Use of a container for medical liquid
Abstract
Abstract: The present invention relates to foil bags used as a primary fluid filling method, and the bags allow fluid to be drawn from them without the use of a large amount of force. The container for the medicinal liquid is removed, as it is a gas-tight gas sealant and liquid-tight and can be stored for many months. The container includes a liquid-tight laminating bag with a fixed flange. The flange is designed to be attached to a discharge connection member, and the container may be placed in a fixed casing casing. The medical liquid does not come into contact with air and is protected from the influence of light. The medicinal fluid may be distributed from the lamellar sac in several partial quantities during a long period of time, as a partial amount of it is transferred to an aerosol solution by an atomizer. ,

Term
No projected expiry on record.
- Priority
- Filed
- Published
- Today
25 claims: 25 independent, 0 dependent
- 11 - A propellant gas-free atomizer containing a discharge connection member for distributing a drug in measured doses that can be inhaled, including:a container containing: A foil bag that is closed at both ends and collapsible at a pressure difference of less than 300 hectopascal (hpa) (300 millibar (mbar)) and contains a welded seam to close one end of the foil bag, where the seam is welded. Said seam is substantially transverse to the longitudinal axis of the foil bag and at least part of said welded seam extends partially in the longitudinal direction of the foil bag, where the foil bag is undermined. The flange is so that it is easily moldable and non-reversible in a pre-determined manner so that it maintains its initial length after unpacking. A flange closes the second end of the foil bag. The flange is placed in a leak-proof manner on the second flange end of the foil bag. The manhole, and the said flange includes a guide passage formed therein, and a sealing location located within the guide passage made for installing the said container on a member. A discharge connection member encased in a watertight form, and a pierceable membrane for sealing said container where said pierceable membrane is breached by said discharge connection member when said container is mounted on said discharge connection member ;An inhalable medicament preparation placed in the aforementioned container, capable of being dispensed in doses ranging from 0 1 microliter (μ1)microliter to 50 microliter. ١ - مرذاذ خالي من الغازات الداسرة propellant gas-free atomizer يحتوي على عضو توصيل للتصريف discharge connection member لتوزيع دواء في جرعات معايرة قابلة للاستشاق، يشتمل على: وعاء container يشتمل على: كيس رقائقي foil bag يغلق عند طرفيه وقابل للتقوض collapsible عند فرق ضغط يقل عن 300 هكتوباسكال (hectopascal (hpa (٣0٠ ملي بار millibar (mbar)) ويحتوي على درزة ملحومة welded seam لإغلاق أحد طرفي الكيس الرقائقي foil bag المنكور، حيث تمت الدرزة الملحومة welded seam المذكورة بشكل مستعرض جوهريا بالنسبة للمحور الطولى للكيس الرقائقى foil bag المنكور ويمتد جزء على الأقل من الدرزة الملحومة welded seam المذكورة بشكل جزئي في الاتجاه الطولي للكيس الرقائقي foil bag المنكور، وحيث يتقوض الكيس الرقائقي foil bag المنكور بحيث يكون قابل للتشكيل بسهولة وغير قابل للانعكاس بكيفية محددة مسبقا بحيث يحافظ على طوله الأولي بعد تفريغه، شفة ناتئة flange تغلق الطرف الثاني للكيس الرقائقي foil bag المذكور، حيث توضع الشفة الناتئة flange المذكورة بشكل مانع للتسرب على الطرف الثاني المنكور للكيس الرقائقي foil bag المنكور، وتشتمل الشفة الناتئة flange المذكورة على ممر توجيه guide passage مشكل فيها، و موقع مانع للشرب sealing location يقع ضمن ممر التوجيه guide passage المنكور لتركيب الوعاء container المذكور على عضو التوصيل للتصريف discharge connection member المنكور بشكل مانع للشرب، و غشاء قابل للخرق pierceable membrane لإحكام سد الوعاء container المذكور حيث يخرق الغشاء القابل للخرق pierceable membrane المذكور بواسطة عضو التوصيل للشريف discharge Connection member المذكور عندما يركب الوعاء container المذكور على عضو التوصيل للتصريف discharge connection member المذكور؛ و مستحضر دوائي قابل للاستشاق inhalable medicament preparation موضوع في الوعاء container المذكور، قابل للتصريف في جرعات يتراوح مقدارها من ٠ ١ ميكرولتر (μ1)microliter إلى ٥٠ ميكرولتر.
- 22 - The atomizer according to protection element 1, where the inhalable medicament preparation is in a solution of ethanol, water, or a mixture of them. ٢ - المرذاذ atomizer وفقا لعنصر الحماية ١، حيث يكون المستحضر الدوائي القابل للاستشاق inhalable medicament preparation في محلول من الإيثانول ethanol، الماء، أو خليط منهما.
- 33 - The atomizer according to protection element 1, where the inhalable medicament preparation includes at least one active ingredient selected from a group consisting of one or more of the following:Berotec (fenoterol-hydrobromide;1-(3,5-dihydroxyphenyl)-2-[[1-(4-hydroxybenzyl)-ethyl]-amino]-ethanol 1-(3,5- dihydroxydphenyl) ) (2-[[l-(4-hydroxybenzyl)-ethyl]-amino]-ethanol-hydrobromide), Atrovent (ipratiopium bromide), Berodual (a combination of fenoterol-hydrobromide and ipratiopium-bromide) Salbutamol (or Albuterol), Combivent, Axivent Oxivent (ba 679), oxitropium bromide (tiotiopium bromide BEA2108), tiotiopium bromide (di-(2-thienyl)-glycol acid tiopenol ester), Flunisolid, Budesonid, and Beclomethason. ٣ - المرذاذ atomizer وفقا لعنصر الحماية ١، حيث يشتمل المستحضر الدوائي القابل للاستشاق inhalable medicament preparation على مادة فعالة واحدة على الأقل تختار من المجموعة التي تتكون من واحد أو أكثر مما يلي: بيروتيك Berotec (هيدروبروميد الفنوترول fenoterol-hydrobromide؛ هيدروبروميد ١-(٣، 5- ثنائي هيدروكسي فنيل)-٢-[[١-(٤-هيدروكسي بنزيل)-إثيل]-أمينو]-إيثانول 1-(3,5- dihydroxydphenyl) (2-[[l-(4-hydroxybenzyl)-ethyl]-amino]-ethanol-hydrobromide)، أتروفنت Atrovent (بروميد الإيبراتروبيوم ipratiopium bromide)، بيروديوال Berodual (توليفة من هيدروبروميد الفنوترول fenoterol-hydrobromide وبروميد الإيبراتروبيوم ipratiopium-bromide)، سالبوتامول Salbutamol (أو ألبوترول Albuterol)، كومبيفنت Combivent، أكسيفنت Oxivent (بروميد الأكسيتروبيوم Ba 679 ،(oxitropium bromide (بروميد التيوتروبيوم BEA2108 ،(tiotiopium bromide (إستر تروبينول لحمض ثنائي- di-(2-thienyl)-glycol acid tiopenol ester)، فلونيسوليد Flunisolid، بودسونيد Budesonid، وبكلوميثاسون Beclomethason.
- 44 - The atomizer, according to Protection Clause 1, where the enclosed container is placed in a casing made of a metal or plastic material, where the aforementioned casing connects to the aforementioned flange. ٤ - المرذاذ atomizer وفقا لعنصر الحماية ١، حيث يوضع الوعاء container المنكور في غلاف casing يصنع من مادة معدنية أو بلاستيكية حيث يتصل الغلاف casing المذكور بالشفة الناتئة flange المذكورة.
- 55 - The atomizer according to protection element 4, where the enclosed casing has a diameter ranging from 0.1 mm (mm) to 0.3 mm. ٥ - المرذاذ atomizer وفقا لعنصر الحماية ٤، حيث يكون للغلاف casing المنكور قطر يتراوح من ٠ ١ ملم (ملي متر) إلى 0 ٣ ملم.
- 66 - The atomizer according to protection element 4, where the aforementioned casing has a diameter ranging from 1.2 mm to 1.7 mm. ٦ - المرذاذ atomizer وفقا لعنصر الحماية ٤، حيث يكون للغلاف casing المذكور قطر يتراوح من ٢ ١ ملم الى ٧ ١ ملم.
- 77 - The atomizer according to protection element 4, where the enclosed casing has a total length ranging from 2.0 mm to 6.0 mm. ٧ - المرذاذ atomizer وفقا لعنصر الحماية ٤، حيث يكون للغلاف casing المنكور طول كلي يتراوح من ٠ ٢ ملم إلى ٠ ٦ ملم.
- 88 - The atomizer according to protection element 4, where the aforementioned casing has a total length ranging from 30 mm to 50 mm. ٨ - المرذاذ atomizer وفقا لعنصر الحماية ٤، حيث يكون للغلاف casing المذكور طول كلي يتراوح من 30 ملم إلى 50 ملم.
- 99 - The atomizer according to claim 4, wherein the casing substantially surrounds it from all directions and contains an opening formed in it. ٩ - المرذاذ atomizer وفقا لعنصر الحماية ٤، حيث يحيط الغلاف casing المنكور به من كل الاتجاهات بشكل جوهري ويحتوي على فتحة مشكلة فيه.
- 1010 - The atomizer in accordance with Protection Clause 4, wherein the vented casing substantially surrounds it from all directions and contains a gap where the flanged casing connects to the aforementioned flange. 10 - المرذاذ atomizer وفقا لعنصر الحماية ٤، حيث يحيط الغلاف casing المنكور به من كل الاتجاهات بشكل جوهري ويحتوي على فجوة عند موقع اتصال الغلاف casing المنكور بالشفة الناتئة flange المذكورة.
- 1111 - The atomizer according to protection element 4, where the aforementioned casing is in the form of a basket with many openings. ١١ - المرذاذ atomizer وفقا لعنصر الحماية ٤، حيث يكون الغلاف casing المذكور على شكل سلة ذات فتحات عديدة.
- 1212 - The atomizer according to Protection Clause 4, wherein the container is configured to be installed in a discharge device containing a connecting portion, and wherein said connecting portion includes a positively locking push-in snap connection that is releasable It is located between said connecting portion of said discharge device and said flange of the container. ١٢ - المرذاذ atomizer وفقا لعنصر الحماية ٤ ، حيث يشكل الوعاء container بحيث يركب في أداة تصريف discharge device تحتوي على جزء توصيل connecting portion، وحيث يشتمل جزء التوصيل connecting portion المذكور على وصلة زنق موجب إطباقية تدفع للداخل positively locking push-in snap connection قابلة للإطلاق تقع بين جزء التوصيل connecting portion المذكور في أداة التصريف discharge device المذكورة والشفة الناتئة flange المذكورة للوعاء container.
- 1313 - The atomizer according to Claim 12, wherein said snap connection includes snap noses and snap hooks, and wherein said flange has a groove extending circumferentially with which said snap noses engage said snap hooks when installed The container is in the aforementioned connecting portion. ١٣ - المرذاذ atomizer وفقا لعنصر الحماية ١٢، حيث تشتمل الوصلة الاطباقية snap connection المذكورة على رؤوس إطباقية snap noses وخطافات إطباقية snap hooks، وحيث يكون للشفة الناتئة flange المذكورة حز groove يمتد محيطيا تتعشق معه الرؤوس الإطباقية snap noses المذكورة للخطافات الإطباقية snap hooks المذكورة عندما يركب الوعاء container في جزء التوصيل connecting portion المذكور.
- 1414 - The atomizer, according to protection element 1, where the aforementioned foil bag is made of a composite material consisting of at least two layers. ١٤ - المرذاذ atomizer وفقا لعنصر الحماية ١، حيث يصنع الكيس الرقائقي foil bag المذكور من مادة مركبة composite material نتكون من طبقتين على الأقل.
- 1515 - The atomizer according to protection element 14, where the first layer of the aforementioned composite material consists of a metallic metal chosen from the group that consists of aluminum, gold, and copper. ١٥ - المرذاذ atomizer وفقا لعنصر الحماية 14، حيث تتكون طبقة اولى من المادة المركبة composite material المذكورة من معدن فلزي يختار من المجموعة التي نتكون من الألومنيوم aluminum، الذهب gold والنحاس .cooper
- 1616 - The atomizer according to Protection Clause 41, where the composite material consists of an inner foil of a plastic material and an outer foil of a metal material. ١٦ - المرذاذ atomizer وفقا لعنصر الحماية ٤ ١، حيث تكون المادة المركبة composite material من رقيقة داخلية inner foil من مادة بلاستيكية ورقيقة خارجية outer foil من مادة معدنية.
- 1717 - The atomizer according to protection element 14, where the aforementioned composite material consists of two foils made of two different plastic materials. ١٧ - المرذاذ atomizer وفقا لعنصر الحماية 14، حيث تتكون المادة المركبة composite material المذكورة من رقيقتين foils من مادتين بلاستيكيتين مختلفتين.
- 1818 - The atomizer, according to Protection Clause 14, where the aforementioned composite material consists of:an inner foil made of a copolymer;diffusion-tight central layer;An outer foil made of a plastic material, where the melting temperature of the aforementioned plastic material is higher than 1 degree. The melting temperature of the aforementioned inner foil. ١٨ - المرذاذ atomizer وفقا لعنصر الحماية 14، حيث تتكون المادة المركبة composite material المذكورة من: رقيقة داخلية inner foil تصنع من بوليمر إسهامي copolymer؛ طبقة وسطية مانعة للانتشار diffusion-tight central layer؛ و رقيقة خارجية outer foil من مادة بلاستيكية، حيث تكون درجة حرارة الانصهار melting temperature للمادة البلاستيكية المذكورة أعلى من درجة. حرارة الانصهار melting temperature للرقيقة الداخلية inner foil المذكورة.
- 1919 - The atomizer, according to protection element 18, where the mentioned diffusion-tight central layer is made of a material chosen from the group that consists of a plastic material, a metal material, a glass material and a ceramic material. ١٩ - المرذاذ atomizer وفقا لعنصر الحماية ١٨، حيث تصنع الطبقة الوسطية المانعة للانتشار diffusion-tight central layer المذكورة من مادة تختار من المجموعة التي تتكون من مادة بلاستيكية، مادة معدنية، مادة زجاجية ومادة خزفية.
- 2020 - The atomizer, according to Protection Clause 14, where the aforementioned composite material consists of an inner layer of plastic material whose thickness ranges from 20 micrometers to 100 micrometers and an outer metal layer whose thickness ranges from 8 micrometers to 20 micrometers. 20 - المرذاذ atomizer وفقا لعنصر الحماية ١٤، حيث نتكون المادة المركبة composite material المذكورة من طبقة داخلية من مادة بلاستيكية تراوح سماكتها من 20 ميكرومتر إلى ١0٠ ميكرومتر وطبقة خارجية معدنية تتراوح سماكتها من ٨ ميكرومتر إلى 20 ميكرومتر.
- 2121 - The atomizer, according to protection element 41, where the aforementioned composite material consists of an inner foil of a plastic material whose thickness ranges from 20 micrometers to 100 micrometers, a central foil of metal whose thickness ranges from 8 micrometers to 20 micrometers, and a thin An outer foil made of a plastic material whose thickness ranges from 10 micrometers to 40 micrometers. ٢١ - المرذاذ atomizer وفقا لعنصر الحماية ٤ ١، حيث نتكون المادة المركبة composite material المذكورة من رقيقة داخلية inner foil من مادة بلاستيكية تتراوح سماكتها من 20 ميكرومتر إلى ١0٠ ميكرومتر، رقيقة وسطية central foil معدنية تتراوح سماكتها من ٨ ميكرومتر إلى 20 ميكرومتر، و رقيقة خارجية outer foil من مادة بلاستيكية تتراوح سماكتها من 10 ميكرومتر إلى 40 ميكرومتر.
- 2222 - The atomizer, according to protection item 14, where the aforementioned composite material consists of a plastic sheet whose thickness ranges from 0.2 micrometers to 100 micrometers. ٢٢ - المرذاذ atomizer وفقا لعنصر الحماية ١٤، حيث نتكون المادة المركبة composite material المذكورة من رقيقة بلاستيكية تتراوح سماكتها من ٠ ٢ ميكرومتر إلى 100 ميكرومتر.
- 2323 - A container for a medicinal liquid is used as an interchangeable cartridge in an inhaler. The container is gas-tight and liquid-tight, and includes:A foil bag is closed at both ends and is collapsible at a pressure difference of less than 300 hectopascals (300 mbar). The foil bag contains a welded seam to close one end of the foil bag, where the aforementioned welded seam extends in a manner Substantially transverse to the longitudinal axis of said foil bag and at least part of said welded seam extending partially in the longitudinal direction of said foil bag, wherein the foil bag is undermined The mentioned foil bag is made of a composite material, and the aforementioned composite material consists of an inner foil made of a copolymer, a layer diffusion-tight central layer, and an outer foil of a plastic material, the melting temperature of which is higher than the melting temperature For the aforementioned inner foil;A flange closes the second end of the corrugated foil bag in a drink-proof manner, wherein said foil bag is welded to said flange at its circumference and the flange contains a guide passage formed therein, wherein the corrugated guide passage includes a means Pairs with a press fit and/or sealing location to attach the container to the discharge connection member of the inhaler. watertight, where a sealing location is required if the sealing effect of the press fit is insufficient;A pierceable membrane placed at the end of or within said guide passage wherein said pierceable membrane is breached by said discharge connection member when the voided container is placed inside the inhaler;The casing is made of a metal or plastic material, where the aforementioned casing is attached to the lip The aforementioned flange protruding so that the aforementioned foil bag is placed inside the aforementioned casing. ٢٣ - وعاء container لسائل طبي medicinal liquid يستخدم كخرطوشة قابلة للتبادل interchangeable cartridge في جهاز استنشاق inhaler، ويكون الوعاء container مانع لشرب الغاز gas-tight ومانع لشرب السائل liquid-tight، ويشتمل على: كيس رقائقي foil bag يغلق عند طرفيه وقابل للتقوض collapsible عند فرق ضغط يقل عن 300 هكتوباسكال (٣0٠ ملي بار)، ويحتوي الكيس الرقائقي foil bag المنكور على درزة ملحومة welded seam لإغلاق أحد طرفي الكيس الرقائقي foil bag المنكور حيث تمتد الدرزة الملحومة welded seam المذكورة بشكل مستعرض جوهريا بالنسبة للمحور الطولي للكيس الرقائقي foil bag المنكور ويمتد جزء على الأقل من الدرزة الملحومة welded seam المذكورة بشكل جزئي في الاتجاه الطولي للكيس الرقائقي foil bag المذكور، وحيث يتقوض الكيس الرقائقي foil bag المذكور بحيث يكون قابل للتشكيل بسهولة وغير قابل للانعكاس بكيفية محددة مسبقا بحيث يحافظ على طوله الأولي بعد تفريغه، ويصنع الكيس الرقائقي foil bag المنكور من مادة مركبة composite material، وتتكون المادة المركبة composite material المذكورة من رقيقة داخلية inner foil تصنع من بوليمر بسهامي copolymer، طبقة وسطية مانعة للانتشار diffusion-tight central layer، ورقيقة خارجية outer foil من مادة بلاستيكية، حيث تكون درجة حرارة الانصهار melting temperahrre لها أعلى من درجة حرارة الانصهار melting temperature للرقيقة الداخلية inner foil المذكورة؛ شفة ناتئة flange تغلق الطرف الثاني للكيس الرقائقي foil bag المنكور بشكل مانع للشرب، حيث يلحم الكيس الرقائقي foil bag المذكور مع الشفة الناتئة flange المذكورة عند محيطه وتحتوي الشفة الناتئة flange على ممر توجيه guide passage مشكل فيها، حيث يشتمل ممر التوجيه guide passage المنكور على وسيلة أزواج بالكيس press fit و/أو موقع مانع للشرب sealing location لتركيب الوعاء container المنكور على عضو توصيل للتصريف discharge connection member لجهاز الاستنشاق inhaler بشكل مانع للشرب، حيث يكون الموقع المانع للتسرب sealing location مطلوبا إذا كان التأثير المانع للتسرب لوسيلة الإزواج بالكبس press fit غير كاف؛ غشاء قابل للخرق pierceable membrane يوضع على طرف أو ضمن ممر التوجيه guide passage المذكور حيث يخرق الغشاء القابل للخرق pierceable membrane المذكور بواسطة عضو التوصيل للتصريف discharge connection member المذكور عندما يوضع الوعاء container المنكور بداخل جهاز الاستنشاق inhaler؛ و غلاف casing يصنع من مادة معدنية أو بلاستيكية، حيث يتصل الغلاف casing المذكور بالشفة الناتئة flange المذكورة بحيث يوضع الكيس الرقائقي foil bag المذكور بداخل الغلاف casing المذكور.
- 2424 - The container, according to Protection Clause 23, where the aforementioned outer foil is made of polyethylene terephthalate. ٢٤ - الوعاء container وفقا لعنصر الحماية ٢٣، حيث نتكون الرقيقة الخارجية outer foil المذكورة من ترفثالات متعدد الإثيلين polyethylene terephthalate.
- 2525 - The container according to claim 23, wherein the copolymer is a copolymer of ethylene-acrylic acid. ٢٥ - الوعاء container وفقا لعنصر الحماية ٢٣، حيث يكون البوليمر الإسهامي copolymer عبارة عن بوليمر إسهامي copolymer من الإثيلين ethylene -حمض الإكريليك acrylic acid.
Independent claims25
151 paragraphs, as filed
A container for medicinal liquid
Full description
Corresponding reference for related requests
This application claims priority over the application serial number 093772/60, filed on July 23, 1998 AD.
Background of the invention
1. Field of invention
The present invention relates to a container for a medicinal liquid, where the container is gas-tight and liquid-tight. 2. Related technology
European Patent No. A2 4 9 0 82 1 0 A bottle-shaped package comprising a fixed-shaped outer container and an inner container placed inside the outer container in the form of an easily deformable bag containing the filling material. The preform is produced by co-extrusion of two coaxial tubular portions. The two parts consist of two thermoplastic materials that are not connected together. The initial shape is expanded into a blow molding mold. A welded seam is provided at the flat bottom of the inner vessel. The flat bottom, formed on the outer bowl, contains a slit-shaped opening. The outer bowl and the inner bowl are connected together by a positive locking relationship in the drain hole area. This packaging is produced in essentially one operation.
The filling material is drained from the container using a pump located in the drain hole.
The inner vessel deforms when its volume shrinks as a result of pumping. The air passes into the space
It is located between the outer vessel and the deformed inner vessel, through an open slit in the flat bottom of the outer vessel, thus preventing a drop in pressure in this intermediate space. The inner bowl is not in constant contact with the outer bowl, except in the area of the drain hole. The package may be provided with a dip tube extending almost to the flat bottom and keeping the inner container in the extended position. This package can only be used acceptably and completely emptied when it is in a certain position in the vacuum.
European Patent No. Al 165 620 0 describes a tubular bag made of composite foil. The composite foil contains a plastic foil placed on the outer side and a metal foil placed on at least one inner side. The tubular sac is closed at both ends in a pouch-like shape. The bag is provided with a desired rupture site, by which the bag can be opened reliably at that point. A tubular bag of this type is suitable for storing hardenable material that is expelled from the tube by means of expulsion.
European Patent No. Al 068653 0 describes a flexible, collapsible container used in one cycle, made of thin film, and used in a suction or feeding bottle that can be used several times. One end of the bowl is open while the other end is closed with a welded seam, and the bowl is provided with a tongue portion. The lingual part is placed in a gap provided at the bottom of the suction or feeding bottle. This ensures that the bag-like container remains in a constantly extended position inside the suction or feeding bottle.
General description of the invention
The invention aims to produce a vessel used in one cycle that is highly economical without adversely affecting its suitability for use, and to facilitate its use.
The object of the present invention is to provide a container for a medical liquid, which is... It is gas-tight and liquid-tight, and has an appropriate filling volume for its intended use. And it is undermined
The vessel is such that it is easily moldable and non-reversible at slightly low pressure
Pre-defined so that it can be substantially unloaded.
According to the present invention, the container contains a foil bag that is closed at both ends. When the pressure difference between the inside of the vessel and its surroundings is less than 3.00 hectopascal (hpa) (300 millibar (mbar), the laminated bag is susceptible to deformation by external pressure and collapses. The vessel also contains a flange that is fixed in shape and mounted in a manner A seal on the foil bag and the flange is a removable connecting element for mounting the receptacle to a discharge connectionmenrber.
The foil bag is closed at at least one end by at least one welded seam extending substantially transversely with respect to the axis of the bag. The protruding lip has a fixed sealing location. It also provides a place for fluid drainage in the protruding lip area, which is fixed in shape.
According to the present invention, the bowl has many advantages over those of traditional bowls. For example, a bowl crown according to the present invention is economically feasible, suitable for use in one cycle and its production requires the use of a small amount of material.
In addition, the vessel according to the present invention may be produced under sterile condition and filled and sealed under sterile conditions. It may also be used for inhalation medications, usually supplied as solutions in ethanol, water, or a mixture of ethanol and water.
The liquid is drained from the vessel according to the present invention under sterile conditions, such that air is not sucked into the vessel upon draining. Thus, the liquid does not come into contact with air, oxygen, or carbon dioxide.
The vessel according to the present invention also allows for the drainage of a medical liquid free of gases and bubbles.
The vessel is sealed in accordance with the present invention so that the diffusion of liquids and gases is as little as possible. The container may be filled and stored for several years, depending on the specific drug used, while meeting the requirements of all official pharmacopoeias.
The vessel is easily deformed at slightly low pressure. The vessel according to the present invention also remains flat and extended in the collapsed position, so that it maintains its initial length after use.
In addition, the vessel of the present invention does not require a valve to equalize pressure after draining part of the liquid, and the vessel can be substantially emptied, even in the receptive position and when inverted.
The foil bag according to the present invention is attached only to the fixed protruding flange and is not secured to any sleeve, if provided.
The container filling volume may be easily adjusted to a predetermined value within a specified range by changing the length and/or diameter of the foil bag. The vessel can also be filled before closing it, and before making the single or second welded seam. Thus, there is no need for a separate closing method.
The container may be used with or without a cover. If the container is placed in a cover, it is protected from external damage.
The liquid is stored in the container according to the present invention, where it is protected from the influence of light by an opaque foil bag or by an opaque cover that is closed in all directions.
In addition, the vessel according to the present invention can be placed in and removed from a drainage device in a simple manner without any rotational movement.
Brief description of fees
The foregoing and other features and advantages of the invention will become apparent from the following more specific description of a preferred embodiment of the invention, as shown in the attached drawings.
Figure 1: A perspective drawing of a first embodiment of a closed foil bag according to the present invention
At both ends.
Figure 2: A perspective drawing of a second embodiment of a sealed foil bag according to the present invention
At both ends.
Figure 3 shows a perspective drawing of a third embodiment of a closed foil bag according to the present invention
At both ends.
Figure 4: A cross-sectional view of a first embodiment of a protruding flange according to the present invention.
Figure 5a: shows a cross-sectional view of a second embodiment of a protruding flange according to the present invention.
Figure 5b: shows a cross-sectional view of a second embodiment of the protruding flange taken along line 5-5 of Figure 5a.
Figure 6: shows a cross-sectional view of a third embodiment of a protruding flange according to the present invention.
Figure 7 shows a cross-sectional view of a fourth embodiment of a protruding flange according to the present invention.
Figure 8a: shows a view of a single-segment protruding flange according to the present invention, which is placed on the side of the foil bag.
Figure 8b: Shows a detailed view of a cross-section of the laminate foil used to make the laminated bag in Figure 8a.
Figure 9a: shows a side view of a first embodiment of a welded seam according to the present invention.
Figure 9b: shows a cross-sectional view of a welded seam taken along line 9-9 of Figure 9a.
Figure 10a: shows a side view of a second embodiment of a welded seam according to the present invention.
Figure 1B: shows a cross-sectional view of a welded seam taken along line 10-10 of the figure.
10a.
Figure 11a: shows a side view of a third embodiment of a welded seam according to the present invention.
Figure 11b: A step view of the welded seam in Figure 11a is shown.
Shapes
12a-12g: show a series of perspective drawings for making and filling a vessel according to a first embodiment of the present invention.
Shapes
13a-13f: Show a series of perspective drawings of making and filling a vessel according to a second embodiment of the present invention.
Figure 14: shows a partial cross-sectional view of a vessel according to the present invention.
Figure E1a: shows a cross-sectional view of a first embodiment of a connecting portion of a receptacle according to the present invention.
Figure 5 1b: A side view of one end of the vessel in Figure 5a shows.
Figure 16a: shows a cross-sectional view of a second embodiment of a connection portion of a receptacle according to the present invention.
Figure 16b: A side view of one end of the vessel in Figure 16a shows.
Detailed description
A preferred embodiment of the present invention is described by reference to figures where similar reference numbers indicate identical or functionally similar elements. While special formations and arrangements are explained, it should be understood that they are for illustrative purposes only. Those skilled in a related technique will realize that other configurations and arrangements can be used without departing from the principle and scope of the invention.
An object of the present invention is to provide a container for a medical liquid, which is gas-tight and liquid-tight, and has a filling volume suitable for the intended purpose of its use. The vessel is collapsed so that it is easily moldable and non-reversible at a slightly low pressure in a predetermined manner so that it can be substantially emptied.
According to the present invention, the container contains a foil bag that is closed at both ends. When the pressure difference between the inside of the container and its surroundings is less than 300 hectopascals (300 mbar), the foil bag is susceptible to deformation by external pressure and collapses. The container also has a fixed, protruding lip that mounts leak-proof on the foil bag. The protruding flange is a releasable coupling element for mounting the vessel to a drainage coupling member.
The laminated bag is closed at at least one end by at least one welded seam running substantially transverse to the axis of the bag. The protruding lip has a fixed shape to prevent scratches. It also provides a location for the liquid lip in the protruding lip area, which is stable in shape.
In another embodiment, the collapsible laminated bag can be deformed and undermined by external pressure at a pressure difference of less than 150 hPa (150 mbar) or preferably less than 0.8 hPa (80 mbar).
The foil bag can be closed with a welded seam at both ends. In this case, a fixed, protruding lip is welded to the side of the foil bag in a way that prevents drinking, and it is preferable to weld it near one end of the foil bag. However, the foil bag can also be closed at one end with a welded seam, and at the other end with a drinking-proof lip. In this case, one end of the foil bag is welded to the flange, preferably at its circumference.
The laminar bag may be made of a tube without a welded seam that extends in the axial direction of the laminar bag. In an alternative embodiment, the foil bag may have one or two welded seams extending in the longitudinal direction. The laminar bag may be in the form of a flat bag or a bag with side folds. Preferably a bag that has a welded seam that stretches in the direction
Longitudinal.
In one embodiment, the foil bag is made of a thin sheet of metal or metal alloy, preferably aluminum, gold or copper, or of a plastic material, preferably a thermoplastic material. In another embodiment, the foil bag is made of a composite film of plastic and metallic material. It is preferable for the composite foil to contain two or three foils connected together. The foil bag may also contain a plastic film on which a layer of metal, glass or ceramic is applied, for example by vapor deposition.
Plastic or metal films are a few micrometers thick. The thickness of the vapor-deposited metal, glass or ceramic layers is in the sub-micrometre range.
We may be a composite chip consisting of two chips made of a metal foil and a plastic foil connected together. In this embodiment, the foil forms the inside or outside of the composite foil. In another embodiment, the composite film consists of two plastic films of different materials,
It is preferable for the three-ply composite film to contain two plastic films.
There is a metal foil between them, connecting the three foils together. Composite foil may contain, instead of metal foil, a layer of glass or ceramic, such as silicon oxide (SiOx), produced by vapor deposition on a plastic foil.
In another embodiment, the inner film of the composite film consists of a copolymer, eg an ethylene-acrylic acid copolymer. It is preferable that the outer plastic sheet of the composite film be made up of a plastic material, for example polyethylene terephthalate, whose melting temperature is higher than the melting temperature of the plastic material that makes up the inner sheet. This flows from the seam welding process of the plastic material that makes up the inner film in the film bag production process.
In a composite film, a bonding layer can be provided between the two films.
The foil bag may include a plastic film with a thickness ranging from 20 micrometers to 100 micrometers. It may also include a composite film consisting of an inner sheet of plastic material with a thickness ranging from 0.2 µm to 100 µm, and an outer sheet of metal with a thickness of between 8 µm and 20 µm. A foil bag may also include a composite film consisting of an inner sheet of plastic material with a thickness of between 0 and 100 micrometers, and a middle sheet of metal with a thickness of between 8
µm and 20 µm, and an outer sheet of plastic material with a thickness of between 0 and 1
µm and 0 4 µm.
The vessel according to the invention is described in greater detail by reference, for example, to the figures.
Figures 1 through 3 represent perspective drawings of various embodiments of the foil bag closed at both ends. Figure 1 shows a tubular bag 1 1 with a fixed, cylindrical flange 2 1 and a u-shaped transverse seam 3 1 closing one end of the tubular bag and extending at least partially in the longitudinal direction of the tubular bag. The edge 4 1 of the protruding flange connects with the other end of the tubular sac. A hole 5 1 is located on the axis of the protruding flange into which a drain connection member can be inserted.
Figure 2 shows a bag with a sealing edge 1 2 containing two films located one on top of the other. The bag contains two welded proteins 22 that extend in the longitudinal direction of the bag, and at one end, a welded seam 23 that extends in the transverse direction. The other end is connected to a fixed protruding flange 4 2 in a fish-like shape. A hole 5 2 is located in the center of the protruding flange through which a drainage connecting member can be inserted.
Figure 3 shows a bag with a side fold 31 that is folded at both its longitudinal sides, and closed at each end by a special welded seam 32 that extends transversely. The protruding flange 33 is welded to maintain the shape of the bag on its flat side. The drain connection portion can be inserted into the hole 34 in the protruding flange.
The protruding lip can be fixed in different shapes. If placed at the end of the foil bag as its sealing device, it can be of a rotationally symmetrical shape and can be adapted to the size of the end of the foil bag. The fixed-shaped protruding flange may be provided with a guide passage into which a drain connection portion can be inserted. When installing the vessel, the valve's connecting member is located in the guide passage.
In one embodiment, the guideway is provided with a piess fit device encircling the discharge coupling member. In one embodiment the bag coupling device is part of the guideway and has a smooth inner wall with an inner diameter that differs only slightly from the outer diameter of the drain coupling member. In another embodiment, a plurality of bulge portions may be provided in a portion of the guide passage on its inner wall. The swollen parts, for example, may have an elongated shape, bend symmetrically and expand in the axial direction. A plurality of bulging parts may also be provided, arranged at axial distances from each other and extending in the azimuthal direction, forming, for example, two rings or comprising a plurality of ring parts. In addition, the bulging parts can extend into a helical configuration; Whereas, it may contain a group of helical parts distributed on the inner wall of the guideway
Or it may contain a helical portion whose length is longer than the circumference of the guideway. It provides a means of pairing
By such pressing the vessel is mounted on the valve connecting member and a sufficiently stable coupling of the protruding flange with the valve connecting member may be provided. Moreover, after emptying, the vessel can be withdrawn from the connecting member for drainage without damaging the latter.
The protruding lip may be single-part or multi-part. The preferred multi-part cantilever flange is the multi-part cantilever flange. A neat, outward portion of the protruding flange connects to the foil bag in a leak-proof manner. The outer part contains an opening that closes with the inner part in a leak-proof manner. The two parts can be screwed together using a screwthread, or they can be connected together with a snap-action connection or ultrasonic welding. The shape of a single-part cantilever flange is similar to that of a two-part cantilever flange, but does not contain any connecting elements. The projecting flange may be manufactured at the same time as a snap coupling, groove for sealing location, and pierceable membrane.
The protruding lip may be made of rubber, metal or plastic, preferably a thermoplastic material. It may be desirable to make the protruding lip from the same plastic material used to form the foil bag or the inner side of the foil bag. A protruding flange made of rubber or metal material can be attached to the foil bag by gluing or possibly vulcanization.
Figures 4 to 7 show cross-sectional views of different embodiments of the cantilever flange. Figure 4 shows a view of a longitudinal section through a single-segment cantilever flange 1 4 containing a cylindrical guide passage of Figure 42, in the form of a bag coupling device, for a cylindrical drainage connection member. The outer end of the guideway is chamfered, while the other end is closed by a diaphragm 43 located diagonally with respect to the axis of the protruding flange. The protruding flange 1 4 is manufactured in one operation, and its edge is connected to a foil bag 4 4 .
Figure 5a shows a longitudinal section of a cylindrical multi-part cantilever flange, and Figure 5b shows a cross section taken along line 5-5 in Figure 5a. A lower portion 51 of the protruding lip is connected to a lamellar bag 53. An upper part 52 of the protruding flange is installed in a slot located in the lower part 051 and the upper part 52 is provided with a guide passage 54 which has three elongated protrusions 55, as shown in Figure 5b, extending in the axial direction of the protruding flange. The elongated prongs 55 serve as a snap-on coupling device for a drain coupling member. An annular protrusion 56 acts as a seal. The lower part 51 and the upper part 52 are welded together at their contact surface 57. The guideway 54 includes an entry hole with an inclined insertion surface. This entry hole is sealed with a sealant film 58.
Figure 6 shows a fixed-shape multi-part cylindrical cantilever flange. A lower portion 61 of the protruding lip is connected to a lamellar bag 63. The upper part 62 of the protruding lip protrudes into the lower annular part 1 6. In the upper part 62, a circular ring 4 6 acts as a seal and is held in place by a gland 65 that is pressed into place. The slot works in a loop
Grouting 65 as a guideway for a drain connecting member. On the inner side of the seal in the upper part 62 is a protrusion extending circumferentially 66, which provides a means of coupling to the bag. A drain coupling member 67 is inserted into the guide passage of the packing ring 65. The vessel is fixed on a drainage connection member 67 by means of coupling to the bag in the form of a protrusion that extends circumferentially 66. The lower part 1 6 and the upper part 2 6 are welded together at their contact surface 8 6.
Figure 7 shows another embodiment of a multi-part cantilever flange according to the present invention.
A lower portion 71 of the protruding flange is connected to a pouch 073 and an upper portion 72 of the protruding flange is located in the lower annular portion 71 with a shoulder. The upper portion 72 includes a flat ring 4 7 acting as a seal, which is held in position by a gasket ring 75 that is pressed into position. A guide passage 76 for a drainage coupling member is placed below the flat ring 074, and two protrusions 77 within the guide passage 76 form a means of coupling to the piston, extending around it in the form of threads. Near the lower end of the guideway 76 is provided a diaphragm 78 perpendicular to the axis of the protruding flange. The membrane 78 is pierced when the vessel is installed on the connecting member for drainage. The membrane 78 and the upper part 72 are manufactured in a single operation. The lower part 71 and the upper part 72 are connected together at their contact surface 79.
Figure 8a shows a cross-section view of a single-segment cantilever flange 81 that is fixed in shape as it lies on the side of a foil bag 82. The protruding flange 81 contains a guide passage 83 that serves as a compression coupling device for a drain coupling member. This protruding flange 81 is sealed at its outer end with a sealing film 084 and when the vessel is installed on a drain connection member 85 with a beveled end, the foil bag is pierced at the inner end 86 of the guideway 83.
Figure 8b shows a detailed view of a cross-section through a commercially available laminated three-ply laminated bag format. The inner foil 87 is composed of polyethylene (4.0 micrometer thick), and the middle foil 88 acts as an anti-diffusion barrier.
It consists of aluminum (1.2 micrometers thick) and the outer layer 89 is composed of polyethylene terephthalate (1.2 micrometers thick).
The welded seam at one or both ends of the foil bag can be V, U or T shaped. The seam runs substantially transverse to the axis of the bag. In one embodiment, the welded connection may extend partially in the direction of the bag axis, where the specific deformation of the laminated bag is enhanced when liquid is drawn from it.
A leak-proof location or spill-proof device may be provided within or at one end of the guideway. The seal location may include a ring located within a groove provided on the inner wall of the guideway. The ring may be circular in shape, or it may have a substantially rectangular cross-section. The ring may be provided with a sealing lip. The ring may be made of an elastomer, a thermoplastic rubber polymer, or rubber. The leak-proof location is attached to the filling space or vessel chamber mounted on the coupling member for drainage in order to prevent gas and liquid leakage from ambient air. In addition, the leak-proof location allows the vacuum vessel to be withdrawn from the coupling member for drainage. A sealing location is required if the sealing effect of the snap-in coupling device is insufficient.
The width of the welded seam on the foil bag may range from 0.7 mm (mm) to 3 mm. The width of the welded seams is chosen according to the requirements for complete sealing and seam durability. Wide and longitudinal seams can be made on the foil bag after the welding process, so that they are placed on the outside of the foil bag, so that the width of the foil bag is only slightly greater than its width in the non-welded part between the welded seams.
The welded seams on the foil bag and the welding site between the foil bag and the protruding flange are made by well-known processes such as heat welding, ultrasonic welding or induction welding in the case of composite foils with a metal layer, where it is preferable to press the welding sites in the heated state. We demonstrate such processes, for example, in two patents
European No. 131 111 0 and No. 239 130 0, as described in this statement in full for reference.
Figures 9a, 9b, 10 or 1b show cross-section views and side views of various embodiments of the welded seam with the foil bag closed at at least one end. Figures 11 or 11b show a side view and a step view of an alternative embodiment of a welded seam on the end of the bag.
Figure 9a shows a U-shaped welded seam 1 9 extending partially in the longitudinal direction of the laminated bag 92. At one side of the foil bag 92, the welded seam 91 merges with the welded seam 93 of the foil bag extending in the longitudinal direction. Figure 9b is a view of a cross section through the film bag taken along line 9-9 in Figure 9a. The inner layer of the multi-layer folded foil 4 9 is welded at the welded seams 91 and 93.
Figure 0 1a shows a V-shaped welded seam 1 0 1 extending partially in the longitudinal direction of the laminated bag 102. In this case, the laminated bag 2 0 1 consists of a tubular film without a longitudinal seam. Figure 1b shows a view of a cross section through the film bag taken along line 10-10 in Figure 10a. The single-layer folded sheet 103 is welded to the welded seam 101.
Figure 1 1a shows a side view of a welded T-shaped seam 1 11, while Figure 1 1b shows a line view of the welded end of the laminated bag 112. In general, the length of the three prongs of the T-seam 111 is the same as the width of the plywood bag, if folded flat, on the outside of the T-seam.
A foil bag welded with a V, U or T-shaped seam in the transverse seam area shall not be larger than the diameter of the shell into which the foil bag may be inserted.
The drainage site should preferably be in the form of a hole or a perforated site. A permeable membrane may be provided at the perforation or perforated site, where the membrane is pierced at
Installing the vessel on the connecting member for drainage. The membrane is preferably arranged between the sealing site and the fluid compartment or space in the laminar bag. The permeable membrane can be placed at one end or within the guideway. It is preferable to place it directly at the end of the guideway or close to this end, which is towards the fluid space. The membrane may be part of the labrum or part of the lamellar sac. If it is part of the flange, it can be made at the same time as the flange, and it can be made from the same plastic material as the flange. The permeable membrane serves as the original sealing device for the filling compartment or compartment in the bag
Lamellar.
In another embodiment, the drain location may be sealed with a sealant film that is pulled before installing the vessel on the drain connecting member or pierced when installing the vessel on the drain connecting member.
The container can be placed in a fixed-shaped feeder consisting of a metal or a plastic material. One end of the casing is connected to the protruding flange in a releasable or non-releasable manner, while the other end of the casing can be closed at the bottom. In one embodiment, the casing is substantially closed on all sides, but has at least one opening. Alternatively, a gap may be provided where the casing connects to the protruding flange. The cover may also be in the form of a fixed basket containing many openings. In an alternative embodiment, instead of the sleeve, the vessel may be placed in a fixed U-shaped holder, each prong of the U-shaped holder being securely attached to a protruding lip, the prong being longer than the foil bag.
In a preferred embodiment, the receptacle placed inside the casing is in contact with the casing itself only at the protruding flange. The end of the foil bag, which is sealed with a welded seam, or its two ends closed with two welded seams, are not in contact with the packaging.
When the liquid is transferred from the vessel to the connecting member for drainage, the film bag collapses flat under the influence of external pressure. The air passes through the hole in the cover or through
The gap between the wrapper and the protruding flange, into the space between the wrapper and the foil bag, ensures pressure equalization. Thus, no valve is needed in the foil bag and the liquid in the foil bag does not come into contact with the air.
A schematic diagram of making and filling the vessel according to the invention is shown in the perspective drawings of Figures 12a-12 and Zo13a-13f.
As shown in Figure 12a, a strip of folded foil containing a welded seam in the longitudinal direction is supplied at both ends, divided into parts and shaped to form a tube. The lower part of the two-part cylindrical flange, made by injection molding, is welded to one end of the tube, as shown in Figure 21b. The other end of the tube is welded with a U-shaped transverse seam, as shown in Figure 12c. The finished vessel is pushed into a cylindrical aluminum housing, as shown in Figure 21d, the edge of which is pressed into a groove or channel in the edge of the cylindrical protruding lip. This way the bowl fits firmly in the casing. The empty container placed in the casing is then filled with liquid through the lower part of the protruding lip equipped with an opening, as shown in Figure 2 1e. After completing the filling process, the upper part of the protruding lip is pressed inside the lower part, as shown in Figure 2 and 1f, and the two parts are connected together in a leak-proof manner. The finished part, as shown in Figure 12g, is ready for installation on a drain connection member.
An alternative manufacturing process is shown in Figures 31a-31f. One end of the pipe is connected to a single-segment protruding flange closed by a sealing film, as shown in Figure 31b. The vessel is filled with liquid through the other open end of the foil tube, as shown in Figure 31c. The open end of the laminated tube is closed by a U-shaped transverse suture, as shown in Figure 3 1d. The filled container is placed inside a plastic cover, as shown in Figure 31d. The edge of the plastic cover is fixed on
The edge of the lip is one-part, folded. The finished part, as shown in Figure 3 and 1, is ready for installation on a drain connection member.
Figure 4 1 shows a partial cross-section view of a typical vessel 141 according to the present invention filled with a fluid and placed in a metal feeder 142. The foil bag is welded at one end with a U-shaped seam, while at the other end it is welded with the edge 144 of the lower part 145 of a two-part, cylindrical protruding flange of fixed shape. The metal sleeve has a bottom 146 in which there is an opening through which air can pass into the space between the metal sleeve 142 and the foil bag. The open end of the metal sleeve 142 is pressed into a groove or channel 147 in the edge of the lower portion 45 1 of the protruding flange. The metal casing 42 1 is fixedly connected to the protruding flange. The upper part 148 of the protruding lip is installed in a hole in the lower part. 145 The lower part 145 and the upper part 148 are connected by a quick-acting closure 149 and are provided with a flat drinking straw 150. Routing lane 151 is closed at its inner end. Using a membrane 152 and sealed at its outer edge with a waterproof film 153.
The metal casing shown in Figure 41 is preferably made of aluminum.
In one embodiment, it has a length of 43 mm, an outer diameter of 1.7 mm, and a wall thickness of 0.5 mm. The two-part flange is made of polyethylene and is manufactured by injection molding process. The upper part of the protruding flange containing the membrane is preferably made in one step in the process. The guide passage at the top of the protruding flange has an internal diameter of 2.5 mm at the piston coupling location and is fixedly mounted on a drainage coupling member.
The foil bag is anti-diffusion for the medical liquid and its components and for gases. The film bag material and composite film structure are selected potentially appropriate for use with liquid. The term “anti-diffusion” according to the present invention refers to the loss of vessel fluid (as measured by ethanol at ambient temperature) due to diffusion
At a rate of less than 0.6 mg (milligrams) per day, preferably less than 0.4 mg per day, and especially preferably less than 0.2 mg per day, and specifically less than 0.1 mg per day.
The inner foil or inner side of the foil bag touches the liquid inserted into the bag.
The material chosen for this film is a material that is not affected by the liquid and does not affect the liquid in a harmful way. It is preferable that this foil be in the form of a weldable foil.
One of the films or a layer placed by vapor deposition, for example, is the anti-diffusion barrier. This barrier prevents the spread of the liquid or its components and prevents the spread of gases from or to the foil bag. It may be desirable to protect the anti-diffusion barrier from mechanical damage and from tearing when the film is bent. One method of protection is to place another plastic sheet on the anti-diffusion barrier so that the spread of liquid or gases continues to be prevented for a long time.
Because the foil bag is diffusion-proof for gases, the drop in pressure that occurs inside the foil bag due to the liquid draining from it cannot be compensated for by the diffusion of gas into it. Thus, the foil bag collapses reliably even if the liquid drains from the vessel very slowly. Also, the liquid can be withdrawn from the foil bag in large partial quantities, for example 200 measured amounts, distributed over a long period of time, for example three months.
The container placed inside a closed feeder shall be essentially impervious to the outside and shall not be damaged when stored or when installed on a connecting member for drainage. An intrinsically sealed cover, a basket-shaped cover with multiple holes, or a fixed shape catcher makes it easy to store the container containing the thin foil bag. These covers also facilitate its use when it is installed on the connecting member for draining and when pulling the empty container from the connecting member for draining.
An example of a discharge coupling member is the hollow plunger for a medical liquid atomizer. Such an atomizer is described in German Patent No. 902.5 36 195 and European Patent No. 2687 97/1, which are described in full herein for reference. An example of an atomizer is shown in Figures 6a and 6b in this description. The hollow piston in this vaporizer is in the form of a connecting member to drain the medicinal liquid inside the container according to the invention. The bowl is mounted on a hollow piston preferably placed on the axis of the atomizer. In this configuration, the hollow plunger tip fits into the drainage site and is thus immersed in the medicinal fluid. The leak-proof location of the protruding lip seals the contents of the container in a way that prevents them from drinking into the outer wall of the hollow piston. The piston coupling device fixes the bowl on the hollow piston mechanically quickly and sufficiently.
It may be desirable, instead of or in addition to the force-locking connection between the bowl and the valve's connecting member, to provide a releasable positive locking connection between the fixed-shaped flange of the bowl and the discharge device, for example an atomizer. Such a connection may be in the form of a push-in snap connection, comprising a set of snap hooks fitted to a connecting portion of the drain device. When the vessel is mounted on a drainer, the snap hooks engage with a slot in the protruding flange, such as with a notch extending circumferentially or beyond the edge of the protruding lip. It is preferable that the snap noses be round in shape or beveled in both directions of movement of the bowl, so that an empty bowl can be removed using a moderate amount of force, and a full bowl can be installed on the drain tool using a moderate amount of force.
Figures 15 or 5 1b show a positive, snap-in, releaseable spring connection located between the fixed-shaped protruding lip of the receptacle and the connecting portion of the drain device.
Figure 5 1a shows a cross-sectional view through a connecting portion 154 disposed in the drain device and including at its axis a drain connecting member 67. Surrounded by a group of
Snap hooks 155, snap heads 156 have a round cross-section, with a drainage connection member 67. The occlusal hooks 155 are separated from each other by an intermediate space
It has an azimuth width ranging from 1.0 degrees to 6.0 degrees. Part 57 1 may be provided no
It has any occlusal head between two occlusal hooks 155. Part 157 rests with a positive clamp on the outer wall of the permeable vessel.
Figure 5 1b shows a side view of the end of a vessel encased in a casing 142 with its fixed-shaped protruding flange 148 protruding out of the casing 142. As shown in Figure 4 1, the casing 142 has a notch extending circumferentially 158, preferably in the region of the portion of the protruding lip that protrudes into the casing 142. The snap heads 156 of the bowl are engaged when installed in the connecting part 154 with the groove 158, while the bowl is connected to the connecting part 154 in a releasable manner with a positive tension relationship.
Figures 61a and 61b show another embodiment of a positive snap-in, push-in, releaseable spring connection.
Figure 6 1a shows a cross-sectional view through a connecting portion 161 disposed in the drain device and including at its axis a drain connecting member 67. A set of snap hooks in the form of tabs 162, with snap heads 163 with beveled sides in both directions of movement of the vessel, surround the drain connection member 67. The snap hooks 162 are placed such that they are separated from each other by azimuthal spacing.
Figure 6 1b shows a side view of the end of a vessel placed in a casing 142 with its fixed-shaped protruding flange 148 protruding out of the casing 142. When the bowl is installed in the connecting portion 154, the occlusal heads 163 engage with the circumferentially extending notch 147 of the portion of the protruding flange 148 that protrudes outside the casing, while the bowl is in releasable contact with the connecting portion with a positive tension relationship.
The vessel according to the invention is particularly suitable as an interchangeable cartridge for inhalable drug solutions in propellant-free atomizers. The filling volume of the vessel may range from 0.5 ml (ml) to 5 ml, preferably from 1 ml to 4 ml, particularly from 1 ml to 3 ml or from 2 ml to 4 ml. These solutions are dispensed in portions, with the specific dose ranging from 1 microliter (μ1) to 5.0 microliters, and preferably from 15 microliters (μl) to 2 microliters.
The diameter of the shell may range from 1.0 mm (mm) to 3.0 mm, preferably from 1.2 mm to 1.7 mm. The length of the vessel, including the portion that protrudes beyond the casing for the fixed flange, may range from 2.0 mm to 6.0 mm, and preferably from 30 mm to 5.0 mm.
According to the invention, the vessel functions as a primary packaging means to contain a medical liquid containing, for example, a medicine dissolved in a solvent. Examples of suitable solvents include water, ethanol, or a mixture of both. Examples of medications used include Berotec (fenoterol-hydrobromide; 1-(3,5-dihydroxyphenyl)-2-[[1-(4-hydroxybenzyl)-ethyl]-amino]-ethanol-3,5-hydrobromide. )-a
dihydroxyphenyl)-2- [ [ 1 -(4-hydroxybenzyl)-ethyl]-amino]-ethanol-hydrobromide),
Ahtrovent (iprateopium bromide), Berodual (a combination of fenoterol-hydrobromide and ipratropium-bromide), Salbutamol (or Albuterol), Combivent, Oxivent (oxifropium bromide, Ba 679). (Bromide Tiotropium BEA 2108, (tioOpium bromide (di-(2-thienyl)-glycol acid tropenol ester), Flunisolid, Budesonid, Beclomethasone and other medicines.
International Patent Publication No. 27959/98 describes stable aqueous medicament preparations for producing gas-free aerosols for inhalation, which are described in full herein for reference. In particular, reference is made to the preparations mentioned in this statement and shown in examples.
For example, suitable pharmaceutical preparations in a solution of ethanol are shown in International Patent Publication No. 01329/97, the description of which is mentioned in this statement in full for reference. In particular, reference is made to the active substances specified in this statement (see pages 2 and 3) and the fixed preparations mentioned in this statement.
1 sheet
Sheet 1
74 members in 40 offices
Priority claims2
| Document | Office | Kind | Date |
|---|---|---|---|
| 19808295 | Germany | A | |
| 198082959 | Germany | – |
Members74
| Document | Office | Kind | |
|---|---|---|---|
| CA2319834A1 | Canada | A1 | |
| DE19808292A1 | Germany | A1 | |
| WO9943571A1 | World Intellectual Property Organization (WIPO) | A1 | |
| AU2930299A | Australia | A | |
| DE19808295A1 | Germany | A1 | |
| UY25401A1 | Uruguay | A1 | |
| ZA991520B | South Africa | B | |
| PE20000509A1 | Peru | A1 | |
| NO20004260D0 | Norway | D0 | |
| ID25514A | Indonesia | A | |
| TW409057B | Taiwan Province of China | B | |
| NO20004260L | Norway | L | |
| BR9908326A | Brazil | A | |
| TR200002494T2 | Türkiye | T2 | |
| EP1058657A1 | European Patent Office (EPO) | A1 | |
| YU52500A | Yugoslavia, later Serbia and Montenegro (until 2006) | A | |
| SK12802000A3 | Slovakia | A3 | |
| BG104691A | Bulgaria | A | |
| AR015239A1 | Argentina | A1 | |
| CN1291957A | China | A | |
| EA200000776A1 | Eurasian Patent Organization (EAPO) | A1 | |
| KR20010041261A | Republic of Korea | A | |
| PL342609A1 | Poland | A1 | |
| HU0101681A2 | Hungary | A2 | |
| HUP0101681A2 | Hungary | A2 | |
| HK1034231A1 | Hong Kong, China | A1 | |
| EA001978B1 | Eurasian Patent Organization (EAPO) | B1 | |
| IL137991D0 | Israel | D0 | |
| CZ20003110A3 | Czechia | A3 | |
| US2002007155A1 | United States of America | A1 | |
| JP2002504411A | Japan | A | |
| EE200000495A | Estonia | A | |
| HU0101681A3 | Hungary | A3 | |
| HUP0101681A3 | Hungary | A3 | |
| EG21987A | Egypt | A | |
| AU757260B2 | Australia | B2 | |
| EP1058657B1 | European Patent Office (EPO) | B1 | |
| AT241528T | Austria | T | |
| ATE241528T1 | Austria | T1 | |
| DE59905739D1 | Germany | D1 | |
| EP1338528A1 | European Patent Office (EPO) | A1 | |
| NZ506759A | New Zealand | A | |
| DK1058657T3 | Denmark | T3 | |
| PT1058657E | Portugal | E | |
| SI1058657T1 | Slovenia | T1 | |
| ES2195549T3 | Spain | T3 | |
| US6685691B1 | United States of America | B1 | |
| UA65606C2 | Ukraine | C2 | |
| IL137991A | Israel | A | |
| US2004143235A1 | United States of America | A1 | |
| EE04335B1 | Estonia | B1 | |
| BG64355B1 | Bulgaria | B1 | |
| CN1222448C | China | C | |
| KR100589298B1 | Republic of Korea | B1 | |
| NO321792B1 | Norway | B1 | |
| SA1259B1This record | Saudi Arabia | B1 | |
| SA99191308B1 | Saudi Arabia | B1 | |
| MY128732A | Malaysia | A | |
| SK285572B6 | Slovakia | B6 | |
| JP3911387B2 | Japan | B2 | |
| PL195731B1 | Poland | B1 | |
| RS49714B | Serbia | B | |
| CZ298854B6 | Czechia | B6 | |
| EP1338528B1 | European Patent Office (EPO) | B1 | |
| AT388906T | Austria | T | |
| ATE388906T1 | Austria | T1 | |
| DE59914692D1 | Germany | D1 | |
| DK1338528T3 | Denmark | T3 | |
| PT1338528E | Portugal | E | |
| ES2303570T3 | Spain | T3 | |
| SI1338528T1 | Slovenia | T1 | |
| CA2319834C | Canada | C | |
| US7963955B2 | United States of America | B2 | |
| CY1108123T1 | Cyprus | T1 |
Numbers
- Publication
- 1259
- Application
- 99191308
Titles2
- Arabic
- وعاء container لسائل طبي medicinal liquid
- English
- A container for medicinal liquid
Classification
- CPC, 8
- A61J1/10
- B65D75/58
- A61J1/1475
- A61M2207/00
- B65D75/5877
- B65D75/5883
- B65D83/62
- B65D2575/583
- IPC, 8
- B65D83 00
- A61J1 00
- A61J1 05
- A61J1 10
- A61J1 14
- B65D33 38
- B65D75 58
- B65D83 14