Classifications

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  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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  • 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
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  • A61K31/16—Amides, e.g. hydroxamic acids
  • A61K31/165—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
  • A61K31/167—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide having the nitrogen of a carboxamide group directly attached to the aromatic ring, e.g. lidocaine, paracetamol
• • A—HUMAN NECESSITIES
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  • A61K31/00—Medicinal preparations containing organic active ingredients
  • A61K31/33—Heterocyclic compounds
  • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
  • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
  • A61K31/4164—1,3-Diazoles
  • A61K31/4178—1,3-Diazoles not condensed 1,3-diazoles and containing further heterocyclic rings, e.g. pilocarpine, nitrofurantoin
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  • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
  • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
  • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
  • A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
• • A—HUMAN NECESSITIES
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  • A61K31/00—Medicinal preparations containing organic active ingredients
  • A61K31/33—Heterocyclic compounds
  • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
  • A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
  • A61K31/551—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
  • A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
  • A61K47/08—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
  • A61K47/10—Alcohols; Phenols; Salts thereof, e.g. glycerol; Polyethylene glycols [PEG]; Poloxamers; PEG/POE alkyl ethers
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
  • A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
  • A61K47/08—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
  • A61K47/12—Carboxylic acids; Salts or anhydrides thereof
• • A—HUMAN NECESSITIES
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  • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
  • A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
  • A61K47/08—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
  • A61K47/14—Esters of carboxylic acids, e.g. fatty acid monoglycerides, medium-chain triglycerides, parabens or PEG fatty acid esters
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  • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
  • A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
  • A61K47/22—Heterocyclic compounds, e.g. ascorbic acid, tocopherol or pyrrolidones
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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  • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
  • A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
  • A61K47/26—Carbohydrates, e.g. sugar alcohols, amino sugars, nucleic acids, mono-, di- or oligo-saccharides; Derivatives thereof, e.g. polysorbates, sorbitan fatty acid esters or glycyrrhizin
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  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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  • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
  • A61K47/44—Oils, fats or waxes according to two or more groups of A61K47/02-A61K47/42; Natural or modified natural oils, fats or waxes, e.g. castor oil, polyethoxylated castor oil, montan wax, lignite, shellac, rosin, beeswax or lanolin
• • 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
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  • A61K9/0012—Galenical forms characterised by the site of application
  • A61K9/0048—Eye, e.g. artificial tears
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  • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
  • A61P1/08—Drugs for disorders of the alimentary tract or the digestive system for nausea, cinetosis or vertigo; Antiemetics
• • A—HUMAN NECESSITIES
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  • A61P29/02—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID] without antiinflammatory effect

Definitions

• the present invention relates to a pharmaceutical oil-in-water nano-emulsion composition for an enhanced delivery o active pharmaceutical substances, particularly, lipophilic and partially lipophilic active pharmaceutical substances and a process for preparing the same.
• Macro-emulsions are widely used to address some of the above issues; in particular, the size distribution and incompatibility of the components or excipients used in the emulsion, which makes it less efficient and tends to undergo separation before reaching the target site; Achieving enhanced bioavailability is a major problem faced while developing many delivery compositions, particularly for pharmaceutical compositions or agents that are ⁇ poorly soluble in water. There is a need tor improved compositions for lipophilic and partiai!y lipophilic active substances that will promote stability in an aqueous environment and allow efficient delivery of such substancesto a desired site of action. . .
• Bioavailability depends on several factors, drug solubility in an aqueous environment and drug .permeability through lipophilic membranes being important ones. Hence, it is important to improve the solubility and/or dissolution rate for lipophilic drugs. More than 40% of NCEs (new chemical entities) developed by the pharmaceutical industry recently are practically insoluble in water. These drugs are associated with slow drug absorption, leading to inadequate and variable bioavailability and mucosal toxicity. Micro-emulsions and nano emulsions offer several advantages, including improved drug solubility, enhanced bioavailability, protection of the drug from the environment, ease of manufacturing, and long .shelf life, [004] When developing such compositions, it is .
• compositions of the present invention are achieved by the compositions of the present invention.
• PCT/GB2002/003005 discloses an emulsion comprising of an oil phase for delivery of benzodiazepine drug.
• the invention further limits the drug loading of the prototype benzodiazepine molecule (Midazolam) only to 10mg/ml.
• the drug loading capacity should be relatively high to allow for administration of the drug via different routes in order to be able to deliver the required therapeutic dose, as the dosing volume will be limited.
• US5993846 discloses oil-in-water emulsions having mucoadhesive properties which are primarily intended for administration of biologically active compounds to mucosal surfaces having particle diameter ranging from 10 nm to 600 nm. Further, the mucoadhesives prolong the residence time in situ.
• the invention disclosed herein describes compositions with a particle size between 10 to 150 nm and its immediate release.
• Another patent CA2347032 entitled 'Gv ' vv emulsion comprising a hydroxyiated oil' describes an oil-in- water emulsion in which the oil phase comprises a hydroxyiated oil preferably castor oil. This describes emulsions with particle size of 200 run; the efficacy of the emulsions has not been established.
• a self emulsifying composition based on oliec acid is disclosed, however, oleic acid content is very high leading to greater viscocity and cause gelling problems upon the addition of water making it unstable unlike the instant invention. Moreover, these compositions potentially are dependent on digestion prior to release of the drug.
• the drawbacks of this system include chemical instabilities of drugs and high surfactant concentrations in compositions.
• Early studies revealed that the selfemulsification process is specific to the nature of the oil/surfactant pair, the surfactant concentration and oil/surfactant ratio, the concentration and nature of co-surfactant and surfactant/co-surfactant ratio and the temperature at which self emulsification occurs. Due to presence of high surfactant and oil concentrations there may be chances of instabilities of drugs. Also the high content of surfactant in self emulsifying compositions irritates the GIT. This also causes less drug loading capabilty.
• Olanzapine micro-emulsion described comprises of a system with 4%> oleic acid content, 30% of surfactant:co-surfactant mix containing Labrasol®, Cremophor RH40, and Transcutol P in ratio of 1:1 :0.3 and 0.5% polycarbophil as a mucoadhesive agent.
• the drug loading of the micro-emulsion was only 8 mg/ml.
• olanzapine 2-rv ethyi-4-(4-methyl- 1 - piperazinyl)-lOFf ⁇ thieno[2,3-b][l,5]benzodiazepine, referred to by the International Nonproprietary Name (INN) olanzapine, is marketed as being useful for the treatment of schizophrenia, schizophreniform disorder, acute mania, bipolar disorder, mild anxiety states, and psychosis.
• US 5,929,070A discloses that olanzapine is also useful in the control of pain associated with migraine.
• olanzapine must be administered orally in the form of tablets or capsules. This results in a substantial delay before the maximum concentration of active drug reaches the target site in the brain (long Tmax). with correspondingly slow onset of therapeutic effects.
• compositions for effective delivery of olanzapine and other therapeutic agents with a faster onset of action.
• the present invention seeks to provide improved compositions with high therapeutic efficacy having an average particle size of less than 200nm for pharmaceutical composition useful for the nasal, oral, intramuscular, ophthalmic, rectal or topical delivery of lipophilic: or partially lipophilic drugs or as therapeutic, monitoring or diagnostic agents.
• the compositions address the aforementioned issues; particularly, they minimize drug degradation and loss, prevent harmful side-effects, increase drug bioavailability, improve solubility of some poorly soluble pharmaceutical components and provide a nano- sized low-viscose monophasic composition.
• the primary object of the present invention is to provide a pharmaceutical oil-in- water nano-emulsion composition for an enhanced delivery of active pharmaceutical substances, particularly, lipophilic and partially lipophilic active pharmaceutical substances.
• An object of the present invention is to provide a a pharmaceutical oil-in-water nano- emulsion composition with a pharmaceutically active substance, encased in monounsaturated fatty acid droplets, the droplets having an average particle size in the range of 60 to 200 rim.
• Another object of the present invention is to provide a pharmaceutical oil-in- water nano-emulsion composition with a pharmaceutically active substance, where a non- ionic surfactant system with a mixture of polyethcrs, macrogolglycerides and polysaccharides is provided.
• the present invention provides a pharmaceutical oil-in-water nano- emulsion, with a pharmaceutically active substance.
• the selected pharmaceutically active substance is encased in monounsaturated tatty acid droplets with the droplets having an average particle size in the range of 60 to 200 nm.
• the nano-emulsion is also provided with a non-ionic surfactant system, which is a mixture of polyethers, macrogolglycerides and polysaccharides, along with pharmaceutically acceptable adjuvants.
• FIG.IA to FIG.1G illustrate particle size distribution in nanometre (nm), polydispersity index (PDI) and zeta potential (MV) of an exemplary composition No. I ' of the present invention, under various conditions.
• FIG. I A depicts particles size distribution under conditions viz., a room temperature with a particle size of 66.36nm and PDl of 0.408 and with a Zeta Potential of -0.0793
• FIG. IB depicts particles size distribution under conditions viz., a temperature 2-8°C with a particle size of 82.76nm and PDl of 0.286 and with a Zeta Potential of -0.152.
• FiG.lC depicts particles size distribution under conditions viz., 25°O ' 60% RK (Relative humidity); Particle size (run): 83.37; PDl: 0.289; ZetaPotential: 0.0278
• FIG. ID depicts particles size distribution under conditions viz., 3Q°C/65%RH; Particle size(nm): 92.7; PDI: 0.2S5; ZetaPotential: 0.0657
• FIG. IE depicts particles size distribution under conditions viz.. 30°C 75%RH; Particle size(nm): 75.02; PDl: 0,31 . 3,; ZetaPotential: 0.0999
• FIG. IF depicts particles size distribution under conditions viz., 40°C/75%RH;Particle size(NM): 81.41; PDl: 0.29; ZetaPotential: 0.00659
• FIG.IG depicts particles size distribution under conditions viz., Heat-Cool cycle;Particle size(nm): 59.78; PDI: 0.415; ZetaPotential: -0.180
• FIG.1H depicts particles size distribution under conditions viz., Freeze-Thaw cycle; Particle size(nm): 70.69; PDI: 0.306: ZetaPotential: -0.234 [028]
• FIG.2A to FIG.2H depict particle size distribution in nanometre (run), polydispersity index (PDI) and zeta potential (iViV) of the exemplary composition No. 2 under various conditions.
• FIG.2A depicts particles size distribution under conditions viz., Initial (Room Temperature); Particle size(nm): 64.32; PDf: 0.372; ZetaPotentiai: -0.0981
• F1G.2B depicts particles size distribution under conditions viz., 2-8°C; Particle size(nm): 64.57; PDI: 0.280; ZetaPotentiai: -0.301
• F1G.2C depicts particles size distribution under conditions viz., 25°C/60%RH (Relative humidity) ;Particle size(nm): 82.50; PDI: 0.284; ZetaPotentiai: -0.0702
• FIG.2D depicts particles size distribution under conditions viz., 30°C/65%R.H; Particle size (nrn): 80.25; PDI: 0.438; ZetaPotentiai: -0.214
• F1G.2E depicts particles size distribution under conditions viz., 30°C/75 RH; Particle size (nm): 68.05; PDI: 0.294; ZetaPotentiai: -0.0437
• FIG.2F depicts particles size distribution under conditions viz., 40°C/75%RH: Particle size (nm): 49.78; PDI: 0.424; ZetaPotentiai: 0.0591
• FIG.2G depicts particles size distribution under conditions viz.. Heat-Cool cycle; Particle size (nm): 75.25; PDI: 0.367; ZetaPotentiai: -0.286
• FIG-.2H depicts particles size distribution under conditions viz., Freeze-Thaw cycle; Particle size(nm): 94.31; PDI: 0.280; ZetaPotentiai: -0.535
• FIG.3A to FIG.3H depict particle size distribution ⁇ nanometre (nm) polydispersity index(PDI) and zeta potential (MV) of the exemplary compostion No. 3 of the present invention under conditions.
• FIG.3A depicts particle size distribution under conditions viz., Room Temperature;Particle size(nm): 164.4; PDI: 0.418; ZetaPotentiai: 0.0991
• F[G.3B depicts particle size distribution under conditions viz., 2-S°C; Particle size( M): 164.6; PDI: 0.375; ZetaPotentiai: 0.0743
• FIG.3C depicts particle size distribution under conditions viz., 25 o C.' ' 60%RH( Relative humidity) ;Partic!e size(nm): 162.0; PDI: 0.286; ZetaPotentiai: -0.0841
• FIG.3D depicts particle size distribution under conditions viz..30°C/65%R.H;Particle size(nm): 165.3; PDI: 0.289; ZetaPotentiai: 0.127
• FIG.3E depicts particle size distribution under conditions viz., 30°C/75%RH:Particle size(nm): 169.5; PDl: 0.293; ZetaPotential: 0.2.11
• FIGJF depicts particle size distribution under conditions viz., 40°C 75%RH;Particle size(nm): 147.3.
• PDl 0.252; ZetaPotential: 0.209
• FIG.3G depicts particle size distribution under conditions viz., Heat-Cool cycle; Particle size(nm): 215.4; PDl: 0.474; ZetaPotential: 0.141
• FIGJfl depicts particle size distribution under conditions viz., Freeze-Thaw cycle;Particle size(nm): 239.2; PDl: 0.485; ZetaPotential: -0.107
• FIG.4A to FIG.4H depict particle size distribution in nanometre(nm) , polyd ispersity index(PDI) and zeta potential (MV) of the exemplary composition No. 4 under various conditions.
• FIG.4A depicts particle size distribution under conditions viz., Initial (Room Temperature);Particle size(NM): 73.55, PDl: 0.304; ZetaPotential: -0.4
• FIG.4B depicts particle size " distribution under conditions viz., 2-SX; Particle size(NM): 71.1; PDl : 0.322; ZetaPoter.]ti,aJ.: .0J 7.5
• FIG.4C depicts particle size distribution under conditions viz., 25°C/'60%RH( Relative humidity) :Particle size(NM): 84.47; PDl: 0.283; ZetaPotential: 0.0954
• FIG.4D depicts particle size distribution under conditions viz., 30°C/65% H;Particle size(nm): 97.15; PDl: 0.276; ZetaPotential: 0.0148
• FIG.4E depicts particle size distribution under conditions viz., 30°C/'75°/oRH;Particle size(nm): 77.79: PDl: 0.289; ZetaPotential: 0.129
• FIG.4F depicts particle size distribution under conditions viz., 40°C/75%RH;Particie size(nm): 80.43; PDl: 0.293; ZetaPotential: 0.0134
• F1G.4G depicts particle size distribution under conditions viz., Heat-Cool cycle;Particle size(nm): 77.02; PDl: 0.410; ZetaPotential: -0.184
• FIG.4H depicts particle size distribution under conditions viz., Freeze-Thaw cycle;Particle size(nm): 91.33; PDl: 0.307; ZetaPotential: -0.186
• FIG.5A to FIG.5E depict particle size distribution in nanometre(nm) , poiydispersity index(PDl) and zeta potential (MV) of the exemplary composition No. 5 of the present invention under various conditions.
• FIG.5A depicts particle size distribution under conditions viz., 25°C/60%RH (Relative humid ity);Particle size(N ): 98.77; PDI: 0.408; ZetaPotential: -0.198
• FiG.58 depicts particle size distribution under conditions viz., 30°C/75%RH;Particle size(NM): 87.18; PDI: 0.31 ; ZetaPotential: 0.24
• FIG.5C depicts particle size distribution under conditions viz., 40°C/75%RH;Partic!e size( M): 84.34; PDI: 0.349; ZetaPotential: 0.0726
• FIG.5D depicts particle size distribution under conditions viz... Heat-Cool cycleT'article size(NM): 61.73; PDI: 0.410; ZetaPotential: -0.169
• FIG.5E depicts particle size distribution under conditions viz., Freeze-Thaw cycleT'article size( M): 77.47; PDI: 0.291 ; ZetaPotential: 0.006
• FIG. A to FIG.6E depict particle size distribution in nanometreinm) .
• FIG.6A depicts particle size distribution ' under conditions viz., 25°C/60 RH( Relative humidity) ;Particle size(NM): 79.66; PDI: 0.4 I 8; ZetaPotential: -0.1 I I
• F1G.6B depicts particle size distribution under conditions viz., 30°C/75% .H;.Rarticle size(NM): 87.65; PDI: 0.311 ; ZetaPotential: -0.0981
• FIG.6E depicts particle size distribution under conditions viz., Freeze-Thaw cycle;Particle size(NM): 90.76; PDI: 0.290; ZetaPotential: -0.358
• F1G.7A to FIG.7F depict particle size distribution in nanometrefnm) , po!ydispersity index(PDl) and zeta potential (MV) of the exemplary composition No. 7 of the present invention under various conditions.
• F5G.7A depicts particle size distribution- under conditions viz., Initial (Room Temperature); Particle size(nm): 143.5; PDI: 0.266; ZetaPotential: 0.0.327
• FIG.7B depicts particle size distribution under conditions viz.. -8°C; Particle size (nm): 144.9; PDI: 0.255; ZetaPotential: -0.0155 [0701]
• FIG.7C depicts particle size distribution under conditions viz., 25°C/60%RH (Relative humidity) ;Particle size(NM): 158.6; PDI: 0.276; ZetaPotential: 0.0863
• FIG.7D depicts particle size distribution under conditions viz., 30°C/65%RH;Particle size(nm): 163.8; PDI: 0.276; ZetaPotential: 0.28
• FIG.7E depicts particle size distribution under conditions viz., °C/75%RH; Particle size (nm): 170.4; PDI: 0.306; ZetaPotential: 0.495
• FIG.7F depicts particle size distribution under conditions viz., 40 o C/75%RH;Particle size(nm): I 56.5; PDI: 0.2S2; ZetaPotential: -0.0123
• FIG.8A to FIG.8F depict particle size distribution in nanometre (nm) , polydispersity index(PDI) and zeta potential (MV) of the exemplary composition No. 8 of the present invention under various conditions.
• FIG.8A depicts particle size distribution under conditions viz.. initial (Room Temperature); Particle size(NM ' ): 98.72; PDI: 0.243; ZetaPotential: -0.101
• FIG.8B depicts particle size distribution under conditions viz., 2-8°C; Particle size(nm): 97.17; PDI: 0.31 : ZetaPotential: -0.526
• FIG.8C depicts particle size distribution under conditions viz.. 25°C/60%RH (Relative humidity) ;Particle size(nm): 109.4; PDI: 0.412: ZetaPotential: -0.376
• FIG.8D depicts particle size distribution under conditions viz., 40°C/75%RH;Particle size(nm): 107.2; PDI: 0.438; ZetaPotential: -0.298
• FIG.8E depicts , particle size distribution under conditions viz., Heat-Cool cycle;Particle size(nm): 86.24; PDI: 0.400; ZetaPotential: -0.136
• F1G.8F depicts particle size distribution under conditions viz., Freeze-Thaw cycte;Partic!e size(nm): ' 9 ' 2.71 ; PDI:O.390; ZetaPotential: -0.0462
• FIG.9A to F1G.9F depict 'particle 'size disiribution in nanometre(nm), polydispersity inde.x(PDl) and zeta potential (MV) of the exemplary composition No. 9 of the present invention under various conditions.
• FIG.9A depicts particle size distribution under conditions viz., Initial (Room Temperature);Particle size(NM): 96.11; PDI: 0.245; ZetaPotential: -0.00741
• FIG.9B depicts particle size distribution under conditions viz.. 2-8°C; Particle size(NM): 87.26; PDI: 0.306; ZetaPotential: -0.0881 (084]
• FIG.9C depicts particle size distribution under conditions viz., 25°C760%RH( Relative humidity) ;Particle size(NM): 74.91; PDI: 0.284; ZetaPotentiai: -0.432
• FIG.9.D depicts particle size distribution .under conditions viz., 40°C/75%RH;Particle size(NM): 91.65; PDI: 0.38S; ZetaPotentiai: -0.0307
• FIG.9E depicts, particle size distribution under conditions viz., Heat-Cool cycle;Particle size(NM): 93.43; PDI: 0.368; ZetaPotentiai: -0.175
• FIG.9E depicts particle size distribution under conditions viz.. Freeze-Thaw cycle;particle size(NM): 82.68; PDI: 0.239; ZetaPotentiai: -0.0868
• FIG.10A to FIG.10F depict particle size distribution in nanometre(nm), polydispersity index(PDI) and zeta potential (MY) of the exemplary composition No. 10 of the present invention under various conditions.
• FIG.10A depicts particle size distribution under conditions viz., initial (Room " femperature);Particle size( M): 79.6; PDI: 0.279; ZetaPotentiai: 0.161
• FIG.10B depicts particle size distribution under conditions viz..2-S°C; Particle size(NM): 84.8; PDI: 0.292; ZetaPotentiai: 0.00795
• FIG. IOC depicts particle size distribution under conditions vi-z.,25°C/60%RHp : - Relative humidity) ;Particle size(NM): 55.79; PDI: 0.241; ZetaPotentiai: -0.2
• FIG.IOD depicts particle size distribution under conditions viz..40°C 75%RH;Particle ' size(NM): 8S.8; PDI: 0.315; ZetaPotentiai: 0.00409
• FIG.10E depicts particle size distribution under conditions viz., Heat-Cool cycle;Particle size(NM): 70.13; PDI: 0.298; ZetaPotentiai; 0.031 I
• FIG.lOF depicts particle size distribution under conditions viz., Freeze-Thaw cyc!e;Particle size(NM): 74.27; PDI: 0.363; ZetaPotentiai: -0.106
• FIG.11A to FIG. I IF depict particle size distribution ⁇ - ⁇ 1 ⁇ 2 nanometre(nm'), polydispersity ' index(PDI) and zeta potential (MV) of the exemplary composition No. 11 of the present invention under various conditions.
• FIG.llA depicts particle size distribution under conditions viz., Initial (Room Temperature):Particle size(NM): 87.53; PDI: 0.242; ZetaPotentiai: -0.176
• FiG.llB depicts particle size distribution under conditions viz.,2-8°C; Particle size(NM): 87.68; PDI: 0.295; ZetaPotentiai: -0.0151 [098]
• FIG. llC depicts particle size distribution under conditions viz., 2_>°C/60% H " (Relative humidity); Particle sizefNM): 85.85; PDI: 0.298; ZetaPotential: -0.506
• FIG.llD depicts particle size distribution under conditions viz.,40°C/75%RH;Particle size(NM): 87.61; PDI: 0.395; ZetaPotential: -0.112
• FIG. HE depicts particle size distribution under conditions viz., Heat-Cool cycle;Particle sizefNM): 78.52; PDI: 0.268; ZetaPotential: 0.0101
• FIG.1 IF depicts particle size distribution under conditions viz., Freeze-Thavv cycle;Particle size(N ): 77.41; PDi: 0.281 ; ZetaPotential: -0.0777
• FIG.12 depicts HPLC assay results to determine the percentage of drug content in the exemplary composition of the present invention.
• F1G.13A to FIG.13F depict particle size distribution in nanometre(nm), poi clispersity index(PDI) and zeta potential ( V) of the exemplary composition No. 13 of the present invention under various conditions.
• FIG.13 A depicts particle size distribution under conditions viz.. Initial (Room Temperature);Particle size(N ): 121.5; PDI: 0.252; ZetaPotential: -0.592
• FIG.13B depicts particle size distribution under conditions viz., 2-8°C; Particle sizefNM): 135.3: PDI: 0.431 ; ZetaPotential: -0.583
• FIG.13C depicts particle size distribution under conditions viz., 25°C/60%RH( Relative humidity) (Particle size(NM): 146.3; PDI: 0.407; ZetaPotential: -0,309
• FIG.13 depicts particle size distribution under conditions viz., 40°C/75%RH;Particle size(N!Vf): 136.8; PDi: 0.287; ZetaPotential: -0.361
• F1G.14A to FIG.14D depict particle size distribution in nanometre(nm), polydispersity index(PDI) and zeta potential (MV) of the exemplary composition No. 14 of the present invention under various conditions.
• FIG.14A depicts particle size distribution under conditions viz., Initial (Room Temperature);Particle sizefNM): 125.3; PDI: 0.311 ; ZetaPotential: -0.341
• FIG.14B depicts particle size distribution under conditions viz.,2-8°C; Particle sizefNM): 123.6; PDI: 0.387; ZetaPotential: -0.219
• FIG.14C depicts particle size distribution under conditions viz.,25°C/60%R.H( Relative humidity) ;Particle sizefNM): 127.7; PDI: 0.317; ZetaPotential: -0.00259 [0112]
• FIG.141 depicts . particle size distribution under conditions viz., 40°C/75%RH;Particle size( M): 130.2; PDI: 0.319; ZetaPotential: -0.364
• FIG. ISA to F1G.15D depict particle size distribution in nanometre(nm), poiydispersity index(PDI) and zeta potential (MV) of the exemplary composition No. 15 of the present invention under various conditions.
• FIG.15A depicts particle size distribution under conditions viz., Initial (Room Temperature);Particle size(NM): 117.5; PDI: 0.274; ZetaPotential: -0.588
• FIG.15B depicts particle size distribution under conditions viz., 2-8°C; Particle sizc(NM): 161: PDI: 0.488; ZetaPotential: 0.0531
• FIG.15C depicts particle size distribution under conditions viz., 25°C/60%RH( Relative humidity) ;Particle size(NiVl): 148.3; PDI: 0.446; ZetaPotential: 0.11
• FIG.15D depicts particle size distribution under conditions viz., 40°C/75%RH;Particle sizc(NM): 158.3: PDI: 0.514; ZetaPotential: 0.157
• FIG.16A to F1G.16D depict particle size distribution in nanometre(riiu), poiydispersity index(PDI) and zeta potential (MV) of .
• the exemplary composition Ko: 6-'of the present invention under various conditions.
• FIG.16A depicts particle size distribution under conditions viz., Initial (Room Temperature);Particle size(NM): 103.5; PDI: 0.194; ZetaPotential: -0.139
• FIG.16 B depicts particle; size distribution under conditions viz., 2-8°C: Particle size(N[ ⁇ 4): 107; PDI: 0.251; ZetaPotential: 0.139
• FIG.16C depicts particle size distribution under conditions viz.,25°C/60%R.H( Relative humidity) -Particle size(NM): 100.6; PDI: 0.233; ZetaPotential: 0.00712
• FIG.16I depicts particle size distribution under conditions viz.,40°C/75°/oRH;Particle size! ⁇ Mr. 107.9; PDI: 0.228; ZetaPotential: 0.973
• FIG.17A to FIG.17D depict particle size distribution in nanometre(nm), poiydispersity index(PDl) and zeta potential (MV) of the exemplary composition No. 17 of the present invention under various conditions.
• FIG.17A depicts particle size distribution under conditions viz.. Initial (Room Tetnperature);Particle size(NM): 146.6; PD!: 0.332; ZetaPotential: -0.254
• F1G.17B depicts particle size distribution under conditions viz., 2-8°C; Particle size(NM): 166.7; PDI: 0.522; ZetaPotential: -0.175
• FIG.17C depicts particle size distribution under conditions viz., 25°C/60%PvH( Relative humidity) ;Particle size(NM): 151.5; PDI: 0.462; ZetaPotential: -0.233 .
• FIG.17D depicts particle size distribution under conditions viz., 40°C/75%RH; Particle size(NM): 154.3; PDI: 0.31 S; ZetaPotential: -0.0449
• FIG.18A to FIG.1BD depict particle size distribution in nanometre(nm), polydispersity index(PDf) and zeta potential (iVfV) of the exemplary composition No. 18 of the present invention under various conditions.
• FIG.18B depicts particle size distribution under conditions viz., initial (Room Temperature);Particle size(N ' ): 142.5; PDI: 0.449; ZetaPotential: -0.248
• FIG.18C depicts particle size distribution under conditions viz., 2-8°C; Particle size(N ): 146.7; PDI: 0.405; ZetaPotential: -0.389
• FIG.18D depicts particle size distribution under conditions viz:, 25°C/60% H( Relative humidity) ;Particle size(NM): 1 1.4; PDI: ' 0.447; ZetaPotential: -0.361
• FIG.18E depicts particle size distribution -under conditions viz., 40°C/75%KH; Particle size(NiVi): 144.9; PDI: 0.331: ZetaPotential: -0.229
• a composition for delivery of lipophilic or partially lipophilic based active pharmaceutical substance and a method for preparing the same, is disclosed.
• the present invention relates to an oil-in-water emulsion comprising an oil phase, the average particle size of which is in the range of 60 to 200 nrn, a method for preparing the composition and the use of the composition for the delivery of the active pharmaceutical substance.
• the composition demonstrates favourable dilution properties without being affected by the solubility characteristics of individual components. , of the composition. Furthermore, the composition exhibits a stable state throughout its shelf life.
• the emulsion of the present invention comprises at least an active pharmaceutical substance, a surfactant, or a mixture of surfactants and additives, wherein the average particle size of the emulsion of the composition is less than 200 nm.
• the invention provides pharmaceutical compositions comprising such compositions and methods of making and using such compositions.
• the active pharmaceutical substance referred herein may also be referred to herein as "drug", “active phamaceutical ingredient” or “therapeut agent”. These terms are used intercahngeably refer to chemical material or compound which, when administered to a species (human or animal), is generally bioavialable and induces the desired pharmacologic effect.
• composition comprising of a lipophilic or partially lipophilic based drugs, an oil phase, surfactants, co- surfactants, adjuvants or other excipients comprising of one or more of stabilizers, antioxidants, preservatives, mucoadhesive agents, buffering agents, absorption enhancers and pH adjusting agents;
• the active pharmaceutical substance is selected from a group of substances that are soluble in oil or partially soluble i water, such as angiotensin-converting enzyme (ACE) inhibitors, antipsychotics, anti-emetics, analgesics and anti-inflammatory drugs including olanzapine, risperidone, ondansetron and paracetamol.
• ACE angiotensin-converting enzyme
• the active pharmaceutical substance can be entrapped in the composition and incorporated into the composition to maintain its stability- and to increase its bioavailability. Olanzapine, risperidone, ondansetron and paracetamol is preferred.
• the term ' ' Partially soluble in water includes sparingly soluble (lgrarn drug gets dissolved in 30 to 1 ⁇ ⁇ solute) slightly soluble (I gram drug gets dissolved in 100 to 1000ml solute) and/or very slightly soluble (I gram drug gets dissolved in 1000 to 10000ml solute) as provided under European Pharmacopeia definitions and as described In biopharmaceutics classification system underclass 11 and class IV.
• the oil phase of the inventive composition comprises one or more fatty acids.
• these are selected from fatty acids having 6 to 22 carbon atoms, more preferably 13 to 21 carbon atoms, more preferably 16 to 20 carbon, atoms, most preferably .1.8..carbon atoms.
• the fatty acids may be saturated, monounsaturated or polyunsaturated. onounsaturated fatty acids are preferred.
• Preferred fatty acids are myristoleic acid, palmitoleic acid, sapienic acid, oleic acid, elaidic acid, and vaccenic acid. Oleic acid is especially preferred. Mixtures of fatty acids are also contemplated, although use of a single fatty acid remains favoured.
• the amount of fatty acid present in the inventive emulsions is in the range of 5 to 25 % w/vv. More preferably, the fatty acid is present in the range of 5 to 15 % vv/w, and still more preferably in the amount of 7.5 to 10 % w/w. f 0 ⁇ 43 J in a further embodiment, the composition further comprises of various surfactants selected from a group of polyether sufactants, macroglyceride surfactants and /or polysaccahride sufactants. Suitable polyethers are paraformaldehyde, polyethylene glycol, polypropylene glycol, Diethylene glycol monoethyl ether ( Transcutol) and polytetramethylene glycol.
• the polyether suitably has a molecular weight in the range of from 50 gmol-l to 1000 gmol-1, more preferably from 100 gmol-1 to 500 gmol-1, still more preferably from 150 gmol-1 to 400 gmol-1, , such as about 200 gmol-1 (PEG 200) and/ or 400gmol-l ( PEG 400).
• the polyether may optionally be end-capped.
• the polyether is present in the emulsion in an amount of from 2.0 to 25 % w/w, preferably from 2.5% to 20 % w/w, for example about 15 % w/w of PEG 200 or 400 and most preferably from 2.5% of Transcutol.
• the oil phase further comprises of a macrogolglyceride surfactant.
• a macrogolglyceride refers to saturated polyglycolized glycerides such as stearoyl-, lauroyl-, oleo!y-, lineoyl-, and caprylocaproyl- macrogol glycerides.
• a preferred " macrogolglyceride is caprylocaproyl macrogoi-8 glycerides, commercially available under the trade name Labrasol® .and acconon® CC6.
• the macrogolglyceride is present in the emulsion in an amount of from 10 to 30 % w/w, preferably from 12 to 25 % w/w. most preferably 15% to 22.5% w/w of labrasol and 15% w/w of acconon CC 6.
• the oil phase fuither comprises a polysaccharide surfactant.
• Preferred polysaccharide surfactants are polyoxyethylene sorbitan fatty acid esters or sorbitan monooleate. Particularly preferred are polysorbate 20 (polyoxyethylene (20) sorbitan monolaurate), polysorbate 40 (polyoxyethylene (20) sorbitan monopalmitate), polysorbate 60 (polyoxyethylene (20) sorbitan monostearate), and polysorbate 80 (polyoxyethylene (20) sorbitan monooleate), with polysorbate 20 (polyoxyethylene (20) sorbitan monolaurate) and polysorbate .80 (polyoxyethylene (80) sorbitan monooleate) being most preferred.
• Polysorbate 20 (polyoxyethylene (20) sorbitan monolaurate) and polysorbate 80 (polyoxyethylene (20) sorbitan monooleate) is commercially available as Tvveen 20® and een 80® and sorbitan monooleate is commercially available as Span 80®
• the polysaccharide surfactant is present in the emulsion in an amount of from 2 to 30 % w/w, preferably from 5 to 25 % w/w and most preferably 5% of span.80 and I 5% to 22.5% w/w of tvveen ® .
• the composition in accordance vvith the present invention can contain one or more additives such as stabilisers, antioxidants, preservatives, miicoadhesive agents, in-situ gelling agents,, buffering agents, absorption enhancers and pH adjusting agents in order to improve the physical and chemical stability of the composition.
• additives are preferably chosen from the group comprising of butylated hydoxytoulene, butylated hydroxyanisole, Kolliphor® HS, Benzyl alcohol, tocopherol. EDTA and ascorbic acid to prevent oxidation, and to form a stable composition.
• the said antioxidants are selected from a aroup comprising of one or more of butylated hydroxytoluene, butylated hydroxyanisole and ascorbic acid.
• the amount of antioxidants in the composition of the invention can preferabl range from 0.01% to 5% by weight and more preferably from 0.01% to 0.2% by . weight with respect to the total weight of the composition.
• the said absorption enhancers are also optionally added to this invention to improve the mucous absorption and bioavailability.
• Preferred absorption enhancers are selected from the group consisting of macrogol fatty acid esters, bile salts, and salts of medium-chain fatty acids.
• macrogol fatty acid esters macrogol- 15 hydroxystearate, commercially available as Kolliphor® HS.
• bile salts sodium glychocoiate is preferred.
• sodium caprylate is preferred.
• the amount of absorption enhancers in the composition of the .invention can preferably range from 0.1% to 10% by weight and more preferably from 1% to 5% by weight with respect to the total weight of the composition.
• miicoadhesive agents may also optionally be added to this invention.
• Preferred miicoadhesive agents are selected from the group comprising of Synthetic polymers including Cellulose derivatives like hydroxy propyl methylcel!ulose, sodium carboxy methylcellulose.
• the different buffering agents that can be used for mainatining the pH are acetate buffer solution, phosphate buffer solution, maleate buffer solution, preferably sodium acetae tryhydarte with glacial acetic acid buffer solution and potassium dihydrogen phosphate with sodium hydroxide buffer solution was used.
• the dispersed phase particles and other ingredients of the composition of the invention have an average size of less than 200 nm and preferably ranging from 40 to 170 nm.
• the composition of the present invention are notable for their low and uniform particle size.
• the decrease in the size of the particles makes it possible to promote the penetration of the drug into the target site more effectively and improves the bioavailability.
• the composition has an excellent stability rate by virtue of the optimum zeta potential, preferably in the range -30m V to ⁇ 30 rnV, preferably in the range -lOrnV to + 10 mV most preferably in the range " -05mV to +05mV.
• the invention provides highly stable composition having drug loading capacity of upto lOOmg/ml , preferably .up to 80mg/ml and leads to quick release of drug to the target site in less than 30 minutes preferablly less than 10 minutes.
• composition of the present invention are further notable for their low viscosity, and a desired degree of chspersibility can be obtained- to increase the (dispersed) Inner phase content to deliver the active ingredient effectively which makes them suitable for administration via e.g. the n sal route.
• the, viscosity of the emulsions is less than 250 cP or lower, more preferably less than 150 cP, or lower
• the composition is a transparent and clear monophasic system with high stability.
• the composition of the invention is substantially free of co- solvents, including monohydric alcohols. However, if required co-solvents may be added in less quantities.
• co-solvents are benzyl alcohol, phenyl ethyl alcohol, chlorobutanol. In this context, "substantially free" or less quantities means less than I % w/w.
• composition of the present invention is further notable for their high stability.
• the composition of the invention provides an advantage of higher drug loading capability in the range of 10 to 80 mg/ml as evidenced in the examples below.
• the drug loading for olanzapine is in the range of 35 to 45 mg/ml, preferably 40 mg/ml, and most preferably 38.46 mg/ml.
• the drug loading for ondansetron is in the range of 10 to 15 mg/ml, preferably 12 mgAni
• the drug loading for paracetamol is between 60 to 80 mg/ml, preferably 75 mg/ml; and for resperidone it is between 20 to 30 mg/ml preferably 25 mg/ml.
• This property of the invention enables improvement of drug bioavailability and reduction of the dosing frequency also suitable for highly potent low-dose drugs,. Even with higher drug content, the invention showed stable and favorable physicochemical characteristics.
• the higher drug loading and the reduction in the particle size indicate the solubility of the lipophilic and partially lipophilic drugs in the instant invention leading to high bioavailability.
• the emulsion of the invention comprises an aqueous phase.
• the aqueous phase is present in an amount greater by weight than any other single component.
• the aqueous phase is present in an amount of between I 5 and 50 % vv/w.
• compositions of the present invention are prepared by conventional methods well known to those skilled in the art.
• the composition of the composition of the invention can be obtained by a process of subjecting the oleic acid, surfactants and co-surfactants or a mixture thereof to homogenization using magnetic stirrer.
• the oil and surfactant mixture is then mixed with a solution containing the required drug and the additives are added and subjected to vigorous stirring at controlled room temperature ranging between 20°C to-25 c C (68 to 77° F) using any suitable mixing apparatus known to those skilled in the art for about 30 minutes or until the entire amount of. " drug is dissolved.
• the homogenized mixture is then subjected to water phase preferably containing ascorbic acid and mixed well to get clear transparent composition, which indicates that the drug has dissolved/incorporated successfully.
• the composition can be used in any pharmaceutical field where this type of composition is useful. While various embodiments herein describe nasal and ocular route of delivery, most preferably nasal delivery of compositions containing the drug, it is further envisaged that the delivery of the drug can be performed by any suitable delivery mechanism that provides therapeutically effective levels of the drug. Accordingly, the system is particularly useful for non-parenteral modes of administration such as buccal, sublingual, rectal, transdermal, topical, nasal, urethral, vaginal, and ocular. When administered by such non-parenteral modes the methods and composition of the present invention can deliver drug both locally and system ica I ly as desired including orai, intramuscular and transcutaneous routes.
• the invention provides composition for intra nasal delivery or ophthalmic route; preferably composition comprises drops, gel composition or aerosol composition.
• the invention provides composition comprising an emulsion as disclosed herein can be administrated preferably as a spray or aerosol or ocular route.
• aerosol we refer to an airborne mist of liquid particles.
• the dispensing system for such a composition ma typically be a can or bottle that contains a liquid pressurized by compressed, propellant gas.
• sprays of liquid particles may be produced by devices in which the liquid is pressurized by a hand-operated pump and forced through an atomizer nozzle.
• a typical nasal spray composition consists of the therapeutic agent suspended or dissolved in an aqueous medium, which is filled into a bottle with a metered spray pump. Pump actuation by the patient delivers the drug in fine droplets into the nasal cavity.
• the composition of ocular suspension consists of the therapeutic agent suspended or dissolved in aqueous medium, which is filled in a bottle for use as eye drops.
• the aforesaid composition confers a synergistic therapeutic effect of high bioavailability compared to the therapeutic effect when a pharmaceutical substance is administered separately or in partial combination of the said ingredients of the said composition.
• the synergistic effect as defined above has been adapted to increase the bioavailability by almost 1.3 times to 12 limes relative to the therapeutic effect when pharmaceutical substance is administered separately and /or in partial combination of the said ingredients of the said composition administered through various routes, preferably intra nasal and ocular route. Increasing the bioavailability plays a very important role in the toxicity of the drugs.
• the composition can help in reduction in the dosage or the frequency of the dosages in the patients due to its higher bioavailability while reducing side effect of the drugs, [n an object, the bioavailibilty of the pharmaceutically active substances is enhanced by atleast 1.3 times ' to 12 times, in another object, the active pharmaceutical substance such as olanzapine when administered to the nasal cavity of a subject establishes a high bioavailability by at least 5 to 6 times in therapeutic plasma concentration within 5 to 10 minutes and bioavailability of 10 to 12 times in brain with in 10 to 30 minutes.
• the table shows drug efficiency of olanzapine through intra nasal route by almost 1.3 times or by 25% in reaching the brain concentration in 5 to 10 minutes and 1.78 times or 45% in attaining the plasma concentration within minutes when compared to intramuscular route of administration.
• the brain concentration was 5.31 times or 80%o better and plasma concentration was almost 10.69 times or 91% higher in.
• the composition has a drug loading capability of between about ID mg/mi and about 80 mg/ml, preferably between 12 mg/ml to 75 mg/ml.
• Bioavailability of a drug in this context means the mount of dose that reaches the site of action (brain and eye in the instant case) in an unchanged form (and usually active) at. a particular time.
• the area under the time versus plasma and brain concentration curve provided in the results below is reflective of the amount of drug that has been absorbed in the brain and plasma using the compositions of the composition provided herein.
• the invention relates to a nasal spray for treatment of pain associated with migraine, headache, cluster headache, psychosis, nausea and vomiting or chemotherapy induced nausea and vomiting, autonomic cephalgia, agitation, sleep disorder, disturbance of mental state and ocular solution for reduction in ocular pressure.
• the method relates to a method of treatment of a mammal suffering from or susceptible to pain associated with migraine, comprising administering an effective amount of a composition according to the invention, wherein the pharmaceutically active ingredient is, or comprises, olanzapine or a pharmaceutically acceptable salt thereof.
• the method involves administration of the composition nasally. Dosing may be once per day (for example, at the onset of symptoms), or may be several times per day as per the requirements. Preferably, the amount is from 0.01 to 20 mg depending upon the severity of symptoms.
• the method relates to a method of treatment of a mammal suffering from or susceptible to pain associated with migraine, comprising administering an effective amount of a composition according to the invention, wherein the pharmaceutically active ingredient is, or comprises, olanzapine or a pharmaceutically acceptable salt thereof.
• the method involves administration of the composition nasally. Dosing may be once per da (for example, at the onset of symptoms), or may be several times per day as per the requirements. Preferably, the amount is from 0.01 to 20 mg depending upon the severity of symptoms.
• the method relates to a method of treatment of suffering from antipsychotic related symptoms including schizophrenia and bipolar disorders, comprising administering an effective amount of a composition according to the invention, wherein the pharmaceutically active ingredient is, or comprises, respiridone or a pharmaceutically acceptable salt thereof.
• the method involves administration of the composition nasally. Dosing may be once per day (for example, at the onset of symptoms), or may be several times per day as per the requirements. Preferably, the amount is from 0.01 to 16 mg depending upon the severity of symptoms.
• the method relates to a method of treatment of a mammal suffering from nausea and vomiting that may be caused by surgery or by medicine, comprising administering an effective amount of a composition according to the invention, wherein the pharmaceutically active ingredient is, or comprises, ondansetron or a pharmaceutically acceptable salt thereof.
• the method involves administration of the composition nasally. Dosing may be once per day (for example, at the onset of symptoms), or may be several times per clay as per the requirements. Preferably, the amount is from 0.01 to 24 mg depending upon the severity of symptoms.
• the method relates to a method of treatment of a mammal suffering from high intraocular pressure, comprising administering an effective amount of a composition according to the invention, wherein the pharmaceutically active ingredient is, or comprises, paracetamol or a pharmaceutically acceptable salt thereof.
• the method involves administrating of the composition through ophthalmic route. Dosing may be once per day (for example, at the onset of symptoms), or may be several times per day.
• the method of treatment involves delivery of a predetermined amount of therapeutic agent (e.g. olanzapine, ondansetron, respirodone) by means of a metered actuation.
• a predetermined amount of therapeutic agent e.g. olanzapine, ondansetron, respirodone
• the method involves administration of from 0.01 to 100 mg of active agent, most preferably 0.1 to 20 mg per metered actuation.
• the methods of the invention in some embodiments involve a second therapeutic agent of known efficacy in the treatment of migraine, for simultaneous, separate of sequential administration with the compositions described (particularly those of olanzapine).
• Preferred second therapeutic agents are selected from the group of almotriptan, eletriptan, flovatriptan, naratriptan. rizatriptan, sumatriptan, zolmitriptan, ergotamine, dihydroergotamine, bosentan and lanepitant.
• the present invention provides a pharmaceutical oil-in- ater nano- emulsion, comprising: a pharmaceutically active substance, encased in monounsaturated fatty- acid droplets, the droplets having an average particle size in the range of 60 to 200 nm; a non- ionic surfactant system comprising a mixture of polyethers, macrogolglycerides and polysaccharides; and pharmaceutically acceptable adjuvants.
• the present invention also provides a process for the preparation of an oil-in-water emulsion composition, by initially forming an oil phase in the presence of a monounsaturated fatty acid, a . polyether surfactant, a macrogolglyceride surfactant and a polysaccharide surfactant, under stirring at an ambient temperature; and adding a therapeutically amount pharmaceutically active substance to the oil phase, under constant stirring and at an ambient temperature, to encase said active substance, in the monounsaturated fatty acid droplets, the droplets with particle size in the range of 60 to 200 nm, to obtain a homogenous oil phase; and adding an aqueous medium to the homogenous oil phase, under stirring to obtain the oil- in-water emulsion.
• Example 2 Composition 2 [0182] To 7.5 % (w vv) of oleic acid, 2.5% (w/vv) of transcutol, 22.5% (w/vv) of Labrasol along with 22.5% (w/vv) of tween 80 and 15% (w/w) PEG 400 were added sequentially under constant stirring. To this 5% (w/vv) Kolliphor HS 15 followed by 3.846% (w/vv) of Olanzapine was added and mixed slowly into the above oil-surfactant mixture under constant stirring at 600-1000 rprn using a magnetic stirrer or overhead stirrer at room temperature (20 to 25°C) for about 30 minutes or until the entire amount of drug was dissolved.
• Example 4 Composition 4 [0186] To 7.5 % (vv/w) of oleic, acid, 2.5% (w/w) of transcutol, 22.5% (vv/w) of Labrasol along with 22.5% (w/w) of t een 80, i 5% (w/w) PEG 400 were added sequentially under constant stirring . To this 5% (w/w) Kolliphor HS 15 followed by 3.846% (w/w) of Olanzapine was added and mixed slowly into the above oil-surfactant mixture under constant stirring at 600-1000 rpm using a magnetic stirrer or any suitable stirrer at room temperature (20 to 25°C) for about 30 minutes or until the entire amount of drug was dissolved.
• Example 9 Composition 9 (01961 To 10 % (w/w) of oleic acid, 22.5 % (vv/vv.) of Labrasol along with 22.5 % (w/w) of ' tween 20 and 15% (w/w) PEG 200 were added. To this, 5% (w/w) Kolliphor HS, 0.01% (w/w) each of BHA and BHT along with 0.1% (w/vv) ascorbic acid were added sequentially under'constant stirring at around 600-1000 rpm on magnetic stirrer or any suifabie stirrer at room temperature (20 to 25°C) until a homogeneous phase was formed.
• Example 11 Composition 11
• Example 12 Composition 12
• Example 15 Composition 15 [0214) To 10% (vv/vv) of oleic acid, 22.5 % (w/w) of Labrasol along with 22.5 % (vv/vv) o tween 20 and 15% (w/w) PEG 200 was added. To this 5% (w/w) olliphor HS 15 and 0.01 (w/w) each of BHA and BHT were added sequentially under constant stirring at around 600- 800 rpm using a magnetic stirrer at room temperature (20 to 25°C) until a homogeneous phase was formed.
• Risperidone 2.5% (w/w) of Risperidone was mixed slowly into the above oil-surfactant mixture followed by addition. of 0.1% (w/w) ascorbic acid dissolved in water under constant stirring at 60Q-1000 rpm using a magnetic stirrer at room temperature (20 to 25°C) for about 30 minutes or until the entire amount of drug was dissolved.
• physiochemical properties such as Particle size distribution and the droplet size of all the emulsions along with polydispersity and Zeta potential was measured and assessed by dynamic light scattering also referred to as photon correlation spectroscopy using a particle size analyser.
• I niL of the diluted composition sample was placed in a clear disposable zeta cuvette.
• the zeta potential analysis at 25 0C in Malvern Zetasizer instrument was performed.
• the zeta potential and polydispersity indices were calculated using the inbuilt software.
• the primary feauture of the nano or micro emulsions is the droplet size, which must be in the nanometer range and is a crucial factor indicating their performance because it determines the rate and extent of drug release as well as drug absorption. Therefore, in the advantagious composition o fthe present invention, the average droplet size of emulsion was found to be around 150 run.
• Polydispersity index (PDi) indicates uniform ity of droplet size within the composition and its stability. The value of PDI was found to be less than 0.3. Low value of PDI indicated uniform distribution of nano droplets within the composition, leading to more rapid absorption and improved bioavailability of the drug.
• figure I to I I for Olanzipine, figure 13 and 14 of Paracetamol, Figure 15 & 16 for Risperidone and figure i7 & 18 for ondansetron respectivlev indicates small and uniform particle size of the emulsion droplets under varoius conditions such as initial, 2- S0C, 25oC/ 60% Tf, 30oC/.65%RH, 30oC/ 75%RH, 40oC/75%RH respectively.
• test samples of the composition containing olanzapine, Paracetomo!, Risperidone.Ondansetron were prepared according to the examples above, and the emulsion was used to determine the stability of the composition and to check, any phase separation or turbidity.
• the compositions were stored and maintained at two different temperatures.
• the amount of drug degraded and remaining in the compositions were determined by withdrawing samples at regular intervals and analysing for drug content by analytical HPLC methods at 0 day and 30 day time interval. The results are as described in the table below.
• the pH of the emulsions according to the invention is an important determinant of how well they are tolerated or favourable when administered-.. into the nasal cavity, ophthalmic or any other preffered route.
• the emulsion may cause irritation and stinging if the pH is too high or low. Therefore, the pH of the aqueous phase of an emulsion according to the invention is preferably in the ' range pH 4.5 to 8.0, more preferably 5 to 7.5.
• the pH of the aqueous phase of the emulsions according to the invention hi ay be adjusted and controlled by means well known to those skilled in the art, such as buffer salts, acids and bases selected from various organic acids or/and alkali metal salts thereof.
• compositions Were centrifuged at 5000 rpm for 30min. After centrifugation, no phase separation or precipitation of the drug was observed which further confirmed the stability of the emulsion. Subsequently, the compositions were further subjected to freeze thaw stress test. Three freeze thaw cycles between ⁇ 20°C and - 15°C with storage at each temperature between 24h and 48h was conducted for the compositions. The values of the particle size, zeta potential and the pH did not vary significantly after the end of the freeze thaw cycle from the initial as per the results in table 7 below, which shows the stability of the composition. Further, the positive results indicated that all the compositions are thermody n am i ca 11 y stable systems and are formed at a particular concentration of oil, surfactant and cosurfactant. with no phase separation, creaming or cracking.
• Composition 6 78.76 0.461 ⁇ -0.158 216.5 7.223
• the components used in the delivery system should have high solubihsation capacity for the drug inorder to ensure its solubihsation in the resultant dispersion.
• solubility of the drug olanzapine was studied using different unsaturated fatty acids. The results of the solubility studies have been provided below.
• Olanzapine has solubilit of less than 40 mg/niL in Labrafil( tradename), Capryol 90( tradename), Acconon CC6( tradename) and Kolliphor HS( tradename). Acconon CC6 and Kolliphor HS are rniscible with water and hence were not used as oil in the development of the micro-emulsions.
• Olanzapine has a solubility of - 60 mg/ml in Capryol 90 but it is lower than oleic acid. The solubility of olanzapine in oleic acid is 3 ⁇ 4 200 mg/ml.
• oleic acid showed highest solubihsation capacity as compared to other unsaturated fatty acids.
• Micro-emulsions were formulated and their in vivo pharmacokinetic performance was evaluated upon intranasal delivery in comparison to oral delivery. Further, the micro- emulsions were explored for relative bioavailability compared with intramuscular administration. Higher drug concentrations were observed in the target organ which is the brain. Direct nose to brain transport indicated more effective and best brain targeting of the micro-emulsions (Drug delivery system). The percentage of relative bioavailability indicated the amount of drug available in the systemic circulation for re-uptake by the brain for prolonged effect. Pharmacokinetic studies conclusively demonstrated rapid brain uptake of dru when compared with intramuscular ' and oral solutions, The results indicated that, the developed micro-emulsion compositions were effective for target organ delivery.
• compositions are control group taken for comparison of p parameters.
• AUC is the area under the plasma concentration versus time. curve from time 0 to time x after nasal route. The relative bioavialbilty was determined by comparing the AUC of nasal administration and oral and intramuscular administration.
• Brain (including olfactory tubercle):
• the Cmax in the brain when " given through the IN route was 2495ng/g with a dose administration of 2mg/kg , but with respect to I and oral administerd dose of 6mg/kg, it was 5615 ng/g and .l40S.36 rig/g respectively. Therefore, in order to achieve the same concentrations reaching the brain one can reduce the close of administration through the nasal route by 25% vis a vis [M and 80% vis a vis oral.
• the Tmax i.e., the time taken to reach the maximum concentration in brain by the nasal composition was attained within 10 mins when compared to 60 n ms through the conventional routes of administration.
• the time taken to reach The maximum concentration in plasma, via the nasal composition was 5mins when compared to 30 mins and GOmins through the intra muscular and oral routes of administration respectively.
• IM & Oral compositions are control group taken for comparison of pK parameters.
• the competitive advantage of the invention described lies in its enhanced drug: ' - delivery mechanism, ease of use, enhanced access, reduced-dosage of administration leading to reduced side effects and high drug loading, which leads to. better patient acceptance and compliance and increased bioavailability.
• the composition of this invention helps in solubilizing higher amounts of drug.
• This invention also provides increased absorption of pharmaceutical agents through endothelial or epithelial membranes.
• the invention with nano-sized oil droplets and the drug dissolved in it, surrounded by surfactant layer aids the lipophilic compounds to be stable in aqueous environment.
• the invention presents a stable composition by preventing oxidation and hydrolysis. This invention also improves the mucous absorption and bioavailability.
• This invention offers clinical advantages over competitor products in a large market of considerable unmet need.
• the drug delivery system is able to enhance the rapid onset of action for lipophilic drugs than the conventional or existing delivery systems.
• the nasal route not only improves the bioavailability by preventing extensive first-pass metabolism but. also targets the receptor site and passes through the blood-brain barrier (BBB).
• BBB blood-brain barrier
• This invention also offers the advantages of the drug being administered simply, non- invasively, cost-effectively, and conveniently.
• One such example showing the ease of treatment is demonstrated by easy sprayability and ease of self-administration with reduced side effects.
• the composition demonstrates improved bioavailability, rapid drug absorption via highly vascularized mucosa, thus demonstrating a superior mode of delivery to the existing treatment options.
• This invention is superior in at least one of the criteria from the similar compositions described in the literature i.e., higher drug loading, better in vivo performance, rapid onset of action etc. Even at this higher drug content, the developed systems sho suitable physicochemical characteristics.
• a benefit of the invention is to prepare a composition of higher drug concentration- for lipophilic and moderately .lipophilic compounds, at concentrations of around 10-80 mg/ml.

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