WO2008001237A2 - Principes actifs peu compatibles contenus dans une poche à deux parties - Google Patents
Principes actifs peu compatibles contenus dans une poche à deux parties Download PDFInfo
- Publication number
- WO2008001237A2 WO2008001237A2 PCT/IB2007/051969 IB2007051969W WO2008001237A2 WO 2008001237 A2 WO2008001237 A2 WO 2008001237A2 IB 2007051969 W IB2007051969 W IB 2007051969W WO 2008001237 A2 WO2008001237 A2 WO 2008001237A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- product
- container
- wrapper
- housing
- apt
- Prior art date
Links
- 230000000144 pharmacologic effect Effects 0.000 claims abstract description 8
- 229940035676 analgesics Drugs 0.000 claims abstract description 4
- 239000000730 antalgic agent Substances 0.000 claims abstract description 4
- 239000004743 Polypropylene Substances 0.000 claims description 5
- -1 polypropylene Polymers 0.000 claims description 5
- 229920001155 polypropylene Polymers 0.000 claims description 5
- BQJCRHHNABKAKU-KBQPJGBKSA-N morphine Chemical compound O([C@H]1[C@H](C=C[C@H]23)O)C4=C5[C@@]12CCN(C)[C@@H]3CC5=CC=C4O BQJCRHHNABKAKU-KBQPJGBKSA-N 0.000 claims description 4
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 3
- 229910052782 aluminium Inorganic materials 0.000 claims description 3
- 239000004411 aluminium Substances 0.000 claims description 3
- 238000000605 extraction Methods 0.000 claims description 3
- 239000012530 fluid Substances 0.000 claims description 3
- 238000007789 sealing Methods 0.000 claims description 3
- TVYLLZQTGLZFBW-ZBFHGGJFSA-N (R,R)-tramadol Chemical compound COC1=CC=CC([C@]2(O)[C@H](CCCC2)CN(C)C)=C1 TVYLLZQTGLZFBW-ZBFHGGJFSA-N 0.000 claims description 2
- OZWKMVRBQXNZKK-UHFFFAOYSA-N ketorolac Chemical compound OC(=O)C1CCN2C1=CC=C2C(=O)C1=CC=CC=C1 OZWKMVRBQXNZKK-UHFFFAOYSA-N 0.000 claims description 2
- 229960004752 ketorolac Drugs 0.000 claims description 2
- 239000000463 material Substances 0.000 claims description 2
- 229960005181 morphine Drugs 0.000 claims description 2
- 229960004380 tramadol Drugs 0.000 claims description 2
- TVYLLZQTGLZFBW-GOEBONIOSA-N tramadol Natural products COC1=CC=CC([C@@]2(O)[C@@H](CCCC2)CN(C)C)=C1 TVYLLZQTGLZFBW-GOEBONIOSA-N 0.000 claims description 2
- 208000002193 Pain Diseases 0.000 description 3
- 230000000202 analgesic effect Effects 0.000 description 3
- 238000001990 intravenous administration Methods 0.000 description 3
- 238000011109 contamination Methods 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 238000004806 packaging method and process Methods 0.000 description 2
- 239000004800 polyvinyl chloride Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 208000004550 Postoperative Pain Diseases 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000001802 infusion Methods 0.000 description 1
- 239000000825 pharmaceutical preparation Substances 0.000 description 1
- 229940127557 pharmaceutical product Drugs 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 230000002980 postoperative effect Effects 0.000 description 1
- 238000004321 preservation Methods 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 238000001356 surgical procedure Methods 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61J—CONTAINERS SPECIALLY ADAPTED FOR MEDICAL OR PHARMACEUTICAL PURPOSES; DEVICES OR METHODS SPECIALLY ADAPTED FOR BRINGING PHARMACEUTICAL PRODUCTS INTO PARTICULAR PHYSICAL OR ADMINISTERING FORMS; DEVICES FOR ADMINISTERING FOOD OR MEDICINES ORALLY; BABY COMFORTERS; DEVICES FOR RECEIVING SPITTLE
- A61J1/00—Containers specially adapted for medical or pharmaceutical purposes
- A61J1/14—Details; Accessories therefor
- A61J1/20—Arrangements for transferring or mixing fluids, e.g. from vial to syringe
- A61J1/2093—Containers having several compartments for products to be mixed
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61J—CONTAINERS SPECIALLY ADAPTED FOR MEDICAL OR PHARMACEUTICAL PURPOSES; DEVICES OR METHODS SPECIALLY ADAPTED FOR BRINGING PHARMACEUTICAL PRODUCTS INTO PARTICULAR PHYSICAL OR ADMINISTERING FORMS; DEVICES FOR ADMINISTERING FOOD OR MEDICINES ORALLY; BABY COMFORTERS; DEVICES FOR RECEIVING SPITTLE
- A61J1/00—Containers specially adapted for medical or pharmaceutical purposes
- A61J1/05—Containers specially adapted for medical or pharmaceutical purposes for collecting, storing or administering blood, plasma or medical fluids ; Infusion or perfusion containers
- A61J1/10—Bag-type containers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61J—CONTAINERS SPECIALLY ADAPTED FOR MEDICAL OR PHARMACEUTICAL PURPOSES; DEVICES OR METHODS SPECIALLY ADAPTED FOR BRINGING PHARMACEUTICAL PRODUCTS INTO PARTICULAR PHYSICAL OR ADMINISTERING FORMS; DEVICES FOR ADMINISTERING FOOD OR MEDICINES ORALLY; BABY COMFORTERS; DEVICES FOR RECEIVING SPITTLE
- A61J1/00—Containers specially adapted for medical or pharmaceutical purposes
- A61J1/14—Details; Accessories therefor
- A61J1/20—Arrangements for transferring or mixing fluids, e.g. from vial to syringe
- A61J1/2003—Accessories used in combination with means for transfer or mixing of fluids, e.g. for activating fluid flow, separating fluids, filtering fluid or venting
- A61J1/202—Separating means
- A61J1/2024—Separating means having peelable seals
Definitions
- the present invention refers to a pharmacological product comprising a container for special pharmacological fluids receiving in separate compartments two or more active principles.
- a patient is usually administered an analgesic cocktail apt to relieve postoperative pain.
- a cocktail is usually obtained with a mixture of two active principles, typically an opioid and a Non-Steroidal Analgesic Drug (so-called NSAD), that are to be suitably diluted and mixed extemporarily at the time of administration, since their mixture is less than stable over time.
- NSAD Non-Steroidal Analgesic Drug
- Such an administration may occur in the form of distinct repeated intravenous (IV) boli performed with a syringe, one per each patient's request during the postoperative course, or by continuous infusion (phleboclysis, best by electronic or elastomeric pump).
- IV intravenous
- the repeated performing of boli causes a discontinuous intervention on the pain peak, by administering an amount of drug that however is generally higher than that theoretically necessary to keep pain itself at acceptable intensity levels.
- the active principles to be mixed are typically contained in very low-dosage phials, (generally 1-ml ones). Accordingly, for each administration the health worker should break and pour a high number of phials, with evident risks of environmental contamination of the end solution, due also to the danger that glass shards, deriving just from the breaking of the phials, get thereinto. Additional problems may be accidental cuts and preparation errors. Therefore, the technical problem underlying the present invention is that of providing an analgesic cocktail in an adequate pharmaceutical form, allowing to overcome the drawbacks mentioned above with reference to the known art.
- the present invention provides several relevant advantages.
- the main advantage lies in that the packaging of the analgesic cocktail in bipartite bag allows to obtain an extemporary solution with optimal properties without the risks associated to current preparation modes.
- FIGS. 2 and 3 show each a respective perspective view of the product of Figure 1 during a clinical use thereof;
- - Figure 4 shows a further perspective view of the product of Figure 1 during the tearing of its pack prior of the clinical use thereof.
- a pharmacological product according to a first embodiment of the invention is generally denoted by 1.
- Product 1 comprises a container 2 substantially in the form of bipartite bag that has just a first and a second separate housing, denoted by 21 and 22, respectively, arranged side-by-side.
- Each of the two housings 21 and 22 contains a respective pharmacological fluid.
- the first housing 21 contains a first active principle 31 of opioid type preferably selected from a group comprising tramadol and morphine
- the second housing 22 contains a second Non-Steroidal Analgesic Drug (NSAD)-type active principle 32- mixable with the first one and preferably selected from a group comprising ketorolac.
- NSAD Non-Steroidal Analgesic Drug
- Said housings 21 and 22 are separated by a dividing septum 23, which is preferably formed by two opposite walls of the container 2 joined by hot-sealing.
- the septum 23 is apt to be permanently torn by exerting a pressure externally to the container 2 itself so as to interconnect the housings 21 and 22 and cause a mixing of the respective active principles 31 and 32.
- the container 2 is externally and internally sterile and see-through and made of a bilaminate material bearing an internal layer, i.e. into contact with the active principles 31 and 32, of polypropylene and an external layer in polyvinyl chloride (PVC).
- PVC polyvinyl chloride
- the container 2 has a self-sealing element 4, per se known, apt to allow the single-dose (at one time) or repeated extraction of the cocktail, by a needle or the like.
- the container 2 has an inserting or collecting element 5 for a multiple- collection connector 6, it also per se known.
- the connecting element 5 is in the form of a channel making a seat for the connector 6 and connecting the internal housings of the container 2 itself to the outside.
- a channel has a transversal septum apt to be torn at the first use, by a mere folding of, or pressure onto the channel-shaped seat.
- the container 2 is completely enclosed in a preferably sterile first external wrapper 7, which is removed at the time of use of the product 1 itself.
- the wrapper 7 may have a preferential tearing region 71.
- the external wrapper 7 is see-through, so as to allow the view of the container 2 and of the active principles 31 and 32, and made of polypropylene .
- product 1 provides a further external wrapper 8, which encloses the first wrapper 7 and is it also removable at the time of using the product 1 itself.
- the second wrapper 8 is apt to shield the active principles 31 and 32 from light and environmental contaminations, and is preferably made of aluminium. It also may have a preferential tearing region.
Landscapes
- Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medical Preparation Storing Or Oral Administration Devices (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Bag Frames (AREA)
- Packages (AREA)
Abstract
L'invention concerne un produit pharmacologique (1) comprenant : un contenant (2) qui se présente sous la forme d'une poche à deux parties, comprenant un premier (21) et un deuxième logement (22) distincts, disposés l'un à côté de l'autre; un premier principe actif, un opioïde (31), qui est disposé dans le premier logement (21); et un deuxième principe actif, un médicament analgésique non stéoroïdien (NSAD) (32), qui peut être mélangé avec ledit premier principe actif (31) et qui est disposé dans le deuxième logement (22). Selon l'invention, le contenant (2) comprend en outre une paroi de séparation (23) entre le premier (21) et le deuxième logement (22), cette paroi pouvant être déchirée définitivement par application d'une pression à l'extérieur du contenant (2), pour relier le premier (21) et le deuxième logement (22) l'un avec l'autre et entraîner le mélange des deux principes actifs (31, 32) dans le contenant (2).
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP20060425350 EP1859771A1 (fr) | 2006-05-24 | 2006-05-24 | Substances actives à compatibilité faible, comprises dans une poche à deux compartiments. |
EP06425350.3 | 2006-05-24 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2008001237A2 true WO2008001237A2 (fr) | 2008-01-03 |
WO2008001237A3 WO2008001237A3 (fr) | 2008-03-13 |
Family
ID=37038340
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/IB2007/051969 WO2008001237A2 (fr) | 2006-05-24 | 2007-05-24 | Principes actifs peu compatibles contenus dans une poche à deux parties |
Country Status (2)
Country | Link |
---|---|
EP (1) | EP1859771A1 (fr) |
WO (1) | WO2008001237A2 (fr) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2019082221A2 (fr) * | 2017-10-23 | 2019-05-02 | Biofarma S.P.A. | Dispositif et procédé pour l'administration orale de principes actifs |
IT201700120081A1 (it) * | 2017-10-23 | 2019-04-23 | Biofarma S P A | Dispositivo e metodo per la somministrazione orale di principi attivi |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4458811A (en) * | 1983-04-21 | 1984-07-10 | Abbott Laboratories | Compartmented flexible solution container |
WO1998010733A1 (fr) * | 1996-09-11 | 1998-03-19 | Baxter International Inc. | Recipients et procedes de stockage et de melange par addition de solutions medicales |
US20040078023A1 (en) * | 2002-10-17 | 2004-04-22 | Paul-Andre Gollier | Peelable seal |
WO2005097040A1 (fr) * | 2004-04-08 | 2005-10-20 | Idd-Eal Manufacturing Company Limited | Contenant permettant de constituer une formulation sous forme liquide |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB9319568D0 (en) * | 1993-09-22 | 1993-11-10 | Euro Celtique Sa | Pharmaceutical compositions and usages |
CA2338327A1 (fr) * | 1998-07-31 | 2000-02-10 | Janus Pharmaceuticals, Inc. | Procedes et compositions d'utilisation de moclobemide |
-
2006
- 2006-05-24 EP EP20060425350 patent/EP1859771A1/fr not_active Withdrawn
-
2007
- 2007-05-24 WO PCT/IB2007/051969 patent/WO2008001237A2/fr active Application Filing
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4458811A (en) * | 1983-04-21 | 1984-07-10 | Abbott Laboratories | Compartmented flexible solution container |
WO1998010733A1 (fr) * | 1996-09-11 | 1998-03-19 | Baxter International Inc. | Recipients et procedes de stockage et de melange par addition de solutions medicales |
US20040078023A1 (en) * | 2002-10-17 | 2004-04-22 | Paul-Andre Gollier | Peelable seal |
WO2005097040A1 (fr) * | 2004-04-08 | 2005-10-20 | Idd-Eal Manufacturing Company Limited | Contenant permettant de constituer une formulation sous forme liquide |
Also Published As
Publication number | Publication date |
---|---|
EP1859771A1 (fr) | 2007-11-28 |
WO2008001237A3 (fr) | 2008-03-13 |
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