JP2002220304A - Whole heating type drug-containing body, container for the same and heating apparatus for drug transpiration - Google Patents

Whole heating type drug-containing body, container for the same and heating apparatus for drug transpiration

Info

Publication number
JP2002220304A
JP2002220304A JP2001020460A JP2001020460A JP2002220304A JP 2002220304 A JP2002220304 A JP 2002220304A JP 2001020460 A JP2001020460 A JP 2001020460A JP 2001020460 A JP2001020460 A JP 2001020460A JP 2002220304 A JP2002220304 A JP 2002220304A
Authority
JP
Japan
Prior art keywords
drug
heating
container
medicine
containing body
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.)
Pending
Application number
JP2001020460A
Other languages
Japanese (ja)
Inventor
Satoshi Yamazaki
聡 山▲崎▼
Kazunori Yamamoto
和則 山本
Tomoko Ishizuka
朋子 石塚
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.)
Fumakilla Ltd
Original Assignee
Fumakilla 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 Fumakilla Ltd filed Critical Fumakilla Ltd
Priority to JP2001020460A priority Critical patent/JP2002220304A/en
Priority to MXPA03006740A priority patent/MXPA03006740A/en
Priority to US10/433,519 priority patent/US7449154B2/en
Priority to BRPI0116528-3A priority patent/BR0116528B1/en
Priority to AU2001284452A priority patent/AU2001284452B2/en
Priority to IL156333A priority patent/IL156333A/en
Priority to NZ526268A priority patent/NZ526268A/en
Priority to PL01363451A priority patent/PL363451A1/en
Priority to EP01963465A priority patent/EP1356731B1/en
Priority to DE60144442T priority patent/DE60144442D1/en
Priority to KR1020037008234A priority patent/KR100746520B1/en
Priority to CA002473552A priority patent/CA2473552A1/en
Priority to AT01963465T priority patent/ATE505080T1/en
Priority to CNB018217141A priority patent/CN1291647C/en
Priority to PCT/JP2001/007728 priority patent/WO2002060254A1/en
Priority to HU0303003A priority patent/HU228096B1/en
Priority to TW090126077A priority patent/TWI225772B/en
Priority to ARP010105057A priority patent/AR031166A1/en
Priority to MYPI20015024A priority patent/MY136846A/en
Priority to PE2001001109A priority patent/PE20020725A1/en
Priority to EG20011189A priority patent/EG23053A/en
Priority to GCP20021829 priority patent/GC0000383A/en
Publication of JP2002220304A publication Critical patent/JP2002220304A/en
Priority to HR20030529A priority patent/HRP20030529A2/en
Priority to HK03109171.9A priority patent/HK1056666A1/en
Pending legal-status Critical Current

Links

Abstract

PROBLEM TO BE SOLVED: To provide a drug-containing body which enables stable drug transpiration for a long time. SOLUTION: The drug-containing body is smaller than the heating surface 15a of a heating body 15, has a thickness of 3 mm or more, and has a heat loss rate L (L=(h-t)/h×100) of 70% or less. In the foregoing equation, (h) is the heating temperature and (t) is the lowest temperature of the drug- containing body.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は、加熱により薬剤を
蒸散させる全体加熱式の薬剤含有体、及びその薬剤含有
体を内包する薬剤含有体用容器、その薬剤含有体用容器
を加熱して薬剤を蒸散させる薬剤加熱蒸散器具に関す
る。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an overall heating type drug-containing substance for evaporating a drug by heating, a container for the drug-containing substance containing the drug-containing substance, and a drug-containing substance by heating the container for the drug-containing substance. The present invention relates to a chemical heating and evaporating apparatus for evaporating a chemical.

【0002】[0002]

【従来の技術】長期間、例えば12時間より長く使用可
能な薬剤加熱蒸散装置としては液体式が知られている。
この液体式の薬剤加熱蒸散装置は薬剤を溶液に溶かし、
被加熱部に吸い上げて部分的に加熱(以下部分加熱式と
いう)することで薬剤を蒸散している。前述の部分加熱
式の場合、常に新鮮な薬液が供給され安定して薬効を持
続させ易いというメリットがある。しかしながら、薬剤
を溶液に溶かした薬液の保持部(液体容器)と被加熱部
が別になる点と、吸い上げるために薬液の粘度を低く保
つために薬液の薬剤濃度が薄く薬液容量が多くなる点の
2点から、概して製剤が大きくなるというデメリットが
ある。
2. Description of the Related Art As a chemical heating and evaporating apparatus which can be used for a long period of time, for example, longer than 12 hours, a liquid type is known.
This liquid-type drug heating and evaporation device dissolves the drug into the solution,
The drug is evaporated by sucking it into the heated part and heating it partially (hereinafter referred to as a partial heating method). In the case of the above-mentioned partial heating type, there is an advantage that a fresh chemical solution is always supplied, and the medicinal effect is easily maintained. However, there is a difference between a holding section (liquid container) for a drug solution in which a drug is dissolved in a solution and a heated section, and a point that the drug concentration of the drug solution is thin and the volume of the drug solution is large in order to keep the viscosity of the drug solution low for sucking up. From the two points, there is a disadvantage that the preparation is generally large.

【0003】薬剤加熱蒸散装置としては、薬剤含有体の
全体を発熱体で加熱して薬剤を蒸散する全体加熱式の装
置が知られている。この全体加熱式の装置の場合、薬剤
保管部と被加熱部が当然一体化されており、製剤がコン
パクトに設計可能である。
[0003] As a drug heating and evaporating apparatus, there is known an overall heating type apparatus for evaporating a drug by heating an entire drug-containing body with a heating element. In the case of this whole heating type apparatus, the medicine storage section and the heated section are naturally integrated, and the formulation can be designed compact.

【0004】また、前述の部分加熱式は、薬剤の濃度を
一定に保たなければ安定して薬剤を蒸散させることがで
きない。すなわち、薬以外に溶剤も空気中に放出しなけ
ればならなくなる。それに対して全体加熱式では、前述
のことが必要がなく、余分な溶剤などを蒸散させないか
ら、環境に対して配慮がなされている。
[0004] Further, in the above-mentioned partial heating method, unless the concentration of the drug is kept constant, the drug cannot be evaporated stably. That is, the solvent must be released into the air in addition to the drug. On the other hand, the whole heating method does not need the above-mentioned operation and does not evaporate excess solvent and the like, so that consideration is given to the environment.

【0005】[0005]

【発明が解決しようとする課題】前述の全体加熱式の薬
剤含有体を用いた全体加熱式の薬剤加熱蒸散装置は、長
期間安定して薬剤を蒸散させることが非常に困難であっ
た。すなわち、従来の全体加熱式の薬剤加熱蒸散装置に
用いる全体加熱式の薬剤含有体は厚みが2mm程度であ
るから、薬剤含有量に限度があり、長期間薬剤を蒸散で
きない。
However, it has been very difficult to stably evaporate the medicine for a long time in the whole-heating-type medicine heating and evaporating apparatus using the above-mentioned whole-heating-type medicine-containing substance. That is, since the whole-heating-type drug-containing material used in the conventional whole-heating-type drug heating and evaporating apparatus has a thickness of about 2 mm, the drug content is limited, and the drug cannot be evaporated for a long time.

【0006】前述の薬剤含有体の平面形状を大きくすれ
ば薬剤含有量が多くなるが、薬剤加熱蒸散装置は家庭に
おいて使用され持ち運びや置き場所のスペースなどの面
から平面形状に大きさの制限があるし、発熱体の消費電
力の関係から発熱体の平面形状に大きさの制限があるの
で、前述の薬剤含有体の平面形状の大きさには限度があ
る。
[0006] If the planar shape of the above-mentioned drug-containing body is increased, the drug content is increased. However, the drug heating and evaporating apparatus is used at home, and its size is limited to a planar shape in view of the space for carrying and placing. In addition, since the size of the planar shape of the heating element is limited due to the power consumption of the heating element, the size of the planar shape of the drug-containing body is limited.

【0007】そこで、本発明は前述の課題を解決できる
ようにした全体加熱式の薬剤含有体及び薬剤含有体用容
器、薬剤加熱蒸散器具を提供することを目的とする。
SUMMARY OF THE INVENTION It is an object of the present invention to provide a whole-heating type medicine-containing body, a medicine-containing body container, and a medicine heating and evaporating apparatus which can solve the above-mentioned problems.

【0008】[0008]

【課題を解決するための手段】本発明者等は、発熱体の
大きさ、発熱温度、薬剤含有体からの薬剤蒸散具合等に
基づき12時間より長く安定して薬剤を蒸散できる全体
加熱式の薬剤含有体を鋭意研究、実験によって見出し
た。
SUMMARY OF THE INVENTION The present inventors have developed an overall heating type that can stably evaporate a drug for more than 12 hours based on the size of the heating element, the heat generation temperature, the degree of drug evaporation from the drug-containing body, and the like. Drug-containing substances have been found through intensive studies and experiments.

【0009】本発明の全体加熱式の薬剤含有体は、厚み
3mm以上で、加熱温度hと薬剤含有体の最低温度tよ
り式1によって求まる熱損率Lが、70%以下であるこ
とを特徴とする全体加熱式の薬剤含有体である。 式1…L=(h−t)/h×100
The whole heating type drug-containing material of the present invention has a thickness of 3 mm or more, and the heat loss rate L obtained by the formula 1 from the heating temperature h and the minimum temperature t of the drug-containing material is 70% or less. It is a drug-containing substance of the whole heating type. Formula 1 L = (ht) / h × 100

【0010】前記薬剤含有体の材質は、無機及び/又は
有機粉末を主材とする粘着体及び/又は焼結体及び/又
は打錠体、パルプを主材とする紙及び/又は不織布、プ
ラスチックを主材とする不織布及び/又は織物、その他
動植物由来物質を主材とする不織布及び/又は織物、プ
ラスチックを主材とするフォーム、プラスチック練り込
み体、植物乾燥体、ゲル、ジェル、シリカゲルの少なく
とも一つから構成されている。
[0010] The material of the drug-containing substance may be an adhesive and / or a sintered and / or tablet made mainly of an inorganic and / or organic powder, a paper and / or non-woven fabric made mainly of pulp, and a plastic. Non-woven fabric and / or woven fabric mainly composed of: non-woven fabric and / or woven fabric mainly composed of animal and plant-derived substances; foam mainly composed of plastic; kneaded plastic, dried plant, gel, gel, silica gel It is composed of one.

【0011】前記薬剤含有体は、一つ以上の通気孔を持
つ薬剤含有体用容器に内包させて使用することが好まし
い。
Preferably, the drug-containing substance is used by being enclosed in a container for the drug-containing substance having one or more air holes.

【0012】本発明の薬剤含有体用容器は、一つ以上の
通気孔を有し、薬剤含有体を内包できる大きさで、その
内面と薬剤含有体の表面との距離が、1〜10mmであ
ること特徴とする薬剤含有体用容器である。
The container for a drug-containing substance of the present invention has at least one vent hole, is large enough to contain the drug-containing substance, and has a distance of 1 to 10 mm between the inner surface and the surface of the drug-containing substance. A container for a drug-containing body, which is characterized in that:

【0013】本発明の薬剤加熱蒸散器具は、請求項4記
載の薬剤含有体用容器が載置される発熱体を備え、この
発熱体の発熱面の角度が0〜70度であること特徴とす
る薬剤加熱蒸散器具である。
According to a fourth aspect of the present invention, there is provided an apparatus for heating and evaporating a medicine, comprising a heating element on which the container for a medicine-containing body according to claim 4 is mounted, wherein an angle of a heating surface of the heating element is 0 to 70 degrees. It is a chemical heating and evaporation device.

【0014】[0014]

【作 用】本発明の全体加熱式の薬剤含有体によれば、
長期間安定して薬剤を蒸散できる。
[Action] According to the drug substance of the present invention which is entirely heated,
Can evaporate drugs stably for a long period of time.

【0015】本発明の薬剤含有体用容器によれば、容器
の内面と薬剤含有体の表面との間を薬剤蒸気がスムーズ
に通過し、通気孔から外部に拡散する。
According to the container for a drug-containing body of the present invention, the drug vapor smoothly passes between the inner surface of the container and the surface of the drug-containing body, and diffuses outside from the vent hole.

【0016】本発明の薬剤加熱蒸散器具によれば、発熱
体によって薬剤含有体の全体を加熱できる。また、発熱
体の発熱面を傾斜させることでコンパクトに設計でき
る。
According to the drug heating and evaporating device of the present invention, the entire drug-containing body can be heated by the heating element. In addition, a compact design can be achieved by inclining the heating surface of the heating element.

【0017】[0017]

【発明の実施の形態】薬剤加熱蒸散装置を図1に基づい
て説明する。薬剤加熱蒸散器具1と、薬剤含有体用容器
2と、全体加熱式の薬剤含有体3で薬剤加熱蒸散装置を
形成する。前記薬剤加熱蒸散器具1は、下部器具10と
上部器具11をビス12で連結した形状である。前記下
部器具10は一側面に開口した薬剤含有体挿入部13
と、この薬剤含有体挿入部13の下部を下面に開口する
空気取入部14を有し、発熱体15が取付けてある。こ
の発熱体15の発熱面15aは水平に対して斜めで、前
記薬剤含有体挿入部13に開口している。前記下部器具
10にスイッチ部16、押釦17、ランプ18が取付け
てある。この押釦17を押すことでスイッチ部16がO
Nして発熱体15に通電されて発熱し、ランプ18が点
灯する。
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS A chemical heating and evaporating apparatus will be described with reference to FIG. The medicine heating and evaporating apparatus 1, the medicine-containing body container 2, and the whole heating-type medicine-containing body 3 form a medicine heating and evaporating apparatus. The drug heating and evaporation device 1 has a shape in which a lower device 10 and an upper device 11 are connected by a screw 12. The lower device 10 has a drug-containing body insertion portion 13 opened on one side.
And an air intake section 14 opening the lower part of the medicine-containing body insertion section 13 on the lower surface, and a heating element 15 is attached. The heat generating surface 15a of the heat generating body 15 is oblique to the horizontal and opens to the medicine-containing body insertion portion 13. A switch unit 16, a push button 17, and a lamp 18 are attached to the lower device 10. When the push button 17 is pressed, the switch section 16
N, the heating element 15 is energized to generate heat, and the lamp 18 is turned on.

【0018】前記薬剤含有体用容器2は、図2〜図7に
示すように、上面板20と下面板21と前面板22と後
面板23と両側面板24で略箱形状で、前面板22に出
口側の通気孔25が形成され、後面板23に入口側の通
気孔26が形成してある。前記下面板21と前面板22
との間に隙間27が有り、その下面板21は着脱自在で
ある。前記下面板21の内面には複数の突起21aが前
後方向に向けて一体的に設けてある。前記前面板22の
内面に複数の前縦片22aが一体的に設けてある。この
前面板22の表面にインジケータ28が取付けてある。
前記後面板23の内面に複数の後縦片23aが一体的に
設けてある。この後縦片23aは前記突片21aの後部
寄りに接する。前記上面板20の内面における両側寄り
に、丸棒形状の杆体20aが下向に一体的に設けてあ
る。この薬剤含有体用容器2は、薬剤含有体挿入部13
内に挿入され、下面板21が発熱体15の発熱面15a
に接するとともに、ストッパ19に当たる。この薬剤含
有体保持容器2は、薬剤含有体挿入部13内に挿入さ
れ、下面板21が発熱体15の発熱面15aに接すると
共に、ストッパ19に当たる。
As shown in FIGS. 2 to 7, the medicine-containing container 2 has a substantially box-like shape including an upper plate 20, a lower plate 21, a front plate 22, a rear plate 23, and both side plates 24. An outlet-side vent hole 25 is formed in the rear panel 23, and an inlet-side vent hole 26 is formed in the rear face plate 23. The lower plate 21 and the front plate 22
And a lower surface plate 21 thereof is detachable. A plurality of protrusions 21a are integrally provided on the inner surface of the lower plate 21 in the front-rear direction. A plurality of front vertical pieces 22a are integrally provided on the inner surface of the front plate 22. An indicator 28 is attached to the surface of the front plate 22.
A plurality of rear vertical pieces 23a are integrally provided on the inner surface of the rear plate 23. Thereafter, the vertical piece 23a contacts the rear portion of the protruding piece 21a. A round bar-shaped rod 20a is integrally provided downward on both sides of the inner surface of the upper surface plate 20. The medicine-containing body container 2 includes a medicine-containing body insertion portion 13.
And the lower surface plate 21 is connected to the heating surface 15 a of the heating element 15.
And contacts the stopper 19. The medicine-containing body holding container 2 is inserted into the medicine-containing body insertion portion 13, and the lower surface plate 21 contacts the heat-generating surface 15 a of the heat-generating body 15 and hits the stopper 19.

【0019】前記薬剤含有体3は加熱することで蒸散す
る薬剤が含浸された矩形板状で、前記下面板21を外す
ことで薬剤含有体用容器2内に設けられる。図8に示す
ように、薬剤含有体3の表面が前縦片22a、後縦片2
3a、両側の杆体20aにそれぞれ接し、この薬剤含有
体用容器2の内面(内壁)と薬剤含有体3の表面との間
に薬剤蒸気が通過するための隙間がある。前記薬剤含有
体3の下面が突起21aに接する。この突起21aの突
出寸法で発熱体15と薬剤含有体3との間の距離を変え
ることで薬剤蒸散量を調整する。また、薬剤蒸散量の調
整は、図示していないが下面板21の下部に突起などを
設けて発熱体15との距離を変化させることでも可能で
ある。
The medicine-containing body 3 has a rectangular plate shape impregnated with a medicine that evaporates when heated, and is provided in the medicine-containing body container 2 by removing the lower plate 21. As shown in FIG. 8, the surface of the drug-containing body 3 has a front vertical piece 22a and a rear vertical piece 2a.
3a, there is a gap between the inner surface (inner wall) of the container 2 for the drug-containing body and the surface of the drug-containing body 3 in contact with the rods 20a on both sides. The lower surface of the drug-containing body 3 contacts the projection 21a. The amount of drug evaporation is adjusted by changing the distance between the heating element 15 and the drug-containing body 3 according to the projection size of the projection 21a. Although not shown, it is also possible to adjust the amount of chemical vaporization by providing a projection or the like below the lower plate 21 to change the distance from the heating element 15.

【0020】前記薬剤含有体用容器2を図1に示すよう
に、薬剤加熱蒸散器具1内に設けた状態で発熱体15を
発熱することで、空気取入部14から空気が流入し、矢
印で示すように入口側の通気孔26から前述の隙間に流
入し、出口側の通気孔25から流出して器具の外部に流
出する。つまり、発熱体15を発熱することで矢印で示
すように空気の上昇気流が発生し、蒸散した薬剤がスム
ーズに拡散される。
As shown in FIG. 1, by heating the heating element 15 with the medicine-containing body container 2 provided in the medicine heating and evaporating apparatus 1, air flows in from the air intake section 14 and is indicated by an arrow. As shown, the gas flows into the above-mentioned gap from the vent hole 26 on the inlet side, flows out of the vent hole 25 on the outlet side, and flows out of the appliance. That is, as the heating element 15 generates heat, an upward airflow of air is generated as shown by an arrow, and the evaporated medicine is smoothly diffused.

【0021】次に、前記薬剤含有体用容器2について詳
細に説明する。形状は、薬剤含有体3を収容できると共
に、一つ以上の通気孔を有すれば良い。つまり、薬剤含
有体用容器2内に通気孔で空気が流通する形状であれば
良い。材質は、ポリオレフィン系、ポリエステル系、ポ
リアミド系、ポリサルフォンから選ばれる一種以上であ
る。薬剤含有体3の表面と容器の内面との間に隙間の大
きさ、つまり距離は1〜10mm、好ましくは1〜5m
mである。つまり、前述の隙間がないと薬剤蒸気が通過
しなくなり、その隙間が大きすぎると保温性が確保でき
なくなるので、前述の距離は薬剤蒸気が通過するための
最低必要な距離で、保温性を確保するために1〜10m
mの範囲で、好ましくは1〜5mmの範囲である。
Next, the medicine-containing container 2 will be described in detail. The shape only needs to be able to accommodate the drug-containing body 3 and have one or more air holes. That is, any shape may be used as long as air can flow through the vent hole in the medicine-containing body container 2. The material is at least one selected from polyolefin, polyester, polyamide, and polysulfone. The size of the gap between the surface of the drug-containing body 3 and the inner surface of the container, that is, the distance is 1 to 10 mm, preferably 1 to 5 m
m. In other words, if there is no gap, the medicine vapor will not pass, and if the gap is too large, it will not be possible to secure heat retention. 1-10m to do
m, preferably in the range of 1 to 5 mm.

【0022】次に、薬剤含有体3の表面と容器の内面と
の距離を変え、下記条件で距離による薬剤蒸散量を測定
した試験例を説明する。 (条件)薬剤含有体3は、打錠体に有効成分としてプラ
レトリンを3000mg配合したものを用いた。薬効成
分量は、シリカゲルにトラップした成分をアセトンで留
去し、ガスクロで定量した。評価は、薬剤蒸散量の対規
定量が90%以上を合格とした。試験結果は下記表1に
示すとおりであった。
Next, a description will be given of a test example in which the distance between the surface of the drug-containing body 3 and the inner surface of the container was changed, and the amount of drug evaporation was measured according to the distance under the following conditions. (Conditions) As the drug-containing material 3, a tableting product containing 3000 mg of praletrin as an active ingredient was used. The amount of the medicinal component was determined by distilling off the component trapped on silica gel with acetone and gas chromatography. In the evaluation, 90% or more of the specified amount of the drug transpiration with respect to the specified amount was passed. The test results were as shown in Table 1 below.

【0023】[0023]

【表1】 [Table 1]

【0024】この試験結果から、前述の薬剤含有体3の
表面と容器の内面との距離は1〜10mmの範囲である
ことが判明した。
From this test result, it was found that the distance between the surface of the drug-containing material 3 and the inner surface of the container was in the range of 1 to 10 mm.

【0025】前記インジケータ28は加熱により色変化
する物質を用いて加熱時間、つまり薬剤残存量を表示す
るものである。このインジケータは、外部から見え易
く、外気温の影響をうけ難く、薬剤蒸散の妨げになり難
い位置に取付けられる。
The indicator 28 displays the heating time, that is, the remaining amount of the medicine, using a substance that changes color by heating. This indicator is mounted at a position that is easily visible from the outside, is not easily affected by the outside air temperature, and is not likely to hinder the evaporation of the drug.

【0026】次に、薬剤加熱蒸散器具1の第2の実施の
形態を図9と図10に基づいて説明する。表面に開口し
た凹陥部30と、この凹陥部30を開閉する蓋31と、
電源用差し込みプラグ32を備えている。前記凹陥部3
0の底面30aは水平に対して斜めで、その底面30a
に発熱体15の発熱面15aが突出している。前記凹陥
部30は通気部33で下面に開口している。
Next, a second embodiment of the chemical heating and evaporating apparatus 1 will be described with reference to FIGS. A concave portion 30 opened on the surface, a lid 31 for opening and closing the concave portion 30,
A power supply plug 32 is provided. The recess 3
0 is inclined with respect to the horizontal, and its bottom surface 30a
The heat generating surface 15a of the heat generating body 15 protrudes. The concave portion 30 is opened at the lower surface by a ventilation portion 33.

【0027】図11に示すように薬剤含有体用容器2を
蓋31を開けて凹陥部30内に挿入し、その下面板21
を発熱体15の発熱面15aに接する。発熱体15を発
熱することで矢印で示すように空気の流れが生じ、薬剤
蒸散がスムーズに行われる。
As shown in FIG. 11, the medicine-containing container 2 is opened and inserted into the recess 30 by opening the lid 31, and the lower plate 21
Is in contact with the heating surface 15a of the heating element 15. By generating heat from the heating element 15, a flow of air is generated as shown by an arrow, and the medicine evaporates smoothly.

【0028】本発明に係る薬剤加熱蒸散器具は、前述の
ように発熱体15が水平に対して傾斜していることによ
って、器具をコンパクトに設計できる。その理由は、加
熱した際に発生する薬剤を乗せた上昇気流上に障害物が
あると薬剤のロスや器具の汚れといったデメリットが発
生し、水平の発熱体上に置いた場合、気流をスムーズに
通すためのアーチが必要になり器具が大きくなるからで
ある。前記発熱体15の最大角度は70度である。ま
た、発熱体15は器具の大きさを考えなければ水平でも
良い。したがって、発熱体15の器具への固定角度は、
0〜70度の範囲であれば良い。
Since the heating element 15 is inclined with respect to the horizontal as described above, the apparatus can be designed to be compact. The reason is that if there is an obstacle on the rising airflow carrying the medicine generated when heated, disadvantages such as loss of medicine and contamination of equipment will occur, and when placed on a horizontal heating element, the airflow will be smoother This is because an arch for passing through is required, and the equipment becomes large. The maximum angle of the heating element 15 is 70 degrees. The heating element 15 may be horizontal if the size of the appliance is not considered. Therefore, the fixing angle of the heating element 15 to the appliance is:
The angle may be in the range of 0 to 70 degrees.

【0029】前記器具の使用時の外郭温度は60℃以下
である。
[0029] The shell temperature during use of the device is 60 ° C or less.

【0030】次に全体加熱式の薬剤含有体3について説
明する。薬剤含有体3は図12に示すように矩形板状
で、平面大きさは発熱体15の発熱面15aの平面大き
さよりも小さい。このことによって、薬剤含有体3の全
体を発熱体によって直接、又は間接に加熱できる。
Next, the whole heating type drug-containing body 3 will be described. As shown in FIG. 12, the medicine containing body 3 has a rectangular plate shape, and the plane size is smaller than the plane size of the heating surface 15 a of the heating body 15. As a result, the entire medicine-containing body 3 can be directly or indirectly heated by the heating element.

【0031】前記薬剤含有体3は薬剤を含有できる材
質、例えば無機及び/又は有機粉末を主材とする粘結体
及び/又は焼結体及び/又は打錠体、パルプを主材とす
る紙及び/又は不織布、プラスチックを主材とする不織
布及び/又は織物、その他動植物由来物質を主材とする
不織布及び/又は織物、プラスチックを主材とするフォ
ーム、プラスチック練り込み体、植物乾燥体、ゲル、ジ
ェル、シリカゲルの少なくとも一つから構成されてい
る。
The drug containing body 3 is made of a material capable of containing a drug, for example, a binder and / or a sintered body and / or a tableted body mainly containing inorganic and / or organic powder, and a paper mainly containing pulp. And / or non-woven fabrics, non-woven fabrics and / or fabrics mainly composed of plastics, non-woven fabrics and / or fabrics mainly composed of animal and plant-derived substances, foams mainly composed of plastics, kneaded plastics, dried plants, gels , Gel and silica gel.

【0032】前記無機及び/又は有機粉末を主材とする
粘結体及び/又は打錠体とは、特開平6−192008
記載の固形体。主材であるカルシウムのリン酸塩類の他
に、粘結時に必要な賦形剤(結晶セルロース)や結合材
(CMC)を、焼結時に必要な結合剤(プラスチック粉
末、ナイロンパウダー)、打錠時に必要な滑沢剤(ステ
アリン酸マグネシウム)などを含む。
The binder and / or tablet containing the inorganic and / or organic powder as a main component is described in JP-A-6-192008.
The solid described. In addition to calcium phosphates, which are the main ingredients, excipients (crystalline cellulose) and binders (CMC) required for caking, binders (plastic powder, nylon powder) required for sintering, tableting Sometimes contains necessary lubricants (magnesium stearate).

【0033】前記パルプを主材とする紙及び/又は不織
布とは、一般的にいうところの紙であるが、プラスチッ
クと混合したものもある。製造方法は、水ですく他、熱
や糊で接着するものがある。
The paper and / or non-woven fabric containing pulp as a main material is generally referred to as paper, but may be mixed with plastic. As for the manufacturing method, there is a method of bonding with heat or glue other than water.

【0034】プラスチックを主材とする不織布及び/又
は織物とは、いわゆる不織布と織物である。不織布の製
造方法は大きく分けて熱や糊を使う乾式と、水や有機溶
剤で繊維を絡める(すく)湿式がある。
The nonwoven fabric and / or woven fabric mainly composed of plastic is a so-called nonwoven fabric and woven fabric. Nonwoven fabric manufacturing methods are roughly classified into a dry method using heat or glue, and a wet method in which fibers are entangled with water or an organic solvent.

【0035】その他、動物由来物質を主材とする不織布
及び/又は織物とは、いわゆる不織布と織物の材料とし
て絹や綿、麻、ケナフ、ゼラチンなどを用いたものであ
る。
In addition, the nonwoven fabric and / or woven fabric mainly composed of an animal-derived substance is a material using so-called nonwoven fabric and woven fabric, such as silk, cotton, hemp, kenaf, and gelatin.

【0036】プラスチックを主材とするフォームとは、
クッション材やスポンジとして主に使用されているポリ
ウレタンフォームやポリエチレンフォーム、ポリプロピ
レンフォームや発泡スチロールを基本的に示すが、広義
にはポーラスなプラスチック全般を意味する。つまり薬
剤を含浸可能な孔のあいたプラスチックのことである。
The foam mainly composed of plastic is as follows.
Polyurethane foam, polyethylene foam, polypropylene foam and styrofoam, which are mainly used as cushioning materials and sponges, are basically shown, but in a broad sense they mean all kinds of porous plastics. In other words, it is a plastic with holes that can be impregnated with a drug.

【0037】プラスチック練り込み体とは、薬剤と、蒸
散や内部移行のための必要に応じて配合する可塑剤を、
プラスチックと混合し成型したものである。
The plastic kneaded body is a chemical compound and a plasticizer compounded as necessary for evaporation and internalization.
It is mixed with plastic and molded.

【0038】植物乾燥体とは、いわゆるドライフラワー
やドライフルーツを指し、ポプリやへちま、木材などが
例示できる。
The dried plant refers to so-called dried flowers and dried fruits, and examples thereof include potpourri, hemp, and wood.

【0039】ゲルとは、ゼラチンやカラギーナン、ジェ
ランガムといったゲル化剤によって固体化したものはも
ちろんのこと、高分子吸水剤や高分子吸油剤によって固
体化したものも含める。
Gels include those solidified by gelling agents such as gelatin, carrageenan and gellan gum, as well as those solidified by polymer water-absorbing agents and polymer oil-absorbing agents.

【0040】ジェルとは、無機及び/又は有機粉末に薬
剤と溶剤を混ぜ、増粘しペースト状にしたもの。これは
加熱によって薬剤と溶剤が蒸散した後に元の粉末に戻り
含有体が崩壊するので、終点(薬効が消滅した時点)が
明確である。
Gel is a paste obtained by mixing an inorganic and / or organic powder with a drug and a solvent to increase the viscosity and paste. Since the drug and the solvent evaporate by heating and return to the original powder and disintegrate, the end point (when the medicinal effect has disappeared) is clear.

【0041】前記薬剤含有体3に含有する薬剤は、蒸気
圧が1.0×10−5mmHg以上を目安とした殺虫
剤、主としてピレスロイド系殺虫剤、殺菌剤、忌避剤、
成長制御剤、芳香剤、消臭剤などである。前記薬剤含有
体3に薬剤と共に配合する物質は、熱安定剤、酸化防止
剤、紫外線吸収剤、染料、顔料、芳香・消臭剤、各種効
力共力剤などである。
The drug contained in the drug substance 3 is an insecticide having a vapor pressure of 1.0 × 10 −5 mmHg or more, mainly a pyrethroid insecticide, a bactericide, a repellent,
Growth regulators, fragrances, deodorants and the like. The substances to be mixed with the medicine in the medicine containing body 3 include a heat stabilizer, an antioxidant, an ultraviolet absorber, a dye, a pigment, an aroma / deodorant, and various synergists.

【0042】次に、本発明の主とする目的である、加熱
によって長期間(12時間より長く)薬剤を蒸散できる
ようにした点について説明する。 (1)薬剤含有体3の厚みは3mm以上である。 (2)熱損率L(L=(h−t)/h×100)は70
%以下である。 但し、hは加熱温度、tは薬剤含有体3の最低温度であ
る。
Next, a description will be given of the main object of the present invention, in which a drug can be evaporated for a long time (more than 12 hours) by heating. (1) The thickness of the drug-containing body 3 is 3 mm or more. (2) The heat loss rate L (L = (ht) / h × 100) is 70
% Or less. Here, h is the heating temperature, and t is the lowest temperature of the drug substance 3.

【0043】前記加熱して蒸散とは、被発熱体の最高温
度が常温より5℃以上となるように加熱して薬剤を空気
中に放出することである。前記薬剤含有体3の厚みと
は、発熱体に最も近い面(下面)から最も離れている面
(天面)までの寸法である。薬剤含有体の最も薄い部分
ではない。例えば図12に仮想線で示すように薬剤含有
体3の薄い側の面3aを発熱体15に乗せて使う場合
は、厚い側の面3bの長さlが厚みとなる。重要なの
は、発熱体から離れても熱を損失しない熱効率の良い薬
剤含有体の材質、物性である。
The above-mentioned heating and transpiration means that the medicine is heated so that the maximum temperature of the object to be heated is 5 ° C. or more higher than the ordinary temperature and the medicine is released into the air. The thickness of the drug-containing body 3 is a dimension from a surface closest to the heating element (lower surface) to a surface farthest away (top surface). Not the thinnest part of the drug substance. For example, as shown by a virtual line in FIG. 12, when the thin side surface 3a of the medicine-containing body 3 is used on the heating element 15, the length 1 of the thick side surface 3b is the thickness. What is important is the material and physical properties of the drug-containing substance having high thermal efficiency that does not lose heat even when it is separated from the heating element.

【0044】前記熱損率とは、熱伝導性と同義である。
使用する発熱体は蒸散させる薬剤に合わせて温度設定す
れば良いが、エネルギーを無駄無く効率的に利用するた
めには熱損率を70%以下とする必要がある。前記熱損
率の算出の基準となる加熱温度hとは、発熱体の最高表
面温度である。
The heat loss ratio is synonymous with the thermal conductivity.
The temperature of the heating element to be used may be set according to the chemical to be evaporated, but the heat loss rate needs to be 70% or less in order to efficiently use energy without waste. The heating temperature h, which is a reference for calculating the heat loss rate, is the maximum surface temperature of the heating element.

【0045】次に、薬剤含有体3の厚みと熱損率を変え
て下記条件で薬剤蒸散時間を測定した試験例を説明す
る。 (条件)マットタイプの加熱蒸散器具を用いた。薬剤含
有体は、発熱体の上に直に置いた。測定には、熱電対式
温度計を用いた。測定は、恒温条件下において行った。
評価は、薬剤蒸散量の対規定量が90%以上で、薬剤蒸
散時間が12時間より長い場合を○としている。薬剤含
有体には、パルプマットに有効成分としてテラレスリン
を配合したものを用いた。有効成分量は、シリカゲルに
トラップした成分をアセトンで留去し、ガスクロロで定
量した。試験結果は下記表2に示すとおりであった。
Next, a description will be given of a test example in which the drug evaporation time was measured under the following conditions while changing the thickness and the heat loss rate of the drug containing material 3. (Conditions) A mat-type heat evaporation device was used. The drug substance was placed directly on the heating element. A thermocouple thermometer was used for the measurement. The measurement was performed under constant temperature conditions.
In the evaluation, a case where the prescribed amount of the drug evaporation amount is 90% or more and the drug evaporation time is longer than 12 hours is indicated by “○”. As the drug-containing material, a pulp mat mixed with terrareslin as an active ingredient was used. The amount of the active ingredient was determined by distilling off the component trapped on the silica gel with acetone and measuring with gas chloro. The test results were as shown in Table 2 below.

【0046】[0046]

【表2】 [Table 2]

【0047】この試験結果から、厚みが3mm未満であ
れば十分な薬剤蒸散量が得られるが、薬剤蒸散時間が1
2時間より短く、厚みが13.8mm(3mm以上)で
あっても熱損失が75.1%(70%以上)であると十
分な薬剤蒸散量が得られなかった。このことから、薬剤
含有体の厚みは3mm以上で、熱損率が70%以下とす
ることで、12時間より長い時間安定して薬剤蒸散でき
ることが判明した。
From this test result, a sufficient amount of drug evaporation can be obtained if the thickness is less than 3 mm.
Even when the heat loss was shorter than 2 hours and the heat loss was 75.1% (70% or more) even when the thickness was 13.8 mm (3 mm or more), a sufficient amount of drug evaporation could not be obtained. From this, it has been found that by setting the thickness of the drug-containing material to 3 mm or more and the heat loss rate to 70% or less, the drug can stably evaporate for more than 12 hours.

【0048】[0048]

【発明の効果】本発明の全体加熱式の薬剤含有体によれ
ば、長期間安定して薬剤を蒸散できる。
According to the whole heating type drug-containing material of the present invention, the drug can be evaporated stably for a long period of time.

【0049】本発明の薬剤含有体用容器によれば、容器
の内面と薬剤含有体の表面との間を薬剤蒸気がスムーズ
に通過し、通気孔から外部に拡散する。
According to the container for a drug-containing body of the present invention, the drug vapor smoothly passes between the inner surface of the container and the surface of the drug-containing body, and diffuses outside from the vent hole.

【0050】本発明の薬剤加熱蒸散器具によれば、発熱
体によって薬剤含有体の全体を加熱できる。また、発熱
体の発熱面を傾斜させることでコンパクトに設計でき
る。
According to the medicine heating and evaporating apparatus of the present invention, the whole medicine-containing body can be heated by the heating element. In addition, a compact design can be achieved by inclining the heating surface of the heating element.

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

【図1】薬剤加熱蒸散装置の断面図である。FIG. 1 is a sectional view of a chemical heating and evaporating apparatus.

【図2】薬剤含有体用容器の平面図である。FIG. 2 is a plan view of a medicine-containing body container.

【図3】薬剤含有体用容器の正面図である。FIG. 3 is a front view of the medicine-containing container.

【図4】薬剤含有体用容器の右側面図である。FIG. 4 is a right side view of the medicine-containing container.

【図5】薬剤含有体用容器の背面図である。FIG. 5 is a rear view of the medicine-containing container.

【図6】薬剤含有体用容器の底面図である。FIG. 6 is a bottom view of the medicine-containing body container.

【図7】図3のA−A断面図である。FIG. 7 is a sectional view taken along the line AA of FIG. 3;

【図8】使用状態の断面図である。FIG. 8 is a sectional view in a use state.

【図9】薬剤加熱蒸散器具の第2の実施の形態を示す平
面図である。
FIG. 9 is a plan view showing a second embodiment of the drug heating and evaporation device.

【図10】図9のB−B断面図である。FIG. 10 is a sectional view taken along line BB of FIG. 9;

【図11】薬剤含有体用容器をセットした状態の断面図
である。
FIG. 11 is a cross-sectional view of a state in which a container for a drug-containing body is set.

【図12】薬剤含有体の斜視図である。FIG. 12 is a perspective view of a drug containing body.

【符号の説明】[Explanation of symbols]

1…薬剤加熱蒸散器具、2…薬剤含有体用容器、3…薬
剤含有体、15…発熱体、15a…発熱面。
DESCRIPTION OF SYMBOLS 1 ... Drug heat evaporation apparatus, 2 ... Drug-containing body container, 3 ... Drug-containing body, 15 ... Heating element, 15a ... Heating surface.

───────────────────────────────────────────────────── フロントページの続き Fターム(参考) 2B121 CA04 CA53 CA54 CC02 CC03 CC13 FA05 FA08 4C080 AA03 BB02 BB03 HH02 KK02 NN06 NN22 QQ14 4H011 AA01 AB03 AC02 AC06 BA01 BB15 BC19 BC22 DA09 DB04 DD05 DE04 DF03 DF04 DH02 DH05 DH10  ──────────────────────────────────────────────────続 き Continued on the front page F term (reference) 2B121 CA04 CA53 CA54 CC02 CC03 CC13 FA05 FA08 4C080 AA03 BB02 BB03 HH02 KK02 NN06 NN22 QQ14 4H011 AA01 AB03 AC02 AC06 BA01 BB15 BC19 BC22 DA09 DB04 DD05 DE04 DF03 DF04 DH04

Claims (5)

【特許請求の範囲】[Claims] 【請求項1】 加熱によって長期間薬剤を蒸散させる厚
み3mm以上の全体加熱式の薬剤含有体であって、加熱
温度[h]と薬剤含有体の最低温度[t]より式(1)
によって求まる熱損率[L]が、70%以下であること
を特徴とする全体加熱式の薬剤含有体。 式1…L=(h−t)/h×100
1. A general heating type drug-containing substance having a thickness of 3 mm or more for evaporating a drug for a long time by heating, wherein a heating temperature [h] and a minimum temperature [t] of the drug-containing substance are used to obtain an equation (1).
The heat loss factor [L] obtained by the method is 70% or less. Formula 1 L = (ht) / h × 100
【請求項2】 前記薬剤含有体の材質は、無機及び/又
は有機粉末を主材とする粘着体及び/又は焼結体及び/
又は打錠体、パルプを主材とする紙及び/又は不織布、
プラスチックを主材とする不織布及び/又は織物、その
他動植物由来物質を主材とする不織布及び/又は織物、
プラスチックを主材とするフォーム、プラスチック練り
込み体、植物乾燥体、ゲル、ジェル、シリカゲルの少な
くとも一つから構成されていることを特徴とする請求項
1記載の全体加熱式の薬剤含有体。
2. The material of the drug-containing body is made of an adhesive and / or a sintered body mainly composed of an inorganic and / or organic powder and / or
Or tableting body, paper and / or non-woven fabric mainly composed of pulp,
Non-woven fabric and / or woven fabric mainly composed of plastic, non-woven fabric and / or woven fabric mainly composed of animal and plant-derived substances,
The whole-heating-type drug-containing substance according to claim 1, wherein the substance is composed of at least one of a foam mainly composed of plastic, a kneaded body of plastic, a dried plant, gel, gel, and silica gel.
【請求項3】 一つ以上の通気孔を持つ薬剤含有体用容
器に内包させて使用することを特徴とする請求項1記載
の全体加熱式の薬剤含有体。
3. The whole-heating-type drug-containing substance according to claim 1, wherein the drug-containing substance is used by being enclosed in a container for the drug-containing substance having one or more air holes.
【請求項4】 一つ以上の通気孔を有し、薬剤含有体を
内包できる大きさで、その内面と薬剤含有体の表面との
距離が、1〜10mmであること特徴とする薬剤含有体
用容器。
4. A drug-containing material having at least one air hole and having a size capable of containing the drug-containing material, wherein the distance between the inner surface and the surface of the drug-containing material is 1 to 10 mm. Container.
【請求項5】 請求項4記載の薬剤含有体用容器が載置
される発熱体を備え、この発熱体の発熱面の角度が0〜
70度であること特徴とする薬剤加熱蒸散器具。
5. A heating element on which the container for a medicine-containing body according to claim 4 is placed, wherein the angle of the heating surface of the heating element is 0 to 5.
An agent for heating and evaporating a medicine characterized by being at 70 degrees.
JP2001020460A 2001-01-29 2001-01-29 Whole heating type drug-containing body, container for the same and heating apparatus for drug transpiration Pending JP2002220304A (en)

Priority Applications (24)

Application Number Priority Date Filing Date Title
JP2001020460A JP2002220304A (en) 2001-01-29 2001-01-29 Whole heating type drug-containing body, container for the same and heating apparatus for drug transpiration
CA002473552A CA2473552A1 (en) 2001-01-29 2001-09-06 Whole heated, chemical containing body, chemical containing body retaining receptacle, chemical heating, volatilizing apparatus and indicator for a heat volatilizing chemical
PCT/JP2001/007728 WO2002060254A1 (en) 2001-01-29 2001-09-06 Chemical-containing formed material of type of heating of whole the material, container for holding chemical-containing formed material, device for heating and transpiring chemical and indicator for chemical to be heated and vaporized
CNB018217141A CN1291647C (en) 2001-01-29 2001-09-06 Chemical-containing formed material of type of heating of whole the material container for holding chemical-containing formed matzrial device for
AU2001284452A AU2001284452B2 (en) 2001-01-29 2001-09-06 Whole-heated, chemical containing body, chemical containing body retaining receptacle, chemical heating, volatilizing apparatus and indicator for a heat volatilizing chemical
US10/433,519 US7449154B2 (en) 2001-01-29 2001-09-06 Chemical-containing formed material of type of heating of whole the material, container for holding chemical-containing formed material, device for heating and transpiring chemical and indicator for chemical to be heated and vaporized
NZ526268A NZ526268A (en) 2001-01-29 2001-09-06 Chemical-containing formed material of type of heating of whole the material, container for holding chemical- containing formed material, device for heating and transpiring chemical and indicator for chemical to be heated and vaporized
PL01363451A PL363451A1 (en) 2001-01-29 2001-09-06 Chemical-containing formed material of type of heating of whole the material, container for holding chemical-containing formed material, device for heating and transpiring chemical and indicator for chemical to be heated and vaporized
HU0303003A HU228096B1 (en) 2001-01-29 2001-09-06 Chemical-containing formed material of type of heating of whole the material container for holding chemical-containing formed material, device for heating and transpiring chemical and indicator for chemical to be heated and vaporized
DE60144442T DE60144442D1 (en) 2001-01-29 2001-09-06 DEVICE FOR HEATING AND EVAPORATING A CHEMICAL
KR1020037008234A KR100746520B1 (en) 2001-01-29 2001-09-06 Chemical heating, volatilizing apparatus
MXPA03006740A MXPA03006740A (en) 2001-01-29 2001-09-06 Chemical-containing formed material of type of heating of whole the material, container for holding chemical-containing formed material, device for heating and transpiring chemical and indicator for chemical to be heated and vaporized.
AT01963465T ATE505080T1 (en) 2001-01-29 2001-09-06 DEVICE FOR HEATING AND VAPORIZING A CHEMICAL
BRPI0116528-3A BR0116528B1 (en) 2001-01-29 2001-09-06 chemical volatilization body, chemical heating volatilization apparatus, and, indicator for a heat volatilization chemical.
IL156333A IL156333A (en) 2001-01-29 2001-09-06 Chemical-containing formed material of type enabling heating of the whole material, container for holding the chemical-containing formed material, device for heating and vaporizing the chemical and indicator of quantity of chemical to be heated and vaporized
EP01963465A EP1356731B1 (en) 2001-01-29 2001-09-06 Apparatus for heating and volatilizing a chemical
TW090126077A TWI225772B (en) 2001-01-29 2001-10-22 Chemical-transpiring body, device for heating and transpiring chemical and indicator for chemical to be heated and vaporized
ARP010105057A AR031166A1 (en) 2001-01-29 2001-10-29 BODY CONTAINING COMPLETELY WARMED CHEMICAL AGENT, BODY RETENTION RECEPTURE CONTAINING CHEMICAL AGENT, HEATING AND VOLATILIZATION DEVICE OF CHEMICAL AGENT AND INDICATOR FOR A CHEMICAL AGENT VOLATILIZABLE BY HEAT
MYPI20015024A MY136846A (en) 2001-01-29 2001-10-30 Whole heated, chemical containing body, chemical containing body retaining receptacle, chemical heating, volatilizing apparatus and indicator for a heat volatilizing chemical
PE2001001109A PE20020725A1 (en) 2001-01-29 2001-11-08 BODY CONTAINING FULLY HEATED CHEMICAL AGENT, RETENTION RECEPTACLE, BODY CONTAINING CHEMICAL AGENT, CHEMICAL AGENT VOLATILIZATION AND HEATING APPARATUS AND INDICATOR FOR A HEAT VOLATILIZABLE CHEMICAL AGENT
EG20011189A EG23053A (en) 2001-01-29 2001-11-10 Whole heated chemical containing body chemical containing body retaining receptacle chemical heatingvolatilizing apparatus and indicator for a heat v olatilizing chemical
GCP20021829 GC0000383A (en) 2001-01-29 2002-01-26 Whole heated, chemical containing body, chemical containing body retaining receptacle, chemical heating, volatilizing apparatus and indicator for a heat volatilizing chemical
HR20030529A HRP20030529A2 (en) 2001-01-29 2003-06-27 Chemical-containing formed material of type of heating of whole the material, container for holding
HK03109171.9A HK1056666A1 (en) 2001-01-29 2003-12-16 Apparatus for heating and volatilizing a chemical

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2001020460A JP2002220304A (en) 2001-01-29 2001-01-29 Whole heating type drug-containing body, container for the same and heating apparatus for drug transpiration

Publications (1)

Publication Number Publication Date
JP2002220304A true JP2002220304A (en) 2002-08-09

Family

ID=18886164

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2001020460A Pending JP2002220304A (en) 2001-01-29 2001-01-29 Whole heating type drug-containing body, container for the same and heating apparatus for drug transpiration

Country Status (1)

Country Link
JP (1) JP2002220304A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007097534A (en) * 2005-10-07 2007-04-19 Koa Corp Element for heat-volatilizing drug and method for heat-volatilizing drug by using the element

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JPH0517307A (en) * 1991-07-09 1993-01-26 Fumakilla Ltd Agent-dissipation material and thermal dissipation apparatus using the same
JPH05194103A (en) * 1992-01-22 1993-08-03 Fumakilla Ltd Chemical agent-containing article for thermal transpiration and method for thermally transpiring chemical agent in the same
JPH06192008A (en) * 1992-12-24 1994-07-12 Fumakilla Ltd Chemical-containing body for long-term heat transpiration and method for carrying out heat transpiration of chemical using the same
JPH06192007A (en) * 1992-12-24 1994-07-12 Fumakilla Ltd Chemical-containing body for long-term heat transpiration and method for carrying out heat transpiration of chemical using the same
JPH0789806A (en) * 1993-09-21 1995-04-04 Fumakilla Ltd Method for thermally transpiring chemical agent

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JPH0517307A (en) * 1991-07-09 1993-01-26 Fumakilla Ltd Agent-dissipation material and thermal dissipation apparatus using the same
JPH05194103A (en) * 1992-01-22 1993-08-03 Fumakilla Ltd Chemical agent-containing article for thermal transpiration and method for thermally transpiring chemical agent in the same
JPH06192008A (en) * 1992-12-24 1994-07-12 Fumakilla Ltd Chemical-containing body for long-term heat transpiration and method for carrying out heat transpiration of chemical using the same
JPH06192007A (en) * 1992-12-24 1994-07-12 Fumakilla Ltd Chemical-containing body for long-term heat transpiration and method for carrying out heat transpiration of chemical using the same
JPH0789806A (en) * 1993-09-21 1995-04-04 Fumakilla Ltd Method for thermally transpiring chemical agent

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007097534A (en) * 2005-10-07 2007-04-19 Koa Corp Element for heat-volatilizing drug and method for heat-volatilizing drug by using the element

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