WO1993000006A1 - Bioactive composition - Google Patents
Bioactive composition Download PDFInfo
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- WO1993000006A1 WO1993000006A1 PCT/US1992/005059 US9205059W WO9300006A1 WO 1993000006 A1 WO1993000006 A1 WO 1993000006A1 US 9205059 W US9205059 W US 9205059W WO 9300006 A1 WO9300006 A1 WO 9300006A1
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Classifications
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- 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
- A61K47/30—Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
- A61K47/32—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. carbomers, poly(meth)acrylates, or polyvinyl pyrrolidone
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/24—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing ingredients to enhance the sticking of the active ingredients
-
- 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
- A61K47/30—Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
- A61K47/36—Polysaccharides; Derivatives thereof, e.g. gums, starch, alginate, dextrin, hyaluronic acid, chitosan, inulin, agar or pectin
- A61K47/38—Cellulose; Derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0019—Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0043—Nose
Definitions
- This invention relates generally to methods and compositions for applying a bioactive agent to a surface upon which enhanced bioeffect is desired.
- bioactive agent-containing composition having a low viscosity which permits the use of conventional spraying equipment for application.
- certain pesticides and herbicides which are employed in the protection of plant life are easily applied by spraying equipment.
- rapid run-off of the low viscosity material results in the need for a high frequency of spraying, with corresponding increase in cost, effort, and environmental damage.
- a delivery method which provides increased retention of the composition on protected surfaces such as the leaves of foliage.
- ingestibles can be protected with a coating which is conveniently applied in liquid form by spraying.
- the coating may reduce the effects of air on the ingestible substance through incorporation of protective bioactive agents, such as preservatives.
- These sprayable compositions generally drain-off or are absorbed into such foods. The protective effect of the initial coating is thereby limited.
- bioactive agents which are commonly applied to surfaces of the bodies of living beings. They include, for example, various forms of therapeutic drugs, cosmetic agents, sun screens, insect repellents, etc. In many instances, it is desired that a liquid formof such materials be applied, especially by spray, and that the material be retained on the substrate to increase the duration of its effectiveness.
- Gels and/or ointments have the capacity to reside for a greater time at a site of application than a sprayable fluid.
- Gels and ointments have three major disadvantages: inconvenience of use, particularly for chronic administration; inconsistency in the amount of drug applied in any given application and reduced area of contact.
- inconvenience of use particularly for chronic administration
- inconsistency in the amount of drug applied in any given application and reduced area of contact.
- This invention provides, in accordance with a first aspect thereof, such a bioactive composition.
- This composition is characterized by a bioactive agent and a hydrophilic polymer in an incompletely hydrated state.
- the agent and polymer are essentially dissolved in a substantially water-miscible solvent system to produce a composition having a viscosity of less than about 350 centipoise (cP), and which increases to in excess of 1000 cP upon dilution with water.
- cP centipoise
- Another aspect of the present invention relates to a method for forming a bioactive coating on a substrate. This method involves the steps of applying the foregoing bioactive composition to a substrate and diluting with water to transform the composition into a gel coating. -4-
- FIG.1 is a graphical illustration showing the apparent viscosity plotted against percentage of water for three solution concentrations of a hydrophilic polymer (Carbopol 934P) in a propylene glycol-water solvent system;
- FIG. 2 is a graphical representation of apparent viscosity plotted against weight percent of Carbopol 934P in a 50%/50% propylene glycol/water mixture;
- FIG. 3 shows temperature effects on apparent viscosity for the Carbopol 934P solution shown in FIG. 2;
- FIG.4 is a graphical representation which illustrates the relationship between viscosity and the concentration of hydroxypropylcellulose in a solvent system comprising 64%/36% methanol/water;
- FIG. 5 is a graphical representation which illustrates the relationship between viscosity and water content for a 1% solution of hydroxypropylcellulose in a methanol/water solvent system
- FIG. 6 is a graphical representation which illustrates the relationship between viscosity and the concentration of sodiumcarboxymethylcellulose in a 64%/36% methanol/water solvent system
- FIG. 7 is a graphical representation which illustrates the relationship between viscosity and water content for a 1% solution of sodium carboxymethylcellulose in methanol/water solvent system
- FIGS. 8 and 9 are graphical plots of plasma level of drug (ng/ml) versus time for the nasal administration of propranolol to two dogs via a specific, illustrative embodiment of a drug delivery system in accordancewith the present invention
- FIGS. 10 and 11 are graphical plots of plasma level of drug (ng/ml) versus time for the nasal administration of propranolol to two dogs of another specific, illustrative embodiment of a drug delivery system in accordance with the present invention
- FIG. 12 is a graphical plot of plasma level of drug (ng/ml)versus time over a two hour period after intranasal administration of progesterone to two dogs via a drug delivery of the present invention
- FIG. 13 is a graphical of the percent of release or loss of miticide from leaf samples versus time over a twenty- four hour accelerated aging study on compositions with and without a hydrophilic polymer of the present invention.
- FIG. 14 is a compound bar graph illustrating the relative distributions of absorbed, washed or residual miticide formulations of the foregoing study after aging.
- the present invention is partially premised on minimizing the run-off of a liquid composition containing a predetermined bioactive agent and extending the residence time thereof at a preselected site of application. This is accomplished by causing the viscosity of the delivery composition to increase in response to the addition of moisture.
- the bioactive compositions of the present invention are free-flowing liquids containing a predetermined bioactive agent and a hydratable, hydrophilic polymer essentially dissolved in a solvent system carrier.
- a hydratable, hydrophilic polymer essentially dissolved in a solvent system carrier.
- the term "essentially dissolved” refers to any substantially homogeneous dispersion.
- the dispersion is a true solution, although a colloid or other liquid composition containing only minute and uniformly distributed solids will suffice.
- the hydrophilic polymer in the present compositions should be in an "incompletely hydrated state".
- the polymer must be susceptible of increasing its degree of hydration. It is hydration, which occurs incident the eventual dilution of the present compositions with water, which spurs the instant increase in viscosity.
- the hydrophilic polymer employed in the present compositions is essentially anhydrous. Hence, it may contain no or virtually no water of hydration. In some embodiments, however, the solvent system is not anhydrous. Such a systemmay even contain a substantial amount of aqueous solvent, including up to 25% water by weight, dependent upon the remaining solvent and polymer selected. In these latter embodiments, the hydrophilic polymer is partially hydrated although not sufficiently for it to uncoil substantially in the manner previously discussed.
- the rheological properties of the bioactive delivery composition should be such that the introduction of water causes a dramatic transition from a free-flowing fluid state into, most desirably, a viscoelastic gel (in excess of 10,000 cP) .
- This dramatic increase in viscosity should be achievable with only a relatively minor input of water, desirably less than 40%, most desirably less than 10%, water by composition weight.
- Any bioactive agent which is dispersed in the composition will be entrapped within the resultant gel matrix and be retained in place for release at the site of application.
- the polymer In order for the polymer to expand in the solvent, thereby resulting in an increase in viscosity or formation of a gel, it is necessary that the polymer also be essentially soluble in the solvent system after addition of water. If the polymer is not then soluble, precipitation will occur and no substantial increase in viscosity is obtained.
- exemplary polymers which may be employed include, without limitation, homopolymers of acrylic acid monomer such as polyacrylic acid; copolymers of acrylic acid obtained by the copolymerization of acrylic acid as a main component with methacrylic acid, styrene, or vinyl ethers as comonomer; vinyl polymers such as polyhydroxyethyl acrylate, polyhydroxyethyl methacrylate, polyvinyl alcohol, or polyvinyl pyrrolidone; cellulose derivatives, such as the lower alkyl cellulose ethers including methyl cellulose, ethyl cellulose, propyl cellulose, hydroxyethyl cellulose, hydroxypropyl cellulose, carboxymethyl cellulose, etc.
- the salts of these polymers are also suitable.
- the hydratable polymer is selected from the group consisting of homopolymers of acrylic acid monomer, copolymers of acrylic acid; vinyl polymers; poly(ethylene oxide) polymers; cellulose derivatives; and the non-toxic, pharmaceutically acceptable salts of these polymers.
- the hydrophilic polymer is ionic (either acidic or basic) and may be subjected to a neutralizing agent to form an acid:base complex or polymer salt.
- the polymer salt is soluble in the solvent system so that it remains essentially dissolved. This ensures that it will be deliverable in a fluid, sprayable form.
- the polymer or its salt must be susceptible of hydration so that introduction of water into the solvent system will cause the polymer salt to uncoil, thereby drastically increasing the viscosity of the system.
- neutralizing agent refers to any agent which will enhance the solubility of polymer in the solvent system employed. This term does not necessarily refer to an agent for bringing the solution to a neutral pH (i.e. approximately 7). The choice of neutralizing agent depends upon whether the polymer is acidic or basic. If a neutral polymer is employed, the choice of neutralizing agent depends on whether an acidic or basic agent is required to increasepolymer solubility in the particular solvent system employed.
- the basic neutralizing agents of the present invention may be either an inorganic base or an organic amine. They are preferably soluble in both the non-aqueous solvent(s) and water.
- the neutralizing agent is an organic amine, especially triethanolamine.
- organic amines such as diisopropanolamine or monoethanolamine; basic amino acids, such as arginine, lysine, or histidine; or amine surfactants, such as Ethomeens or Jeffamines (trademarks of Jefferson Chemical Co.), can be employed in lieu of triethanolamine with similar results.
- the neutralizing agent should be an acid, such as an inorganic acid.
- the neutralizing agent is an organic amine and is selected from the group consisting of triethanolamine, diisopropanolamine, monoethanolamine, basic amino acids and amine surfactants. This agent is preferably present in an amount approximately between 0.3 and 10 percent by weight of the composition.
- the preferred neutralizing agent is triethanolamine.
- the acidic ionic polymer is Carbopol 934 or 934P (934P is the pharmaceutical grade of the Carbopol designated 934) .
- Carbopol is a registered trademark of the B. F. Goodrich Company, SpecialtyPolymers & Chemical Div. , Cleveland, OH 44131.
- Carbopol 934P generically known as Carbomer, is a synthetic highmolecular weight polymer of acrylic acid (MW 3,000,000) approved for human usage by the Food and Drug Administration. It is typically used in the pharmaceutical industry in controlled release tablets, oral suspensions, EKG gels and topical products.
- Carbopol 934P is a cross-linked acrylic acid-allyl sucrose copolymer (the preparation and description of Carbopol 934/934P are reported to be set forth in United States Patent Numbers 2,798,053 and 2,909,462).
- the hydrophilic polymer (most desirably Carbopol)is an acidic ionic polymer neutralized with an inorganic base and an organic amine.
- the neutralizing agent is an organic amine and is selected from the group consisting of triethanolamine, diisopropanolamine, monoethanolamine, basic amino acids and amine surfactants.
- the hydrophilic polymer employed is a basic polymer, and the neutralizing agent is an inorganic acid.
- the solvent system must contain a non-aqueous solvent.
- a non-aqueous solvent is propylene glycol
- a second solvent is a parenteral vehicle selected from the group consisting of dimethylacetamide, ethyl lactate, ethyl carbonate, dimethylformamide, dimethyl sulfoxide, and dioxolanes.
- the pharmaceutically- approved compound propylene glycol is a preferred solvent.
- propylene glycol can be an irritant at high concentrations. Therefore, in particularly preferred embodiments, the propylene glycol content of the non-aqueous solvent system is limited to approximately 55 percent by total weight. This limitation requires at least a second pharmaceutically acceptable solvent which does not materially increase the viscosity of the system or adversely alter the viscoelastic properties thereof.
- dimethylacetamide a known solvent currently used in parenteral formulations
- a second non-aqueous solvent in a propylene glycol system.
- Other non-aqueous parenteral vehicles such as ethyl lactate, ethyl carbonate, dimethylformamide, dimethyl sulfoxide, and dioxolanes are also acceptable co-solvents.
- the solvent system includes an oil.
- This oil solvent is selected from the group consisting of hydrophobic organic substances, such as hexadecane or benzyl alcohol, and oils derived from vegetable and animal sources, including an oil selected from the group consisting of vegetable oils, fixed oils, and essential oils.
- the oil may be selected from the group consisting of oils and hydrophobic organic substances, the oil being present in an amount of up to approximately 30 percent by weight of the composition.
- the oil may be selected from the group consisting of benzyl alcohol, hexadecane, and olive oil, and is preferably present in an amount approximately between 2 and 25 percent by weight of the composition.
- the solvent system may, in some embodiments, be an emulsion containing an oil phase and optional emulsifying agent.
- the oil of that phase may constitute any of the foregoing oils.
- Emulsification may be aided by the addition of a detergent or surfactant, synthetic or otherwise, which has the capacity to form micelles.
- the resulting non-aqueous emulsion should have a sprayable viscosity, i.e., less than about 350 cP.
- the solvent system of the bioactive agent delivery composition is provided with an emulsifying agent that agent is desirably a non-ionic surfactant of HLB less than about 15.
- the non-ionic surfactant is selected from the group consisting of Span 80, Span 65, Span 40, Tween 80 and Tween 65.
- the emulsifying agent may be Span 80, a sorbitan ester surfactant with an HLB of 4.3. Additionally any of many other non-ionic surfactants having a relatively low HLB (less than about 15), including without limitation.
- Span 65, Span 40, Tween 80 and Tween 65 may be employed in the practice of the invention.
- the invention contemplates a method of forming a coating on a substrate.
- This method comprises the steps of applying a bioactive agent and a hydrophilic polymer in an incompletely hydrated state which are essentially dissolved in a substantially water-miscible solvent system to a substrate, the composition having a viscosity of less than 350 centipoise; and diluting the composition with water, whereby the water interacts with the polymer to form a gel coating on the substrate, the gel having a viscosity in excess of 1000 centipoise.
- the step of applying includes spraying the liquid composition onto the substrate.
- Such a dual compartment dispenser is particularly useful in a situation where the bioactive agent delivery composition is being applied to a dry surface or where an aqueous polymer system is employed to a dry surface.
- the importance of the characteristics of the polymer (or its neutralized salt) may be seen from the following representative study.
- FIG. 1 is a graphical illustration showing apparent viscosity plotted against percentage of water in a propylene glycol-water system for three concentrations of Carbopol 934P (CBP 934 P).
- CBP 934 P Carbopol 934P
- the viscosities of solutions of Carbopol 934P in pure propylene glycol do not change to any significant degree with increasing Carbopol 934P concentration.
- the viscosities of water-rich mixtures increase linearly with Carbopol 934P concentration as seen in FIG.2 which is a graphical representation of apparent viscosity plotted against weight percent Carbopol 934 P in a 50/50 propylene glycol/water mixture.
- the viscosities for aqueous solvent system were consistently higher than the corresponding non-aqueous propylene glycol systems. Moreover, the increase in aqueous solution viscosity over the corresponding viscosity in propylene glycol solution increased as a function of polymer concentration. It also was discovered that for a given concentration of Carbopol 934P, an increase in thewater content inamixture increased the viscosity. The increase in viscosity ranged from about two-fold for 0.2 percent Carbopol 9334P to about ten-fold for a 1.0 percent Carbopol concentration.
- FIG. 3 shows temperature effects on apparent viscosity for the Carbopol 934P solution shown in FIG.2. These temperature effects are essentially minor and reversible.
- the increase in viscosity upon changing solvent composition from pure propylene glycol to a water-containing system is substantial, particularly at higher concentrations of Carbopol 934P.
- Carbopol 934P concentrations result in a more viscous non-aqueous solution.
- This goal may be achieved by altering the solubility of the Carbopol 934P-triethanolamine salt in propylene glycol by the addition of chemical components which are very soluble in propylene glycol.
- Solubility-adjusting components may form an oil phase emulsion and comprise hyrophobic additives and/or emulsifying agents which are miscible in propylene glycol, all as previously described.
- a specific illustrative composition of the bioactive agent delivery compositions of the present invention is as follows, all percentages are by weight:
- Bioactive Agent This formulation has a viscosity of around 100-200 cP.
- the formulation can be delivered consistently and without difficulty using commercially available mechanical delivery systems, such as ametered dose nebulizer for intranasal delivery.
- Each spray from a typical nebulizer delivers a total of about 0.1 g of the formulation and, hence, about 5 mg of the bioactive agent.
- the density of this formulation is about 1.001 g/cc.
- Hydrophilic Polymer 0.1% to 10% by weight of the composition
- Second Solvent 0% to 99% of the solvent system
- Oil Solvent 0% to 30% by weight of the composition
- Bioactive Agent 0.05% to 20% by weight of the composition
- Emulsifying Agent 0% to 5% by weight of the composition
- Neutralizing Agent 0% to 20% by weight of the composition
- Carbopol 934P 0.60% to 2.00% Propylene glycol 30.00% to 55.00% Dimethylacetamide 30.00% to 55.00% Benzyl Alcohol 2.00% to 25.00% Bioactive Agent (Drug) 1.00% to 10.00% Span 80 0.50% to 2.00% Triethanolamine 0.03% to 10.00%
- Examples 2 and 3 are similar in composition to Example 1, but incorporate hexadecane and olive oil, respectively, as the oil solvent instead of benzyl alcohol as set forth in Example 1.
- the enhancement in viscosity can be as much as about thirty-fold at low shear rate.
- the enhancement in viscosity for the two formulations at 25°C and 35°C at a shear rate of 10 per second is set forth in Table 4. Apparent viscosity is a function of shear rate and this low shear rate (10 per second) is typical of ciliary beat frequencies in the nasal cavity.
- Example 3 31 25 + 30% Water
- a hydrophilic polymer and non-aqueous solvent system having the appropriate rheological characteristics for use in the practice of the present invention are given below:
- Example 5 sodium carboxy methylcellulose (CMC) 20 g methanol qs 1000 ml
- compositions incorporate non-ionic polymers and exhibit increases in viscosity upon being subjected to the presence of water.
- the viscosity effect in the presence of water is tabulated herein below:
- FIG.4 is a graphical representation which illustrates the relationship between viscosity and the concentration of hydroxypropyl cellulose (HPC H) in a solvent system comprising 36% water in methanol. Viscosity is seen to increase linearly for greater polymer concentrations.
- FIG. 5 is a graphical representation which illustrates the relationship between viscosity of a 1% solution of HPC H in methanol and the amount of water in the solvent system. A substantial increase in viscosity is observed upon introduction of greater than about 35 percent water to the solvent system.
- HPC H hydroxypropyl cellulose
- FIG.6 is a graphical representation which illustrates the relationship between viscosity and the concentration of sodium carboxyy methylcellulose (sod. CMC) in a solvent system comprising 36% water in methanol. The viscosity is seen to increase linearly with increasing polymer concentration.
- FIG. 7 is agraphical representationwhich illustrates the relationship between the viscosity of 1% of sodium CMC suspended in methanol and the amount of water introduced into the solvent system. A substantial increase in viscosity is seenforwater concentrations in excess of 20 percent.
- the method of preparation of the non-aqueous liquid carrier or vehicle includes the steps of dissolving or otherwise dispersing the hydrophilic polymer in at least one solvent and adding a bioactive agent to the resultant dispersion.
- the bioactive agent may be added directly to the dispersion, or may first be first dispersed in solvent.
- the neutralizing agent is normally added to polymer in the solvent system.
- the solution or emulsion thus formed should be a free-flowing liquid having a low viscosity of less than 350 cP, and preferably about 100 to 200 cP.
- these agents are broadly classified in three categories: a) cationic agents, such as propranolol hydrochloride, which interact with the hydratable polymer such as the acrylic acid polymer Carbopol 934P; b) hydrophobic agents, such as progesterone, which could alter the solubility characteristics in the non-aqueous solvent or the oil phase; and c) all other agents which are not included in category (a) or (b).
- cationic agents such as propranolol hydrochloride
- the hydratable polymer such as the acrylic acid polymer Carbopol 934P
- hydrophobic agents such as progesterone
- e ulsifier e.g. Span 80, 1.1.5 g
- hydrophobic bioactive e.g. progesterone, 5-6 g
- solvent e.g. propylene glycol, 35 g
- a neutralizing agent e.g. triethanolamine, 0.3 to 0.35 g
- an emulsifying agent e.g. Span 80, 1-1.2 g
- oil solvent e.g. benzyl alcohol or olive oil, 4-5 g
- bioactive agent e.g. 1.1 bis(p-chlorophenyl) - 2,2,2-trichloroethanol 5- 6 g
- emulsifying agent e.g. Tween 80, 2-3 g
- the temperature range for the preparation of the formulations in accordance with the foregoing is from ambient temperature to about 70°C or higher depending upon the thermal stability of the components. Heating Carbopol 934P, for example, above the 70°C range can irreversibly degrade the polymer and result in loss of its viscosity-enhancement properties. Many drugs are also adversely affected by elevated temperatures.
- the emulsions and/or solution of the present invention may be stable over extended periods of time (at least 4 months). Exposure to light may result in slight discoloration. Therefore, it is preferable to store the present compositions in opaque containers.
- the drug selected was propranolol, an adrenergic drug which undergoes extensive first-pass metabolism in the liver, and therefore, has very low bioavailability when administered orally.
- Specific formulations used in the experiment are given below, expressed in terms of weight percentages:
- the experiments were carried out on male beagle dogs, each roughly 10 kg in weight.
- the dogs were fasted overnight before each study and food was withheld until the end of the experiment.
- the dogs were restrained in a dog sling.
- Approximately 10 mg of propranolol was administered nasally to each dog by spraying an appropriate amount of the present formulations containing propranolol into both nostrils of the dog using a metered dose dispenser (typically 2 sprays over a two minute period) .
- the amount of drug administered nasally was obtained by weighing the dispenser before and after spraying.
- Blood samples were withdrawn at desired intervals from each dog through a cannula inserted in the cephalic vein. The blood samples were centrifuged immediately after the collection and the plasma samples were stored frozen until assayed.
- the assay for propranolol consisted of HPLC separation and UV/fluorescence detection.
- FIGS. 8 through 11 are plots of plasma level (ng/ml) of drug versus time curves. Specifically, FIGS. 8 and 9 are graphical plots of the plasma level of propranolol as a function of time for two dogs following nasal administration of the propranolol delivery system of Formulation 1. FIGS. 10 and 11 are graphical plots of the plasma level of propranolol versus time for the same two dogs following nasal administration of the propranolol delivery system of Formulation 2.
- the nasal bioavailability is presented as a fraction of the bioavailability of an equivalent dose of propranolol (lOmg) administered intravenously.
- the area under the curve (AUC) has been normalized to the amount of propranolol administered. It is evident from the results that the enhancement in bioavailability of propranolol administered nasally using the formulations of the present invention is about ten-fold greater than that obtained by oral administration of propranolol in tablet form.
- Progesterone As a specific example of a bioactive agent delivery system containing a category (b), or hydrophobic, drug, the following composition incorporating progesterone as the bioactive agent was produced. This formulation was tested _in_ vivo for blood level in comparison to a non-aqueous solution of progesterone (Formulation 4) which was not prepared in accordance with the principles of the invention and which, therefore, does not exhibit the advantageous viscosity augmentation characteristic of Formulation 3 upon administration to themucosa.
- Formulation 4 a non-aqueous solution of progesterone
- Formulation 3 was produced by dissolving progesterone in a solvent system of propylene glycol and benzyl alcohol.
- the Carbopol 934P polymer was dissolved in dimethylacetamide and combined with the progesterone-containing solution.
- Triethanolamine and Span 80 were then added to form a fluid, low viscosity emulsion.
- Test formulations 3 and 4 were administered into the nostrils of four male beagles in an atomized form on three separate days to assess the absorption of the formulations by the mucosa.
- the dogs received two sprays in each nostril (10 mg) and blood samples were withdrawn and analyzed as set forth in the propranolol studies discussed hereinabove.
- the nostrils of the dogs were examined before dosing and following dosing at the same intervals at which the blood samples were obtained for the progesterone assays. No nasal irritation was observed in the progesterone treated animals.
- FIG. 12 shows the plasma levels of progesterone in ng/ml versus time over a two hour period post dosing for Formulations 3 and 4.
- FIG. 12 graphically demonstrates the superior bioavailability achievable by use of the novel progesterone delivery system of the present invention.
- Miticide Comparative formulations of a miticide solution for use in the protection of plant foliage were prepared. They differed essentially by whether or not they contained Carbomer 934P so as to comprise a bioactive agent delivery composition in accordance with the present invention. Their formulas were as follows: Weight (%)
- Keltane EC Dimethyl Acetamide Propylene Glycol Benzyl Alcohol Carbomer 934P Triethanolamine Span 80
- the formulation of Formula A was prepared in accordance with the present invention by forming a first solution by dissolving the Keltane EC in benzyl alcohol and then adding the propylene glycol. Separately, the Carbomer 934P was slowly added to the dimethyl acetamide in a magnetic stirrer to form a second solution. After combining the solutions, while continuing mixing, the triethanolamine and Span 80 were added sequentially.
- the formulation of Formula B (the placebo or control to Formula A) was prepared in the same manner, except for omission of the step of adding the Carbomer 934P. To compare the relative effectiveness of these two formulations, squares (10 cm by 10 cm) were cut from the center of peace lily leaves. These test squares were then placed in a humidifier (Model HC 22, Soundesign, Jersey City, NJ) and exposed to maximum humidification (6 mL/ in) for 5 minutes.
- a humidifier Model HC 22, Soundesign, Jersey City, NJ
- test squares were sprayed with 0.1 mL respectively of Formula A or B. This deposited 105 mg of formula on each square.
- the test squares were then placed 10 centimeters in front of the humidifier spout, arranged so that their planes formed an angle of 45 degrees from the horizontal.
- the humidifier was then operated at maximum with its output stream being directed onto the top surfaces of the test squares.
- the condensed drippings from the test square surfaces were monitored periodically for 24 hours by ultraviolet spectroscopic analysis for miticide washed from the leaf test squares. The results of these periodic analyses were as follows:
- hydrophilic polymer of the present invention is responsible for an eleven (11) fold increase in topical retention.
- the present invention affords a method of plant treatment which will achieve a given effect both at a lower application level for the bioactive agent and over a lengthened period of effective bioactivity on a plant.
- the bioactive agent can be more economically utilized, with reduced danger of adverse ecological impact beyond its desired site of activity.
- analgesic and anti-inflammatory agents include, without limitation, analgesic and anti-inflammatory agents, anti-inflammatory enzyme preparations, anti-inflammatory steroids, antihistamines, antibiotics, antibacterial agents, chemotherapeutic agents, local anesthetics, cardiac tonics, vasodilators, antitussive and expectorants, oral antiseptics, hemostats, hormones, hypotensive agents, sedative or tranquilizers, anti-tumor
- bioactive agents may be used singly or as a mixture of two or more such agents, and in amounts sufficient to prevent, cure, or treat a disease, as the case may be, to which the pharmaceutical preparation delivered in accordance with the principles of the invention is to be applied.
- bioactive agent delivery composition of the present invention is applicable to other routes of drug administration such as transdermal, parenteral, rectal, vaginal, ophthalmic, otic, etc.
- bioactive agents include, all plant treatment chemicals such as pesticides; non-therapeutic materials which are applied to the surfaces of the bodies of living beings, such as cosmetic agents, sun screens, skin softeners, acne treating agents, perfumes, etc.
- certain foods or other ingestibles can be protected with a coating which is applied in liquid form, but which gels to produce a protective layer which excludes air and may incorporate other materials such as preservatives, antioxidants, and nutritional agents, such as vitamins and/or minerals.
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Abstract
Description
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Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SK13693A SK13693A3 (en) | 1991-06-27 | 1992-06-17 | Bioaktive composition |
BR9205313A BR9205313A (en) | 1991-06-27 | 1992-06-17 | Bioactive composition |
CZ93252A CZ25293A3 (en) | 1991-06-27 | 1993-02-22 | Biologically active preparation |
NO93930620A NO930620L (en) | 1991-06-27 | 1993-02-23 | BIOACTIVE COMPOSITION |
FI930847A FI930847A (en) | 1991-06-27 | 1993-02-25 | BIOACTIVE ACTIVITIES |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US07/722,511 US5221698A (en) | 1991-06-27 | 1991-06-27 | Bioactive composition |
US722,511 | 1991-06-27 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1993000006A1 true WO1993000006A1 (en) | 1993-01-07 |
Family
ID=24902155
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US1992/005059 WO1993000006A1 (en) | 1991-06-27 | 1992-06-17 | Bioactive composition |
Country Status (12)
Country | Link |
---|---|
US (2) | US5221698A (en) |
EP (1) | EP0555427A4 (en) |
JP (1) | JPH06501029A (en) |
AU (1) | AU2302592A (en) |
BR (1) | BR9205313A (en) |
CA (1) | CA2090480A1 (en) |
FI (1) | FI930847A (en) |
HU (1) | HUT63539A (en) |
MX (1) | MX9203477A (en) |
PL (1) | PL298146A1 (en) |
SK (1) | SK13693A3 (en) |
WO (1) | WO1993000006A1 (en) |
Cited By (3)
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1991
- 1991-06-27 US US07/722,511 patent/US5221698A/en not_active Expired - Fee Related
-
1992
- 1992-06-17 PL PL29814692A patent/PL298146A1/en unknown
- 1992-06-17 HU HU9300864A patent/HUT63539A/en unknown
- 1992-06-17 BR BR9205313A patent/BR9205313A/en not_active Application Discontinuation
- 1992-06-17 CA CA002090480A patent/CA2090480A1/en not_active Abandoned
- 1992-06-17 JP JP5501535A patent/JPH06501029A/en active Pending
- 1992-06-17 EP EP19920914868 patent/EP0555427A4/en not_active Withdrawn
- 1992-06-17 WO PCT/US1992/005059 patent/WO1993000006A1/en not_active Application Discontinuation
- 1992-06-17 SK SK13693A patent/SK13693A3/en unknown
- 1992-06-17 AU AU23025/92A patent/AU2302592A/en not_active Abandoned
- 1992-06-26 MX MX9203477A patent/MX9203477A/en unknown
-
1993
- 1993-02-25 FI FI930847A patent/FI930847A/en not_active Application Discontinuation
-
1994
- 1994-08-02 US US08/284,171 patent/US5455286A/en not_active Expired - Fee Related
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US3920436A (en) * | 1972-08-07 | 1975-11-18 | Minnesota Mining & Mfg | Artificial protective environment for plants |
EP0143297A1 (en) * | 1983-10-21 | 1985-06-05 | Fearing Manufacturing Co., Inc. | In situ insecticide |
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Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6617293B2 (en) | 2001-08-06 | 2003-09-09 | 3M Innovative Properties Company | Thickening on dilution liquid soap |
US11083796B2 (en) | 2005-07-26 | 2021-08-10 | Durect Corporation | Peroxide removal from drug delivery vehicle |
US11400019B2 (en) | 2020-01-13 | 2022-08-02 | Durect Corporation | Sustained release drug delivery systems with reduced impurities and related methods |
US11771624B2 (en) | 2020-01-13 | 2023-10-03 | Durect Corporation | Sustained release drug delivery systems with reduced impurities and related methods |
Also Published As
Publication number | Publication date |
---|---|
CA2090480A1 (en) | 1992-12-28 |
FI930847A (en) | 1993-04-05 |
JPH06501029A (en) | 1994-01-27 |
EP0555427A4 (en) | 1994-07-06 |
HUT63539A (en) | 1993-09-28 |
FI930847A0 (en) | 1993-02-25 |
AU2302592A (en) | 1993-01-25 |
MX9203477A (en) | 1993-12-01 |
US5455286A (en) | 1995-10-03 |
PL298146A1 (en) | 1993-11-02 |
EP0555427A1 (en) | 1993-08-18 |
SK13693A3 (en) | 1993-07-07 |
BR9205313A (en) | 1994-06-21 |
HU9300864D0 (en) | 1993-07-28 |
US5221698A (en) | 1993-06-22 |
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