liquid can be administered to an affected part via a discharge part, without taking a hand. However, since the discharge part has a unique shape such as a circle, there is a problem that it is difficult to spread the content liquid when the liquid agent is administered to an uneven part such as a joint. Moreover, since such a liquid agent contacts the discharge part and the skin, not only the discharge part is contaminated by resident bacteria of the skin, but also there is a problem accompanied by tenderness when administered to the inflamed site.
一方、手や吐出部を介することなく、離れた位置から炎症部位に内容液を投与できる剤形としては、NSAIDs含有のスプレー剤があり、液化ガスや圧縮ガスを使用したエアゾール剤が多く販売されている。エアゾール剤は、液化ガスや圧縮ガスを使用し、これらと共に内容液を離れた位置から所望する患部に向かって噴霧できるため、手や吐出部が汚染されず、患部の形状にかかわらず投与しやすく、かつ、圧痛を伴わない利点がある。また、エアゾール剤を使用する際は、ガスと共に内容液をミスト状に噴射できるため、液状に噴射するよりも患部に内容液が集中せず、液だれが起こりにくくなる。さらに、内容液が噴霧された時に生じる液滴は、表面積が大きいため気化しやすくなっている。そのため、エアゾール剤は、スポーツ時の打撲や捻挫、筋肉痛などの症状に対して、炎症部位を冷やす効果も期待できることから夏季に汎用される剤形である。このように、ミスト状に噴霧できるエアゾール剤の有用性は、使用上および治療上の観点から着目されている。 On the other hand, NSAIDs-containing sprays are available as dosage forms that can administer the content liquid to the inflamed site from a remote location without going through the hand or discharge part, and many aerosols using liquefied gas or compressed gas are sold. ing. Aerosols use liquefied gas or compressed gas, and together with these, the liquid contents can be sprayed from a remote location toward the desired affected area, so that the hands and discharge parts are not contaminated and are easy to administer regardless of the shape of the affected area. And there is an advantage without tenderness. In addition, when using an aerosol agent, the content liquid can be ejected in a mist form together with the gas, so that the content liquid does not concentrate on the affected area and the dripping is less likely to occur than when it is ejected in liquid form. Further, the droplets generated when the content liquid is sprayed are easy to vaporize because of the large surface area. Therefore, the aerosol is a dosage form that is widely used in summer because it can be expected to cool the inflammatory site against symptoms such as bruises, sprains, and muscle pain during sports. Thus, the usefulness of the aerosol which can be sprayed in mist form attracts attention from the viewpoint of use and treatment.
しかし、エアゾール剤は、液化ガスや圧縮ガスを使用しているため、高温環境下での保管による容器の破裂や患部の凍傷など、従来からその保管または使用時の危険性が指摘されており、特に夏季においてはこれらの危険性は増大する。また、エアゾール剤で使用される容器は一般的に金属製で円筒形が汎用されているが、大気中の水分などにより金属が腐食しやすく、円筒形のため転がりやすい形状である。そのため、金属が腐食した際は容器が脆くなり内容液が滲出し、容器が転がった際は捻挫や筋肉痛などの痛みを伴っている使用者が製剤を拾うために歩き回り、更なる苦痛を与える恐れがある。
エアゾール剤で金属を使用せず腐食を防止することができる技術として、特許文献1に示すように、ポリエチレンテレフタレートなどを使用したプラスチック容器が開発されているが、円筒形であるため転がりやすい課題は解決されていない。
However, since aerosols use liquefied gas or compressed gas, there have been traditionally pointed out dangers during storage or use, such as rupture of containers due to storage in high temperature environments and frostbite of affected areas. Especially in summer, these risks increase. Moreover, although the container used with an aerosol agent is generally made of metal and has a cylindrical shape, the metal is easily corroded by moisture in the atmosphere, and the shape is easy to roll because of the cylindrical shape. Therefore, when the metal is corroded, the container becomes brittle and the content liquid oozes out. There is a fear.
As a technique that can prevent corrosion without using a metal with an aerosol agent, as shown in
そこで、液化ガスや圧縮ガスを使用せず、容器の腐食が防止でき、容器が転がりにくく、内容液をミスト状に投与できるNSAIDs含有スプレー剤が望まれていた。 Therefore, there has been a demand for an NSAIDs-containing spray agent that does not use liquefied gas or compressed gas, can prevent corrosion of the container, is difficult to roll, and can administer the content liquid in a mist form.
本発明の目的は、上述の状況を鑑みてなされたもので、液化ガスや圧縮ガスを使用せず、容器の腐食が防止でき、容器が転がりにくく、内容液をミスト状に投与できるNSAIDs含有スプレー剤を提供することである。 An object of the present invention has been made in view of the above-described circumstances, and does not use liquefied gas or compressed gas, can prevent corrosion of the container, the container is difficult to roll, and can contain the NSAIDs containing the liquid in a mist form. Is to provide an agent.
本発明者らは、上述の課題を解決すべく鋭意検討した結果、NSAIDsを含有する内容液を、底面と平行に切断した際の胴部の水平断面が長円形状または略長方形状であり、かつ合成樹脂製のボトル本体と液化ガスや圧縮ガスを使用せずに内容液をミスト状に噴霧可能なディスペンサーにより構成されるスプレー容器に充填することで、液化ガスや圧縮ガスを使用せず、容器の腐食が防止でき、容器が転がりにくく、内容液をミスト状に投与できることを見出し、本発明を完成するに至った。
すなわち、本発明は以下の(1)〜(4)に示したものである。
(1)液化ガスや圧縮ガスを使用せず、容器の腐食が防止でき、容器が転がりにくく、内容液をミスト状に投与できるNSAIDs含有スプレー剤であって、
前記スプレー剤は、合成樹脂製のボトル本体および液化ガスや圧縮ガスを使用せずに内容液をミスト状に噴霧可能なディスペンサーからなり、
該ボトル本体は、内側に内容液の充填空間と、上端に形成され開口を有する首部を有し、かつ該ボトル本体の胴部を底面と平行に切断した際の水平断面の重心を通る長径と短径の比が最大で1.3〜10.0の長円形状または長辺と短辺の比が最大で1.3〜10.0の略長方形状であることを特徴とするNSAIDs含有スプレー剤。
(2)前記合成樹脂が、ポリエチレン、ポリプロピレン、ポリエステルまたはポリスチレンのいずれか一種以上である上記(1)に記載のNSAIDs含有スプレー剤。
(3)前記ボトル本体の胴部の外周が最大で100〜150mmであり、かつ、該ボトル本体の底面から首部までの高さが50〜200mmである上記(1)〜(2)のいずれかに記載のNSAIDs含有スプレー剤。
(4)前記ディスペンサーが、エアポンプ式である上記(1)〜(3)のいずれかに記載のNSAIDs含有スプレー剤。
As a result of intensive studies to solve the above-mentioned problems, the inventors of the present invention have a horizontal cross section of the trunk when the content liquid containing NSAIDs is cut in parallel with the bottom surface, or an oval shape or a substantially rectangular shape. And by filling the spray container composed of a dispenser that can spray the liquid contents in a mist form without using a synthetic resin bottle body and liquefied gas or compressed gas, liquefied gas or compressed gas is not used, It has been found that the corrosion of the container can be prevented, the container is difficult to roll, and the content liquid can be administered in the form of a mist, and the present invention has been completed.
That is, this invention is shown to the following (1)-(4).
(1) NSAIDs-containing spray agent that does not use liquefied gas or compressed gas, can prevent corrosion of the container, the container is difficult to roll, and can administer the content liquid in mist form,
The spray agent consists of a bottle body made of synthetic resin and a dispenser capable of spraying the liquid contents in a mist form without using liquefied gas or compressed gas,
The bottle body has a content liquid filling space inside, a neck formed at the top and having an opening, and a long diameter passing through the center of gravity of the horizontal section when the body of the bottle body is cut parallel to the bottom surface. NSAIDs-containing spray, characterized in that it has an oval shape with a maximum minor axis ratio of 1.3 to 10.0 or a substantially rectangular shape with a maximum ratio of long side to short side of 1.3 to 10.0 Agent.
(2) The NSAIDs-containing spray agent according to (1), wherein the synthetic resin is one or more of polyethylene, polypropylene, polyester, or polystyrene.
(3) Any of the above (1) to (2), wherein the outer circumference of the body of the bottle body is 100 to 150 mm at the maximum, and the height from the bottom surface to the neck of the bottle body is 50 to 200 mm. NSAIDs-containing sprays described in 1.
(4) The NSAIDs-containing spray according to any one of (1) to (3), wherein the dispenser is an air pump type.
以上述べたように、本発明は、液化ガスや圧縮ガスを使用せず、容器の腐食が防止でき、容器が転がりにくく、内容液をミスト状に投与できるNSAIDs含有スプレー剤を提供することができる。 As described above, the present invention can provide an NSAIDs-containing spray that does not use liquefied gas or compressed gas, can prevent corrosion of the container, is difficult to roll, and can administer the liquid in a mist form. .
以下、本発明のNSAIDs含有スプレー剤を詳細に説明する。なお、本明細書に記載の例示は、本発明を特に限定するものではない。 Hereinafter, the NSAIDs-containing spray of the present invention will be described in detail. Note that the examples described in the present specification do not particularly limit the present invention.
本発明の「転がりにくい」とは、NSAIDs含有スプレー剤を用いて、傾斜角度7°、平面からの高さが3cmの斜面に横倒しに設置させたときに、平面に着地してからの転がりにくさをいう。つまり、転がった距離が10cm以上の時、「転がった」とし、10cm未満の時、「転がらなかった」とした。 The term “difficult to roll” in the present invention refers to the rolling after landing on a flat surface when the NSAIDs-containing spray agent is installed on a slope with an inclination angle of 7 ° and a height of 3 cm from the flat surface. Say it. That is, when the rolled distance was 10 cm or more, it was “rolled”, and when it was less than 10 cm, it was “not rolled”.
図1に示すように、本発明のNSAIDs含有スプレー剤は、ボトル本体AとディスペンサーBからなっており、ディスペンサーBは液化ガスや圧縮ガスを使用せずに内容液をミスト状に噴霧可能であり、その上部には、キャップCを装着することができる。 As shown in FIG. 1, the NSAIDs-containing spray of the present invention comprises a bottle body A and a dispenser B. The dispenser B can spray the content liquid in a mist form without using liquefied gas or compressed gas. The cap C can be attached to the upper part.
本発明におけるボトル本体Aの容量は、特に制限されないが、50mL未満であるとボトル本体Aが小さく手に持った際のフィット感が悪くなり、200mLを超えると容器がかさばり携帯性に欠くため、50〜200mLであることが好ましい。 The capacity of the bottle main body A in the present invention is not particularly limited, but if the bottle main body A is less than 50 mL, the fit when the bottle main body A is small and held in hand is poor, and if it exceeds 200 mL, the container is bulky and lacks portability. It is preferable that it is 50-200 mL.
図2〜3に示すようにボトル本体Aは、底部1、胴部2、肩部3および首部4からなっており、合成樹脂を基礎樹脂として単層もしくは積層として成形され、底面5から首部4までの高さは特に制限されないが、50〜200mmが好ましい。合成樹脂としては、高密度ポリエチレン、低密度ポリエチレンなどのポリエチレン、ポリプロピレン、ポリエステル、ポリスチレンなどが挙げられ、単独または2種以上組み合わせて用いることができる。
As shown in FIGS. 2 to 3, the bottle main body A includes a
図2〜3に示すように底部1は、ボトル本体Aの着地面となる底面5を構成している。
As shown in FIGS. 2 to 3, the
図2〜3に示すように胴部2は、底部1と肩部3との間にあり、図4〜5に示すように底面5と平行に切断した水平断面が長円形状もしくは略長方形状を形成している。より詳しくは、図4に示すように長円形状の重心を通る長径6および短径7は各々10〜100mm、かつ、長径6と短径7の比が最大で1.1〜15.0であることが好ましいが、より好ましくは長円形状の重心を通る長径6および短径7は各々20〜50mm、かつ、長径6と短径7の比が最大で1.3〜10.0である。また、図5に示すように略長方形状の重心を通る長辺8および短辺9は各々10〜100mm、かつ、長辺8と短辺9の比が最大で1.1〜15.0であることが好ましいが、より好ましくは略長方形状の重心を通る長辺8および短辺9は各々20〜50mm、長辺8と短辺9の比が最大で1.3〜10.0である。図6〜7に示すように、胴部2のコーナー部10を丸面取りし、更に外周を100〜150mmの大きさとすることで、手に持った際のボトル本体Aとのフィット感が向上でき、使用者がボトル本体Aをより一層持ちやすくさせることができる。
2-3, the trunk |
肩部3は胴部2の上部に位置し、図2に示すように胴部2と同一の形状および大きさを有するように形成されている、もしくは図3に示すように、胴部2から首部4にかけて徐々に縮径し、なで肩状に形成されている。肩部3は底部1および胴部2と同様に、全体として長円形状もしくは略長方形状に形成されており、その外周は胴部2より小さく、首部4より大きい。
The
図2〜3に示すように首部4はボトル本体Aの上端部に位置し、首部4の外周には、ディスペンサーを着脱可能に構成されたネジ11が螺設されていてもよい。また、図6〜7に示すように首部4は、上端が開口しており、内容液の供給口として機能する。 As shown in FIGS. 2 to 3, the neck 4 is positioned at the upper end of the bottle main body A, and a screw 11 configured to be detachable from the dispenser may be screwed around the outer periphery of the neck 4. Moreover, as shown in FIGS. 6-7, the neck part 4 has opened the upper end, and functions as a supply port of a content liquid.
本発明のNSAIDs含有スプレー剤に使用するボトル本体の成形方法としては、ブロー成形法を挙げることができ、ブロー成形を採用することにより、容易に各種形状のボトル本体を自由自在に製造することができる。ここで、ブロー成形法としては、ダイレクトブロー成形、インジェクションブロー成形のいずれを用いてもよい。また、コールドパリソン法、ホットパリソン法のいずれであっても構わない。 As a molding method of the bottle body used for the NSAIDs-containing spray of the present invention, a blow molding method can be mentioned. By adopting blow molding, bottle bodies of various shapes can be easily produced freely. it can. Here, either direct blow molding or injection blow molding may be used as the blow molding method. Further, either the cold parison method or the hot parison method may be used.
本発明におけるディスペンサーBは、液化ガスや圧縮ガスを使用せずに内容液をミスト状に噴霧できれば形状、構造、材質などは特に制限されないが、エアポンプ式、トリガー式などが挙げられる。好ましくは、ディスペンサー本体が大きくなく携帯性に優れたエアポンプ式である。 The dispenser B in the present invention is not particularly limited in shape, structure, material and the like as long as the liquid content can be sprayed in a mist form without using liquefied gas or compressed gas, but examples include an air pump type and a trigger type. Preferably, the dispenser main body is not large and is an air pump type excellent in portability.
本発明におけるディスペンサーBを1回作動させた際に噴霧される内容液の量は、0.05mL未満であると十分な消炎鎮痛効果が得られず、また、0.5mLを超えると過剰投与となり副作用の発現のリスクが高くなるため、0.05〜0.5mLであることが好ましい。さらに、本発明のNSAIDs含有スプレー剤は、炎症部位などに使用されるため、ディスペンサーBを1回作動させた際に、内容液が炎症部位全体に噴霧された方が好ましい。そのため、10cm離れた垂直板面にむけて内容液を噴霧した際、その板面における濡れた部分の最大径が5〜30cmであり、かつ、濡れた部分の面積が、10〜700cm2であることが好ましい。濡れた部分の面積が10cm2未満であると所望される範囲に噴霧できず、700cm2を超えると所望される範囲以外にも噴霧されて無駄を生じるため好ましくない。また、本発明のNSAIDs含有スプレー剤は、逆さまの状態で使用される可能性もあるため、ディスペンサーBは正立状態で噴霧されるだけでなく、倒立状態でも噴霧されることが好ましい。 When the dispenser B in the present invention is operated once, the amount of the content liquid sprayed is less than 0.05 mL, and a sufficient anti-inflammatory analgesic effect cannot be obtained. Since the risk of developing side effects increases, it is preferably 0.05 to 0.5 mL. Furthermore, since the NSAIDs-containing spray of the present invention is used for an inflammatory site or the like, it is preferable that the content liquid is sprayed on the entire inflammatory site when the dispenser B is operated once. Therefore, when the content liquid is sprayed toward a vertical plate surface 10 cm away, the maximum diameter of the wet portion on the plate surface is 5 to 30 cm, and the area of the wet portion is 10 to 700 cm 2 . It is preferable. When the area of the wet portion is less than 10 cm 2 , spraying cannot be performed in a desired range, and when the area exceeds 700 cm 2 , spraying is performed outside the desired range, resulting in waste. Further, since the NSAIDs-containing spray of the present invention may be used upside down, the dispenser B is preferably sprayed not only in an upright state but also in an inverted state.
本発明のNSAIDs含有スプレー剤に使用されるディスペンサーの成形方法としては、通常行われている方法であれば特に制限されないが、射出成形法、圧縮成形法などの公知の成形方法が適用できる。 The method of molding the dispenser used for the NSAIDs-containing spray of the present invention is not particularly limited as long as it is a commonly used method, but known molding methods such as injection molding and compression molding can be applied.
本発明に用いるNSAIDsとしては、たとえば、インドメタシン、イブプロフェン、ケトプロフェン、イブプロフェンピコノール、ピロキシカム、アセチルサリチル酸、アスピリン、フェルビナク、アルクロフェナック、クリダナク、サルサラート、ナプロキセン、フェンブフェン、フルフェナム酸、フルルビプロフェン、メチアジン酸、メフェナム酸、ベンダザック、ブフェキサマク、ウフェナマート、ロキソプロフェンおよびこの塩、グリチルレチン酸およびこの塩、サリチル酸メチル、サリチル酸グリコールなどが挙げられ、単独または2種以上組み合わせて用いることができる。NSAIDsの含量は、内容液の全体に対して、0.01質量%未満であると十分な消炎鎮痛効果が得られず、また、10質量%を超えると副作用を発現するリスクが高くなるため、0.01〜10質量%であることが好ましいが、より好ましくは0.5〜5質量%である。 Examples of NSAIDs used in the present invention include indomethacin, ibuprofen, ketoprofen, ibuprofen piconol, piroxicam, acetylsalicylic acid, aspirin, felbinac, alclofenac, clidanac, salsalate, naproxen, fenbufen, flufenamic acid, flurbiprofen, methiazine. Acid, mefenamic acid, bendazac, bufexamac, ufenamate, loxoprofen and its salt, glycyrrhetinic acid and its salt, methyl salicylate, glycolic salicylate and the like can be mentioned, and these can be used alone or in combination of two or more. If the content of NSAIDs is less than 0.01% by mass relative to the entire content liquid, a sufficient anti-inflammatory analgesic effect cannot be obtained, and if it exceeds 10% by mass, the risk of developing side effects increases. Although it is preferable that it is 0.01-10 mass%, More preferably, it is 0.5-5 mass%.
本発明に用いる水としては、たとえば、精製水、滅菌水、天然水、常水、注射用水などが挙げられ、単独または2種以上組み合わせて用いることができるが、好ましくは精製水である。 Examples of the water used in the present invention include purified water, sterilized water, natural water, normal water, and water for injection. These can be used alone or in combination of two or more, but purified water is preferred.
本発明のNSAIDs含有スプレー剤には、本発明の効果を損なわない範囲で医薬品を製造するにあたって許容される各種成分、すなわち、アルコール、界面活性剤、増粘剤、保湿剤、油性成分、pH調整剤、キレート剤、香料・清涼化剤、酸化防止剤、防腐剤、吸収促進剤などを適宜配合することができる。 The NSAIDs-containing spray of the present invention has various components that are acceptable for producing pharmaceuticals within the range that does not impair the effects of the present invention, that is, alcohol, surfactant, thickener, moisturizer, oily component, pH adjustment An agent, a chelating agent, a fragrance / cooling agent, an antioxidant, an antiseptic, an absorption accelerator, and the like can be appropriately blended.
本発明に用いるアルコールとしては、たとえば、エタノール、無水エタノール、各種変性エタノール、n−プロパノール、イソプロパノール、n−ブタノール、イソブタノールなどが挙げられ、単独または2種以上組み合わせて用いることができる。アルコールの含量は、内容液の全体に対して、5質量%未満であるとNSAIDsを十分に溶解または分散させることが困難であり、また、60質量%を超えると皮膚刺激性が高くなるため、5〜60質量%であることが好ましいが、より好ましくは15〜40質量%である。 Examples of the alcohol used in the present invention include ethanol, absolute ethanol, various denatured ethanol, n-propanol, isopropanol, n-butanol, and isobutanol, and these can be used alone or in combination of two or more. If the alcohol content is less than 5% by mass with respect to the entire content liquid, it is difficult to sufficiently dissolve or disperse NSAIDs, and if it exceeds 60% by mass, skin irritation becomes high. Although it is preferable that it is 5-60 mass%, More preferably, it is 15-40 mass%.
界面活性剤としては、たとえば、ポリオキシエチレンアルキルエーテル、ポリオキシエチレンポリプロピレンアルキルエーテルなどのエーテル系化合物、ソルビタン脂肪酸エステル、ポリオキシエチレンソルビタン脂肪酸エステル、グリセリン脂肪酸エステル、ポリグリセリン脂肪酸エステル、ポリオキシエチレングリセリン脂肪酸エステル、ポリエチレングリコール脂肪酸エステル、ショ糖脂肪酸エステルなどのエステル系化合物、ポリオキシエチレンヒマシ油・硬化ヒマシ油、ポリオキシエチレンポリオキシプロピレン重合体などのノニオン界面活性剤、ラウリルジメチルベタインなどのアルキルベタイン、ヤシ油脂肪酸アミドプロピルベタインなどのアルキルアミドベタイン、アルキルスルホベタイン、イミダゾリンなどの両性界面活性剤、飽和高級脂肪酸塩、アルキルスルホン酸塩、アルキルエーテルスルホン酸塩、ポリオキシエチレンアルキルエーテルリン酸塩などのアニオン界面活性剤が挙げられ、単独または2種以上組み合わせて用いることができる。 Examples of the surfactant include ether compounds such as polyoxyethylene alkyl ether and polyoxyethylene polypropylene alkyl ether, sorbitan fatty acid ester, polyoxyethylene sorbitan fatty acid ester, glycerin fatty acid ester, polyglycerin fatty acid ester, polyoxyethylene glycerin. Fatty acid esters, polyethylene glycol fatty acid esters, ester compounds such as sucrose fatty acid esters, nonionic surfactants such as polyoxyethylene castor oil / hardened castor oil, polyoxyethylene polyoxypropylene polymer, and alkylbetaines such as lauryl dimethyl betaine , Amphoteric surfactants such as alkylamide betaines such as coconut oil fatty acid amidopropylbetaine, alkylsulfobetaines and imidazolines Agents, saturated higher fatty acid salts, alkyl sulfonates, alkyl ether sulfonates, anionic surfactants such as polyoxyethylene alkyl ether phosphate and the like, may be used alone or in combination of two or more.
増粘剤としては、たとえば、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、カルメロース、クロスカルメロース、メチルセルロースなどのセルロース誘導体、部分α化澱粉などの加工澱粉、ポリビニルアルコール、ポリビニルピロリドン、クロスポピドン、ポリエチレングリコール、カルボキシビニルポリマー、アクリル酸・メタクリル酸アルキル共重合体、キサンタンガム、カラギーナン、アルギン酸ナトリウム、アラビアゴム、グアーガム、ローカストビーンガム、プルラン、ゼラチン、ポリアクリル酸ナトリウムなどが挙げられ、単独または2種以上組み合わせて用いることができる。 Examples of the thickener include cellulose derivatives such as hydroxypropylcellulose, hydroxypropylmethylcellulose, carmellose, croscarmellose and methylcellulose, modified starches such as partially pregelatinized starch, polyvinyl alcohol, polyvinylpyrrolidone, crospovidone, polyethylene glycol, carboxy Vinyl polymers, acrylic acid / alkyl methacrylate copolymers, xanthan gum, carrageenan, sodium alginate, gum arabic, guar gum, locust bean gum, pullulan, gelatin, sodium polyacrylate, etc. are used alone or in combination of two or more. be able to.
保湿剤としては、たとえば、エチレングリコール、ジエチレングリコール、プロピレングリコール、ブチレングリコール、ジブチレングリコール、グリセリン、ジグリセリン、ポリグリセリンやショ糖、乳糖、マルロース、マンニトール、エリスリトール、キシリトールなどの糖類および糖アルコールなどが挙げられ、単独または2種以上組み合わせて用いることができる。 Examples of the humectant include ethylene glycol, diethylene glycol, propylene glycol, butylene glycol, dibutylene glycol, glycerin, diglycerin, polyglycerin and sucrose, lactose, malose, mannitol, erythritol, xylitol and other sugars and sugar alcohols. Can be used alone or in combination of two or more.
油性成分としては、たとえば、パルミトオレインアルコール、オレインアルコール、エイコソニルアルコール、エライジルアルコール、リノレイルアルコールなどの不飽和脂肪族アルコール、オレイン酸、エライジン酸、リノール酸、ウンデシレン酸、ミリストレイン酸、パルミトレイン酸、リンデル酸、ラウロレイン酸、ツズ酸、ペテロセリン酸、バセニン酸、ゴンドイン酸などの不飽和脂肪酸、グリセリンモノオレイン酸エステルグリセリン、ジオレイン酸エステル、オレイン酸オクチルドデシル、オレイン酸オレイルなどの不飽和脂肪酸エステル、オレイルアルコール、エライジルアルコール流動パラフィン、ワセリン、マイクロクリスタリンワックスなどの炭化水素類、メチルポリシロキサン、メチルフェニルポリシロキサン、ジメチルシクロポリシロキサンなどのシリコン油類、ミツロウなどのロウ類、セチルアルコール、ステアリルアルコールなどの高級アルコール類、コレステロールなどのステロール類、オレイン酸オクチルドデシル、オレイン酸オレイル、オクタン酸セチル、ミリスチン酸イソプロピル、ミリスチン酸ミリスチルなどの脂肪酸エステル類、ステアリン酸アルミニウム、ステアリン酸マグネシウムなどの金属石鹸類などが挙げられ、単独または2種以上組み合わせて用いることができる。 Examples of the oil component include unsaturated fatty alcohols such as palmitooleic alcohol, oleic alcohol, eicosonyl alcohol, elaidyl alcohol, linoleyl alcohol, oleic acid, elaidic acid, linoleic acid, undecylenic acid, myristoleic acid, Unsaturated fatty acids such as palmitoleic acid, lindelic acid, lauroleic acid, tuzuic acid, peteroselic acid, bassenic acid, gondonic acid, glyceryl monooleate glycerin, dioleate, octyldodecyl oleate, oleyl oleate Fatty acid esters, oleyl alcohol, elidyl alcohol liquid paraffin, petrolatum, hydrocarbons such as microcrystalline wax, methylpolysiloxane, methylphenylpolysiloxane, dimethyl Silicon oils such as lucyclopolysiloxane, waxes such as beeswax, higher alcohols such as cetyl alcohol and stearyl alcohol, sterols such as cholesterol, octyldodecyl oleate, oleyl oleate, cetyl octanoate, isopropyl myristate, Examples include fatty acid esters such as myristyl myristate, and metal soaps such as aluminum stearate and magnesium stearate, which can be used alone or in combination of two or more.
pH調整剤としては、たとえば、酢酸、ギ酸、乳酸、酒石酸、シュウ酸、グリコール酸、リンゴ酸、クエン酸、コハク酸、フマル酸、リン酸、塩酸、硝酸、硫酸およびこれらの塩、水酸化ナトリウム、水酸化カリウム、水酸化カルシウム、アルギニン、メチルアミン、エチルアミン、プロピルアミン、ジメチルアミン、ジエチルアミン、ジプロピルアミン、トリメチルアミン、トリエチルアミン、トリプロピルアミン、モノメタノールアミン、モノエタノールアミン、モノプロパノールアミン、ジメタノールアミン、ジエタノールアミン、ジプロパノールアミン、トリメタノールアミン、トリエタノールアミン、イソプロパノールアミン、ジイソプロパノールアミン、トリプロパノールアミン、アンモニンア水、炭酸グアニジン、炭酸水素ナトリウム、炭酸アンモニウムなどが挙げられ、単独または2種以上組み合わせて用いることができる。 Examples of pH adjusters include acetic acid, formic acid, lactic acid, tartaric acid, oxalic acid, glycolic acid, malic acid, citric acid, succinic acid, fumaric acid, phosphoric acid, hydrochloric acid, nitric acid, sulfuric acid and their salts, sodium hydroxide , Potassium hydroxide, calcium hydroxide, arginine, methylamine, ethylamine, propylamine, dimethylamine, diethylamine, dipropylamine, trimethylamine, triethylamine, tripropylamine, monomethanolamine, monoethanolamine, monopropanolamine, dimethanol Amine, diethanolamine, dipropanolamine, trimethanolamine, triethanolamine, isopropanolamine, diisopropanolamine, tripropanolamine, ammonia water, guanidine carbonate, bicarbonate Potassium, and ammonium carbonate and the like, may be used alone or in combination of two or more.
キレート剤としては、たとえば、ピロリン酸、ヘキサメタリン酸、グルコン酸などが挙げられ、単独または2種以上組み合わせて用いることができる。 Examples of the chelating agent include pyrophosphoric acid, hexametaphosphoric acid, gluconic acid and the like, and can be used alone or in combination of two or more.
香料・清涼化剤としては、たとえば、ハッカ油、ハッカハク油、ケイヒ油、チョウジ油、ウイキョウ油、ヒマシ油、テレピン油、ユーカリ油、オレンジ油、ラベンダー油、レモン油、ローズ油、レモングラス油、ダイウイキョウ油、チアミン油、ヘノポジ油、ヤマジン油、トウカ油、ベルガモット油、シトロネラ油、樟脳油、セラニウム油などやローズマリーやセージをはじめとする植物抽出物などの香料、l−メントール、カンフル、チモール、N−エチル−p−メンタン−カルボキシアミド、p−メンタン−3,8−ジオール、l−イソプレゴール、l−メンチルグリセリルエーテルなどの清涼化剤が挙げられ、単独または2種以上組み合わせて用いることができる。 Examples of fragrances and refreshing agents include mint oil, mint oil, cinnamon oil, clove oil, fennel oil, castor oil, turpentine oil, eucalyptus oil, orange oil, lavender oil, lemon oil, rose oil, lemongrass oil, Fragrances such as daikyo oil, thiamine oil, henoposi oil, yamadine oil, touka oil, bergamot oil, citronella oil, camphor oil, cerium oil and plant extracts such as rosemary and sage, l-menthol, camphor, Cooling agents such as thymol, N-ethyl-p-menthane-carboxamide, p-menthane-3,8-diol, l-isopulegol, l-menthyl glyceryl ether, and the like may be used alone or in combination of two or more. Can do.
酸化防止剤としては、たとえば、アスコルビン酸、没食子酸プロピル、ブチルヒドロキシアニソール、ジブチルヒドロキシトルエン、ノルジヒドログアヤレチン酸、トコフェロール、酢酸トコフェロールなどが挙げられ、単独または2種以上組み合わせて用いることができる。 Examples of the antioxidant include ascorbic acid, propyl gallate, butylhydroxyanisole, dibutylhydroxytoluene, nordihydroguaiaretic acid, tocopherol, and tocopherol acetate, which can be used alone or in combination of two or more. .
防腐剤としては、たとえば、チモール、イソプロピルメチルフェノール、安息香酸、安息香酸メチル、パラオキシ安息香酸エチル、パラオキシ安息香酸プロピル、パラオキシ安息香酸ブチル、ベンジルアルコール、塩化ベンザルコニウム、塩化ベンゼトニウムなどが挙げられ、単独または2種以上組み合わせて用いることができる。 Examples of preservatives include thymol, isopropylmethylphenol, benzoic acid, methyl benzoate, ethyl paraoxybenzoate, propyl paraoxybenzoate, butyl paraoxybenzoate, benzyl alcohol, benzalkonium chloride, benzethonium chloride, and the like. It can be used alone or in combination of two or more.
吸収促進剤としては、たとえば、ジイソプロピルアジペート、レシチン、スクワラン、スクワレン、エイゾン、l−メントール、ポリエチレングリコール、ミリスチン酸イソプロピル、ジメチルスルホキシド、ハッカ油、ユーカリ油、d−リモネン、dl−リモネンなどが挙げられ、単独または2種以上組み合わせて用いることができる。 Examples of the absorption promoter include diisopropyl adipate, lecithin, squalane, squalene, azone, l-menthol, polyethylene glycol, isopropyl myristate, dimethyl sulfoxide, peppermint oil, eucalyptus oil, d-limonene, dl-limonene and the like. These can be used alone or in combination of two or more.
本発明のNSAIDs含有スプレー剤は、従来公知の常法または今後新しく提供される方法で製造することができる。その代表的な方法としては、NSAIDs、アルコールを精製水に十分に溶解または分散させ、さらに界面活性剤、増粘剤、保湿剤、油性成分、pH調整剤、キレート剤、香料・清涼化剤、酸化防止剤、防腐剤、吸収促進剤などを加え、十分に溶解または分散させて、内容液を調製する。調製した内容液を、合成樹脂製のボトル本体と液化ガスや圧縮ガスを使用せずにミスト状に噴霧可能なディスペンサーからなるスプレー容器に充填し、本発明のNSAIDs含有スプレー剤を製造することができる。 The NSAIDs-containing spray of the present invention can be produced by a conventionally known conventional method or a method newly provided in the future. As typical methods, NSAIDs and alcohol are sufficiently dissolved or dispersed in purified water, and further surfactants, thickeners, moisturizers, oil components, pH adjusters, chelating agents, fragrances / cooling agents, Antioxidants, preservatives, absorption promoters, etc. are added and sufficiently dissolved or dispersed to prepare the content liquid. The prepared content liquid can be filled in a spray container consisting of a synthetic resin bottle body and a dispenser that can be sprayed in a mist form without using liquefied gas or compressed gas to produce the NSAIDs-containing spray of the present invention. it can.
以下に、実施例により更に詳細に本発明を説明するが、本発明は、これに限定されるものではない。
(実施例1)
表1に示す配合に基づき、後述する調製法1の方法により調製し、本発明のNSAIDs含有スプレー剤1を得た。得られたNSAIDs含有スプレー剤1を用いて、試験例1に従って転がり試験を実施した結果、4cmとなり、転がらなかった。結果を表2に示す。
Hereinafter, the present invention will be described in more detail with reference to examples, but the present invention is not limited thereto.
Example 1
Based on the formulation shown in Table 1, it was prepared by the method of
(調製法1)
精製水に、ジイソプロパノールアミン、フェルビナク、エタノール、グリセリンを順次加え、撹拌・溶解して得た内容液を、ポリプロピレンを主成分とし、底面と平行に切断した際の胴部の水平断面が長円形状で、水平断面の重心を通る長径が48mm、短径が31mm(長径と短径の比が1.5)、外周が120mm、底面から首部までの高さが146mmであるボトル本体(本多プラス(株)製、NOC−120)に100mL充填し、液化ガスや圧縮ガスを使用せずにミスト状に噴霧可能なエアポンプ式ディスペンサー((株)三谷バルブ製、Z−155)を装着し、本発明のNSAIDs含有スプレー剤1を得た。
(Preparation method 1)
The horizontal cross section of the body when the content liquid obtained by adding diisopropanolamine, felbinac, ethanol, and glycerin to purified water in order, stirring and dissolving, with polypropylene as the main component and parallel to the bottom surface is an ellipse. The main body of the bottle with a major axis of 48 mm, a minor axis of 31 mm (ratio of major axis to minor axis is 1.5), an outer circumference of 120 mm, and a height from the bottom to the neck of 146 mm. Filled with 100 mL of NOC-120 made by Plus Co., Ltd. and equipped with an air pump dispenser (Z-155, manufactured by Mitani Valve Co., Ltd.) that can be sprayed in a mist form without using liquefied gas or compressed gas, The NSAIDs-containing
(試験例1)
転がり試験
前述した実施例1のNSAIDs含有スプレー剤1、後述する実施例2のNSAIDs含有スプレー剤2および比較例1のスプレー剤1を用いて、転がり試験を実施した。
各スプレー剤を傾斜角度7°、平面からの高さが3cmの斜面に横倒しに設置した。各スプレー剤が平面に着地してからの転がった距離を測定し、この距離が10cm以上の時、「転がった」とし、10cm未満の時、「転がらなかった」とした。
(Test Example 1)
Rolling test A rolling test was carried out using the NSAIDs-containing
Each spray was placed on a slope with an inclination angle of 7 ° and a height from a plane of 3 cm. The rolling distance after each spray agent landed on a flat surface was measured. When this distance was 10 cm or more, it was “rolled”, and when it was less than 10 cm, it was “not rolled”.
(実施例2)
実施例1において使用するボトル本体を、底面と平行に切断した際の胴部の水平断面が略長方形状(隅が湾曲するR長方形状)で、水平断面の重心を通る長辺の長さが44mm、短辺の長さが34mm(長辺と短辺の比が1.3)、外周が130mm、底面から首部までの高さが134mmであるボトル本体(本多プラス(株)製、MRC−120)とした以外、実施例1と全く同じ調製法を繰り返し、NSAIDs含有スプレー剤2を得た。得られたNSAIDs含有スプレー剤2用いて、試験例1に従って転がり試験を実施した結果、5cmとなり、転がらなかった。結果を表2に示した。
(Example 2)
When the bottle body used in Example 1 is cut in parallel with the bottom surface, the horizontal cross section of the body portion is substantially rectangular (R rectangular shape with curved corners), and the length of the long side passing through the center of gravity of the horizontal cross section is 44mm, the length of the short side is 34mm (the ratio of the long side to the short side is 1.3), the outer periphery is 130mm, and the height from the bottom to the neck is 134mm (manufactured by Honda Plus Co., Ltd., MRC -The same preparation method as Example 1 was repeated except that it was set to -120), and the NSAIDs containing
(比較例1)
実施例1において使用するボトル本体を、底面と平行に切断した際の胴部の水平断面が直径39mm、外周が120mmの真円形で、底面から首部までの高さが121mmであるボトル本体(本多プラス(株)製、NCC−100)とした以外、実施例1と全く同じ調製法を繰り返し、スプレー剤1を得た。得られたスプレー剤1を用いて、試験例1に従って転がり試験を実施した結果、80cmとなり、転がった。結果を表2に示した。
(Comparative Example 1)
When the bottle body used in Example 1 is cut in parallel with the bottom surface, the horizontal section of the trunk portion is a true circle with a diameter of 39 mm and the outer periphery is 120 mm, and the height from the bottom surface to the neck portion is 121 mm. Except for using NCC-100 (manufactured by Multiplus Co., Ltd.), the same preparation method as in Example 1 was repeated to obtain a
本発明は、NSAIDs含有の内容液を、底面と平行に切断した際の胴部の水平断面が長円形状または略長方形状であり、かつ合成樹脂製のボトル本体と液化ガスや圧縮ガスを使用せずに内容液をミスト状に噴霧可能なディスペンサーにより構成されるスプレー容器に充填することで、液化ガスや圧縮ガスを使用せず、容器の腐食が防止でき、容器が転がりにくく、内容液をミスト状に投与できるNSAIDs含有スプレー剤に関するものであり、産業上十分に利用できるものである。 The present invention uses a liquid body containing liquefied gas or compressed gas, and the horizontal section of the body when the content liquid containing NSAIDs is cut parallel to the bottom surface is an oval shape or a substantially rectangular shape. By filling the spray container with a dispenser that can spray the contents liquid in a mist form without using liquefied gas or compressed gas, corrosion of the container can be prevented, the container is difficult to roll, and the contents liquid is not The present invention relates to a spray containing NSAIDs that can be administered in the form of a mist, and can be used industrially.
A ボトル本体
B ディスペンサー
C キャップ
1 底部
2 胴部
3 肩部
4 首部
5 底面
6 長径
7 短径
8 長辺
9 短辺
10 コーナー部
11 ネジ
A Bottle body B
Claims (4)
前記スプレー剤は、合成樹脂製のボトル本体および液化ガスや圧縮ガスを使用せずに内容液をミスト状に噴霧可能なディスペンサーからなり、
該ボトル本体は、内側に内容液の充填空間と、上端に形成され開口を有する首部を有し、かつ該ボトル本体の胴部を底面と平行に切断した際の水平断面の重心を通る長径と短径の比が最大で1.3〜10.0の長円形状、または長辺と短辺の比が最大で1.3〜10.0の略長方形状であることを特徴とするNSAIDs含有スプレー剤。 NSAIDs-containing spray agent that does not use liquefied gas or compressed gas, can prevent corrosion of the container, is difficult to roll, and can administer the content liquid in mist form,
The spray agent consists of a bottle body made of synthetic resin and a dispenser capable of spraying the liquid contents in a mist form without using liquefied gas or compressed gas,
The bottle body has a content liquid filling space inside, a neck formed at the top and having an opening, and a long diameter passing through the center of gravity of the horizontal section when the body of the bottle body is cut parallel to the bottom surface. NSAIDs-containing, characterized in that it has an elliptical shape with a short diameter ratio of 1.3 to 10.0 at the maximum, or a substantially rectangular shape with a long to short side ratio of 1.3 to 10.0 at the maximum Spray agent.
The NSAIDs-containing spray according to any one of claims 1 to 3, wherein the dispenser is an air pump type.
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JP2015192400A JP2017065717A (en) | 2015-09-30 | 2015-09-30 | NSAIDs-CONTAINING SPRAY AGENT |
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Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
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JP2002346442A (en) * | 2001-05-25 | 2002-12-03 | Daizo:Kk | Spraying product |
JP2010155630A (en) * | 2008-12-26 | 2010-07-15 | Yoshino Kogyosho Co Ltd | Container for pump |
JP2014195626A (en) * | 2013-03-29 | 2014-10-16 | 三笠製薬株式会社 | Nsaids-containing liquid drug |
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2015
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Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
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JP2002346442A (en) * | 2001-05-25 | 2002-12-03 | Daizo:Kk | Spraying product |
JP2010155630A (en) * | 2008-12-26 | 2010-07-15 | Yoshino Kogyosho Co Ltd | Container for pump |
JP2014195626A (en) * | 2013-03-29 | 2014-10-16 | 三笠製薬株式会社 | Nsaids-containing liquid drug |
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