[go: up one dir, main page]
More Web Proxy on the site http://driver.im/

JPH07157427A - Dental surface anesthetic - Google Patents

Dental surface anesthetic

Info

Publication number
JPH07157427A
JPH07157427A JP5303016A JP30301693A JPH07157427A JP H07157427 A JPH07157427 A JP H07157427A JP 5303016 A JP5303016 A JP 5303016A JP 30301693 A JP30301693 A JP 30301693A JP H07157427 A JPH07157427 A JP H07157427A
Authority
JP
Japan
Prior art keywords
anesthetic
dental surface
surface anesthetic
gingiva
water
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.)
Withdrawn
Application number
JP5303016A
Other languages
Japanese (ja)
Inventor
Masataka Shiki
政孝 信貴
Daizaburo Sanuki
大三郎 佐貫
Mitsuji Higashide
充志 東出
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Fujisawa Pharmaceutical Co Ltd
Teika Pharamaceutical Co Ltd
Original Assignee
Fujisawa Pharmaceutical Co Ltd
Teika Pharamaceutical Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Fujisawa Pharmaceutical Co Ltd, Teika Pharamaceutical Co Ltd filed Critical Fujisawa Pharmaceutical Co Ltd
Priority to JP5303016A priority Critical patent/JPH07157427A/en
Publication of JPH07157427A publication Critical patent/JPH07157427A/en
Withdrawn legal-status Critical Current

Links

Landscapes

  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

PURPOSE:To obtain such a dental surface anesthetic as to evidently realize the coated side, i.e., the site to which a local anesthetic is to be injected, when this anesthetic is applied onto the gingiva. CONSTITUTION:This anesthetic contains a total of >=0.01wt.% of an anesthetic active ingredient, a water-soluble polymeric base and a medium color- or a cold color-based colorant and has a viscosity at 40 deg.C of 300-1000cps.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】この発明は歯科用表面麻酔剤、さ
らに詳しくは塗布した際に歯肉から流れ落ちたり広範囲
に広がったりせず、配合されている着色料により塗布位
置が明瞭にわかる歯科用表面麻酔剤に関するものであ
り、歯科医療の分野で利用される。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a dental surface anesthetic, more specifically, a dental surface whose application position can be clearly seen by a coloring agent that does not run off the gums or spread over a wide area when applied. It relates to anesthetics and is used in the field of dentistry.

【0002】[0002]

【従来の技術】歯科の領域において、抜歯等の前処置と
して局所麻酔剤の注射を実施する際、その注射部位の歯
肉に予め表面麻酔を施すことが行なわれている。この表
面麻酔には、局所麻酔剤であるアミノ安息香酸エチルを
有効成分とし、ポリエチレングリコールを基剤とする無
色または黄色あるいは若干青色に着色されたゲル製剤が
用いられており、このゲル製剤が注射部位に塗布されて
いる。
2. Description of the Related Art In the field of dentistry, when a local anesthetic is injected as a pretreatment for tooth extraction or the like, the gingiva at the injection site is subjected to surface anesthesia in advance. For this surface anesthesia, a colorless or yellow or slightly blue-colored gel preparation based on polyethylene glycol, which is a local anesthetic, ethylaminobenzoate as an active ingredient, is used. It is applied to the part.

【0003】[0003]

【発明が解決しようとする課題】表面麻酔の効果を発現
するには、表面麻酔剤を塗布後5分間程度の時間が必要
であるが、この間歯科医師は他の患者の治療をしたりし
て多忙である。従来の表面麻酔剤は無色であったり、歯
肉と同系統の色(黄色)に着色されていたり、あるいは
青色であっても非常に薄く着色されているために、歯肉
に塗布した際にその塗布部位が不明瞭となり、歯科医師
は表面麻酔剤を塗布していない部位、すなわち表面麻酔
を施していない部位に局所麻酔剤を注射し、患者に痛み
を与えることがあった。そのため、表面麻酔を施した部
位、すなわち局所麻酔剤を注射すべき部位(刺入点)が
分かりやすい歯科用表面麻酔剤の開発が望まれている。
In order to bring out the effect of surface anesthesia, it takes about 5 minutes after applying the surface anesthetic, but during this time, the dentist may treat other patients. I'm busy. Conventional surface anesthetics are colorless, colored in the same system as gingiva (yellow), or very lightly colored even in blue. The site became unclear, and the dentist sometimes gave pain to the patient by injecting a local anesthetic into a site where the surface anesthetic was not applied, that is, a site where the surface anesthetic was not applied. Therefore, there is a demand for the development of a dental surface anesthetic agent in which it is easy to understand the site where the surface anesthesia is applied, that is, the site where the local anesthetic agent should be injected (point of insertion).

【0004】[0004]

【課題を解決するための手段】この発明の発明者は、表
面麻酔剤を調製する際に、基剤として水溶性高分子基剤
を用いて40℃における粘度を300〜1000センチ
ポイズとし、さらに中間色系または寒色系の着色料を
0.01重量%以上配合することによって、この表面麻
酔剤を歯肉に塗布した際に歯肉から表面麻酔剤が流れ落
ちたり広範囲に広がったりせず、しかも配合されている
着色料により塗布部位が明瞭になることを見い出してこ
の発明を完成した。この発明の歯科用表面麻酔剤は、局
所麻酔作用を有する有効成分、水溶性高分子基剤および
中間色系または寒色系の着色料を0.01重量%以上含
有し、40℃において粘度が300〜1000センチポ
イズであることを特徴とする。
Means for Solving the Problems The inventor of the present invention, when preparing a surface anesthetic, uses a water-soluble polymer base as a base to adjust the viscosity at 40 ° C. to 300 to 1000 centipoise, and further By blending 0.01% by weight or more of a systemic or cold colorant, when the surface anesthetic is applied to the gingiva, the surface anesthetic does not run off from the gingiva or spread over a wide range, and it is mixed. The present invention has been completed by finding that the applied portion becomes clear by the coloring agent. The dental surface anesthetic of the present invention contains 0.01% by weight or more of an active ingredient having a local anesthetic effect, a water-soluble polymer base and a neutral or cold colorant, and has a viscosity of 300 to 40 ° C. It is characterized by being 1000 centipoise.

【0005】この発明の歯科用表面麻酔剤に用いられる
有効成分としては、例えばアミノ安息香酸エチル、塩酸
パラブチルアミノ安息香酸ジエチルアミノエチル、リド
カインなどが挙げられ、製剤中に通常5〜30重量%配
合される。
Examples of the active ingredients used in the dental surface anesthetic of the present invention include ethyl aminobenzoate, parabutylaminoaminobenzoic acid diethylaminoethyl, lidocaine and the like, and usually 5 to 30% by weight in the preparation. To be done.

【0006】水溶性高分子基剤としては、製剤の歯肉へ
の塗布のしやすさおよび塗布した際に歯肉から流れ落ち
たり広範囲に広がったりしないために、40℃において
粘度が300〜1000センチポイズ、さらに好ましく
は400〜700センチポイズになるようなものを選択
する必要がある。粘度が300センチポイズ未満では、
歯肉に塗布した際歯肉から流れ落ちたり広範囲に広が
る。また、粘度が1000センチポイズを超えると、歯
肉への付着性が悪くなる。
The water-soluble polymer base has a viscosity of 300 to 1000 centipoise at 40 ° C., because it is easy to apply the preparation to the gingiva and does not run off the gingiva or spread widely when applied. It is necessary to select a material having a pressure of preferably 400 to 700 centipoise. If the viscosity is less than 300 centipoise,
When applied to gingiva, it runs off the gingiva or spreads over a wide area. If the viscosity exceeds 1000 centipoise, the adhesiveness to the gingiva becomes poor.

【0007】このような粘度に調製するための好ましい
水溶性高分子基剤の例としては常温で液状であるポリエ
チレングリコール(例えばポリエチレングリコール40
0)と、常温で固体状であるポリエチレングリコール
(例えばポリエチレングリコール1500、ポリエチレ
ングリコール4000、ポリエチレングリコール600
0、ポリエチレングリコール20000)との混合物
や、ポリエチレングリコール、ポリビニルピロリドン、
ポリビニルアルコール、ヒドロキシプロピルメチルセル
ロース、ヒドロキシエチルセルロース、ヒドロキシプロ
ピルセルロース、カルボキシメチルセルロース、デキス
トリン、ゼラチン、アラビアゴムなどの1種または2種
以上の混合物を溶融し、水と混合したものが挙げられ
る。これらの水溶性高分子基剤は製剤中に通常60〜9
0重量%配合される。
An example of a preferred water-soluble polymer base for adjusting such a viscosity is polyethylene glycol which is liquid at room temperature (for example, polyethylene glycol 40).
0) and polyethylene glycol that is solid at room temperature (for example, polyethylene glycol 1500, polyethylene glycol 4000, polyethylene glycol 600).
0, a mixture of polyethylene glycol 20000), polyethylene glycol, polyvinylpyrrolidone,
Examples include polyvinyl alcohol, hydroxypropylmethyl cellulose, hydroxyethyl cellulose, hydroxypropyl cellulose, carboxymethyl cellulose, dextrin, gelatin, gum arabic and the like, which are melted and mixed with water. These water-soluble polymer bases are usually used in the formulation in the range of 60-9.
0% by weight is compounded.

【0008】着色料としては、歯肉の色と明瞭に区別す
るために、中間色系または寒色系の着色料を添加する必
要があり、好ましい着色料としては、中間色系の着色料
として例えば緑色色素(例えば、緑色3号、緑色201
号、緑色202号、緑色204号、緑色205号な
ど)、銅クロロフィル、銅クロロフィルナトリウム、酸
化チタン、薬用炭などが挙げられ、寒色系の着色料とし
ては、例えば青色色素(例えば青色1号、青色2号、青
色201号、青色202号、青色203号、青色204
号、青色205号など)、紫色201号などが挙げられ
る。これらの着色料はその種類によっても異なるが、塗
布位置を明瞭にするため、製剤中に0.01重量%以
上、好ましくは0.05重量%以上配合する。着色料が
0.01重量%未満では、歯肉の着色が薄く塗布位置が
明瞭にならない。
[0008] As the coloring agent, it is necessary to add an intermediate-colored or cold-colored coloring agent in order to clearly distinguish it from the color of gingiva. As a preferable coloring agent, an intermediate-colored coloring agent such as a green pigment ( For example, Green No. 3, Green 201
No., Green No. 202, Green No. 204, Green No. 205, etc.), copper chlorophyll, sodium copper chlorophyll, titanium oxide, medicinal charcoal, and the like, and examples of cold colorants include blue dyes (for example, Blue No. 1, Blue No. 2, Blue No. 201, Blue No. 202, Blue No. 203, Blue No. 204
No. 205, blue No. 205, etc.), purple No. 201, etc. Although these coloring agents vary depending on their types, 0.01% by weight or more, and preferably 0.05% by weight or more are blended in the preparation in order to clarify the application position. If the amount of the colorant is less than 0.01% by weight, the gingiva will be less colored and the application position will not be clear.

【0009】この発明の歯科用表面麻酔剤には、味と香
りをつけるためにサッカリンナトリウム、サッカリン、
白糖などの甘味料、バナナオイル、チェリーオイル、オ
レンジオイル、バニラエッセッスなどの香料を配合する
ことが好ましく、さらにメチルパラベン、エチルパラベ
ン、プロピルパラベンなどの防腐剤、Tween80な
どの界面活性剤、精製水などを適宜配合してもよい。
The dental surface anesthetic of the present invention contains saccharin sodium, saccharin,
It is preferable to add sweeteners such as sucrose, flavoring agents such as banana oil, cherry oil, orange oil and vanilla essence, and further preservatives such as methylparaben, ethylparaben, propylparaben, surfactants such as Tween80, purified water and the like. You may mix | blend suitably.

【0010】この発明の歯科用表面麻酔剤は、水溶性高
分子基剤を適宜加熱して溶融し、そこに局所麻酔作用を
有する有効成分および適宜精製水に溶解した着色料を混
合撹拌し、さらに必要に応じて上記の甘味料、香料、防
腐剤などを混和撹拌することによって調製できる。この
ようにして得られるこの発明の歯科用表面麻酔剤は、歯
肉に塗布することにより使用に供される。
In the dental surface anesthetic of the present invention, a water-soluble polymer base is appropriately heated and melted, and an active ingredient having a local anesthetic action and a colorant appropriately dissolved in purified water are mixed and stirred therein. Furthermore, it can be prepared by mixing and stirring the above-mentioned sweeteners, flavors, preservatives and the like, if necessary. The dental surface anesthetic of the present invention thus obtained is used by applying it to the gingiva.

【0011】試験例1 粘度測定 サンプル 後記実施例1で得られたこの発明の歯科用表面麻酔剤 使用機器 ・E型粘度計 タイプEM(VISCONIC EM
D,TOKYO SEIKI) 設定条件 ・温度 40℃(恒温水循環方式,2時間以上の安定化
の後使用) ・スリット巾:5.6 試料のサンプリングおよび測定方法 サンプル1.5mlを、気泡をいれない様にしながら注
射筒にとった。次いで試料受器を粘度計から外し、試料
を注射筒から試料受器に試料が平均的になる様、気泡が
混入しない様にゆっくりと移した。試料受器を粘度計に
セットし、20分間以上安定させた後、5.0RPMで
測定した。サンプルの粘度は460センチポイズであっ
た。
Test Example 1 Viscosity measurement sample Dental surface anesthetic agent of the present invention obtained in Example 1 described later Equipment used ・ E type viscometer type EM (VISCONIC EM)
D, TOKYO SEIKI) Setting conditions-Temperature 40 ° C (constant temperature water circulation system, use after stabilization for 2 hours or more) -Slit width: 5.6 Sample sampling and measurement method While taking it, I took it in a syringe. Then, the sample receiver was removed from the viscometer, and the sample was slowly transferred from the injection cylinder to the sample receiver so that the sample was uniform and no bubbles were mixed. The sample receiver was set on a viscometer and allowed to stabilize for 20 minutes or longer, after which it was measured at 5.0 RPM. The viscosity of the sample was 460 centipoise.

【0012】[0012]

【発明の効果】この発明の歯科用表面麻酔剤の効果を調
べるために次の実験を行なった。 試験例2 実験対象は成人ボランティア10名とし、試料塗布部位
は浸潤麻酔施行時の刺入点を想定し、上顎前歯部歯肉頬
移行部の粘膜とした。なお、粘膜への後記実施例1で得
られた製剤の塗布は次の手順で実施した。上口唇を歯科
用ミラーで翻転し、歯肉頬移行部粘膜部位に、綿棒ある
いは歯科用ピンセットを用いて塗布した。その結果、こ
の発明の歯科用表面麻酔剤は、歯肉への接着性が良好で
製剤が流れ落ちたり広範囲に広がったりせず、着色料の
色(青色)が明瞭に見えた。そのため、局所麻酔剤の注
射の際に刺入点が明瞭になる利点があり使いやすい。
The following experiment was conducted to examine the effect of the dental surface anesthetic of the present invention. Test Example 2 Ten adult volunteers were used as test subjects, and the sample application site was the mucosa of the anterior maxillary anterior part, gingiva-cheek transition part, assuming the puncture point when performing infiltration anesthesia. The preparation obtained in Example 1 below was applied to the mucosa by the following procedure. The upper lip was turned over with a dental mirror and applied to the mucous membrane part of the gingiva-cheek transition part using a cotton swab or dental tweezers. As a result, the dental surface anesthetic of the present invention had good adhesiveness to the gingiva, the formulation did not flow down or spread over a wide area, and the color (blue) of the coloring agent was clearly visible. Therefore, there is an advantage that the insertion point becomes clear when the local anesthetic is injected, and it is easy to use.

【0013】[0013]

【実施例】【Example】

実施例1 真空式練合機(みずほ工業製)にポリエチレングリコー
ル4000(64kg)を入れて70℃に加熱して融解
させ、ポリエチレングリコール400(88kg)を均
一に混合し70℃に保つ。70℃に保ったままアミノ安
息香酸エチル(40kg)およびメチルパラベン(0.
4kg)を加えて混合し溶解する。精製水(4.5k
g)に青色1号(0.1kg)およびサッカリンナトリ
ウム(2kg)を加えて室温で撹拌して溶解し、この溶
液をバナナオイル(1kg)とともに上記ポリエチレン
グリコール溶液に加えて均一に混合し、室温まで冷却し
て、100g中に以下の組成を有する歯科用表面麻酔剤
を得る。
Example 1 Polyethylene glycol 4000 (64 kg) was placed in a vacuum kneader (manufactured by Mizuho Industry Co., Ltd.) and heated to 70 ° C. to melt it, and polyethylene glycol 400 (88 kg) was uniformly mixed and kept at 70 ° C. While maintaining at 70 ° C, ethyl aminobenzoate (40 kg) and methylparaben (0.
4 kg) is added and mixed to dissolve. Purified water (4.5k
Blue No. 1 (0.1 kg) and sodium saccharin (2 kg) were added to g) and dissolved by stirring at room temperature, and this solution was added to the above polyethylene glycol solution together with banana oil (1 kg) and uniformly mixed, and the mixture was allowed to reach room temperature. Upon cooling, 100 g of dental surface anesthetic having the following composition is obtained.

【表1】 [Table 1]

Claims (4)

【特許請求の範囲】[Claims] 【請求項1】 局所麻酔作用を有する有効成分、水溶性
高分子基剤および中間色系または寒色系の着色料を0.
01重量%以上含有し、40℃において粘度が300〜
1000センチポイズであることを特徴とする歯科用表
面麻酔剤。
1. An active ingredient having a local anesthetic effect, a water-soluble polymer base, and a neutral or cold colorant are added in an amount of 0.
Contains at least 01% by weight and has a viscosity of 300 to 40 ° C.
A dental surface anesthetic, which is 1000 centipoise.
【請求項2】 有効成分がアミノ安息香酸エチルである
請求項1に記載の歯科用表面麻酔剤。
2. The dental surface anesthetic according to claim 1, wherein the active ingredient is ethyl aminobenzoate.
【請求項3】 着色料が青色色素である請求項2に記載
の歯科用表面麻酔剤。
3. The dental surface anesthetic according to claim 2, wherein the colorant is a blue pigment.
【請求項4】 水溶性高分子基剤が常温で液状および固
体状のポリエチレングリコールを混合したものである請
求項2または3に記載の歯科用表面麻酔剤。
4. The dental surface anesthetic according to claim 2, wherein the water-soluble polymer base is a mixture of liquid and solid polyethylene glycol at room temperature.
JP5303016A 1993-12-02 1993-12-02 Dental surface anesthetic Withdrawn JPH07157427A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5303016A JPH07157427A (en) 1993-12-02 1993-12-02 Dental surface anesthetic

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5303016A JPH07157427A (en) 1993-12-02 1993-12-02 Dental surface anesthetic

Publications (1)

Publication Number Publication Date
JPH07157427A true JPH07157427A (en) 1995-06-20

Family

ID=17915927

Family Applications (1)

Application Number Title Priority Date Filing Date
JP5303016A Withdrawn JPH07157427A (en) 1993-12-02 1993-12-02 Dental surface anesthetic

Country Status (1)

Country Link
JP (1) JPH07157427A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2006096913A1 (en) 2005-03-15 2006-09-21 Animal Ethics Pty Ltd A topical anaesthetic composition

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2006096913A1 (en) 2005-03-15 2006-09-21 Animal Ethics Pty Ltd A topical anaesthetic composition
US8822416B2 (en) 2005-03-15 2014-09-02 Animal Ethics Pty Ltd. Topical analgesic composition
US8960128B2 (en) 2005-03-15 2015-02-24 Animal Ethics Pty Ltd Topical anesthetic composition
US9592318B2 (en) 2005-03-15 2017-03-14 Animal Ethics Pty Ltd Topical analgesic composition

Similar Documents

Publication Publication Date Title
US6031007A (en) Pharmaceutical composition with anaesthetic effect
JPH0820527A (en) In-keratin-reserving type antimycotic composition for external use
JP2004517092A5 (en)
EP0608361A1 (en) Root canal filling material and adhesive composition
JPS6185305A (en) Root canal filler
WO2006070578A1 (en) Band seal for hard capsule
HU196706B (en) Process for producing aqueous dispersion suitable for preparing plaster
KR101659896B1 (en) Peel-off type eyebrow coloring composition and the manufacturing method thereof
JP3908275B2 (en) Cold seat
JPH092925A (en) Two agent-mixing type cosmetic
DK164770B (en) Neutral Topical Sodium Fluoride Gel
EP1553915B1 (en) Dental masking product for teeth and gum
JPH07157427A (en) Dental surface anesthetic
JPS63201119A (en) Plaster composition
JPS63130541A (en) Antimicrobial composition
JPS58185514A (en) Novel antiphlogistic and analgesic gel cream for local application
WO2019066583A1 (en) Fluorine coating agent having enhanced dental tubule permeability and coating endurance and method for preparing same
JP3916194B2 (en) Acid hair dye composition
JPH0369323B2 (en)
KR100214714B1 (en) A novel gel composition used for local anesthetic
JP2004043431A (en) Hair dyeing agent
US20070184410A1 (en) Method of preparing dentition for the taking of a dental impression
CA2570346C (en) Method of preparing dentition for dental impression
AU2005293842A1 (en) Self-adhesive dental floss
Bingham et al. The use of anaesthetic EMLA cream in minor otological surgery

Legal Events

Date Code Title Description
A300 Application deemed to be withdrawn because no request for examination was validly filed

Free format text: JAPANESE INTERMEDIATE CODE: A300

Effective date: 20010206