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A6 B6 214513 五、發明説明() (請先閲讀背面之注音?寧項再項寫本頁) 本發明係有鬨於一用以貯存一液態醫藥物質和用以施 用包含此一醫藥物質之眼藥水之裝置,其中該裝置傷包含 有一用以容納該醫藥物質之剛固圔筒狀容器,和一被裝置 ,在此一容器之一端部上之分配器,此一分配器上偽被提供 有一施加用嘴口,該嘴口上是被裝設有一被設計來形成和 置放該眼藥水於一患者眼睛上之孔口。 很多如此作用之装置:全部是被設計來貯存和施用一 醫藥物質以來以水珠狀態來被置放至患者眼睛上之裝置是 已為人們所習知。在這些裝置之大部分設計中,該貯存容 器偽包含有二由具彈性合成材料所製成之壁牆•或是以一 具有折疊式壁牆之伸縮軟管之形式出現,如此以使一使用 者可對該貯存容器施加壓力以來造成該液體是以水珠狀之 形式來被排出。 當該壓力是被釋放時,該具彈性可變形之容器是在該 施加用嘴口上建立起回吸力量,此一回吸力量偽會偉形成 ^— 、.+ 該嘴Q、末绱上之該最-後一滴藥水被吸回至該容器中。 經濟部中央標準局貝工消费合作社印- 然面,因為在該眼藥水被施用之時,基於該腾口和該 眼睛、該眼險或該眼睫毛之接近,該施加甩嘴口之細菌污 染是持別無法被避免。最接近於該嘴口末端之該藥水•特 別是形成在該嘴口末端之該最竽一適眼水是特興容易爱 到上述情況之污染。除此之外,該潮濕的環境是待別有利 於細菌之滋長,而該細菌之進入該容器之内部是無法被避 本紙张尺度这叫中家桴毕(CNS)甲4汉鉻CMO X ) 82.3. 40,000 21451^ A6 B6 經濟部中央標準局貝工消費合作社印¾ 五、發明説明() 免。當該最後一滴之眼藥水是被吸回至該嘴口内部時*此 一細菌之進入速度是被加速。 為了來避免包含在容器内之該醫藥物質之全部被污染 ,同時為了避免該細菌污染之進一步發展,一適當的防腐 .劑是被添加至此一醫藥樹質中。 然而,在此應被注意的是,該防腐劑之殺菌效用是有 其受限之有效期限。為了此一原因·該被用來作為眼藥水 之醫藥溶液是僅被考慮有一自該第一方、使用後大約有3 0 天之無菌期間。此一限制係導至金錢上之損失,同時會提 高患者眼睛受到感染之危險,當該患者並不導守該使用說 明書來使用該眼藥水時。 該已知之具有由合成材料撓性容器之糸統,其是不適 用於傳統的高壓蒸氣鍋殺菌*因為該高溫是為該習用之合 成材料所不能忍受。此一事實偽造成須要有細菌防腐劑使 用之第二原因。 不幸的是,太過高濃度之防腐劑的出現偽是會造成一 可觀的不方便,因為該防腐劑係會對該患者産生某些重要 的問題。它們偽會造成眼角膜之變質,刺激或過敏... 等等。 為了來消除由該防腐劑所造成之副作用,該防腐劑在 該眼藥水被施加至該患者之眼睛中前是須自該眼藥水中來 被排除。 一為所知的方法偽是在該裝置中來安置有一薄膜,一 (請先閱功背面之注竞¥^再堉寫本頁) 丨裝. 訂_ .泉. -?<·«.< :!ί tL«S'S^:a· (CNS) ψ i JVij (2ι,ι X 297 ) 82.3. 40.000 21451^ a6 ____B6 五、發明説明() (請先閱讀背面之注意事項再項寫本頁) 襯墊或一過濾器,其是當該眼藥水被施用之時來特定地吸 收該防腐劑。如此之一方法之一例是為被掲示在美國專利 第5, 056, 689號中。然而,如此之吸收方法是很 難來被設計成只待定地來對該被使用之防腐劑作用而來避 •免對該醫療活性物質産生作用之危險。 該吸收方法之有效作用之可行性是受限制,且其之研 究和發展偽須要一大額度的投資。該美國專利前案之裝置 是被裝設有一單向閥體,如此以來避免該眼藥水經由該施 用器嘴口而被直接地吸回至該容器中,且該嘴口上是被安 装有另一單向閥體以來使非無菌空氣可被允許進入該容器 中。該二單向閥體之設置並無法來解決該嘴口和溶液等二 者之污染問題。除了該吸收材料和該防腐劑本身之成本之 外,此一設計係産生有額外的成本。在實際運用上,該防 腐劑是被保留在該眼藥水溶液中,因為事實證明基於容器 彈性變形所産生之眼藥水回吸是無法被避免,且事實上沒 有一種方法是可被設計來防止在該嘴口施用器上之細菌之 繁殖。 經濟部中央標準局貝工消費合作社印- 同樣的問題是發生在揭示在國際專利申諳案第W Ο 91/16868號案之装置中。除此之外,由該專利申 謗菜所提出之装置對於一使用者而言是有一多數之缺點, 該缺點之範圍偽包括自不方便於簡單的使用而至會對健康 發生危險。 在此為一事實的是,當包含有一彈性可變形之容器之 本紙Kf適引中國:¾家找芈(CNS)甲4规珞(210 X 297么D 82.3. 40,000 A6 21451^ _B6_ 五、發明説明() 裝置是被裝置有一殺菌用過濾器時,該過濾器是必須保持 潮濕狀態以來能夠有效地作甩,如此之一潮濕過濾器會造 成一愈來愈大的真空被建立在該容器之内部中,且該藉由 在該容器主體内之壓力而被排出之眼藥水,其在被施用之 後是會部分地被吸回至該殺_用之過濾器上,如此傜防止 外部空氣來穿透進入該容器中。在使用過後,在該容器上 之具撓性或可折叠壁牆所須要來形成眼藥水水珠之力量是 變得很大,如此偽使一使用者是不方便來使用此一裝置。 更進一步者,該眼藥水回吸之現象是無法來排除所有可能 發生之危險,因為假如該嘴口是已為眼睛所污染的話,如 此之污染是會朝向該装置之内部來散佈,且是來可能會感 染該殺菌用過濾器。 另外一膣未為該已知糸統所解決之問題是為該形成眼 藥水水珠之規則性和精確度。 在此已為人所知悉的是,一滴的眼藥水水珠是須有少 於30微公升(micro 1 i ter s)之體積以防止 眼睛的被”氾濫"("f 1 〇 〇 d e d 〃)。更進一步者 ,由該使闬者所施加之力量以來使他能夠自一分配裝置來 産生一眼藥水珠之較佳力量是已被量測。此一力量是大約 為3 0 0公克之力量,且該力量在多重分配量裝置中之使 用全部期間中是瞜為一定的。除此之外,該装置無論是被 旋加有多大之力量,其瞜該是不會有一水柱噴流的産生。 大部分習知之裝置是無法允許具規則性之水珠的産生,同 82.3. 40.000 -------------------------裝------,玎------·" (請先閱諱背面之注意事項再塡寫本頁) 經濟部中央標準局員工消费合作钍印" A6 B6 五、發明説明() 時其亦無法來一定力量之施加,如此偽導至該眼藥水之一 可觀的損失和在使用時之缺點。某一些裝置是藉由一薄膜 之導入而欲霣試來克服上述這些缺點,其中該薄膜是用來 吸收該防腐劑,然而在該眼藥水溶液中仍然發現有部分的 .防腐劑,是該裝置並無法完全地滿足所須之搽件。一沒有 被回吸之眼藥水水珠之精確形成,或一不為所須之第二滴 眼藥水之形成是無法藉由上述所提供之解決方案而被保證 ,不管上述之解決方案之眼藥水溶液中是否包含有一防腐 劑之存在。 在此已披注意的是,為了要保護患者之健康,所有的 防腐劑是須要來自該眼藥水溶液中除排掉,而以吸收防腐 _之方法來排除掉防腐劑是無法成功地來克服該裝置嘴口 部分污染的問題,或者是無法來克服以——定之力量和一 定之精確度來分配眼藥水水珠的問題,是故,習用裝置是 無法讓人來方便地使用。同時,以下的事實亦是須被考量 :因為該回吸作用,某些眼藥水溶液並不是保持為一均勻 的狀態而是形成為一泡沫狀態,此一泡沫狀態之形成在施 甩眼藥水時是為一無法被接受的變化。 經濟部中央標準居R工消费合作社印^ (請先閱讀背面之注意';·,項再堉寫木頁} 一可栾完全消除在眼藥水溶液中和在該眼藥水珠中之 防腐劑之裝置之詳細規格(同時該裝置是可保證包含在容 器内和被保持在該分配機構通道中之眼藥水溶液之連續殺 菌作用),其較佳地是有以下所述方法之出現: ——方法是可以一 一定的力量來自一容器中排出該眼 本呔银尺Λ迻用中SS家疗退(CNS)甲4現洛(21〇 X 2S7公分) S2.3. 40.000 214513 A6 B6 五、發明説明() 液 溶 水 藥 態 狀 空 真1 起 立 &Ε a 中 器 容 該 在 免 避 來 可 是 法 方 水1 有 會 不 而 度 .i'-l 3 之 出 流 水 藥 眼 制 控 來 可 是 法 方 成 形 的 柱 該珠 在水 去水 移藥 來眼 後滴 加二 施第 確免 精被 被以 水此 藥如 眼 , 滴力· 一 壓; 在餘部 可剩外 是之之 法内口 方器嘴 一 容該 I 水在 藥成 眼形 安嘴 和在 密含 緊包 1 和 供力 提壓 來的 下多 險過 危成 的造 ., 誤會流 錯不回 有是一 沒法之 在方液 可該溶 是時水 法同藥 方,眼 一 封之 I 密分 的部 全 口 氣 會 空不 及而 流珠 紊水 之藥 部眼 内的 口勻 嘴均 器成 配形 分來 該以 在此 止如 防 ,.* 可生沫 是産泡 法之的 方合何 一 混任 I 液有 溶生 \ 産 中 β. 0 内 之 器 容 該 於 入 移 之 菌 細 止 防 來 可 是 法 方 (請先閲讀背面之注意丨項再塡寫本頁) 装. 訂. 及 殖 繁 之 部 内□ 嘴 器 配 分 該 在 菌 細 止 防 來 可 是 法 方 專公 國利 英專 在洲 示歐 掲和 為號 例 1 一 8 由 6 藉 可 ο 是 1 些 ο 某 之 2 中 I 法Α 方 1 些 Β 這G 逑第 上告 公 利 經濟部中央標準局貝工消費合作社印轚 -技 供知 提習 所決 器解 注只 之是 號案 4 方 4 決 5 解 之 7 供 ο 提 2 所 利 ο 專 -二 Α 上 - 以 P 由 E , 第而 告然 述眼 上之 ’ 劑 此腐 因防 , 須 要無 須 一 之為 上受 度接 程被 部來 金法 足無 滿並 法置 無装 而之 難示 困掲 之所 分置 部裝 藝二 中苒另家桴爭(cxs)甲4 (21fi χ 公兮) S2.3. 40.〇〇〇 214513 Δβ Α6 __ Β6 五、發明説明() 烴濟部中央標準肩員工消費合作杜印製 一 和之缺 物而為之 而 α器和之可此不。來殘亦 有 口制因 藥然因器 ,性射置物是如而險器因其 證 嘴控菌 充,,用 式菌注裝含接由水危射卻時 保 器被無 填免中施 型無該制内連,藥之注器同 可 量法之 了避器該 之之至控中之 _ 該部該射, 方 計無珠 。為被用且 用其接率器間明配内使注珠 制 珠和水證用法施置 使持連速射塞說分置可該水 控 水確水保作無水裝 重保被動注活被來装該而水 和 水精藥被〃而藥之。多來可流該其已地該應然藥 現 藥不眼法吸在眼式菌為以器為在和中滴染良 ,眼 出 眼一該無回存在型無須式濾用止塞述一污改上該 之 有以 ,而〃 之止用的是型過作防柱上著有一 口配 法 置可此件該液禁使全置之用可來器在接會此嘴分 方 裝是在筷 -血被重完装用作亦以射 ί 滴不之之地 述 ,其 ,分中試對多為之使菌眉器注點一亦用器確 上是,珠部器測絶一持水一殺it..檔於缺可時作配精 有。的器水大射了 是為保藥單有過阻介之是同部分來 只配實射水之注為用是被眼一偽之流良用置 ,全水法 , 分事注藥中一和作器須用為此此回改作裝成之藥無 置之一之眼法在中〃 用被施須在如之由吸之形器眼而 裝水為器成方 ,器吸施是於是 ,,用藉回得之射一故 用藥此濾形逑時射回水部用器後時作 α 該獲柱注在之 施眼在過來上同注〃藥内一射最同腐染止所水一置因 水菌 菌法有 該 一眼子 注 。防污防計有管装壓 藥無 殺方乏 至此該瓶 一 上具受來設會儘被餘 --------------------------裝------#-----\^· (請先閱#背面之注奇:)_項再塡寫本頁) H尺Λιΐΐ中3:«孓怜準(CN.S)甲4規洛(2!〇 X 297公穿 82.3. 40.000 214513 A6 B6_ 五、發明説明() (請先閲讀背面之注意¥項再瑣寫本頁) 無法來消除介於二次施用之間産生在該過濾器下游處之污 染和細菌繁殖之危險。此一S現亦是發生在所有習用之装 置中,甚至是那些在其内部中裝設有可吸收在醫藥物質中 防腐劑機構之装置,因為該嘴口之受污染是無法被避免且 ,在該防腐劑吸收機構下游處之細菌污染是無法被避免的。 更進一步者,該無法被控制之殘餘壓力一旦被移去後 ,其立即地是會産生眼藥水不為所須流動發生之危險,在 此該不為所須之流動是被須馬上來被消除以能精確地分離 該眼藥水水珠。如此一之流動消除是無法由傳統的活塞來 達成之。 本發明是被闬來克服上迖之習用裝置之缺點,且是提 供一装置可來滿足在上述規格中所訂定之要求和大部分最 近的要求,在此同時,本g明是可來簡化製造和方便患者 之使用。 經濟部中央橒準局貝工消費合作社印*''代 為了達成上述之目標,依據本發明之裝置偽是有以下 之持徵:該容器偽在其之一消部上被密封,該在端部上該 分配器是被装設有一流量控制装置,該流量控制裝置傷包 含有一 di mL:該調整元俘之打開程度是依據旅力至該 S藥流體物質上之起始力而被決定,且該容器之另一端 部是藉由一和該容器相喔合之滑動活塞而被密封,該滑動 活塞是被安排以來産生該起始壓力,且該流量速率控制裝 置是被連接至一具防腐作用之裝置上,該防腐作用装置對 於位在孔口上游處之一設定諄積之醫藥物質是有一徽活動 82.3. 40,000 ρΛ 4513 Α6 Β6 五、發明説明() 的(〇1 igodynamic)作用。 依據本發明實施之形式,該流動速率控制裝置係可包 含有至少為一之在其上具有披調制微孔洞之薄膜,和至少 為一之被調制孔口或是至少為一之狹長孔道。 ’ 較佳地,該容器偽額外地包含有一額外可移動之密封 方法,該密封方法是被安排來在醫藥物質貯存期間防止該 醫藥物質和該流動速率控裝置之接觸。 此一額外可移動之密封方法是可為一可移動之密封柱 塞,且該容器是可包含有一旁通容室以在當該醫藥物質被 使用時來至少部分地接纳此一柱塞。 在本發明之一較佳實施形式上,該可移動柱塞係包含 有至少為一之環狀外綠以來確保該容器在貯存期間之不可 穿透性,和包含有至少為一之横向凹樯以來確保該裝置在 使用期間該醫藥用物質之流動,其中,該至少為一之橫向 K槽是被安排來和被形成在該容器底部上之至少為一之凹 槽相連通。 依據該實施例之形式,該旁通容室之高度是可較小於 或較大於該可移動密封柱塞之高度。 經濟部中央標準局3工消費合作a印- (請先閱讀背面之注意萼項再填寫本頁) 較佳地,該可移動密封柱塞是包含有一較小厚度之中 央區間,且該容器内是被設置有一剌針以來穿透此一柱塞 之該中央區間。 較佳地,該剌針亦是可為移動的且是被安置在一可移 動刺針承載支撐上。 -1 2- 司中(CNS〉甲4規必(2l·〕X 二、殳) 82.3. 40,000 經濟部中夹標準局員工消費合作社印" 21451^ 五、發明説明() 在本發明之另一形式之實施例中,該可移動密封柱塞 偽包含有一單一方向閥體。 為了來使該容器内之剩餘體積減至有一最小的體積, 該可移動密封柱塞和該可移動活塞是可分別地包含有至少 ’為一之凹槽和一和該凹槽有互補形狀和尺寸之凸出物。 在所有之變化實施例中,該流動速率控制裝置是被安 排在該分配器之基部上,且較佳地是在此一分配器之該施 用器嘴口之基部上。 在本發明之一較佳形式之實施例中,該裝置偽包含有 至少為一之通口,該通口是被安排在該容器之端部上且是 導引進入該旁通容器之内部中,如此以能夠在使用此一裝 置之前來將包含在此一容室内之氣醱排出至容室之外。 該容器是可包含有二由一可移動中間柱塞所分離之隔 室,該二隔室中之一者是包含有一溶液,且另一隔室中偽 包含有一被設計來溶解在該溶液中或和該溶液相混合之物 質。 在此一形式之實施例中,該容器較佳地偽包含有一中 央擴大部分,該中央擴大部分偽披安排在當此中間可移動 柱塞是被移動至此一擴大部分之附近時來做為可使液態溶 液流通通過之通道。 在本發明該装置之一較佳形式之實施例中,一罩蓋偽 限制該柱塞之行程以來確定該二成分之混合。 為了來消除該液體在使用後殘除部餘部分之排出,該 -13- 本,,燸準(CNS)甲 4 (210 X 297 ) 82.3. 40,000 ---------------------------裝------.玎-----# { 一 (諳先閲?一好面之注意^項再塡寫本頁) A6 B6 214513 五、發明説明() 活塞是可包含有一剛固的保持止動器和一界定有一内部孔 穴之柔軟内襯,此一保持止動器偽包含有一支撐短捍,且 該止動器和該支撐短捍一起之金部高度是至少大約相同於 該内部孔穴之高度。 • 在本發明裝置之該較佳實施例形式中,該活塞偽包含 有一彈簧環狀物,該彈簧環狀物係被安排以來施加一漸增 的推力。 較佳地,在所有形式之簧施例中,該容器係包含有一 圓茼形狀之封套,該封套偽構成了該容器之内部壁牆。 在一特別經濟和有效率之實施例形式中,該圖筒狀容 器是由一第一管狀物和一第二管狀物所形成,其中該第二 管狀物是套設在該第一管狀物之内部,該第一管狀物是由 一固定密封物和一可移動活塞而被密封,而該第二管狀物 則是包含有一中空剛固元件,該剛固元件偽機械地和該可 移動活塞及該滑動活塞相連结,該固定之密封物傜包含有 一允許該醫藥物質朝向該分配器流動之單一方向閥體,且 該第二管狀元件之_底部是被密封的。 該圓筒狀容器較佳地是較由一滑動活塞而被密封,其 中,該滑動活塞是被剛固地連结至一被安裝在一殼套底部 上之中空剛固元件上,在此該圓筒狀容器是被部分地插置 在該殼套之内部中,且該中空空元件係經由一過濾器及/ 或該防腐殺菌裝置而和該分配器相連通。 在依據本發明實施例之一較佳方法,該流動速率控制 -14- 82.3. 40,000 ----------------------------裝------#------ ^ (請先閱讀背面之注意事項再填寫本頁) 經濟部中失標準局8工消費合作社印- 214513 A6 B6 五、發明説明() 裝置傜包含有一具一厚度之過濾器。 此一具有厚度之過濾器偽可包含有一燒結材料,該燒 结材料偽包含有至少為一之元件,該元件具制菌之微活動 效果,其中,該元件係可選自重金屬、這些金屬之化合物 .或混合物和這些化合物之混合物。 上述之具有防腐殺菌作用裝置偽包括有銀及/或銀之 氧化物。 依據本發明實施例之一較佳方法,該裝置是被如此地 安排以使該預定之體積是小於一滴眼藥水珠之體積,且較 佳地,介於該以微公升(mi cor 1 eters)來量 測之該預定體積和該以平方毫米來量測之該防腐殺菌裝置 之表面面積之比例是小於1。 為了來避免該装置在使後殘餘醫_物質之排出,該活 塞上較佳地是被提供有具彈性之裝置以被安排來吸收殘餘 的壓力。 經濟部中央標準局员工消費合作社印κ (請先閱讀背面之注意?;項再螭寫本頁> 上述之該具彈性裝置.其較佳地是包含有一具低阻力 之區間,該具低阻力區間是被裝設在和該醫藥物質相接觸 之活塞之側邊上,且該具低阻力區間是被安排來改變其之 形狀當有一推力是被施加至該活塞上時,而在當該推力是 結束時該具低阻區間是回復至其之原來狀態。 本發明將會籍由參考於實施例之揭示和所附相鬨圔示 之說明而被較佳地了解,其中:— 圖示1A和1表示依據本發明之該装置之較佳實 -15- 大 中 4半(CNS)甲 4 (:M0 X 297 ) 813. 40,000 214513 A6 B6_ 五、發明説明() 施例之一形式之一軸向剖面視画, 圏示2和3偽表示依據本發明之該装置之較佳賁施例 之另一形式之一軸向剖面視圖,其中,丨該二圖示偽分別表 示在一貯存位置和在一被使用之位置, 圖示4和5偽表示依據本發明之該裝置之一變化實施 例,其中,該二圖示偽分別表示在一貯存位置和在一被使 用之位置, 圖示6和7偽表示依據本發明之該裝置之詳細視圔, 圖示8和9偽表示依據本發明之該裝置之另一變化實 施例,其中,該二圖示偽|分別表示在一貯存位置和在一被 使招之位置, 圆示1 0和1 1偽表示依據本發明之該裝置之另一變 化實施例,其中,該二圖示偽分別表示在一貯存位置和在 一被使用之位置, 圖示1 2至2 0偽說明用來獲得依據本發明之已可來 貯存藥水之裝置之元件準備之各種不同階段和這些元件之 組合, 圖示2 1偽表示砍據本發明之該裝置之一特別形式之 實施例,其中,該容器偽包含有二容室,在此,此一裝置 是被表示在其之貯存位置中, 圔示22偽表示画示21之該装置在一中間位置之狀 況, 圖示2 3偽表示依據本發明之該裝置在使用位置之狀 -1 5 - --------------------------裝------1T-----J 球 (請先閱分背面之注龙卜項再塡寫本頁) 經濟部中央標準局3工消費合作社印" 衣f m邊用中萏围家(C‘VS)甲4坨洛(210 X 29m ) S2.3. 40.000 A6 B6 214513 五、發明説明() 況, 圖示24至3 3偽說明這些元件和由這些元件之組合 以獲得依據本發明之一裝置之各種不同程序,在此,該装 置之容器偽包含有如圖示2 1至2 3所表示之二部分, 圔示34至3 6偽説明該活塞之實施之一較佳形式, 其中,該活塞偽分別在靜止狀態和在使用狀態, 圔示3 7至3 8偽為二視圖以詋明本發明裝置在實施 上之二値形式,其中,本發明之該裝置是處於一貯存之狀 態, 圖示3 9偽為本發明之該裝置之一特別有利形式之一 橫剖面斷面視圆,其中,該裝置是處在一貯存之狀態, 画不4 0和4 1偽說明圖不3 9之實施例,其分別表 示該實施例裝置是處在一驅動狀態和在一分配狀態, 圖示4 2偽表示由圖示3 9所掲示之該實施例之一變 化, 圖示4 3和44係為一詳細視圖以說明依據圖示4 2 之該裝置之該滑動活塞,在此該/活塞分別是在一貯存狀況 和在一使用狀況5 参考圔示1 A和1B,表示在此一較佳實施例形式之 該装置,其係完金地包含有一圓筒狀容器10, —被置放 在該容器一端部上之一分配器1 1和一滑動活塞1 2是和 該容器相噁合而在和該分配器相對之位置上。一保護性罩 蓋1 3是被安裝在該分配器1 1之上。 -1 7 - (請先閲讀背面之注意"項再塡寫本頁) --° 丁 經濟部中央標準局3工消費合作钍印- 中茬溥孓丨 甲 4 wje· (210 X 297 公嗲 A6 B6 214513 五、發明説明() (請先閱讀背面之注意'-'>項再塡寫本頁) 此一分配器1 1偽由一施用器嘴口 1 4所組成,該施 用器嘴口偽有一孔口15,該孔口15傜被設計來可形成 該眼藥水水珠,在此該眼藥水水珠是要被施加至患者之眼 睛上。此一孔口 1 5是和一被形成在該施用器嘴口 1 4 一 端部上之容室1 6相連通,而該容室1 6是經由一側邊通 道1 7和經由一流動速率控制装置1 9而和該容器之内部 相連接,在此該側邊通道1 7是被形成介於該施加器嘴口 内部壁牆和一嵌入物18之間,在此,該流動速率控制裝 置1 9在以下會有掲示。 在此一實施例中之該流動速率控制裝置係包含有在其 上有被調制徹孔洞之薄膜,該薄膜偽密封了該容器1 ◦之 一端,而該容器1 0之另一端則是由該活塞1 2所密封。 此一活塞12是被裝設在一活塞捍柱20之端部上, 或是經由一彈簧元件2 1而被裝設在一柱塞之端部上,以 下會對該彈簧元件2 1之作用做一說明。 經濟部中央標準局R工消費合作社印- 該活塞12事實上是由一密封栓塞22所組成,其中 ,該密封栓塞是22為一具有由一彈性體材料所製成之一 画環狀外_,該彈性體材料所製成之外綜是被固定在一剛 固止動器2 3之周圍上,而該止動器2 3則是經由該彈餐 元件2 1而被連接至該柱塞2〇上。 在上述所表示之賓施形式中,該孔口15是由一軸向 通道之一端部所形成,該軸向通道偽延伸於該施用器嘴口 之上半部上。在該通道中較佳地是詖插置有—銀製尖片2 18- 82.3. 40,000 本闲中國家作芈(CNS)甲!規洛(210 X 297 y分) 經濟部中央標準局员工消费合作钍印¾ 五、發明説明() 4’該銀製尖片24籍由其之陽離子釋出而具有抑制細菌 胃果’且該銀製尖片偽維持該施用器嘴口之孔口是在—防 胃2狀態。在圔示1 B中傜更持定地說明該銀製尖片24 是ϋ由至少為二之徑向薄片2 5而被維持在一軸向之中心 位5±。在此,該銀製尖片24是可由任何具有相等作用 料來取代之,甚至該尖片24是由藉由在此一通道接 Ϊ5該孔口 1 5部分之内側壁牆上來鍍上具有相同性質材料 之塗層以取代之。 當該保護性罩蓋13是被置放在該裝置上時,亦就是 當該罩蓋是以螺紋接合在該施加器嘴口 (該嘴口上置有陽 螺紋26,而該罩蓋之内部是被置有相對的陰螺紋27) 上時,事實上形成該施用器嘴口頂部之該通道之端部,其 在界定了一緊接於該孔口 1 5之一徹小容室2 8 ,在此, 當該裝置是被第一次使用後,包含在該容室1〇内之醫藥 物質2 9是可被包存在該微小容室2 8内。此一微量之醫 療梭)質是藉由其和該銀製尖片之瞬時接觸或繼續保持接觸 而被達成殺菌防腐之作用。 該流動速率控制裝置1 9偽是由一或更多之在其上包 含有被調制徹孔洞之薄膜所組成,該薄膜傜可以來精5萑地 控制該醫藥物質經由該側邊通道流向該施用器嘴□之孔口 1 5之流動速率。此一装置偽可在當醫藥物質通過其上時 來使該翳藥物質有一壓力負載上之損失,其中該損失是和 由該活室1 2施加在該醫藥物質溶液上之壓力成正比。在 -19- !t: (CSS) ψ 4 «.«δ- (210 X 29: ) 82.3. 40.000 ----------------(--------裝------.ΤΓ-----二 f锖先閲讀背面之注意::··項再域·寫本頁) A6 B6 214513 五、發明説明() (請先閱讀背面之注意事項再瑣寫本頁) 此該圓筒之斷面積是有一相當大的面積,例如像是為25 0mm2 ,因此在此偽須要施加一為2. 5公斤之推力以 來達成該溶液上有一為1巴(bar)之壓力。然而,在 實際上是可接受一為1公斤之推力,因為該推力是已被考 盧足夠高地來驅動此一条統,亦就是可以以一食指來推動 該活塞。該最大的壓力是大約有〇. 4巴之壓力,而實驗 顯示甚至是施加有一等於2公斤之力量,在此是不可能在 該施加器嘴口之末端上産生一水柱狀之噴流,而是會依據 本發明之設計來産生一均勻的水珠。實驗是可顯示,因為 該流動控制裝置所造成之結果,眼藥水水珠是以每一秒或 毎二秒一滴的速率形成在該孔口 1 5之外部。這些眼藥水 水珠是有一介於2 0和4 0微公升間之體積。 該不可被考盧為一定須要之彈簧元件21,其卻可使 該装置之使用變得更為容易,同時其是可使一使用者之推 力來漸漸地施加至該活塞捍柱或柱塞上。以口語的方式來 說明之,該彈簧係補助該流動速率控制裝置之功能以防止 一瞬時過大之推力之被施加至包容在該容器10内部之醫 藥物質2 9上。 經濟部中央標準居员工消費合作社印- 圖示2和3偽說明一實施本發明之一形式,其中該容 器10是為一長條狀且其是藉由一可移動之密封栓塞30 而被密封在其之一遠方端部上(亦就是在該分配器1 1之 附近),在當一使用者藉由壓迫該柱塞20而推動該活塞 1 2時,該密封拴塞3 0是被設計來至少部分地被推入至 -2 0- 本坟涞义文違引中围國孓缥芈(CN-S)甲4悅洛(2〖0 X 29了 H ) 82.3. 40,000 經濟部中央標準局3工消費合作社印κ 214513 A6 B6 五、發明説明() 一旁通容室3 1中 該旁通容室3 1偽包含有側邊凹槽32,該凹槽32 偽使被包容在容器10中該醫藥物質可來經由一或多之軸 向通道33而自該容器10中流出,其中,該軸向通道3 3是形成介於該可移動密封拴塞3 0和該容器1 0之内側 壁牆之間,這些和該凹稽32相連通之通道33,其本身 是和一或更多之徑向管道34相連通,而該徑向管道34 則是連通至一位在該流動速率控制裝置1 9上游處之中央 區間3 5 ,其中,該流動速宰控制裝置1 9是藉由一薄膜 過濾器所溝建而成。 在此,本發明之此一簧施例形式是用於當包含在該容 器内之該醫藥物質是無法來忍受長期(一例為三年)和該 流動速率控制裝置(亦就是該薄膜過濾器)接觸之狀況下 ,其中該接觸一般而言是很可能持绩有一個月之久。該可 移動密封拴塞是有一項單一之任P :保持該醫藥物質2 9 於一由該容器1 0之壁牆、該密封柱塞2 2之環狀外綠和 該可移動密封栓塞3 0所形成之一密封空間中。 圖示4和5偽詋明此一實施之形式和前述實施形式之 不同偽在於:此一實施形式之容器是為具有内襯的,換言 之,此一容器偽包含有一玻璃材料所製成之圓筒狀襯套4 ◦包覆在該容器之内部壁牆上。在此一實施例中,該醫藥 按質是被圍封在一由該玻璃襯套40、該可移動密封拴塞 3 0和該活塞1 2之密封拴塞2 2所形成之空間中。 82.3. 40,000 ------------------^-------裝------,玎-----τπ (請先閱讀背面之注告τ::項再堉寫本頁) A6 B6 214513 五、發明説明() 為了來便利由位在該容器1 0主體内部之三値元件所 界定此一獨立容器之設置,該容器之壁牆較佳地是有一第 —區間4 1和一第二區間4 2 ,該第一區間4 1之内部表 面是有一直徑大約相同於該襯套40之外部直徑,而該第 ‘二區間4 2之内部直徑是大於該襯套4 0之外部直徑。此 —設計之結果是為,該襯套40是僅會藉由其抵靠在該第 ~區間41内部壁牆上之摩擦力和可能藉由其抵靠在形成 在該第二區間4 2上之定中心舌狀物4 3上而被固定在其 位置上,如此該襯套4 0是可在無須過多推力之形狀下來 被容易地定位在其位置上。 在此一實施例中,其係有可能來逹成該獨立容器之完 金自動裝填,此一自動装填將在以下參考於圔示12至1 7而被說明,在此,該容器是在裝填有醫藥物質後來被導 人該装置之主體中,如此以使得該裝置是成為立卽可被使 用。 圖示6和7是為放大視圖,其以更詳細的方式來說明 頴示在圔示4和5中之該裝置之可移動密封栓塞3 0之實 施形式和操作方法。此一密封柱塞偽是以一至少為一之環 狀珠綠44之形式出現,當此一密封栓塞是在其之貯存位 置時(亦就是該密封栓塞和該容器10之襯套4 0相喔合 時),該環狀珠緣44是部分地被壓平以在使用該装置時 來形成醫藥锪質流通之通道。由於該凹槽3 2偽相同於參 考於圆示2所界定之凹槽之結果,旦由於該珠綠4 4位置 -22- ----------------j-------裝------.訂------j (請先閱讀背面之注意事項再塥寫本頁) 經濟部中央標準局S工消費合作社印κ 本*氏m及用中^;与家戍準(CNS)甲4規洛(210 X 297公殳) 82.3. 40,000 A6 B6 314513 五、發明説明() 之结果,該旁通容室31之高度是較低於該可移動密封栓 塞之高度,如此偽使得該容器1 0之全部高度在相對於其 它實施例時是可有一較低之高度,其中,其它之實施例之 旁通容室是必須有充分的高度以來完全地接纳該可移動密 _封栓塞。 由画示8和9所掲示之該設計是不同時前述之實施例 ,在此,圖示8和9之設計中是以一密封栓塞50來取代 該可移動密封栓塞,該密封栓塞50是設計要來被剌穿的 。為了達成此一目的,此一密封栓塞包含有一薄厚度的中 央區間5 1,且一剌針5 2是被裝置在該容器底部相對於 詨施加器嘴口之位置上。該活室之環狀外绉是有二凸出物 5 3 ,該二凸出物5 3是有一形狀大約互補於該可移動密 封栓塞在該薄厚度中央區間5 1之凹槽5 4之形狀。 在貯存期間藉由該保護性罩蓋1 5而被密封之作用為 通氣孔之橫向孔口 5.. 5 ,其在當該栓塞移動時且當該罩蓋 是被旋鬆時是可使起初包含在該容器内部而位在該可移動 密封拴塞50下游處之空氣被排洩出去。在事實上,這些 開口 5 5是籍由該保護性罩蓋之一下方部分而被密封,此 一下方部分偽構成一防止擅自打開環5 6,其藉由連接桿 臂而被附接至該罩蓋之蓋口部分上,在此當該使用者欲來 使用該装置時,該捍臂是會被打斷以來打開這些孔口。 在此亦可來改變此一設計:在一可移動刺針承載架支 撐上來安裝該剌針5 2 ,其中,該承載架支撐是被推動進 -2 3 _ (CNH) ψ 4 (210 X 25: ) {請先W讀背面之注夺.:V項再塡寫本頁) —装· *π. 經濟部中央標準局κχ工消費合作社印友 S2.3. 40.000 214513 A6 B6 經濟部中央標準局员工消贫合作社印- 五、發明説明() 入該容器之内部以來確保該密封栓塞之被剌穿。 圖示1 0和1 1傜說明本發明實施之另一種形式,此 一形式傜導自於圖示8和9,其中,該可移動密封栓塞5 7之中央區間被装設有一藉由一狹長之孔洞所構建之單向 閥體5 8 ,在此當沒有任合壓力是被施加在該醫藥物質2 9上時,該閥體58是被封閉,且當只有該壓力是足夠大 到使此一單向閥匾之唇口部分打開時,該閥髅58才會打 開以使該醫藥物質通過而流向該流動速率控制裝置1 9。 在此一實施例中之該活塞之該環狀外綠,其下方是有 一凸出物5 9,該凸出物之形狀較佳地是互補於形成介於 該單向閥體之唇口部分之該凹槽之形狀,如此在當本装置 是被使用之後,此一凸出物是會穿透進入該凹槽中以來使 該容器之终了體積或剩餘體體是被減少至有一最小的體積 〇 在上述全部之實施例中,該流動控制裝置是以一在其 上包含有一預定數量被調制微孔洞之薄膜形式出現。在此 .應被注意的是,此一形式之流動速率控制裝置是可由任何 其它合適之機構來取代之,例如,一充分小的被調制孔口 ,一直線形狀或螺旋線形狀之狹長孔道或是其它可來調制 該流動速率之任何合適機構,如此無論施加在該本装置活 塞上之壓力大小是為如何,本裝置是可避免一水柱之形成 和來加強規則性眼藥水水珠的形成。 該薄膜過濾器較佳地是為一殺菌過濾器,該過濾器上 -24- (請先閲讀背面之注音->.項再塡寫本頁) —裝· 訂- 琛· 82.3. 40.000 Α6 Β6 214513 五、發明説明() (請先《讀背面之注音::¥項再項寫本頁) 之孔洞是可有一介於〇 · 1和〇 · 4 5徹米(m i c r 〇 ns)之直徑,且較佳地,該孔洞直徑是在〇. 22徹米 之範圍,如此以可來阻止所有尺寸大於0. 22微米的固 態顆粒,和細菌及其它異物。 在上述所有之實施例中,至少有一主要作用為控制流 動速率之過濾器是被裝設,且同時是有一作用為一防止顆 粒物流過之防腐過濾器是來吸收該防腐劑。該裝置是可包 含有一第二元件,例如一薄膜過濾器或一襯塾以來吸收該 防腐劑。 經濟部中央標準局员工消費合作社印5农 來使用以上之設計是可直接地得到很多的優點。在這 些優點中可由使用者所直接察覺的是,當該柱塞是被推動 而形成在該施用器嘴口绱部上之該眼藥水水珠精確度之規 則性是有很大的規則性。在此為事實的是,該有一預定體 饅積眼藥水水珠在經由本装置之使用是有一完全一定的體 積。該@來做為制止和預防該醫藥物質來以一水柱形狀來 被排出之流動速率控制過濾器偽提供該眼藥水水珠之規則 性。此一規則性同時亦經由一具有一彈簧之柱塞而被獲得 ,其中該彈簧偽形成一機構以來使該柱塞之衝程相對於該 活塞之衝程為一缓慢的移動。在實際應用上,當該使用來 推動該柱塞時,基於該彈簧彈性作用之結果,該使用者可 在造成該彈簧移動之前來壓縮該彈簧有——定之距離。該 過濾器本身是有一壓縮設定值,當施加力量超過該壓縮設 定值時,該醫藥物質偽會通過該過濾器而形成被調制之水 -25- 82.3. 40,000 214513 A6 B6_ 五、發明説明() 珠。更進一步者,此一過濾器亦有一防止顆粒锪質通過之 作用,其中,該顆粒物質是來自作為該醫療作用之醫藥物 質之藥品混合物,或者是來自該裝置之元件上。在這些來 自醫藥物質本身中之顆粒物質,其可能是為那些在産品製 •造程序中無法溶解在溶劑中之顆粒物質或是無法和溶劑有 良好混合之顆粒物質,或者,那些顆粒物質可能是由於貯 存期間聚合作用所産生之顆粒物質。 最後,某一些醫藥物質是無法承受高溫的殺菌作用, 如此它們的保存除非是可接受一具防腐殺菌作用之過濾, 否者的話,在這些醫藥物質之貯存期間勢必要加入有至少 為一之防腐劑。一待別被設計來在使用該醫藥物質前來吸 收其中之防腐劑之過濾器,或一襯墊,其是可被插置在該 施用器嘴口中。在此為一事實的是,這些防腐劑是可能提 高過敏之可能而造成不舒服或是副作用,是故這些防腐劑 在施用該醫藥物質於患者眼睛之前是必須來I該醫藥物質 中來被排除掉。 該被置放在該施用器嘴口端部上之過濾器,其係預防 基於自細_自該嘴口外部之移入和在該施加器嘴口内部擴 散所造成之污染。最後,該在其上裝設有一銀製尖片或任 其它合適材料之護罩,其係確保了該施用器嘴口之該遠方 端部之永久活性的不會受到感染作用。 本發明該装置之製造之優點,其偽由部分掲示在圔示 4至7中之該實施例所説明,其中,在該圔上之容器之詳 -2 6 - ----------------^ --------裝------.玎------- (请先閱讀背面之注意事項再填寫本頁)A6 B6 214513 V. Description of the invention () (please read the phonetic notation on the back? Ning Xiang then write this page) The present invention is coveted by an eye for storing a liquid pharmaceutical substance and for administering the drug A device for potions, wherein the device includes a rigid cylindrical container for containing the medicinal substance, and a device, a dispenser on one end of the container, the dispenser is pseudo provided with a The mouth for application is provided with an orifice designed to form and place the eye drops on a patient's eye. Many devices that work in this way: all are devices designed to store and administer a medicinal substance to be placed on the patient's eyes in the form of drops of water are known. In most designs of these devices, the storage container pseudo-contains two walls made of elastic synthetic materials or appears in the form of a telescopic hose with folding walls, so as to make one use The pressure can be applied to the storage container to cause the liquid to be discharged in the form of water droplets. When the pressure is released, the elastically deformable container establishes a sucking force on the mouth of the application, and this sucking force will pseudo-form ^ —,. + The mouth Q, the end The last-drop of medicine is sucked back into the container. Printed by the Beigong Consumer Cooperative of the Central Bureau of Standards of the Ministry of Economic Affairs, because when the eye drops are applied, based on the proximity of the mouth and the eye, the eye hazard, or the eyelashes, the bacterial contamination of the mouth flap is Holding farewell cannot be avoided. The potion closest to the end of the mouth and mouth • Especially the most suitable eye water formed at the end of the mouth and mouth is the pollution that Texing easily loves the above situation. In addition, the humid environment is not conducive to the growth of bacteria, and the entry of the bacteria into the container cannot be avoided from this paper standard. This is called Zhongjiazhenbi (CNS) A 4 Han Chromium CMO X) 82.3. 40,000 21451 ^ A6 B6 Printed by the Beigong Consumer Cooperative of the Central Bureau of Standards of the Ministry of Economy ¾ V. Invention Instructions () Exempt. When the last drop of eye drops is sucked back into the mouth, the entry speed of this bacterium is accelerated. In order to avoid all contamination of the pharmaceutical substance contained in the container, and in order to avoid the further development of the bacterial contamination, an appropriate preservative is added to this pharmaceutical tree. However, it should be noted here that the bactericidal effect of this preservative has its limited validity period. For this reason, the medical solution used as eye drops is only considered to have a sterile period of about 30 days after use from the first party. This restriction leads to financial loss and increases the risk of infection of the patient's eyes when the patient does not follow the instructions for use of the eye drops. This known system with flexible containers made of synthetic materials is not suitable for the sterilization of conventional high-pressure steam cookers * because the high temperature is unbearable for the conventional synthetic materials. This fact pretends to be the second reason for the use of bacterial preservatives. Unfortunately, the presence of preservatives at too high a concentration can actually cause considerable inconvenience because the preservatives cause certain important problems for the patient. They can cause deterioration of the cornea, irritation or allergies ... and so on. In order to eliminate the side effects caused by the preservative, the preservative must be eliminated from the eyedrop before the eyedrop is applied to the patient's eye. One known method is to place a film in the device, one (please read the note on the back of the merit first ¥ ^ and then write this page) 丨 Install. Order_. 泉.-? < · «. <:! ί tL «S'S ^: a · (CNS) ψ i JVij (2ι, ι X 297) 82. 3. 40. 000 21451 ^ a6 ____B6 V. Description of the invention () (Please read the precautions on the back before writing this page) A liner or a filter that specifically absorbs the preservative when the eye drops are applied. An example of such a method is shown in U.S. Patent No. 5,056,689 for being trapped. However, it is very difficult to design such an absorption method so as to act only on the preservative to be used to avoid the danger of acting on the medically active substance. The feasibility of the effective function of this absorption method is limited, and its research and development require a large amount of investment. The device of the previous US patent is equipped with a one-way valve body, so that the eye drops are prevented from being directly sucked back into the container through the mouth of the applicator, and another mouth is installed on the mouth The one-way valve body allows non-sterile air to be allowed into the container. The arrangement of the two one-way valve bodies cannot solve the pollution problem of the mouth and the solution. In addition to the cost of the absorbent material and the preservative itself, this design incurs additional costs. In practical application, the preservative is retained in the aqueous solution of eye drops, because it has been proved that the back suction of eye drops based on the elastic deformation of the container cannot be avoided, and in fact there is no method that can be designed to prevent The propagation of bacteria on the mouth and mouth applicator. Printed by the Beigong Consumer Cooperative of the Central Bureau of Standards of the Ministry of Economic Affairs-The same problem occurred in the device disclosed in the International Patent Application No. W Ο 91/16868. In addition, the device proposed by the patent application has a majority of disadvantages for a user. The scope of the disadvantages includes the inconvenience of simple use and danger to health. What is true here is that when the original paper Kf containing an elastically deformable container is suitable for China: ¾ 家 找 芈 (CNS) A 4 gauge Luo (210 X 297 M D 82. 3. 40,000 A6 21451 ^ _B6_ 5. Description of the invention () When the device is equipped with a filter for sterilization, the filter must be kept in a moist state to be able to effectively throw away, such a wet filter will cause an increasingly large Vacuum is established in the interior of the container, and the eye drops that are expelled by the pressure in the body of the container are partially sucked back to the killing filter after being applied , So prevent external air from penetrating into the container. After use, the strength of the flexible or collapsible walls on the container to form the eye drops drops becomes so great that it is inconvenient for a user to use this device. Furthermore, the phenomenon of the eye drops being sucked back cannot eliminate all possible dangers, because if the mouth is already contaminated by the eyes, such contamination will spread toward the inside of the device and come The filter for sterilization may be infected. Another problem that has not been solved by the known system is the regularity and accuracy of the formation of eye drops. What is known here is that a drop of eye drops must have a volume of less than 30 microliters (micro 1 iter s) to prevent the eyes from being "flooded" (" f 1 〇ded 〃). Further, the best force that has been applied by the messenger to enable him to produce an eyedrop from a dispensing device has been measured. This force is about 300 grams Power, and the power is constant during the entire period of use of the multiple distribution device. In addition, no matter how much power is applied to the device, there will not be a jet of water. Most of the conventional devices are unable to allow regular water droplets to be produced, as in 82. 3. 40. 000 ------------------------- installed ------, 玎 ------ " (please read the back first (Notes on this page will be written on this page) Employee Consumption Cooperation of the Central Bureau of Standards of the Ministry of Economic Affairs “A6 B6” V. Invention Description () It cannot be applied with a certain amount of power, so it is perverted to one of the eye drops. Losses and shortcomings in use. Some devices are intended to overcome these shortcomings by introducing a film, in which the film is used to absorb the preservative, but some are still found in the aqueous solution of eye drops. Preservative is the device that the device can not completely meet the required paint. The precise formation of a drop of eye drops that has not been sucked back, or the formation of a second drop of eye drops that is not required cannot be guaranteed by the solution provided above, regardless of the eye drops of the above solution Whether the aqueous solution contains a preservative. It has been noted here that in order to protect the health of the patient, all preservatives need to be removed from the aqueous solution of eye drops, and the method of absorbing preservatives to exclude preservatives cannot successfully overcome this The problem of partial contamination of the mouth of the device, or it is impossible to overcome the problem of distributing eye drops with a certain power and a certain accuracy, so the conventional device cannot be easily used by people. At the same time, the following facts must also be considered: because of the resorption effect, some aqueous eye drops are not maintained in a uniform state but form a foam state, the formation of this foam state when applying eye drops It is an unacceptable change. Printed by the Ministry of Economic Affairs, Central Standard Ju Rong Consumer Cooperative Society ^ (please read the notes on the back '; ·, Xiang Zaiyu writes a wooden page} Yi Ke Luan completely eliminates the preservatives in the eye drops aqueous solution and the eye drops The detailed specifications of the device (at the same time, the device is capable of ensuring the continuous sterilization of the aqueous ophthalmic solution contained in the container and held in the channel of the dispensing mechanism), which preferably has the following methods: ——Method It is possible to discharge the eye from a container with a certain force from the silver ruler Λ shift with the Chinese SS Home Retreat (CNS) Jia 4 Xianluo (21〇X 2S7 cm) S2. 3. 40. 000 214513 A6 B6 V. Description of the invention () Liquid-dissolved medicinal state Void 1 Stands up & E a The container should be avoided, but French water 1 may not be enough. i'-l 3's outflow water medicine eye is controlled but it is a column formed by the method. The bead is added after the water is removed from the water and the medicine is added to the eye. One pressure; the rest can be left in the mouth. The mouth of the square device should contain the I water in the eye shape of the medicine and the mouth and the tight package 1 and the pressure to increase the pressure. Make. , Misunderstanding and wrong, there is no way to be in the prescription liquid can be dissolved is the same as the prescription, the part of the eye with a dense part of the mouth will be empty and the bead turbulent water in the eye The mouth uniforms are evenly shaped and should be stopped here. * Can produce foam is a method of producing foam. The device within 0 should be used for the prevention of the bacteria in the migration, but it is a French method (please read the note on the back first before writing this page). Order. In the Ministry of Propagation and Propagation □ The mouthparts should be distributed to prevent the bacteria, but the French Principality Li Yingzhuo showed the name in the European Union. Example 1 1 8 from 6 can be borrowed ο Yes 1 some ο 2 of the I method Α Party 1 Some Β This G was reported to the Ministry of Public Affairs and Economics Central Bureau of Standards Beigong Consumer Cooperative Printed-Technical knowledge and knowledge of the decision-making solution Note only the case 4 party 4 decision 5 solution 7 offer ο mention 2利利 专-二 Α 上-With P by E, the first to tell the eyes of the 'reagent for the prevention of this rot, need not need to be one of the highest degree of access to be received by the Ministry of gold law is not full and set It's difficult to show without disguise. The division of the distressed department is divided into two parts. The other family is struggling (cxs) A 4 (21fi χ 公 兮) S2. 3. 40. 〇〇〇 214513 Δβ Α6 __ Β6 Fifth, the invention description () Hydrocarbon Economy Ministry of Central Standards staff consumption cooperation to print the lack of a sum of things and the alpha device can not. There are also oral systems for medicines and medicines. Sex shots are the same as dangerous devices because of their mouths. They are filled with bacteria. There is no interlinkage of the system, the medicine injection device is the same as the measurable method, and the avoidance device should be controlled to the _ the part should be shot, and the count is no beads. In order to be used and use the connection between the connector and the bead injection system to make beads and use the water certificate, the use of a continuous-speed injection plug says that the separation can be used to control the water and ensure that the water is guaranteed to be waterless, and the passive injection is coming. The water and the water essence medicine were taken as medicine. It ’s easy to get the right place, the proper medicine, the current medicine, not the eye method, the eye type bacteria is used as a device, and the medium is dripping well, and the eye is out of the eye. The pollution reform should be appropriate, and the only thing used is that the anti-pillar is equipped with a mouthpiece. This piece of liquid is forbidden to be used for the whole set. When the mouth is connected, it is installed separately. The chopsticks-blood was re-installed and used as a drop-off. It is divided into the pilot test for the most eyebrow device. The device is indeed the same. The bead device is absolutely tested. Water kills it. . It is used as a match when there is a shortage. The water of the device is shot to prevent the drug form from being over the same. The same part is used to match the injection of the real water only. It is used by the eye and the false flow. The whole water method is used to divide the medicine into one. The implement must use the eye method which is changed to make medicine for this time. In the 〃, the water must be filled by the shape of the shape of the shape of the shape of the shape. , Use the borrowed shot to take the medicine, the filter shape is used to shoot back to the back of the device, and the alpha is to be used. The shot is applied to the eye, and the same injection 〃 the shot is the same as the decay of the water. A set of due to water bacteria bacteria method should have a glance. The anti-fouling and anti-counterfeit drugs are available in tubes and pressure killers. -装 ------ # ----- \ ^ · (Please read #Notes on the back of the first:) _ Item and then write this page) H rule Λιll 1 in 3: «孓 惜 准 (CN. S) A 4 gauge Luo (2! 〇 X 297 male wear 82. 3. 40. 000 214513 A6 B6_ V. Description of the invention () (please read the note on the back first and then write down this page). It is impossible to eliminate the risk of contamination and bacterial reproduction downstream of the filter between the second application. This S is also happening in all conventional devices, even those with a preservative mechanism that can be absorbed in medical substances in its interior, because the contamination of the mouth cannot be avoided and, in Bacterial contamination downstream of the preservative absorption mechanism cannot be avoided. Furthermore, once the uncontrollable residual pressure is removed, it will immediately cause the danger that the eye drops will not flow unnecessarily. Here, the undesirable flow is to be eliminated immediately. In order to accurately separate the eye drops. Such a flow elimination cannot be achieved by traditional pistons. The present invention is designed to overcome the shortcomings of conventional devices, and to provide a device that can meet the requirements stipulated in the above specifications and most recent requirements. At the same time, the present invention can simplify the manufacturing And convenient for patients. In order to achieve the above goals, the device according to the present invention has the following characteristics: the container is sealed on one of its consumer parts, which is on the end The distributor is equipped with a flow control device. The flow control device contains a di mL: the opening degree of the adjustment element is determined according to the initial force on the S-fluid substance. And the other end of the container is sealed by a sliding piston which is in line with the container, the sliding piston is arranged to generate the starting pressure, and the flow rate control device is connected to a corrosion resistant On the device of action, the anti-corrosion device for a set of medicinal substances located upstream of the orifice is a emblem activity 82. 3. 40,000 ρΛ 4513 Α6 Β6 Fifth, the description of the invention () (〇1 igodynamic) role. According to an implementation form of the present invention, the flow rate control device may include at least one thin film having modulated micropores thereon, and at least one modulated orifice or at least one elongated channel. Preferably, the container additionally contains an additional removable sealing method that is arranged to prevent contact between the medical substance and the flow rate control device during storage of the medical substance. This additional removable sealing method may be a removable sealed plunger, and the container may contain a bypass volume to at least partially receive the plunger when the medicinal substance is used. In a preferred embodiment of the present invention, the movable plunger includes at least one ring-shaped outer green to ensure the impermeability of the container during storage, and at least one lateral recess To ensure the flow of the medicinal substance during use of the device, the at least one transverse K-groove is arranged to communicate with at least one groove formed on the bottom of the container. According to the form of this embodiment, the height of the bypass chamber may be smaller or larger than the height of the movable sealing plunger. The Ministry of Economic Affairs, Central Bureau of Standards, 3 Industrial and Consumer Cooperation a-print (please read the note on the back before filling in this page) Preferably, the movable sealing plunger contains a central section with a smaller thickness, and the container It is the central section that has been provided with a stab needle that penetrates this plunger. Preferably, the stab needle is also movable and is placed on a movable lancet bearing support. -1 2- Sizhong (CNS> A 4 rules must (2l ·) X II, Shi) 82. 3. 40,000 Printed by the Staff Consumer Cooperative of the China Bureau of Standards, Ministry of Economic Affairs " 21451 ^ V. Description of the Invention () In another form of embodiment of the invention, the movable sealing plunger pseudo contains a single directional valve body. In order to reduce the remaining volume in the container to a minimum volume, the movable sealing plunger and the movable piston may respectively include at least a groove and a groove with a complementary shape and Protrusions of size. In all variant embodiments, the flow rate control device is arranged on the base of the dispenser, and preferably on the base of the applicator mouth of the dispenser. In a preferred form of embodiment of the invention, the device pseudo contains at least one port which is arranged on the end of the container and which leads into the interior of the bypass container In this way, the gas contained in the chamber can be discharged out of the chamber before using the device. The container may contain two compartments separated by a movable intermediate plunger, one of the two compartments contains a solution, and the other compartment contains a pseudo designed to dissolve in the solution Or mixed with the solution. In this form of embodiment, the container preferably pseudo-contains a central enlarged portion, the central enlarged portion is pseudo-arranged when the middle movable plunger is moved to the vicinity of the enlarged portion to act as The channel through which the liquid solution circulates. In an embodiment of the preferred form of the device of the present invention, a cover pseudo-limits the travel of the plunger to determine the mixing of the two components. In order to eliminate the discharge of the remaining part of the liquid after use, the -13- this, 燸 准 (CNS) A 4 (210 X 297) 82. 3. 40,000 --------------------------- installed ------. 玎 ----- # {a (read first? Attention to a good side ^ item and then write this page) A6 B6 214513 V. Description of invention () The piston can contain a rigid holding stopper and a A soft lining defining an internal cavity is defined, and this holding stopper pseudo includes a support short, and the height of the gold portion of the stopper and the support short is at least approximately the same as the height of the internal cavity. • In the preferred embodiment form of the device of the present invention, the piston pseudo contains a spring ring, which is arranged to exert an increasing thrust since it was arranged. Preferably, in all forms of spring embodiments, the container includes a round chrysanthemum-shaped envelope that pseudo-forms the inner wall of the container. In a particularly economical and efficient embodiment form, the cylindrical container of the figure is formed by a first tube and a second tube, wherein the second tube is sleeved on the first tube Inside, the first tubular body is sealed by a fixed seal and a movable piston, and the second tubular body contains a hollow rigid element, which is pseudo-mechanically connected to the movable piston and The sliding piston is connected, the fixed sealant contains a unidirectional valve body that allows the medical substance to flow toward the dispenser, and the bottom of the second tubular element is sealed. The cylindrical container is preferably sealed by a sliding piston, wherein the sliding piston is rigidly connected to a hollow rigid element mounted on the bottom of a casing, here the The cylindrical container is partially inserted in the interior of the shell, and the hollow element is in communication with the dispenser via a filter and / or the antiseptic sterilization device. In a preferred method according to an embodiment of the present invention, the flow rate control -14- 82. 3. 40,000 ---------------------------- installed ------ # ------ ^ (please read the back Matters needing attention and then fill out this page) Printed by the Workers ’Consumers Cooperative of the China Bureau of Loss of Standards, Ministry of Economic Affairs-214513 A6 B6 5. Description of the invention () The device contains a filter with a thickness. The filter with a thickness may include a sintered material, the sintered material may include at least one element, the element has a micro-activation effect of bacteria, wherein the element may be selected from heavy metals, these metals Compound. Or mixtures and mixtures of these compounds. The above-mentioned antiseptic and sterilizing device includes silver and / or silver oxide. According to a preferred method of an embodiment of the present invention, the device is so arranged that the predetermined volume is less than the volume of a drop of eye drops, and preferably, between the microliters (mi cor 1 eters) The ratio of the predetermined volume measured to the surface area of the antiseptic sterilization device measured in square millimeters is less than 1. In order to avoid the discharge of residual medical substances from the device, the piston is preferably provided with a flexible device to be arranged to absorb residual pressure. Printed by the Ministry of Economic Affairs, Central Bureau of Standards and Staff Consumer Cooperative κ (please read the note on the back ?; Xiang Zai writes this page> the above flexible device. It preferably includes a section with low resistance, the section with low resistance is installed on the side of the piston in contact with the medicinal substance, and the section with low resistance is arranged to change its shape When a thrust force is applied to the piston, and when the thrust force is over, the low-resistance section returns to its original state. The present invention will be better understood by referring to the disclosure of the embodiments and the accompanying description, where:-Figures 1A and 1 show the preferred implementation of the device according to the present invention-15- Big Middle 4 and a half (CNS) A 4 (: M0 X 297) 813. 40,000 214513 A6 B6_ V. Description of the invention () One of the forms of the embodiment is an axial cross-sectional view, and the 2 and 3 pseudo shows the other form of the preferred embodiment of the device according to the invention. A cross-sectional view, wherein, the two pictorial symbols respectively represent a storage position and a used position, and pictorial diagrams 4 and 5 pseudo represent a variant embodiment of the device according to the present invention, wherein the two pictorial diagrams Pseudo indicates a storage position and a used position, Figures 6 and 7 indicate detailed views of the device according to the invention, Figures 8 and 9 indicate another variation of the device according to the invention Embodiments, wherein the two pictorial pseudo | represents a storage position and a recruited position, respectively, and the circular representations 10 and 11 pseudo represent another variant embodiment of the device according to the present invention, wherein, The two pictograms respectively represent a storage position and a used position. Pictograms 12 to 20 pseudo-describe the various stages of preparation of the components used to obtain the device that can store the medicinal solution according to the present invention. The combination of these components, picture 2 1 It shows an embodiment of a special form of the device according to the present invention, in which the container pseudo contains two compartments, here, this device is shown in its storage position, 圔 示 22 pseudo indicates drawing 21 is the state of the device in an intermediate position, the figure 2 3 pseudo represents the state of the device according to the invention in the use position -1 5------------------- -------- Equipment ------ 1T ----- J ball (please read the note on the back and write the page first) " Clothing fm side with Zhonglianweijia (C'VS) Jia 4 Tuoluo (210 X 29m) S2. 3. 40. 000 A6 B6 214513 V. Description of the invention (), the figures 24 to 3 3 pseudo-describe these components and the combination of these components to obtain various procedures of a device according to the present invention. Here, the container of the device pseudo-contains As shown in the two parts shown in Figures 2 1 to 2 3, Ps 34 to 3 6 pseudo-illustrates a preferred form of implementation of the piston, wherein the pss pseudo respectively at rest and in use, P 3 Pseudo 3 to 3 8 are two views to illustrate the implementation of the device of the present invention, wherein the device of the present invention is in a stored state, Figure 39 is pseudo one of the device of the present invention is particularly advantageous One of the forms is a cross-sectional cross-sectional view of a circle, where the device is in a stored state, without drawing 4 0 and 4 1 pseudo-illustration of the embodiment of FIG. 3 9, which indicates that the device of this embodiment is in a Driving state and a distributing state, Figure 42 pseudo-represents a change of one of the embodiments shown by Figure 39, Figure 43 and 44 are a detailed view to illustrate the device according to Figure 42 The sliding piston, where the / piston is in a storage Status and a usage status 5 Refer to the indications 1 A and 1B, indicating that the device in the form of a preferred embodiment includes a cylindrical container 10, which is placed on one end of the container. One of the dispenser 11 and a sliding piston 12 is in misalignment with the container and is in a position opposite to the dispenser. A protective cover 13 is mounted on the dispenser 11. -1 7-(Please read the note on the back " item before writing this page)-° Ding, Ministry of Economic Affairs, Central Standards Bureau, 3 industrial and consumer cooperation, thorium printing-middle stubble, prince 4 wje (210 X 297嗲 A6 B6 214513 V. Description of the invention () (Please read the note on the back '-'> first and then write this page) This dispenser 1 1 pseudo consists of an applicator mouth 1 4, the applicator The mouth mouth has an orifice 15, which is designed to form the eye drops, where the eye drops are to be applied to the patient's eyes. This hole 15 is a The container chamber 16 formed on one end of the mouth of the applicator 14 communicates with the container chamber 16 through a side channel 17 and through a flow rate control device 19 to the interior of the container Connected, here the side channel 17 is formed between the inner wall of the applicator mouth and an insert 18, here, the flow rate control device 19 will be shown below. Here In one embodiment, the flow rate control device includes a thin film with modulated holes on it, which pseudo-seales the container 1 End, and the other end of the container 10 is sealed by the piston 12 2. The piston 12 is installed on the end of a piston cylinder 20, or is installed via a spring element 2 1 Set on the end of a plunger, the function of the spring element 21 will be described below. The Central Bureau of Economic Affairs of the Ministry of Economic Affairs R-Consumer Cooperative Printing-The piston 12 is actually composed of a sealing plug 22, of which The sealing plug 22 is a ring-shaped outer frame made of an elastomer material. The outer heald made of the elastomer material is fixed around a rigid stop 23 , And the stopper 23 is connected to the plunger 20 via the bullet element 21. In the above-mentioned Binsch form, the orifice 15 is formed by one end of an axial channel The portion is formed, the axial channel extends pseudo on the upper half of the mouth of the applicator. In the channel is preferably inserted into the 詖-silver tip 2 18- 82. 3. 40,000 copies of the country's idle work (CNS) Jiaruo Luo (210 X 297 y points) Ministry of Economic Affairs Central Standards Bureau employee consumption cooperation thorium seal ¾ V. Description of the invention () 4 'the silver sharp film 24 from its cation It is released and has a bacteriostatic gastric fruit ', and the silver pointed piece pseudo-maintains the orifice of the mouth of the applicator to be in the state of preventing stomach 2. In Fig. 1B, Wu stated more firmly that the silver tip 24 is maintained at a central position of 5 ± in an axial direction by a radial sheet 25 of at least two. Here, the silver tip 24 can be replaced by any material with equal effect, even the tip 24 is plated with the same properties by connecting the inner wall of the hole 15 part of the opening 15 in this channel The coating of the material replaces it. When the protective cover 13 is placed on the device, that is, when the cover is screwed on the mouth of the applicator (the mouth is provided with a male thread 26, and the inside of the cover is When placed on the opposite female thread 27), in fact it forms the end of the channel at the top of the mouth of the applicator, which defines a small chamber 2 8 immediately adjacent to the orifice 15 Therefore, after the device is used for the first time, the medical substance 29 contained in the chamber 10 can be contained in the tiny chamber 28. This trace amount of medical shuttle is sterilized and antiseptic by its instantaneous contact or continued contact with the silver tip. The flow rate control device 19 is composed of one or more thin films containing modulated holes on it, and the thin film can control the flow of the medicinal substance to the application through the side channel. The flow rate of the orifice 15 of the nozzle □. This device can make the pangolin substance have a loss of pressure load when the medicinal substance passes therethrough, wherein the loss is proportional to the pressure exerted on the medicinal substance solution by the chamber 12. On -19-! T: (CSS) ψ 4 «. «Δ- (210 X 29:) 82. 3. 40. 000 ---------------- (-------- install ------. ΤΓ ----- 二 f 锖 Read the notes on the back first :: · Item then domain · write this page) A6 B6 214513 V. Description of invention () (Please read the notes on the back before writing this page) This The cross-sectional area of the cylinder is a relatively large area, such as 25 0mm2, so in this pseudo need to apply a 2. A thrust of 5 kg is used to achieve a pressure of 1 bar on the solution. However, in practice, a thrust of 1 kg is acceptable, because the thrust is high enough to be driven by Kaulu to drive the system, that is, the piston can be pushed with one index finger. The maximum pressure is about 〇. The pressure of 4 bar, and experiments show that even a force equal to 2 kg is applied, it is not possible to produce a jet of water at the end of the mouth of the applicator, but will produce a Even water drops. Experiments can show that, as a result of the flow control device, drops of eye drops are formed outside the orifice 15 at a rate of one drop per second or every two seconds. These drops of eye drops have a volume between 20 and 40 microliters. The spring element 21, which cannot be taken by Kaulu as an indispensable element, makes the use of the device easier, and at the same time, it allows a user ’s thrust to be gradually applied to the piston or plunger . To explain in a colloquial way, the spring supplements the function of the flow rate control device to prevent an instantaneous excessive thrust force from being applied to the medical substance 29 contained in the container 10. Printed by the Ministry of Economic Affairs, Central Standard Resident Employee Consumer Cooperative-Figures 2 and 3 pseudo-describe a form of implementing the present invention, in which the container 10 is a long strip and it is sealed by a removable sealing plug 30 At one of its distal ends (that is, near the dispenser 11), when a user pushes the piston 12 by pressing the plunger 20, the sealing plug 30 is designed To be at least partly pushed to -2 0- Lai Yiwen of this grave violates the Zhongwei country 劓 犈 (CN-S) A 4 Yue Luo (2 〖0 X 29 了 H) 82. 3. 40,000 Printed by the Central Bureau of Standards of the Ministry of Economic Affairs 3 Industrial and Consumer Cooperatives κ 214513 A6 B6 V. Description of the invention () A bypass chamber 3 1 The bypass chamber 3 1 pseudo contains a side groove 32, the groove 32 is a fake The pharmaceutical substance contained in the container 10 can flow out of the container 10 through one or more axial channels 33, wherein the axial channel 33 is formed between the movable sealing plug 30 and the Between the inner side walls of the container 10, the channels 33 that communicate with the recess 32 are themselves connected to one or more radial pipes 34, and the radial pipes 34 are connected to one bit In the central section 3 5 upstream of the flow rate control device 19, the flow rate control device 19 is constructed by a membrane filter. Here, the spring embodiment of the present invention is used when the medicinal substance contained in the container cannot tolerate long-term (for example, three years) and the flow rate control device (that is, the membrane filter) Under the condition of contact, the contact is generally likely to last for a month. The movable sealing plug has a single task P: keep the medical substance 2 9 on a wall formed by the container 10, the ring-shaped outer green of the sealing plunger 2 2 and the movable sealing plug 3 0 One of the formed sealed spaces. Figures 4 and 5 show that the difference between this implementation form and the previous implementation form is that the container of this implementation form is lined, in other words, this container contains a circle made of glass material. Cylindrical liner 4 ◦Wrapped on the inner wall of the container. In this embodiment, the medical substance is enclosed in a space formed by the glass bush 40, the movable sealing plug 30, and the sealing plug 22 of the piston 12. 82. 3. 40,000 ------------------ ^ ------- installed ------, 玎 ----- τπ (please read the note on the back first τ :: Xiang Zaiyu wrote this page) A6 B6 214513 V. Description of the invention () In order to facilitate the installation of this independent container defined by the three-valued components located inside the body of the container 10, the walls of the container are relatively Preferably, there is a first interval 41 and a second interval 4 2, the inner surface of the first interval 41 has a diameter approximately the same as the outer diameter of the bushing 40, and the inner portion of the second interval 4 2 The diameter is larger than the outer diameter of the bush 40. The result of this design is that the bushing 40 can only be formed on the second section 42 by its friction against the inner wall of the section 41 and possibly by it. The centering tongue 43 is fixed at its position, so that the bush 40 can be easily positioned at its position in a shape that does not require excessive thrust. In this embodiment, it is possible to complete the automatic filling of the individual container. This automatic filling will be explained below with reference to the indications 12 to 17; here, the container is being filled Some medical substances were later introduced into the main body of the device, so that the device became stand-alone and could be used. Figures 6 and 7 are enlarged views, which illustrate in a more detailed manner the implementation form and method of operation of the movable sealing plug 30 of the device shown in Figures 4 and 5. The sealing plunger is actually in the form of an at least one ring green 44, when the sealing plug is in its storage position (that is, the sealing plug and the liner 40 phase of the container 10 (When it is closed), the ring-shaped bead 44 is partially flattened to form a channel for the circulation of the medical spot when using the device. Since the groove 3 2 is pseudo-same as the result of the groove defined with reference to the circle 2, once the bead green 4 4 position-22 ----------------- j ------- install ------. Order ------ j (please read the precautions on the back before writing this page) Printed by the Ministry of Economic Affairs, Central Standards Bureau, S Industry and Consumer Cooperative Society κ ** m and in use ^; 4 gauge Luo (210 X 297 Gong Shi) 82. 3. 40,000 A6 B6 314513 5. As a result of the description of the invention, the height of the bypass volume 31 is lower than the height of the movable sealing plug, so that the total height of the container 10 is relative to other embodiments It is possible to have a lower height, in which the bypass chamber of other embodiments must have a sufficient height to fully receive the movable seal plug. The design shown by the drawings 8 and 9 is the aforementioned different embodiment. Here, the design of the illustrations 8 and 9 replaces the movable sealing plug with a sealing plug 50. The sealing plug 50 is a design It's going to be pierced. For this purpose, the sealing plug includes a central section 51 with a thin thickness, and a needle 52 is mounted at the bottom of the container relative to the mouth of the crotch applicator. The annular outer crepe of the chamber has two protrusions 53, and the two protrusions 53 have a shape approximately complementary to the shape of the groove 5 4 of the movable sealing plug in the central section 51 of the thin thickness . During storage, the protective cover 15 is sealed as a lateral orifice of the vent 5. . 5. When the plug is moved and when the cap is unscrewed, the air initially contained inside the container and located downstream of the movable sealing plug 50 can be discharged. In fact, these openings 55 are sealed by one of the lower parts of the protective cover, this lower part falsely constitutes an unauthorized opening of the ring 56, which is attached to the On the cover part of the cover, when the user wants to use the device, the protection arm will be broken to open these openings. This design can also be changed here: the needle 5 2 is mounted on a movable lancet carrier support, where the carrier support is pushed into -2 3 _ (CNH) ψ 4 (210 X 25: ) (Please read the back note first. : V-item and then write this page) — Install · * π. Yin You, Central Bureau of Standards, Ministry of Economic Affairs κχ 工 consumer cooperative S2. 3. 40. 000 214513 A6 B6 Printed by the Poverty Alleviation Cooperative of the Central Bureau of Standards of the Ministry of Economic Affairs-V. Description of the invention () Since entering the inside of the container, ensure that the sealing plug is penetrated. Figures 10 and 11 illustrate another form of implementation of the present invention. This form is derived from Figures 8 and 9, in which the central section of the movable sealing plug 5 7 is provided with a slit The one-way valve body 5 8 constructed by the hole, where no pressure is applied to the medicinal substance 29, the valve body 58 is closed, and when only the pressure is large enough to make this When the lip of a one-way valve plaque is partially opened, the valve 58 will be opened to allow the medical substance to pass through and flow to the flow rate control device 19. In the ring-shaped outer green of the piston in this embodiment, there is a protrusion 5 9 below, the shape of the protrusion is preferably complementary to the lip portion formed between the one-way valve body The shape of the groove, so that after the device is used, the protrusion will penetrate into the groove so that the final volume of the container or the remaining body is reduced to a minimum volume 〇In all the above embodiments, the flow control device appears in the form of a thin film containing a predetermined number of modulated micropores on it. here . It should be noted that this type of flow rate control device can be replaced by any other suitable mechanism, for example, a sufficiently small modulated orifice, a straight or spiral shaped elongated channel or other available Any suitable mechanism for modulating the flow rate, so that regardless of the amount of pressure applied to the piston of the device, the device can avoid the formation of a water column and enhance the formation of regular eye drops. The membrane filter is preferably a sterilization filter, the filter -24- (please read the Zhuyin on the back-> first. Xiang Zaicheng wrote this page) — Binding · Order-Chen · 82. 3. 40. 000 Α6 Β6 214513 V. Description of invention () (please first read the phonetic note on the back: ¥ item and then write this page) The hole can have a range between 〇. 1 and 〇. 4 5 chemi (micr 〇ns) The diameter, and preferably, the hole diameter is at 〇. 22 Chemi range, so as to prevent all sizes greater than 0. 22 micron solid particles, bacteria and other foreign matter. In all of the above-mentioned embodiments, at least one filter whose main function is to control the flow rate is installed, and at the same time, a anti-corrosion filter that prevents the particles from flowing through is used to absorb the antiseptic. The device may contain a second element, such as a membrane filter or a liner, to absorb the preservative. The use of the above design by the Staff Consumer Cooperative of the Central Bureau of Standards of the Ministry of Economic Affairs can directly obtain many advantages. Among these advantages, what is directly perceivable by the user is that the regularity of the accuracy of the drop of eye drops formed on the mouth of the applicator when the plunger is pushed is very regular. What is true here is that there is a predetermined volume of buns of eye drops that have a completely constant volume when used by this device. The @ 来 as a flow rate control filter that suppresses and prevents the medicinal substance from being discharged in the shape of a water column pseudo provides the regularity of the eye drops. This regularity is also obtained through a plunger with a spring, where the spring pseudo-forms a mechanism so that the stroke of the plunger moves slowly relative to the stroke of the piston. In practical applications, when the push is used to push the plunger, based on the result of the spring's elastic action, the user can compress the spring by a certain distance before causing the spring to move. The filter itself has a compression setpoint, when the applied force exceeds the compression setpoint, the medicinal substance will pass through the filter to form modulated water -25- 82. 3. 40,000 214513 A6 B6_ V. Invention description () beads. Furthermore, this filter also has a function of preventing the passage of particulate matter, wherein the particulate matter comes from a drug mixture that is a medicinal substance for the medical action, or from an element of the device. The particulate matter from the pharmaceutical substance itself may be the particulate matter that cannot be dissolved in the solvent during the product manufacturing process or the particulate matter that cannot be well mixed with the solvent, or the particulate matter may be Particulate matter due to polymerization during storage. Finally, some medical substances cannot withstand the sterilization effect of high temperature, so they are preserved unless it is acceptable to filter with a preservative sterilization effect, otherwise, it is necessary to add at least one antiseptic during the storage of these medical substances Agent. A filter designed to absorb the preservatives before using the medicinal substance, or a liner, can be inserted in the mouth of the applicator. It is a fact that these preservatives may increase the possibility of allergies and cause discomfort or side effects, so these preservatives must come to the medical substance before they are applied to the patient's eyes. Off. The filter placed on the end of the mouth of the applicator is to prevent contamination based on self-fine movement from the outside of the mouth and spreading inside the mouth of the applicator. Finally, the shield with a silver tip or any other suitable material on it ensures that the permanently active end of the distal end of the mouth of the applicator will not be infected. The advantages of the manufacturing of the device of the present invention are illustrated by the embodiments shown partially in Figures 4 to 7, in which the details of the container on the Figure 2-6 --------- -------- ^ -------- Install ------. 玎 ------- (Please read the notes on the back before filling this page)
經濟部中央標準局员工消費合作社印S 本用中 as 孓 π準(CN'-S) τ 4 «洛(210 X 297 二’公) 82.3. 40,000Printed by the Staff Consumer Cooperative of the Central Bureau of Standards of the Ministry of Economic Affairs. Used as a standard π quasi (CN'-S) τ 4 «Luo (210 X 297 2’) 82.3. 40,000
A 2A 2
ΛΛ 1 AΛΛ 1 A
6 B 經濟部中央標準局貝工消費合作社印說 五、發明説明() 細狀況是可由圖示12至20而被進一步了解。這些画示 傷說明了該裝置之全部製造程序,亦就是該各餹不同元件 之準備和組裝。 圖示1 2偽說明包含有以下程序之步驟:使用可抽取 ,式噴嘴尖端來清潔該圓筒狀殼套4 0及在該毅套4 Ο上來 塗佈上一層矽其中,該圓筒狀殼套40是藉由一夾具 6 1之操作而被保持在其位置上。此一圔筒狀殻套40事 前是藉由熱衝擊和在沒有持殊妥形下而自一玻璃管子上切 下而成。然後.如圖示13所示,此一圓筒狀殼套是在一 爐子6 2中來以3 0 Ot:之溫度來進行再加熱和去焦處理 (depyrogenat ion)。圖示 14 係說明利 用一軸向可移動柱塞6 3來置放該可移動密封栓塞3 0。 画示1 5偽詋明該容器之填充步驟,或更精確而言之,該 殼套4 ◦藉由一彼拉下之可抽取注入器6 4之填充而被填 充有該醫藥物質29。圖示1 6偽詋明該活塞1 2經由一 軸向可移動柱塞65而被裝設之情形。在此假設該容器是 有一完全為圓筒狀之外部形戕,事先填充好有醫藥物質之 一大量容器是可以彼此之間一邊接者一邊之方式來被置放 在一容匣中以便於後續之使用。在這些後續之程序中,該 最有用之者是為高壓蒸氣鍋殺菌作用,此一作用是被提 供在該醫藥物質2 9是可承受在溫度上相對昇高之條件下 〇 _示1 8偽說明該容器在該裝置中之置放情形,其中 -27- 82.3. 40,000 (請先閲讀背面之注意事項再塡寫本頁) —裝· .11. A6 B6 214513 五、發明説明() 該装置事先是以適當的方法來被殺菌處理過。在此一装設 後,該柱塞2 0是被帶至其之位置上並且是如圖示19所 示被連接至該活塞上。圖示20係顯示該裝置之一完全裝 配和反置之情形。在此情況下,該裝置亦可以單一或集合 ,包装之情況來被貯存在一容匣中。 圖示2 1至2 3偽表示甩於眼藥水水珠之貯存和分配 裝置,其中,該容器1 0 Z是被分別地區分成二個隔室1 0 z a和10 ' b,該容器10 /之下方隔室10 ' a是 可包含有一親水性鹽7 0 (如圖所示)、或一粉末、或一 液體,而該上方隔室1 0 / b必須包含有一在液體狀態之 溶液。如先前所述者,該容器1 0 '是藉由一可移動密封 栓塞30而被密封在其之一绡部上,同時是藉由一活塞而 被密封在其之一上方端部上。一中間可移動栓塞7 2偽分 隔該二隔室1 ϋ z &和1 〇 ' b。在此一實施例之形式中 ,該容器10 1之該圖筒狀殼套40偽有一中央擴大部分 73,該中央擴大部分在此一条統被使時偽包含有一旁通 通道,關於此點以下有進一步揭不。 其它之元件,例如是該柱塞2 0和該施用器嘴口 1 4 相關於以上所掲示者是沒有改變。 該装置之驅動是披1¾明在圔示2 2中。在該柱塞2 Q 上之一第一推力傜造成該可移動中間栓塞7 2在該容器之 該中央區間中移動,其中/該圔筒狀殼套偽包含有該放大 部分7 3。該中間检塞7 2移動之结果偽造成該溶液流動 -28- 、-dh (C+VS)甲 4 (210 X 297 公*# ) ----------------一-- 裝------,1T-----{ % (請先閲讀背面之注意事項再填寫本頁) 經濟部中央標準局貝工消費合作社印κ 82.3. 40,000 經濟部中央標準局貝工消費合作社印¾ 五、發明説明() 進入該隔室1 0 z a中而來溶解該粉末或該親水性鹽70 。藉由此一方法,該醫藥锪質偽披組成或是被再組成,然 後該醫藥物質是被用來形成該要被施用在患者眼睛上之眼 藥水水珠。該柱塞2 0上是可被安裝有一以一罩蓋7 4形 ,式存在之可移動止動器,以來限制混合該二組成成份所須 之行程。 以下之步驟,亦就是本裝置利用之步驟是被說明在圔 示2 3中。在前述步驟之最後(當所有之溶液是己進入該 隔室1 〇 / a後),該活塞20是被向上推動而抵住該可 移動中間密封物7 2 ,在此時,該可移動中間密封物7 2 偽成形成一作用如同一活塞之單一元件。在抽拉該可移動 止動器後,該裝置在使用時之操作係完全相同於如先前所 述之該用於單一組成成份之装置之操作。一在該活塞上之 推力P 2在初始排出包含在該旁通氣室中之氣體後,而在 該可移動密封栓塞是未完全移動進入該旁通容室之前,該 推力P 2是有推動該可移動密封栓塞3 0進入該旁通容室 31之作用,然後可來使該先前已被組成之醫藥物質來流 通而形成眼藥水水珠。 圖示2 4至3 3偽說明先前所述之該裝置之元件之準 備和組合之步驟,其中,該容器是為二组成成份混合之形 式。由圔示24所說明之該第一步驟傜如先前所詋明者, 是為事先自一圓筒狀玻璃管中之所切下之該殼套4 0之淸 洗和塗谛上一層矽膠薄膜,其中該中央放大部分偽藉由一 -29- (CNS) r 4 (210 X 29: ) 82.3. 40,000 ----------------^--------裝-------玎-----„球 (請先閱讀背面之注意事項再填寫本頁) A6 B6 五、發明説明() 區域性加熱步驟而披形成,在此,該加熱步驟偽可來獲得 所須之合適變形。由圖示2 5所說明之下一値步驟,其係 為使該殼套4 0在一爐子6 2中以大约為3 0 0亡之溫度 來進行再加熱和去焦處理(depyrogenat io η)。由圓示26所説明之下一個步驟偽相同於参考圖示 14所掲示之步驟。圖示27偽說明在該裝置中來裝填一 第一組成成份,在此,該第一組成成份在以後偽會接受有 一親水化處理步驟。此一第一组成成份7 0 ~在接受由圔 示2 8所表示之該親水化處理步驟之後,其結果偽會得到 被包含在隔室1 0 < a中之該親水性鹽70。在此應被注 意的是,在該親水化處理步驟實施期間,該中間可移動栓 塞7 2是和該圓筒狀殼套4 0相喔合以來充分地密封該圓 茼狀殼套4 0。 在由圖示3 0所說明之該操作步驟期間,一柱塞偽推 動該中間可移動密封物72進入其之中央位置上,在此在 (請先閲讀背面之注意事項再墙寫本頁) —裝. 訂. 經濟邨中央標準局貝工消費合作社印汉 該裝形後套之見續 據被所隨毅質參後 佔} 物該狀物 ί 的 會 2 封 之筒藥 ο 同 將 7 密 明圓醫8不 2 物動說該有匣種 7 封移所保充容各 物密可 2 確«或或 封動間 3 來被匣理 密移中示以該卡處 •動可該圖設 ,在之 移間由由装下置同 可中於在被況..安不 間該入 。是情;被種 中 {注上 ο 一 可各 該件被部 2 此其於 ,元是底塞在後甩 間 一 1 之活 。然來 期此 7 室該封 ,以 存在液隔 ,密成中 貯 。溶方中後形丨 之 置該上 驟最被 3 置位 ,該步之是 3 装央後之作 ο 器示 該中 設成操 4 容圔 乂中囚:¾’孓(CNS) Y 4 ni洛(2ic X 297 公分) 82.3. 40,000 214513 A6 B6 五、發明説明() 操作。在此為清楚的是,在此一情況下基於該親水性鹽之 存在該容器之殺菌作用是為不可能的,因為該親水性鹽是 無法來承受如此之一操作。 該容器在該装置主體之裝設,和當此一容器是在其之 •位置上時該栓塞之組合以使該裝置可來被貯存等搡作步驟 ,其是相同於參考圔示18至20所掲示之搡作。 如先前所述者,該親水性鹽是可由一粉末或是一液體 所取代。該被設計來將該醫藥物質置放在該二隔室中之操 作步驟中之大部分,其是相同於參考画示24至33所掲 示之操作步驟。然而,當該隔室中之一者是包含一粉末時 ,在此偽須要栾先將該溶肢置放在該上方隔室中,然後再 來定位該中間可移動密封物,最後再來置入該粉末於該下 方隔室中。此一相關於置放該親水性盥和該溶液之反向操 作偽為須要的以來避免該上方隔室為該粉末所污染。一容 器之不受污染操作之步驟是進一步被要求來消除該粉末之 頼粒,其中該顆粒是可能散佈在此一容器之外部。在此一 賁施例中應該要被注意的是,該粉末之一殺菌操作通常是 不可能的,因為此一粉末是無法來接受如此之一操作。 在另一方面,當分別被包含在該下方和上方隔室中之 -------------------------裝------ΤΓ-----•線 一 ^ (諳先閲讀背面之注意事項再項寫本頁) 烴濟部中央標準扃we工消费合作社印¾ 可就下會 是亦該不 充 ,自是 琪施是時 之實或昇 質來始上 物上開度 0 向室溫 醫方隔在 二一方液 該另上溶 - 在該該 時是自要 液者:可只 溶或是 , 態 ,充外 掖施填之 為實之此 是被質除 質來物 α 物上藥始 藥向醫開 _ 方該室 二一 ,隔 該在是方 明中基甲.1悅烙(21ΰ X 297公殳) 82.3. 40,000 214513 A6 B6_ 五、發明説明() 有任何化學轉變或分解的話,該容器之一完全殺菌作用是 為可能的。 此二實施例之使用方式是為完全相同於前述之實施例 ,其中,前述之實施例之二隔室中之一者係包含有一親水 .性鹽。 對於上述所有實施例而言,其傺可能會産生有下述之 問題。當該使用者推動該活塞時,包含在該容器内之空氣 之一小體積之壓縮,其在一眼藥水水珠是被施加之後係可 能推動某一定量之液體使其流出該施該施用器嘴口,如此 而産生有具大之缺點。為了來避免此一缺點,一小型的回 吸作用是被建立在眼藥水使用之终了期間以來回吸該不受 控制地流出之眼藥水液體》此一效果是由該活塞1 2之一 持別設計之結果而被獲得。如圖示3 4所示,該活塞1 2 偽包含有一剛固保持制動器1 2 a ,該制動器1 2 a是和 該活塞桿柱連結成同一元件,同時該活塞1 2偽包含有一 環繞此一制動器1 2 a之可撓曲之環狀側綠部分1 2 b。 一支撐用短桿1 2c偽被安排在該保持制動器1 2a之底 部,如此當該活塞在靜止時,包含該短桿1 2 c之該制動 器之全部高度偽大约相同於該環狀側緣1 2 b之該内部孔 穴12 d之高度。當該活塞是被壓下時,如圖示35所示 ,該短桿1 2 c係造成該環狀側綠在該底部之一變形。在 使用後,當該環狀側綠回復至其原來形狀時,如画示3 6 所示,建立在該容器内之該獲縮偽導至一小型的回吸作用 -32- 82.3. 40,000 ------------------------裝------.玎------^ (請先閲讀背面之注意#項再壜寫本頁) 經濟部中央標準局員工消費合作钍印5代 經濟部中央標準局員工消費合作社印- A6 B6 五、發明説明() 。如此上述之目的偽被達成。 參考於圔示3 7,該裝置傜包含有一被裝置在該施用 器嘴口基部上之過濾器9 0。此一過濾器偽有一相當大的 面積。在該施用器嘴口之内部偽装設有一具殺菌作用之燒 結氣化銀之插置物9 1。 在由圔示3 8所表示之該實施例中,該較佳地是有殺 菌作用之過濾器9 2是有一較小之表面積。一銀製插置物 9 3是較佳地被置放在該施用器嘴口之内部。在上述之二 實施例中,該插置物偽界定有一軸向通道以允許該醫藥物 質之流通。 圖示3 9偽說明本發明裝置之另一形式之實施例,其 包含有一第一管狀元件100,該第一管狀元件100偽 部分地被裝設在一具有一密封底部之第二管狀元件1 0 1 之内部。該第一管狀元件是藉由一固定密封物10 2和一 可移動活塞104而被密封,其中,該固定密封物102 是被安排該二端部中接近於該装置之一施用器嘴口 1 0 3 之一端部上。在該第一管狀元件中由該固定密封物10 2 和該可移動活室1 0 4所形成之該内部空間是來包容該醫 藥物質。該第二管狀元件偽包含有一滑動活塞105,該 滑動活塞1 05偽籍由一中空剛固元件1 06而和該可移 動活塞1 ◦ 4機械連結,其中,該中空剛固元件1 0 6偽 界定有一通道以讀該醫藥物質可自該通道中流出。 該第一管狀元件1 0 0是被插立在一封套上1 0 7 , -3 3 - 82.3. 40,000 ------------------一----------裝------.订-------- (請先閑讀背面之注意事項再塡寫本頁) 214513 五、發明説明() 該封套1 07本身之一端部偽為一由可移動保護罩蓋1 0 8所套蓋住之施用器嘴口 1 03。該第二管狀元件1 0 1 像是由一罩蓋109所套蓋住,其中,該罩蓋109俗有 一被置放在該封套1 0 7内部之密封底部。此一罩蓋1 0 9上係包含有切槽1 1 〇或是周圍槽道,而該封套1 〇7 上傜包含有二或更多之被裝設在一斜槽上之具彈性舌狀物 1 1 1以和該切稽1 10 —起作用,如此以防止該罩蓋1 〇9離開該封套107之相對移動,而在此同時可來允許 其相反方向之移動。 如圖示40和41所顯示者,為了來使用該裝置,在 此偽須要藉由壓動該罩蓋1 0 9之底部以充分地推動該第 二管狀元件來朝向該第一管狀元件移動。如此偽産生使該 剛固元件1 0 6向前移動之效果,然後此一剛固元件之該 尖端1 1 2偽在該可移動活塞1 〇 4之該事先已被剌穿之 中央區間來穿過該可移動活塞,同時因該滑動活塞 移動之結果,該醫藥物質是被推動回流至在該第=管狀元 件105後方現在已為自由之一容室中。此一作用之結果 偽使全部之丨夜態竪藥拽質是自該、^置2前方而被·移_至該 装置之後方。該可移動活塞傷.移動至前方且是來阻塞抵靠 經濟部中央標準局具工消費合作社印*''代 (請先閲讀背面之注意事項再塡寫本頁) 當一 g外的推力是被施加在該裝置之該底部時,其偽造成 該醫藥物質之一滴接著一滴之流動。 _示4 2偽說明本發明裝置依圔不3 9至4 1之一變 -34- 82.3. 40,000 814513 A6 B6 五 '發明説明( 化實施例。 2〇是藉由 2是被喔合 上述圖示( 7。該滑動 部上之剛固 且該封套1 之中央凹槽 固定在此一 2 7 ,該周 S形成之保 在該封套之 該滑動 4 4中,該 態。在此將 1 2 1 a 是 固元件1 2 打開該單向 在此一實施例中,一容納該醫藥 一滑動活塞12 1而被密封,同 在一封套122中,該封套12 ,4 0和4 1 )中該裝 1是藉由一固定在此一 圖示3 9 活塞1 2 元件1 2 3而和該封套 1 2 2機 用器嘴口 2 2偽界定ή 一和一施 5和一銀製帽狀 一過濾器1 2 中。該容器包含有一周 分1 2 7係和一和該封 物1 2 8 —起作用,以6 B Printed by the Beigong Consumer Cooperative of the Central Bureau of Standards of the Ministry of Economy V. Description of the invention () The detailed status can be further understood from the illustrations 12 to 20. These pictures show the entire manufacturing process of the device, that is, the preparation and assembly of the different components. Figure 1 2 Pseudo-instructions include the steps of the following procedure: use an extractable nozzle tip to clean the cylindrical shell 4 0 and apply a layer of silicon on the Yi shell 4 Ο, the cylindrical shell The sleeve 40 is held in place by the operation of a clamp 61. The cylindrical sleeve 40 was previously cut from a glass tube by thermal shock and without a special shape. Then, as shown in Figure 13, this cylindrical shell is reheated and depyrogenated at a temperature of 30 Ot: in a furnace 62. Figure 14 illustrates the use of an axially movable plunger 63 to place the movable sealing plug 30. Drawing 15 shows the filling procedure of the container, or more precisely, the shell 4 is filled with the medicinal substance 29 by the filling of the extractable injector 6 4 under a pull. Fig. 16 shows the situation where the piston 12 is installed via an axially movable plunger 65. It is assumed here that the container has a completely cylindrical outer shape, and a large number of containers filled with medicinal substances can be placed in a container in a way to be connected to each other for subsequent use Use. In these subsequent procedures, the most useful one is the sterilization effect of the high-pressure steam cooker. This effect is provided under the condition that the medicinal substance 29 can withstand a relative increase in temperature. Explain the placement of the container in the device, of which -27- 82.3. 40,000 (please read the precautions on the back before writing this page) —install · .11. A6 B6 214513 V. Description of the invention () The device It was sterilized in an appropriate way beforehand. After this installation, the plunger 20 was brought to its position and connected to the piston as shown in Figure 19. Figure 20 shows one of the devices fully assembled and reversed. In this case, the device can also be stored in a container in a single or collective package. Figure 2 1 to 2 3 pseudo-symbolizes the storage and distribution device of the eyedrops, wherein the container 10 Z is divided into two compartments 10 za and 10'b respectively, the container 10 / The lower compartment 10'a may contain a hydrophilic salt 70 (as shown), or a powder, or a liquid, and the upper compartment 10 / b must contain a solution in a liquid state. As previously mentioned, the container 10 'is sealed on one of its threads by a movable sealing plug 30, and is sealed on one of its upper ends by a piston. An intermediate movable embolism 7 2 pseudo-separates the two compartments 1 ϋ z & 10 ′ b. In the form of this embodiment, the cylindrical casing 40 of the figure of the container 101 has a central enlarged portion 73, and the central enlarged portion includes a bypass channel when the entirety is used, and the following There is no further disclosure. Other components, such as the plunger 20 and the applicator mouth 14 have not changed in relation to those shown above. The drive of the device is shown in Figure 22. A first thrust force on the plunger 2 Q causes the movable intermediate plug 72 to move in the central section of the container, in which the swollen cylindrical shell pseudo contains the enlarged portion 73. The result of the movement of the intermediate plug 7 2 forged the flow of the solution -28-, -dh (C + VS) A4 (210 X 297 male * #) --------------- -一-installed ------, 1T ----- {% (please read the notes on the back before filling in this page) Printed by Beigong Consumer Cooperatives, Central Bureau of Standards, Ministry of Economic Affairs κ 82.3. 40,000 Central Ministry of Economic Affairs Printed by Beigong Consumer Cooperative of Standards Bureau. V. Description of the invention () Enter the compartment 10 za to dissolve the powder or the hydrophilic salt 70. By this method, the medical antimicrobial pseudomask is composed or reconstituted, and then the medical substance is used to form the eye drops to be applied to the patient's eye. The plunger 20 can be installed with a movable stopper in the form of a cover 74 to limit the travel required to mix the two components. The following steps, which are the steps used by this device, are described in Figure 23. At the end of the previous step (after all the solution has entered the compartment 10 / a), the piston 20 is pushed upward against the movable intermediate seal 7 2, at this time, the movable intermediate The seal 7 2 is pretended to form a single element that acts as the same piston. After pulling the movable stopper, the operation of the device in use is exactly the same as that of the device for a single component as previously described. A thrust P 2 on the piston initially discharges the gas contained in the bypass chamber, and before the movable sealing plug is completely moved into the bypass chamber, the thrust P 2 pushes the The movable sealing plug 30 enters the bypass volume 31, and then the previously formed medical substance can be circulated to form eye drops. Figures 2 4 to 3 3 pseudo-describe the steps of preparation and assembly of the components of the device previously described, where the container is in the form of a mixture of two components. The first step described by 圔 示 24, as described earlier, is to wash and apply a layer of silicone film to the shell 40 previously cut from a cylindrical glass tube. Among them, the central magnified part is faked by a -29- (CNS) r 4 (210 X 29:) 82.3. 40,000 ---------------- ^ ------- -Installation ------- 玎 ----- "Balls (please read the precautions on the back before filling in this page) A6 B6 5. Description of the invention () Regional heating steps are formed, here, this The heating step can be used to obtain the desired deformation. The next step is illustrated by the illustration 25, which is to make the shell 40 in a furnace 6 2 at a temperature of about 300. Perform reheating and defocusing (depyrogenat io η). The next step illustrated by circle 26 is pseudo-same as the one illustrated with reference to figure 14. Figure 27 pseudo-describes that a first component is filled in the device Components, here, the first component will be subjected to a hydrophilization treatment step in the future. This first component 70 ~ ~ after receiving the hydrophilization treatment step represented by 圔 示 28 It is possible to obtain the hydrophilic salt 70 contained in the compartment 10 < a. It should be noted here that during the implementation of the hydrophilization treatment step, the intermediate movable plug 72 and the cylinder Since the 40-phase casing is fully sealed, the round chrysanthemum-shaped casing 40 is fully sealed. During the operation step illustrated by the diagram 30, a plunger pseudo-pushes the middle movable seal 72 into it Central location, here (please read the precautions on the back and then write this page on the wall)-installed. Ordered. Economic Village Central Bureau of Standards, Beigong Consumer Cooperative Society, India and Han. After the quality of the ginseng} The thing and the thing will be the 2 seals of the tube medicine ο The same will be 7 密 明 圆 医 8 No 2 The thing is said to have the box type 7 Sealing and the preservation of the contents can be dense 2 OK «or Or seal the moving room 3 to be shown by the card in the case of moving the box secretly. The moving can be set in the picture, and the moving room can be set by the device and can be used in the state of the quilt .. ; Be planted in the {note on ο one can each piece of this piece is part of the other, the yuan is the bottom plug in the back of the room a 1 to live. Then in the coming 7 rooms the seal, in order to exist liquid It is stored in a dense mixture. The top shape of the fused side is set by the uppermost step 3, the step is the work after 3 installations. The instrument shows that the middle is set to operate 4 Rong Xiqi prisoner: ¾ ' (CNS) Y 4 ni Luo (2ic X 297 cm) 82.3. 40,000 214513 A6 B6 V. Description of the invention () Operation. It is clear here that in this case based on the presence of the hydrophilic salt in the container Sterilization is impossible because the hydrophilic salt cannot withstand such an operation. The installation of the container in the main body of the device, and the combination of the plug when the container is in its position so that the device can be stored and the steps are the same, which is the same as reference 18 to 20 The show is shown. As previously mentioned, the hydrophilic salt can be replaced by a powder or a liquid. Most of the operation steps designed to place the medical substance in the two compartments are the same as the operation steps shown in reference drawings 24 to 33. However, when one of the compartments contains a powder, it is necessary for Luan to place the dissolving limb in the upper compartment first, then to locate the middle movable seal, and finally to place Into the lower compartment. This is related to the reverse operation of placing the hydrophilic toilet and the solution as necessary to avoid contamination of the upper compartment with the powder. The steps of a non-contaminated operation of a container are further required to eliminate the particles of the powder, wherein the particles may be scattered outside the container. It should be noted in this Ben application that sterilization of one of the powders is usually impossible, because this powder cannot accept such an operation. On the other hand, when it is contained in the lower and upper compartments --------------------------------------------- ΤΓ ----- • Line 1 ^ (Read the precautions on the back and then write this page) The Central Standard of the Ministry of Hydrocarbon Economy is printed by the Consumer Welfare Cooperative Society. It is the real time or the quality is improved. The opening on the object is 0. To the room temperature, the medical solution is separated from the other side. The other should be dissolved-at this time, it is the liquid required: it can only be dissolved or, state, charge The fact that the filling of the outer nipple is true is that the substance is removed from the substance, the substance is α, the medicine is prescribed, and the medicine is prescribed to the doctor _ Fang the room 21, the other is the Fang Mingzhong base. 1 Yue Luo (21ΰ X 297 Gong Shi) 82.3. 40,000 214513 A6 B6_ V. Description of the invention () If there is any chemical transformation or decomposition, it is possible for one of the containers to be completely sterilized. The two embodiments are used in the same way as the previous embodiment, wherein one of the two compartments of the previous embodiment contains a hydrophilic salt. For all the above-mentioned embodiments, the following problems may arise from Ye. When the user pushes the piston, a small volume of air contained in the container is compressed, which may push a certain amount of liquid to flow out of the mouth of the applicator after the eye drops are applied This has big disadvantages. In order to avoid this shortcoming, a small sucking effect is established to suck back the uncontrolled eyedrop liquid since the end of the eyedrops. This effect is held by one of the pistons 12 The result of the design is obtained. As shown in FIG. 3 4, the piston 1 2 pseudo includes a rigid holding brake 1 2 a, the brake 1 2 a is connected with the piston rod to form the same element, and the piston 1 2 pseudo includes a surrounding one The green portion 1 2 b of the flexible ring side of the brake 1 2 a. A supporting short rod 1 2c is arranged at the bottom of the holding brake 1 2a, so that when the piston is at rest, the total height of the brake including the short rod 1 2 c is approximately the same as the annular side edge 1 The height of the internal cavity of 2 b is 12 d. When the piston is depressed, as shown in Fig. 35, the short rod 12c causes the annular side green to deform at one of the bottoms. After use, when the ring-shaped side green returns to its original shape, as shown in Figure 36, the shrinkage established in the container leads to a small suction effect -32- 82.3. 40,000- ----------------------- 装 ------. 玎 ------ ^ (Please read the note # on the back first, then 壜Write this page) Employee consumption cooperation of the Central Bureau of Standards of the Ministry of Economic Affairs Thorium seal 5th generation Employee consumption cooperative of the Central Bureau of Standards of the Ministry of Economic Affairs-A6 B6 V. Description of invention (). In this way, the above-mentioned purpose is falsely achieved. Referring to Figure 3 7, the device contains a filter 90 which is mounted on the base of the mouth of the applicator. This filter has a considerable area. Inside the mouth of the applicator is camouflaged a sterilized silver sintered insert 91. In the embodiment indicated by the reference 38, the filter 92, which preferably has a bactericidal effect, has a small surface area. A silver insert 93 is preferably placed inside the mouth of the applicator. In the above two embodiments, the insert pseudo-defines an axial channel to allow the circulation of the medical substance. Figure 39 pseudo-illustrates another form of embodiment of the device of the present invention, which includes a first tubular element 100 which is pseudo-partially mounted on a second tubular element 1 having a sealed bottom 0 1 inside. The first tubular element is sealed by a fixed seal 102 and a movable piston 104, wherein the fixed seal 102 is arranged in one of the two ends close to the applicator mouth 1 of the device 0 3 on one end. The internal space formed by the fixed seal 10 2 and the movable chamber 104 in the first tubular element is to contain the medical substance. The second tubular element pseudo includes a sliding piston 105, which is mechanically connected to the movable piston 1 ◦ 4 by a hollow rigid element 106, wherein the hollow rigid element 106 is pseudo A channel is defined to read that the medical substance can flow out of the channel. The first tubular element 100 is inserted into a sleeve 1 0 7, -3 3-82.3. 40,000 ------------------ 一 ---- ------ Install ------. Order -------- (please read the precautions on the back before writing this page) 214513 V. Description of the invention () The envelope 1 07 itself One of the ends is an applicator mouth 103 covered by a removable protective cover 108. The second tubular element 101 appears to be covered by a cover 109, wherein the cover 109 generally has a sealed bottom placed inside the envelope 107. The cover 1 0 9 includes a cut groove 1 1 〇 or a surrounding channel, and the upper cover of the envelope 1 0 7 includes two or more elastic tongues mounted on a chute The object 1 1 1 acts in conjunction with the cut 1 10, so as to prevent the relative movement of the cover 10 9 from the envelope 107, while at the same time allowing its movement in the opposite direction. As shown in Figures 40 and 41, in order to use the device, it is necessary to move towards the first tubular element by pressing the bottom of the cover 109 sufficiently to push the second tubular element. This pseudo-generates the effect of moving the rigid element 106 forward, and then the tip 1 12 of the rigid element is pseudo-pierced in the central section of the movable piston 104 that has been penetrated beforehand After the movable piston, as a result of the movement of the sliding piston, the medicinal substance is pushed back into a chamber that is now free behind the third tubular element 105. As a result of this action, if all the night-state vertical medicine dragging properties were moved from the front of the device to the back of the device. The movable piston is injured. Move to the front and it is to block against the stamp printed by the Ministry of Economic Affairs Central Standards Bureau Tooling Consumer Cooperative * (please read the precautions on the back before writing this page). When the thrust is 1g When applied to the bottom of the device, it fakes a drop-by-drop flow of the medical substance. _Show 4 2 pseudo description of the device according to the present invention is not changed from 3 9 to 4 1 -34- 82.3. 40,000 814513 A6 B6 5 'Description of the invention (in the embodiment. 2 is by 2 is combined with the above figure Show (7. The sliding part is rigid and the central groove of the envelope 1 is fixed in this 2 7, the cycle S is formed in the slide 4 4 of the envelope, this state. Here will be 1 2 1 a is a solid element 1 2 opens the one-way. In this embodiment, a sliding piston 12 1 containing the medicine is sealed, the same in an envelope 122, the envelopes 12, 40 and 41) The device 1 is fixed by a picture 3 9 piston 1 2 element 1 2 3 and the envelope 1 2 2 machine mouth 2 2 pseudo-definition one and one application 5 and a silver cap-shaped one filter器 1 2. The container contains a week 1 2 7 series and one and the seal 1 2 8-to function, to
中央凹槽 圍放大部 持用舌狀 内部D 锪質之 時該容 2是大 置之封 封套1 械地相 12 4 物1 2 圍放大 套1 2 來保持 容器1 器1 0 致相同 套1 0 2 2底 連結, 相連通 6是被 部分1 2為一 該容器 活塞1 2 1之詳細形狀是被掲示在圖示4 3和 二圖示偽分別說該裝置是在貯存和在使用之狀 被注意到的是,該滑動活塞1 2 1之中央部分 為一薄膜,當在使用期間(圖示4 4 )自該剛 3之推力係使該薄膜之形狀變形,如此係有一 閥Β 1 2 1 b之效杲而來允許該醫藥物質流動 ------------------------裝------tr-----《4: I- - (锖先Mit背面之注意事項再填寫本頁) 經濟部中央標準局员工消費合作社印3衣 看 一先允 被 有書可 可 用明該 中使 說為 式地案是 形分本中 例部如搆 施或有機 實地可些 部部是這 全 全置在 之是裝 α 示 例..之果 〇 揭施;明效 b 和實發之 1 明之本置 2 詋置肋裝 1 所裝幫想 II示明以理 閥圖發構一 向上本機之 單以 ,之示 該由 是量揭 過 的數所 通 到定前 82.3. 40,000 1 2 e /-When the central groove surrounds the tongue-shaped inner part with a tongue-shaped inner D, the volume 2 is a large-sized envelope 1 mechanical phase 12 4 objects 1 2 surround the enlargement sleeve 1 2 to hold the container 1 container 1 0 to the same sleeve 1 0 2 2 bottom connection, connected 6 is part 1 2 is a container piston 1 2 1 The detailed shape of the container piston is shown in the picture 4 3 and the two pictures pseudo said that the device is in storage and in use It is noticed that the central part of the sliding piston 1 2 1 is a film. When the thrust force from the rigid 3 during use (shown in FIG. 4 4) deforms the shape of the film, there is a valve B 1 2 1 The effect of b comes to allow the flow of the medicinal substance ------------------------ installed ------ tr ----- 4: I--(Import the precautions on the back of Mit first, then fill out this page) Printed by the Ministry of Economic Affairs, Central Bureau of Standards, Employee Consumer Cooperatives, 3 clothes, a copy of the first permission is available. The examples in this book are the construction or the organic field, but these parts are all placed in it. It is a case of installing α. The fruit of the 〇 reveals; the effect of b and the fact that the 1 is the original position 2 the ribs are installed 1 The installed helper II shows justification The structure of the valve diagram is as follows: the list of the machine is up, and the indication is that it should be communicated to the pre-determination 82.3. 40,000 1 2 e /-
6 6 A B 經濟部中央標準局κκ工消費合作社印- 五、發明説明() 許眼藥水水珠是被形成在一定之力量下。這些機搆包含有 一可移動活塞,其在軸向之一方向上移動以來在一貯存醫 藥物質之容器内建立起有一體積之眼藥水水滴,或是包含 有一固定活塞和一在該固定活塞上方滑動之可移動容器, 並且來確保該容室是包含有該醫藥物質之一具一體積之水 滴之形成,其中,該醫藥物質是被貯存在此一可移動容器 之中。 在此同時亦有機構以來預防一真空被建立在該容器内 部之可能性。這些機構包含有一可移動之活塞和一活塞桿 柱,其中該活塞和該活塞桿柱並不為機械連結在一起,或 是S含有一可移動活塞和一單方向閥體,其中當該可移動 容器是被拉動時該單方向閥體是被封閉,或是包含有一固 定閉封物和一單方向閥體或是一覆蓋於該可移動容器上而 未和該可移動容器相連结之可移動柱塞,該可移動柱塞係 防止因拉動該可移動容器而來拉伸該可移動容器之所有可 能性,如此以使該容器偽只能有藉推力所造成之單一方向 之移動。 在此同時亦有機溝可來控制該醫藥物質之流動速率以 來産生規則而精確的眼藥水水滴而不會有形成一水柱之危 險。這些機構包含有一流動速率控制器,其偽依據該眼_ 水溶液之壓力和粘度為比例..而來建立起一負載上之損失, ' ;·' 該流動速率控制器偽是為一人造多孔而具一厚度之過滹器 形式,其是藉由一 Μ壓縮粉末或金屬球體然後再燒結而得 36- (請先閱讀背面之注意事項再填寫本頁} 丨裝. 訂· 線. 本 中:¾¾’家(CXS)甲 格(210 X 297 ) 82.3. 40,000 A6 B6 五、發明説明( ,如此在該過 孔。此一機構 的之元 基於該 •移動一 積之水 服後且 之滑動 式而來 在 逹率控 之一具 在 件,因 活塞抵 毫米之 珠是為 在此亦 是不可 自由地 此應該 制器是 撓性容 此本發 在一滴眼藥水 ,此一剩餘壓 力和該藉由該 造成。本發明 成之同時在該 滴之形成。這 遽器上 是被考 為在此 靠在該 十分之 不可能 無任何 避免, 流出。 要被注 和壓力 器之壁 明之裝 被精確 力是棊 流動速 之這些 施用器 些機構 是被形成有穿透的被調制孔洞或是狹 盧來獲得該所須精確水滴所不可或缺 是不可能精確地控制該活塞之移動( 容器壁牆上之摩擦力,該活塞之精確 一之距_以來産生一為3 0微公升體 的)。因為一旦當此一摩擦力是被克 流動速率控制器之設置的話,該活塞 如此而造成該溶液可來以一水柱之形 意的是 被施加 牆上是 置亦有 施用後 於該活 率控制 機構是 嘴口之 包含有 ,在一活 習用裝置 有一相同 機構可來 殘餘在該 塞抵靠在 器所導致 用來避免 未端部分 以一具彈 塞装置上之此一流動 中目前已被廣為使用 之效果。 消除因該活塞移動而 容器内部之剩餘壓力 該容器壁牆上之摩擦 之負載損失等因素所 在該第一滴眼藥水形 上有第二滴眼藥水水 性膜片形式存在之一 ‘先閲讀背面之注意事項再填寫本頁)6 6 A B Printed by the Central Standards Bureau of the Ministry of Economic Affairs κκIndustry and Consumer Cooperatives-V. Description of the Invention () Xu Yanye drops are formed under a certain force. These mechanisms include a movable piston that has moved in one of the axial directions to establish a volume of eye drops in a container for storing medicinal substances, or includes a fixed piston and a slidable slide over the fixed piston Move the container, and ensure that the chamber is formed of a volume of water droplets containing one of the medicinal substances, wherein the medicinal substance is stored in this movable container. At the same time, there is also the possibility of preventing a vacuum from being established inside the container. These mechanisms include a movable piston and a rod rod, where the piston and the rod rod are not mechanically connected together, or S contains a movable piston and a unidirectional valve body, where the movable When the container is pulled, the one-way valve body is closed, or contains a fixed closure and a one-way valve body, or a movable covering the movable container without being connected to the movable container Plunger, the movable plunger prevents all possibilities of stretching the movable container by pulling the movable container, so that the container can only move in a single direction caused by thrust. At the same time, the organic ditch can be used to control the flow rate of the medicinal substance to produce regular and precise eye drops without the risk of forming a water column. These mechanisms include a flow rate controller, which is based on the pressure and viscosity of the eye_aqueous solution in proportion to the establishment of a load loss, '; ·' The flow rate controller is a pseudo-porous and It has the form of a filter with a thickness, which is obtained by compressing a powder or metal sphere with a Μ and then sintering to get 36- (please read the precautions on the back before filling out this page) 丨 installed. Order · line. In this: ¾¾ 'Home (CXS) Jiage (210 X 297) 82.3. 40,000 A6 B6 V. Description of the invention (, so in the via. The element of this organization is based on the movement of a large amount of water and sliding Here comes one of the most important things in the rate control, because the piston is against the millimeter beads. It is also not free here. The device should be flexible. This should be a drop of eye drops. This residual pressure and the borrow Caused by this. The invention is formed at the same time that the drop is formed. This device is considered to be leaning on this very unlikely to flow out without any avoidance. The equipment to be injected and the wall of the pressure device is accurate Power is the speed of flow It is indispensable to obtain the required precise water droplets by using a mechanism that is formed with a modulated hole or a narrow hole penetrating. It is impossible to accurately control the movement of the piston (friction force on the wall of the container, the piston The precise distance between them has produced a volume of 30 microliters. Because once the friction force is set by the flow rate controller, the piston causes the solution to come in the shape of a water column. It means that it is placed on the wall and also included after the application. The rate control mechanism is included in the mouth. There is a same mechanism in a living device that can be left in the plug against the device. The end part is an effect that has been widely used in this flow on a bullet device. Eliminating the residual pressure inside the container due to the movement of the piston, the load loss of the friction on the wall of the container and other factors are the first There is one of the second eye drops aqueous film on the form of eye drops. First read the precautions on the back and then fill out this page)
經濟部中央標準局3工消费合作社印K 區 間 中 之 塞 活 ^janw 滑 該 在 放 置 被 是 片 膜 該 中 其 間 區 〇 央上 中間 部ii 端穿 其可 在不 口的 嘴證 該保 使有 來具 可是 構封 機密 有 一 亦此 置 , 裝封 該密 之的 明透 發穿 本可 此不 在有 具 上 S2.3. 40.000 % A6 B6 五、發明説明() 性,或是不會産生過多的壓力,或是不會將在該施用器嘴 口内之液體水柱驅動回流至該容器之内部。這些機構包含 有一不具螺旋之罩蓋。在習知之条統中,該具螺旋之罩蓋 通常是具有一密封環狀物以在該罩蓋被完全旋緊前來密封 .該瓶子,如此以避免因該罩蓋之未能完全鎖緊至該瓶子時 來建立有具缺陷的不可穿透性。此一習用設計是有以下之 缺點:其會産生有過大之壓力和迪成眼藥水來被醒動朝向 該容器之内部回流,如此係會造成細菌之污染,或是因為 空氣滲穿至該容器内部之結果而在容器内部産生有泡沫。 同時,本發明之該裝置亦有額外機構可來消除在該施 用器嘴口内紊流之産生。在這些機構中是包含有一單向閥 體和一單向移動之活塞,其偽用來防止液體被回吸至該容 器之内部。 最後,本發明之裝置是有機構以來消除細菌之繁殖, 其中,該細菌是可能在一滴眼藥水被施用之後來移動進入 該施用器嘴口之内部中。這些機構是藉由具有殺菌作用或 制菌自動殺菌作用之材料之出現而被獲得,其中,該材料 是藉由一徹/if動的作甩或水解性.釣恨甩面來抑制组菌之滋 .長。這些機構包含有一元件,一鍍層或是一插置物,其是 乂〆' 可為具多孔性或是不以重金屬來製造之,例如像是為一例 為銀、金、白金、鍚、銅.·.等等之貴金屬或半貴金屬 等,或是為上逑金屬之一化合物,特別地是為氧化物或是’ 氧化物之混合,例如像是氣化銀或是一例為鐵氟龍(R) -38« 82.3. 40,000 ------------------------裝------ΤΓ-----~ ^ f 一 (绮先閲讀背面之注意事項再填寫本頁) 經濟部中央標準局0®工消費合作钍印¾ X ) A6 B6 五、發明説明() 之陶磁或其它具有相似非結晶待性和防腐殺菌效果之任合 其它物質,或是最終地,上述金屬,化合物或物質之一混 合或是組合。在這些機構中亦是包含有該施用器嘴口之一 待別設計。此一待別設計傜使該施用器可來在一眼藥水水 珠被形成和排出後來僅保留有一極端小的殘餘眼藥水體積 。闋於此點,在此應被注意到的是,該殘餘眼藥水體積理 想地是為一滴眼藥水體積之10至20%,如此該損失可 減至最小,且該施甩之眼藥水劑量是可足夠大地來補償上 述殘餘體積之具作用成分在其部分上所失去之具防腐殺菌 作用之持性。 經濟部中央橒準局貝工消費合作钍印发 一茴較佳之解決方案偽包含有在該施用器嘴口内部上 來插入一具有多孔性之桿狀物,此一捍狀係藉由壓縮氧化 銀然化來烷結之而為獲得,如此以來提供一具一厚度之過 濾器。在實際上,由微生物學之觀點上來視之,要來得到 ..有最佳效果之形式是為該表面積/髏積之比例是有一可能 最大之比例。位在該分佈器接近於該施用器孔口之醫藥物 質之預定e積,較佳地是小於一滴眼藥水水珠之體積。介 於以徹公升量測之該預定b積和以平方毫米量測之該防腐 作用裝置之表面積之比例,其在任何情況下是小於1 ,且 較佳地是小於0 . 5。 總而言之,基於本發明装置之整體設計和其間單獨元 件之設計和單獨元件間交互作用之結果,本發明對於製造 者和使用者而言是可獲有一多數新穎特性之®點。 -3 9 - 82.3. 40,000 (請先閱讀背面之注意事項再塡寫本頁) (CNS) ^ 4 ¢210 X 2S7 ^ ) 明 説 明 發 Ψ 五The Ministry of Economic Affairs, Central Bureau of Standards, 3 Industrial and Consumer Cooperatives printed K in the interval ^ janw sliding in the place is placed in the film in the middle of the area. The upper middle part ii can wear it in the mouth. Comes with a secret, but there is also a place to set the secret. The transparent and transparent hairdresser that encapsulates the secret may not have S2.3. 40.000% A6 B6. V. The description of the invention (), or will not produce too much Pressure, or will not drive the liquid water column in the mouth of the applicator back to the inside of the container. These mechanisms include a non-spiral cover. In the conventional system, the screw cap is usually provided with a sealing ring to seal the cap before the cap is fully tightened. The bottle is thus avoided to prevent the cap from being fully locked By the time of the bottle, a defective impermeability was established. This conventional design has the following disadvantages: it will generate excessive pressure and Dicheng eye drops to be awakened and flow back toward the inside of the container, which will cause bacterial contamination, or the air penetrates into the container As a result of the inside, foam is generated inside the container. At the same time, the device of the present invention also has additional mechanisms to eliminate turbulence in the mouth of the applicator. These mechanisms include a one-way valve body and a one-way moving piston, which is used to prevent liquid from being sucked back into the container. Finally, the device of the present invention has mechanisms to eliminate the propagation of bacteria, wherein the bacteria may move into the mouth of the applicator after a drop of eye drops is applied. These mechanisms are obtained by the emergence of materials that have a bactericidal effect or bactericidal automatic sterilization effect, in which the material is shaken or hydrolyzed by a full / if action. .long. These mechanisms include a component, a coating or an interposer, which can be porous or not made of heavy metals, such as silver, gold, platinum, tin, copper, for example. .Noble metals or semi-precious metals, etc., or a compound of the upper metal, especially oxides or mixtures of oxides, such as vaporized silver or Teflon (R) for example -38 «82.3. 40,000 ------------------------ installed ------ ΤΓ ----- ~ ^ f one (Qi Xian Read the precautions on the back and fill in this page) Central Bureau of Standards of the Ministry of Economic Affairs 0® Industrial and Consumer Cooperation Thorium Seal ¾ X) A6 B6 V. Description of the invention () Ceramics or any combination with similar non-crystalline hospitality and antiseptic sterilization effect Other substances, or ultimately, one of the above metals, compounds or substances are mixed or combined. One of the mouths of the applicator is also included in these mechanisms. This wait-and-see design allows the applicator to be formed and discharged after a drop of eye drops only retains an extremely small volume of residual eye drops. At this point, it should be noted here that the volume of the residual eye drops is ideally 10 to 20% of the volume of a drop of eye drops, so that the loss can be minimized, and the dose of the eye drops applied is It is large enough to compensate for the persistence of the anti-corrosion and sterilization effect of the above-mentioned residual volume of the active component on its part. The Ministry of Economic Affairs Central Bureau of Industry and Fisheries Consumer Cooperation Thorium issued a better solution of fennel. Pseudo-containment consists of inserting a porous rod inside the mouth of the applicator. It is obtained by conversion to alkane, thus providing a filter with a thickness. In fact, from the point of view of microbiology, it is necessary to obtain .. The form with the best effect is that the ratio of the surface area to the cross-sectional area is the largest possible ratio. The predetermined e product of the medicinal substance located in the dispenser close to the orifice of the applicator is preferably less than the volume of a drop of eye drops. The ratio between the predetermined b product measured in liters and the surface area of the anticorrosive device measured in square millimeters is in any case less than 1, and preferably less than 0.5. In summary, based on the overall design of the device of the present invention and the design of the individual components therebetween and the interaction between the individual components, the present invention provides a number of novel features for manufacturers and users. -3 9-82.3. 40,000 (Please read the notes on the back before writing this page) (CNS) ^ 4 ¢ 210 X 2S7 ^)
6 6 A B 任完該結 在是,連 且氣是地 動空的固 推之實堅 前用事塞 向作為活 被菌此該 可殺在和 只披 α 有 塞未部沒 活是内而 該 ,之上 為動器之 因拉容塞 - 後該活 言向至該 而被入在 者可吸設 用不被裝 使皆來被 於下能僅 對況可是 情不塞 何全柱 後滯 最 留 且能 , 可 隔後 阻用 腐使 防始 的初 效在 有置 常裝 非明 1 發 成本 形證 傜保 器傜 濾置 過裝 該菌 〇 殺 起腐 1 防 在該 明用 發使 本之 〇 置 菌裝 殺本 之由 質經 物在 藥質 翳物 滴藥 1 醫 何該 任使 之偽 部果 内結 口 之 嘴歡 器特 用述 施上 該置 在裝 方殺 種溫 各高 之受 述接 所能 上不 以保 案確 本來 得下 使況 偽狀 杲的 結劑 其腐 , 防 的用 菌 使 無有 為沒 持在 保可 仍偽 後法 排 來 係 其 中 置 裝 明 〇 發 裝本 包於 菌造 無製 之被 液來 溶地 質外 物額 藥是 0 塞 之活 理該 處 菌6 6 AB is the end of the knot is, even if the qi is the ground and the air is solid and solid, before using it, it should be used as a living quilt. It should be killed and only covered with α. Above is the actuator's pulling capacity-after that, the words can be absorbed by those who can be used without being installed, so they can be used only by the situation, but the situation is not jammed. Yes, it is possible to prevent the initial effect of the use of rot to prevent the initiation. In the case of a regular installation of non-ming 1, the cost of proof is to protect the device. The bacterium is killed. 〇Put the bacteria and kill the roots of the meridian in the medicine. The medicine should be used in the pseudo part of the mouth of the mouth. The special device is applied to the device. The acceptance of the description of the connection can not be used to ensure that the case is actually able to use the causal agent of the pseudo-hypocrite to prevent its rot, and the use of anti-bacteria makes it useless. 〇The package is contained in the bacterium-made untreated liquid to dissolve the geological foreign material. The medicine is 0.
之滲 質菌 物細 藥之 醫生 該産 防所 預後 以用 此使 如次 丨 一 力第 壓在 餘為 殘因 之 〇 中動 置流 裝之 明須 發所 本為 在不 除 I 果氧 效為 動是 活例 微 一 一 或 著屬 有金 多重 更同 或.不 一 由 為一 因此 其 0 ,決 題解 問被 染而 污甩 之採 成之 造件 而元 透之 所装 們菌 人殺 為腐 是防 其逑 , 上 果 -效果 動效 活菌 微殺 之之 生其 産 揮 所發 物地 化效 氧有 屬來 金 了 重為 之 0 銀悉 化知 (請先«讳背面之注意^-項存填寫本頁) 丨裝. 訂. Λ球. 蛵濟部中央標準局爵工消費合作钍印^ 被每 要在 該 , 而為 - 是 好果 愈結 大其 愈 〇 須好 必愈 是小 積愈 面要 表是 觸積 接體 之之 表質 質物 物藥 藥醫 醫之 和理 置處 被積銀 須體由 必之是 是珠件 積水元 體水菌 餘藥殺 殘眼性 之滴活 口 一 一 孔毎是 該於的 於,.小佳 近.須較 接必為 , 是 此 後且在 用積 , 施體的 被之目 水定一 藥一此 眼為了 滴證為 1 保 0 〜、人:乂又茂这片]中^ :¾家(C\S)甲.1 (21,〕X 297二、分) 82.3. 40.000 A6The doctor of the osmotic bacteria fine medicine has the prognosis of the obstetric prevention institute to use this to make the first place the first pressure is still the residual cause. The clear liquid must be made in the first place. In order to move is a living example, one is one or one, and the one with gold is more or less the same. The one is not one, so its 0, the problem is solved by the stained and smeared artifacts and the penetrating people who are installed. Killing for decay is to prevent it, the fruit of the effect of the micro-killing of the effect of the active bacteria, the production of the effective oxygen of the ground, there is a gold to the gold, and the weight is 0. Attention ^ -item fill in this page) 丨 installed. Ordered. Λ ball. The Central Department of Economics and Trade Department of the Ministry of Economics and Consumer Affairs thorium printing ^ printed by the ^ every need to be in the, and for-is the good fruit grows bigger It is better to be a small product, and the surface is to be the surface quality of the contact body. The medicine and the doctor are treated by the silver accumulator body. It must be a bead of water accumulation. Every hole of the drop eye of the residual eye is due to. Xiaojia is close. It must be more close, it is after and in Accumulate, apply the medicine by the eyes of the body to set a medicine for this purpose. It is guaranteed to be 1 to protect 0 ~, people: Xie Youmao]] ^: ¾ home (C \ S) A.1 (21,) X 297 Second, points) 82.3. 40.000 A6
五、發明説明() 經濟部中央標準局員工消費合作社印鬏 用裝 使制 披控 來率 c 式 S 形動 器流 濾 一 過為 之做 度可 厚亦 一 外 具用 之作 成菌 製殺 所了 物除 化件 氧元 銀該 結此 燒如 。 和 ,置 -----------------(-----------裝------.玎------- (請先W讀背面之注意事項再碭寫本頁) 本乜t適明中围:¾家m (CNS)甲4規仏a)i〇 X 37 ) 8^.3. 40,000Fifth, the invention description () Ministry of Economic Affairs, Central Bureau of Standards, Employee and Consumer Cooperatives, the use of equipment to control the rate of use of c-type S-shaped actuator flow filter can be done thick and can also be used for external control All the oxygen-removing silver should be burned like this. And, set ----------------- (----------- install ------. 玎 ------- (please Read the precautions on the back first and then write this page) This is suitable for the mid-range: ¾ home m (CNS) A 4 regulations (a) i〇X 37) 8 ^ .3. 40,000
Claims (1)
Applications Claiming Priority (1)
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FR9200728 | 1992-01-21 |
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TW214513B true TW214513B (en) | 1993-10-11 |
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TW82102551A TW214513B (en) | 1992-01-21 | 1993-04-07 |
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Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
TWI453008B (en) * | 2006-11-27 | 2014-09-21 | Hologic Inc | Biological sample container and method of obtaining an aliquot of a liquid-based biological sample disposed in a container |
TWI828265B (en) * | 2022-07-28 | 2024-01-01 | 日商納奇健康科技股份有限公司 | Blood storage containers and blood collection equipment |
-
1993
- 1993-04-07 TW TW82102551A patent/TW214513B/zh active
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
TWI453008B (en) * | 2006-11-27 | 2014-09-21 | Hologic Inc | Biological sample container and method of obtaining an aliquot of a liquid-based biological sample disposed in a container |
TWI828265B (en) * | 2022-07-28 | 2024-01-01 | 日商納奇健康科技股份有限公司 | Blood storage containers and blood collection equipment |
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