JP2798272B2 - Interface for iontophoresis - Google Patents

Interface for iontophoresis

Info

Publication number
JP2798272B2
JP2798272B2 JP22316689A JP22316689A JP2798272B2 JP 2798272 B2 JP2798272 B2 JP 2798272B2 JP 22316689 A JP22316689 A JP 22316689A JP 22316689 A JP22316689 A JP 22316689A JP 2798272 B2 JP2798272 B2 JP 2798272B2
Authority
JP
Japan
Prior art keywords
drug
water
interface
iontophoresis
present
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 - Fee Related
Application number
JP22316689A
Other languages
Japanese (ja)
Other versions
JPH0386176A (en
Inventor
敬一郎 岡部
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.)
Hisamitsu Pharmaceutical Co Inc
Original Assignee
Hisamitsu Pharmaceutical Co Inc
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 Hisamitsu Pharmaceutical Co Inc filed Critical Hisamitsu Pharmaceutical Co Inc
Priority to JP22316689A priority Critical patent/JP2798272B2/en
Priority to CA 2026885 priority patent/CA2026885C/en
Priority to DE69026323T priority patent/DE69026323T2/en
Priority to PCT/JP1990/000144 priority patent/WO1990008571A1/en
Priority to EP90902704A priority patent/EP0411146B1/en
Priority to AU50327/90A priority patent/AU624481B2/en
Publication of JPH0386176A publication Critical patent/JPH0386176A/en
Application granted granted Critical
Publication of JP2798272B2 publication Critical patent/JP2798272B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Landscapes

  • Electrotherapy Devices (AREA)

Description

【発明の詳細な説明】 本発明はイオントフォレーゼ用のインタフェース(皮
膚・粘膜当接体)に関する。
Description: The present invention relates to an interface (skin / mucosa abutment) for iontophoresis.

イオントフォレーシスに於けるインタフェースは、薬
液を保持する為のリザーバと電流分散用の電極とを組み
合わせた構造を有する。
The interface in iontophoresis has a structure in which a reservoir for holding a chemical solution and an electrode for current distribution are combined.

このリザーバの構造は、薬液を生体皮膚界面迄、経時
的に所定量を確実に到達せしめるものでなければならな
いが、リザーバ自体が立体的であり、しかも水を介する
為、薬物の希釈化が生じる等、未だ充分な構造が提案さ
れるに至っていない。
The structure of this reservoir must ensure that the drug solution reaches a predetermined amount over time up to the biological skin interface, but since the reservoir itself is three-dimensional and passes through water, dilution of the drug occurs. For example, a sufficient structure has not yet been proposed.

上記に鑑み本発明は、イオントフォレーシスに適し
た、即ち特にペプチド等の微量用量薬物の局所高濃度維
持による効率適投薬を行ない得る構造を有するインタフ
ェースを提供することを目的とする。
In view of the above, an object of the present invention is to provide an interface having a structure suitable for iontophoresis, that is, an interface having a structure capable of performing efficient and appropriate administration by maintaining a local high concentration of a small amount of a drug such as a peptide.

即ち、カルシトニン、インスリン、生長ホルモン等の
特にペプチド系の薬物は微少用量で有効であるが、これ
をイオントフォレーシスにより経皮乃至経粘着的に有効
投与するためには、その濃度を充分高く維持しなければ
ならない。
That is, particularly peptide-based drugs such as calcitonin, insulin, and growth hormone are effective in small doses, but in order to effectively administer them transdermally or transadhesively by iontophoresis, their concentrations must be sufficiently high. Must be maintained.

本発明は、これを薬物不透性且つ水透過性の半透性膜
の生体当接面上に薬物をスプレードライ、散布等により
付着乃至貼着せしめたインタフェースを提案することに
より、効果的に解決したものである。
The present invention effectively proposes an interface in which a drug is attached or stuck to the living body contacting surface of a drug-impermeable and water-permeable semipermeable membrane by spray-drying, spraying, or the like. It is a solution.

治療時、水分保持部からの水分(電解質液、緩衝液
等)は半透性膜を介して、例えば粉末等の固体状に半透
性膜外面に付着していた薬物を皮膚に面して溶解し、局
所高濃度を長時間維持するものである。
During treatment, the water (electrolyte solution, buffer solution, etc.) from the water retention unit passes through the semi-permeable membrane, causing the drug, which has adhered to the outer surface of the semi-permeable membrane in a solid state such as powder, to the skin. It dissolves and maintains local high concentration for a long time.

尚、本発明における薬物の貼着・付着形態の他の1態
様としては、適当な水溶性高分子と薬物との結合物、即
ち薬物含有水溶解性層の形態を例示し得る。
In another embodiment of the present invention, a drug-adhered form of a drug-containing water-soluble layer can be exemplified as another embodiment of the mode of sticking / adhering a drug.

即ち、薬物含有水溶解性層は、所定の薬物を保持・付
着・包含した水溶性高分子より形成されるものであり、
水溶性高分子としては可溶性澱粉(オブラート)、ポリ
アクリル酸ソーダ、ポリビニルアルコール等々、任意の
水溶性高分子を使用し得、通常、薄フィルム状に形成さ
れる。又、その水溶性の程度も、使用目的に応じて適宜
調節され得る。
That is, the drug-containing water-soluble layer is formed of a water-soluble polymer that retains, adheres to, and contains a predetermined drug,
As the water-soluble polymer, any water-soluble polymer such as soluble starch (oblate), sodium polyacrylate, polyvinyl alcohol and the like can be used, and is usually formed into a thin film. Further, the degree of water solubility can be appropriately adjusted according to the purpose of use.

ここにおいて、水分保持部は、容器構造又は層状体
で、綿、PVAスポンジ、セルローストリアセテート等の
水分浸透性繊維より成る層、あるいは水を保持した膨潤
ゲル、多孔性セラミック材等が例示される。又、必要に
応じて周囲を硬質性樹脂で形成したカップで覆い、外部
への蒸散を防ぐ構造、あるいは用時のみ溶液が導入され
る構造をも適宜取り得る。
Here, the moisture retaining portion is a container structure or a layered body, and is exemplified by a layer made of moisture permeable fibers such as cotton, PVA sponge, and cellulose triacetate, a swelling gel retaining water, a porous ceramic material, and the like. If necessary, a structure in which the periphery is covered with a cup made of a hard resin to prevent evaporation to the outside, or a structure in which the solution is introduced only at the time of use, may be appropriately adopted.

半透性膜は、半透性セルロース酢酸塩、ポリビニルク
ロライド、又は再生セルロースの素材より成るものが例
示されるが、特に限定されない。
Examples of the semipermeable membrane include those made of semipermeable cellulose acetate, polyvinyl chloride, or regenerated cellulose, but are not particularly limited.

次に、本発明の実施例を図面を参照して詳細に説明す
る。
Next, embodiments of the present invention will be described in detail with reference to the drawings.

第1図に於いて、1は水分保持部であり、上述した如
く多孔質体に水乃至電解質液を含浸させたもの、あるい
は上述した膨潤ゲル状のもの、又は単なる容器構造等で
ある。
In FIG. 1, reference numeral 1 denotes a water holding unit, which is a porous body impregnated with water or an electrolyte solution as described above, a swollen gel-like body described above, or a simple container structure.

2は半透性膜(例えば、Spectrum medical industrie
s−inc社製(スペクトラム メディカル インダストリ
ーズ インコーポレイティド社製)Spectra−Por 3又は
Spectra−Por 6)であり、3はその一方の面上に配置さ
れた薬物である。半透性膜2の内面側には、導電性ゴ
ム、導電性ポリマー、カーボンフィルム、アルミ箔他、
金属箔よりなる多孔性乃至メッシュ状等の電極4が配置
されている。これら構造物全体は、柔軟性支持部材6に
よって覆われ、支持固定されている。
2 is a semipermeable membrane (for example, Spectrum medical industrie
Spectra-Por 3 manufactured by s-inc (Spectrum Medical Industries, Inc.) or
Spectra-Por 6), 3 is the drug located on one side. On the inner surface side of the semipermeable membrane 2, conductive rubber, conductive polymer, carbon film, aluminum foil, etc.
A porous or mesh-shaped electrode 4 made of metal foil is arranged. The whole of these structures is covered and supported and fixed by the flexible support member 6.

支持部材6は、更に生体皮膚表面01迄延びており、生
体皮膚表面01との接触面には各種貼着剤、接着剤11が付
設されている。
The support member 6 further extends to the living skin surface 01, and various adhesives and adhesives 11 are provided on the contact surface with the living skin surface 01.

使用薬物としては、その分子量等に限定されるもので
はないが、本発明インタフェースは、特に用量が微量に
も拘らず、イオントフォレーシスの効率上、可及的高濃
度を維持し且つ充分な水の存在を要する、主としてイン
スリン等のペプチド系薬物に有用である。
Although the drug used is not limited to its molecular weight, etc., the interface of the present invention maintains the highest possible concentration and maintains a sufficient concentration on the efficiency of iontophoresis, even though the dose is particularly small. It is mainly useful for peptide drugs such as insulin which require the presence of water.

鎮咳去痰剤 クロモグリク酸ナトリウム、フマール酸ケトチフェン 気管支拡張剤 フマル酸ホルモテロール 鎮痛剤 塩酸ナルブフィン、乳酸ペンタゾシン、ジクロフェナ
ックナトリウム 強心剤 塩酸ドパミン 精神神経安定剤 ペルフェナジン、フェノチアジン 抗生物質 セフォテタン二ナトリウム、硫酸ジベカシン、硫酸ア
ミカシン、硫酸ネチルマイシン、硫酸シソマイシン 抗悪性腫瘍剤 アドリアマイシン、マイトマイシンC、塩酸ブレオマ
イシン、レンチナン、ピシバニール、硫酸ビンクリスチ
ン、シスプラチン 循環機能改善剤 クエン酸ニカメタート、塩酸メクロフェノキサート、
マレイン酸リスリド、ホパンテン酸カルシウム 痛風治療剤 アロプリノール その他ペプタイド類 LHRH,エンケファリン、エンドルフィン、インターフ
ェロン、インシュリン、カルシトニン、TRH,オキシトシ
ン、リプレシン、バソプレシン、グルカゴン、脳下垂体
ホルモン(HGH,HMG,HCG,酢酸デスモプレシン)、卵胞黄
体ホルモン 以上詳述の如く本発明は、半透性膜の介在により、そ
の外面に保持された薬物が希釈されることなく、適当な
水分が補給でき、しかも生体表面乃至外部から浸入する
細胞の水分保持部への浸入を阻止でき、長期間効率的且
つ正確な投薬を行なえる等の効果を有するものである。
Antitussive expectorant Sodium cromoglycate, Ketotifen fumarate Bronchodilator Formoterol fumarate Analgesic Nalbuphine hydrochloride, Pentazocine lactate, Diclofenac sodium Cardiotonic agent Dopamine hydrochloride Psychiatric nerve stabilizer Perphenazine, Phenothiazine Antibiotics Cefotetan disodium sulfate, Dibecacin sulfate, Amino acid Netilmycin, sisomicin sulfate Antineoplastic agent Adriamycin, Mitomycin C, Bleomycin hydrochloride, Lentinan, Picibanil, Vincristine sulfate, Cisplatin Circulating function improver Nicametate citrate, Meclofenoxate hydrochloride,
Lisulide maleate, Calcium hopantenate Gout treatment Allopurinol Other peptides LHRH, Enkephalin, Endorphin, Interferon, Insulin, Calcitonin, TRH, Oxytocin, Ripressin, Vasopressin, Glucagon, Pituitary hormone (HGH, HMG, HCG, Desmopressin acetate) As described in detail above, the present invention can provide an appropriate water supply without diluting a drug held on the outer surface thereof by the interposition of a semipermeable membrane, and furthermore, the drug penetrates from the surface of a living body or outside. This has the effect of preventing cells from infiltrating into the water holding portion and enabling efficient and accurate administration for a long period of time.

【図面の簡単な説明】[Brief description of the drawings]

第1図は、本発明の実施例を示す図である。 1……水分保持部、 2……半透性膜、 3……配置薬物、 4……電極、 6……支持部材、 01……生体皮膚表面。 FIG. 1 is a diagram showing an embodiment of the present invention. DESCRIPTION OF SYMBOLS 1 ... Moisture holding | maintenance part, 2 ... Semi-permeable membrane, 3 ... Drug arrangement | positioning, 4 ... Electrode, 6 ... Support member, 01 ... Body skin surface.

Claims (1)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】その生体当接面上に薬物を貼着乃至付着せ
しめた半透性膜を有することを特徴とするイオントフォ
レーゼ用インタフェース。
1. An interface for iontophoresis, comprising a semipermeable membrane on which a drug is stuck or adhered on the living body contacting surface.
JP22316689A 1989-02-06 1989-08-31 Interface for iontophoresis Expired - Fee Related JP2798272B2 (en)

Priority Applications (6)

Application Number Priority Date Filing Date Title
JP22316689A JP2798272B2 (en) 1989-08-31 1989-08-31 Interface for iontophoresis
CA 2026885 CA2026885C (en) 1989-02-06 1990-02-06 Interface for iontophorese
DE69026323T DE69026323T2 (en) 1989-02-06 1990-02-06 INTERFACE FOR IONTOPHORESIS
PCT/JP1990/000144 WO1990008571A1 (en) 1989-02-06 1990-02-06 Interface for iontophoresis
EP90902704A EP0411146B1 (en) 1989-02-06 1990-02-06 Interface for iontophoresis
AU50327/90A AU624481B2 (en) 1989-02-06 1990-02-06 Interface for iontophoresis

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP22316689A JP2798272B2 (en) 1989-08-31 1989-08-31 Interface for iontophoresis

Publications (2)

Publication Number Publication Date
JPH0386176A JPH0386176A (en) 1991-04-11
JP2798272B2 true JP2798272B2 (en) 1998-09-17

Family

ID=16793835

Family Applications (1)

Application Number Title Priority Date Filing Date
JP22316689A Expired - Fee Related JP2798272B2 (en) 1989-02-06 1989-08-31 Interface for iontophoresis

Country Status (1)

Country Link
JP (1) JP2798272B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4732881B2 (en) * 2005-12-07 2011-07-27 Tti・エルビュー株式会社 Iontophoresis device

Also Published As

Publication number Publication date
JPH0386176A (en) 1991-04-11

Similar Documents

Publication Publication Date Title
KR950013631B1 (en) Plaster structural assembly for iontophoresis
JP2542792B2 (en) User-operated iontophoretic device
KR100453132B1 (en) Device and method for enhancing transdermal agent flux
KR100601776B1 (en) Anhydrous drug reservoir for electrolytic transdermal delivery device
JPH0614980B2 (en) Device for transdermal administration of protein and peptide drugs
JP4321966B2 (en) Electrotransport devices containing compatible antimicrobial agents
JP2818075B2 (en) Interface for iontophoresis
WO1996010439A1 (en) Interface for iontophoretic percutaneous administration, and agent and method for treating the skin for that purpose
WO1999043382A1 (en) Iontophoresis device
KR20040012744A (en) Transdermal electrotransport delivery device including an antimicrobial compatible reservoir composition
CA2026885C (en) Interface for iontophorese
US20050169976A1 (en) Insulin administration apparatus
JP2845509B2 (en) Interface for iontophoresis
JP2009509682A (en) Pulsed delivery of gonadotropin-releasing hormone from pre-filled combined electrical delivery patches
US6587717B1 (en) Iontophoresis device and method of assembling the same
EP0586666B2 (en) User activated iontophoretic device
JP2798272B2 (en) Interface for iontophoresis
JP2795452B2 (en) Interface for iontophoresis
JP2818771B2 (en) Interface for iontophoresis
JP2792661B2 (en) Interface for iontophoresis
JP2795453B2 (en) Interface for iontophoresis
JP2792660B2 (en) Interface for iontophoresis
JPH07213628A (en) Matrix for ionto-phoresis
JPH0312173A (en) Interface for iontophoresis
JPH0616535A (en) Interface for iontophoresis

Legal Events

Date Code Title Description
R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

FPAY Renewal fee payment (prs date is renewal date of database)

Year of fee payment: 10

Free format text: PAYMENT UNTIL: 20080703

LAPS Cancellation because of no payment of annual fees