JP2008194288A - Needle-like body and method for producing needle-like body - Google Patents

Needle-like body and method for producing needle-like body Download PDF

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JP2008194288A
JP2008194288A JP2007033373A JP2007033373A JP2008194288A JP 2008194288 A JP2008194288 A JP 2008194288A JP 2007033373 A JP2007033373 A JP 2007033373A JP 2007033373 A JP2007033373 A JP 2007033373A JP 2008194288 A JP2008194288 A JP 2008194288A
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substrate
needle
intaglio
protrusion
applying
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JP4959363B2 (en
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Hiroshi Sugimura
浩 杉村
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Toppan Inc
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Toppan Printing Co Ltd
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M37/00Other apparatus for introducing media into the body; Percutany, i.e. introducing medicines into the body by diffusion through the skin
    • A61M37/0015Other apparatus for introducing media into the body; Percutany, i.e. introducing medicines into the body by diffusion through the skin by using microneedles
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M37/00Other apparatus for introducing media into the body; Percutany, i.e. introducing medicines into the body by diffusion through the skin
    • A61M37/0015Other apparatus for introducing media into the body; Percutany, i.e. introducing medicines into the body by diffusion through the skin by using microneedles
    • A61M2037/0046Solid microneedles
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M37/00Other apparatus for introducing media into the body; Percutany, i.e. introducing medicines into the body by diffusion through the skin
    • A61M37/0015Other apparatus for introducing media into the body; Percutany, i.e. introducing medicines into the body by diffusion through the skin by using microneedles
    • A61M2037/0053Methods for producing microneedles

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  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Dermatology (AREA)
  • Medical Informatics (AREA)
  • Anesthesiology (AREA)
  • Biomedical Technology (AREA)
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  • Veterinary Medicine (AREA)
  • Media Introduction/Drainage Providing Device (AREA)

Abstract

<P>PROBLEM TO BE SOLVED: To provide a needle-like body with sufficient mechanical strength which allows sustained-release transdermal administration, and also to provide a method for producing the needle-like body. <P>SOLUTION: The needle-like body has a projection on an easily decomposing section. The easily decomposing section is decomposed faster within a living body than the projection. With such a configuration, the needle-like body keeps sufficient mechanical strength before puncturing the skin and breaks selectively within a living body to leave the projection within the living body. The needle-like body thus provided has the sufficient mechanical strength and allows sustained-release transdermal administration. <P>COPYRIGHT: (C)2008,JPO&INPIT

Description

本発明は、微細な針状体および該針状体の製造方法に関するものである。   The present invention relates to a fine needle-like body and a method for producing the needle-like body.

生理活性物質の生体内への供給方法として、非経口投与が広く用いられている。非経口投与としては、注射針による投与、経皮投与、などが知られている。このとき、生体内の生理活性物質血中濃度を長時間にわたり適正且つ安定的に維持するために、徐放性を有することが好ましい。   As a method for supplying a physiologically active substance into a living body, parenteral administration is widely used. As parenteral administration, administration with an injection needle, transdermal administration, and the like are known. At this time, in order to maintain the blood concentration of the physiologically active substance in the living body appropriately and stably for a long time, it is preferable to have sustained release properties.

注射針による投与にて徐放性を付与する場合、生理活性物質をマイクロカプセル化して投与し、生理活性物質をマイクロカプセルから徐々に放出させる方法が知られている。このとき、徐放性マイクロカプセルは生体内に保持されるため、カプセル材は人体に悪影響を及ぼさない材料であることが望ましく、この材料としてはポリグリコール酸、ポリ乳酸、ポリリンゴ酸、ポリクエン酸、乳酸とグリコール酸の共重合体等の生体内分解性材料が有望視されている(特許文献1参照)。   In the case of imparting sustained release by administration with an injection needle, a method is known in which a physiologically active substance is administered in microcapsules and the physiologically active substance is gradually released from the microcapsules. At this time, since the sustained-release microcapsules are held in the living body, it is desirable that the capsule material is a material that does not adversely affect the human body, such as polyglycolic acid, polylactic acid, polymalic acid, polycitric acid, Biodegradable materials such as a copolymer of lactic acid and glycolic acid are considered promising (see Patent Document 1).

一方、近年、生理活性物質を経皮投与する方法として、微細な針状体を用いて経皮投与する方法が注目を集めている。微細な針状体を用いてバリア性の高い角質層を穿孔することで、生理活性物質の通過経路を形成し、経皮投与の効率を向上することが出来る。このとき、微細な針状体が角質層を貫通し、毛細血管や神経まで到達しないように設計することで、使用時に出血や痛みを伴わないようにすることが出来る。   On the other hand, in recent years, as a method for transdermal administration of a physiologically active substance, a method of transdermal administration using a fine needle-like body has attracted attention. By perforating a stratum corneum having a high barrier property using a fine needle-like body, a passage route for a physiologically active substance can be formed, and the efficiency of transdermal administration can be improved. At this time, by designing the fine needle-like body so as not to penetrate the stratum corneum and reach the capillaries and nerves, it is possible to prevent bleeding and pain during use.

上記経皮投与の目的で微細な針状体を用いる場合、微細な針状体は、皮膚を穿孔するための十分な細さ、および先端角、皮膚の最外層である角質層を貫通し、かつ神経層へ到達しない長さ、を有していることが望ましく、具体的には、針状体の直径は数μmから100μm程度、針状体の先端角度は30°以下、針状体の長さは数十μmから数百μm程度、であることが望ましいとされている。   When a fine needle-like body is used for the purpose of transdermal administration, the fine needle-like body penetrates through the stratum corneum, which is thin enough to perforate the skin, and the tip corner, the outermost layer of the skin, It is desirable that the needle does not reach the nerve layer. Specifically, the diameter of the needle-like body is about several to 100 μm, the tip angle of the needle-like body is 30 ° or less, The length is preferably about several tens of μm to several hundreds of μm.

また、上述した微細な針状体を構成する材料としては、仮に破損した針状体が体内に残留した場合でも、人体に悪影響を及ぼさない材料であることが望ましく、材料としては医療用シリコン樹脂や、マルトース、ポリ乳酸、デキストラン等の生体適合性材料が有望視されている(特許文献2参照)。   In addition, the material constituting the fine needle-shaped body is preferably a material that does not adversely affect the human body even if the damaged needle-shaped body remains in the body. In addition, biocompatible materials such as maltose, polylactic acid, and dextran are considered promising (see Patent Document 2).

また、上述した微細な針状体を製造する方法として、機械加工により針状体の原版を作成し、原版から複製版を作り、転写加工成形を行う製造方法が提案されている(特許文献3参照)。   Further, as a method for manufacturing the fine needle-shaped body described above, a manufacturing method has been proposed in which an original plate of a needle-shaped body is created by machining, a duplicate plate is made from the original plate, and transfer processing is performed (Patent Document 3). reference).

また、上述した微細な針状体を用いた経皮投与にて、徐放性を向上させる方法として、括れ、段差、矢じり形状などの破損しやすい形状をした微細な糖質からなる針状体に機能性物質を内包し、角質層に挿入後、針状体を折って角質層内に残留させるという方法が提案されている(特許文献4参照)。
特開平6−192068号公報 特開2005−21677号公報 特表2006−513811号公報 特開2003−238347号公報
In addition, as a method for improving sustained release by transdermal administration using the fine needle-like body described above, a needle-like body made of a fine carbohydrate having a shape that is easily damaged such as a constriction, a step, or an arrowhead shape. A method has been proposed in which a functional substance is encapsulated and inserted into the stratum corneum, and then the needle-like body is folded and left in the stratum corneum (see Patent Document 4).
Japanese Patent Application Laid-Open No. 6-192068 Japanese Patent Laid-Open No. 2005-21677 JP-T-2006-513811 JP 2003-238347 A

しかしながら、括れ、段差、矢じり形状などの破損しやすい形状をした微細な糖質からなる針状体のように、機械的強度が不足した針状体では、押圧したとき、皮膚に穿刺する前に針状体が破損しやすく、皮膚内部に穿刺することが困難である。   However, in the case of needles with insufficient mechanical strength, such as needles made of fine carbohydrates that are easily damaged such as constrictions, steps, arrowheads, etc., when pressed, before puncturing the skin The needle-like body is easily damaged, and it is difficult to puncture the inside of the skin.

特に、角質層より内側の表皮層や真皮層への生理活性物質の投与を行う場合、角質層へ針状体を挿入する場合と比べてより大きな押圧が必要なため、針状体の機械的強度の不足の問題はより顕著となる。一般的に角質層よりも、より内側の表皮層や真皮層の方が生理活性物質の吸収効率が高いことが知られている。   In particular, when a physiologically active substance is administered to the epidermis layer or dermis layer inside the stratum corneum, a larger pressure is required than when the needle-like body is inserted into the stratum corneum. The problem of lack of strength becomes more prominent. In general, it is known that the inner skin layer and dermis layer have higher absorption efficiency of physiologically active substances than the stratum corneum.

そこで、本発明は、上述の問題を解決するためになされたものであり、徐放性を有する経皮投与が可能となり、充分な機械的強度を有した針状体および針状体の製造方法を提供することを目的とする。   Accordingly, the present invention has been made to solve the above-mentioned problems, and enables the transdermal administration having sustained release, and a method for producing a needle-like body having sufficient mechanical strength. The purpose is to provide.

請求項1に記載の本発明は、微細な針状体において、基板と、前記基板上に設けられた易分解部と、前記易分解部上に設けられた突起部と、を備え、前記易分解部は、突起部よりも生体内での溶解速度が速いことを特徴とする針状体である。
なお、本明細書において、「針状体」とは、突起部が一本の場合に限定されず、突起部が複数本規則的に配列(例えば、アレイ状に配列)された構造体をも含むものとして定義する。
The present invention according to claim 1 is a fine needle-like body, comprising a substrate, an easily disassembled portion provided on the substrate, and a protrusion provided on the easily disassembled portion, The decomposition part is a needle-like body characterized in that the dissolution rate in the living body is faster than the protrusion part.
In the present specification, the term “needle-like body” is not limited to the case where there is a single protrusion, but also includes a structure in which a plurality of protrusions are regularly arranged (for example, arranged in an array). Define as including.

請求項2に記載の本発明は、微細な針状体の製造方法において、所望する針状体の形状を凹凸反転させた凹版を形成する工程と、基板に易分解部材料を塗布する工程と、前記易分解部材料を塗布した基板に、突起部材料を塗布する工程と、前記基板に前記凹版を押圧する工程と、前記基板から凹版を剥離する工程と、を含むことを特徴とする針状体の製造方法である。   According to a second aspect of the present invention, in the method for producing a fine needle-like body, a step of forming an intaglio in which the shape of the desired needle-like body is inverted, and a step of applying an easily decomposable part material to the substrate; A needle comprising: a step of applying a protrusion material to a substrate coated with the easily decomposable portion material; a step of pressing the intaglio on the substrate; and a step of peeling the intaglio from the substrate. It is a manufacturing method of a shape.

請求項3に記載の本発明は、請求項2に記載の針状体の製造方法であって、突起部材料を塗布する工程は、基板と凹版を押圧するとき凹版の凹部に対応する位置のみに選択的に突起部材料を塗布する工程であることを特徴とする針状体の製造方法である。   The present invention according to claim 3 is the method for manufacturing the needle-shaped body according to claim 2, wherein the step of applying the protrusion material is performed only at a position corresponding to the concave portion of the intaglio when pressing the substrate and the intaglio. This is a method for producing a needle-like body, which is a step of selectively applying a projection material to the surface.

請求項4に記載の本発明は、請求項2に記載の針状体の製造方法であって、突起部材料を塗布する工程は、易分解部材料を塗布した基板全面に突起部材料を塗布する工程であり、基板から凹版を剥離する工程の後、前記基板全面にエッチング処理を行う工程を行うことを特徴とする針状体の製造方法である。   According to a fourth aspect of the present invention, there is provided the needle-shaped body manufacturing method according to the second aspect, wherein the step of applying the protruding portion material includes applying the protruding portion material to the entire surface of the substrate to which the easily decomposable portion material has been applied. In the method of manufacturing a needle-like body, a step of etching the entire surface of the substrate is performed after the step of peeling the intaglio from the substrate.

請求項5に記載の本発明は、微細な針状体の製造方法において、所望する針状体の形状を凹凸反転させた凹版を形成する工程と、易分解部材料と突起部材料とを攪拌する工程と、前記攪拌した易分解部材料と突起部材料とを基板上に塗布する工程と、前記基板に前記凹版を押圧する工程と、前記基板から凹版を剥離する工程と、を含むことを特徴とする針状体の製造方法である。   According to a fifth aspect of the present invention, in the method for producing a fine needle-like body, the step of forming an intaglio plate having the shape of the desired needle-like body reversed, and the easily decomposable portion material and the protrusion portion material are agitated. Including the steps of: applying the agitated easily decomposable portion material and protrusion material onto the substrate; pressing the intaglio on the substrate; and peeling the intaglio from the substrate. It is the manufacturing method of the needle-shaped body characterized.

本発明の針状体は、易分解部上に突起部を備え、前記易分解部は突起部よりも生体内での溶解速度が速いことを特徴とする。これにより、充分な機械的強度を有した形状、材質を用いても、生体内部で選択的に破損し、突起部を生体内に残留させることが出来る。このため、徐放性を有する経皮投与が可能であり、かつ充分な機械的強度を有した針状体を提供することが可能となる。   The needle-shaped body of the present invention is characterized in that a protrusion is provided on the easily decomposable part, and the easily decomposable part has a faster dissolution rate in vivo than the protrusion. As a result, even when a shape and material having sufficient mechanical strength are used, they can be selectively damaged inside the living body, and the protrusions can remain in the living body. For this reason, it becomes possible to provide a needle-like body that can be transdermally administered with sustained release and has sufficient mechanical strength.

以下、本発明の針状体の説明を行う(図2)。
本発明の針状体は、
基板と、
前記基板上に設けられた易分解部と、
前記易分解部上に設けられた突起部と、を備え、
前記易分解部は、突起部よりも生体内での溶解速度が速いこと
を特徴とする。
Hereinafter, the acicular body of the present invention will be described (FIG. 2).
The needle-shaped body of the present invention is
A substrate,
An easily disassembling part provided on the substrate;
A protrusion provided on the easy disassembly part,
The easily decomposable part has a faster dissolution rate in the living body than the protruding part.

基板は、易分解部、突起部を支持するために設けられる。基板は、易分解部、突起部を支持するだけの機械的強度があれば、特に限定はされない。また、生体に対して低刺激の材質であることが好ましい。また、曲面に対しても面に対して均一な押圧が出来るように柔軟性を持つことが好ましい。   A board | substrate is provided in order to support an easily decomposable part and a projection part. The substrate is not particularly limited as long as it has sufficient mechanical strength to support the easily decomposable portion and the protruding portion. Moreover, it is preferable that it is a material with low irritation to a living body. Moreover, it is preferable to have flexibility so that the surface can be uniformly pressed against the curved surface.

易分解部は、基板表面に層上に形成され、突起部を支持するために設けられる。また、易分解部は、針状体が生体内に穿刺後、生体内で分解することで、生体内に突起部を残留させる。このため、易分解部は、突起部よりも生体内での溶解速度が速いことが求められる。ここで、「生体内で分解する」とは、針状体が皮膚に刺突後の環境で分解することであり、例えば、体液により溶解、融点が生体温度以下などの条件のいずれかを満たせば良い。
具体的には、突起部としてポリ乳酸グリコール酸共重合体を適用した場合、易分解部として、例えば、ポリビニルアルコール、ポリビニルピロリドン、カルボキシメチルセルロース、メチルセルロースなどを用いて良い。
The easily decomposable part is formed on the layer on the substrate surface, and is provided to support the protruding part. Further, the easy-decomposition unit causes the protrusion to remain in the living body by decomposing in a living body after the needle-like body punctures the living body. For this reason, the easily decomposable part is required to have a faster dissolution rate in the living body than the protruding part. Here, “decomposes in vivo” means that the acicular body decomposes in the environment after piercing the skin. For example, it can be dissolved by body fluids and satisfy any of the conditions such as melting point below living body temperature. It ’s fine.
Specifically, when a polylactic acid glycolic acid copolymer is applied as the protruding portion, for example, polyvinyl alcohol, polyvinyl pyrrolidone, carboxymethyl cellulose, methyl cellulose, or the like may be used as the easily decomposable portion.

突起部は、易分解部上に形成され、生体内部へ穿刺するために設けられる。このとき、前記易分解部が生体内で分解することで、突起部は生体内部に残留することが出来る。突起部は、生体内で緩やかに溶解および分解が進行する材料が好ましく、例えば、ポリ乳酸、ポリグリコール酸、ポリ乳酸グリコール酸共重合体、ポリクエン酸、ポリリンゴ酸、ポリアミノ酸などを主材料として用いても良い。突起部は生体内部に残留することが出来るため、突起部に生理活性物質を含むことで、生理活性物質が、突起部の分解や溶解に伴って徐々に放出される。このとき、生理活性物質は、突起部に塗布されていても良いし、内部に含有されていても良い。また、主材料の種類や、主材料の割合を変更することで、生体内における主材料の分解速度や溶解速度を制御すること出来、処方にあわせた生理活性物質の徐放期間、濃度などに対応することが出来る。   The protrusion is formed on the easily decomposable portion and is provided for puncturing into the living body. At this time, the easily decomposable portion is decomposed in the living body, so that the protruding portion can remain inside the living body. The protrusion is preferably made of a material that slowly dissolves and decomposes in the living body. For example, polylactic acid, polyglycolic acid, polylactic glycolic acid copolymer, polycitric acid, polymalic acid, polyamino acid, etc. are used as the main material. May be. Since the protrusion can remain inside the living body, when the protrusion includes a physiologically active substance, the physiologically active substance is gradually released as the protrusion is decomposed or dissolved. At this time, the physiologically active substance may be applied to the protrusions or contained inside. In addition, by changing the type of the main material and the ratio of the main material, the degradation rate and dissolution rate of the main material in the living body can be controlled, and the sustained release period and concentration of the physiologically active substance according to the prescription can be adjusted. Can respond.

本発明の針状体は、易分解部上に突起部を備え、前記易分解部は突起部よりも生体内での溶解速度が速いことを特徴とする。これにより、充分な機械的強度を有した形状、材質を用いても、生体内部で選択的に破損し、突起部を生体内に残留させることが出来る。このため、徐放性を有する経皮投与が可能となり、充分な機械的強度を有した針状体を提供することが可能となる。   The needle-shaped body of the present invention is characterized in that a protrusion is provided on the easily decomposable part, and the easily decomposable part has a faster dissolution rate in vivo than the protrusion. As a result, even when a shape and material having sufficient mechanical strength are used, they can be selectively damaged inside the living body, and the protrusions can remain in the living body. For this reason, percutaneous administration having sustained release becomes possible, and a needle-like body having sufficient mechanical strength can be provided.

また、充分な機械的強度を持った針状体とすることが出来ることにより、突起部を角質層より内側の表皮層や真皮層に残留させることが出来る。このとき、易分解部は生体内で溶解されるため、針状体を用いることで皮膚に形成された穿孔は皮膚の再生機能によって塞がる。このため、角質層のバリア機能を回復した状態で生体内に生理活性物質を封入することが出来、処方後、皮膚の穿孔からの二次感染を抑制することが出来る。   In addition, since the needle-like body having sufficient mechanical strength can be obtained, the protrusion can be left in the epidermis layer or dermis layer inside the stratum corneum. At this time, since the readily decomposable portion is dissolved in the living body, the perforation formed in the skin by using the needle-like body is closed by the skin regeneration function. For this reason, a physiologically active substance can be encapsulated in the living body with the barrier function of the stratum corneum restored, and secondary infection from skin perforation can be suppressed after prescription.

以下、本発明の針状体の製造方法について図1を用いながら、具体的に説明を行う。
本発明の針状体の製造方法は、
所望する針状体の形状を凹凸反転させた凹版を形成する工程と、
基板に易分解部材料を塗布する工程と、
前記易分解部材料を塗布した基板に、突起部材料を塗布する工程と、
前記基板に前記凹版を押圧する工程と、
前記基板から凹版を剥離する工程と、を含むこと
を特徴とする。
Hereinafter, the manufacturing method of the acicular body of the present invention will be specifically described with reference to FIG.
The method for producing the needle-shaped body of the present invention comprises:
Forming an intaglio in which the shape of the desired needle-like body is inverted, and
Applying a readily decomposable part material to the substrate;
Applying a protrusion material to a substrate coated with the easily decomposable material;
Pressing the intaglio on the substrate;
And a step of peeling the intaglio from the substrate.

<凹版を形成する工程>
まず、所望する針状体の形状を凹凸反転させた凹版を形成する。針状体の形状を決定する原版の製造方法としては、針状体の形状に応じて適宜公知の製造方法を用いて良い。このとき、微細加工技術を用いて原版を形成してよく、微細加工技術として、例えば、リソグラフィ法、ウェットエッチング法、ドライエッチング法、サンドブラスト法、レーザー加工法、精密機械加工法などを用いても良い。原版から凹版を形成する方法としては、適宜公知の形状転写法を用いてよい。例えば、Ni電鋳法により、Niの凹版を形成しても良い。
<Process for forming intaglio>
First, an intaglio plate is formed by reversing the shape of the desired needle-like body. As a method for producing the original plate for determining the shape of the needle-like body, a known production method may be appropriately used according to the shape of the needle-like body. At this time, the original plate may be formed using a fine processing technique. For example, a lithography method, a wet etching method, a dry etching method, a sand blasting method, a laser processing method, or a precision machining method may be used as the fine processing technology. good. As a method for forming the intaglio from the original plate, a known shape transfer method may be used as appropriate. For example, a Ni intaglio may be formed by Ni electroforming.

<基板に易分解部材料を塗布する工程>
次に、基板に易分解部材料を塗布する。基板および易分解部材料については、上述した要件を満たすものであれば良い。塗布方法としては、適宜公知の薄膜形成法を用いて良い。例えば、PVD法、CVD法、スピンコート法、スリットコート法、スプレーコート法、ディップコート法などを用いても良い。
<The process of applying the easily decomposable material to the substrate>
Next, the easily decomposable portion material is applied to the substrate. About a board | substrate and an easily decomposable | degradable part material, what is necessary is just to satisfy | fill the requirements mentioned above. As a coating method, a known thin film forming method may be used as appropriate. For example, a PVD method, a CVD method, a spin coating method, a slit coating method, a spray coating method, a dip coating method, or the like may be used.

<突起部材料を塗布する工程>
次に、易分解部材料を塗布した基板に、突起部材料を塗布する。突起部材料としては上述した要件をみたすものであればよく、生理活性物質、生体内で分解する材料など複数の材料を積層/混合しても良い。塗布方法としては、適宜公知の薄膜形成法を用いて良い。例えば、PVD法、CVD法、スピンコート法、スリットコート法、スプレーコート法、ディップコート法などを用いても良い。
<Process for applying protrusion material>
Next, the protrusion material is applied to the substrate to which the easily decomposable material is applied. The protrusion material may satisfy any of the above requirements, and a plurality of materials such as a physiologically active substance and a material that decomposes in vivo may be laminated / mixed. As a coating method, a known thin film forming method may be used as appropriate. For example, a PVD method, a CVD method, a spin coating method, a slit coating method, a spray coating method, a dip coating method, or the like may be used.

また、突起部材料を塗布する工程は、基板と凹版を押圧するとき凹版の凹部に対応する位置のみに選択的に突起部材料を塗布する工程であることが好ましい(図1(a))。基板と凹版を押圧するとき凹版の凹部に対応する位置のみに選択的に突起部材料を塗布することで、針状体先端部に選択的に突起部を形成することが出来る。このとき、突起部材料を塗布する量を調整することで、製造される針状体について、突起部の高さを調整することが出来る。突起部の高さは、皮膚内部の残留深さに対応するため、処方により、薬物を投与する位置が指定された場合(例えば、角質層、表皮層、真皮層など)であっても対応することが出来る。この場合、塗布方法としては、選択的に塗布し、かつ塗布量の調整が可能な方法が望ましい。例えば、液滴吐出法などを用いても良い。   Moreover, it is preferable that the process of apply | coating a projection part material is a process of apply | coating a projection part material selectively only to the position corresponding to the recessed part of an intaglio when pressing a board | substrate and an intaglio (FIG. 1 (a)). When the substrate and the intaglio are pressed, the protrusion can be selectively formed at the tip of the needle-like body by selectively applying the protrusion material only to the position corresponding to the recess of the intaglio. At this time, by adjusting the amount of the protrusion material applied, the height of the protrusion can be adjusted for the manufactured needle-like body. Since the height of the protrusion corresponds to the residual depth inside the skin, it corresponds even when the position to administer the drug is specified by the prescription (eg, stratum corneum, epidermis layer, dermis layer, etc.) I can do it. In this case, as a coating method, a method capable of selectively coating and adjusting the coating amount is desirable. For example, a droplet discharge method or the like may be used.

<基板に凹版を押圧する工程>
次に、基板に凹版を押圧する(図1(b))。このとき、基板と凹版は接触面に均一な負荷がかかるように押圧されることが好ましい。また、用いた材料に応じて、材料の硬化処理(例えば、温度変化など)を行っても良い。
<Step of pressing the intaglio on the substrate>
Next, the intaglio is pressed against the substrate (FIG. 1B). At this time, it is preferable that the substrate and the intaglio are pressed so that a uniform load is applied to the contact surface. Further, depending on the material used, the material may be cured (for example, temperature change).

<凹版を剥離する工程>
次に、基板から凹版を剥離し、針状体を製造する(図1(c))。
このとき、凹版の剥離性を向上させるために、押圧の工程以前に、凹版の表面上に離型効果を増すための離型層を形成してもよい(図示せず)。離型層としては、例えば広く知られているフッ素系の樹脂を用いることが出来る。また、離型層の形成方法としては、適宜公知の薄膜形成法を用いて良い。例えば、PVD法、CVD法、スピンコート法、スリットコート法、スプレーコート法、ディップコート法などを用いても良い。
<Process for peeling intaglio>
Next, the intaglio is peeled from the substrate to produce a needle-like body (FIG. 1 (c)).
At this time, in order to improve the peelability of the intaglio, a release layer for increasing the release effect may be formed on the surface of the intaglio before the pressing step (not shown). As the release layer, for example, a well-known fluorine-based resin can be used. Further, as a method for forming the release layer, a known thin film forming method may be used as appropriate. For example, a PVD method, a CVD method, a spin coating method, a slit coating method, a spray coating method, a dip coating method, or the like may be used.

また、本実施の形態において、突起部材料を塗布する工程は、易分解部材料を塗布した基板全面に突起部材料を塗布する工程であり、基板から凹版を剥離する工程の後、前記基板全面にエッチング処理を行う工程を行うことが好ましい。基板全面に突起部材料を塗布することにより、アライメントを簡略化することが出来る。また、エッチング処理を行うことにより、易溶解部を表出することが出来、図3に示す針状体を製造することが出来る。   Further, in the present embodiment, the step of applying the protrusion material is a step of applying the protrusion material to the entire surface of the substrate to which the easily decomposable portion material has been applied. After the step of peeling the intaglio from the substrate, the entire surface of the substrate is applied. It is preferable to perform an etching process. By applying the protrusion material to the entire surface of the substrate, the alignment can be simplified. Moreover, by performing an etching process, an easily soluble part can be exposed and the acicular body shown in FIG. 3 can be manufactured.

以下、本発明の針状体の製造方法について、別の実施の形態について説明を行う。
本発明の針状体の製造方法は、
所望する針状体の形状を凹凸反転させた凹版を形成する工程と、
易分解部材料と突起部材料とを攪拌する工程と、
前記攪拌した易分解部材料と突起部材料とを基板上に塗布する工程と、
前記基板に前記凹版を押圧する工程と、
前記基板から凹版を剥離する工程と、を含むこと
を特徴とする。
Hereinafter, another embodiment of the method for manufacturing a needle-shaped body of the present invention will be described.
The method for producing the needle-shaped body of the present invention comprises:
Forming an intaglio in which the shape of the desired needle-like body is inverted, and
A step of stirring the easily decomposable part material and the protrusion part material;
Applying the agitated easily decomposable part material and the protrusion part material onto the substrate;
Pressing the intaglio on the substrate;
And a step of peeling the intaglio from the substrate.

<凹版を形成する工程>
<凹版を押圧する工程>
<凹版を剥離する工程>
上記工程については、上述の実施の形態と同様に行って良い。
<Process for forming intaglio>
<Step of pressing intaglio>
<Process for peeling intaglio>
About the said process, you may carry out similarly to the above-mentioned embodiment.

<易分解部材料と突起部材料とを攪拌する工程>
<易分解部材料と突起部材料とを基板上に塗布する工程>
易分解部材料と突起部材料とを攪拌し、基板上に塗布することで、図4に示すような、易分解部内に生理活性物質を内包した構成の針状体を製造することが出来る。塗布方法としては、適宜公知の薄膜形成法を用いて良い。例えば、PVD法、CVD法、スピンコート法、スリットコート法、スプレーコート法、ディップコート法などを用いても良い。
<Step of stirring easily decomposable part material and protrusion part material>
<The process of apply | coating an easily decomposable part material and protrusion part material on a board | substrate>
By stirring the easily decomposable portion material and the protrusion portion material and applying them on the substrate, a needle-like body having a structure in which a physiologically active substance is included in the easily decomposable portion as shown in FIG. 4 can be manufactured. As a coating method, a known thin film forming method may be used as appropriate. For example, a PVD method, a CVD method, a spin coating method, a slit coating method, a spray coating method, a dip coating method, or the like may be used.

以上より、本発明の針状体を製造することが出来る。   From the above, the acicular body of the present invention can be produced.

以下、本発明の針状体の製造方法の実施の一例として、具体的に図1を用いながら説明を行う。当然のことながら、本発明の針状体の製造方法は下記実施例に限定されず、類推できる他の製造方法をも含むものとする。
また、本発明の針状体は、下記の実施例にて作成された針状体に限定されるものではない。
Hereinafter, as an example of an embodiment of the method for manufacturing a needle-shaped body of the present invention, description will be given with reference to FIG. Naturally, the manufacturing method of the needle-shaped body of the present invention is not limited to the following examples, and includes other manufacturing methods that can be analogized.
Moreover, the acicular body of this invention is not limited to the acicular body created in the following Example.

まず、シリコン基板に精密機械加工を用いて、正四角垂(高さ:150μm、底面:60μmx60μm)が、1mm間隔で、6列6行の格子状に36本配列した針状体を形成した。   First, by using precision machining on a silicon substrate, needle-like bodies in which 36 squares (height: 150 μm, bottom surface: 60 μm × 60 μm) were arranged in a grid of 6 columns and 6 rows at 1 mm intervals were formed.

次に、前記シリコン基板で形成された針状体に、メッキ法によりニッケル膜を500μmの厚さに形成し、90℃に加熱した重量パーセント濃度30%の水酸化カリウム水溶液によって前記シリコン基板をウェットエッチングして除去し、ニッケルから成る凹版を作成した。   Next, a nickel film having a thickness of 500 μm is formed on the needle-like body formed of the silicon substrate by plating, and the silicon substrate is wetted with a 30% by weight potassium hydroxide aqueous solution heated to 90 ° C. An intaglio plate made of nickel was prepared by etching.

次に、アクリル基板(厚さ:1mm)に、易分解部材料としてカルボキシメチルセルロースを100μm塗布した。   Next, 100 μm of carboxymethyl cellulose as an easily decomposable part material was applied to an acrylic substrate (thickness: 1 mm).

次に、前記易分解部材料上に、突起部材料として生理活性物質を分散したポリ乳酸グリコール酸共重合体を、基板と凹版を押圧するとき凹版の凹部に対応する位置のみに選択的に突起部材料を塗布した。このとき、突起部材料は液滴吐出法を用いて塗布し、塗布量は7000μmとした(図1(a))。 Next, a polylactic acid glycolic acid copolymer in which a physiologically active substance is dispersed as a protrusion material is selectively protruded only on the position corresponding to the concave portion of the intaglio when pressing the substrate and the intaglio. Part materials were applied. At this time, the protrusion material was applied using a droplet discharge method, and the application amount was set to 7000 μm 3 (FIG. 1A).

次に、易分解部材料および突起部材料を塗布した基板に、凹版を押圧した(図1(b))。   Next, the intaglio was pressed against the substrate coated with the easily decomposable part material and the protrusion part material (FIG. 1B).

次に、基板から凹部を剥離し、針状体を製造した(図1(c))。
このとき、製造された針状体は、針状体先端部から易分解部表面までの距離が50μmであった。
Next, the concave portion was peeled off from the substrate to produce a needle-like body (FIG. 1 (c)).
At this time, the manufactured needle-like body had a distance of 50 μm from the tip of the needle-like body to the surface of the easily decomposable portion.

本発明の針状体は、徐放性を有する経皮投与が求められる分野に対して広範に用いることが期待され、例えば、医療、創薬、化粧品などの様々な分野に用いることが期待できる。   The needle-shaped body of the present invention is expected to be used in a wide range of fields requiring transdermal administration with sustained release, and can be expected to be used in various fields such as medicine, drug discovery, and cosmetics. .

本発明の針状体の製造方法の概略工程図である。It is a schematic process drawing of the manufacturing method of the acicular body of the present invention. 本発明の針状体の一例である。It is an example of the acicular body of this invention. 本発明の針状体の一例である。It is an example of the acicular body of this invention. 本発明の針状体の製造方法により製造可能な針状体の一例である。It is an example of the acicular body which can be manufactured with the manufacturing method of the acicular body of this invention.

符号の説明Explanation of symbols

1……針状体
2……基板
3……突起部
4……易分解部
5……凹版
6……生理活性物質
7……突起部材料
DESCRIPTION OF SYMBOLS 1 ... Needle-like body 2 ... Board | substrate 3 ... Protrusion part 4 ... Decomposable part 5 ... Intaglio 6 ... Bioactive substance 7 ... Protrusion part material

Claims (5)

微細な針状体において、
基板と、
前記基板上に設けられた易分解部と、
前記易分解部上に設けられた突起部と、を備え、
前記易分解部は、突起部よりも生体内での溶解速度が速いこと
を特徴とする針状体。
In fine needles,
A substrate,
An easily disassembling part provided on the substrate;
A protrusion provided on the easy disassembly part,
The easy-to-decompose part has a faster dissolution rate in the living body than the protrusion part.
微細な針状体の製造方法において、
所望する針状体の形状を凹凸反転させた凹版を形成する工程と、
基板に易分解部材料を塗布する工程と、
前記易分解部材料を塗布した基板に、突起部材料を塗布する工程と、
前記基板に前記凹版を押圧する工程と、
前記基板から凹版を剥離する工程と、を含むこと
を特徴とする針状体の製造方法。
In the method for producing fine needles,
Forming an intaglio in which the shape of the desired needle-like body is inverted, and
Applying a readily decomposable part material to the substrate;
Applying a protrusion material to a substrate coated with the easily decomposable material;
Pressing the intaglio on the substrate;
And a step of peeling the intaglio from the substrate.
請求項2に記載の針状体の製造方法であって、
突起部材料を塗布する工程は、基板と凹版を押圧するとき凹版の凹部に対応する位置のみに選択的に突起部材料を塗布する工程であること
を特徴とする針状体の製造方法。
It is a manufacturing method of the acicular body according to claim 2,
The method of manufacturing a needle-like body, wherein the step of applying the protrusion material is a step of selectively applying the protrusion material only to a position corresponding to the concave portion of the intaglio when pressing the substrate and the intaglio.
請求項2に記載の針状体の製造方法であって、
突起部材料を塗布する工程は、易分解部材料を塗布した基板全面に突起部材料を塗布する工程であり、
基板から凹版を剥離する工程の後、
前記基板全面にエッチング処理を行う工程を行うこと
を特徴とする針状体の製造方法。
It is a manufacturing method of the acicular body according to claim 2,
The process of applying the protrusion material is a process of applying the protrusion material to the entire surface of the substrate to which the easily decomposable material is applied,
After the process of peeling the intaglio from the substrate,
A method of manufacturing a needle-like body, comprising performing an etching process on the entire surface of the substrate.
微細な針状体の製造方法において、
所望する針状体の形状を凹凸反転させた凹版を形成する工程と、
易分解部材料と突起部材料とを攪拌する工程と、
前記攪拌した易分解部材料と突起部材料とを基板上に塗布する工程と、
前記基板に前記凹版を押圧する工程と、
前記基板から凹版を剥離する工程と、を含むこと
を特徴とする針状体の製造方法。
In the method for producing fine needles,
Forming an intaglio in which the shape of the desired needle-like body is inverted, and
A step of stirring the easily decomposable part material and the protrusion part material;
Applying the agitated easily decomposable part material and the protrusion part material onto the substrate;
Pressing the intaglio on the substrate;
And a step of peeling the intaglio from the substrate.
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Cited By (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2010069270A (en) * 2008-09-17 2010-04-02 Yoshiichi Tobinaga Device for administration of functional medicine and method and apparatus for manufacturing the same
WO2011043085A1 (en) * 2009-10-08 2011-04-14 株式会社バイオセレンタック Stamper for microneedle sheet, method for manufacturing the stamper, and method for manufacturing microneedle using the stamper
JP2012065826A (en) * 2010-09-22 2012-04-05 Terumo Corp Biological-adhesive sheet and device for bonding sheet
CN102727989A (en) * 2011-04-12 2012-10-17 上海林静医疗器械有限公司 Environmental-friendly and energy-saving degradable disposable vagina dilator and preparation method thereof
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JP2013517907A (en) * 2010-01-29 2013-05-20 アイコン メディカル コーポレーション Biodegradable protrusions on inflatable devices
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US9114238B2 (en) 2007-04-16 2015-08-25 Corium International, Inc. Solvent-cast microprotrusion arrays containing active ingredient
JP2015208479A (en) * 2014-04-25 2015-11-24 凸版印刷株式会社 Stylet device
US9498524B2 (en) 2007-04-16 2016-11-22 Corium International, Inc. Method of vaccine delivery via microneedle arrays
WO2017043627A1 (en) * 2015-09-11 2017-03-16 株式会社バイオセレンタック Microneedle preparation
US9962534B2 (en) 2013-03-15 2018-05-08 Corium International, Inc. Microarray for delivery of therapeutic agent, methods of use, and methods of making
US10195409B2 (en) 2013-03-15 2019-02-05 Corium International, Inc. Multiple impact microprojection applicators and methods of use
US10245422B2 (en) 2013-03-12 2019-04-02 Corium International, Inc. Microprojection applicators and methods of use
US10384046B2 (en) 2013-03-15 2019-08-20 Corium, Inc. Microarray for delivery of therapeutic agent and methods of use
US10384045B2 (en) 2013-03-15 2019-08-20 Corium, Inc. Microarray with polymer-free microstructures, methods of making, and methods of use
KR102042572B1 (en) * 2017-09-29 2019-12-02 아이큐어 주식회사 Micro-structure for non-patch type micro-needle device, and Non-patch type micro-needle device
US10624843B2 (en) 2014-09-04 2020-04-21 Corium, Inc. Microstructure array, methods of making, and methods of use
KR20200122629A (en) * 2019-04-18 2020-10-28 아이큐어 주식회사 Manufacturing method of micro-structure for delivery of bioactive materials to skin
US10857093B2 (en) 2015-06-29 2020-12-08 Corium, Inc. Microarray for delivery of therapeutic agent, methods of use, and methods of making
KR20210010595A (en) * 2019-04-18 2021-01-27 아이큐어 주식회사 Manufacturing method of micro-structure for delivery of bioactive materials to skin
US11052231B2 (en) 2012-12-21 2021-07-06 Corium, Inc. Microarray for delivery of therapeutic agent and methods of use
US11419816B2 (en) 2010-05-04 2022-08-23 Corium, Inc. Method and device for transdermal delivery of parathyroid hormone using a microprojection array

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2002064193A2 (en) * 2000-12-14 2002-08-22 Georgia Tech Research Corporation Microneedle devices and production thereof
WO2006018642A1 (en) * 2004-08-16 2006-02-23 Functional Microstructures Limited Method of producing a microneedle or microimplant
JP2006341089A (en) * 2005-05-13 2006-12-21 Fujikura Ltd Instrument for carrying medicinal material and manufacturing method of the same

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2002064193A2 (en) * 2000-12-14 2002-08-22 Georgia Tech Research Corporation Microneedle devices and production thereof
WO2006018642A1 (en) * 2004-08-16 2006-02-23 Functional Microstructures Limited Method of producing a microneedle or microimplant
JP2006341089A (en) * 2005-05-13 2006-12-21 Fujikura Ltd Instrument for carrying medicinal material and manufacturing method of the same

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