JP3050413B2 - Patch for treating skin diseases - Google Patents
Patch for treating skin diseasesInfo
- Publication number
- JP3050413B2 JP3050413B2 JP3020012A JP2001291A JP3050413B2 JP 3050413 B2 JP3050413 B2 JP 3050413B2 JP 3020012 A JP3020012 A JP 3020012A JP 2001291 A JP2001291 A JP 2001291A JP 3050413 B2 JP3050413 B2 JP 3050413B2
- Authority
- JP
- Japan
- Prior art keywords
- ointment
- patch
- support
- separation layer
- treating
- 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.)
- Expired - Lifetime
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- Medicinal Preparation (AREA)
Description
【0001】[0001]
【産業上の利用分野】本発明は、患者の苦痛を和らげ、
施療の効率を高める皮膚疾患治療用の貼付剤に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relieves patient pain,
The present invention relates to a patch for treating skin diseases which improves the efficiency of treatment.
【0002】[0002]
【従来の技術】軟膏は外用医薬として種々用いられてい
るが、軟膏含有の皮膚疾患治療用貼付剤は未だ開発され
ていない。2. Description of the Related Art Ointments have been variously used as external medicines, but no ointment-containing patches for treating skin diseases have been developed yet.
【0003】[0003]
【発明が解決しようとする課題】軟膏は患部に塗布する
場合、指が患部に触れると患者が痛みを訴えるため、使
用しづらい欠点があるほか、患部面が広い場合は軟膏を
全面に均一塗布するのに時間がかかる不便もある。更
に、軟膏は塗布した後、塗布面をガーゼ、脱脂綿、油紙
等で覆って衣服への付着を防ぐ必要があり、施療者にと
っては手間がかかるという不満もあった。そのため、予
め軟膏を塗布した貼付剤の開発が望まれていた。When the ointment is applied to the affected area, the patient complains of pain when the finger touches the affected area, so there is a drawback that it is difficult to use. In addition, when the affected area is wide, the ointment is applied evenly over the entire surface. There is also inconvenience that it takes time to do. Furthermore, after the ointment is applied, it is necessary to cover the applied surface with gauze, absorbent cotton, oil paper, or the like to prevent the ointment from adhering to clothes, and there is also a complaint that the practitioner takes time and effort. Therefore, development of a patch to which an ointment has been applied in advance has been desired.
【0004】そこで、先ず従来のパップ剤のように、不
織布等の支持体に軟膏を塗布し、ポリエチレン、ポリプ
ロピレン等のプラスチックフィルム(保護ライナー)で
軟膏面を保護した貼付剤の作製を試みたが、剥離時、軟
膏が保護ライナーへ付着したまま、支持体と軟膏のあい
だに剥離がみられる問題のあることがわかった。この問
題を解決するため種々検討したところ、軟膏と保護ライ
ナーのあいだに、支持体よりも軟らかく、又は伸びやす
い性質のシート状の層(本発明では分離層という)を介
在させればよいことを見出し、本発明を完成した。[0004] Therefore, first, an ointment was applied to a support such as a non-woven fabric, and a patch was prepared by protecting the ointment surface with a plastic film (protective liner) such as polyethylene or polypropylene, like a conventional cataplasm. At the time of peeling, it was found that there was a problem that peeling was observed between the support and the ointment while the ointment remained attached to the protective liner. Various investigations have been made to solve this problem. As a result, it was found that a sheet-like layer (hereinafter, referred to as a separation layer in the present invention) having a property of being softer or more easily stretchable than the support may be interposed between the ointment and the protective liner. Heading, the present invention has been completed.
【0005】[0005]
【課題を解決するための手段】すなわち、本発明は図1
に示すように、支持体1、軟膏の層2、分離層3及び保
護ライナー4を順次積層した構造の皮膚疾患治療用貼付
剤である。本発明で用いる支持体は患部面への均一な密
着性を第一に考慮して、綿、セルロース、スフ、化学繊
維等の織布又は不織布や軟質塩化ビニル、ポリエチレ
ン、ポリウレタン等の発泡体シート等が適当である。特
に、通気性を兼ね備えた綿、スフ、セルロース等からな
る織布あるいは不織布が良い。これらの材質は更に、人
体への密着性をよくするため、伸縮性とドレープ性をも
たせることもできる。That is, the present invention relates to FIG.
As shown in Fig. 1, a patch for treating a skin disease has a structure in which a support 1, an ointment layer 2, a separation layer 3, and a protective liner 4 are sequentially laminated. The support used in the present invention is made of a woven or non-woven fabric such as cotton, cellulose, staple fiber, chemical fiber, or a non-woven fabric, soft vinyl chloride, polyethylene, polyurethane, or the like in consideration of uniform adhesion to the affected surface. Etc. are appropriate. In particular, a woven or non-woven fabric made of cotton, staple, cellulose or the like having air permeability is preferable. These materials can also have elasticity and drape to improve the adhesion to the human body.
【0006】本発明で用いる分離層は、上記の支持体よ
りも軟らかく、又は伸びやすい物理的性状をもつことが
必要である。しかし、その化学的性状は支持体と同じで
あっても、あるいは異なるものでもよい。これらの分離
層としては、例えば、綿、セルロース、スフ、化学繊維
等の織布又は不織布や軟質塩化ビニル、ポリエチレン、
ポリウレタン等の発泡体シート等が用いられる。分離層
が支持体よりも軟らかく、又は伸びやすい性質をもって
いるものであるか否かは、下記の方法で両者の剛軟度、
伸び率(30%モジュラス)又は空隙率を測定し、比較
することによって知ることができる。The separation layer used in the present invention needs to have physical properties that are softer or easier to expand than the above-mentioned support. However, its chemical nature may be the same as or different from that of the support. As these separation layers, for example, woven or non-woven fabric such as cotton, cellulose, staple fiber, chemical fiber, soft vinyl chloride, polyethylene,
A foam sheet such as polyurethane is used. Whether the separation layer is softer than the support or has a property of being easily stretched is determined by the following method.
It can be known by measuring the elongation (30% modulus) or the porosity and comparing them.
【0007】剛軟度、伸び率(30%モジュラス)及び
空隙率の測定方法は以下のとおり。剛軟度の測定:幅2
cm、長さ15cmの試験片を、45゜の斜面をもつカ
ンチレバ形試験装置の水平台上にのせ、試験片の短辺を
スケールの基線に合わせたのち、斜面の方向に試験片を
ゆるやかに滑らせ、試験片の一端(中央部)が斜面に接
したときの試験片の押し出された長さを求める。伸び率
(30%モジュラス)の測定:幅5cm、長さ20cm
の試験片を、JIS L1068織物の引張り試験方法
に準じ、つかみ間隔10cm、引張り速度30±2cm
/minで引張り、試験片が30%伸びたときの荷重を
求める。空隙率の測定:試料の紋様が鮮明に写るように
適当な色の台紙上に置いて、拡大コピーする。次いで、
これにトレーシング用のグラフ用紙を重ね、空隙部分の
面積を実測する。上記の測定方法から明らかなように、
剛軟度及び伸び率(30%モジュラス)の値は小さいほ
ど、また空隙率は大きいほど軟らかく、伸びやすいと言
える。[0007] The methods for measuring the softness, elongation (30% modulus) and porosity are as follows. Measurement of bending resistance: width 2
cm and a 15 cm length of the test piece are placed on a horizontal stand of a 45 ° cantilever type test device, and the short side of the test piece is adjusted to the base line of the scale. Then, the test piece is gently moved in the direction of the slope. Slide and determine the extruded length of the test piece when one end (center) of the test piece contacts the slope. Measurement of elongation (30% modulus): width 5 cm, length 20 cm
Specimens of the above, according to JIS L1068 woven fabric tensile test method, gripping interval 10cm, pulling speed 30 ± 2cm
/ Min, and the load when the test piece is elongated by 30% is determined. Measurement of porosity: Place the sample on a mount of an appropriate color so that the pattern of the sample can be clearly seen, and make an enlarged copy. Then
Graph paper for tracing is superimposed on this, and the area of the void is measured. As is clear from the above measurement method,
It can be said that the smaller the value of the bending resistance and the elongation percentage (30% modulus) and the higher the porosity, the softer and more easily the elongation.
【0008】分離層として、支持体よりも軟らかく、伸
びやすい材料を用いることにより、貼付剤から保護ライ
ナーを剥離する時、支持体と軟膏の界面で剥離が起こら
ず、保護ライナーに分離層が付着したまま、軟膏と分離
層の界面で剥離が起こるのである。分離層を保護するた
めの保護ライナーとしては、ポリエチレン、ポリプロピ
レン、ポリ塩化ビニル、ポリエステル等のプラスチック
フィルム、それらをエンボス加工したもの等を用いるこ
とができる。By using a material that is softer and more stretchable than the support as the separation layer, when the protective liner is peeled off from the patch, the separation does not occur at the interface between the support and the ointment, and the separation layer adheres to the protective liner. As it is, peeling occurs at the interface between the ointment and the separation layer. As a protective liner for protecting the separation layer, a plastic film of polyethylene, polypropylene, polyvinyl chloride, polyester, or the like, or an embossed plastic film thereof can be used.
【0009】軟膏は慣用の方法、例えば日本薬局方製剤
総則軟膏剤の項に準じて調製された油脂性軟膏、乳剤性
軟膏又は水溶性軟膏を用いることができる。例えば、基
剤、一部の乳化剤及び安定剤を加温して融解し、混和
し、約75℃に保ち、これに水溶性の安定剤及び乳化剤
を水で溶かし、約75℃に加温したものを添加し、かき
混ぜ、適当な温度に冷却し、主薬(有効成分)を加え、
かき混ぜ全質均等化した軟膏(医薬用バルク)である。As the ointment, an oil-based ointment, an emulsion-based ointment or a water-soluble ointment prepared according to a conventional method, for example, according to the general ointment of the Japanese Pharmacopoeia, can be used. For example, the base, some emulsifiers and stabilizers were heated and melted, mixed and kept at about 75 ° C, and the water-soluble stabilizers and emulsifiers were dissolved in water and heated to about 75 ° C. Add the ingredients, stir, cool to an appropriate temperature, add the active ingredient (active ingredient),
It is an ointment (pharmaceutical bulk) that has been stirred and homogenized.
【0010】主薬(有効成分)として用いられるものは
特に限定されないが、試験したところではリゾチームが
好ましい。プラスミン、ブロメライン、上皮細胞生長因
子(EGF)、カリクレイン等のタンパク質性薬物も用
いられる。また、その他の例として、スルフィゾミジ
ン、スルファジアジン等のサルファ剤、カナマイシン、
エリスロマイシン、クロラムフェニコール、ゲンタマイ
シン等の抗生物質、ハイドロコーチゾン、デキサメタゾ
ン、フルオシノニド等の副じん皮質ホルモン、ジフェン
ヒドラミン、インドメタシン等の消炎鎮痛剤、トコフェ
ロール等のビタミン剤等も挙げられる。Although what is used as the main drug (active ingredient) is not particularly limited, lysozyme is preferred in the tests. Proteinaceous drugs such as plasmin, bromelain, epidermal growth factor (EGF), and kallikrein are also used. Further, as other examples, sulfisomidines, sulfa drugs such as sulfadiazine, kanamycin,
Antibiotics such as erythromycin, chloramphenicol, and gentamicin; corticosteroids such as hydrocortisone, dexamethasone, and fluocinonide; anti-inflammatory analgesics such as diphenhydramine and indomethacin; and vitamins such as tocopherol are also included.
【0011】支持体への軟膏の展延、塗布は、室温又は
室温以下の温度で、通常のドクターナイフ法、Tダイ
法、ロールコート法などにより行えばよい。軟膏の塗布
厚さは0.5〜5mmが適当であるが、治療効果を十分
に発揮させるには、1mm以上にするのが好ましい。ま
た、人体への適用時の作業性を考慮して、貼付剤の辺縁
2〜4mmは軟膏を塗布しない状態に保持してもよい。
支持体として空隙率の大きいシートを用いる場合、その
シートの開口部から軟膏が浸みだすことがあるので、こ
の防止のため支持体の外側を更に布、不織布、紙等で覆
ってもよい。貼付剤の大きさは特に制限されないが、種
々の大きさの用途に応じられるよう、A6〜A3版の大
きさとするのが好ましい。これら貼付剤は、アルミ接着
フィルム等でつくられた密封容器中に封じて使用時まで
保管される。The spreading and coating of the ointment on the support may be carried out at room temperature or at a temperature lower than room temperature by a usual doctor knife method, T-die method, roll coating method or the like. The coating thickness of the ointment is suitably 0.5 to 5 mm, but is preferably 1 mm or more in order to sufficiently exert the therapeutic effect. In addition, in consideration of workability at the time of application to the human body, the margin of the patch from 2 to 4 mm may be kept in a state where the ointment is not applied.
When a sheet having a large porosity is used as the support, the ointment may seep out from the opening of the sheet. To prevent this, the outside of the support may be further covered with cloth, nonwoven fabric, paper or the like. The size of the patch is not particularly limited, but is preferably A6 to A3 size so that it can be used for various sizes. These patches are sealed in a sealed container made of an aluminum adhesive film or the like and stored until use.
【0012】[0012]
【実施例】実施例により、本発明を更に具体的に説明す
る。 実施例1 支持体として、1平方m当り100gの重さで、剛軟度
が200mm、伸び率が0.1kgの不織布、分離層と
して1平方m当り30gの重さで、剛軟度が50mm、
伸び率が0.1kgの不織布を用いた。支持体上に25
℃で1昼夜保管したリゾチーム軟膏(リフラップ軟膏、
日立化成製)をナイフドクターを用いて14cmの幅で
1.5mmの厚さに展延し、その上に分離層を積層し、
更に分離層の上にポリエステルフィルム(25μm)を
積層した。軟膏塗布部の片側に1.5cmの耳部を設
け、10cmの長さに裁断し、軟膏部分の大きさが10
×14cm、支持体、分離層及び保護ライナーの大きさ
が10×15.5cmの皮膚疾患治療用貼付剤を作製し
た。このものの剥離時のフェーシング(分離層+保護ラ
イナー)への軟膏付着率は5%と良好であった。EXAMPLES The present invention will be described more specifically with reference to examples. Example 1 A nonwoven fabric having a rigidity of 200 mm and an elongation percentage of 0.1 kg as a support at a weight of 100 g per 1 m2 and a rigidity of 50 mm at a weight of 30 g per 1 m2 as a separation layer. ,
A nonwoven fabric having an elongation of 0.1 kg was used. 25 on support
Lysozyme ointment (reflap ointment,
Hitachi Chemical) was spread using a knife doctor to a width of 14 cm and a thickness of 1.5 mm, and a separation layer was laminated thereon,
Further, a polyester film (25 μm) was laminated on the separation layer. An ear portion of 1.5 cm was provided on one side of the ointment application portion, and cut into a length of 10 cm.
A patch for treating a skin disease having a size of × 14 cm and a size of the support, the separation layer and the protective liner of 10 × 15.5 cm was prepared. The ointment adhesion rate to the facing (separation layer + protective liner) at the time of peeling was as good as 5%.
【0013】実施例2 支持体として、剛軟度が20mm、伸び率が 0.5k
gのポリエチレンネットを用い、分離層として、剛軟度
が10mm、伸び率が0.01kgの不織布を用いた。
支持体上に、25℃で1昼夜保管したリフラップ軟膏を
2本ロールを用いて3mmの厚さに展延し、その上に分
離層を積層し、更に分離層の上に25μmのポリエチレ
ンフィルムを積層した。この時、支持体開口部から軟膏
がにじみ出るのを防ぐため、支持体側に更に1平方m当
り100gの重さの不織布を積層した。支持体側の不織
布は、使用時、取り除くことなくそのままカバー材とす
ることが可能である。これを実施例1と同様に裁断し、
皮膚疾患治療用貼付剤を作製した。このものの剥離時の
フェーシングへの軟膏付着率は1%と良好であった。Example 2 The support had a bending resistance of 20 mm and an elongation of 0.5 k.
g of polyethylene net, and a nonwoven fabric having a stiffness of 10 mm and an elongation of 0.01 kg was used as a separation layer.
On a support, reflap ointment stored at 25 ° C. for one day and night was spread to a thickness of 3 mm using two rolls, a separation layer was laminated thereon, and a 25 μm polyethylene film was further placed on the separation layer. Laminated. At this time, in order to prevent the ointment from oozing from the opening of the support, a nonwoven fabric weighing 100 g per square meter was further laminated on the support. At the time of use, the nonwoven fabric on the support side can be used as a cover material without being removed. This was cut in the same manner as in Example 1,
A patch for treating skin diseases was prepared. The ointment adherence rate to the facing at the time of peeling was as good as 1%.
【0014】実施例3 支持体として、剛軟度20mm、伸び率2.0kgのガ
ーゼ、分離層として、剛軟度20mm、伸び率0.1k
gの不織布を用いたほかは、実施例2と同様に操作し、
皮膚疾患治療用貼付剤を作製した。このものの剥離時の
フェーシングへの軟膏付着率は3%と良好であった。Example 3 A gauze having a stiffness of 20 mm and an elongation of 2.0 kg was used as a support, and a stiffness of 20 mm and an elongation of 0.1 k were used as a separation layer.
g in the same manner as in Example 2 except that
A patch for treating skin diseases was prepared. The ointment adhesion rate to the facing at the time of peeling was as good as 3%.
【0015】実施例4 支持体として、空隙率20%のポリエチレンネット、分
離層として、空隙率50%のポリエチレンネット(剛軟
度20mm、伸び率0.5kgは両者とも同じ)を用い
たほかは、実施例2と同様に操作し、皮膚疾患治療用貼
付剤を作製した。このものの剥離時のフェーシングへの
軟膏付着率は3%と良好であった。Example 4 A polyethylene net having a porosity of 20% was used as a support, and a polyethylene net having a porosity of 50% (a rigidity of 20 mm and an elongation of 0.5 kg were the same in both cases). In the same manner as in Example 2, a patch for treating skin diseases was prepared. The ointment adhesion rate to the facing at the time of peeling was as good as 3%.
【0016】比較例 支持体として、1平方m当り100gの重さ、剛軟度2
0mm、伸び率0.1kg、空隙率30%の不織布を用
い、分離層として、上記支持体に用いたものと同じ不織
布を用いたほかは、実施例1と同様に操作した。このも
のの剥離時のフェーシングへの軟膏付着率は40%と高
かった。COMPARATIVE EXAMPLE As a support, a weight of 100 g per square meter and a softness of 2
The same operation as in Example 1 was performed except that a nonwoven fabric having a thickness of 0 mm, an elongation of 0.1 kg, and a porosity of 30% was used, and the same nonwoven fabric as that used for the support was used as a separation layer. The ointment adhesion rate to the facing at the time of peeling was as high as 40%.
【0017】[0017]
【発明の効果】軟膏の投与量は貼付剤の大きさにより容
易かつ確実に定まるので、患部の大きさなどに応じ、所
定の大きさの貼付剤を選んで貼付すれば良い。そのため
本発明は、患者の苦痛を和らげ、施療の効率を高める効
果がある。The dose of the ointment is easily and reliably determined by the size of the patch, so that a patch having a predetermined size may be selected and applied according to the size of the affected part. Therefore, the present invention has the effect of relieving the patient's pain and increasing the efficiency of treatment.
【図1】本発明における皮膚疾患治療用貼付剤の一例を
示す断面図である。FIG. 1 is a cross-sectional view showing an example of a patch for treating a skin disease in the present invention.
1:支持体 2:軟膏の層 3:分離層 4:保護ライナー 1: Support 2: Ointment layer 3: Separation layer 4: Protective liner
───────────────────────────────────────────────────── フロントページの続き (72)発明者 大字 祥仁 香川県大川郡大内町三本松567番地 帝 國製薬株式会社内 (72)発明者 石原 学 香川県大川郡大内町三本松567番地 帝 國製薬株式会社内 (58)調査した分野(Int.Cl.7,DB名) A61K 9/70 305 ──────────────────────────────────────────────────続 き Continuing on the front page (72) Inventor: Shoji Oji-machi, Okawa-gun, Ogawa-gun, Kagawa Prefecture Incorporated (58) Field surveyed (Int.Cl. 7 , DB name) A61K 9/70 305
Claims (4)
かく、または伸びやすい物理的性状を有する分離層、更
に保護ライナーを順次積層してなる皮膚疾患治療用貼付
剤。1. A patch for treating a skin disease, comprising a support, a layer of an ointment, a separating layer having physical properties softer or more stretchable than the support, and a protective liner sequentially laminated thereon.
布、不織布又は紙で覆われている請求項1記載の皮膚疾
患治療用貼付剤。2. The surface of the support opposite to the surface in contact with the ointment,
The patch for treating a skin disease according to claim 1, which is covered with a cloth, a nonwoven fabric, or paper.
に記載の皮膚疾患治療用貼付剤。3. The separation layer according to claim 1, wherein the separation layer is in the form of a sheet.
The patch for treatment of a skin disease according to item 1.
項1〜3のいずれかに記載の皮膚疾患治療用貼付剤。4. The patch for treating skin diseases according to claim 1, wherein the active ingredient of the ointment is lysozyme.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3020012A JP3050413B2 (en) | 1991-02-13 | 1991-02-13 | Patch for treating skin diseases |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3020012A JP3050413B2 (en) | 1991-02-13 | 1991-02-13 | Patch for treating skin diseases |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH04257516A JPH04257516A (en) | 1992-09-11 |
| JP3050413B2 true JP3050413B2 (en) | 2000-06-12 |
Family
ID=12015203
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP3020012A Expired - Lifetime JP3050413B2 (en) | 1991-02-13 | 1991-02-13 | Patch for treating skin diseases |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP3050413B2 (en) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2843957B2 (en) * | 1993-08-04 | 1999-01-06 | マルホ株式会社 | Ointment patch |
| JP4584381B2 (en) * | 1999-07-30 | 2010-11-17 | 久光製薬株式会社 | Felbinac-containing patch |
| CN1188116C (en) | 2000-06-06 | 2005-02-09 | 帝人株式会社 | Membr for application of ointment and ointment patch employing the same |
| WO2017219334A1 (en) * | 2016-06-23 | 2017-12-28 | 彭鹏 | Dressing |
-
1991
- 1991-02-13 JP JP3020012A patent/JP3050413B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPH04257516A (en) | 1992-09-11 |
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