WO2004062461A2 - Therapeutic microfoam - Google Patents
Therapeutic microfoam Download PDFInfo
- Publication number
- WO2004062461A2 WO2004062461A2 PCT/GB2004/000026 GB2004000026W WO2004062461A2 WO 2004062461 A2 WO2004062461 A2 WO 2004062461A2 GB 2004000026 W GB2004000026 W GB 2004000026W WO 2004062461 A2 WO2004062461 A2 WO 2004062461A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- gas
- microfoam
- foam
- sclerosing
- blood
- Prior art date
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/10—Dispersions; Emulsions
- A61K9/12—Aerosols; Foams
- A61K9/124—Aerosols; Foams characterised by the propellant
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/075—Ethers or acetals
- A61K31/08—Ethers or acetals acyclic, e.g. paraformaldehyde
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K33/00—Medicinal preparations containing inorganic active ingredients
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0019—Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
Definitions
- the present invention relates to a therapeutic microfoam comprising a sclerosing material, particularly a sclerosing liquid, which is suitable for use in the treatment of various medical conditions involving blood vessels, particularly varicose veins and other disorders involving venous malformation.
- the invention relates also to the method and apparatus for the generation of such a microfoam.
- Sclerosis of varicose veins is based on the injection into the veins of liquid sclerosant substances which, by mter alia causing a localised inflammatory reaction, favour the elimination of these abnormal veins.
- sclerotherapy was a technique selected in cases of small and medium calibre varicose veins, those with diameters equal to or greater than 7 mm being treated by surgery.
- the preparation of such a microfoam may be carried out with a solution of any sclerosing substance, particularly polidocanol.
- the method of preparation is to use a small brush attached to a high-speed motor to whip a dilute aqueous solution of the preferred sclerosant to a firm mousse-like consistency in a period of 1-2 minutes under a gas atmosphere containing physiologically acceptable gas mixes.
- this known method requires extemporaneous production of microfoam by the physician, pharmacist or an assistant immediately prior to administration to the patient.
- Such procedure allows for variation of microfoam sclerosing agent depending upon the person preparing it; microfoam density, gas makeup, bubble size and foam stability all needing attention with respect to the condition being treated.
- WO 00/72821-A1 BCG International Limited
- WO 00/72821-A1 BCG International Limited
- This microfoam is made with a relatively low concentration of a foamable sclerosing agent and a significant amount of a blood dispersible gas in sterile fashion without volatile liquid propellants or the need for the operator to directly be concerned in the control of its parameters.
- This application also addresses the perception that large volumes of nitrogen should not unnecessarily be introduced into patients. This is particularly an issue where large vessels are being filled with foam, if air is used as the gas for producing the foam.
- a preferred form of gas described in WO 00/72821-Al comprises 50% vol/vol or more oxygen, the remainder being carbon dioxide, or carbon dioxide, nitrogen and trace gases in the proportion found in atmospheric air.
- the sclerosing agent is a solution of polidocanol or sodium tetradecyl sulfate in an aqueous carrier, e.g. water, particularly in a saline.
- sclerosing fluid for example, aqueous polidocanol
- WO 02/41872-A1 BCG International Limited
- WO 02/41872-A1 offers a solution to this potential problem by storing the sclerosant liquid and the oxygen-rich physiologically acceptable blood dispersible gas in separate containers until immediately prior to use, when the blood-dispersible gas is introduced into the container holding the sclerosant liquid.
- the mixture of blood-dispersible gas and sclerosant liquid is then released, the components of the mixture interacting upon release of the mixture to form a sclerosing foam.
- the present inventors have identified another issue with long-term storage of physiologically acceptable blood dispersible gases under pressure in a sealed canister, namely the need to ensure that potential leaks are minimised. They have determined that the introduction of helium into a physiologically acceptable blood dispersible gas gives a similarly physiologically acceptable mixture that is capable of being detected at very small quantities by a suitable sensor.
- helium Although helium has very low solubility in water or blood, the helium gas molecules are small enough to readily diffuse across pulmonary gas exchange membranes and be exhaled. The safety of helium in respirable gas mixtures is well established and widely exploited (namely Heliox mixtures for deep sea divers containing up to 70% helium).
- helium in respirable gas mixtures results from its extremely low solubility in water or blood, even under high ambient pressures.
- Helium can also be shown to diffuse very rapidly across pulmonary gas exchange membranes, and therefore presents no danger of pulmonary gas embolism.
- Helium can also be used as an efficient marker of gas bubble arrival in the pulmonary circulation, following breakdown of a microfoam that has helium as a constituent gas.
- the first aspect of the present invention provides a sclerosing foam comprising a physiologically acceptable gas that is readily dispersible in blood together with an aqueous sclerosant liquid, characterised in that the foam is a microfoam further including helium in an amount from 0.01 % to 40% of the total volume of gas.
- a commercially available leak detector is the VeecoTM MS-40 portable automatic leak detector, provided by the Vacuum Instrument Corporation, Ronkonkoma, New York. This is said to detect a helium leakage level expressed in units of std cc/sec down to 4 x 10 ⁇ n , i.e. 4 x 10 _n cm 3 s -1 at standard temperature conditions.
- a pressure loss of 0.15 bar in 3 years shelf life may be tolerated from a pressurised single-canister microfoam generator of 300 ml capacity, initially at 3.5 bar absolute, and containing
- the limits of the present invention are a sclerosing foams including helium in an amount from 0.01% to 40% of the total volume of gas. Similar calculations to the above show that the leakage level that has to be detected is 1 x 10 ⁇ 10 cm 3 s _1 to
- the microfoam includes helium in an amount from 0.1% to 40% of the total volume of gas. More preferably the microfoam includes helium in an amount from 0.5%) to 20%) of the total volume of gas. More preferably the microfoam includes helium in an amount from 1% to 10% of the total volume of gas. More preferably the microfoam includes helium in an amount from 1%> to 5% of the total volume of gas.
- the gas mixture may be regarded as made up of three components:
- Suitable further inert gases include neon, argon, and nitrogen.
- the gas mixture includes less than 10% vol/vol nitrogen.
- the gas mixture comprises at least 50%> of the physiologically acceptable gases oxygen and/or carbon dioxide, more preferably 75% or more oxygen and/or carbon dioxide and most preferably at least 99%> oxygen or carbon dioxide.
- oxygen or carbon dioxide is medical grade.
- a method for producing a microfoam suitable for use in scleropathy of blood vessels comprising introducing a physiologically acceptable blood-dispersible gas into a container holding an aqueous sclerosant liquid and releasing the mixture of blood-dispersible gas and sclerosant liquid, whereby upon release of the mixture the components of the mixture interact to form a microfoam, characterised in that the physiologically acceptable blood-dispersible gas is stored in the presence of helium in an amount from 0.01%) to 40% of the total volume of gas.
- the pressurised gas mixture may be stored long term in the same container as the aqueous sclerosant liquid, if long term stability tests show no degradative reaction between the gas mixture and the aqueous sclerosant liquid.
- the oxygen component of the final gas mix is stored in a separate container from the aqueous sclerosant liquid and introduced immediately prior to use.
- the oxygen component of the gas may thereby be stored in a container provided with engaging means for the container holding the aqueous sclerosant liquid.
- engaging means is disclosed in WO 02/41872-A1
- a device for producing a microfoam suitable for use in scleropathy of blood vessels comprising a housing in which is situated a pressurisable chamber containing a solution of the sclerosing agent in a physiologically acceptable solvent; a pathway with one or more outlet orifices by which the solution may pass from the pressurisable chamber to the exterior of the device through said one or more outlet orifices and a mechanism by which the pathway from the chamber to the exterior can be opened or closed such that, when the container is pressurised and the pathway is open, fluid will be forced along the pathway and through the one or more outlet orifices; said housing incorporating an inlet for the admission of a pressurised source of physiologically acceptable gas that is dispersible in blood; the gas being in contact with the solution on activation of the mechanism such as to produce a gas-solution mixture; said pathway to the exterior of the housing including one or more foaming elements; characterised in that the housing is charged with blood-dispersible gas stored
- a method of treating a patient in need of sclerotherapy of a blood vessel comprising administering a microfoam as described above.
- a microfoam as described above.
- the sclerosant liquid utilised in the invention may be any of those discussed in WO 00/72821-Al and WO 02/41872-A1.
- the sclerosant liquid is a solution of polidocanol or sodium tetradecyl sulfate in an aqueous carrier, e.g. water, particularly in a saline.
- the solution is from 0.25 to 5%>Nol/vol polidocanol, preferably in sterile water or a physiologically acceptable saline, e.g. in 0.5 to 2% vol/vol saline. More preferably still, the concentration of polidocanol is from 0.5 to 5%> vol/vol in the liquid, preferably 0.5 to 3%> vol/vol polidocanol and most preferably being 1%> vol/vol in the liquid. Concentration of sclerosant in the solution will be advantageously increased for certain abnormalities such as Klippel- Trenaunay syndrome.
- the sclerosant may also contain additional components, such as stabilising agents, e.g. foam stabilising agents, e.g.
- glycerol such as glycerol.
- Further components may include alcohols such as ethanol. Even though this can reduce foam stability, inclusion of a few percent of ethanol is thought to aid in solubilising low-molecular- weight oligomers of polidocanol and also prevent degradation of the polidocanol.
- the water or saline also may contain 2-5% vol/vol physiologically acceptable alcohol, e.g. ethanol.
- the polidocanol solution is preferably phosphate buffered.
- Physiologically acceptable blood dispersible gas is a gas that is capable of being substantially completely dissolved in or absorbed by blood.
- a sclerosant liquid is a liquid that is capable of sclerosing blood vessels when injected into the vessel lumen.
- Scleropathy or sclerotherapy relates to the treatment of blood vessels by injection of a sclerosing agent to eliminate them.
- An aerosol is a dispersion of liquid in gas.
- Half- life of a microfoam is the time taken for half the liquid in the microfoam to revert to unfoamed liquid phase, under the influence of gravity, and at a defined temperature.
- the mixture of blood-dispersible gas and sclerosant liquid is preferably pressurised to a pre-determined level.
- Preferred pressures are in the range 800 mbar to 4.5 bar gauge (1.8 bar to 5.5 bar absolute). Pressures in the range of 1 bar to 2.5 bar gauge have been found to be particularly effective — over this range of pressures, there is very little change in either the density or the half-life of the resulting foam as the canister empties.
- the microfoam is such that less than 20%o of the bubbles are less than 30 ⁇ m diameter, greater than 75% are between 30 and 280 ⁇ m diameter, less than 5 %> are between 281 and 500 ⁇ m diameter, and there are substantially no bubbles greater than 500 ⁇ m diameter.
- the gas/liquid ratio in the mix is controlled such that the density of the microfoam is 0.07 g/ml to 0.19 g/ml, more preferably 0.10 g/ml to 0.15 g/ml.
- the microfoam has a half-life of at least 2 minutes, more preferably at least 2.5 minutes. The half-life may be as high as 1 or 2 hours or more, but is preferably less than 60 minutes, more preferably less than 15 minutes and most preferably less than 10 minutes.
- Figure 1 shows a cross-sectional view of a pre-pressurised container for the generation of therapeutic microfoam according to the invention, as disclosed in WO 00/72821-Al and further described in Example 1 below.
- Figure 2 shows a shows a cross-sectional view of a device comprising a container provided with engaging means and a mesh stack shuttle according to the invention, as disclosed in WO 02/41872-A1 and further described in Example 2 below.
- Figure 3 shows an apparatus for use in then helium detection technique as further described in Example 3 below.
- FIG. 1 A typical apparatus for the generation of therapeutic microfoam according to the invention, as disclosed in WO 00/72821-Al, is shown in Figure 1.
- the canister has an aluminium wall (1), the inside surface of which is coated with an epoxy resin.
- the bottom of the canister (2) is domed inward.
- the canister inner chamber (4) is pre-purged with 100% oxygen for 1 minute, containing 15 ml of a 1%) vol/vol polidocanol / 20 mmol phosphate buffered saline solution / 4%> ethanol, of composition as given in Table 1 below, then filled with an oxygen-helium mixture at 2.7 bar gauge (1.7 bar over atmospheric).
- a standard 1 inch diameter EcosolTM aerosol valve (5) (Precision Valve, Peterborough, UK) is crimped into the top of the canister after sterile part filling with the solution and may be activated by depressing an actuator cap (6) to release content via an outlet nozzle (13) sized to engage a Luer fitting of a syringe or multi-way connector (not shown).
- a further connector (7) locates on the bottom of the standard valve and mounts four Nylon 66 meshes held in high density polyethylene (HDPE) rings (8), all within an open-ended polypropylene casing. These meshes have diameter of 6 mm and have a 14% 0 open area made up of 20 ⁇ m pores, with the meshes spaced 3.5 mm apart.
- HDPE high density polyethylene
- a further connector (9) locates on the bottom of the connector holding the meshes and receives a housing (10) which mounts the dip tube (12) and includes gas receiving holes (11a, l ib) which admit gas from chamber (4) into the flow of liquid which rises up the dip-tube on operation of the actuator (6).
- gas receiving holes (11a, l ib) which admit gas from chamber (4) into the flow of liquid which rises up the dip-tube on operation of the actuator (6).
- Holes (11a, lib) have cross-sectional area such that the sum total ratio of this to the cross-sectional area of the liquid control orifice at the base of the valve housing (at the top of the dip-tube) is controlled to provide the required gas/liquid ratio.
- Example 2 container with engaging means and mesh stack shuttle
- a device comprising a container provided with engaging means and a mesh stack shuttle according to the invention, as disclosed in WO 02/41872 -Al, is shown in Figure 2.
- the device comprises a low pressure container (1) for an aqueous sclerosant liquid and an unreactive gas atmosphere, a container (2) for a physiologically acceptable blood-dispersible gas and an engaging means comprising a connector (3).
- the container (2) for a physiologically acceptable blood-dispersible gas is charged at 5.8 bar absolute pressure with an oxygen-helium mixture containing 3%> helium, whereas the container (1) is charged with a carbon dioxide-helium mixture containing 3%> helium.
- Container (2) is used to pressurise container (1) at the point of use to approx 3.5 bar absolute and is then discarded, just before the microfoam is required.
- the two containers will thus be referred to hereinafter as the PD [polidocanol] can (1) and the O 2 can (2).
- Each of the cans (1, 2) is provided with a snap-fit mounting (4, 5). These may be made as identical mouldings.
- the snap-fit parts (4, 5) engage the crimped-on mounting cup (6, 7) of each can (1, 2) with high frictional force.
- the connector is made in two halves (8, 9), and the high frictional force allows the user to grip the two connected cans (1, 2) and rotate the connector halves (8, 9) relative to each other without slippage between connector (3) and cans.
- Each of these can mountings (6, 7) has snap-fit holes (10, 11) for engaging mating prongs (12, 13) which are on the appropriate surfaces of the two halves (8, 9) of the connector.
- the connector (3) is an assembly comprising a number of injection mouldings.
- the two halves (8, 9) of the connector are in the form of cam track sleeves which fit together as two concentric tubes. These tubes are linked by proud pins (14) on one half that engage sunken cam tracks (15) on the other half.
- the cam tracks have three detented stop positions.
- the first of these detents is the stop position for storage. An extra security on this detent is given by placing a removable collar (16) in a gap between the end of one sleeve and the other. Until this collar (16) is removed it is not possible to rotate the sleeves past the first detent position. This ensures against accidental actuation of the connector.
- the cam track sleeves (8, 9) are injection moulded from ABS as separate items, and are later assembled so that they engage one another on the first stop of the detented cam track.
- the assembled sleeves are snap-fitted as a unit onto the O 2 can (2) mounting plate (5) via four locating prongs.
- the security collar is added at this point to make an O can subassembly.
- the connector (3) includes in its interior a series of foaming elements comprising a mesh stack shuttle (17) on the connector half (8) adjacent to the PD can (1).
- the mesh stack shuttle (17) is comprised of four injection moulded disk filters with mesh hole size of 20 ⁇ m and an open area of approx. 14%, and two end fittings, suitable for leak-free connection to the two canisters. These elements are pre- assembled and used as an insert in a further injection moulding operation that encases them in an overmoulding (18) that provides a gas-tight seal around the meshes, and defines the outer surfaces of the mesh stack shuttle.
- the end fittings of the stack (17) are designed to give gas-tight face and/or rim seals against the stem valves (19, 20) of the two cans (1, 2) to ensure sterility of gas transfer between the two cans.
- the mesh stack shuttle (17) is assembled onto the PD can valve (19) by push- fitting the components together in a aseptic environment.
- the PD can (1) and attached shuttle (17) are offered up to the connector (3) and the attached O 2 can (2), and a sliding fit made to allow snap-fitting of the four locating prongs (12) on the PD can side of the connector (3) into the mating holes (10) in the mounting plate (4) on the PD can (1).
- PD can valve (19) opens fully.
- the gas flow from the O 2 can (2) is restricted by a small outlet hole (21) in the stem valve (20). It takes about 45 seconds at the second detent position for the gas pressure to (almost) equilibrate between the two cans to a level of 3.45 bar ⁇ 0.15 bar.
- the connector (3) is rotated further to the third detent position by the user. At this position, the two cans
- a standard 1 inch diameter aerosol valve (19) (Precision Valve, Peterborough, UK) is crimped into the top of the PD can (1) before or after sterile filling with the solution and may be activated by depressing the mesh stack shuttle (17), which functions as an aerosol valve actuator mechanism, to release the contents via an outlet nozzle (22) sized to engage a Luer fitting of a syringe or multi-way connector (not shown).
- a leak detector incorporating an apparatus for the generation of therapeutic microfoam according to the invention is shown in Figure 3.
- the device uses a commercially available leak detector, the VeecoTM MS-40 portable automatic leak detector, provided by the Vacuum Instrument Corporation, Ronkonkoma, New York.
- the leak detector uses a large capacity internal mechanical pump and a mass spectrometer comprising a 180-degree deflection dual magnetic sector mass spectrometer tube with built-in high vacuum ion gauge.
- the mass spectrometer is sensitive to Helium Mass 3 or Mass 4 and is operator selectable.
- An apparatus for the generation of therapeutic microfoam according to the invention is placed is a sealed chamber.
- the space between the generator and the sealed chamber is then evacuated using the internal mechanical pump, and helium levels, emanating from the generator into the sealed, evacuated space around it, are detected using the mass spectrometer.
- Table 1 Composition of 1% Polidocanol solution
Abstract
Description
Claims
Priority Applications (8)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2006500177A JP2006517428A (en) | 2003-01-10 | 2004-01-07 | Therapeutic microfoam |
AU2004204373A AU2004204373A1 (en) | 2003-01-10 | 2004-01-07 | Therapeutic microfoam |
DK04700472.6T DK1597171T3 (en) | 2003-01-10 | 2004-01-07 | THERAPEUTIC MICROSUM |
ES04700472T ES2399390T3 (en) | 2003-01-10 | 2004-01-07 | Therapeutic microfoam |
EP04700472A EP1597171B1 (en) | 2003-01-10 | 2004-01-07 | Therapeutic microfoam |
CA002512801A CA2512801A1 (en) | 2003-01-10 | 2004-01-07 | Therapeutic microfoam |
SI200431993T SI1597171T1 (en) | 2003-01-10 | 2004-01-07 | Therapeutic microfoam |
US10/890,267 US20050002873A1 (en) | 2003-01-10 | 2004-07-14 | Therapeutic microfoam |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB0300586.5 | 2003-01-10 | ||
GBGB0300586.5A GB0300586D0 (en) | 2003-01-10 | 2003-01-10 | Therapeutic microfoam |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US10/890,267 Continuation-In-Part US20050002873A1 (en) | 2003-01-10 | 2004-07-14 | Therapeutic microfoam |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2004062461A2 true WO2004062461A2 (en) | 2004-07-29 |
WO2004062461A3 WO2004062461A3 (en) | 2004-10-28 |
Family
ID=9950957
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/GB2004/000026 WO2004062461A2 (en) | 2003-01-10 | 2004-01-07 | Therapeutic microfoam |
Country Status (11)
Country | Link |
---|---|
US (1) | US20050002873A1 (en) |
EP (1) | EP1597171B1 (en) |
JP (1) | JP2006517428A (en) |
CN (1) | CN1735544A (en) |
AU (1) | AU2004204373A1 (en) |
CA (1) | CA2512801A1 (en) |
DK (1) | DK1597171T3 (en) |
ES (1) | ES2399390T3 (en) |
GB (1) | GB0300586D0 (en) |
SI (1) | SI1597171T1 (en) |
WO (1) | WO2004062461A2 (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2005048976A2 (en) * | 2003-11-17 | 2005-06-02 | Btg International Limited | Foams comprising a sclerosing and a viscosity enhancing agent, methods for production thereof |
WO2006120465A2 (en) * | 2005-05-13 | 2006-11-16 | Btg International Limited | Therapeutic sclerosing foam made preferably xenon |
WO2006120469A2 (en) * | 2005-05-13 | 2006-11-16 | Btg International Limited | Therapeutic sclerosing foam made preferably xenon |
DE112007003084T5 (en) | 2006-12-21 | 2009-10-29 | Btg International Ltd. | Apparatus and method for the production of therapeutic foam |
US7780695B2 (en) * | 2005-06-30 | 2010-08-24 | Codman & Shurtleff, Inc. | Chemically based vascular occlusion device deployment |
US20130189192A1 (en) * | 2005-10-21 | 2013-07-25 | Btg International Limited | Aerosol valve |
IT201800006109A1 (en) * | 2018-06-07 | 2019-12-07 | POLIDOCANOL FOR USE AS AN IMMUNOMODULATOR |
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GB9912356D0 (en) * | 1999-05-26 | 1999-07-28 | Btg Int Ltd | Generation of microfoam |
GB0028692D0 (en) * | 2000-11-24 | 2001-01-10 | Btg Int Ltd | Generation of therapeutic microform |
US8512680B2 (en) * | 2001-08-08 | 2013-08-20 | Btg International Ltd. | Injectables in foam, new pharmaceutical applications |
US8048439B2 (en) * | 2003-11-17 | 2011-11-01 | Btg International Ltd. | Therapeutic foam |
GB0509824D0 (en) * | 2005-05-13 | 2005-06-22 | Btg Int Ltd | Therapeutic foam |
WO2010005959A1 (en) * | 2008-07-07 | 2010-01-14 | Rich Products Corporation | Method for treatment and storage of platelets |
CA2860037C (en) | 2011-09-26 | 2019-09-24 | Advanced Preservations Technologies, Llc | Method for living tissue preservation |
EP2982444B1 (en) * | 2014-08-05 | 2019-11-13 | Goizper, S. Coop. | Pressure spray device |
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FR2795644B1 (en) * | 1999-07-02 | 2004-07-30 | Air Liquide Sante Int | THERAPEUTIC USES OF A HELIUM / OXYGEN MIXTURE, PARTICULARLY IN THE TREATMENT OF ASTHMA |
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2003
- 2003-01-10 GB GBGB0300586.5A patent/GB0300586D0/en not_active Ceased
-
2004
- 2004-01-07 AU AU2004204373A patent/AU2004204373A1/en not_active Abandoned
- 2004-01-07 SI SI200431993T patent/SI1597171T1/en unknown
- 2004-01-07 JP JP2006500177A patent/JP2006517428A/en active Pending
- 2004-01-07 CN CNA2004800020423A patent/CN1735544A/en active Pending
- 2004-01-07 ES ES04700472T patent/ES2399390T3/en not_active Expired - Lifetime
- 2004-01-07 CA CA002512801A patent/CA2512801A1/en not_active Abandoned
- 2004-01-07 EP EP04700472A patent/EP1597171B1/en not_active Expired - Lifetime
- 2004-01-07 WO PCT/GB2004/000026 patent/WO2004062461A2/en active Application Filing
- 2004-01-07 DK DK04700472.6T patent/DK1597171T3/en active
- 2004-07-14 US US10/890,267 patent/US20050002873A1/en not_active Abandoned
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WO2002041872A1 (en) * | 2000-11-24 | 2002-05-30 | Btg International Limited | Generation of therapeutic microfoam |
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EP1597171B1 (en) | 2012-12-19 |
AU2004204373A1 (en) | 2004-07-29 |
JP2006517428A (en) | 2006-07-27 |
US20050002873A1 (en) | 2005-01-06 |
SI1597171T1 (en) | 2013-04-30 |
CN1735544A (en) | 2006-02-15 |
GB0300586D0 (en) | 2003-02-12 |
WO2004062461A3 (en) | 2004-10-28 |
CA2512801A1 (en) | 2004-07-29 |
EP1597171A2 (en) | 2005-11-23 |
DK1597171T3 (en) | 2013-02-11 |
ES2399390T3 (en) | 2013-04-01 |
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