JPH04257516A - Plaster for treatment of dermatosis - Google Patents

Plaster for treatment of dermatosis

Info

Publication number
JPH04257516A
JPH04257516A JP2001291A JP2001291A JPH04257516A JP H04257516 A JPH04257516 A JP H04257516A JP 2001291 A JP2001291 A JP 2001291A JP 2001291 A JP2001291 A JP 2001291A JP H04257516 A JPH04257516 A JP H04257516A
Authority
JP
Japan
Prior art keywords
ointment
support
separation layer
plaster
substrate
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP2001291A
Other languages
Japanese (ja)
Other versions
JP3050413B2 (en
Inventor
Hitoshi Higuchi
樋口 仁
Masaaki Kobi
向尾 正昭
Yoshihito Ooaza
大字 祥仁
Manabu Ishihara
学 石原
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.)
Teikoku Seiyaku Co Ltd
Resonac Corp
Original Assignee
Teikoku Seiyaku Co Ltd
Hitachi Chemical 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 Teikoku Seiyaku Co Ltd, Hitachi Chemical Co Ltd filed Critical Teikoku Seiyaku Co Ltd
Priority to JP3020012A priority Critical patent/JP3050413B2/en
Publication of JPH04257516A publication Critical patent/JPH04257516A/en
Application granted granted Critical
Publication of JP3050413B2 publication Critical patent/JP3050413B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Abstract

PURPOSE:To provide a plaster for the treatment of dermatosis, having uniformly coated ointment and free from the adhesion of the ointment to a protection liner in the peeling of the liner to ensure easy application to the skin. CONSTITUTION:An ointment is uniformly applied to a substrate such as woven fabric or nonwoven fabric. The coated layer is successively laminated with a sheet layer (separation layer) having softness or extensibility higher than those of the substrate and with a protection liner such as a plastic film to obtain the objective plaster. The outside of the substrate may be covered with cloth, paper, etc., to prevent the extrusion of the ointment from a side of the substrate. The plaster is stored until use in the form sealed in an air-tight container made of aluminum adhesive film, etc.

Description

【発明の詳細な説明】[Detailed description of the invention]

【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。
[Industrial Application Field] The present invention alleviates patient pain,
This invention relates to a patch for treating skin diseases that increases 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。
BACKGROUND OF THE INVENTION Ointments are used in various ways as external medicines, but a patch containing an ointment for treating skin diseases has not yet been developed.

【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。
[Problems to be solved by the invention] When applying ointment to the affected area, the patient complains of pain when touching the affected area with a finger, so it is difficult to use, and if the affected area is large, it is difficult to apply the ointment evenly over the entire surface. There is also the inconvenience that it takes time to do so. Furthermore, after applying the ointment, it is necessary to cover the applied surface with gauze, absorbent cotton, oiled paper, etc. to prevent it from adhering to clothing, which has caused complaints that it is time-consuming for the practitioner. Therefore, it has been desired to develop a patch to which an ointment is applied in advance.

【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] First, an attempt was made to create a patch in which ointment was applied to a support such as non-woven fabric, and the ointment surface was protected with a plastic film (protective liner) made of polyethylene, polypropylene, etc., as in conventional poultices. It was found that there was a problem in which, when peeled off, the ointment remained attached to the protective liner and peeling occurred between the support and the ointment. After conducting various studies to solve this problem, we found that it is sufficient to interpose a sheet-like layer (referred to as a separation layer in the present invention) that is softer or more stretchable than the support between the ointment and the protective liner. 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。
[Means for Solving the Problems] That is, the present invention
As shown in FIG. 1, this patch for treating skin diseases has a structure in which a support 1, an ointment layer 2, a separation layer 3, and a protective liner 4 are laminated in this order. The support used in the present invention is a woven fabric or non-woven fabric made of cotton, cellulose, staple fiber, chemical fiber, etc., or a foam sheet made of soft vinyl chloride, polyethylene, polyurethane, etc., with the primary consideration of uniform adhesion to the affected area. etc. are appropriate. In particular, woven or non-woven fabrics made of breathable cotton, cotton, cellulose, etc. are preferred. These materials can also be made to have stretchability and drapability in order to improve their 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。
[0006] The separation layer used in the present invention needs to have physical properties that are softer or easier to stretch than the above-mentioned support. However, its chemical properties may be the same as the support or different. These separation layers include, for example, woven or non-woven fabrics such as cotton, cellulose, staple fiber, and chemical fibers, soft vinyl chloride, polyethylene,
A foam sheet made of polyurethane or the like is used. Whether or not the separation layer is softer or more stretchable than the support can be determined by determining the bending resistance,
This can be determined by measuring and comparing the elongation rate (30% modulus) or porosity.

【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±2c
m/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。
The methods for measuring bending resistance, elongation (30% modulus) and porosity are as follows. Measuring bending resistance: Width 2
A test piece with a length of 15 cm and a length of 15 cm was placed on the horizontal table of a cantilever type test device with a 45° slope, and after aligning the short side of the test piece with the base line of the scale, the test piece was gently moved in the direction of the slope. Determine the length of the specimen pushed out when one end (center) of the specimen touches the slope. Measurement of elongation rate (30% modulus): width 5 cm, length 20 cm
A test piece was prepared according to the JIS L1068 textile tensile test method, with a grip interval of 10 cm and a tensile speed of 30 ± 2 c.
The test piece is pulled at m/min and the load is determined when the test piece is elongated by 30%. 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. Next, graph paper for tracing was placed on top of this, and the area of the gap was actually measured. As is clear from the above measurement method, it can be said that the smaller the values of bending resistance and elongation rate (30% modulus) and the larger the porosity, the softer and easier it is to stretch.

【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, peeling does not occur at the interface between the support and the ointment, and the separation layer adheres to the protective liner. Peeling occurs at the interface between the ointment and the separation layer. As the protective liner for protecting the separation layer, plastic films such as polyethylene, polypropylene, polyvinyl chloride, polyester, etc., and embossed films 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。
[0009] The ointment can be used in a conventional manner, for example, an oil-based ointment, an emulsion ointment, or a water-soluble ointment prepared according to the Japanese Pharmacopoeia, General Preparations section, Ointments. For example, a base, some emulsifiers and stabilizers are heated, melted, mixed and kept at about 75°C, and water-soluble stabilizers and emulsifiers are dissolved in water and heated to about 75°C. It is an ointment (medicinal bulk) in which the ingredients are added, stirred, cooled to an appropriate temperature, the main drug (active ingredient) is added, and the quality is equalized by stirring.

【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。
[0010] Although there are no particular restrictions on what is used as the main drug (active ingredient), lysozyme is preferred according to tests. Protein drugs such as plasmin, bromelain, epidermal growth factor (EGF), and kallikrein are also used. Other examples include sulfa drugs such as sulfizomidine and sulfadiazine, antibiotics such as kanamycin, erythromycin, chloramphenicol, and gentamicin, corticosteroids such as hydrocortisone, dexamethasone, and fluocinonide, and anti-inflammatory analgesics such as diphenhydramine and indomethacin. , vitamin preparations such as tocopherol, and the like.

【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。
[0011] The ointment may be spread and coated onto the support at room temperature or below by a conventional 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 in order to fully exhibit its therapeutic effect, it is preferably 1 mm or more. In addition, in consideration of workability when applying to the human body, the edges of the patch
~4 mm may be kept without ointment. When a sheet with a large porosity is used as a support, the ointment may seep out from the openings of the sheet, so to prevent this, the outside of the support may be further covered with cloth, nonwoven fabric, paper, etc. Although the size of the patch is not particularly limited, it is preferably A6 to A3 size so that it can be used in various sizes. These patches are stored in sealed containers made of aluminum adhesive film or the like until they are used.

【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。
[Example] The present invention will be explained in more detail with reference to Examples. Example 1 A nonwoven fabric with a weight of 100 g per square meter, a bending resistance of 200 mm, and an elongation rate of 0.1 kg is used as a support, and a separation layer is a nonwoven fabric with a weight of 30 g per square meter and a bending resistance of 50 mm. ,
A nonwoven fabric with an elongation rate of 0.1 kg was used. 25 on the support
Lysozyme ointment (Reflap ointment,
(manufactured by Hitachi Chemical) was spread to a width of 14 cm and a thickness of 1.5 mm using a knife doctor, and a separation layer was laminated on top of it.
Furthermore, a polyester film (25 μm) was laminated on the separation layer. Place a 1.5cm ear on one side of the ointment application area, cut it into a 10cm length, and make sure the size of the ointment area is 10x.
A skin disease treatment patch with a size of 14 cm and a support, separation layer and protective liner of 10 x 15.5 cm was prepared. The adhesion rate of the ointment 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  0.5
kg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 A support material with bending resistance of 20 mm and elongation rate of 0.5
A nonwoven fabric having a bending resistance of 10 mm and an elongation rate of 0.01 kg was used as a separation layer. A refrap ointment that had been stored for one day at 25°C was spread on a support 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 top of the separation layer. Laminated. At this time, in order to prevent the ointment from seeping out from the opening of the support, a nonwoven fabric weighing 100 g per square meter was further laminated on the support side. The nonwoven fabric on the support side can be used as a cover material without being removed during use. This was cut in the same manner as in Example 1,
We created a patch for treating skin diseases. The adhesion rate of ointment to the facing when this product was peeled off 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 As a support, gauze with a bending resistance of 20 mm and an elongation rate of 2.0 kg was used, and as a separation layer, a gauze with a bending resistance of 20 mm and an elongation rate of 0.1k was used.
The procedure was carried out in the same manner as in Example 2, except that the nonwoven fabric of g was used.
We created a patch for treating skin diseases. The ointment adhesion rate to the facing when this product was peeled off 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 with a porosity of 20% was used as the support, and a polyethylene net with a porosity of 50% was used as the separation layer (bending resistance of 20 mm and elongation rate of 0.5 kg were the same for both). The same procedure as in Example 2 was carried out to prepare a patch for treating skin diseases. The ointment adhesion rate to the facing when this product was peeled off 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。
[0016] As a comparative example support, the weight was 100 g per square meter, and the bending resistance was 2.
The same procedure as in Example 1 was carried out except that a nonwoven fabric having a length of 0 mm, an elongation rate 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 the separation layer. The rate of ointment adhesion to the facing when this product was peeled off 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。
[Effects of the Invention] Since the dosage of ointment can be easily and reliably determined by the size of the patch, it is sufficient to select and apply a patch of a predetermined size depending on the size of the affected area. Therefore, the present invention has the effect of alleviating patient pain and increasing the efficiency of treatment.

【図面の簡単な説明】[Brief explanation of the drawing]

【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 sectional view showing an example of a skin disease treatment patch according to the present invention.

【符号の説明】[Explanation of symbols]

1:支持体 2:軟膏の層 3:分離層 4:保護ライナー 1: Support 2: Layer of ointment 3: Separation layer 4: Protective liner

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】支持体上に軟膏の層、分離層及び保護ライ
ナーを順次積層してなる皮膚疾患治療用貼付剤。
Claims: 1. A patch for treating skin diseases, comprising a support, a layer of ointment, a separation layer and a protective liner laminated in sequence.
【請求項2】分離層が支持体よりも軟らかく、又は伸び
やすいシート状のものである請求項1記載の貼付剤。
2. The adhesive patch according to claim 1, wherein the separation layer is in the form of a sheet that is softer or more stretchable than the support.
【請求項3】軟膏の有効成分がリゾチームである請求項
1又は請求項2記載の貼付剤。
3. The patch according to claim 1 or 2, wherein the active ingredient of the ointment is lysozyme.
JP3020012A 1991-02-13 1991-02-13 Patch for treating skin diseases Expired - Lifetime JP3050413B2 (en)

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 true JPH04257516A (en) 1992-09-11
JP3050413B2 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)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0797315A (en) * 1993-08-04 1995-04-11 Maruho Kk Ointment pasting agent
JP2001039864A (en) * 1999-07-30 2001-02-13 Hisamitsu Pharmaceut Co Inc Felbinac-containing plaster
US7074421B2 (en) 2000-06-06 2006-07-11 Teijin Limited Member for application of ointment and ointment patch employing the same
WO2017219334A1 (en) * 2016-06-23 2017-12-28 彭鹏 Dressing

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0797315A (en) * 1993-08-04 1995-04-11 Maruho Kk Ointment pasting agent
JP2001039864A (en) * 1999-07-30 2001-02-13 Hisamitsu Pharmaceut Co Inc Felbinac-containing plaster
JP4584381B2 (en) * 1999-07-30 2010-11-17 久光製薬株式会社 Felbinac-containing patch
US7074421B2 (en) 2000-06-06 2006-07-11 Teijin Limited Member for application of ointment and ointment patch employing the same
WO2017219334A1 (en) * 2016-06-23 2017-12-28 彭鹏 Dressing

Also Published As

Publication number Publication date
JP3050413B2 (en) 2000-06-12

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