JPS605159A - Production of medical band - Google Patents

Production of medical band

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Publication number
JPS605159A
JPS605159A JP58114035A JP11403583A JPS605159A JP S605159 A JPS605159 A JP S605159A JP 58114035 A JP58114035 A JP 58114035A JP 11403583 A JP11403583 A JP 11403583A JP S605159 A JPS605159 A JP S605159A
Authority
JP
Japan
Prior art keywords
water
film
polymer substance
powder
soluble polymer
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
Application number
JP58114035A
Other languages
Japanese (ja)
Inventor
柳橋 憲夫
小野 富士夫
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.)
Lion Corp
Original Assignee
Lion Corp
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 Lion Corp filed Critical Lion Corp
Priority to JP58114035A priority Critical patent/JPS605159A/en
Publication of JPS605159A publication Critical patent/JPS605159A/en
Pending legal-status Critical Current

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Abstract

(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。
(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 本発明は、高分子物質を主体としてなり、+5’lえぼ
口腔内、轟腔内等の体腔内の患部にこの体腔内の粘液の
作用で貼着して使用Jる医療用バンドの製造方法に関し
、更に詳述すると患部にり・1ηる(;J着力が強く、
患部に長時間付着し、しかも柔軟で使用性に優れ、患部
に対して強い刺激を!jえることのない医療用バンドの
製造方法に1Iliする。
DETAILED DESCRIPTION OF THE INVENTION The present invention is mainly composed of a polymeric substance, and is used by being attached to an affected area in a body cavity such as the inside of the oral cavity or the inside of the cavity by the action of mucus in the body cavity. Regarding the manufacturing method of the Jru medical band, in more detail, it will stick to the affected area.
It sticks to the affected area for a long time, is flexible and easy to use, and provides strong stimulation to the affected area! This is a timeless method for manufacturing medical bands.

従来より、口腔内、0腔内等の1本腔内の患部に粘液の
作用でイ」着さ「、止血剤ヤ)薬剤の基祠簀として使用
される医療用基材として、ゼラ1−ン、メチルセルロ−
ス カルボキシメチルセルローフナ1〜リウム等の水溶性高
分子物質をスポンジ上の膜に形成したもの、ポリアクリ
ル酸塩、ヒドロキシプロピルセルロース等の水溶性高分
子物質を錠剤に形成したものなどが知られている。これ
らの医療旦材は、水溶性高分子物質の溶液を凍結乾燥し
たり、粉末を打錠する等の方法で製造されるものである
が、従来のものは種々の問題点を有している。即ち、前
者のスポンジ状基材は、柔軟で、しかも素早く患部に付
着するため、使用性には優れているが、付着力が弱く、
付着時間も短かいという欠点を有し、又後右の錠剤状の
基材は、付着力が強く、付着時間も長いが、錠剤である
ために硬く、患部に初期の刺激を与えるおそれがあり、
しかも使用する部位に応じて大きさ、形状を変えること
が不可能であると共に、歯肉部等の湾曲した部位には適
用しにくいなど、使用性の面で欠点があり、アフタのよ
うな小さな疾患にしか使用できないものであった。
Conventionally, Zera 1-1 has been used as a medical substrate used as a base for drugs that adhere to affected areas within the oral cavity, the intracavity, etc. due to the action of mucus. Methyl cellulose
Some known tablets include water-soluble polymeric substances such as carboxymethylcellulose sodium chloride formed into a film on a sponge, and tablets formed from water-soluble polymeric substances such as polyacrylate and hydroxypropyl cellulose. ing. These medical materials are manufactured by freeze-drying a solution of a water-soluble polymer substance or compressing a powder into tablets, but conventional materials have various problems. . That is, the former sponge-like base material is flexible and quickly adheres to the affected area, so it is easy to use, but the adhesive strength is weak.
It has the disadvantage that the adhesion time is short, and the tablet-shaped base material on the back right has strong adhesion and a long adhesion time, but because it is a tablet, it is hard and may cause initial irritation to the affected area. ,
Moreover, it has disadvantages in terms of usability, such as the fact that it is impossible to change the size and shape depending on the area where it is used, and it is difficult to apply it to curved areas such as the gingival area. It could only be used by

本発明者らは、上記事情に鑑み、付着力が強く、付着時
間が長く、しかも柔軟で使用性に優れたバンド状の医療
用基材を得るために種々検討を行なった結果、ヒドロキ
シプロピルセルロース、ポリビニルピロリドン等の造膜
性高分子物質をエタノール等の有機溶媒に溶解し、この
溶液にポリアクリル酸す1〜リウム、メチルセルロース
、カルボキシメチルセルロースナトリウム等の前記有機
溶媒に不溶で、かつ水に溶解もしくは水でゲル化して粘
着性を示す水溶性高分子物質の粉末を分散混合し、この
水溶性高分子物質の粉末が分散した造膜性高分子物質の
溶液を台上等に適宜厚さに展延して造膜し、これを乾燥
することにより、上記目的が効果的に達成され、口腔用
薬品基材、口腔用絆ぷj膏、鼻腔用薬品基材、膣腔用薬
品基材、止血剤等として好適に使用し得る医療用バンド
を製造できることを知見し、本発明をなすに至ったもの
である。
In view of the above circumstances, the present inventors conducted various studies in order to obtain a band-shaped medical base material that has strong adhesion, long adhesion time, flexibility, and excellent usability, and found that hydroxypropyl cellulose , dissolve a film-forming polymeric substance such as polyvinylpyrrolidone in an organic solvent such as ethanol, and add to this solution a substance that is insoluble in the organic solvent and soluble in water, such as sodium to lithium polyacrylate, methylcellulose, sodium carboxymethylcellulose, etc. Alternatively, a powder of a water-soluble polymer substance that becomes sticky when gelled with water is dispersed and mixed, and a solution of a film-forming polymer substance in which the powder of the water-soluble polymer substance is dispersed is spread on a table to an appropriate thickness. By spreading and forming a film and drying it, the above objectives are effectively achieved, and the above-mentioned purpose is effectively achieved, and the drug base material for the oral cavity, the adhesive plaster for the oral cavity, the drug base material for the nasal cavity, the drug base material for the vaginal cavity, The inventors have discovered that it is possible to produce a medical band that can be suitably used as a hemostatic agent, etc., and have arrived at the present invention.

以下、本発明につき詳しく説明する。The present invention will be explained in detail below.

本発明に係る医療用バンドの製造方法は、右(幾溶媒に
造膜性高分子物質を溶解してなる溶液に前記有機溶媒に
不溶でかつ水に溶解もしくは水でゲル化して粘着性を示
す水溶性高分子物質の粉末を分散混合し、次いでこの水
溶性高分子物質の粉末が分散した造膜性高分子物質の溶
液を所定厚さに造膜し、これを乾燥して造膜性高分子物
質のシート中に水溶性高分子物質の粉末が分散した医療
用バンドを得ることを特徴とするものである。
The method for manufacturing a medical band according to the present invention is as follows. A powder of a water-soluble polymer substance is dispersed and mixed, and then a solution of a film-forming polymer substance in which the powder of a water-soluble polymer substance is dispersed is formed into a film to a predetermined thickness, and this is dried to form a film-forming polymer substance. The present invention is characterized in that a medical band is obtained in which powder of a water-soluble polymer substance is dispersed in a sheet of a molecular substance.

この場合、上記造膜性高分子物質としては、有(幾溶媒
に溶解してこれを乾燥させた場合に造膜性を示す高分子
物質であればいずれのものでも使用し得るが、特に親水
性のもの、水溶性のものを使用することが好ましく、こ
れによりバンドの患部に対づる付着性をより高めること
ができる。
In this case, the film-forming polymeric substance may be any polymeric substance that exhibits film-forming properties when dissolved in a solvent and dried; however, it is particularly hydrophilic. It is preferable to use a water-soluble material or a water-soluble material, which can further improve the adhesion of the band to the affected area.

また、上記水溶性高分子物質の粉末としては、水に溶解
もしくは水でゲル化して粘着性を示づ高分子物質の粉末
であればいずれのものでも使用し得るが、特に粘着性の
強いものが好ましい。
Furthermore, as the water-soluble polymer substance powder, any polymer substance powder can be used as long as it dissolves in water or gels with water and exhibits stickiness, but particularly those with strong stickiness can be used. is preferred.

なJ3、上記造膜性高分子物質及び水溶性高分子物質ど
しては天然高分子物質、半合成高分子物質、合成高分子
物質の別を問わず用いることができ、両者に共通して使
用し得る水溶性の高分子物質を例示すると、天然高分子
物質としてはアラビアガム、トラガントガム、ローカス
トビーンズガム、グアーガム、寒天、カラゲナン、アル
ギン酸ナトリウム、デキストリン、デキストン、ゼラチ
ン、アミロース等、半合成高分子物質としてはカルボキ
シメチルセルロースナトリウム、メチルセルロース、ヒ
ドロキシ化されたアルキルセルロースエーテル等、合成
高分子物質としては親水性ポリビニル化合物、例えばポ
リビニルビ[lリドン、ビニルピロリドンとアクリル酸
のエステル、ポリビニルアルコール、部分的に加水分解
されたポリビニルアセテート又はスチレン、酢酸ビニル
と共重合体し得る甲量体例えばアクリル酸、メタクリル
酸、クロトン酸、又はそれらのエステルとのバ小含体、
酢酸アリル、メチルビニルエーテルとマレイン酸無水物
との共重合体、ポリビニルスルiJ\ン酸、ポリイタコ
ン酸、ポリビニルカルボキシアミド例えばポリアクリル
アミド、スチレンとマレイン酸無水物との共重合体、エ
チレンと7レイン酸無水物との共重合体、アクリルアミ
ドとアクリル酸との共重合体、高分子電解質例えばアル
ギン酸、アルギン酸塩等を使用し得る。
J3, the above-mentioned film-forming polymeric substances and water-soluble polymeric substances can be used regardless of whether they are natural polymeric substances, semi-synthetic polymeric substances, or synthetic polymeric substances; Examples of water-soluble polymer substances that can be used include semi-synthetic polymers such as gum arabic, gum tragacanth, locust bean gum, guar gum, agar, carrageenan, sodium alginate, dextrin, dextone, gelatin, and amylose. Substances include sodium carboxymethylcellulose, methylcellulose, hydroxylated alkylcellulose ethers, etc. Synthetic polymeric substances include hydrophilic polyvinyl compounds such as polyvinylvinylidene, esters of vinylpyrrolidone and acrylic acid, polyvinyl alcohol, partially hydrated Decomposed polyvinyl acetate or styrene, polymers copolymerizable with vinyl acetate, such as acrylic acid, methacrylic acid, crotonic acid, or esters thereof;
Allyl acetate, copolymer of methyl vinyl ether and maleic anhydride, polyvinyl sulfuric acid, polyitaconic acid, polyvinyl carboxamide such as polyacrylamide, copolymer of styrene and maleic anhydride, ethylene and 7-leic acid Copolymers with anhydrides, copolymers of acrylamide and acrylic acid, polyelectrolytes such as alginic acid, alginates, etc. may be used.

これらの中で、上記造膜性高分子物質としては半合成高
分子物質、合成高分子物質が好ましく、特にヒドロキシ
プロピルセルロース、ポリビニルピロリドンが好適に使
用し得る。また、上記水溶性高分子物質の粉末としては
ポリアクリル酸、ポリアクリル声ナトリウム等のポリア
クリル酸の塩、メチルセルロース、カルボキシメチルセ
ルロースナトリウム専の粘着性の強いものの粉末が好適
に使用し得る。なJ′3、これら高分子物質は単独で用
いても良く、2種以」二を混合して用いても良い。
Among these, semi-synthetic polymeric substances and synthetic polymeric substances are preferable as the film-forming polymeric substance, and hydroxypropylcellulose and polyvinylpyrrolidone can be particularly preferably used. Further, as the powder of the water-soluble polymer substance, powders of strongly adhesive substances such as polyacrylic acid, salts of polyacrylic acid such as sodium polyacrylic acid, methyl cellulose, and sodium carboxymethyl cellulose can be suitably used. J'3, these polymeric substances may be used alone or in combination of two or more.

本発明においては、上記造膜性高分子物質を有機溶媒に
溶解した溶液を調製するものであるが、この場合使用す
る有機溶媒に溶解する造膜性高分子物質を適宜選択して
用いるものである。なお、有機溶媒としてはエタノール
、アセ1ヘン等の適宜なものを用いることができる。ま
た、上記溶液は造膜性高分子物質が有機溶媒の1〜30
%(重量%、以下同じンとなるように調製することが作
業性等の点から好ましい。
In the present invention, a solution is prepared by dissolving the film-forming polymeric substance in an organic solvent, but in this case, a film-forming polymeric substance that dissolves in the organic solvent used may be appropriately selected and used. be. Incidentally, as the organic solvent, an appropriate one such as ethanol, acetylene, etc. can be used. In addition, in the above solution, the film-forming polymer substance is 1 to 30% of the organic solvent.
% (weight %, hereinafter the same) is preferable from the viewpoint of workability and the like.

本発明にJ3い−Cは、上記有機溶媒に溶解しない水溶
性高分子物質の粉末を適宜選択し、この水溶性高分子物
質の粉末を上記溶液に分散混合し、この分散液を台上等
の適宜な基台上に所定厚さに展延して造膜し、この茄膜
物を乾燥して造膜性高分子物質のシー1〜中に水溶性高
分子物質の粉末が分散した医療用バンドを得るものであ
る。この場合、造IIIする厚さは医療用バンドの用途
等により異なり、特に制限はないが、通常乾燥時のバン
ドの厚さが0.5〜3m+n4’1度となるように展延
することが好ましい。また、乾燥方法としては自然乾燥
、低温乾燥、減圧乾燥等の適宜な方法を採用し得る。
In J3-C of the present invention, a powder of a water-soluble polymer substance that does not dissolve in the organic solvent is appropriately selected, the powder of the water-soluble polymer substance is dispersed and mixed in the above solution, and the dispersion is placed on a bench or the like. A film is formed by spreading it to a predetermined thickness on an appropriate base, and this film is dried to form a medical product in which powder of a water-soluble polymeric substance is dispersed in a sheet of film-forming polymeric substance. This is what you get for your band. In this case, the thickness to be formed varies depending on the purpose of the medical band and is not particularly limited, but it is usually spread so that the thickness of the band when dried is 0.5 to 3 m + n4'1 degree. preferable. Further, as a drying method, an appropriate method such as natural drying, low temperature drying, reduced pressure drying, etc. can be adopted.

なa3、本発明においては、J−記造膜性凸分子物質の
溶液中或いは上記水溶性高分子物質のわ)米中に必要に
応じて有効成分、界面活性剤等の他の成分を配合しても
差支えない。
a3. In the present invention, other ingredients such as active ingredients and surfactants are blended as necessary in the solution of the J-described film-forming convex molecular substance or in the rice of the water-soluble polymer substance described above. I don't mind if you do that.

而して、本発明に係る医療用バンドの製造方法は、有機
溶媒に造膜性高分子物質を溶解してなる溶液に前記有機
溶媒に不溶でかつ水に溶解もしくは水でゲル化して粘着
性を示す水溶性高分子物質の粉末を分散混合し、次いで
この水溶性高分子物質の粉末が分散した造膜性高分子物
質の溶液を所定厚さに造膜し、これを乾燥して造膜性高
分子物質のシート中に水溶高分子物質の粉末が分散した
医療用バンドを得るよう構成したことにより、本発明製
造方法によれば付着力が強く、付着時間も長く、しかも
柔軟−で患部に対して刺激を与えることがなく、かつ使
用に際して任意の大きさ、形状に形成することができて
体腔内のどの部位にでも適用することができ、種々の用
途に好適に使用し1gる@療用バンドを製造することが
できるものである。
Accordingly, the method for manufacturing a medical band according to the present invention involves adding a film-forming polymer substance to a solution obtained by dissolving a film-forming polymer substance in an organic solvent, which is insoluble in the organic solvent, and dissolved in water or gelled with water to make it sticky. A powder of a water-soluble polymer substance exhibiting the above is dispersed and mixed, and then a solution of a film-forming polymer substance in which the powder of the water-soluble polymer substance is dispersed is formed into a film to a predetermined thickness, and this is dried to form a film. By constructing a medical band in which powder of a water-soluble polymeric substance is dispersed in a sheet of a water-soluble polymeric substance, the manufacturing method of the present invention has strong adhesion, a long adhesion time, and is flexible enough to easily adhere to the affected area. It does not cause any irritation to the skin, can be formed into any size and shape when used, and can be applied to any part of the body cavity, making it suitable for a variety of applications. It is possible to manufacture medical bands.

以下実施例を示し、本発明を具体的に説明する。EXAMPLES The present invention will be specifically explained below with reference to Examples.

なお、%はすべて重量%を示ず。Note that all percentages do not indicate weight percent.

〔実施例1〕 合 計 100.0% 上記材料のうちAを混合し、これをエタノールにヒドロ
キシプロピルセルロース(造膜性高分子物質)がエタノ
ールの20%となるように溶解して造膜性溶液を得た。
[Example 1] Total 100.0% Among the above materials, A was mixed and dissolved in ethanol so that hydroxypropyl cellulose (film-forming polymeric substance) was 20% of the ethanol to obtain film-forming property. A solution was obtained.

次に、この造膜性溶液にBを混合したちのく水溶性高分
子物質の粉末)を加え、撹拌して粉末を分散し、この分
散液を台上に厚さ1關に展延して造膜し、これを乾燥し
て医療。
Next, a powder of a water-soluble polymer substance mixed with B) was added to this film-forming solution, stirred to disperse the powder, and the dispersion was spread to a thickness of 1 inch on a table. to form a film and dry it for medical treatment.

用バンドを得た。I got a band for it.

次に、上記実施例1の医療用バンドを用いて下記の実験
を行なった。
Next, the following experiment was conducted using the medical band of Example 1 above.

裏−−1 実施例1で[311した医療用バンドの片面に1デルセ
ルロース溶液をスプレーコーティングしてエチルセルロ
ースの被膜を形成した。次にパネル5名を用い、上記医
療用バンドのエチルセルロース被膜を形成していない面
を各パネルの下記表に示す口腔内置部位に貼着し、バン
ドがはがれるまでの付着時間を測定した。結果を表に示
す。なお、バンドはそれぞれ 1010X10Tの大きさのものを用いた。また、各パ
ネルには貼着してから3時間後から4時間後の間に食事
を取らせるようにした。
Back side--1 One side of the medical band prepared in Example 1 was spray coated with a 1delcellulose solution to form an ethyl cellulose film. Next, using five panelists, the side of the medical band on which the ethyl cellulose coating was not formed was adhered to each panel at the intraoral placement site shown in the table below, and the adhesion time until the band was peeled off was measured. The results are shown in the table. Note that each band used had a size of 1010×10T. Furthermore, the subjects were asked to eat a meal between 3 and 4 hours after each panel was pasted.

表 表の結果より、本発明方法により得られた医療用バンド
は、3〜6.5時間という長い付着時間を右することが
認められた。
From the results shown in the table, it was confirmed that the medical band obtained by the method of the present invention has a long attachment time of 3 to 6.5 hours.

(実施例2) 合 計 ioo、o% 上記材料のうらAを混合し、これをエタノールにヒドロ
キシプロピルセルロース(造膜性高分子物質)がエタノ
ールの5%となるように溶解して造膜性溶液を得た。次
に、この造膜性溶液に8を混合したもの(水溶性高分子
物質の粉末)を加え、撹拌して粉末を分散し、この分散
液を台上に厚さ0.7鴫に展延して造膜し、これを乾燥
して医療用バンドを得た。
(Example 2) Total ioo, o% The back A of the above materials was mixed, and this was dissolved in ethanol so that hydroxypropyl cellulose (film-forming polymeric substance) was 5% of the ethanol to determine film-forming property. A solution was obtained. Next, a mixture of 8 (powder of a water-soluble polymer substance) is added to this film-forming solution, stirred to disperse the powder, and the dispersion is spread on a table to a thickness of 0.7 mm. A film was formed, and this was dried to obtain a medical band.

〔実施例3〕 ←(PEG−400) 合 計 ioo、o% 上記材料のうちAを混合し、これをエタノールにポリビ
ニルピロリドン(造膜性高分子物質)がエタノールの1
0%となるように溶解して造膜性溶液を得た。次に、こ
の造膜性溶液に88混合したちのく水溶性高分子物質の
粉末ンを加え、撹拌して粉末を分散し、この分散液を台
−Fに厚さ1關に展延して造膜し、これを減圧乾燥して
医療用バンドを得た。
[Example 3] ←(PEG-400) Total ioo, o% Among the above materials, A was mixed, and polyvinylpyrrolidone (film-forming polymeric substance) was mixed with ethanol in an amount of 1% of the ethanol.
A film-forming solution was obtained by dissolving the solution to a concentration of 0%. Next, 88% of mixed Chinoku water-soluble polymer material powder was added to this film-forming solution, stirred to disperse the powder, and the dispersion was spread to a thickness of 1 inch on table F. This was dried under reduced pressure to obtain a medical band.

なお、上記実施例2.3の@療用バンドを用いて実施例
1の場合と同様の実験を行なったところ、やはり長い付
着時間を有するものであった。
When the same experiment as in Example 1 was conducted using the medical band of Example 2.3, it was found that the band also had a long attachment time.

出願人 ラ イ オ ン 株式会社 代理人 弁理士 小 島 隆 司Applicant: Laion Co., Ltd. Agent: Patent Attorney Takashi Kojima

Claims (1)

【特許請求の範囲】 1、有機溶媒に造膜性高分子物質を溶解してなる溶液に
前記有機溶媒に不溶でかつ水に溶解もしくは水でゲル化
して粘着性を示す水溶性高分子物V(の粉末を分散混合
し、次いでこの水溶性高分子物質の粉末が分散した造膜
性高分子物質の溶液を所定厚さに造n桑し、これを乾燥
して造膜性高分子物質のシート中に水溶性高分子物質の
粉末が分散した医療用バンドを得ることを特徴どする医
療用バンドの製造方法。 2、造膜性高分子物デ1がヒドロキシプロピルセルロー
ス及びポリビニルピロリドンから選ばれるものである特
ム′1請求の「む間第1項記載の製造方法。 3、水で溶解もしくは水でゲル化して粘着性を示す水溶
性高分子物質がポリアクリル酸、ポルアクリル酸の塩、
メチルセルロース及びカルボキシメチルセルロースナト
リウムから選ばれるものである特許請求の範囲第1項又
は第2項記載の’!<j jjff方法。
[Scope of Claims] 1. A water-soluble polymer V which is insoluble in the organic solvent and exhibits stickiness when dissolved in water or gelled with water in a solution prepared by dissolving a film-forming polymeric substance in an organic solvent. The powder of the water-soluble polymer substance is dispersed and mixed, and then a solution of the film-forming polymer substance in which the water-soluble polymer substance powder is dispersed is formed to a predetermined thickness, and this is dried to form a film-forming polymer substance. A method for manufacturing a medical band, characterized by obtaining a medical band in which a powder of a water-soluble polymer substance is dispersed in a sheet. 2. Film-forming polymer substance 1 is selected from hydroxypropylcellulose and polyvinylpyrrolidone. 3. The water-soluble polymer substance that exhibits adhesive properties when dissolved or gelled in water is a salt of polyacrylic acid or polyacrylic acid. ,
'! according to claim 1 or 2, which is selected from methylcellulose and sodium carboxymethylcellulose. <j jjff method.
JP58114035A 1983-06-24 1983-06-24 Production of medical band Pending JPS605159A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58114035A JPS605159A (en) 1983-06-24 1983-06-24 Production of medical band

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58114035A JPS605159A (en) 1983-06-24 1983-06-24 Production of medical band

Publications (1)

Publication Number Publication Date
JPS605159A true JPS605159A (en) 1985-01-11

Family

ID=14627395

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58114035A Pending JPS605159A (en) 1983-06-24 1983-06-24 Production of medical band

Country Status (1)

Country Link
JP (1) JPS605159A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0250187A2 (en) * 1986-06-16 1987-12-23 JOHNSON &amp; JOHNSON CONSUMER PRODUCTS, INC. Bioadhesive extruded film for intra-oral drug delivery and process
WO1998055079A3 (en) * 1997-06-06 1999-03-04 Procter & Gamble A delivery system for an oral care substance using a strip of material having low flexural stiffness
WO1999056724A3 (en) * 1998-05-02 2000-02-17 Lohmann Therapie Syst Lts Therapeutic system for applying at least one care or active agent topically or transmucosally, on or through the nasal mucosa, and method for using the system
US9554976B2 (en) 2002-09-11 2017-01-31 The Procter & Gamble Company Tooth whitening product
US10285915B2 (en) 2012-10-17 2019-05-14 The Procter & Gamble Company Strip for the delivery of an oral care active and methods for applying oral care actives

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0250187A2 (en) * 1986-06-16 1987-12-23 JOHNSON &amp; JOHNSON CONSUMER PRODUCTS, INC. Bioadhesive extruded film for intra-oral drug delivery and process
WO1998055079A3 (en) * 1997-06-06 1999-03-04 Procter & Gamble A delivery system for an oral care substance using a strip of material having low flexural stiffness
WO1999056724A3 (en) * 1998-05-02 2000-02-17 Lohmann Therapie Syst Lts Therapeutic system for applying at least one care or active agent topically or transmucosally, on or through the nasal mucosa, and method for using the system
US9554976B2 (en) 2002-09-11 2017-01-31 The Procter & Gamble Company Tooth whitening product
US10493016B2 (en) 2002-09-11 2019-12-03 The Procter & Gamble Company Tooth whitening product
US10285915B2 (en) 2012-10-17 2019-05-14 The Procter & Gamble Company Strip for the delivery of an oral care active and methods for applying oral care actives
US10285916B2 (en) 2012-10-17 2019-05-14 The Procter & Gamble Company Strip for the delivery of an oral care active and methods for applying oral care actives

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