WO2000078301A1 - Anesthetic composition for intravenous injection comprising propofol - Google Patents
Anesthetic composition for intravenous injection comprising propofol Download PDFInfo
- Publication number
- WO2000078301A1 WO2000078301A1 PCT/KR2000/000649 KR0000649W WO0078301A1 WO 2000078301 A1 WO2000078301 A1 WO 2000078301A1 KR 0000649 W KR0000649 W KR 0000649W WO 0078301 A1 WO0078301 A1 WO 0078301A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- composition
- propofol
- poloxamer
- formulation
- surfactant
- Prior art date
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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
- A61K9/107—Emulsions ; Emulsion preconcentrates; Micelles
- A61K9/1075—Microemulsions or submicron emulsions; Preconcentrates or solids thereof; Micelles, e.g. made of phospholipids or block copolymers
-
- 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
- A61K31/045—Hydroxy compounds, e.g. alcohols; Salts thereof, e.g. alcoholates
- A61K31/05—Phenols
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P23/00—Anaesthetics
Definitions
- the present invention relates to an anesthetic composition for intravenous injection comprising 2,6-diisopropylphenol (hereinafter, referred to as "propofol") More specifically, the present invention relates to an anesthetic composition for intravenous injection, characterized in that it contains propofol and a poloxamer as the surfactant
- Propofol is highly lipid-soluble and has a characteristic property that it can readily permeate biomembranes such as blood brain barrier (BBB) Therefore, it has been used as a useful anesthetic agent.
- BBB blood brain barrier
- anesthetic agents are eliminated through their metabolism and excretion in living body
- an anesthetic agent having a long half-life When an anesthetic agent having a long half-life is repeatedly administered in a large amount, it may be greatly accumulated into storage tissues such as skeletal muscles, adipose tissues, etc., so that the recovery may be delayed
- storage tissues such as skeletal muscles, adipose tissues, etc.
- the recovery rate of patients may be delayed and the psychomotor function may also be damaged over long period
- an alkylphenol derivative, propofol has a short half-life and thus, has some clinical characteristic features that it can be rapidly migrated into the brain to show a rapid onset of anesthetic effect and further, rapidly re-distributed into other tissues and then metabolized so that the patients can be rapidly recovered from the anesthetic state
- propofol may cause less side effects such as headache, nausea, vomiting, etc , than other anesthetic agents in patients and its accumulation into human body can be minimized in spite of its administration for a long period Therefore, it has been known that propofol is the most ideal anesthetic agent for intravenous injection
- anesthetic agents commonly used in the clinical field are in a gaseous state
- propofol is useful for intravenous injection and therefore, can be very effectively used as a local analgesic adjuvant due to its hypnotic and sedative activities, an anesthetic agent for patients for whom pulmonary respiration should be cared, an anesthetic agent used under conscious state, etc , or for patients under medical treatment in intensive care unit (ICU) or patients in serious state, etc
- ICU intensive care unit
- water may substantially be an essential solvent in preparing all pharmaceutical formulations including anesthetic agents
- hpid-soluble drugs such as propofol
- water water as the solvent
- hpid-soluble drugs which are generally poorly soluble in water have been developed into such forms as emulsions, microemulsions, micelles, etc , using a surfactant
- it also possesses a limitation
- Zeneca Inc has prepared and sold the formulation wherein 1% propofol is dissolved in 16% Cremophor EL as a non-ionic surfactant
- this formulation causes some side effects such as anaphylactoid reaction as an allergic reaction in some patients, which is believed to be caused by Cremophor EL contained therein in an excessive amount Therefore in order to overcome such side effects caused by the surfactant
- Zeneca Inc has developed the injectable formulation (trade name Dip ⁇ van) in the form of a novel fat emulsion, wherein 1% propofol is dissolved in 10% soybean oil and then stabilized with 1 25% egg phosphatide
- the emulsion is thermodynamically unstable and therefore, is fused in the course of time to make the formulation unstable
- the active ingredient and hpid components may cause a pain when the formulation is injected
- hpid component may serve as a cause of the acceleration of microorganism growth in the absence of any preservative, strict aseptic techniques must be maintained when handling these formulation Finally, the administration of hpid components as the main ingredient may result in hyperhpidemia
- Zeneca Inc has developed the formulation comprising a novel composition having an antiseptic activity by addition of a preservative (EDTA) in order to inhibit the microorganism growth due to pid components amongst the above-mentioned problems (U S Patent No 5,714,520)
- EDTA preservative
- this formulation still has the unsolved problems including phvsical unstabihty, pain at injection site, embolism, hyperhpidemia.
- the formulations have recently been studied using inclusion complexation of propofol with biodegradable surfactants or cyclodextrin (Giuseppe Trapani et al , J.
- the technical subject of the present invention is to provide a useful anesthetic composition for intravenous injection which can be efficiently converted into the desired formulation and further, can minimize the side effects, with overcoming the above- mentioned problems involved in the prior art.
- the technical subject of the present invention is to provide a useful anesthetic composition for intravenous injection which can be efficiently converted into the desired formulation and further, can minimize the side effects, with overcoming the above- mentioned problems involved in the prior art.
- an anesthetic composition for intravenous injection which comprises propofol and a poloxamer as the surfactant
- propofol is contained in an amount of 1 to 2% by weight of the total composition
- the composition of the present invention may additionally contain at least one co-surfactant selected from the group consisting of Solutol HS 15, egg lecithin, Labrasol, polyoxy 10 oleyl ether, tween, ethanol and polyethylene glycol, in addition to a poloxamer as the surfactant
- poloxamer 407 it is particularly preferred to use poloxamer 407 as the poloxamer It is desirable to have poloxamer 407 in an amount of 0 1 to 5% by weight of the total composition
- composition of the present invention is preferably present in the form of an oil-in- water microemulsion having a particle size of lOOnm and below
- composition of the present invention may contain Solutol HS 15 in an amount of 0 1 to 10%) by weight of the total composition, egg lecithin in an amount of 0 1 to 5%> by weight of the total composition, and ethanol and polyethylene glycol in an amount of 0 1 to 5% by weight of the total composition
- composition of the present invention can additionally contain an agent for pH adjustment and an agent for isotonicity
- agent for pH adjustment is preferably sodium hydroxide and the agent for isotonicity is particularly preferable to use glycerol
- composition of the present invention is characterized in that it contains propofol and a poloxamer as the surfactant
- the poloxamers are a block copolymer composed of hydrophilic polyoxyethylene and hydrophobic polyoxypropylene, which allows that in the aqueous solution the lipid- soluble portion formed from polyoxypropylene can include the drug therein and the hydrophilic polyoxyethylene portion is placed on the outside of the core so that it can be hydrated with water
- All of poloxamers have a substantially similar composition to each other and are classified into many varieties depending on the ratio of polyoxyethylene/polyoxypropylene content
- the poloxamers are a very stable material to exist in a stable state in an aqueous solution containing acids, alkalis and even the metals In addition, they have been known as being a non-toxic and non-irritant material which is not metabolized in a living body Poloxamers are described in USP XXIII and have been once used as a stable excipient by U S Food and Drug Administration (FDA) Further, they have been known as having less side effects than others when they are intravenously injected.
- the present invention provides an anesthetic composition for intravenous injection which contains propofol and poloxamer alone or in combination with other co-surfactant.
- the content of propofol amounts to 1 to 2% by weight of the total composition and the content of poloxamer amounts to 0 1 to 10% by weight of the total composition
- the poloxamer which can be preferably used in the present invention include poloxamer 407 and poloxamer 188, with poloxamer 407 being particularly preferable in providing the effect of the present invention In case of poloxamer 407, it is preferably contained in an amount of 0 1 to 5% by weight of the total composition
- poloxamers used in the present invention can allow the microemulsification of the composition even by using a smaller amount than prior surfactants, the toxicity of anesthetic composition containing propofol as the active ingredient can be significantly reduced
- composition of the present invention can additionally contain at least one co- surfactant selected from the group consisting of Solutol HS 15, egg lecithin, Labrasol, polyoxy 10 oleyl ether, tween, ethanol and polyethylene glycol, with Solutol HS 15 and egg lecithin being particularly preferable
- Solutol HS 15 is added in an amount of 0 1 to 10%) by weight of the total composition or egg lecithin is added in an amount of 0 1 to 5% by weight of the total composition, they can show the most excellent effect
- the composition of the present invention is in the form of an oil-in-water microemulsion having a particle size of lOOnm and below
- the microemulsions have the particle size of lOOnm and below, are thermodynamically stable and do not cause any phase separation in the course of time
- the micromeulsions are classified into an oil-in-water and a water-in-oil forms, wherein the former is preferable in the present invention
- the oil-in-water microemulsion means ultrafine elementary particles protected in the water phase, which is formed by dissolving the drug in the oil phase and then enclosing the drug in the surfactant and/or co-surfactant when the drug is hydrophobic
- They have physico-chemical properties that they are thermodynamically stable, allow to disperse the immiscible two liquid phases into a single phase, can be prepared spontaneously without putting external energy into the procedures for their preparation, and are apparently transparent since the incident light is totally reflected on the surface of particles due to the low concentration and small size of the enclosed particles as finally prepared, and the like.
- thermodynamic stability of microemulsions can be ensured by selecting a suitable surfactant to reduce the surface tension and further by adding the co-surfactant to increase the fluidity of particle membrane.
- poloxamers used as the surfactant have a high hydrophilic/lipophilic balance and therefore, can allow that the composition can be readily prepared in the form of an oil-in-water microemulsion
- the microemulsion thus prepared can overcome the problem of emulsions due to a unstability of the formulation since it has characteristic features that it is thermodynamically stable in comparison to the known emulsions, can be readily prepared spontaneously at room temperature and is a transparent solution.
- the hvdrophilicity of the stably enclosed drug can sufficiently contribute for reducing the pain when it is injected, since when it is injected via intravenous route, it is dispersed by rapid blood flow to reduce the direct contact with the membrane of blood vessel Moreover, since it does not contain any lipid component which is used in lipid emulsions, it also reduce the risk of hyperhpidemia which may be raised due to lipid components
- composition of the present invention can be prepared by further adding an agent for pH adjustment Although any agent for pH adjustment conventionally used in this may can be used without any special limitation, sodium hydroxide (NaOH) is particularly preferably used.
- the composition of the present invention can also contain an agent for isotonicity, if appropriate Similarly, although any agent for isotonicity conventionally used in this art can be irrespectively used, it is preferable to select glycerol
- composition of the present invention is typically a sterile, aqueous preparation and has a very small particle size (lOOnm and below) Therefore, it can be formulated into an injectable solution in a sterile state by a simple filtration, rather than the final sterilization using autoclave It is preferred to practice all the procedures for preparation under nitrogen
- the present invention is more specifically explained by the following examples However, it should be understood that the scope of the present invention is not limited by the examples in any manner It will be appreciated by any person skilled in this art that the present invention includes the following examples and further can be variously modified and altered within the technical concept of the present invention Example 1
- the surfactant 4g of poloxamer 407 was added and dissolved in about 80g of purified water for injection at room temperature While stirring, lg of propofol was added dropwise to the resulting solution and the stirring was continued until the single phase is formed
- the co-surfactant 1 5g of ethanol and 0 5g of polyethylene glycol 400 were added thereto Purified water for injection was added to make lOOm-0 of the final volume The resulting microemulsion was filtered through 0 22/tm filter to remove the particulate materials and microorganisms The product thus obtained was introduced into a suitable container which was filled with nitrogen and then, sealed
- test samples were prepared by combining each of 3%, 4%, 6%, 8% and 10% poloxamer 407 with 1%) porpofol, 1 5% ethanol and 0 5% polyethylene glycol 400 to compare the anesthetic effect and toxicity with each other
- 5 male Sprague-Dawley rats 160+ 10g
- propofol was administered in an amount of 10mg/kg
- the control group received Diprivan which has been currently used in the clinical field
- the time from the point immediately after the administration to the point at which the righting response disappears and the animal is recovered was maintained at the mean level of approximately 1 1 + 1 minutes
- the clinical symptoms and the weight were daily observed during one week after recovery from anesthesia and as the result, it was identified that they were uniform and normal
- poloxamer 407 has no effect on the anesthetic effect of propofol and further, does not show any symptom of toxicity
- test group received only the formulation of Example 6 and the control group received Diprivan Rats were placed in the fixed cage Each formulation was injected into tail vein within 5 to 15 seconds. Rats were then removed from the fixed cage and laid flat Each of time to unconsciousness, time to startle response, time to righting response and time to full recovery was recorded from the test animals and compared from each other
- test group received only the formulation of Example 6 and the control group received Diprivan Rabbits were placed in the fixed cage Each formulation was injected into tail vein within 30 seconds Rabbits were then removed from the fixed cage and laid flat Each of time to unconsciousness, time to startle response, time to righting response and time to full recovery was recorded from the test animals and compared from each other
- the test was practiced to determine the anesthetic effect of the formulation of Example 6 in laparotomy 8 weeks-old rats were anesthetized with ether and then the hair was cut from the abdominal portion After rabbits were recovered from ether anesthesia, the formulation was administered through the catheter inserted into tail vein After 5 minutes from anesthesia induction, the abdominal portion was incised to about 3 cm and the formulation was repeatedly injected to maintain the anesthetic state for about 60 minutes At the time of 45 minutes of anesthetic maintenance, the incised portion was gated and then, each of time to unconsciousness, time to startle response, time to righting response and time to full recovery was recorded
- the total dosage of the formulation required to maintain the anesthetic state was about 38 9mg/kg 5 and the time to full recovery was recorded as 71 5 minutes After laparotomy, any abnormal change was not observed in rabbits
- Example 6 The formulation of Example 6 was injected into ear vein of each of three rabbits in a total amount of 3m ⁇ at the rate of l ⁇ /min After 30 minutes, and 1, 1 5, 2, 4, 6 and 24 hours, each injection site was macroscopically observed for the responses caused by pain and phlebitis As the result, the resistant behaviour caused by pain from injection, and any change of phlebitis such as rubor, erythema, edema, etc could not be observed
- Example 6 albino rat was incised with scissor at the upper part of left femoral region, at which each of vein and artery was cannulated, and then 10mg/kg of the formulated drug was intravenously injected over one minute After 0, 5, 10 15, 30, 45 and 60 minutes, blood was collected from femoral artery in an amount of 100 t ⁇ each time Blood was obtained after heparin- physiological saline and some blood filled in the catheter were removed few seconds before collecting blood each time After blood was collected, a small amount of heparin- physiological saline was introduced into the catheter connecting tube to prevent blood coagulation 100 ⁇ of the collected blood were mixed with 500/ ⁇ of physiological saline and then centrifuged with 3000 rpm for 10 minutes 100 ⁇ of the supernatant were transferred into microplate and the absorbance of released hemoglobin was measured at 540 nm Hemolysis (%) was calculated according to the following equation The control group used 70% propylene glycol (
- Hemolysis % (A f - Ao)/(A 100 - ,) x 100
- a 100 is the absorbance at the time of 100% hemolysis (100 ⁇ of blood was mixed with 500 - ⁇ of water)
- a ⁇ is the absorbance at the time of 0% hemolysis as the blank (Before injection of the drug, normal blood was mixed with 500 ⁇ of physiological saline for the blank test)
- a f is the absorbance of each specimen
- Example 6 shows the similar absorbance to the blank test and thus, does substantially not cause hemolysis whereas 70% PG as the control group shows the absorbance 80-90 times as high as the formulation of Example 6 and causes hemolysis Experiment 8
- test material Example 1
- positive comparative material Diprivan
- the symptoms including intoxication, dyspnea, abnormal behaviour, appearance and death were continuously observed.
- the blood pressure and heart rate were measured by connecting the catheter with the measuring equipment (data acquisition system, Biopak, USA) After the stabilization of blood pressure for about 20 minutes was identified, the test material (Example 1) and the positive comparative material (Diprivan) were administered for 12 hours During the total period of the experiment, the test animal was maintained under continuous ventilation by inserting the tracheal tube into the test animal and controlling the stroke volume as 200- 250 and spm as 20-30 by means of a ventilator The blood pressure and heart rate were measured for 12 hours and represented by the change percent (%) relative to the values measured before drug administration 3) Blood biochemical examination
- Blood was collected from right femoral artery before administration of the drug and at interval of one hour for 12 hours after administration and then, measured O 2 and CO 2 partial pressure and pH of arterial blood using a blood gas analyzer
- both the group receiving the test formulation (Example 1) and the group receiving the positive comparative formulation (Diprivan) maintained the constant pH level
- the CO 2 partial pressure exhibited a tendency to slightly increase in the course of time in the group receiving the positive comparative formulation (Diprivan) but maintained at the constant level in the group receiving the test formulation (Example 1)
- the O 2 partial pressure was somewhat lowered in the course of time both in the group receiving the test formulation (Example 1) and the group receiving the positive comparative formulation (Diprivan) but was generally somewhat higher in the group receiving the test formulation (Example 1)
- the present invention provides an anesthetic composition for intravenous injection, which is prepared in the form of a microemulsion by adding a ploxamer and optionally, at least one selected from the group consisting of Solutol HS 15, egg lecithin, Labrasol, polyoxy 10 oleyl ether, tween, ethanol and polyethylene glycol, to propofol
- the composition of the present invention is composed of small particles of lOOnm and below, thermodynamically stable, and does not cause the phase separation in the course of time Further, since it can be aseptically filtered to remove the microorganisms contamination, it has advantages that a separate sterilization procedure is unnecessary so that it can be readily prepared at a low cost by a simple procedure In addition, since the composition of the present invention is hydrophilic and is composed of small particles so that it can be dispersed by rapid blood flow in the case of intravenous injection, it results in a little pain at injection site does substantially not cause embolism and does also not cause hemolysis
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Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10/018,663 US6743436B1 (en) | 1999-06-21 | 2000-06-20 | Anesthetic composition for intravenous injection comprising propofol |
AU55742/00A AU5574200A (en) | 1999-06-21 | 2000-06-20 | Anesthetic composition for intravenous injection comprising propofol |
DE60028384T DE60028384T2 (en) | 1999-06-21 | 2000-06-20 | PROPOFOL-CONTAINING ANESTHETIC COMPOSITION FOR INTRAVENOUS INJECTION |
JP2001504365A JP2003502363A (en) | 1999-06-21 | 2000-06-20 | Anesthetic composition for intravenous injection containing propofol |
CA002377614A CA2377614C (en) | 1999-06-21 | 2000-06-20 | Anesthetic composition for intravenous injection comprising propofol |
EP00940958A EP1202719B1 (en) | 1999-06-21 | 2000-06-20 | Anesthetic composition for intravenous injection comprising propofol |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1999/23336 | 1999-06-21 | ||
KR19990023336 | 1999-06-21 |
Publications (1)
Publication Number | Publication Date |
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WO2000078301A1 true WO2000078301A1 (en) | 2000-12-28 |
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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PCT/KR2000/000649 WO2000078301A1 (en) | 1999-06-21 | 2000-06-20 | Anesthetic composition for intravenous injection comprising propofol |
Country Status (11)
Country | Link |
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US (1) | US6743436B1 (en) |
EP (1) | EP1202719B1 (en) |
JP (1) | JP2003502363A (en) |
KR (1) | KR100410937B1 (en) |
CN (1) | CN1149984C (en) |
AT (1) | ATE327741T1 (en) |
AU (1) | AU5574200A (en) |
CA (1) | CA2377614C (en) |
DE (1) | DE60028384T2 (en) |
ES (1) | ES2261210T3 (en) |
WO (1) | WO2000078301A1 (en) |
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WO2001064187A2 (en) * | 2000-02-29 | 2001-09-07 | Maelor Pharmaceuticals Limited | Anaesthetic formulations |
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- 2000-06-20 US US10/018,663 patent/US6743436B1/en not_active Expired - Fee Related
- 2000-06-20 EP EP00940958A patent/EP1202719B1/en not_active Expired - Lifetime
- 2000-06-20 DE DE60028384T patent/DE60028384T2/en not_active Expired - Fee Related
- 2000-06-20 AT AT00940958T patent/ATE327741T1/en not_active IP Right Cessation
- 2000-06-20 ES ES00940958T patent/ES2261210T3/en not_active Expired - Lifetime
- 2000-06-20 WO PCT/KR2000/000649 patent/WO2000078301A1/en active IP Right Grant
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Also Published As
Publication number | Publication date |
---|---|
KR20010039671A (en) | 2001-05-15 |
EP1202719A1 (en) | 2002-05-08 |
KR100410937B1 (en) | 2003-12-18 |
CN1149984C (en) | 2004-05-19 |
EP1202719B1 (en) | 2006-05-31 |
DE60028384T2 (en) | 2007-05-16 |
EP1202719A4 (en) | 2004-03-17 |
US6743436B1 (en) | 2004-06-01 |
CN1356896A (en) | 2002-07-03 |
ATE327741T1 (en) | 2006-06-15 |
DE60028384D1 (en) | 2006-07-06 |
CA2377614C (en) | 2008-07-29 |
CA2377614A1 (en) | 2000-12-28 |
JP2003502363A (en) | 2003-01-21 |
AU5574200A (en) | 2001-01-09 |
ES2261210T3 (en) | 2006-11-16 |
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