EP2884964A2 - Pharmazeutische zusammensetzung von propofol - Google Patents

Pharmazeutische zusammensetzung von propofol

Info

Publication number
EP2884964A2
EP2884964A2 EP13833549.2A EP13833549A EP2884964A2 EP 2884964 A2 EP2884964 A2 EP 2884964A2 EP 13833549 A EP13833549 A EP 13833549A EP 2884964 A2 EP2884964 A2 EP 2884964A2
Authority
EP
European Patent Office
Prior art keywords
emulsion
propofol
water
oil
coarse
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP13833549.2A
Other languages
English (en)
French (fr)
Other versions
EP2884964A4 (de
Inventor
Sougata Pramanick
Keshav Gurjar Mukund
Satish MEHTA Samit
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Emcure Pharmaceuticals Ltd
Original Assignee
Emcure Pharmaceuticals Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Emcure Pharmaceuticals Ltd filed Critical Emcure Pharmaceuticals Ltd
Publication of EP2884964A2 publication Critical patent/EP2884964A2/de
Publication of EP2884964A4 publication Critical patent/EP2884964A4/de
Withdrawn legal-status Critical Current

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
    • A61K9/107—Emulsions ; Emulsion preconcentrates; Micelles
    • 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
    • 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
    • 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
    • A61K9/0053—Mouth and digestive tract, i.e. intraoral and peroral administration
    • 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 pharmaceutical composition(s) containing a lipophilic therapeutic agent.
  • the invention provides pharmaceutical compositions containing the compound 2,6-diisopropylphenol (propofol) and methods of preparing the same.
  • Propofol is an intravenous short- acting anaesthetic agent, which since its introduction in the late 80s has gained wide acceptance for inducing and maintaining anesthesia, as well as for sedation.
  • the drug exhibits many notable advantages such as minimal side effects, controllable anaesthetic state, quick onset and rapid emergence from general anesthesia.
  • Propofol is lipophilic in nature and helps in providing rapid anesthetic action.
  • the lipophilicity of Propofol which is a liquid at room temperature, renders it relatively insoluble in water.
  • the molecule has a calculated partition coefficient (Log Pcalc) of 3.83 and presents little opportunity for solubilization through salt formation. Therefore, it is formulated as an oil-in-water emulsion, in which the disperse phase is soya-oil containing dissolved Propofol with emulsification using lecithin.
  • Such formulations because of their lipid component are good substrates for bacterial growth. Further, the parenteral administration of large volumes of lipid emulsions and/or the administration of lipid emulsions over prolonged periods of time may result in hyperlipidemia.
  • Diprivan injectable emulsion is a white, oil-in- water emulsion containing 10 milligrams propofol per milliliter of emulsion, 100 mg soybean oil per mL, 22.5 mg glycerol per mL, 12 mg egg lecithin per mL, 0.005% disodium edetate and sodium hydroxide.
  • Diprivan ® injectable emulsion is indicated as a single-use parenteral product. The said formulation is the subject matter of US 5,714,520 filed by Jones et al.
  • PropoFlo ® another oil-in water emulsion, contains 10 milligrams propofol per milliliter of emulsion, contains 100 mg soybean oil per mL, 22.5 mg glycerol per mL, 12 mg egg lecithin per mL, benzyl alcohol 20 mg per mL, oleic acid 0.6 mg per mL and sodium hydroxide which is adequately disclosed in US 6,140,373 of May et al.
  • Rapinovet ® anesthetic injection is a white, oil-in-water emulsion containing 10 milligrams propofol per milliliter of emulsion, 100 mg soybean oil/mL, 22.5 mg glycerol/mL, 12 mg egg lecithin/mL, 0.25 mg sodium metabisulfite/mL, and sodium hydroxide.
  • the said formulation was disclosed by Mirejovsky et al in US 6,147,122.
  • Emulsions intended for intravenous use should have an extremely small droplet size as this has a direct effect on both toxicity and stability. Any large droplet placed in the circulation may lodge in the pulmonary capillaries and could potentially lead to an embolism. The exact size at which this phenomenon becomes important is widely debated and pharmacopoeial limits on particulates in parenterals are vague, although 5 ⁇ is generally accepted as an upper limit. Emulsions containing droplets ranging in size from 0.5 to 1.0 ⁇ are utilized more rapidly by the body than emulsions with 3-5 ⁇ droplets.
  • Emulsions are thermodynamically unstable and various processes lead to changes in the drop size-distribution and/or emulsion structure.
  • the most common processes of emulsion destabilization are drop-drop coalescence, flocculation, creaming, and the Ostwald ripening.
  • the emulsion structure changes, while drop-size distribution may remain unaltered.
  • the drop-drop coalescence and the Ostwald ripening lead to changes in the drop-size distribution with time.
  • the intravenous emulsions must be sterile and steam sterilization is the preferred sterilization method on commercial scale.
  • the sterilization process supplies energy which can further destabilize the thermodynamically unstable emulsion system causing coalescence and flocculation.
  • sterilization conditions must be selected carefully to ensure both the stability and particle size of the final product.
  • the classical method for manufacture of Propofol emulsion employs a rotary autoclave.
  • the rotary cycle ensures that the product is in constant motion during the cycle, preventing separation of the two phases.
  • the rotary sterilizer, during the sterilization cycle facilitates heat transfer and maintains emulsion integrity because of the continuous agitation of the product.
  • the shaking cycle the product must be agitated lying on its side providing oscillatory movement along the container centroidal axis.
  • the agitation frequency maintained throughout the cycle must be, e.g., 70 rpm.
  • the product must be agitated throughout the sterilization process with the containers being horizontally positioned in rack(s) in a fixed manner and the rack(s) being rotated to result in an agitation.
  • a further object of the present invention is to provide a process for preparation of a stable injectable formulation of propofol, wherein the said process has minimal destabilization effect on propofol formulation.
  • the present invention provides a stable injectable emulsion formulation of propofol having uniform droplet size.
  • the present invention provides a simple, commercially viable process for manufacture of injectable emulsion formulation.
  • the process used in production of injectable emulsion formulation of propofol involves formation of an aqueous phase and oil phase.
  • Water soluble and oil-soluble ingredients are generally dissolved in the aqueous phase and oil phase, respectively.
  • Emulsifiers such as phosphatides, can be dispersed in either oil or an aqueous phase. Both phases are adequately heated and stirred to disperse or dissolve the ingredients.
  • the lipid phase is then generally added to the aqueous phase under controlled temperature and agitation (using high-shear mixers) to form a homogenously dispersed coarse emulsion.
  • the coarse emulsion is then homogenized (using a microfmidizer or a high-pressure homogenizer) at optimized pressure, temperature, and number of cycles to further reduce the droplet size and form fine emulsion.
  • Factors such as type and concentration of oil phase and surfactants, operating temperature, pressure, number of cycles, etc. has influence on the mean droplet size during high-pressure homogenization and microfluidization, hence need to control critically.
  • the pH of the resulting fine emulsion is then adjusted to the desired value and the emulsion is filtered through 0.45 to 5 urn filters.
  • the fine emulsions are usually packed in USP Type I glass containers. The packed vials are then sterilized terminally by autoclaving.
  • one aspect of the present invention relates to a method for preparation of a stable injectable emulsion formulation of propofol having uniform droplet size.
  • the main requirement of all injectable emulsions formulation is uniform droplet size.
  • the present invention achieves this requirement by suitably modifying the pH during the process of emulsification.
  • the present invention relates to a stable injectable formulation of propofol obtained from coarse propofol emulsion having alkaline pH, preferably above 8.
  • coarse emulsion means a crude mixture of the aqueous phase and oil phase.
  • the main difference between coarse emulsions and the final emulsion lies in the" droplet size of the dispersed phase.
  • Final emulsion has droplets
  • coarse emulsion typically in the size range 100-300 nm whereas coarse emulsion has the particle size in the range of 300 to 3000 nm.
  • Emulsions are thermodynamically unstable systems and various processes lead to changes in the drop size-distribution and/or emulsion structure.
  • the most essential parameters influencing the particle size are homogenization pressure, number of cycles, homogenization temperature, pH value and steam sterilization procedure could affect the particle size of an emulsion.
  • the classical method for manufacture of emulsions employ a rotary autoclave as it is believed that the rotary cycle ensures the constant motion of the product, preventing separation of the two phases.
  • the present inventors have surprisingly found out that if the pH of the coarse emulsion is adjusted in the alkaline range, preferably above 8, then stationary or normal conventional steam autoclave could be used for sterilization of the emulsion without affecting its stability.
  • the composition of the present invention comprises from 0.1 to 5%, by weight, of propofol.
  • the composition comprises from 1 to 3 % by weight of propofol and, in particular, about 1% or about 2%.
  • propofol alone is emulsified with water by means of a surfactant.
  • the propofol is dissolved in a water-immiscible solvent prior to emulsification.
  • the water-immiscible solvent is suitably present in an amount that is up to 30% by weight of the composition, more suitably 5-25%, preferably 10-20% and in particular about 10%.
  • a wide range of water-immiscible solvents can be used in the compositions of the present invention.
  • the water-immiscible solvent is a vegetable oil, for example soy bean, safflower, cottonseed, corn, sunflower, castor or olive oil.
  • the vegetable oil is soy bean oil.
  • the water-immiscible solvent is an ester of a medium or long-chain fatty acid for example a mono-, di-, or triglyceride; or is a chemically modified or manufactured material such as ethyl oleate, isopropyl myristate, isopropyl palmitate, a glycerol ester or polyoxy hydrogenated castor oil.
  • the compositions of the present invention may comprise a mixture of two or more of the above water- immiscible solvents.
  • Suitable surfactants include synthetic non-ionic surfactants, for example ethoxylated ethers and esters and polypropylene-polyethylene block co-polymers, and phosphatides for example naturally occuring phosphatides such as egg and soya phosphatides and modified or artificially manipulated phosphatides (for example prepared by physical fractionation and/or chromatography), or mixtures thereof.
  • Preferred surfactants are egg and soya phosphatides.
  • Additives such as tonicity modifiers, antioxidants and preservatives are usually added to the aqueous phase (water for injection). Tonicity adjustment can be achieved with glycerin, sorbitol or xylitol. Antioxidants such as a-tocopherol, ascorbic acid, and deferoxamine mesylate are generally added to prevent oxidation of the oil and drug substance. Additionally, antimicrobial agents such as EDTA, sodium benzoate and benzyl alcohol, are added to the aqueous phase to prevent microbial growth.
  • the oil-in-water emulsion of the present invention is prepared by homogenizing the oil and aqueous phases.
  • the oil phase is prepared by dissolving propofol and other oil-soluble ingredients in a water-immiscible solvent whereas the aqueous phase comprises of water-soluble ingredients.
  • Emulsifiers such as phosphatides, can be dispersed in either oil or aqueous phase. Both phases are adequately heated and stirred to disperse or dissolve the ingredients.
  • the lipid phase is then generally added to the aqueous phase under controlled temperature and agitation (using high-shear mixers) to form a homogenously dispersed coarse emulsion.
  • the process of preparing emulsion is as follows:
  • aqueous phase by mixing water soluble ingredients such as glycerine, egg lecithin, disodium EDTA in water ;
  • Preparing oil phase by dissolving propofol in solvent for propofol;
  • the obtained Emulsion has a globule size in the range of 100 to 300 nm.
  • the emulsion is then filtered through 0.45 to 5.0 ⁇ filters and packed in suitable containers such as USP type I glass containers. Siliconized containers could also be used. Additionally, teflon-coated vial plugs/stoppers are useful to prevent oxygen permeation and softening on contact with the oil phase.
  • the entire process (filtration/ coarse and fine emulsion preparation) is preferably carried out under nitrogen atmosphere whenever possible and especially in cases where the excipients and drugs are sensitive to oxidation.
  • compositions of the present inventions are typically sterile aqueous formulations and are prepared according to conventional manufacturing techniques using for example aseptic manufacture or terminal sterilization by conventional stationary autoclaving apparatus and procedure.
  • the present inventors have surprisingly found that if the pH of the coarse emulsion is adjusted well above 8, preferably in the pH range of 8.5 to 11.0, more preferably in the range of 10.0 to 11.0, then the terminal sterilization has very minimal influence on droplet size of the emulsion. In other words, the droplet size is not at all affected by the temperature and time of the conventional steam sterilization methods (121 C for 45 minutes). Moreover, by adjusting the pH, recourse to rotary sterilizer is also avoided.
  • composition of the present invention is suitably formulated as follows:
  • a sterile aqueous oil-in-water emulsion for parenteral administration was prepared as follows. All processing stages were carried out under nitrogen and weights, refer to weight in the final volume.
  • An aqueous phase was prepared by adding glycerin, edetate disodium and egg lecithin in water.
  • the oil phase was prepared by adding propofol to the soybean oil.
  • the oil phase was added to the aqueous phase at a temperature below 25°C and homogenized at high pressures to get a coarse emulsion.
  • the pH of the coarse emulsion was adjusted to pH in the range of 10.5 to 11.0 by using 0.2 N sodium hydroxide solution and the solution was brought to final volume with water and homogenized at high pressure.
  • Table -1 Effect of pH on droplet size of emulsion sterilized by autoclaving

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Epidemiology (AREA)
  • Dispersion Chemistry (AREA)
  • Nutrition Science (AREA)
  • Physiology (AREA)
  • Anesthesiology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Organic Chemistry (AREA)
  • Dermatology (AREA)
  • Medicinal Preparation (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
EP13833549.2A 2012-08-16 2013-08-13 Pharmazeutische zusammensetzung von propofol Withdrawn EP2884964A4 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
IN2373MU2012 2012-08-16
PCT/IN2013/000495 WO2014033751A2 (en) 2012-08-16 2013-08-13 Pharmaceutical composition of propofol

Publications (2)

Publication Number Publication Date
EP2884964A2 true EP2884964A2 (de) 2015-06-24
EP2884964A4 EP2884964A4 (de) 2016-01-06

Family

ID=50184537

Family Applications (1)

Application Number Title Priority Date Filing Date
EP13833549.2A Withdrawn EP2884964A4 (de) 2012-08-16 2013-08-13 Pharmazeutische zusammensetzung von propofol

Country Status (2)

Country Link
EP (1) EP2884964A4 (de)
WO (1) WO2014033751A2 (de)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104490780B (zh) * 2015-01-16 2017-04-19 河北一品制药有限公司 一种丙泊酚脂肪乳注射液的制备方法

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6028108A (en) * 1998-10-22 2000-02-22 America Home Products Corporation Propofol composition comprising pentetate
US6177477B1 (en) * 1999-03-24 2001-01-23 American Home Products Corporation Propofol formulation containing TRIS
GB0012597D0 (en) * 2000-05-25 2000-07-12 Astrazeneca Ab Formulation
KR100459025B1 (ko) * 2002-05-02 2004-12-03 (주) 에프디엘 프로포폴을 함유하는 신규한 주사제용 조성물
WO2007052288A2 (en) * 2005-08-05 2007-05-10 Bharat Serums & Vaccines Ltd. Intravenous propofol emulsion compositions having preservative efficacy
BRPI0604377A (pt) * 2006-10-27 2008-06-24 Cristalia Prod Quimicos Farm microemulsão óleo/água de propofol estável e pronta-para-uso
DE102009003980A1 (de) * 2009-01-07 2010-07-08 B. Braun Melsungen Ag Propofol in triheptanoinhaltiger Trägeremulsion
US9132090B2 (en) * 2009-01-13 2015-09-15 Chetan Majmudar Propofol based anesthetic with preservative
CN102552136B (zh) * 2012-02-09 2013-05-01 清远嘉博制药有限公司 一种丙泊酚中/长链注射液及其制备方法

Also Published As

Publication number Publication date
WO2014033751A3 (en) 2014-05-30
WO2014033751A2 (en) 2014-03-06
EP2884964A4 (de) 2016-01-06

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