The present invention discloses a nano-cluster that includes a plurality of nano-particles, wherein the nano-particles can disperse in response to an environmental cue. Also disclosed is a method of preventing, treating, or diagnosing a disease or condition in a subject comprising administering a therapeutically effective amount of a composition comprising nano-clusters of the present invention.

Description of the Invention

SUMMARY OF THE INVENTION

The present invention overcomes the deficiencies in the art by providing effective drug delivery systems that can: (1) formulate nano-particles as a nano-cluster to facilitate handling, administering, or targeting, for example; and (2) maintain the cluster or disperse the nano-particles at the targeted site.

In one aspect of the present invention, there is disclosed a nano-cluster comprising a plurality of nano-particles. In certain non-limiting aspects, the nano-cluster is maintained at the targeted site (e.g., the nano-cluster does not disperse into separate nano-particles). In other aspects, the nano-particles disperse in response to an environmental cue. The nano-cluster, in certain non-limiting embodiments, can have a size of about 1 to about 200 microns. In certain aspects, the nano-cluster size is 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 100, 110, 120, 130, 140, 150, 160, 170, 180, 190, or 200 microns. In other aspects, the size of the nano-cluster can be greater than 200 microns (e.g., 210, 220, 230, 240, 250, 300, 350, 400, 450, 500, 600, 700, or more microns in size.) The nano-cluster of the present invention can also have a variety of shapes (e.g, spherical and non-spherical shapes). In certain embodiments, the nano-cluster can be solid or hollow. A person of ordinary skill in the art will recognize that a solid nano-cluster can be completely solid throughout or can have spaces, such as pores or a hollow core, that are created by the packing of the nano-particles within the nano-cluster. The size of these packing spaces can be from about 1 nm to about 1000 nm, in non-limiting aspects. In certain aspects, the size of the packing spaces can be about 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 20, 30, 40, 50, 60, 70, 80 , 90, 100, 150, 200, 250, 300, 350, 400, 450, 500, 550, 600, 650, 700, 750, 800, 850, 900, 950, 1000 or more nanometers, in non-limiting aspects. Hollow nano-clusters can have an empty space or cavity. The size of the cavity can vary, for example, from about 50 m to about 20 .mu.m, in non limiting aspects. The size of the cavity, for example, can be 50, 100, 150, 200, 250, 300, 3500, 400, 450, 500, 550, 600, 650, 700, 750, 800 . . . 20 .mu.m, and any range derivable therein.

The nano-particles that are included in the nano-cluster, in some embodiments, are not held (e.g., adhered or chemically bound (e.g., covalent bond, non-covalent bond, van der waals forces)) together by a functional group on the nano-particles. The nano-particles can be in direct contact with one another in some aspects. In other aspects, the nano-particles are not in direct contact with one another. In certain embodiments of the present invention, the nano-particles are not encapsulated. In other embodiments, the nano-particles do not include a functional group. In other aspects, however, the nano-particles can include a functional group such as, for example, a carboxyl, sulhydryl, hydroxyl, or amino group. All types of functional groups that can be used to bind other nano-particles together, active ingredients to the surface of nano-particles, or other compounds are contemplated as being useful with the present invention.

In certain embodiments, the nano-cluster can include an active ingredient. Non-limiting examples of active ingredients that are contemplated as being useful in the context of the present invention include those known to a person of ordinary skill and those described throughout this specification. By way of example only, active ingredients can include medical pharmaceuticals and specialties such as preventive agents, for example vaccines, diagnostic agents, for example tracers of various types and imaging enhancers, therapeutic agents, for example small molecules (e.g., nucleic acids, proteins, peptides, polypeptides, etc.), drugs, peptides, and radiation, immuno-modulators, vaccine and virus vectors, and combinations of these classes. The nano-particles can include particular embodiments, respirable non-medical specialties such as physiochemical agents, for example gas antidotes, biophysical modulators, for example paramagnetics, emitters, for example electromagnetic wave emitters, and imaging enhancers. The active ingredients, in certain embodiments, can be associated with the nano-particles. For example, the active ingredients can be entangled, embedded, incorporated, encapsulated, bound to the surface (e.g., covalently or non-covalently bonded), or otherwise associated with the nano-particle. In certain preferred aspects, the active ingredient is the nano-particle. In other aspects, the nano-particles can include a polymer material (including, for example, biodegradable and non-biodegradable polymers). Non-limiting examples of polymer materials that can be used include those known to a person of ordinary skill and those described throughout this specification. In certain embodiments, the nano-particles can include a mixture of a polymer and an active ingredient.

In other non-limiting embodiments, the nano-cluster or nano-particles, or both, can include at least one, two, three, four, five, six, seven, or more different active ingredients. In a preferred embodiment, the nano-cluster or nano-particles include a first drug on its surface, and a second active ingredient encapsulated within the nano-cluster or nano-particles or other incorporated into the nano-cluster or nano-particle material. It is contemplated that a nano-cluster can release the active ingredients in a given environment, or after a given period of time in a controlled manner. For example, a nano-cluster having at least one active ingredient can be released in response to an environmental cue or after a pre-determined amount of time. Also by way of example only, a nano-cluster having at least two different active ingredients can be released in response to different environmental cues or after pre-determined periods of time. For example, active ingredient 1 can be released first and then active ingredient 2 can be released second. In certain non-limiting aspects, the release of the first active ingredient can improve the performance of the second active ingredient.

In other particular aspects, the nano-clusters of the present invention can include a dispersing material that holds the plurality of nano-particles together and/or disperses the nano-particles in response to an environmental cue. The dispersing materials that can be used with the present invention include those materials that are known to a person of skill in the art and those that are disclosed throughout this specification. Non-limiting examples of dispersing material include liquid sensitive materials (e.g., water-soluble materials (e.g., polymers)), biodegradable polymers, polyelectrolytes, metals, surfactants, polymeric cross-linkers, small molecule cross-linkers, pH sensitive materials, pressure sensitive materials, enzymatic sensitive materials, and temperature sensitive materials. Non-limiting examples of environmental cues that can be used with the present invention include liquid (e.g., water, blood, mucous, solvent, etc.), a selected pH range, a selected temperature range, an electric current, a selected ionic strength, pressure, the presence of a selected enzyme, protein, chemical, electromagnetic wavelength range (e.g., visible light, UV light, infrared, ultraviolet light, microwaves, X-rays, and gamma-rays), or the presence of an external force (e.g., vibration, shearing, shaking, etc.). In certain aspects, the dispersing material can be coated onto the surface of the nano-particles before or after nano-cluster formation. In certain embodiments, the dispersing material can be between the nano-particles or link the nano-particles together (e.g., covalently or non-covalently couple a first nano-particle to a second nano-particle). The dispersing material can be adhered to or covalently or non-covalently coupled to the nano-particles.

In particular embodiments of the present invention, the nano-cluster can include from about 1% to about 99% by weight or volume of the nano-particles or dispersing materials. The nano-cluster can also be completely made up of nano-particles (i.e., 100%). In preferred embodiments, the nano-cluster includes from about 10% to about 90%, 15% to about 80%, 20% to about 70%, 30% to about 60%, and about 40% to about 50% of nano-particles or dispersing materials. In certain embodiments, the nano-cluster includes at least 50% of the nano-particles or dispersing material.

Another embodiment to the present invention is a composition comprising a nano-cluster of the present invention. The composition in certain non-limiting aspects can have a plurality (e.g., at least 2, 3, 4, 5, 6, 7, 8, 9, 10, 20, 30, 40, 50 , 60, 70, 80, 90, 100, 200, 300, 400, 500, or more nano-clusters. The composition can further include an active ingredient. As discussed throughout this specification, the composition can be formulated into a dry powder, an aerosol, a spray, a tablet, or a liquid. The compositions of the present invention can include at least about 1%, 2%, 3%, 4%, 5%, 6%, 7%, 8%, 9%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, or 100% of the nano-clusters of the present invention. In certain aspects, the compositions of the present invention can include a plurality of identical or similar nano-clusters. In other aspects, the compositions of the present invention can include at least 2, 3, 4, 5, 6, 7, 8, 9, 10, or more nano-clusters that have different characteristics (e.g., different active ingredients attached, different shapes, hollow or solid, etc.). The compositions of the present invention can be formulated into a pharmaceutically acceptable carrier.

In another embodiment, there is disclosed a method of preventing or treating a disease or condition in a subject comprising administering a therapeutically effective amount of a composition comprising a nano-cluster of the present invention to a subject (e.g., human, pigs, horses, cows, dogs, cats, mouse, rat, rabbit, or any other mammal and non-mammals) in need of the composition. The method can further include a method for determining whether a subject is in need of the prevention or treatment. The disease or condition can include all types of diseases or conditions known to a person of skill in the art and discussed throughout this specification. In certain preferred aspects, the disease or condition can be a pulmonary associated disease or condition (e.g., common cold, flu, cystic fibrosis, emphysema, asthma, tuberculosis, severe acute respiratory syndrome, pneumonia, lung cancer, etc.), a circulatory disease or condition, a muscular disease or condition, a bone disease or condition, an infection, a cancer, etc. In certain embodiments, the method can include the administration of a second therapy used to treat or prevent the disease (e.g., combination therapy). In preferred embodiments, the compositions of the present invention are administered nasally. Other modes of administration known to those of skill in the art or discussed in this specification are also contemplated. In particular aspects, the nano-clusters within the composition are delivered to the deep lung (e.g., bronchiole or alveolar regions of the lung).

In certain preferred aspects of the present invention, the nano-clusters of the present invention can be used to deliver vaccines or components of vaccines. For instance, cells of the immune system, especially macrophages and dendrocytes, are targets for immunization. These "professional" antigen-presenting cells (APCs) can elicit a desired T-cell response to vaccine components. APCs are typically capable of phagocytosis of particles in the range of 1 to 10 .mu.m. By generating in this size range nano-clusters or nano-particles containing vaccine components, one can passively target delivery of the vaccine to APCs. U.S. Pat. No. 6,669,961, for example, provides a non-limiting explanation of this process.

The nano-clusters of the present invention can also have a particular mass density. In certain preferred embodiments, for example, the mass density can be greater than, equal to, or less than 0.1 g/cm.sup.3. In particular embodiments, the mass density of the nano-clusters of the present invention can be about 0.01, 0.02, 0.03, 0.04, 0.05, 0.06, 0.07, 0.08, 0.09, 0.1, 0.2, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8, 0.9, 1.0, 1.1, 1.2, 1.3, 1.4, 1.5, 1.6, 1.7, 1.8, 1.9, 2.0 g/cm.sup.3, or greater.

Also disclosed is a method of preparing a nano-cluster comprising: (i) obtaining a plurality of nano-particles; (ii) obtaining a dispersion material (when desired); and (iii) admixing (i) and (ii), wherein the admixture is formulated into a nano-cluster. In certain aspects, obtaining a plurality of nano-particles comprises: (i) obtaining an aqueous suspension of nano-particles; (ii) emulsifying the suspension into a non-aqueous phase; (iii) allowing water in the aqueous suspension to absorb into the non-aqueous phase; (iv) allowing the nano-particles to aggregate together; and (v) retrieving the aggregated nano-particles. In other non-limiting embodiments, obtaining a plurality of nano-particles includes: (i) obtaining a non-aqueous suspension of nano-particles; (ii) emulsifying the suspension into an aqueous phase; (iii) allowing liquid in the non-aqueous suspension to absorb into the aqueous phase; (iv) allowing the nano-particles to aggregate together; and (v) retrieving the aggregated nano particles. The disclosed method represents a non-limiting method with other methods being evident by one skilled in the art (e.g. emulsion/solvent evaporation, extraction, spray-drying, spray freeze-drying, self-assembly in solution, etc.). In certain aspects, it is contemplated that the nano-clusters can be prepared in a solution without using spray and/or freeze dry techniques. It is also contemplated that the nano-clusters can be recovered from the solution by using freeze dry or spray dry techniques that are known to those of skill in the art. As noted throughout this specification, the nano-cluster can be included within a composition. The composition can be formulated into a liquid, a spray, an aerosol, or a dry powder in non-limiting embodiments.

Also disclosed is a method of delivering an active ingredient to a subject in need comprising obtaining composition comprising a nano-cluster of the present invention and an active ingredient and administering the composition to the subject. In non-limiting aspects, the active ingredient is encapsulated in the nano-particle, incorporated within the nano-particle material, conjugated to the nano-particle, absorbed or coupled to the nano-particle.

In yet another embodiment of the present invention, there is disclosed a method of preparing a nano-cluster comprising: (i) obtaining a first nano-particle and a second nano-particle; and (ii) admixing the first and second nano-particles, wherein the nano-particles self assemble to form a nano-cluster. The first and second nano-particles, for example, can have hydrophobic properties, hydrophilic properties, or a mixture of both. In other aspects, the first or second nano-particles can have an electrostatic charge. For example, the first nano-particle can be positively charged and the second nano-particle negatively charged, and vice versa. The self-assembly, in particular embodiments can be based on an electrostatic interaction between the first and second nano-particles. In other non-limiting aspects, the self-assembly can be based on a hydrophobic or hydrophilic interaction between the first and second nano-particles. The first and second nano-particles can self assemble in solution to form the nano-cluster in certain embodiments. In particular aspects, preparation of the nano-clusters does not require the use of spray and/or freeze dry techniques; rather nano-cluster formation can occur in solution. The nano-clusters can be recovered from the solution by using freeze dry or spray dry techniques that are known to those of skill in the art. In other aspects, the method of preparing the nano-cluster can further comprise obtaining a dispersion material and admixing the dispersion material with the first and second nano-particles.

As disclosed is a method of storing nano-particles comprising forming the nano-particles into a nano-cluster. The nano-particles, for instance, can be stored as a liquid, a spray, and aerosol, or a dry powder. The method of storing the nano-particles can further comprise returning the nano-cluster to nano-particles. In certain aspects, returning the nano-cluster to nano-particles can include subjecting the nano-cluster to an environmental cue. As noted above and throughout this specification, non-limiting examples of environmental cues include water, a selected pH, a selected temperature, a selected enzyme, a selected chemical, a selected electromagnetic wavelength range, vibration, or shearing. In certain particular aspects, the nano-cluster can include a dispersing material that holds the nano-particles together and/or disperses the nano-particles in response to an environmental cue. Non-limiting examples of dispersing materials include a water soluble polymer, a biodegradable polymer, a polyelectrolyte, a metal, a polymeric cross-linker, a small molecule cross-linker, a pH sensitive material, a surfactant, or a temperature sensitive material.

It is contemplated that any embodiment discussed in this specification can be implemented with respect to any method or composition of the invention, and vice versa. Furthermore, compositions of the invention can be used to achieve methods of the invention.

The terms "inhibiting," "reducing," or "prevention," or any variation of these terms, when used in the claims and/or the specification includes any measurable decrease or complete inhibition to achieve a desired result.

The term "effective," as that term is used in the specification and/or claims, means adequate to accomplish a desired, expected, or intended result.

The use of the word "a" or "an" when used in conjunction with the term "comprising" in the claims and/or the specification may mean "one," but it is also consistent with the meaning of "one or more," "at least one," and "one or more than one."

The term "about" or "approximately" are defined as being close to as understood by one of ordinary skill in the art. In one non-limiting embodiment the terms are defined to be within 10%, preferably within 5%, more preferably within 1%, and most preferably within 0.5%.

The use of the term "or" in the claims is used to mean "and/or" unless explicitly indicated to refer to alternatives only or the alternatives are mutually exclusive, although the disclosure supports a definition that refers to only alternatives and "and/or."

As used in this specification and claim(s), the words "comprising" (and any form of comprising, such as "comprise" and "comprises"), "having" (and any form of having, such as "have" and "has"), "including" (and any form of including, such as "includes" and "include") or "containing" (and any form of containing, such as "contains" and "contain") are inclusive or open-ended and do not exclude additional, unrecited elements or method steps.

DESCRIPTION OF ILLUSTRATIVE EMBODIMENTS

Current drug delivery treatment options can often be ineffective due to inefficient delivery of an active ingredient to a targeted site. Many of the current drug delivery systems are limited in their ability or efficiency to access a specifically targeted site. Although nano-particles offer several advantages for delivering drugs (e.g. improved dissolution of low solubility API, intracellular and transcellular transport, etc.), the use of nano-particles, for example, can be hindered by the inability to deliver nano-particles to the site of drug action (e.g. dried nano-particles are too small to deposit efficiently in the lungs, can avoid detection by APCs, etc.). In addition, nano-particles are often difficult to handle at an industrial scale and a controlled clustering process may ease handling and allow facile reconstitution and formulation of nano-particles or nano-clusters for delivering drugs.

The nano-clusters of the present invention can be used to deliver active ingredients to a targeted site. The size and distribution of the disclosed nano-clusters and nano-particles can be designed for a desired route of administration and/or for the treatment of a particular disease or condition. In one aspect, for example, the nano-clusters provide an effective and efficient drug delivery system that can carry nano-particles to a targeted site via the nano-cluster. In certain aspects, the nano-cluster is maintained at the targeted site. In other aspects, the nano-cluster can disperse the nano-particles at the targeted site. Additionally, the nano-clusters can be formulated with the appropriate physicochemical properties to carry and controllably release therapeutic nano-particles or active ingredients to a targeted site.

Another aspect of the invention is that the nano-clusters can be prepared in a solution without using standard spray and/or freeze dry techniques known to those of ordinary skill in the art.

These and other aspects of the present invention are described in further detail in the following sections.

A. Nano-Clusters

In certain non-limiting aspects, a nano-cluster of the present invention can include a plurality of nano-particles with or without a dispersing material that holds the plurality of nano-particles together. The dispersing material can also be used to disperse the nano-particles in response to an environmental cue. An active ingredient can also be incorporated into the nano-cluster. In other aspects, the nano-particle can be the active ingredient. FIG. 1 (see Original Patent), for example, illustrates a nano-cluster having a therapeutic nanoparticle and a dispersing material. This delivery system provides the advantage of particle clusters appropriately sized for delivery (e.g., lung, nasal passage, M-cells in the digestive tract, uptake by antigen presenting cells, etc.) with the benefits of nano-particles, such as improvements in drug solubility, bioavailability, transport through biological barriers, intracellular delivery, etc. As described in more detail throughout this specification, changing the nature of the dispersing material allows for the development of an environmentally responsive nano-particle delivery system and/or biosensors. In addition, the special arrangement of nano-particles within the cluster can allow discrete control over the duration and concentration of an active ingredient, a concept that can also be facilitated by the independent formulation of each nano-particle type before cluster formation.

The inventors have successfully formulated nanoclusters from a variety of nanoparticulate materials and have controlled the dispersion of clusters into constituent nanoparticles in aqueous solution (see Examples 1-3 below). In a non-limiting aspect, the inventors obtained a colloidal suspension of nanoparticles in deionized water which is subsequently emulsified into octanol. Water in the dispersed droplets then absorbs into the octanol phase. Nanoparticles can pack together as water is extracted from individual droplets until an aggregate of nanoparticles remains (FIG. 2 (see Original Patent)). The size of the droplet, in certain non-limiting embodiments, can serve as a template for controlling the size of the resulting nanoclusters depending on the concentration of nanoparticles within the droplet. In other aspects, the clustered nanoparticles in FIG. 2 (see Original Patent) can be held together by hydrophobic, coulombic, and/or Van der Waals forces and can resist dispersion into aqueous media.

These and other aspects of the nano-clusters of the present invention are described in further detail in the following subsections.

The term "nano-cluster," as that term is used in the specification and/or claims, means a cluster of nano-particles arranged such that the surface of the nano-particles are in contact with one another as shown in FIG. 2.

1. Nano-Particles

A nano-particle is a microscopic particle whose size is measured in nanometers. In preferred embodiments, the nanoparticles of the present invention have a size of from about 1 to about 3000 nanometers. In more particular aspects, the nano-particle has a size of 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 100, 110, 120, 130, 140, 150, 175, 200, 225, 250, 275, 300, 325, 350, 375, 400, 425, 450, 475, 500, 550, 600, 650, 700, 750, 800, 850, 900, 950, 1000, 1100, 1200, 1300, 1400, 1500, 1600, 1700, 1800, 1900, 2000, 2100, 2200, 2300, 2400, 2500, 2600, 2700, 2800, 2900, 3000, or more nanometers, or any range derivable therein.

It is contemplated that all types of materials and structures, including inorganic and organic materials, can be used for the nano-particles of the present invention. Non-limiting examples of these materials and structures include active ingredients (see specification), polymersomes, liposomes, and polyplexes. Additional non-limiting materials include poly(orthoesters), poly(anhydrides), poly(phosphoesters), poly(phosphazenes) and others. In preferred aspects, the material is the biodegradable polymer poly(lactic-co-glycolic acid) (PLGA). PLGA is a well-studied polymer for drug delivery and is FDA-approved for a number of in vivo applications. Other non-limiting materials include, for example, polyesters (such as poly(lactic acid), poly(L-lysine), poly(glycolic acid) and poly(lactic-co-glycolic acid)), poly(lactic acid-co-lysine), poly(lactic acid-graft-lysine), polyanhydrides (such as poly(fatty acid dimer), poly(fumaric acid), poly(sebacic acid), poly(carboxyphenoxy propane), poly(carboxyphenoxy hexane), copolymers of these monomers and the like), poly(anhydride-co-imides), poly(amides), poly(ortho esters), poly(iminocarbonates), poly(urethanes), poly(organophasphazenes), poly(phosphates), poly(ethylene vinyl acetate) and other acyl substituted cellulose acetates and derivatives thereof, poly(caprolactone), poly(carbonates), poly(amino acids), poly(acrylates), polyacetals, poly(cyanoacrylates), poly(styrenes), poly(vinyl chloride), poly(vinyl fluoride), poly(vinyl imidazole), chlorosulfonated polyolefins, polyethylene oxide, copolymers, polystyrene, and blends or co-polymers thereof. In certain preferred aspects, the nano-particles include hydroxypropyl cellulose (HPC), N-isopropylacrylamide (NIPA), polyethylene glycol, polyvinyl alcohol (PVA), polyethylenimine, chitosan, chitin, dextran sulfate, heparin, chondroitin sulfate, gelatin, etc. and their derivatives, co-polymers, and mixtures thereof. A non-limiting method for making nano-particles is described in U.S. Publication 2003/0138490, which is incorporated by reference.

In certain embodiments, the nano-particles can be associated with an active ingredient (e.g., entangled, embedded, incorporated, encapsulated, bound to the surface, or otherwise associated with the nano-particle). In certain preferred aspects, the active ingredient is the nano-particle. In a preferred but non-limiting aspect, the active ingredient is a drug such as a pure drug (e.g., drugs processed by crystallization or supercritical fluids, an encapsulated drug (e.g., polymers), a surface associated drug (e.g., drugs that are absorbed or bound to the nano-particle surface), a complexed drugs (e.g., drugs that are associated with the material used to form the nano-particle).

The nano-particles of the present invention, in certain embodiments, do not include a functional group. In other aspects, however, the nano-particles can include a functional group such as, for example, a carboxyl, sulhydryl, hydroxyl, or amino group. All types of functional groups that can be used to bind other nano-particles together, active ingredients to the surface of nano-particles, or other compounds are contemplated as being useful with the present invention. For instance, the functional groups can be available for drug binding (covalent or electrostatic).

2. Dispersing Material

In certain aspects of the present invention, the dispersing material can serve several functions. For example, it can be used to hold (e.g., adhere or chemical bind (e.g., covalent bond, no-covalent bond, van der wall forces) the nano-particles to one another via the dispersing material. In other aspects, the dispersing material can disperse the nano-particles at a targeted site in response to an environmental cue. This dispersing can occur, for example, when the dispersing material breaks-down, disintegrates, or other changes in such a way that it is no longer capable of holding the nano-particles together.

Non-limiting examples of dispersing materials that are contemplated as being useful with the present invention include liquid sensitive materials (e.g., water-soluble materials) such as polyoxyethylene sorbitan fatty acid esters, polyglycerol fatty acid esters, polyoxyethylene deriviatives, and analogues thereof, sugar esters, sugar ethers, sucroglycerides, (e.g. sucrose, xylitol and sorbitol) etc., biodegradable polymers (see list of polymers for nano-particle preparation), polyelectrolytes such as dextran sulfate, polyethylenimine, chitosan, chondroitin sulfate, heparin, heparin sulfate, poly(L-lysine), etc., metals (calcium, zinc, etc.), polymeric cross-linkers (polymethacrylate or similar derivatives with this functionality, poly(glutamic acid), poly(phosphorothioates), poly(propylene fumarate)-diacrylate, etc. and/or polymers with appropriate terminal or side chain reactive groups, small molecule cross-linkers (di-expoxies, di-acids, di-amines, etc.) such as 2-methylene-1,3-dioxepane, gluteraldehyde, dithiobis succinimidyl propionate, pH sensitive materials such as poly(.gamma.-glutamic acid), enzymatic sensitive materials such as poly(amino acids) (peptides, proteins, etc.) like poly(N-substituted alpha/beta-asparagine)s, polysaccharides, lipids, oils, etc., and temperature sensitive material such as (2-hydroxyethyl methacrylate), poly(N-isopropylacrylamide), poly(2-ethylacrylic acid-co-N-[4-(phenylazo)phenyl]methacrylamide), polymers of acrylic acid or acrylamide and related polymers including and co-polymers or blends of these in addition to those previously mentioned as nano-particle forming materials, and surfactants (e.g., nonionic, cationic, anionic, cryptoanionic, and zwitterionic surfactants (See McCutcheon's Emulsifiers & Detergents (2001); U.S. Pat. Nos. 5,011,681; 4,421,769; 3,755,560, 6,117,915)). Non-limiting examples of surfactants include esters of glycerin, esters of propylene glycol, fatty acid esters of polyethylene glycol, fatty acid esters of polypropylene glycol, esters of sorbitol, esters of sorbitan anhydrides, carboxylic acid copolymers, esters and ethers of glucose, ethoxylated ethers, ethoxylated alcohols, alkyl phosphates, polyoxyethylene fatty ether phosphates, fatty acid amides, acyl lactylates, soaps, TEA stearate, DEA oleth-3 phosphate, polyethylene glycol 20 sorbitan monolaurate (polysorbate 20), polyethylene glycol 5 soya sterol, steareth-2, steareth-20, steareth-21, ceteareth-20, PPG-2 methyl glucose ether distearate, ceteth-10, cetyl phosphate, potassium cetyl phosphate, diethanolamine cetyl phosphate, polysorbate 20, polysorbate 60, polysorbate 80, glyceryl stearate, PEG-100 stearate, tyloxapol, cetyltrimethylammonium bromide (CTAB), pluronic-68, and mixtures thereof.

Non-limiting examples of environmental cues that can cause the dispersing material to no longer be capable of holding the nano-particles together include liquid (e.g., water, blood, mucous, solvent, etc.), a selected pH range, a selected temperature range, an electric current, a selected ionic strength, pressure, the presence of a selected enzyme, protein, DNA, chemical, electromagnetic wavelength range (e.g., visible light, UV light, infrared, ultraviolet light, microwaves, X-rays, and gamma-rays), or the presence of an external force (e.g., vibration, shearing, shaking, etc.).

3. Active Ingredients

In certain non-limiting aspects, the nano-clusters of the present invention can include an active ingredient. Active ingredients include, but are not limited to, any component, compound, or small molecule that can be used to bring about a desired effect. Non-limiting examples of desired effects of the present invention include diagnostic and therapeutic effects. For example, a desired effect can include the diagnosis, cure, mitigation, treatment, or prevention of a disease or condition. An active ingredient can also affect the structure or function of body part or organ in a subject.

Active ingredients which can be used by the present invention include but are not limited to nucleic acids, proteins and peptides, hormones and steroids, chemotherapeutics, NSAIDs, vaccine components, analgesics, antibiotics, anti-depressants, etc. Non-limiting examples of nucleic acids that can be used include DNA, cDNA, RNA, iRNA, siRNA, anti-sense nucleic acid, peptide-nucleic acids, oligonucleotides, or nucleic acids that are modified to improve stability (e.g., phosphorothioates, aminophosphonates or methylphosphonates).

Proteins and peptides that can be used with the present invention include but are not limited to human growth hormone, bovine growth hormone, vascular endothelial growth factor, fibroblast growth factors, bone morphogenic protein, tumor necrosis factors, erythropoietin, thrombopoietin, tissue plasminogen activator and derivatives, insulin, monoclonal antibodies (e.g., anti-human epidermal growth factor receptor2 (Herceptin), anti-CD20 (Rituximab), anti-CD 18, anti-vascular endothelial growth factor, anti-IgE, anti-CD 11a) and their derivatives, single-chain antibody fragments, human deoxyribonuclease I (domase alfa, Pulmozyme), type-1 interferon, granulocyte colony-stimulating factor, leuteinizing hormone releasing hormone inhibitor peptides, leuprolide acetate, endostatin, angiostatin, porcine factor VIII clotting factor, interferon alfacon-1, pancrelipase (pancreatic enzymes), ovalbumin, nifedipine, loratadine, etc.

Non-limiting examples of hormones and steroids (e.g., corticosteroids) that can be used include norethindrone acetate, ethinyl estradiol, progesterone, estrogen, testosterone, prednisone and the like.

Chemotherapeutics that can be used include but are not limited to taxol (Paclitaxel), vinblastine, cisplatin, carboplatin, tamoxifen and the like.

Non-limiting examples of NSAIDs include piroxicam, aspirin, salsalate (Amigesic), diflunisal (Dolobid), ibuprofen (Motrin), ketoprofen (Orudis), nabumetone (Relafen), piroxicam (Feldene), naproxen (Aleve, Naprosyn), diclofenac (Voltaren), indomethacin (Indocin), sulindac (Clinoril), tolmetin (Tolectin), etodolac (Lodine), ketorolac (Toradol), oxaprozin (Daypro), and celecoxib (Celebrex).

Vaccine components that can be used include but are not limited to Hepatitis B, polio, measles, mumps, rubella, HIV, hepatitis A (e.g., Havrix), tuberculosis, etc.

Non-limiting examples of analgesics include but are not limited to aspirin, acetaminophen, ibuprofen, naproxen sodium and the like.

Antibiotics include but are not limited to amoxicillin, penicillin, sulfa drugs, erythromycin, streptomycin, tetracycline, clarithromycin, tobramycin, ciprofloxacin, terconazole, azithromycin and the like.

Anti-depressants include but are not limited to Zoloft, fluoxetine (Prozac), paroxetine (Paxil), citalopram, venlafaxine, fluvoxamine maleate, imipramine hydrochloride, lithium, nefazodone and the like.

Other active ingredient that can be used with the present invention include but are not limited to sildenafil (Viagra), acyclovir, gancyclovir, fexofenidine, celecoxib (Celebrex), rofecoxib, androstenedione, chloroquine, diphenhydramine HCl, buspirone, doxazocin mesylate, loratadine, clomiphine, zinc gluconate, zinc acetate, hydrocortisone, warfarin, indinavir sulfate, lidocaine, novacaine, estradiol, norethindrone acetate, medroxyprogesterone, dexfenfluramine, dextroamphetamine, doxycycline, thalidomide, fluticasone, fludarabine phosphate, etanercept, metformin hydrochloride, hyaluronate, tetrazocin hydrochloride, loperamide, ibogaine, clonazepam, ketamine, lamivudine (3TC), isotretinoin, nicotine, mefloquine, levofloxacin, atorvastatin (Lipitor), miconazole nitrate (Monistat), ritonavir, famotidine, simvastatin (Zocor), sibutramine HCl monohydride, ofloxacin, lansoprozole, raloxifene (Evista), zanamivir (Relenza), oseltamivir phosphate, 4-phenylbutyric acid sodium salt, chlorpromazine, nevirapine, zidovudine, and cetirizine hydrochloride (Zyrtec).

Non-limiting examples of additional active ingredients can be found in Physician's Desk Reference 2000, 54th Edition, ISBN: 1563633302, AHFS 99 Drug Information, Amer. Soc. of Health System, ISBN: 1879907917 and U.S. Pat. No. 5,019,400, all of which are incorporated by reference.

B. Nano-Cluster Formulation Variables and Tunability

Varying nanoparticle type or size, dispersion properties, dispersing materials, and processing conditions, for example, can be used to tune the nano-cluster to a targeted size, density, and/or dispersability. For example, FIGS. 3 and 4 (see Original Patent) illustrate that varying processing conditions can be used to create nano-clusters with a broad or narrow size range and also allows for the formation of solid or hollow nano-clusters. Controlling the droplet size in an emulsion or sprayed from a nozzle can facilitate the formation of uniform nano-clusters. Varying the solvent and extraction phase, temperature, humidity, etc. as well as the properties of the nano-particles can control the morphology of the nano-cluster. For example, rapid extraction of the nanoparticle-carrying solution may result in a core/shell structure while slow remove of this phase allows time for nano-particles to diffuse from the interface and form a more dense nano-cluster structure. In another example, controlling nanoparticle physicochemical properties can provide a driving force for the nanoparticle towards or away from the droplet interface, thus, leading to a core/shell structure or solid matrix, respectively. Additionally, based on an adaptation of the inventors' reported precision particle fabrication methodology (Berkland 2001, Berkland 2001, Berkland 2002, Berkland 2004) or similar technologies, the inventors can produced a wide range of monodisperse nano clusters (FIG. 4 (see Original Patent)).

A variety of techniques can be used to characterize nanoclusters that have been created by varying nanoparticle type or size, dispersion properties, dispersing materials, and processing conditions. These techniques can be used to mechanistically determine how processing parameters affect particle physicochemical properties. For example, the aerodynamic diameter of a dried nanocluster powder can be determined by an Aerosizer LD (available at the Center for Drug Delivery Research, KU), which will also provide supportive data on dry particle geometric diameter, size distribution, aggregation and density. A helium pycnometer (Micromeritics AccuPyc 1330 helium gas pycnometer) located in Dr. Eric Munson's lab (Pharmaceutical Chemistry, KU) can be used to more accurately determine the density of different nanocluster formulations. For example, a sample of nanocluster powder is measured into a 1 cm.sup.3 sample holder and weighed. The density of the sample is determined by helium displacement of the sample compared to a secondary empty chamber. Measurements are conducted in triplicate for each of three samples and the average and standard deviation calculated. Particle exterior and interior morphology (interior viewed via cryo-fracturing (Berkland 2004)) can be investigated via scanning electron microscopy (LEO 1550).

C. Pharmaceutical Compositions and Routes of Administration

One embodiment of this invention includes methods of treating, preventing, or diagnosing a particular disease or condition by administering the disclosed nano-clusters to a subject. In many instances, the nano-clusters are administered alone or can be included within a pharmaceutical composition. An effective amount of a pharmaceutical composition, generally, is defined as that amount sufficient to ameliorate, reduce, minimize or limit the extent of the disease or condition. More rigorous definitions may apply, including elimination, eradication or cure of the disease or condition.

1. Pharmaceutical Compositions

Pharmaceutical compositions of the present invention can include a nano-cluster of the present invention. The phrases "pharmaceutical or pharmacologically acceptable" can include but is not limited to molecular entities and compositions that do not produce an adverse, allergic or other untoward reaction when administered to a subject, such as, for example, a human. The preparation of a pharmaceutical composition is generally known to those of skill in the art. Remington's Pharmaceutical Sciences, 18th Ed. Mack Printing Company, 1990. Moreover, for animal (e.g., human) administration, it is preferred that the preparations meet sterility, pyrogenicity, general safety and purity standards as required by FDA Office of Biological Standards.

"Therapeutically effective amounts" are those amounts effective to produce beneficial results in the recipient. Such amounts may be initially determined by reviewing the published literature, by conducting in vitro tests or by conducting metabolic studies in healthy experimental animals. Before use in a clinical setting, it may be beneficial to conduct confirmatory studies in an animal model, preferably a widely accepted animal model of the particular disease to be treated. Preferred animal models for use in certain embodiments are rodent models, which are preferred because they are economical to use and, particularly, because the results gained are widely accepted as predictive of clinical value.

"Pharmaceutically acceptable carrier" includes any and all solvents, dispersion media, coatings, surfactants, antioxidants, preservatives (e.g., antibacterial agents, antifungal agents), isotonic agents, absorption delaying agents, salts, preservatives, drugs, drug stabilizers, gels, binders, excipients, disintegration agents, lubricants, sweetening agents, flavoring agents, dyes, such like materials and combinations thereof, as would be known to one of ordinary skill in the art (Remington's, 1990).

The actual dosage amount of a composition of the present invention administered to a subject can be determined by physical and physiological factors such as body weight, severity of condition, the type of disease being treated, previous or concurrent therapeutic interventions, idiopathy of the patient and on the route of administration. The practitioner responsible for administration will, in any event, determine the concentration of active ingredient(s) in a composition and appropriate dose(s) for the individual subject.

In certain non-limiting embodiments, pharmaceutical compositions may comprise, for example, at least about 0.1% of an active ingredient or a nano-cluster, for example. In other embodiments, the an active ingredient or nano-cluster may comprise between about 2% to about 75% of the weight of the unit, or between about 25% to about 60%, for example, and any range derivable therein. In other non-limiting examples, a dose may also comprise from about 1 microgram/kg/body weight, about 5 microgram/kg/body weight, about 10 microgram/kg/body weight, about 50 microgram/kg/body weight, about 100 microgram/kg/body weight, about 200 microgram/kg/body weight, about 350 microgram/kg/body weight, about 500 microgram/kg/body weight, about 1 milligram/kg/body weight, about 5 milligram/kg/body weight, about 10 milligram/kg/body weight, about 50 milligram/kg/body weight, about 100 milligram/kg/body weight, about 200 milligram/kg/body weight, about 350 milligram/kg/body weight, about 500 milligram/kg/body weight, to about 1000 mg/kg/body weight or more per administration, and any range derivable therein. In non-limiting examples of a derivable range from the numbers listed herein, a range of about 5 mg/kg/body weight to about 100 mg/kg/body weight, about 5 microgram/kg/body weight to about 500 milligram/kg/body weight, etc., can be administered, based on the numbers described above.

The composition may also include various antioxidants to retard oxidation of one or more active ingredient or nano-cluster. The prevention of the action of microorganisms can be brought about by preservatives such as various antibacterial and antifungal agents, including but not limited to parabens (e.g., methylparabens, propylparabens), chlorobutanol, phenol, sorbic acid, thimerosal or combinations thereof.

The compositions of the present invention may include different types of carriers depending on whether it is to be administered in solid, liquid or aerosol form, and whether it need to be sterile for such routes of administration as injection.

The compositions may be formulated into a composition in a free base, neutral or salt form. Pharmaceutically acceptable salts, include the acid addition salts, e.g., those formed with the free amino groups of a proteinaceous composition, or which are formed with inorganic acids such as for example, hydrochloric or phosphoric acids, or such organic acids as acetic, oxalic, tartaric or mandelic acid. Salts formed with the free carboxyl groups can also be derived from inorganic bases such as for example, sodium, potassium, ammonium, calcium or ferric hydroxides; or such organic bases as isopropylamine, trimethylamine, histidine or procaine.

In embodiments where the composition is in a liquid form, a carrier can be a solvent or dispersion medium comprising but not limited to, water, ethanol, polyol (e.g., glycerol, propylene glycol, liquid polyethylene glycol, etc.), lipids (e.g., triglycerides, vegetable oils, liposomes) and combinations thereof. The proper fluidity can be maintained, for example, by the use of a coating, such as lecithin; by the maintenance of the required particle size by dispersion in carriers such as, for example liquid polyol or lipids; by the use of surfactants such as, for example hydroxypropylcellulose; or combinations thereof such methods. In many cases, it will be preferable to include isotonic agents, such as, for example, sugars, sodium chloride or combinations thereof.

In other embodiments, one may use eye drops, nasal solutions or sprays, aerosols or inhalants in the present invention. Such compositions are generally designed to be compatible with the target tissue type. In a non-limiting example, nasal solutions are usually aqueous solutions designed to be administered to the nasal passages in drops or sprays. Nasal solutions are prepared so that they are similar in many respects to nasal secretions, so that normal ciliary action is maintained. Thus, in preferred embodiments, the aqueous nasal solutions usually are isotonic or slightly buffered to maintain a pH of about 5.5 to about 6.5. In addition, antimicrobial preservatives, similar to those used in ophthalmic preparations, drugs, or appropriate drug stabilizers, if required, may be included in the formulation. For example, various commercial nasal preparations are known and include drugs such as antibiotics or antihistamines.

In certain embodiments, the compositions are prepared for administration by such routes as oral ingestion. In these embodiments, the solid composition may comprise, for example, solutions, suspensions, emulsions, tablets, pills, capsules (e.g., hard or soft shelled gelatin capsules), sustained release formulations, buccal compositions, troches, elixirs, suspensions, syrups, wafers, or combinations thereof. Oral compositions may be incorporated directly with the food of the diet. Preferred carriers for oral administration comprise inert diluents, assimilable edible carriers or combinations thereof. In other aspects of the invention, the oral composition may be prepared as a syrup or elixir. A syrup or elixir, and may comprise, for example, at least one active agent, a sweetening agent, a preservative, a flavoring agent, a dye, a preservative, or combinations thereof.

In certain embodiments, an oral composition may comprise one or more binders, excipients, disintegration agents, lubricants, flavoring agents, and combinations thereof. In certain embodiments, a composition may comprise one or more of the following: a binder, such as, for example, gum tragacanth, acacia, cornstarch, gelatin or combinations thereof; an excipient, such as, for example, dicalcium phosphate, mannitol, lactose, starch, magnesium stearate, sodium saccharine, cellulose, magnesium carbonate or combinations thereof; a disintegrating agent, such as, for example, corn starch, potato starch, alginic acid or combinations thereof; a lubricant, such as, for example, magnesium stearate; a sweetening agent, such as, for example, sucrose, lactose, saccharin or combinations thereof; a flavoring agent, such as, for example peppermint, oil of wintergreen, cherry flavoring, orange flavoring, etc.; or combinations thereof the foregoing. When the dosage unit form is a capsule, it may contain, in addition to materials of the above type, carriers such as a liquid carrier. Various other materials may be present as coatings or to otherwise modify the physical form of the dosage unit. For instance, tablets, pills, or capsules may be coated with shellac, sugar or both.

Sterile injectable solutions are prepared by incorporating the active compounds in the required amount in the appropriate solvent with various of the other ingredients enumerated above, as required, followed by filtered sterilization. Generally, dispersions are prepared by incorporating the various sterilized active ingredients into a sterile vehicle which contains the basic dispersion medium and/or the other ingredients. In the case of sterile powders for the preparation of sterile injectable solutions, suspensions or emulsion, the preferred methods of preparation are vacuum-drying or freeze-drying techniques which yield a powder of the active ingredient plus any additional desired ingredient from a previously sterile-filtered liquid medium thereof. The liquid medium should be suitably buffered if necessary and the liquid diluent first rendered isotonic prior to injection with sufficient saline or glucose. The preparation of highly concentrated compositions for direct injection is also contemplated, where the use of DMSO as solvent is envisioned to result in extremely rapid penetration, delivering high concentrations of the active agents to a small area.

The composition should be stable under the conditions of manufacture and storage, and preserved against the contaminating action of microorganisms, such as bacteria and fungi. It will be appreciated that exotoxin contamination should be kept minimally at a safe level, for example, less that 0.5 ng/mg protein.

In another aspect of the present invention, a person of ordinary skill will recognize that the compositions of the present invention can include any number of combinations of nano-particles, dispersion materials, active ingredients, and other components. It is also contemplated that that the concentrations of these ingredients can vary. For example, in one-non-limiting aspect, a composition of the present invention can include at least about 0.0001% to about 0.001%, 0.001% to about 0.01%, 0.01% to about 0.1%, 0.2%, 0.3%, 0.4%, 0.5%, 0.6%, 0.7%, 0.8%, 0.9%, 1.0%, 1.1%, 1.2%, 1.3%, 1.4%, 1.5%, 1.6%, 1.7%, 1.8%, 1.9%, 2.0%, 2.1%, 2.2%, 2.3%, 2.4%, 2.5%, 2.6%, 2.7%, 2.8%, 2.9%, 3.0%, 3.1%, 3.2%, 3.3%, 3.4%, 3.5%, 3.6%, 3.7%, 3.8%, 3.9%, 4.0%, 4.1%, 4.2%, 4.3%, 4.4%, 4.5%, 4.6%, 4.7%, 4.8%, 4.9%, 5.0%, 5.1%, 5.2%, 5.3%, 5.4%, 5.5%, 5.6%, 5.7%, 5.8%, 5.9%, 6.0%, 6.1%, 6.2%, 6.3%, 6.4%, 6.5%, 6.6%, 6.7%, 6.8%, 6.9%, 7.0%, 7.1%, 7.2%, 7.3%, 7.4%, 7.5%, 7.6%, 7.7%, 7.8%, 7.9%, 8.0%, 8.1%, 8.2%, 8.3%, 8.4%, 8.5%, 8.6%, 8.7%, 8.8%, 8.9%, 9.0%, 9.1%, 9.2%, 9.3%, 9.4%, 9.5%, 9.6%, 9.7%, 9.8%, 9.9%, 10%, 11%, 12%, 13%, 14%, 15%, 16%, 17%, 18%, 19%, 20%, 21%, 22%, 23%, 24%, 25%, 26%, 27%, 28%, 29%, 30%, 35%, 40%, 45%, 50%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, or 99% or any range derivable therein, of at least one of the nano-particles, dispersion materials, active ingredients, or other components that are mentioned throughout the specification and claims. In non-limiting aspects, the percentage can be calculated by weight or volume of the total composition. A person of ordinary skill in the art would understand that the concentrations can vary depending on the addition, substitution, and/or subtraction of nano-particles, dispersion materials, active ingredients, and other components.

2. Routes of Administration

The present invention can be administered intravenously, intradermally, intraarterially, intraperitoneally, intralesionally, intracranially, intraarticularly, intraprostaticaly, intrapleurally, intratracheally, intranasally, intravitreally, intravaginally, intrauterinely, intrarectally, intrathecally, topically, intratumorally, intramuscularly, intraperitoneally, subcutaneously, subconjunctival, intravesicularlly, mucosally, intrapericardially, intraumbilically, intraocularally, orally, topically, locally, inhalation (e.g., aerosol inhalation), injection, infusion, continuous infusion, localized perfusion bathing target cells directly, via a catheter, via a lavage, in cremes, in lipid compositions (e.g., liposomes), or by other method or any combination of the forgoing as would be known to one of ordinary skill in the art (Remington's, 1990).

D. Combination Therapies

In order to increase the effectiveness of a treatment with the nano-clusters of the present invention, it may be desirable to combine these nano-clusters with other therapies effective in the treatment of a particular disease or condition.

The compositions of the present invention, for example, can precede or follow the other agent treatment by intervals ranging from minutes to weeks. It is contemplated that one may administer both modalities within about 12-24 h of each other and, more preferably, within about 6-12 h of each other. In some situations, it may be desirable to extend the time period for treatment significantly, where several days (2, 3, 4, 5, 6 or 7), several weeks (1, 2, 3, 4, 5, 6, 7 or 8) or even several months (1, 2, 3, 4, 5, 6, or more) lapse between the respective administrations.

Various combinations may be employed where a compositions including a nano-cluster is "A" and the secondary agent, is "B" -- see Original Patent.

E. Source of Nano-Particles, Dispersion Materials, Active Ingredients, and Other Components

The nano-particles, dispersion materials, active ingredients, and other components described in the claims and specification can be obtained by any means known to a person of ordinary skill in the art. In a non-limiting embodiment, for example, these ingredients can be isolated by obtaining the source of such nano-particles, dispersion materials, active ingredients, and other components. Additionally, the ingredients can be purified by any number of techniques known to a person of ordinary skill in the art. Non-limiting examples of purification techniques include Polyacrylamide Gel Electrophoresis, filtration, centrifugation, dialysis, High Performance Liquid Chromatography (HPLC), Gel chromatography or Molecular Sieve Chromatography, and Affinity Chromatography. In other aspects, the compounds, agents, and active ingredients can be obtained by chemical synthesis or by recombinant means by using conventional techniques. See, for example, Stewart and Young, (1984); Tam et al., (1983); Merrifield, (1986); and Barany and Merrifield (1979), Houghten (1985).

F. Kits

In further embodiments of the invention, there is a provided a kit. The kit can include, in non-limiting aspects, the nano-particles, dispersion materials, active ingredients, and other components described in the claims and the specification. In preferred embodiments, the kit can include a composition that includes a nano-cluster. The nano-cluster can include, for example, a plurality of nano-particles and a dispersing material that holds the plurality of nano-particles together and/or disperses the nano-particles in response to an environmental cue.

Containers of the kits can include a bottle, dispenser, package, compartment, or other types of containers, into which a component may be placed. The container can include indicia on its surface. The indicia, for example, can be a word, a phrase, an abbreviation, a picture, or a symbol.

The containers can dispense a pre-determined amount of the component (e.g. compositions of the present invention). The composition can be dispensed in a spray, an aerosol, or in a liquid form or semi-solid form. The containers can have spray, pump, or squeeze mechanisms. In certain aspects, the kit can include a syringe for administering the compositions of the present invention.

Where there is more than one component in the kit (they may be packaged together), the kit also will generally contain a second, third or other additional containers into which the additional components may be separately placed. The kits of the present invention also can include a container housing the components in close confinement for commercial sale. Such containers may include injection or blow-molded plastic containers into which the desired bottles, dispensers, or packages are retained.

A kit can also include instructions for employing the kit components as well the use of any other compositions, compounds, agents, active ingredients, or objects not included in the kit. Instructions may include variations that can be implemented.

Claim 1 of 62 Claims

1. A nano-cluster comprising a plurality of nano-particles, wherein the nano-particles include an active ingredient and a polymer, and wherein the nano-cluster is not hollow.

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