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
• • 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
  • A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
  • A61K9/50—Microcapsules having a gas, liquid or semi-solid filling; Solid microparticles or pellets surrounded by a distinct coating layer, e.g. coated microspheres, coated drug crystals
  • A61K9/51—Nanocapsules; Nanoparticles
  • A61K9/5107—Excipients; Inactive ingredients
  • A61K9/5123—Organic compounds, e.g. fats, sugars
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K48/00—Medicinal preparations containing genetic material which is inserted into cells of the living body to treat genetic diseases; Gene therapy
• • 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
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
  • A61P31/12—Antivirals
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P37/00—Drugs for immunological or allergic disorders
  • A61P37/02—Immunomodulators
  • A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
• • C—CHEMISTRY; METALLURGY
  • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
  • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
  • C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
  • C12N15/09—Recombinant DNA-technology
  • C12N15/87—Introduction of foreign genetic material using processes not otherwise provided for, e.g. co-transformation
  • C12N15/88—Introduction of foreign genetic material using processes not otherwise provided for, e.g. co-transformation using microencapsulation, e.g. using amphiphile liposome vesicle
• • 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
  • A61K9/127—Liposomes
  • A61K9/1271—Non-conventional liposomes, e.g. PEGylated liposomes, liposomes coated with polymers
  • A61K9/1272—Non-conventional liposomes, e.g. PEGylated liposomes, liposomes coated with polymers with substantial amounts of non-phosphatidyl, i.e. non-acylglycerophosphate, surfactants as bilayer-forming substances, e.g. cationic lipids

Definitions

• the present invention relates to oil-in-water lipid emulsions, a complex between the emulsion and genes, and emulsions loaded with hydrophobic or amphiphilic drugs using biocompatible and biodegradable fats and oils.
• the present invention also relates to a method of preparing oil-in-water lipid emulsions, a complex between the emulsion and genes, and emulsions loaded with hydrophobic or amphiphilic drugs using biocompatible and biodegradable fats and oils.
• the present invention also relates to a method of transferring genes efficiently into cells by using said lipid emulsions.
• Figure 1 is a graph showing a correlation between the average droplet size of the lipid emulsion for different oils and the interfacial tension between water and oil;
• Figure 2a is a graph showing a correlation between the average droplet size of the lipid emulsion using different triglycerides and the concentration of DLPC
• Figure 2b is a graph showing a correlation between the changes in the average droplet size of the lipid emulsion using tributyrin and the concentration of DLPC;
• Figure 2c is a graph showing a correlation between the changes in the average droplet size of the lipid emulsion using tricaproin and the concentration of DLPC;
• Figure 2d is a graph showing a correlation between the changes in the average droplet size of the lipid emulsion using tricaprylin and the concentration of DLPC;
• Figure 3a is a graph showing a correlation between the average droplet size l of the lipid emulsion using tributyrin and the concentration of the emulsifiers;
• Figure 3b is a graph showing a correlation between the average droplet size of the lipid emulsion using tricaproin and the concentration of the emulsifiers;
• Figure 3c is a graph showing a correlation between the average droplet size of the lipid emulsion using tricaprylin and the concentration of the emulsifiers;
• Figure 4 is an electrophoresis photograph showing a complex formation between DNA and lipid emulsion of the present invention.
• One microgram of pCMV-beta plasmid and different amounts of lipid emulsion were used to form a complex;
• Lane 1 DNA molecular weight marker;
• Lane 2 1 ⁇ g of pCMV-beta plasmid [7164 base pairs (bp)]; Lane 3: 2 ⁇ l of Lipofectamine and 1 ⁇ g of pCMV-beta plasmid; Lane 4: 4 ⁇ g of DOTAP liposome and 1 ⁇ g of pCMV-beta plasmid; Lanes 5, 6, 7 and 8: 1 ,2,4 and 6 ⁇ g, respectively, of DOTAP/squalene lipid emulsion and 1 ⁇ g of pCMV-beta plasmid;
• Lane 9 4 ⁇ g of DOTAP/soybean oil lipid emulsion and 1 ⁇ g of pCMV-beta plasmid
• Lane 10 4 ⁇ g of DOTAP/linseed oil lipid emulsion and 1 ⁇ g of pCMV-beta plasmid.
• Figure 5 is an electrophoresis photograph of pCMV-beta after the carrier/DNA complexes underwent an exchange reaction with poly-L-aspartic acid;
• Lane 1 DNA molecular weight marker;
• Lane 2 1 ⁇ g of pCMV-beta plasmid [7164 base pairs (bp)];
• Lanes 4-13 carrier/ pCMV-beta complex incubated with 0.625, 1 .25, 2.5, 5.0, 25, 50, 100, 200, 400 and 800 equivalency of poly-L-aspartic acid for an hour.
• Equivalency in the present invention represents the charge ratio between phosphate group of DNA and carboxylic group of PLAA.
• Figure 6 is a transmission electron micrograph of cationic solid lipid nanoparticle, DNA and their complex.
• Figure 7 is a graph showing the effect of a helper lipid DOPE on the transfection efficiency of liposome and emulsion carriers; A) DOTAP/DOPE liposome, B) DOTAP/DOPE squalene lipid emulsion ⁇ : no serum, j 80 % serum.
• Figure 8 is a graph showing the effect of a helper lipid diolein on the transfection efficiency of liposome and emulsion carriers; A) DOTAP/DOPE liposome, B) DOTAP/DOPE squalene iipid emulsion
• Figure 9 is a graph showing the changes in the transfection efficiency of liposome and emulsion carriers by adding a non-ionic surfactant, Tween 80; A) DOTAP/DOPE/Tween 80 liposome, B) DOTAP/DOPE/Tween 80 squalene lipid emulsion
• Figure 10 is a graph showing the stability of the lipid emulsion by adding
• Tween 80 ⁇ DOTAP/DOPE squalene lipid emulsion
• ⁇ DOTAP/DOPE/Tween 80 squalene lipid emulsion.
• Figure 11 is a graph showing the changes in the transfection efficiency using the lipid carriers by adding protamine sulfate
• Figure 12 is a graph showing the transfection efficiency using different lipid gene carriers with various cell-lines
• ⁇ no serum, ⁇ : 80 % serum.
• Figure 13 is a graph showing the difference in in vitro release rates of rifampicin from different lipid emulsions; v : PBS, ⁇ :linseed oil emulsion, ⁇ : soybean oil emulsion, ⁇ : squalene emulsion.
• Figure 14 is a graph showing the difference in in vitro release rates of diclofenac from different lipid emulsions; v : PBS, ⁇ :linseed oil emulsion, ⁇ : soybean oil emulsion, ⁇ squalene emulsion.
• Figure 15 is a graph comparing the in vivo transfection efficiencies when 10 ⁇ g of DNA was administered intravenously by using different lipid gene carriers.
• Figure 16 is a graph comparing the in vivo transfection efficiencies when 50 ⁇ g of DNA was administered intravenously by using different lipid gene carriers.
• Figure 17 is a graph comparing the in vivo transfection efficiencies when DNA was administered intravenously by using different lipid gene carriers: effect of emulsifiers with PEG moiety.
• Figure 18 is a graph comparing the in vivo transfection efficiencies when DNA was administered intravenously by using different lipid gene carriers: effect of protamine sulfate.
• Figure 19 is a graph comparing the in vivo transfection efficiencies when DNA was administered by intranasal instillation by using different lipid gene carriers.
• Figure 20 is a graph showing the difference in the in vitro release rates of diclofenamic acid from different lipid emulsions; v : PBS, ⁇ : linseed oil emulsion, ⁇ : soybean oil emulsion, ⁇ : squalene emulsion.
• Another object of the present invention is to provide a complex between biologically active material and lipid emulsion comprising non-triglyceride oils and a complex between biologically active material and solid lipid nanoparticle comprising a fat selected from the group comprising triglycerides and ethyl stearate, and the preparation method thereof.
• Another object of the present invention is to provide lipid emulsions comprising squalene or squalane loaded with drugs or to provide ethyl stearate solid lipid nanoparticles loaded with drugs and the preparation methods thereof.
• the present invention also concerns the method of transferring genes and drugs efficiently into cells by using the lipid emulsions.
• Liposome and emulsion are the two of the well-known non-viral gene carriers. Gene therapy using liposomes are under clinical trials. There are many reports in the past several years regarding liposome-mediated gene delivery.
• Triglycehde lipid emulsion which has been developed recently, may form a complex that maintains physical stability and delivers genes in the presence of serum. These triglyce de emulsions, however, has a low physical stability and loses the ability to transfer genes without a polymeric lipid such as 1-palmitoyl-2- oleoyl-st7-glycero-3-phosphoethanolamine-N[-poly(ethyleneglycol)2000](PEG 20 ooPE).
• the polymeric lipids that may provide physical stability of emulsions include Span, Tween, and Brij series lipids having polyethylene glycol moiety in the lipid headgroup.
• polymeric lipids may attenuate the interaction between the lipid emulsion and the gene since the polymeric moiety provides a steric hindrance. Therefore, the cationic lipid emulsion containing polymeric lipid could form a complex with DNA when there are 3-4 excess positive charges of emulsions.
• an object of the present invention is to prepare a stable lipid emulsion without or with a minimal amount of polymeric lipid. Accordingly, we have used different oils that are known to be biocompatible with an acceptable toxicity. Among the lipid emulsions when egg phosphatidylcholine (PC) was used as an emulsifier, we have discovered that the oils that have higher interfacial tension against water forms more stable emulsions than those with a lower interfacial tension. We also have discovered that the correlation between emulsion stability and the oil/water (o/w) interfacial tension has not been systemically studied.
• PC egg phosphatidylcholine
• Lipid emulsions are generally prepared by dispersing oil in water by use of an emulsifier. There are many theoretical works on how emulsions can be stabilized.
• oils were selected to form emulsions by using egg PC as an emulsifier.
• the lipid emulsions having 10 %(v/v) of oils and 1.2 %(w/v) of egg PC were obtained by 1 ) preparing a liposome solution by sonicating egg PC in water and 2) adding oil in the liposome solution to sonicate the mixture for 2 min for three times (total 6 min).
• the size of the particles in the emulsion was measured by photon correlation spectroscopy.
• the emulsion made with linseed oil has the biggest emulsion droplet sizes whereas the squalene and jojoba bean oil formed emulsions with the smallest droplet sizes.
• the relationship between the size of the emulsion and the o/w interfacial tension of the oils is shown in Figure 1. The results show that the oil that has bigger o/w interfacial tension forms an emulsion with smaller droplet size.
• the oils are mainly mixtures of triglycerides and esters of fatty acid/alcohols, except squalene.
• emulsions made with squalene or squalane are stable without the use of polymeric lipids.
• the squalene emulsions are used as vaccine adjuvants (US patent 5,376,369).
• Squalene was selected as an oil phase in o/w emulsion since it has a low cytotoxicity and is biodegradable.
• Squalene emulsion was also formulated as a Taxol carrier (US patent 5,407,683).
• this Taxol- loaded squalene emulsion is formulated by forming a self-emulsifying glass by adding surfactant or alcohols and by dispersing it in water. A large amount of ethanol is included in the formulation.
• composition and the preparation method are completely different form those of the present invention.
• squalene emulsions known up to now are 1) vaccine adjuvants to deliver antigens and 2) Taxol-loaded emulsions having different composition and preparation method from the present invention. Therefore, the lipid emulsion of the present invention to deliver genes and lipophilic or amphiphilic drugs differs from the pre-existing squalene emulsion formulas.
• Squalene emulsion shows a far superior stability to the emulsions made by castor, soybean, and safflower or sunflower oil. The release rate of lipophilic drug is slower from more stable emulsions.
• the present invention is also related to the ethyl stearate solid lipid nanoparticles.
• Solid lipid nanoparticles made with ethyl stearate, or more broadly the ethyl esters of fatty acid or alcohols with C10-18 straight chains, have never been used as gene carriers.
• the ethyl stearate solid lipid nanoparticles have not been used as a carrier of a lipophilic or amphiphilic drug.
• the present invention provides the lipid emulsion made of non-triglycerides including squalene or squalane and 1 ) cationic emulsifier and 2) phospholipids and lipid with PEG moiety, and the preparation methods thereof. Also, the present invention provides cationic solid lipid nanoparticles to deliver genes or other biologically active materials and the preparation method thereof.
• the solid lipid nanoparticles of the present invention are suspension of solid fat particles in water. Therefore, it may be freeze-dried to remove water from the system to preserve the fat particles. It has an advantage of preparing drug-loaded solid lipid nanoparticles that can be freeze-dried to increase storage time.
• Cationic solid lipid nanoparticle is composed of t glyceride, having C12-18 straight chain hydrophobic tail, which exists as a solid at room and body temperatures and cationic emulsifier. There are no current reports on the positively charged solid lipid nanoparticle as a gene carrier.
• Lipid emulsions made of triglycerides have been widely used as a drug delivery system. For instance, there are many different emulsion formulations for cyclosporin, an oligopeptide immunosurppresant. Medium chain triglycerides with C8-12 carbons were used to solubilize cyclosporin in o/w emulsions (US patent 5,660,858). Emulsions, made by alcohol, alkanol, polysorbate 80 and cyclosporin with submicron particle sizes, are reported to be stable and have high bioavailability (WO 97/35,603).
• cyclosporin dissolved in medium chain triglycerides was dispersed in water easily by using propylene carbonate as a co-emulsifier with an average droplet size of ca. 100 nm.
• propylene carbonate as a co-emulsifier with an average droplet size of ca. 100 nm.
• cyclosporin formulations there are no reports or patents on the emulsion formulation using squalene or squalane, highly pure branched hydrocarbons.
• solid lipid nanoparticles made of ethyl stearate Squalene, squalane and ethyl stearate are mono-component oil systems. Therefore, unlike vegetable oils made of many components, the physical and chemical properties do not vary.
• Mono-component system provides a better quality control in mass-production.
• squalene emulsion is more stable having smaller average particle sizes than many other vegetable emulsions.
• the in vitro drug release experiment also shows that the release of drugs such as rifampicin is sustained with a zero-order release pattern from the squalene emulsion.
• the squalene and squalane emulsions and the ethyl stearate solid lipid nanoparticle can be used as a carrier of negatively-charged biologically active materials including DNA when cationic emulsifier was used and as a drug delivery system for lipophilic or amphiphilic drugs.
• the cationic emulsion or solid lipid nanoparticle, loaded with lipophilic anticancer drugs can form a complex with a therapeutic gene in cancer therapy.
• the present invention provides a lipid emulsion to deliver genes or other biologically active materials comprising a) 2-30 % of oil of non-triglycerides, b) 0.01-20 % of one or more emulsifiers including a cationic surfactant and c) water to 100 %.
• the lipid emulsion of the present invention can include other additives.
• the emulsifier in the present invention is required to make the surface charge of the emulsion positive and therefore, it is selected from an emulsifier having a positive charge to form a complex with a negatively charged biologically active material including DNA.
• a non-ionic surfactant, phospholipid, fatty acid, fatty alcohol, bile salt or cholesterol may be additionally used as an emulsifier.
• the present invention provides a solid lipid nanoparticle to deliver genes or other biologically active materials comprising a) 2-30 % of triglycerides having 10-18 carbons in each hydrophobic tails or ethyl stearate, b) 0.01-20 % of one or more emulsifiers including a cationic surfactant and c) water to 100 %.
• the lipid emulsion of the present invention can include other additives.
• the emulsifier in the present invention is required to make the surface charge of the emulsion positive and therefore, it is selected from an emulsifier having a positive charge to form a complex with a negatively charged biologically active material including DNA.
• a non-ionic surfactant, phospholipid, fatty acid, fatty alcohol, bile salt or cholesterol may be additionally used as an emulsifier.
• the present invention provides a drug-loaded lipid emulsion to deliver a lipophilic or amphiphilic drug comprising a) 2-30 % non-triglycerides oil such as squalene or squalane, b) 0.01- 20 % of one or more emulsifiers, c) 0.1-10 % lipophilic or amphiphilic drug and d) water to 100 %.
• the drug-containing emulsion of the present invention can include other additives.
• the surface charge of the drug-containing emulsion of the present invention may be positive, zero or negative.
• the present invention provides a drug-loaded solid lipid nanoparticle to deliver a lipophilic or amphiphilic drug comprising a) 2-30 % of ethyl stearate, b) 0.01 -20 % of one or more emulsifiers, c) 0.1-10 % lipophilic or amphiphilic drug and d) water to 100 %.
• the drug- containing solid lipid nanoparticle of the present invention can include other additives.
• the surface charge of the drug-containing solid lipid nanoparticle of the present invention may be positive, zero or negative.
• the present invention is also related to the method of preparing the lipid emulsion to deliver gene or other biologically active materials to cells.
• the preparation method of the lipid emulsion according to the present invention include a) a first step of preparing an aqueous phase by mixing 0.01-20 % of one or more emulsifiers including a cationic emulsifier and b) a second step of preparing emulsion by mixing said aqueous phase with 2-30 % of non-triglycerides oil.
• the present invention is also related to a method of preparing the solid lipid nanoparticle to deliver gene or other biologically active materials to cells.
• the preparation method of the solid lipid nanoparticle according to the present invention include a) a first step of preparing an aqueous phase by mixing 0.01-20 % of one or more emulsifiers including a cationic emulsifier and b) a second step of preparing emulsion by mixing said aqueous phase with 2-30 % of fat of triglycerides having
• the present invention is also related to a method of preparing the lipid emulsion to deliver lipophilic or amphiphilic drugs to cells.
• the preparation method of the drug-loaded lipid emulsion according to the present invention include a) a first step of preparing an aqueous phase by mixing 0.01-20 % of one or more emulsifiers, b) a second step of preparing oil phase by mixing 0.1-10 % of lipophilic or amphiphilic drug and 2-30 % of non-triglycerides oil and b) a third step of preparing drug-loaded emulsion by mixing the aqueous and oil phases prepared in the first and second steps, respectively.
• the present invention is also related to a method of preparing the solid lipid nanoparticle to deliver lipophilic or amphiphilic drugs to cells.
• the preparation method of the drug-loaded solid lipid nanoparticle according to the present invention include a) a first step of preparing an aqueous phase by mixing 0.01 -20 % of one or more emulsifiers, b) a second step of mixing 0.1 -10 % of lipophilic or amphiphilic drug and 2-30 % of fat such as ethyl stearate and b) a third step of preparing drug- loaded solid lipid nanoparticle by mixing the aqueous and oil phases prepared in first and second steps, respectively.
• lipid emulsion or solid lipid nanoparticle by first preparing an oil or fat phase, respectively, comprising oil or fat, respectively, emulsifier and drugs and subsequently by mixing the oil phase with water.
• the present invention is related to the preparation method of the lipid emulsion to deliver biologically active materials including genes to cells.
• the preparation method includes a) a first step of preparing an oil phase by mixing 2-30 % of one or more emulsifier including a cationic emulsifier with 0.1 -20 % of non-triglycerides oil and b) a second step of mixing the oil phase with water.
• the present invention is also related to the preparation method of the solid lipid nanoparticle to deliver biologically active materials including genes to cells.
• the preparation method includes a) a first step of preparing a fat phase by mixing 0.1 -20 % of one or more emulsifier including a cationic emulsifier with 2-30 % fat of triglycerides having 10-18 carbons in each hydrophobic tails and ethyl stearate and b) a second step of mixing the fat phase with water.
• the present invention is related to a method of preparing the drug-loaded lipid emulsion.
• the preparation method includes a) a first step of preparing an oil phase by mixing 0.1 -20 % of one or more emulsifier and 0.1 -10 % of lipophilic or amphiphilic drug with 2-30 % of non-triglycerides oil and b) a second step of mixing the oil phase with water.
• the present invention is also related to a method of preparing the drug-loaded solid lipid nanoparticle.
• the preparation method includes a) a first step of preparing an fat phase by mixing 0.1 -20 % of one or more emulsifier and 0.1 -10 % of lipophilic or amphiphilic drug with 2-30 % fat such as ethyl stearate and b) a second step of mixing the oil phase with water.
• the lipid emulsion according to the present invention represents a heterogeneous mixture of two or more immiscible liquid stabilized by the use of a surfactant or an emulsifier.
• the solid lipid nanoparticle according to the present invention represents a solid-state fat dispersed in a liquid stabilized by the use of a surfactant or an emulsifier.
• the non-triglycerides of the present invention include squalene and squalane.
• the fat in the solid lipid nanoparticle of the present invention includes ethyl ester of alcohol or acid having a straight chain having 10-18 carbons, and preferably ethyl stearate.
• the emulsifier according to the present invention may additionally include phospholipid or non-ionic surfactant.
• the cationic surfactant used as emulsifiers of the present invention include 1 ,2-dimyristoyl-3-trimethylammonium-propane (DMTAP), 1 ,2-dipalmitoyl-3-trimethylammonium-propane (DPTAP), 1 ,2-distearoyl-3- trimethylammonium-propane (DSTAP), 1 ,2-dioleoyl-3-trimethylammonium-propane (DOTAP), 1 ,2-dimyristoyl-3-dimethylammonium-propane (DMDAP), 1 ,2-dipalmitoyl- 3-dimethylammonium-propane (DPDAP), 1 ,2-dilauroyl-3-dimethylammonium- propane (DLDAP), 1 ,2-distearoyl-3-dimethylammonium-propane (DS
• the cationic emulsifiers are required to deliver genes since they may not only interact with negatively charged DNA to form a complex but also enhance the interaction with cells with an excess positive charge.
• the phospholipids according to the present invention include phosphatidylcholine (PC) and derivatives thereof, phosphatidylethanolamine (PE) and derivatives thereof and phosphatidylserine (PS).
• PC phosphatidylcholine
• PE phosphatidylethanolamine
• PS phosphatidylserine
• DOPE L- ⁇ -dioleoyl phosphatidylethanolamie
• a fusogenic lipid including DOPE or diolein may be additionally used as an emulsifier.
• fatty acid, fatty alcohol, cholesterol or bile salt may be additionally used as an emulsifier to increase the physical stability of the lipid emulsion or solid lipid nanoparticle.
• Non-ionic surfactants in the present invention include poloxamers (also known as a pluronic: a copolymer of polyoxyethylene and polyoxypropylene), sorbitan esters (Span), polyoxyethylene-sorbitan fatty acid esters (Tween) and polyoxyethylene ethers (Brij).
• the present invention may comprise hydrophilic polymers, polymeric lipid where the hydrophilic polymers are covalently bonded to a phospholipid or polymerizable lipid such as diacetylated phospholipid.
• hydrophilic polymers examples include polyoxyethylene, polyethyloxazoline and polyethyleneglycol (PEG).
• PEG polyethyleneglycol
• the polymeric lipids enhance the steric stability of the emulsion, and also PEG with a small molecular weight is a well-known fusogenic agent.
• compositions of the present invention may also comprise an osmotic pressure regulator such as glycerol.
• the present invention may also comprise low-molecular weight polyethylene glycol (average molecular weight in the range of 500-1000) and fusogenic peptide, such as HA gp 41 , to improve the transfection efficiency.
• low-molecular weight polyethylene glycol average molecular weight in the range of 500-1000
• fusogenic peptide such as HA gp 41
• the present invention may also comprise materials such as glycolipid, lipopeptide, antibody, and ligand for receptors, viral protein to target specific cells or organs.
• the present invention may also comprise polycations such as protamine sulfate, histone and polylysine to condense DNA.
• the present invention may comprise mono- or poly-anions to alter the interaction between lipid carrier and DNA.
• the biologically active material which can be used in the present invention include DNA, ribonucleic acid (RNA), antisense nucleic acid, ribosome, polynucleotide, oligonuclotide, or other pharmaceutical drugs.
• RNA ribonucleic acid
• antisense nucleic acid ribosome
• polynucleotide oligonuclotide
• other pharmaceutical drugs include DNA, ribonucleic acid (RNA), antisense nucleic acid, ribosome, polynucleotide, oligonuclotide, or other pharmaceutical drugs.
• a carrier In the case the biologically active material to be deliver is a nucleic acid such as DNA, a carrier must have a positive charge to form a complex with the nucleic acid and also must be within the appropriate size range.
• the positively charged lipid emulsion or solid lipid nanoparticle of the present invention may be loaded with lipophilic or amphiphilic drugs.
• the lipid emulsion or solid lipid nanoparticle of the present invention may additionally include a hydrophilic drug in the aqueous phase.
• the lipid emulsion of the present invention is physically stable and has high transfection efficiency in the presence of serum.
• the lipid emulsion that can deliver biologically active materials such as DNA is prepared by mixing a) 2-30 % of non- triglycerides oil and b) an aqueous phase comprising 0.01 -20 % of one or more emulsifiers including a cationic surfactant and additionally 0.01 -10% of hydrophilic polymer or phospholipid having a hydrophilic polymeric moiety.
• the solid lipid nanoparticle that can deliver biologically active materials such as DNA according to the present invention is prepared by mixing a) 2-30 % of triglycerides having 10 -18 carbons in the hydrophobic tail or ethyl stearate which is heated above its melting temperature and b) a heated aqueous phase comprising
• emulsifiers including a cationic surfactant and additionally
• hydrophilic polymer or phospholipid having a hydrophilic polymeric moiety Upon mixing, the temperature of the aqueous and oil phases must be maintained above the melting temperature of the oil phase.
• the present invention also provides a method of preparing drug-loaded lipid emulsion for the in vivo delivery of lipophilic or amphiphilic drugs.
• the drug loaded lipid emulsion of the present invention is prepared by mixing a) an oil phase comprising 2-30 % of non-triglycerides oil and 0.1 -10 % of lipophilic or amphiphilic drug and b) an aqueous phase comprising 0.01 -20 % of one or more emulsifiers and additionally 0.01 -10% of hydrophilic polymer or phospholipid having a hydrophilic polymeric moiety.
• the present invention also provides a method of preparing drug-loaded solid lipid nanoparticle for the in vivo delivery of lipophilic or amphiphilic drugs.
• the drug loaded solid lipid nanoparticle of the present invention prepared by mixing a) an oil phase comprising 2-30 % of triglycerides oil having 10-18 carbons in the hydrophobic tail or ethyl stearate which is heated above its melting temperature and 0.1 -10 % of lipophilic or amphiphilic drug and b) an aqueous phase comprising
• the lipid emulsion that can deliver biologically active materials such as DNA is prepared by mixing a) an oil phase composed of 2-30 % of non-triglycerides oil and 0.01-20 % of one or more emulsifiers including a cationic surfactant and b) an aqueous phase comprising 0.01-10% of hydrophilic polymer or phospholipid having a hydrophilic polymeric moiety.
• the solid lipid nanoparticle that can deliver biologically active materials such as DNA is prepared by mixing a) an oil phase comprising 2-30 % of fat of triglycerides having 10-18 carbons in the hydrophobic tail or ethyl stearate which is heated above its melting temperature, and 0.01-20 % of one or more emulsifiers including a cationic surfactant and b) a heated aqueous phase comprising 0.01-10% of hydrophilic polymer or phospholipid having a hydrophilic polymeric moiety.
• the temperature of the aqueous and oil phases must be maintained above the melting temperature of the oil phase.
• the present invention also provides a method of preparing drug-loaded lipid emulsion for the in vivo delivery of lipophilic or amphiphilic drugs.
• the drug loaded lipid emulsion of the present invention is prepared by mixing a) an oil phase comprising 2-30 % of non-triglycerides oil, 0.01-20 % of one or more emulsifiers and 0.1-10 % of lipophilic or amphiphilic drug and b) an aqueous phase comprising 0.01-10% of hydrophilic polymer or phospholipid having a hydrophilic polymeric moiety.
• the present invention also provides a method of preparing drug-loaded solid lipid nanoparticle for the in vivo delivery of lipophilic or amphiphilic drugs.
• the drug loaded solid lipid nanoparticle of the present invention is prepared by mixing a) an oil phase comprising 2-30 % of triglycerides oil having 10-18 carbons in the hydrophobic tail or ethyl stearate which is heated above its melting temperature, 0.01-20 % of one or more emulsifiers and 0.1-10 % of lipophilic or amphiphilic drug and b) an aqueous phase comprising 0.01-10% of hydrophilic polymer or phospholipid having a hydrophilic polymeric moiety.
• the temperature of the aqueous and oil phases must be maintained above the melting temperature of the oil phase.
• the aqueous phase is prepared by preparing liposome according to the method well known in the field.
• the aqueous and oil phases are mixed by using the method well known in the field.
• the prepared aqueous and oil phases are heated to solubilize the components and mixed by using tools such as a homogenizer, sonicator or microfluidizer.
• the present invention also is related to a method of transferring biologically active materials such as DNA into cells by using lipid emulsions made of non- triglycehde and solid lipid nanoparticles made of saturated triglycerides or ethyl stearate.
• the present invention also relates to a method of in vivo delivery of lipophilic or amphiphilic drugs by using lipid emulsions made of non-triglyceride and solid lipid nanoparticles made of saturated triglycerides or ethyl stearate.
• the lipid emulsion and solid lipid nanoparticle according to the present invention deliver the biologically active materials into cells wherein the cell is selected from the group consisting of white blood cells, fibroblasts, cancer cells, cells infected with virus, epithelial cells, endothelial cells, muscle cells, liver cells, endocrine cells, neural cells, dermal cells, germ cells, oocytes, sperms, hematopoietic cells, fetal cells, M cells, Langerhans islet cells, macrophages, plant cells, animal cells, and immortalized cell lines.
• the cell is selected from the group consisting of white blood cells, fibroblasts, cancer cells, cells infected with virus, epithelial cells, endothelial cells, muscle cells, liver cells, endocrine cells, neural cells, dermal cells, germ cells, oocytes, sperms, hematopoietic cells, fetal cells, M cells, Langerhans islet cells, macrophages, plant cells,
• the method of delivering the biologically materials into the target cells according to the present invention is to form a complex between the lipid emulsion or solid lipid nanoparticle with biologically active material.
• the lipid emulsion of the present invention can be administered intravenously, intramuscularly, intranasally, intratracheally, subcutaneously, parenterally, by a topical administration, or direct administration to a specific organ.
• the lipophilic and/or amphiphilic drug that may be loaded in the lipid emulsion or the solid lipid nanoparticle includes antivirals, steroidal anti-inflammatory drugs
• SAID non-steroidal anti-inflammatory drugs
• NSAID non-steroidal anti-inflammatory drugs
• antibiotics antibiotics
• antifungals vitamins, hormones, retinoic acid, prostaglandins, prostacyclins, anticancer drugs, antimetabolitic drugs, miotics, cholinergics, adrenergic antagonists, anticonvulsants, antianxiety agents, major tranquilizers, antidepressants, anesthetics, analgesics, anabolic steroids, estrogens, progesterones, glycosaminoglycans, polynucieotides, immunosuppressants and immunostimulants.
• Example 1 Preparation of lipid emulsion using egg phosphatidylcholine as an emulsifier
• eggPC egg phosphatidylcholine
• water water at a concentration of 12 mg/ml
• probe type sonicator High intensity ultrasonic processor, 600- Watt
• Lipid emulsions were prepared with 10 %(v/v) different oils as listed in and the liposome solution by sonication for 2 minutes for 3 times (6 minutes total).
• the size of the emulsion particles were measured by using Malvern Zetasizer(Malvem Instruments Limited, England) after diluting the emulsion by 300 times in deionized distilled water.
• the size of the emulsiion particles one day and 20 days after preparation is presented in Table 1 to show the size change of the emulsion droplets with time.
• the values represent an average from 3 measurements with a single sample.
• squalene a non-triglyceride lipid forms more stable emulsion with a smaller average droplet size than other emulsions listed.
• the emulsions so prepared were stored at 4 °C until further experiments.
• Lipid emulsions were prepared using various oils (10 %(v/v)) and DOTAP as an emulsifier DOTAP was mixed with water at a concentration of 24 mg/ml to solubihze the lipids at 37 °C
• the lipid solution was sonicated by using a probe type sonicator for 2 minutes to form a liposome solution
• Various oils (10 %(v/v)) were added to the liposome solutions and sonicated for 2 minutes 3 times (total 6 minutes) to form lipid emulsions
• the lipid emulsion made of oils having higher o/w interfacial tension has a smaller average droplet sizes than those made of oils having lower o/w interfacial tension
• the emulsion particle sizes were below 200 nm with an exception of lin
• Example 3 Stability of lipid emulsions made of various oils in the presence of serum.
• the stability of the DOTAP liposomes and emulsions were compared by measuring the emulsion particle sizes in the presence of serum. The result of the measurements was listed in Table 3. Even with 0.5 % of serum, the sizes of the liposomes increased by 2.7 times. In the case of lipid emulsions, there are no apparent changes in the sizes in the presence of serum.
• One of the problems in delivering genes using liposomes was the formation of large insoluble aggregates that can attenuate the transfection efficiency.
• the lipid emulsions of the present invention overcame such a problem by maintaining the small size with narrow size distribution in the presence of serum.
• Lipid emulsions were prepared using various oils (10 %(v/v)) and DOTAP as an emulsifier.
• DOTAP was mixed with water at a concentration of 24 mg/ml to solubilize the lipids at 37 °C.
• the lipid solution was sonicated by using a probe type sonicator for 2 minutes to form a liposome solution.
• Trilaurin or ethyl stearate according to Table 1 were heated to 50 °C.
• Melted oils (10 %(v/v)) were added to the liposome solutions and sonicated for 2 minutes for 3 times (total 6 minutes) to form lipid emulsions at 50 °C.
• the lipid emulsion was slowly cooled at room temperature to solidify melted oils and as a resultant to form solid lipid nanoparticles.
• COS-1 cells (kidney, SV40 transformed, African green monkey) were grown in 5 % CO 2 incubator in DMEM supplemented with 10 % fetal bovine serum (FBS), 100 units/ml penicillin, and 100 ⁇ g/ml streptomycin.
• FBS fetal bovine serum
• a plasmid pCMV-CAT encoding a chloramphenicol acetyl transferase driven by a human cytomegalovirus immediate-early promoter was purchased from
• the plasmids were amplified in a E. coli DH5- ⁇ strain and purified by using a Quiagen mega-kit (Quiagen Inc., Chatsworth, CA) according to the manufacturer's instruction. DNA purity was determined by agarose gel electrophoresis and by measuring optical density. DNA having O.D. 26( O.D. 28 o ⁇ 1 -8 were used in this study.
• Example 6 Complex formation between cationic lipid emulsion and DNA The complex formation between DNA and the lipid emulsion prepared in Example 2 was observed by using a gel electrophoresis technique. Lipofectamine and DOTAP liposomes were used as controls. DNA (1 ⁇ g) was mixed with appropriate amounts of lipid carriers in a test tube, and the complexes were incubated for 30 minutes at room temperature. The complexes were loaded on a 1 % agarous gel containing ethidium bromide and electrophoresed in Tris-acetate-EDTA buffer solution at pH 8.0. The gel was visualized under a UV light as shown in Figure 4.
• DNA complexes were formed with the Lipofectamine, DOTAP liposomes and cationic lipid emulsions as in example 6. Different concentrations of poly-L-aspartic acid (PLAA) were added to the complex. Since PLAA is an anionic polymer, it can dissociate the anionic DNA from the complex. Therefore, the dissociation of DNA from the complex in the presence of PLAA is an indicator of the strength of the complex. DNA was dissociated from the Lipofectamine/DNA and DOTAP liposome/DNA complexes at or above the equivalency between PLAA/DNA of 1.25. On the other hand, the BRC 001 -DNA complex remained stable in at the equivalence of 640.
• PLAA poly-L-aspartic acid
• the lipid emulsion/DNA complex is stronger than liposome/DNA complexes in the presence of an anionic competitor. Therefore, it is expected that the emulsion carrier can exhibit superior transfection efficiency in the presence of biological barriers including serum or mucus layer.
• Example 8 Gene transfection efficiency in COS-1 cell line by cationic lipid emulsions
• COS-1 cells were seeded at 1 x 10 4 cells in a 96-well plate ca. 12 hours prior to transfection.
• pCMV-beta plasmid DNA (0.5 ⁇ g) were mixed with DOTAP liposome and lipid emulsions as example 2 at amounts to contain 2 ⁇ g of DOTAP.
• the mixtures were diluted in 2 ⁇ l of serum free DMEM medium. The mixtures were completely shaken 10 times by inversion during 30 min incubation period. After cleaning the COS-1 cells with serum free RPMI 1640, 160 ⁇ l serum free media and carrier-DNA mixture were added to cells.
• the cells were washed with serum free DMEM to remove the remaining carrier-DNA complex in the solution.
• the cells were incubated in DMEM containing 10% serum for 24 hours.
• the transfected cells were harvested after the incubation.
• Cells were washed with 200 ⁇ l PBS, harvested with 50 ⁇ l of lysis solution (0.1 % Triton X-100, 250 mM Tris, pH8.0), and lysed by means of a freeze-thaw cycle.
• 50 ⁇ l of PBS contained 0.5 % of bovine serum albumin.
• the substrate solution 150 ⁇ l of 1mg/ml chloramphenicol red galactopyranoside was added at room temperature for an hour for enzymatic reaction.
• a recombinant ⁇ -galactosidase was used as a standard.
• the transfection efficiency is expressed as the relative ⁇ -galactosidase activity as shown in Table 5.
• carrier-DNA complexes were prepared in DMEM without serum. The cells were washed with DMEM without serum. Transfection was performed in the presence of 80 % serum (in 160 ⁇ l of DMEM) according to the method in Example 8. The transfection efficiency in the presence of 80 % serum is listed in Table 5.
• Live cells is quantified by using a 3-(4,5-dimethylthiazol-2-yl)-
• TMTT 2,5-diphenyl- tetrazolium bromide
• the COS1 cells were harvested from exponential phase culture by trypsinization, counted and plated in 96-well microplates. A concentration of 1 x 10" cells/well was found suitable. Plates were incubated at 37°C for 1 day under a humidified atmosphere. The lipid emulsions were diluted in growth medium to a final volume of 200 ⁇ l and added to the cells and incubated for 24 hours. After exposure with a lipid emulsion, the cells were washed twice with PBS. MTT was dissolved in PBS, filter-sterilized and stored at 4°C until further experiment.
• the transfection efficiency is lower for the lipid emulsions than for the liposomes without serum.
• the transfection efficiency of the liposome decreased by 18.2 times upon adding serum.
• the transfection efficiency of the lipid emulsion decreased on by 1.6-2.7 times upon adding serum.
• the transfection efficiency of the squalene emulsion was better than other emulsion carriers with or without serum.
• the squalene emulsion has a superior physical stability with or without serum. This physical stability may provide an ability to deliver genes to cells in the presence of many destabilizing factors as in vivo applications.
• the cytotoxicity of the emulsions was lower than liposomes.
• the squalene emulsion had a lowest cytotoxicity having more than 89 % of cell proliferation rate.
• Example 11 Complex formation between cationic solid lipid nanoparticle and DNA
• the cationic solid lipid nanoparticle made of trilaurin in Example 4 and DNA were mixed at different ratios in a buffer solution and negatively stained with 1 % uranyl acetate to observe the complex under transmission electron microscope at a magnification ratio of 50,000.
• Figure 6A is pure DNA.
• Figures 6C and 6D represents the solid lipid nanoparticle/DNA complexes.
• Example 12. Transfection with cationic solid lipid nanoparticle
• Cationic solid lipid nanoparticle prepared with trilaurin was used for the in vitro transfection.
• the ⁇ -galactosidase activity was 0.24 ⁇ 0.07 and 0.11 ⁇ 0.02 mU/well without or with 80 % serum, respectively.
• the cell proliferation rate was 82.6 ⁇ 15.6 % indicating low cytotoxicity of the solid lipid nanoparticles.
• the results indicate that the solid lipid nanoparticles can be used as a gene carrier.
• Example 13 Increase in the transfection efficiency by adding DOPE as a helper lipid to the cationic lipid emulsion.
• Squalene emulsions were prepared by using an additional emulsifier, DOPE to increase transfection efficiency.
• the helper lipid, DOPE has a fusogenicity at room temperature and is known to disturb endosomal membrane to increase the transfection efficiency.
• the liposome and squalene emulsion were prepared as in Example 2, except the emulsifier was 24 mg/ml DOTAP/DOPE mixtures instead of pure DOTAP.
• the weight ratio between DOTAP and DOPE were 1 1 :1 , 7:1 , 5:1 , 3:1 , 5:3, 1 :1 , 1 :3 and 1 :5.
• Transfection was performed by following the method in Example 8. Also, the serum effect was studied using the method in Example 9. The results are illustrated in Figure 7.
• the transfection efficiency was maximum at DOTAP/DOPE ratio of 5: 1 for liposome and lipid emulsion. At a higher DOPE concentration, the transfection efficiency decreases probably due to the instability of the lipid carriers and the complexes resulted by the addition of the DOPE.
• Example 14 Increase in the transfection efficiency by adding diolein as a helper lipid to the cationic lipid emulsion.
• Squalene emulsions were prepared by using an additional emulsifier, diolein, to increase transfection efficiency.
• the present inventors have tested the possibility of using diolein, which has not been used as a helper lipid, to increase the transfection activity.
• the liposome and squalene emulsion were prepared as in Example 2, except the emulsifier was DOTAP/diolein mixture (9:1 by weight) instead of pure DOTAP. Transfection was performed by following the method in Example 8. Also, the serum effect was studied using the method in Example 9. The results are illustrated in Table 6. The transfection efficiency was increased by adding diolein for liposome and lipid emulsion. Interestingly, cytotoxicity of the liposome decreased upon adding diolein.
• diolein activates protein kinase C which regulates cell function. Therefore, unlike DOPE, diolein may be a better helper lipid that increases the transfection efficiency with a lowered cytotoxicity.
• Example 15 Increase in the transfection efficiency by adding DOPE and diolein simultaneously as helper lipids to the cationic lipid emulsion.
• DOPE and diolein in Examples 13 and 14, respectively were used as helper lipids to DOTAP in squalene emulsions in transfection.
• the weight ratio between DOTAP and DOPE was set at 5:1 and the amount of diolein was changed.
• the squalene emulsion was prepared as in Example 2, except the emulsifiers were
• DOTAP DOTAP
• DOPE DOPE
• diolein mixtures instead of pure DOTAP.
• the weight ratio between (DOTAP+DOPE) and diolein were 1 :0, 7:1 , 5:1 , 3:1 , 1 :1 and 1 :3.
• the transfection efficiency was maximum at (DOTAP+DOPE)/DOPE ratio of
• DOPE and diolein may have provided fusogenicity and diolein may have acted as a protein kinase C activator. Transfection activity, however, decreased at higher concentrations indicating that diolein changes the stability of emulsion/DNA complex.
• Example 16 Transfection efficiency and cytotoxicity by adding an emulsifier with polyethylene glycol moiety.
• Emulsifier with polyethylene glycol (PEG) moiety may increase the stability of emulsions by providing a steric hindrance. Also, low molecular weight PEG unit may also provide a fusogenicity. Therefore, different PEG-lipids were used as a co-emulsifier to form emulsions. Squalene emulsions were prepared by using 24 mg/ml DOTAP/DOPE (5:1 by weight) and different polymeric emulsifiers.
• the transfection efficiency in the presence of 80 % serum decreased significantly by adding polymeric lipids.
• the transfection efficiency with 80 % serum was at least 50 % of that without serum when lipid emulsions were used as gene carriers.
• the transfection efficiency increased for liposome and emulsion upon adding Tween 80.
• other polymeric lipids lowered the transfection efficiency due to the steric hindrance of the polymeric moiety.
• larger amounts of the carrier were needed for the interaction between cationic lipid and DNA with an increased cytotoxicity. Therefore, Tween 80 was the lipid of choice that provides emulsion stability without hindering the interaction between emulsion and DNA.
• Example 17 Increase in the transfection efficiency by adding Tween 80 Squalene emulsions were prepared by using 24 mg/ml DOTAP/DOPE (5 1 by weight) and different polymeric Tween 80 The amount of Tween 80 was 0, 5, 10, 15 and 20 %(w/w) in addition to DOTAP/DOPE Transfection and was performed by following the method in Example 8 The results are shown in Figure 9 The transfection efficiency increased as the amount of Tween 80 increased up to 10 % At higher than 10 % of Tween 80, however, the efficiency decreased probably due to an increase of the steric hindrance of the polyethylene glycol moiety
• Example 18 Increase in the emulsion stability by adding Tween 80
• Example 19 Preparation methods Lipid emulsion having 10 %(w/w) Tween 80 of Example 17 was prepared by two different preparation methods; microfluidization and sonication. Size and transfection efficiency were compared. Preparation method of the sonicated emulsion was same as Example 2. The method using microfluidization was as follows. Oil and aqueous phases were heated to 70 °C to solubilize the components completely before mixing the two phases. The emulsion was prepared by mixing the two solutions with a high-speed homogenizer (T-25-Ultra-Turrax, S25-18G, IKA Werke, Janke & Kunkel GmbH & Co KG, Germany) at 8000 rpm for 10 min.
• a high-speed homogenizer T-25-Ultra-Turrax, S25-18G, IKA Werke, Janke & Kunkel GmbH & Co KG, Germany
• the mixture was passed 10 times through a Microfluidizer (Microfluidics Co., Newton, MA) with an exit air pressure of 80 psi.
• the emulsion so prepared was stored at 4 °C until further use.
• the size of the emulsion particles was measured by using Malvern Zetasizer after diluting the emulsion by 300 times in water as in Example 1. Transfection was performed as in Example 8. The results are listed in Table 8. Table 8. Characteristics of lipid emulsions made by different preparation methods.
• Example 20 Effect of pre-treatment with protamine sulfate on the size of the complex
• Protamine sulfate is a polycationic protein and forms a protamine sulfate/DNA complex by interacting with and condensing anionic DNA. Also protamine sulfate has a nucleus targetting moiety that can promote a transfer of the complex to nucleus to increase the transfection activity.
• protamine sulfate was mixed with DNA before adding an emulsion solution.
• Protamine sulfate at amounts of 0.5, 1.0 and 1.5 ⁇ g/well, were added to DNA 15 min before adding the emulsion.
• the size of the emulsion particles was measured by using Malvern Zetasizer after diluting the emulsion by 300 times in water as in Example 1. Table 9 shows that the size of the complex does not increase by adding protamine sulfate. Addition of protamine sulfate may lower the amount of cationic lipid emulsion and as a result may lower the emulsion related cytotoxicity.
• Example 21 Increase in transfection efficiency by adding protamine sulfate.
• Emulsion/DNA complex was made after pre-treatment with protamine sulfate as in Example 20, and transfection was performed as in Example 8. Transfection efficiency in the presence of serum was also determined by following the method in Example 9. The results are shown in Figure 11. Transfection efficiency by using emulsion or protamine sulfate alone was 7-10 times lower than that by using emulsion/DNA complex pre-treated with DNA. The highest transfection efficiency was obtained with 1.0 ⁇ g protamine sulfate.
• Example 22 Transfection efficiency in different cell lines Lipid emulsion containing DOTAP/DOPE/Tween80 as in Example 19 was used as a transfection reagent in different cell lines using the method in Example 8 except that CV-1 or NIH3T3 cell lines was used instead of COS-1.
• Figure 12 shows that the lipid emulsion may be used as gene carriers for these cell lines.
• Oil phase comprising 1g of oils in Table 10, 100 mg egg PC and 80 mg
• PEG 2000 PE were heated to 55 °C to solubilize the components completely.
• Rifampicin (10 mg) was added to the oil phase.
• the emulsion was prepared by adding 10 ml PBS and by sonicating for 2 min.
• the size of the emulsion particles was measured by using Malvern Zetasizer after diluting the emulsion by 300 times in water as in Example 1 (Table 10)
• Example 24 In vitro release of rifampicin from lipid emulsions
• Example 23 Three miliiiters of emulsions prepared in Example 23 were put in dialysis bags, each end tightened by closures. The emulsion-filled bags were sunk in 10 ml PBS contained in 50 ml conical tubes. The conical tubes were put in shaking water bath at 37 °C. As a comparative example, release rate of rifampicin in PBS was compared. Concentration of rifampicin was measured by fluorescence spectroscopy.
• the release rate was slowest from squalene emulsion by showing 0 th order release pattern. Release rate was fastest for the rifampicin solution followed by linseed oil emulsion and by soybean oil emulsion.
• Example 25 Preparation of lipid emulsion loaded with diclofenac sodium
• Emulsions were prepared as in Example 23 except that 3 mg diclofenac sodium was loaded instead of rifampicin.
• the size of the emulsion particles was measured by using Malvern Zetasizer after diluting the emulsion by 300 times in water as in Example 1 Table 11.
• Example 26 In vitro release of diclofenac sodium from lipid emulsions In vitro release of diclofenac sodium from the emulsions prepared in Example
• Example 25 was performed by following the method in Example 26.
• release rate of diclofenac sodium in PBS was compared. Concentration of diclofenac sodium was measured by HPLC. Release of diclofenac was faster than that of rifampicin since diclofenac was more hydrophilic. As shown in Figure 14, the release rate was slowest from squalene emulsion than other emulsions. However, the difference in the release rate is much less pronounced than in case of rifampicin release. Also, release of diclofenac solution was the fastest of all.
• Example 27 Estimation of lethal dose
• Squalene emulsion prepared in Exmaple 2 was used to estimate the lethal dose. 200 micoliters of emulsions diluted by 1/2, 1/4, 1/8 and 1/16 were injected intravenously to Balb/C mice (groups of 6 mice) to observe the survival rate after 24 hours. The results are shown in Table 12. The dose where half of the mice in the group die (LD 50 ) is approximately 1.6 g DOTAP/kg.
• Example 28 Systemic gene delivery by intraveous administration of emulsion/DNA complex (In vivo experiment)
• Emulsion/DNA complexes as well as liposome/DNA complexes were delivered systemically by intravenous administration.
• Complexes between 1.7 ⁇ l lipid emulsions prepared in Example 2 and10 ⁇ g pCMV-luc + were injected intravenously through the tail vein of 30 g Balb/C mouse.
• liposome/DNA complex and naked DNA were also administered.
• the mice were sacrificed 22 hours after the injection to analyze the expression of luciferase in each organ.
• Heart, liver, lung, kidney and spleen were obtained for analysis. Expression of luciferase was measured by following the protocols provided by Promega. Briefly, each organ was homogenized after adding 4 ⁇ l of lysis buffer per 1 mg tissue.
• Example 29 Systemic gene delivery by intraveous administration of emulsion/DNA complex (In vivo experiment)
• Example 28 In vivo experiments were performed as in Example 28 except that complexes having 10.5 ⁇ l lipid emulsions and 50 ⁇ g DNA was used. For comparison, liposome/DNA complexes and naked DNA were also administered. The mice were sacrificed 22 hours after the injection to analyze the expression of luciferase in each organ. Heart, liver, lung, kidney and spleen were obtained for analysis. As shown in Figure 16, the expression rate in each organ, especially in the lung, was pronounced with squalene emulsion as a gene carrier.
• Example 30 Systemic gene delivery by intraveous administration of emulsion/DNA : Effect of emulsifiers with PEG moiety
• Example 28 In vivo experiments were performed by following the method in Example 28. DNA (10 ⁇ g) was complexed with lipid emulsions prepared as in Example 18. Amount of emulsions in the complexes was controlled to show maximum transfection efficiency in vitro in Example 18. For comparison, lipsomes having same lipid composition was complexed with DNA for the intraveous injection. The mice were sacrificed 22 hours after the injection to analyze the expression of luciferase in each organ. Heart, liver, lung, kidney and spleen were obtained for analysis. When DOTAP/DOPE and DOTAP/DOPE/Tween 80 were used as emulsifier systems, emulsions showed higher transfection efficiency than the liposomes used. The DOTAP/DOPE/Tween 80 emulsion, had a high in vivo transfeciton efficiency especially in the lung.
• Example 31 Systemic gene delivery by intraveous administration of emulsion/DNA : Effect of emulsifiers with PEG moiety
• Example 28 In vivo experiments were performed by following the method in Example 28. DNA (pCMV-luc+, 10 ⁇ g) was complexed with 30 ⁇ g of protamine sulfate and incubated for 15 min at room temperature. Appropriate amount of lipid emulsion prepared as in Example 18 was added by following the method in Example 21 to form a complex. Amount of emulsions in the complex was controlled to show maximum transfection efficiency in vitro in Example 18. For comparison, lipsomes having same lipid composition was complexed with DNA for the intraveous injection. The mice were sacrificed 22 hours after the injection to analyze the expression of luciferase in each organ. Heart, liver, lung, kidney and spleen were obtained for analysis.
• DOTAP/DOPE and DOTAP/DOPE/Tween 80 were used as emulsifier systems, emulsions showed higher transfection efficiency than the liposomes used.
• the DOTAP/DOPE/Tween 80 emulsion had a high in vivo transfeciton efficiency especially in the lung.
• Example 32 Gene delivery by nasal instillation of emulsion/DNA
• Emulsion/DNA complexes in Examples 2, 13 and 16 were administered by nasal administration.
• Complex between DNA (pCMV-luc+, 20 ⁇ g) and emulsion was administered to Balb/c Mice (30 g).
• lipsome/DNA complex as well as naked DNA were administered.
• the mice were sacrificed 20 hours after the injection to analyze the expression of luciferase in the nasal cavity and lung. Expression of luciferase was measured by following the protocols provided by Promega. As shown in Figure 19, squalene emulsions showed prominently higher luciferase expression rate than liposome or naked DNA.
• squalene emulsion made with DOTAP/DOPE had higher luciferase expression in nasal cavity whereas DOTAP/DOPE/Tween 80 was more efficient in the lung.
• Emulsions were prepared as in Example 23 except that 3 mg diclofenamic acid was loaded instead of rifampicin.
• the size of the emulsion particles was measured by using Malvern Zetasizer after diluting the emulsion by 300 times in water as in Example 1. Table 13
• Example 34 In vitro release of diclofenac sodium from lipid emulsions
• Example 32 In vitro release of diclofenac sodium from the emulsions prepared in Example 32 was performed by following the method in Example 24. As a comparative example, release rate of diclofenac sodium in PBS was compared. Concentration of diclofenac sodium was measured by HPLC.
• Diclofenamic acid are more hydrophobic than its salt form. As shown in Figure 20, the release rate was slowest from squalene emulsion than other emulsions.
• Example 35 Preparation of solid lipid nanoparticles loaded with cyclosporin
• Oil phase comprising 1 g of ethyl stearate, 100 mg egg PC and 80 mg PEG 2000 PE was heated to 55 °C to solubilize the components completely.
• Cyclosporin (20 mg) was added to the oil phase at 55 °C.
• the solid lipid nanoparticles were prepared by adding 10 ml PBS and by sonicating for 2 min. The size of the emulsion particles was measured by using Malvern Zetasizer after diluting the emulsion by 300 times in water as in Example 1 (Table 10). Also, emulsions were prepared as in Example 23 except that 20 mg cyclosporin was loaded instead of rifampicin.
• Example 36 Freeze-drying of solid lipid nanoparticles loaded with cyclosporin
• the solid lipid nanoparticles loaded with cyclosporin were freeze dried for convenient storage.
• Solid lipid nanoparticles resuspended in water had an average particle size of ca. 500 nm.

Landscapes

• Health & Medical Sciences (AREA)
• Life Sciences & Earth Sciences (AREA)
• Chemical & Material Sciences (AREA)
• Engineering & Computer Science (AREA)
• General Health & Medical Sciences (AREA)
• Medicinal Chemistry (AREA)
• Pharmacology & Pharmacy (AREA)
• Animal Behavior & Ethology (AREA)
• Bioinformatics & Cheminformatics (AREA)
• Public Health (AREA)
• Veterinary Medicine (AREA)
• Genetics & Genomics (AREA)
• Epidemiology (AREA)
• Organic Chemistry (AREA)
• Molecular Biology (AREA)
• Biotechnology (AREA)
• Biomedical Technology (AREA)
• Immunology (AREA)
• Physics & Mathematics (AREA)
• Zoology (AREA)
• Biophysics (AREA)
• General Chemical & Material Sciences (AREA)
• General Engineering & Computer Science (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
• Dispersion Chemistry (AREA)
• Wood Science & Technology (AREA)
• Plant Pathology (AREA)
• Biochemistry (AREA)
• Microbiology (AREA)
• Transplantation (AREA)
• Virology (AREA)
• Communicable Diseases (AREA)
• Oncology (AREA)
• Nanotechnology (AREA)
• Optics & Photonics (AREA)
• Medicinal Preparation (AREA)
• Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
• Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Priority Applications (3)

Applications Claiming Priority (2)

Publications (1)

Family

ID=19546046

Family Applications (1)

Country Status (5)

Cited By (38)

Families Citing this family (4)

Citations (5)

• 1999
  • 1999-07-30 JP JP2000561977A patent/JP2002521423A/ja not_active Withdrawn
  • 1999-07-30 WO PCT/KR1999/000414 patent/WO2000006120A1/en active Application Filing
  • 1999-07-30 AU AU50689/99A patent/AU5068999A/en not_active Abandoned
  • 1999-07-30 EP EP99935145A patent/EP1100464A1/en not_active Withdrawn
• 2002
  • 2002-01-30 KR KR10-2002-0005448A patent/KR100374482B1/ko not_active IP Right Cessation

Patent Citations (5)

Non-Patent Citations (2)

Also Published As

Similar Documents

Legal Events