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
  • A61K9/0012—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
  • A61K9/0029—Parenteral nutrition; Parenteral nutrition compositions as drug carriers
• • 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
  • A61K31/21—Esters, e.g. nitroglycerine, selenocyanates
  • A61K31/215—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids
  • A61K31/22—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acyclic acids, e.g. pravastatin
  • A61K31/23—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acyclic acids, e.g. pravastatin of acids having a carboxyl group bound to a chain of seven or more carbon atoms

Definitions

• Emulsion for parenteral administration Emulsion for parenteral administration
• Fat emulsions which are intended, inter alia, for intra ⁇ venous, nutrient supply and which exhibit insignificant secondary effects have been available since the beginning 5 of the 196 ⁇ 's ( retlind, A. Development of fat emulsions, JPEN 5: No. 3, 230.235, 1981).
• This development work has investigated the effect of emulsions which contain a num ⁇ ber of mutually different fats (olive oil, cottonseed oil, soyabean oil, maize oil, safflower oil, coconut oil, etc.) 10 and several mutually different emulsifiers (soyabean phos- pholipids, egg yolk phospholipids, cerebrosides , diglyce- rides etc.).
• the fats or oils used comprise triglycerides of fatty acids.
• the present invention now makes it possible to prepare emulsions which will satisfy the aforesaid desiderata, with the use of alkyl esters, and then preferably ethyl esters of fatty acids deriving from synthetic, animal or vegetable origins.
• alkyl esters can be obtained either by esterification of triglycerides with ethyl alco ⁇ hol or other alcohols in the presence of a catalyst, such as sodium alcoholate and certain zinc compounds.
• fatty acids can be prepared by complete hydrolysis of triglycerides with sodium hydroxide or potassium hydro ⁇ xide, whereafter the solution containing the salt compound of the fatty acids is extracted with hexane or some other organic solvent, so as to remove unsaponifiable residues.
• the free fatty acids are obtained subsequent to adding hydrochloric acid or some other acid.
• the free fatty acids can then be converted to ethyl esters or some other alkyl esters in some suitable way, by treating the fatty acids with ethyl alcohol or some other alkyl alcohol having one or two hydroxyl groups capable of esterification.
• Suitable esters can also be obtained by esterifying synthetic or otherwise produced fatty acids having an even or an odd number of carbon atoms.
• the present invention thus relates to an emulsion intended for parenteral administration and including a hydrophobic phase emulsified in a water phase, this emulsion being characterized in that a substantial part of the hydropho ⁇ bic phase comprises one or more alkyl esters of pharmaco ⁇ logically acceptable fatty acids.
• the alkyl esters will preferably comprise low-molecular alkyl esters having 2-4 carbon atoms in the alkyl groups, and then primarily ethyl esters.
• the fatty acids are preferably of vegetable, animal or synthetic origins, and will preferably have from 9 to 22 carbon atoms in their carbon chains.
• the carbon chain of the fatty acids will contain predominantly or exclusively an even or odd number of carbon atoms. This has been found significant with respect to certain usages of the emul- sions prepared. For instance, fatty acids having an odd number of carbon atoms will produce a high percentage of glucose when metabolized, a fact which can have signifi ⁇ cance when using the emulsion for nutrient administration.
• the alkyl ester content of the emulsion will suitably be from 5 to 60 percent by weight, calculated on the total emulsion, and preferably from 5 to 30 percent by wei ⁇ ht. Future reference to percentages made in this description and appended claims refers to weight/volume percent (w/v) , unless otherwise stated.
• the hydrophobic phase of the emulsion may also include glyceryl esters of fatty acids.
• the weight ratio of the alkyl esters to the glyceryl esters will then suitably be from 10:1 to 1:10.
• ethyl esters or other alkyl esters of fatty acids will afford, inter alia, the following advantages: l:o homogenization is simplified as a result of the lower viscosity; 2:o the lower viscosity will also result in a lower visco ⁇ sity of the prepared emulsion;
• the present emulsion will thus contain one or more pharma ⁇ cologically active substances dissolved or dispersed in the hydrophobic phase.
• These substances, or agents may be of very different types, as will be made apparent in the 5 following, and the type of active substance used is not intended to limit the scope of the present invention.
• inventive emulsions may contain X-ray contrast agents, particularly in the form of one or more iodized fats or contrast substances for such investigative procedures as datortomography and NMRI (Nuclear Magnetic 10 Resonance Imaging). These substances or agents may be pre ⁇ sent in a quantity of 1-60 percent by weight, calculated on the whole emulsion.
• inventive emulsion has two essential areas of use. The first of these areas is
• the use of the emulsion as a nutrient source intended for parenteral nutrient supply is the use of the emulsion as a vehicle for carrying pharma ⁇ cologically active substances, including X-ray contrast substances or media, these substances being dissolved or
• 25 intended for nutrient supply can include one or more phar ⁇ macologically active substances in the hydrophobic phase.
• the inventive emulsions are primarily intended for intra ⁇ venous administration, particularly when used for nutrient supply.
• the emulsions can also be administered ⁇ ⁇ parenterally in any other manner, the manner in which the emulsions are administered bein ⁇ determined bv the effect and function of the pharmacologically active substances included and by the indications or symptoms of the patient.
• compositions prepared in accordance with the invention may also contain various additives, i.e. in addition to the active substance (or substances) and the hydrophilic component, comprising water, optionally with substances dissolved therein, and the hydrophobic component, compri ⁇ sing alkyl esters, and then particularly ethyl esters of fatty acids.
• these further additives may, for instances, comprise preserving agents, pH-adjusters and agents for achieving a suitable ozmotic pressure.
• one of the most important additives will comprise one or more suitable emulsifiers capable of providing a stable dispersion. A multiple of emulsifying and suspension agents of both natural and synthetic origin can be used in this respect.
• agents examples include phospholi- pids deriving from eggs or soyabeans, and polyethylene polypropylene glycol.
• phospholi- pids deriving from eggs or soyabeans examples include phospholi- pids deriving from eggs or soyabeans, and polyethylene polypropylene glycol.
• Many useable emulsifiers are known from the literature and are commercially available, and the person skilled in this particular art will have no problem in selecting one or more agents suitable for the purpose intended.
• the emulsion may also contain nutrients dissolved or dis ⁇ persed in the aqueous phase.
• nutrients include, for instance, amino acids, glycerol, glucose, fructose, xylitol, sorbitol or other sugars or alcohols, water-soluble vitamins, salts and trace elements.
• the emulsion may contain several of these substances at one and the same time.
• the aqueous phase may also contain water-soluble, pharmacologically active substances,
• All of the. particles nresent in an inventive emulsion will have a diameter considerably smaller than 1 micron, there ⁇ by obviating the risk of the particles fastening in the capillaries.
• An emulsion having a particle size of 0.1-0.3 micron can be produced without any great difficulty. This renders the system stable.
• the inventive emulsions can be prepared in a manner to prevent the particles from forming agglomerates in the blood.
• the inventive emulsions will withstand being auto- claved and can be stored for long periods without degreda- tion or decomposition.
• the actual vehicle system is well tolerated and will not result in secondary effects, when administered intrave ⁇ nously.
• Emulsions prepared in accordance with the present inven ⁇ tion exhibit a high degree of tolerance in experiments carried out on animals.
• Ethyl esters of fatty acids obtai ⁇ ned from soyabean oil have been examined in infusion expe ⁇ riments on rats.
• the volume used corresponded approximately to the energy consumed each minute by the animal concerned.
• the amount of alcohol administered to the animals in the aforesaid experiments corresponds to only 10 % of the total energy requirement of the body.
• the emulsion itself was prepared in a conventional manner, i.e. a manner well known to the skilled person from, for instance, the aforecited literature.
• the hydrophobic phase, the emulsifier and the aqueous phase can be mixed together to form a "coarse emulsion", which is then homo ⁇ genized in some suitable apparatus to a "suitable particle size with regard to the hydrophobic phase.
• Those substan- ces intended to be in solution or dispersion in the hydro- phobic phase, and/or the aqueous phase are normally first dissolved in respective phases prior to mixing said phases together. Subsequent to homogenization, the emulsion is poured into suitable containers and then sterilized.
• the quality of the emulsion ingredients is such as to be free from pharmacological complaint, and that this quality is sus ⁇ tained through the whole of the process of preparation.
• the components must be free from contaminants capab- le of causing harmful secondary effects, such as pyrogens, and must also be protected from the harmful effect, for instance, of oxidation, prior to, during and subsequent to the process of preparation, all of which is well known to the person skilled in this art.
• soyabean oil 100 g were mixed with 1 liter of absolute alcohol. It was found that the oil did not dissolve, but lay in a layer beneath the alcohol. Sodium alcoholate was then added in an amount corresponding to 0.25 g metallic sodium. A clear solution was obtained after 2C-30 minutes, subsequent to tran ⁇ -esterification of the so2abean oil taking place. Three volumes of water were added and the resultant oil layer was then isolated and washed with some small volumes of water. The resultant oil comprised the ethyl esters of the fatty acids of the soyabean oil. i.
• the viscosity of the ethyl esters is significantly lower than the viscosity of the original soyabean oil.
• the spe ⁇ cific weight is also lower than the specific weight of corresponding triglyceride.
• ethyl esters 50 g were mixed with 6 g phospholi- pids, 12.5 g glycerol and water to a volume of 500 ml. 1 M NaOH was added to obtain a pH between 7 and 10.5, where ⁇ after the mixture was homogenized in a conventional man ⁇ ner, e.g. in a Moulin-Gaulin homogenizer. The resultant emulsion was heat sterilized at 120 * C for 20 minutes. Sub ⁇ sequent to being analyzed for control purposes, the emul ⁇ sion was ready for intravenous administration. The measu ⁇ red particle size was 0.15-0.30 micron.
• the emulsion was administered in quantities of 150 ml per kilogram and day to rats under a planned 14 day course of administration.
• the rats exhibited a good increase in weight. No signs of secondary effects were observed.
• the amount administered corresponded to about 40 to 50 % of the energy requirements of the rats.
• oil 100 g of oil (soyabean oil, safflower oil, olive oil or some other vegetable or animal oil) were mixed with 2 liters of 0.2 M NaOH and 0.5 liter of hexane while slowly stirring the mixture.
• the hexane fraction was separated, subsequent to ail fat having been saponified.
• the aqueous solution was neutralized with 1 liter of 0.5 M HC1.
• the resultant layer of free fatty acids was separated and washed with water.
• the fatty acids were esterified with ethyl alcohol or some other alkyl alcohol in a manner similar to that described, for instance, by CH. Rogers (A method for manufacturing oenanthylate. J. Amer. Pharmaceut. Assoc. Sci. Ed. Voi 12:503-506, No. 6,
• esters obtained were used to prepare fat emulsion.
• the ingredients used were as follows:
• the ingredients were mixed in a Turmix, Turrax or a simi- lar mixer.
• the resultant "coarse emulsion" was homogenized in an ho ogenizer of the type Moulin-Gaulin microfluidizer or the like.
• the emulsion obtained was sterilized in an autoclave at 120°C for 20 minutes.
• Example 3 Ethyl esters of fatty acids obtained from animal or vege ⁇ table fat were mixed with phospholipids from eggs or soya ⁇ bean oil and glycerol in the following proportions:
• Diazepam was dissolved in ethyl esters of fatty acids obtained from animal or vegetable fat, and an emulsion was prepared from the solution.
• the ingredients were used in the following proportions:
• the emulsion was poured into bottles of desired volume and the emulsion then heat sterilized at 120 * C.
• the diazepam/ethyl-ester emulsion of this example was com- pared with a diazepam/soyabean emulsion with regard to creaming in vitro with plasma and serum derived from seriously ill patients under intensive care.
• the method by which creaming is determined is given in Swedish Patent Application No. 8505047-4 filed 25 October 1985.
• the results obtained are set forth in Tables 1 and 2 below. It will be seen from the results that the creaming activity decreased dramatically (i.e. the creaming time had increa ⁇ sed) when ethyl ester was used as the hydrophobic phase in diazepa -containing emulsions, instead of soy-oil.
• An emulsion was prepared from the following ingredients
• Example 2 Homogenization was effected in the same manner as that described in Example 2. The emulsion was poured into bottles and heat sterilised at 120'C for 20 minutes.
• the mixture was homogenized in the same manner as that described in Example 2 and the emulsion was poured into bottles and then heat sterilized at 120 ° C for 20 minutes.
• the particle size of the emulsion was determined in a con- ventional manner and found to lie between 0.15-0.20 micron
• a photericin 3 is an antifungal antibiotic.
• the substance is soluble in dimethyl aceta ide and dimethylsulfoxide , but very difficult to dissolve in water and common orga- nic solvents.
• An infusion suspension can be prepared with sodium deoxychoiate. This suspension, however, is highly unstable and must therefore be used within ⁇ hours from the time of its preparation. It has now been found that a stable emulsion having the following composition can be prepared when ethyl ester from vegetable oil is used as a solution promotor.
• the emulsion was prepared and sterilized in the same way as that described in Example 2.
• Perfluorodecalin (Flutec PP5 from ISC Chemicals Ltd.) 28 g Ethyl ester of fatty acids from soyabean oil 10 g
• Glycerol 2.5 g Sterile and pyrogen-free water to an amount of 100 ml
• the emulsion was prepared and sterilized in the same manner as that described in Example 2.

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• Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

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Citations (5)

• 1987
  • 1987-12-18 SE SE8705064A patent/SE467861B/sv not_active IP Right Cessation
• 1988
  • 1988-12-13 CA CA000585715A patent/CA1334281C/en not_active Expired - Fee Related
  • 1988-12-14 EP EP89900673A patent/EP0353267B1/en not_active Expired - Lifetime
  • 1988-12-14 JP JP1500461A patent/JP2930242B2/ja not_active Expired - Fee Related
  • 1988-12-14 EP EP88850423A patent/EP0321429A1/en active Pending
  • 1988-12-14 ES ES89900673T patent/ES2059827T3/es not_active Expired - Lifetime
  • 1988-12-14 DE DE89900673T patent/DE3884945T2/de not_active Expired - Fee Related
  • 1988-12-14 AU AU28214/89A patent/AU2821489A/en active Granted
  • 1988-12-14 WO PCT/SE1988/000680 patent/WO1989005638A1/en active IP Right Grant
• 1989
  • 1989-08-16 FI FI893867A patent/FI99080C/fi not_active IP Right Cessation
  • 1989-08-17 DK DK198904052A patent/DK173596B1/da not_active IP Right Cessation
  • 1989-08-17 NO NO893303A patent/NO176745C/no unknown

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