JPS6311942Y2 - - Google Patents
Info
- Publication number
- JPS6311942Y2 JPS6311942Y2 JP18503183U JP18503183U JPS6311942Y2 JP S6311942 Y2 JPS6311942 Y2 JP S6311942Y2 JP 18503183 U JP18503183 U JP 18503183U JP 18503183 U JP18503183 U JP 18503183U JP S6311942 Y2 JPS6311942 Y2 JP S6311942Y2
- Authority
- JP
- Japan
- Prior art keywords
- water
- film
- small particles
- bandage
- mucosal
- 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
Links
- 239000002245 particle Substances 0.000 claims description 43
- 239000000126 substance Substances 0.000 claims description 16
- 230000001070 adhesive effect Effects 0.000 claims description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 10
- 229920003169 water-soluble polymer Polymers 0.000 claims description 9
- 210000004400 mucous membrane Anatomy 0.000 claims description 7
- 239000000843 powder Substances 0.000 description 11
- 239000003814 drug Substances 0.000 description 7
- 239000000853 adhesive Substances 0.000 description 6
- 229940079593 drug Drugs 0.000 description 6
- 230000028327 secretion Effects 0.000 description 5
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 4
- 239000004372 Polyvinyl alcohol Substances 0.000 description 4
- 229920002125 Sokalan® Polymers 0.000 description 4
- 238000004090 dissolution Methods 0.000 description 4
- 229920002451 polyvinyl alcohol Polymers 0.000 description 4
- 229920002153 Hydroxypropyl cellulose Polymers 0.000 description 3
- 206010052428 Wound Diseases 0.000 description 3
- 208000027418 Wounds and injury Diseases 0.000 description 3
- 239000001863 hydroxypropyl cellulose Substances 0.000 description 3
- 235000010977 hydroxypropyl cellulose Nutrition 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 210000000214 mouth Anatomy 0.000 description 3
- 239000002985 plastic film Substances 0.000 description 3
- 229920006255 plastic film Polymers 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 206010061218 Inflammation Diseases 0.000 description 2
- 229920002472 Starch Polymers 0.000 description 2
- DPXJVFZANSGRMM-UHFFFAOYSA-N acetic acid;2,3,4,5,6-pentahydroxyhexanal;sodium Chemical compound [Na].CC(O)=O.OCC(O)C(O)C(O)C(O)C=O DPXJVFZANSGRMM-UHFFFAOYSA-N 0.000 description 2
- 239000001768 carboxy methyl cellulose Substances 0.000 description 2
- 238000009792 diffusion process Methods 0.000 description 2
- 239000000499 gel Substances 0.000 description 2
- 235000011187 glycerol Nutrition 0.000 description 2
- 230000004054 inflammatory process Effects 0.000 description 2
- 230000003993 interaction Effects 0.000 description 2
- 230000007774 longterm Effects 0.000 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
- 229920001495 poly(sodium acrylate) polymer Polymers 0.000 description 2
- 239000011148 porous material Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 2
- 229920001027 sodium carboxymethylcellulose Polymers 0.000 description 2
- NNMHYFLPFNGQFZ-UHFFFAOYSA-M sodium polyacrylate Chemical compound [Na+].[O-]C(=O)C=C NNMHYFLPFNGQFZ-UHFFFAOYSA-M 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 239000008107 starch Substances 0.000 description 2
- 235000019698 starch Nutrition 0.000 description 2
- LNAZSHAWQACDHT-XIYTZBAFSA-N (2r,3r,4s,5r,6s)-4,5-dimethoxy-2-(methoxymethyl)-3-[(2s,3r,4s,5r,6r)-3,4,5-trimethoxy-6-(methoxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6r)-4,5,6-trimethoxy-2-(methoxymethyl)oxan-3-yl]oxyoxane Chemical compound CO[C@@H]1[C@@H](OC)[C@H](OC)[C@@H](COC)O[C@H]1O[C@H]1[C@H](OC)[C@@H](OC)[C@H](O[C@H]2[C@@H]([C@@H](OC)[C@H](OC)O[C@@H]2COC)OC)O[C@@H]1COC LNAZSHAWQACDHT-XIYTZBAFSA-N 0.000 description 1
- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 description 1
- 229920002126 Acrylic acid copolymer Polymers 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 239000001856 Ethyl cellulose Substances 0.000 description 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
- 229920000084 Gum arabic Polymers 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 241000978776 Senegalia senegal Species 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 235000010489 acacia gum Nutrition 0.000 description 1
- 239000000205 acacia gum Substances 0.000 description 1
- WPKYZIPODULRBM-UHFFFAOYSA-N azane;prop-2-enoic acid Chemical compound N.OC(=O)C=C WPKYZIPODULRBM-UHFFFAOYSA-N 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 210000005178 buccal mucosa Anatomy 0.000 description 1
- 125000002057 carboxymethyl group Chemical group [H]OC(=O)C([H])([H])[*] 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 230000001010 compromised effect Effects 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 229920000591 gum Polymers 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 230000007794 irritation Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 210000002200 mouth mucosa Anatomy 0.000 description 1
- 210000003928 nasal cavity Anatomy 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- 239000012466 permeate Substances 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920006267 polyester film Polymers 0.000 description 1
- -1 polyethylene Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 210000003296 saliva Anatomy 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 235000010413 sodium alginate Nutrition 0.000 description 1
- 239000000661 sodium alginate Substances 0.000 description 1
- 229940005550 sodium alginate Drugs 0.000 description 1
- 238000009827 uniform distribution Methods 0.000 description 1
Landscapes
- Materials For Medical Uses (AREA)
- Medicinal Preparation (AREA)
Description
【考案の詳細な説明】
この考案は粘膜包帯に係り、口腔内、鼻孔内等
の体腔内の粘膜面に体腔内の分泌液の作用で付着
せしめて使用する粘膜包帯の構造に関するもので
ある。[Detailed Description of the Invention] This invention relates to a mucosal bandage, and relates to the structure of a mucosal bandage that is used by being attached to the mucosal surface of a body cavity such as the oral cavity or nasal cavity by the action of secretions within the body cavity.
口腔内、鼻孔内等の体腔内粘膜面は一般に軟ら
かく運動性が高い。 Mucosal surfaces in body cavities such as the oral cavity and nasal passages are generally soft and highly motile.
また常に唾液等の分泌液で湿潤されているた
め、その表面は絶えず洗われている状態にある。 Also, since it is constantly moistened with secretions such as saliva, its surface is constantly being washed.
このため、体腔内粘膜面への薬物の持続的な投
与や粘膜に生じた創傷や炎症の被覆保護は非常に
困難である。 For this reason, it is extremely difficult to continuously administer drugs to the mucosal surfaces of body cavities and to protect wounds and inflammation caused in the mucous membranes.
近時、口腔等の粘膜面での薬物の滞留性および
薬理効果を高めることを目的とした製剤が考案さ
れ、使用されている(特開昭54−41320号、特開
昭57−58615号、特公昭56−25210号、特公昭56−
27491号)。 Recently, preparations aimed at increasing drug retention and pharmacological effects on mucosal surfaces such as the oral cavity have been devised and used (Japanese Patent Application Laid-Open No. 54-41320, JP-A No. 57-58615, Special Publication No. 56-25210, Special Publication No. 56-
No. 27491).
これらの製剤は、その中に薬剤を含有したもの
であつて、水溶性高分子物質が水に溶解あるいは
膨潤した際に、接着性を示すことを利用したもの
がほとんどである。 These preparations contain a drug therein, and most take advantage of the fact that water-soluble polymeric substances exhibit adhesive properties when dissolved or swollen in water.
しかして創傷や炎症を被覆保護したり、任意の
薬物を粘膜面に固定することを目的とした粘膜包
帯については、あまり検討されておらず、実用化
されているものもないというのが現状である。 However, mucosal bandages for the purpose of covering and protecting wounds and inflammation, or for fixing arbitrary drugs on mucosal surfaces, have not been studied much, and currently there are none that have been put to practical use. be.
というのは、体腔内粘膜面に用いる粘膜包帯に
は、湿潤面への長時間にわたる接着性ばかりでな
く、複雑な形状を有し、かつ運動性の高い面に十
分に密着する柔軟性と被覆保護に十分な強靭性が
必要であるが、これらの性質をあわせ持つことが
困難なためであると考えられる。 This is because mucosal bandages used for mucosal surfaces in body cavities not only have the ability to adhere to wet surfaces for a long time, but also have flexibility and coverage that allow them to adhere well to surfaces with complex shapes and high mobility. This is thought to be because sufficient toughness is required for protection, but it is difficult to have both of these properties.
この考案は上記したような条件を満たした実用
的効果の大なる粘膜包帯を提供することを目的と
するものである。 The purpose of this invention is to provide a mucosal bandage that satisfies the above-mentioned conditions and has great practical effects.
即ち、この考案は湿潤粘膜に付着して、該粘膜
を被覆する粘膜包帯であつて、水に溶解あるいは
膨潤して接着性を示す水溶性高分子物質の空気を
含有する多数の小粒が柔軟かつ強靭なフイルム表
面または内部互いに接することなくそれぞれに独
立して存在することを特徴とする粘膜包帯に関す
るものである。 That is, this device is a mucosal bandage that adheres to and covers a moist mucous membrane, and is made of a flexible and air-containing large number of air-containing particles of a water-soluble polymeric substance that exhibits adhesive properties when dissolved or swollen in water. The present invention relates to a mucosal bandage characterized by strong film surfaces or interiors that exist independently without contacting each other.
この考案による粘膜包帯においては、上述した
包帯剤としての必要条件のうち、湿潤面への長時
間にわたる接着性は水に溶解あるいは膨潤して接
着性を示す水溶性高分子物質の空気を含んだ小粒
が担い、被覆性、柔軟性に加えて強靭性をフイル
ムが担うものである。また空気を含んだ水溶性高
分子物質の多数の小粒はフイルムの表面または内
部に互いに接することなくそれぞれ独立して存在
するためにフイルムの柔軟性を損なわないのであ
る。 In the mucosal bandage according to this invention, among the above-mentioned requirements for a bandage, long-term adhesion to wet surfaces is achieved by containing air in a water-soluble polymer substance that exhibits adhesive properties when dissolved or swollen in water. The small particles are responsible for this, and the film is responsible for covering properties, flexibility, and toughness. Furthermore, since the large number of small particles of water-soluble polymeric material containing air exist independently on the surface or inside of the film without contacting each other, the flexibility of the film is not impaired.
一般に、高分子物質は低分子物質に比べて溶媒
に対する溶解速度が遅いことはよく知られてい
る。 In general, it is well known that polymeric substances have a slower dissolution rate in solvents than low molecular weight substances.
特に水溶性高分子物質は、溶解速度がおそいの
で、これを速やかに溶解して均一な溶液を得る方
法として粉末を一旦アルコールなどの非溶媒に分
散したのちに水中に投じて溶解する方法が行なわ
れている。 In particular, water-soluble polymer substances have a slow dissolution rate, so a method of quickly dissolving them and obtaining a uniform solution is to first disperse the powder in a non-solvent such as alcohol and then pour it into water to dissolve it. It is.
このように、水溶性高分子物質の溶解速度がお
そいのは、水に膨潤してゲル化する、あるいは溶
解しても高粘度であるために、分子の拡散がおそ
いこととともにブロツキングを起した粉末の表面
だけが内部に空気を含んだままゲル化あるいは溶
解するので内部への溶媒の拡散が著しく抑制され
たいわゆる継粉の状態を生じるためである。 In this way, the dissolution rate of water-soluble polymer substances is slow because they swell in water and turn into gels, or even when dissolved, they have a high viscosity, which slows the diffusion of molecules and causes blocking in powders. This is because only the surface of the powder gels or dissolves while containing air inside, resulting in a so-called joint powder state in which diffusion of the solvent into the interior is significantly suppressed.
この考案は上述の現象を逆に利用することによ
りなされたものである。 This invention was made by utilizing the above-mentioned phenomenon in reverse.
即ち、この考案の粘膜包帯の構成要素である水
に溶解あるいは膨潤して接着性を示す水溶性高分
子物質の空気を含んだ小粒が湿潤粘膜に接する
と、該小粒の表面付近が毛細管現象により分泌液
を吸収し、すばやく溶解あるいはグル化して接着
性を示すとともに、小粒内は継粉を形成するた
め、その溶解は著しく抑制されて長時間にわたる
接着性を示すのである。 That is, when the small air-containing particles of the water-soluble polymeric substance, which is a component of the mucosal bandage of this invention and exhibits adhesive properties when dissolved or swollen in water, come into contact with a moist mucous membrane, the area near the surface of the small particles becomes sticky due to capillary action. It absorbs secretions and quickly dissolves or forms adhesives, exhibiting adhesive properties, and forms joint powder within the small grains, which significantly suppresses dissolution and exhibits adhesive properties over a long period of time.
この考案において水溶性高分子物質の小粒内に
含まれる空気の適性量は、高分子物質の種類や空
気の粒子内での分散の程度によつて異なるが、体
積百分率で10〜60%が適当である。 In this invention, the appropriate amount of air contained in small particles of water-soluble polymeric material varies depending on the type of polymeric material and the degree of dispersion of air within the particles, but the appropriate volume percentage is 10 to 60%. It is.
これは空気量が10%以下では分泌液の小粒によ
る吸収がおそく、初期の接着力が弱くなると共
に、継粉としての性質が弱く、接着時間が短くな
つて好ましくないためであり、また60%以上では
小粒の機械的強度が弱くなり、安定な粘膜包帯を
得ることが困難となるためである。 This is because if the air content is less than 10%, the absorption by small particles of secreted liquid is slow, the initial adhesion strength is weak, the properties as joint powder are weak, and the adhesion time is shortened, which is undesirable. This is because the mechanical strength of the small particles becomes weaker and it becomes difficult to obtain a stable mucosal bandage.
そして小粒の形状は、球形、円柱、円板、楕円
体、棒状など何れであつてもよい。 The shape of the small particles may be any shape such as a sphere, a cylinder, a disk, an ellipsoid, or a rod.
またこの空気を含んだ水溶性高分子物質の小粒
はその粒径が大きくなるに従つて接着時間が長く
なり、小さくなるに従つて使用感が良好となる傾
向があるので、これを考慮して使用部位、目的等
により大きさを決定すればよい。因みに口腔内粘
膜に使用する場合において小粒の形状が球形の時
の粒径0.1〜1.0mmφ程度が適当である。 In addition, the larger the particle size of the air-containing water-soluble polymer particles, the longer the adhesion time, and the smaller the particle size, the better the feeling of use. The size may be determined depending on the site of use, purpose, etc. Incidentally, when used on the oral mucosa, it is appropriate that the particle size is about 0.1 to 1.0 mmφ when the shape of the small particles is spherical.
この考案の粘膜包帯に用いられる水溶性高分子
物質としては、水に溶解あるいは膨潤して接着性
を示すものであればよく、そのような物質として
は例えばポリアクリル酸、ポリアクリル酸ナトリ
ウム、ポリアクリル酸アンモニウム、カルボキシ
ビニルポリマーなどのアクリル酸重合体または共
重合体あるいはそれらの塩、ポリビニルアルコー
ル、ポリビニルピロリドンなどの合成物、メチル
セルロース、エチルセルロース、カルボキシメチ
ルセルロースナトリウム、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
キシメチル澱粉などの半合成物、澱粉、アルギン
酸ナトリウム、アラビヤゴム、トラガガントゴム
などの天然物、およびそれらの混合物などがあ
る。 The water-soluble polymeric substance used in the mucosal bandage of this invention may be any substance that dissolves or swells in water and exhibits adhesive properties. Examples of such substances include polyacrylic acid, sodium polyacrylate, and polyacrylate. Acrylic acid polymers or copolymers or their salts such as ammonium acrylate and carboxyvinyl polymer, synthetic products such as polyvinyl alcohol and polyvinylpyrrolidone, methylcellulose, ethylcellulose, sodium carboxymethylcellulose, hydroxyethylcellulose, hydroxypropylcellulose, carboxymethyl starch These include semi-synthetic products such as starch, natural products such as sodium alginate, gum arabic, gum tragaganth, and mixtures thereof.
この考案において用いられるフイルムとして
は、柔軟で強靭なものであれば水溶性、非水溶性
を問わずいかなるものでも用いることができる。 As the film used in this invention, any film can be used as long as it is flexible and strong, regardless of whether it is water-soluble or water-insoluble.
例えば水溶性のフイルムとしてはポリビニルア
ルコール、ヒドロキシプロピルセルロースなど、
非水溶性のフイルムとしてはポリエチレン、ポリ
塩化ビニル、ポリウレタンなどがある。 For example, water-soluble films include polyvinyl alcohol, hydroxypropyl cellulose, etc.
Examples of water-insoluble films include polyethylene, polyvinyl chloride, and polyurethane.
また非水溶性のフイルムを用いた場合には、包
帯剤の背面からの分泌液の透過がなく、従つてよ
り長時間の包帯が可能であるが、その反面、小粒
とフイルムの間の相互作用が弱いため、包帯剤と
しての接着力は弱くなる傾向がある。 Furthermore, when a water-insoluble film is used, there is no permeation of secretions from the back side of the dressing, and therefore a longer dressing time is possible, but on the other hand, the interaction between the small particles and the film is Because of its weak adhesive strength as a bandage, its adhesive strength tends to be weak.
逆に水溶性のフイルムを用いた場合には、包帯
剤としての接着力は強くなるが、包帯剤の背面か
ら分泌液が浸透するために接着時間が短くなる傾
向がある。 On the other hand, when a water-soluble film is used, the adhesive force as a dressing becomes stronger, but the adhesion time tends to be shorter because secretions permeate from the back side of the dressing.
次に、この考案の一実施例を図面に基づいて説
明する。 Next, one embodiment of this invention will be described based on the drawings.
第1図A、B乃至第3図A、Bはこの考案の粘
膜包帯Dの基本的な構成の数例を示す平面図およ
び側面図である。 FIGS. 1A, B to 3A, B are a plan view and a side view showing several examples of the basic structure of the mucosal bandage D of this invention.
第1図A、Bは水溶性高分子物質の空気を含ん
だ小粒と粘膜との接着性を重視した形態であつ
て、小粒1と相互作用の強い水溶性フイルム2を
用いる場合に適している。そしてこの場合はフイ
ルム面2と粘膜面(図示せず)の間に若干の隙間
3があるので薬粉を固定する目的に用いるのに好
適である。 Figures A and B are configurations that emphasize adhesion between air-containing small particles of a water-soluble polymer substance and mucous membranes, and are suitable when using a water-soluble film 2 that strongly interacts with the small particles 1. . In this case, since there is a slight gap 3 between the film surface 2 and the mucous membrane surface (not shown), it is suitable for use for the purpose of fixing medicine powder.
第2図A、Bは小粒1とフイルム2′間の付着
力を重視した形態であつて、この場合フイルム
2′としては、小粒1と相互作用の弱い非水溶性
のフイルムを用いる場合に適している。 Figures 2A and 2B are configurations that place emphasis on the adhesion between the small particles 1 and the film 2'; in this case, the film 2' is suitable when using a water-insoluble film that has weak interaction with the small particles 1. ing.
第3図A、Bは第1図と第2図の中間の形態、
即ち小粒1と粘着の接着性、および小粒1とフイ
ルム2の接着性の双方を満足しうる形態を示すも
のである。 Figure 3 A and B are intermediate forms between Figures 1 and 2;
That is, it shows a form that can satisfy both the adhesion between the small particles 1 and the adhesive and the adhesion between the small particles 1 and the film 2.
しかして第1図乃至第3図では小粒はフイルム
上に均一に分布せしめたものであるが、この均一
分布は必要条件とするものではなく、例えば第4
図、第5図に示すように包帯剤Dのフイルム2の
一定区域4には小粒1を存在させないようなもの
であつてもよく、このような包帯剤Aは創傷部が
特に刺激に弱い場合や局所的に大量の薬物を投与
する場合には特に好適である。 However, although the small particles are uniformly distributed on the film in FIGS. 1 to 3, this uniform distribution is not a necessary condition;
As shown in Fig. 5, the small particles 1 may not be present in a certain area 4 of the film 2 of the dressing D, and such a dressing A may be used when the wound area is particularly sensitive to irritation. It is particularly suitable for locally administering large amounts of drugs.
またこの考案の粘膜包帯は第6図に示すように
フイルム2の層を2a,2bの2層あるいはそれ
以上の多層とすることもよく、これは特に水溶性
のフイルム2aの背面に非水溶性のフイルム層2
bをうすく設けると、強い接着力と長時間にわた
る薬物の滞留の双方を同時に満足させることがで
きる。 In addition, in the mucosal bandage of this invention, the film 2 may have two layers 2a and 2b, or more than two layers, as shown in FIG. film layer 2
By providing b thinly, both strong adhesive force and long-term drug retention can be satisfied at the same time.
この考案の粘膜包帯の構成要素である水溶性高
分子物質の小粒は、適度の粒度の粉末を圧着、熱
圧着、場合によつては湿潤状態で圧着することに
より得ることができる。 The small particles of the water-soluble polymeric substance, which are the constituent elements of the mucosal bandage of this invention, can be obtained by compressing, thermocompressing, or, in some cases, compressing in a wet state, powders of appropriate particle size.
またこの小粒を有する粘膜包帯は、小粒とフイ
ルムを圧着、熱圧着することにより、あるいは湿
潤状態で圧着することにより得ることができる。 Further, a mucosal bandage having the small particles can be obtained by press-bonding or thermocompression bonding the small particles and a film, or by press-bonding the small particles and a film in a wet state.
このほかフイルム上にパターン状に散布した高
分子物質の粉末を圧着によつて一度に粘膜包帯と
して形成することも可能である。要するにこの考
案の粘膜包帯は小粒が独立して存在するために、
包帯の柔軟性が損なわれない。即ち、水溶性高分
子の小粒は一般に柔軟性を有しないので、小粒が
フイルム上あるいはフイルム内部に互いに接触し
て存在すると、たとえフイルムが柔軟であつて
も、小粒がフイルムの変形を妨げるために柔軟性
が損なわれて、包帯としての特性を失う。しかし
この考案のように小粒が互いに接することなく独
立に存在すると、間隙が存在するためにフイルム
の柔軟性は十分に保たれるのである。 In addition, it is also possible to form a mucosal bandage all at once by compressing polymer powder powder spread in a pattern on a film. In short, the mucosal bandage of this invention has small particles that exist independently, so
The flexibility of the bandage is not compromised. That is, since small particles of water-soluble polymers generally do not have flexibility, if small particles are present on the film or inside the film in contact with each other, even if the film is flexible, the small particles will prevent the film from deforming. It becomes less flexible and loses its properties as a bandage. However, when the small particles exist independently without touching each other as in this invention, the flexibility of the film is maintained sufficiently due to the presence of gaps.
以下、この考案を実施例により説明する。 This invention will be explained below using examples.
実施例 1
平均重合度1600のポリビニルアルコールの粉末
を圧縮成型して直径2mm、厚さ500μmの円盤状の
空気含有率40%の小粒を得る。この小粒100個を、
10%のグリセリンをふくむ平均重合度1600のポリ
ビニルアルコールのフイルム(厚さ=100μm)上
に第1図のように配置し、加湿下で加圧して接着
し、25mm×25mmの矩形の第1図に示す本考案の粘
膜包帯を得た。Example 1 Polyvinyl alcohol powder with an average degree of polymerization of 1600 is compression molded to obtain disc-shaped small particles with a diameter of 2 mm and a thickness of 500 μm and an air content of 40%. 100 of these small grains,
It is placed as shown in Figure 1 on a polyvinyl alcohol film (thickness = 100 μm) with an average degree of polymerization of 1600 containing 10% glycerin, and adhered under pressure under humidified conditions. The mucosal bandage of the present invention shown in Figure 1 was obtained.
該包帯を10人のパネラーの頬粘膜に貼付したと
ころ、平均で40分にわたつて良好に付着した。 When the bandage was applied to the buccal mucosa of 10 panelists, it adhered well for an average of 40 minutes.
実施例 2
カルボキシビニルポリマーを加圧成型して空気
含有率60%、厚さ100μmのシートを得る。このシ
ートを砕き、孔径1mmのふるいを通して、不定形
の小粒を得る。この小粒を厚さ200μmの平均重合
度800の酢酸ビニル樹脂のフイルム上にその面積
の約50%を覆うように散布し、50℃にてプレスし
て小粒をフイルム内に埋め込み、第2図に示す本
考案の粘膜包帯を得た。Example 2 A carboxyvinyl polymer is pressure molded to obtain a sheet with an air content of 60% and a thickness of 100 μm. This sheet is crushed and passed through a sieve with a pore size of 1 mm to obtain irregularly shaped small particles. These small particles were scattered on a vinyl acetate resin film with a thickness of 200 μm and an average degree of polymerization of 800 so as to cover about 50% of the area, and pressed at 50°C to embed the small particles in the film, as shown in Figure 2. A mucosal bandage of the present invention as shown was obtained.
該包帯を10mm×10mmの矩形に切断し、10人のパ
ネラーの上歯茎部前面に貼付したところ、平均で
60分にわたつて良好に付着した。 The bandage was cut into a 10 mm x 10 mm rectangle and applied to the front surface of the upper gums of 10 panelists.
Good adhesion was achieved over 60 minutes.
実施例 3
ポリアクリル酸ナトリウム3g、カルボキシメ
チルセルロースナトリウム6g、グリセリン10
g、及び水30gからなる混合液をポリエステルフ
イルム上に流延乾燥して、厚さ100μmのフイルム
を得る。このフイルムの片面にコロジオンを塗布
乾燥して、柔軟なフイルムを得る。もう一方の面
に孔径0.5mmの円形の穴が1cm2当たり100個あいた
プラスチツクフイルムを被せ、その上からヒドロ
キシプロピルセルロースの粉末を1cm2当たり10mg
散布した後、プラスチツクフイルムを取り除い
て、パターン状散布を行なう。これを100℃でプ
レスして半分埋設した小粒を形成し、第6図に示
す本考案の粘膜包帯を得た。Example 3 Sodium polyacrylate 3g, sodium carboxymethylcellulose 6g, glycerin 10
g and 30 g of water was cast onto a polyester film and dried to obtain a film with a thickness of 100 μm. Collodion is applied to one side of this film and dried to obtain a flexible film. Cover the other side with a plastic film with 100 circular holes with a pore size of 0.5 mm per square centimeter, and add 10 mg of hydroxypropyl cellulose powder per square centimeter over the plastic film.
After spraying, the plastic film is removed and patterned spraying is performed. This was pressed at 100°C to form half-embedded small particles to obtain the mucosal bandage of the present invention shown in FIG.
該包帯をφ20mmの円形に切断し、10人のパネラ
ーの上顎内面に貼付したところ、平均で110分に
わたつて良好に付着した。 The bandage was cut into a circle with a diameter of 20 mm and applied to the inner surface of the upper jaw of 10 panelists, and the bandage adhered well for an average of 110 minutes.
第1図AおよびBはこの考案の粘膜包帯の基本
的な構成例を示す平面図および側面図、第2図
A、Bおよび第3図A、Bは同じく他の構成例を
示す平面図と側面図、第4図および第5図はこの
考案の粘膜包帯においてフイルム上への高分子物
質の小粒の分布状態の他例を示す平面図、第6図
はフイルム層を2層とせる粘膜包帯を示す側面図
である。
1……水溶性高分子物質よりななる空気を含ん
だ小粒、2……フイルム。
Figures 1A and B are plan views and side views showing basic configuration examples of the mucosal bandage of this invention, and Figures 2A and B and Figures 3A and B are plan views showing other configuration examples. A side view, FIGS. 4 and 5 are plan views showing other examples of the distribution of small particles of polymer material on the film in the mucosal bandage of this invention, and FIG. 6 is a mucosal bandage with two film layers. FIG. 1...Small particles containing air made of a water-soluble polymer substance, 2...Film.
Claims (1)
膜包帯であつて、水に溶解あるいは膨潤して接
着性を示す水溶性高分子物質の空気を含有する
多数の小粒が柔軟かつ強靭なフイルム表面また
は内部に互いに接することなくそれぞれ独立し
て存在することを特徴とする粘膜包帯。 (2) 水に溶解あるいは膨潤して接着性を示す水溶
性高分子物質よりなる小粒中の空気含有量が10
〜60%であることを特徴とする実用新案登録請
求の範囲第1項記載の粘膜包帯。[Scope of Claim for Utility Model Registration] (1) A mucosal bandage that adheres to moist mucous membranes to cover and protect the mucous membranes, which contains air of a water-soluble polymer substance that exhibits adhesive properties when dissolved or swollen in water. A mucosal bandage characterized by a large number of small particles existing independently on the surface or inside of a flexible and strong film without touching each other. (2) Air content in small particles made of a water-soluble polymer substance that exhibits adhesive properties when dissolved or swells in water is 10
60%.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP18503183U JPS6092517U (en) | 1983-11-29 | 1983-11-29 | mucosal bandage |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP18503183U JPS6092517U (en) | 1983-11-29 | 1983-11-29 | mucosal bandage |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6092517U JPS6092517U (en) | 1985-06-24 |
JPS6311942Y2 true JPS6311942Y2 (en) | 1988-04-06 |
Family
ID=30400031
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP18503183U Granted JPS6092517U (en) | 1983-11-29 | 1983-11-29 | mucosal bandage |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6092517U (en) |
-
1983
- 1983-11-29 JP JP18503183U patent/JPS6092517U/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS6092517U (en) | 1985-06-24 |
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