CA2315256A1

CA2315256A1 - Needle-free injection of formulated nucleic acid molecules

Info

Publication number: CA2315256A1
Application number: CA002315256A
Authority: CA
Inventors: Lou Smith; Russ Mumper; Michael Barry
Original assignee: Individual
Current assignee: Baylor College of Medicine; Urigen Pharmaceuticals Inc
Priority date: 1997-12-16
Filing date: 1998-12-16
Publication date: 1999-06-24
Also published as: AU1922999A; WO1999031262A3; WO1999031262A2; JP2003528024A; EP1038016A2

Abstract

A novel method is provided for delivering nucleic acid molecules through and/or to the skin of mammals by needle-free injection. The method involves the incorporation of formulated nucleic acid molecules with devices for injecting the molecules by air, fluid and/or mechanical pressure. Disclosed are compositions and methods for enhancing the administration to and uptake of nucleic acids in a mammal. The methods disclosed provide an increased immune response by allowing the uptake of formulated nucleic acid molecules by a wide variety of cell types simultaneously. Also disclosed are examples which demonstrate that the combination of formulated nucleic acid molecules and needle-free injection methods results in immune responses which are superior to those obtained by conventional means of delivery. Methods for delivery, as well as methods for formulating nucleic acid molecules with various compounds, such as cationic complexing agents, polymeric and non-polymeric formulations, protective, interactive, non-condensing systems are also disclosed.

Description

WO 99/312b2 PCTNS981Z6823 NEEDLE FREE INJECTION OF FORMULATED NUCLEIC ACID MOLECULES
Statement of Related Applications This application is related to U.S. Patent Application entitled "NUCLEIC ACID
TRANSPORTERS FOR DELIVERY OF NUCLEIC ACIDS INTO A CELL" Serial Nwnber 08/484,777, filed June 7,1995, International Patent Application entitled '~1TJCLEiC ACID TRANSPORTERS FOR DELIVERY OF NUCLEIC ACIDS INTO A
CELL" No. PCT/US96/05579 filed April 23, 1996 and U.S. Patent Application "TRANSPORTERS FOR SPECIFIC DELIVERY OF MACROMOLECULES TO
CELLS" Serial Number 60/045,295, filed May 2, 1997 all of which are incorpon~ted herein by reference in their entirety, including any drawings.
Introduction The present invention relates to products and methods useful for delivering formulated nucleic acid molecules by needle-free injection.
The following information is presented solely to assist the understanding of the reader, and none of the information is admitted to describe or constitute prior art to the claims of the prescnt invention.
In the past, non-viral administration of nucleic acids ~n vivo has been pursued by a variety of methods. These include lipofectin/liposome fusion: Proc. Natl. Acad Sci., Volume 84, pp. 7413-7417 (1993); polylysine condensation with and without adenovirus enhancement: Human Gene Therapy, Volume 3, pp. 147-154 {1992); and ..a transferrinaraasferrin receptor delivery of nucleic acid to cells: Proc. Natl.
Acad Sci., Volume 87, pp. 3410-3414 (1990). The use of a specific composition consisting of polyacrylic acid has been disclosed in WO 94/24983. Naked DNA has been administered as disclosed in International Patent Publication No. WO 90/11092.

Since the introduction of the needle-syringe, injection technology has remained virtually unchanged. Once considered a simple and innocuous part of medical therapy, injections now take oa ominous consequences. Needlestick injuries can be a life threatening event. Jet injection, or the injection of proteins by aerosol pressure, was introduced into clinical use in 1947 (Military~l~Iedicine, June, S 16-524, 1963), and a base of scientific data has validated the safety and effcacy of this method of injection (New Zealand Medical Journal, Vol. 95. p.815, 1983). Current aerosol pressure injectors are calibrated to allow the user to select the accurate depth of penetration, and are available with syringes designed for intramuscular, subcutaneous or epidermal injections.
Use of aerosol pressure injections to immunize rabbits to HbsAg protein has been shown to be superior to classical syringe and needle methods, and resulted in a nearly 4 fold increase in antibody production at eight weeks when compared with a nornial syringe and needle (Davis et al., Vaccine vo1.12(16):1503-91994). In the Davis et al., study the DNA was suspended in endotoxin free Dulbeccos's PBS and the area to be injected was not pretreated.
The transfection of tissue by aerosol injection has been reported as being superior to needle injection methods (Kerr et al., Journal of Cellular Biochemistry Supplement 0 (21A). 1995). It has also been shown that aerosol injection of rabbit papilloma virus genome into rabbit epithelium results in the induction of papillomas (Brandsma et al., Proc. natl. Acad Sci. USA 88. 4816-4820. 1991). Aerosol injection has been use to introduce human cytomegalovirus immediate early gene i enhancer/ promoter sequences, bacterial chloramphenicol acetyltransferase, whey acidic protein promoter sequences, and the bacterial -galactosidase gene through the skin surface so as to transfect skin, muscle, fat and mammary tissue of living animals (Forth et al., Analytical biochemistry, 205, 365-368, 1992). It has been stated that suspending aerosol-injected DNA constructs in solutions which enhance cellular uptake of DNA may increase the number of cells transfected in a single injection (Forth et al., supra).
DNA bound by precipitation methods to inert particles have been delivered by needle-free injection. Coating inert particles, such as gold microprojectiles, and injecting.
them by needle-free devices offers direct injection into the cells due to the projectile carrier penetrating the cell. Tang et al., inoculated mice with DNA encoding human growth hormone coated gold micropmjectiles and stated that this method was superior to needle injection of plasmids encoding human growth hormone. Tang et al, reports that this technique simplifies the procedure and shortens the time required to produce antibodies to particular proteins by eliminating steps for protein purification and adjuvant-administration. (Tang et ai., Nature, Vol. 356152-154 1992) Summary Of the Invention This invention features compositions and methods for enhancing the administration to and uptake of nucleic acids in a mammal. An efficient strategy for enhancing needle-free delivery of nucleic acids in vivo is to protect the nucleic acid from degradation, thereby maintaining the administered nucleic acid at the target site in order to further increase its cellular uptake. The data presented herein demonstrates that the combinaxion of formulated nucleic acid molecules and needle free injection methods are synergistic, providing the desired antibody response to the resulting expressed protein that is unexpectedly high when compared with either needle-free injection of non-formulated nucleic acids or needle injection of formulated nucleic acids.
The invention provides a method to deliver formulated nucleic acid molecules through and/or to the skin of a mammal by using an apparaxus configured and arranged to administer molecules by air, or mechanical pressure through and/or to the skin of a mammal. Thus, the present invention allows for superior delivery of nucleic acid molecules into cells in vivo by the combination of a needle free device and formulated nucleic acid molecules. Furthermore, the present invention also allows for treatment of diseases, vaccination, and treatment of muscle disorder and serum protein deficiencies.
In a first aspect, the present invention features a method for delivering a nucleic acid molecule formulated with a tramsfection facilitating agent through and/or to the skin of a mammal by the use of a needle-free injection device. Preferably, the needle-free device is configured and arranged to cause aerosol delivery of the formulated nucleic acid through and/or to the skin of the marnmal.
By "delivery" or "delivering" is meant transportation of nucleic acid molecules to desired cells or any cells. The nucleic acid molecules will be delivered to multiple cell lines, including the desired target. Delivery results in the nucleic acid molecules coming in contact with the cell surface, cell membrane, cell endosome, within the cell membrane, nucleus or within the nucleus, or any other desired area of the cell from which transfection can occur within a variety of cell lines which can include but are not limited to; epithelial cells, Langerhan cells, Langhans' cells, littoral cells, keratinocytes, dendritic cells, S macrophage cells, kupffer cells, lymphocytes and lymph nodes. Preferably, the nucleic acid molecule can be delivered thmugh and/or to the skin by aerosol pressure and is not significantly sheared.
The term "nucleic acid" as used herein refers to both RNA and DNA including:
cDNA, genomic DNA, plasmid DNA or condensed nucleic acid, nucleic acid formulated with cationic lipids, nucleic acid formulated with peptides, antisense molecule, cationic substances, RNA or mRNA. In a preferred embodiment, the nucleic acid administered is plasmid DNA which comprises a "vector". The nucleic acid can be, but is not limited to, a plasmid DNA vector with a eukaryotic promoter which expresses Human Growth Hormone, such as in the example provided.
The term "formulated" as used herein means the process by which nucleic acid molecules are combined with a transfection facilitating agent in a manner which makes the nucleic acid molecules more stable, protected, and therefore, more easily transferable.
The term "transfection facilitating agent" as used herein refers to an agent that forms a complex with the nucleic acid. This molecular complex is associated with nucleic acid, molecule in either a covalent or a non-covalent manner. The transfection facilitating agent should be capable of h~ansporting nucleic acid molecules in a stable state and of releasing the bound nucleic acid molecules into the cellular interior. The transfection facilitating agent should also be capable of being bound to nucleic acid molecules and lyopholized or freeze dried and either rehydrated prior to needle-free delivery or delivered as a fine powder via needle-free delivery.
in addition, the transfection facilitating agent may prevent lysosomal degradation of the nucleic acid molccules by endosomal lysis. Furthermore, the transfection facilitating agent allows for efficient transport of the nucleic acid molecule through the cytoplasm of the cell to the nuclear membrane and into the nucleus and provide protection.
In a preferred embodiment transfection facilitating agents are non-condensing polymers, oils and surfactants. These may be suitable for use as compounds which prolong the localized bioavailability of a nucleic acid:
polyvinylpyrrolidones;
poiyvinylalcohols; propylene glycols; polyethylene glycols; polyvinylacetates;
poloxamers (Pluronics)(block copolymers of propylene oxide and ethylene oxide, relative amounts of the two subunits may vary is different poloxamers); poloxamines (Tetronics);
ethylene vinyl acetates; celluloses, including salts of c~rboxymethylcelluloses, methylcelluloses, hydroxypropylcelluloses, hydroxypropylmethylcelluloses; salts of hyalumnates;
salts of alginates; heteropolysaccharides (pectins); dextrans; chitosans;
phosphatidylcholines (lecithins); miglyols; polylactic acid; polyhydroxybutyric acid. Some of these compounds may be used as protective, interactive, non-condensing compounds and others as sustained release compounds, while some may be used in either manner under the respectively appropriate conditions.
In another embodiment cationic condensing agents such as cationic lipids, peptides, or lipopetides may associate with the nucleic acid molecule and may facilitate transfection.
In a further embodiment some of these compounds may be covalently attached to gold particles and thereby bind with nucleic acid molecules of the present invention. Gold particles coated with a polymer or polymers of the present invention can deliver nucleic acid molecules into cells by penetrating the cell when delivered by needle-free injection device.
The term "protects" or "protective" or "protected" as used herein refers to an effect of the interaction between such a compound and a nucleic acid such that the rate of degradation of the nucleic acid is decreased in a particular environment, thereby prolonging the localized bioavailability of the nucleic acid molecule. Such degradation may be due a variety of different of factors, which specifically include the enzymatic action of a nuclease. The protective action may be provided in different ways, for example, by exclusion of the nuclease molecules or by exclusion of water.
The compounds which protect the nucleic acid and/or prolong the localized bio-availability of a nucleic acid may achieve one or more of the following effects, due to their physical, chemical or rheological properties: ( 1 ) Protect nucleic acid, for example plasmid DNA, from nucleases due to steric, viscosity, or other effects such as shearing; (2) increase the area of contact between nucleic acid, such as plastnid DNA, through extracellular b matrices and over cellular membranes, into which the nucleic acid is to be taken up; (3) concentrate nucleic acid, such as plasmid DNA, at cell surfaces due to water cxclusion; (4) indirectly facilitate uptake of nucleic acid, such as plasmid DNA, by disrupting cellular membranes due to osmotic, hydrophobic or lytic effects; and (5) indirectly facilitate uptalo~
of nucleic acids by allowing diffusion of protected nucleic acid chains through tissue at the administration site.
By "prolonging the localized bioavailability of a nucleic acid" is meant that a nucleic acid when administered to an organism in a composition comprising such a compound will be available for uptake by cells for a longer period of time than if administered in a composition without such a compound, for example when administered in a saline solution. This increased availability of nucleic acid to cells could occur, for example, due to increased duration of contact between the composition containing the nucleic acid and a cell or due to protection of the nucleic acid fiom attack by nucleases.
The compounds which prolong the localized bioavailability of a nucleic acid are suitable for internal administration.
By "suitable for internal administration" is meant that the compounds are suitable to be administered within the tissue of an organism, for example within a muscle or within a joint space, epidermally, intradermaily or subcutaneously. Properties making a compound suitable for internal administration can include, for example, the absence of a high level of toxicity to the organism as a whole.
The term "needle-free injection device" as used herein relates to an apparatus that is capable of injecting an aerosol through and/or to the skin of a marnmal into the tissue by air and/or mechanical pressure. It is understood that conventional devices of this type are calibrated to allow one of ordinary skill in the art to select and/or adjust the desired injection depth and therefore it is expected that future devices that perform this function will also be calibrated in the same manner. It is also understood that devices of this type may have a needle which is only used io collect a solution which is subsequently aerosolized, and delivered by needle-free means. The type of injection device is not considered a limiting aspect of the present invention. The primary importance of a needle-flee device is, in fact, the capability of the device to deliver an aerosol of formulated nucleic acid molecules through and/or to the skin of a mammal. The needle-flee injection device can include, for example, a Gene Gun or a Needle-Less Injector as described in U.S. Patent S,4$0,381 or a powder delivery device such as in PCT
W0/097/134652.
The term "apparatus" as used herein relates to the set of components that upon combination allow the delivery of an aerosol through andlor to the skin of a mammal. The;
S components can be a nozzle or needle-free syringe with which one can collect and/or administer the formulated nucleic acid molecules, and a pump or spring for creating air pressure which forcibly evacuates the formulated nucleic acid molecules from the nozzle or needle-free syringe in a manner that creates an aerosol capable of penetrating the skin of a mammal. To create air pressure the apparatus can employ gas pressure, gas spring or spring force.
Preferably, the apparatus is capable of being calibrated to allow selection of depth of delivery. Hence, delivery can occur through the skin or to the skin.
The term "aerosol" as used herein is a suspension of formulatcd nucleic acid molecules in the form of a particulate mist. Aerosols have been defined as colloidal 1 S systems consisting of very finely subdivided liquid or solid particles dispersed in and surrounded by a gas. The aerosol of the present invention can depend upon the power of a liquified or compressed gas or mechanical spring to generate the fine mist of formulated nucleic acid molecules. Particles of an aerosol can range from less than 1 to SO m. The particles are said to remain suspended in the air for relatively long periods of time. The size of the particles can be measured by conventional methods such as the Milken Oil Drop Experiment for measuring aerosol particle size, but the need to determine specific size is falling into disuse (Sciarra, et al., in Remington's Pharmaceutical Sciences, 18th ed.
chapter 92, 1990). The aerosol can be a liquid, a powder, or a heterogeneous mist comprising both a liquid and solid phase.
2S The term "skin" refers to the outer covering of a mammal consisting of epidermal and den~rral tissue and appendages such as sweat ducts and hair folicles. Skin can comprise the hair of a mammal in cases where the mammal has an epidermis which is covered by hair. In mammals which have enough hair to be considered fiu or a pelt it is preferable to shave the hair, leaving primarily skin.
The team "mammal" refers to any warm blooded organism. Preferably the mammal is a human.

In preferred embodiments the method results in an immune response, preferably a humoral immune response targeted for the protein product encoded by the nucleic acid molecule, such as an antibody response that is preferably at least 3 times greater than an antibody response caused by needle injection of a protein product encoded by a nucleic acid molecule suspended in saline, and at lean 10 times greater than an antibody response caused by needle injection of a nucleic acid molecule formulated with a transfection facilitating agent. In other situations the immune response preferably is a cytotoxic T-lymphocyte response.
The term "immune response" as used herein refers to the mammalian natural defense mechanism which can occur when foreign material is internalized. The immune response can be a global immune response involving the immune system components in their entirety. Preferably the immune response results from the protein product encoded by the formulated nucleic acid molecule. The immune response can be, but is not limited to; antibody production, T-cell proliferation /differentiation, activation of cytotoxic T-lymphocytes, and/or activation of natural killer cells. Preferably the immune response is a humoral immune response. However, as noted abave, in other situations the immune response, preferably, is a cytotoxic T-lymphocyte response.
The term "humoral immune response" refers to the production of antibodies in response to internalized foreign material. Preferably the foreign material is the protein product encoded by a formulated nucleic acid molecule internalized by injection with a needle free device.
In an additional embodiment the needle-free device is selected from the group consisting of Mediject, Bioject, Gent Gun, Mesoflash, Ped-O-ject and Powder-Ject.
Generally, it is understood that such a device is accompanied by directions for usage.
In another aspect the invention features a kit. The kit includes a provider for providing a nucleic acid molecule formulated with a transfection facilitating agent and a needle-free means for delivering the nucleic acid molecule through and/or to the skin of a The "provider" can be ions furnished to allow one of ordinary skill in the art to make formulated nucleic acid molecules. The instructions will furnish steps to make the compounds used for formulating nucleic acid molecules. Additionally, the instructions will include methods for testing the formulated nucleic acid molecules that entail establishing if the formulated nucleic acid molecules are damaged upon injection from the needle-free device. The provider can also be the formulated nucleic acid molecules themselves.
The term "transfection" as used herein, refers to the process of introducing DNA
(e.g., formulated DNA expression vector) into a cell, thcreby, allowing cellular transformation. Following entry into the cell, the transfected DNA may: ( 1 ) recombine with that of the host; (2) replicate independently as a plasmid or temperate phage; or (3) be maintained as an episome without replication prior to elimination.
As used herein, "transformation" relates to transient or permanent changes in the characteristics (expressed phenotype) of a cell induced by the uptake of a vector by that cell. Genetic material is introduced into a cell in a form where it expresses a specific gene product or alters the expression or effect of endogenous gene products.
Transformation of the cell may be associated with production of a variety of gene products including protein and RNA. These products may function as intracellular or extracellular structural elements, ligands, hormones, neurotransmitters, growth regulating factors, enzymes, chemotaxins, serum proteins, receptors, carriers for small molecular weight compounds, drugs, immunomodulators, oncogenes, cytokines, tumor suppressers, toxins, tumor antigens, antigens, antisense inhibitors, triple strand forming inhibitors, ribozymes, or as a ligand recognizing specific structural determinants on cellular structures for the purpose of modifying their activity. This list is only an example and is not meant to be limiting.
In another aspect, the invention features a method for making a kit.
Preferably the method involves the step of combining a provider for providing a nucleic acid formulated with a transfection facilitating agent and a needle-free means for delivering the nucleic acid to a mammal. The provider for providing a nucleic acid can be instructions for formulating nucleic acid molecules or simply the formulated nucleic acid molecules.
In yet another aspect, the invention also features a method for treating a mammal that is suffering from a disorder conventionally treated by administering human growth hormone. The method requires administering a nucleic acid molecule encoding human WO 99131262 pCT/US98/26823 gmwth hormone and formulated with a transfection facilitating agent through and/or to the skin of the mammal by use of a needle-free device.
In another aspect, the invention features a method for treating a mammal that is suffering from a cancer by administering a nucleic acid molecule encoding the appropriate;

5 cancer antigen. The method requires administering a nucleic acid molecule encoding a cancer antigen and formulated with a transfection facilitating agent thmugh and/or to the skin of the mammal by use of a needle-free device.
Preferably, the cancer is melanoma and the appropriate cancer antigen is MAGE
1.
In yet another aspect, the invention also features a method for treating a mammal 10 that is suffering from an infectious disease by administering a nucleic acid molecule encoding an antigen for the infectious disease. The method requires administering a nucleic acid molecule encoding an antigen for the infectious disease and formulated with a transfection facilitating agent through andlor to the skin of the mamznal by use of a needle-free device.
In a preferred embodiment the infectious disease is chronic hepatitis and the antigen is HBV core antigen.
Administration as used herein refers to the mute of introducing the formulated nucleic acid molecules of the invention into the body of cells or organisms.
Administration includes the use of aerosol pressure as provided by a needle free device to targeted areas of the mammalian body such as the muscle and the lymph nodes.
Prior to administration, the nucleic acid molecules of the invention can be formulated with at least one other type of molecule. For example, the molecular complexes can be formulated with other molecules such as polyvinyl-pyrrolidone as described herein. Formulation techniques are provided herein by example.
In a prefen~ed embodiment administration is directed through the epiden~nis, intradermis, and subcutaneous layer to the muscle tissue. The present invention administers formulated nucleic acid molecules in a manner which causes contact with various mammalian cell types which are not contacted by conventional needle injection techniques during one injection. Cell lines contacted by injection with the present invention are, but are not limited to, epithelial cells, langerhan cells, keratinocytes, dendritic cells, macrophage cells, kupfer cells, lymphocytes and lymph nodes.

Another aspect of the present invention features a mcthod for modifying inert particles by first washing the inert particles in fuming nitric acid solutions or in solutions of nitric acid mixed with sulfuric acid, and then combining the inert particles with cysteine terminated cationic DNA binding peptides to form a monolayer peptide coating.
Preferably, the DNA binding peptide recognizes and binds a specific nucleic acid sequence of a designed plasmid. Hence, one molecule of DNA binding peptide binds with an inert particle and a plasmid, therefore reducing the amount of crosslinking between inert particles. The inert particles can be but are not limited to gold particles.
Preferably, the inert particles are combined with nucleic acid molecules and delivered through the skin of a mammal to cells by a needle-free device.
The term "inert particles" refers to biologically inactive particles which can be but are not limited to particles from the group consisting of, ferrite crystals, gold particles or beads, tungsten spheres, other metals or biologically inactive compounds which are of a density of roughly I S - 20g/cm3 and a size of mughly 1-3 m. Generally, the optimum particle is small enough to produce minimal cell damage. The size of particles is not a limiting aspect. It is known by those of ordinary skill in the art that the particle must be large enough to acquire sufficient momentum to penetrate the cell: momentum being a function of size density and velocity, and by convention particle size should be roughly 10 times smaller than the target cell.
A further aspect of the invention features a method for delivering a nucleic acid molecule formulated with a modified inert particle through and/or to the skin of a mammal by the use of a needle-free injcction device. Preferably, the needle-free device is configured and arranged to cause aerosol delivery of the formulated nucleic acid through and/or to the skin of the mammal.
. The summary of the invention described above is not limiting and other features and advantages of the invention will be apparent from the Following detailed description of the invention and from the claims.
Brief Descri 'on c~f'Ifie Drawings The drawings will herein briefly be described.

WO 99/31262 PCTlUS98/26823 Figure 1 shows the humoral immune response to hGH in dogs after needle and needle-free injection of transfection facilitating agent formulated pCMV-hGH
in dogs.
The antibody titer for each data point is an average for two dogs.
Figure 2 shows a comparison between pCMV-hGH suspended in saline and transfection facilitating agent formulated pCI~V-hGH for the elicitation of humoral immune response to hGH in dogs after needle-free injection. The antibody titer for each data point is an average for two dogs.
Figure 3 shows the amounts of expressed Luciferase in conditions where a plasmid encoding CMV-Luciferase is formulated with modified gold particles that are coated or uncoated with Cys-Tyr-Lys-ala- (Lys)g -Trp-Lys (CK8). The formulations are then loaded on a Kapton carrier membrane in ethanol, water or precipitated with Ca2+ and then loaded in ethaaol.
fled Description of the Preferred Embodiments The delivery of formulated nucleic acid molecules by the use of a needle free device represents a novel approach to gene delivery. The present invention offers a nucleic acid delivery apparatus that provides an increased immune response when compared to previous methods. The invention provides the advantage of allowing the uptake of formulated nucleic acid molecules by a wide variety of cell types simultaneously. Injecting formulated nucleic acid molecules by needle free device results in the formulated nucleic acid molecules directly contacting many more cell types than in conventional needle injection. Thus, the present invention provides an enhanced delivery of nucleic acid molecules and also provides a more e~cient gene delivery system which can be used to generate an immune response.
Needle-free delivery of formulated nucleic acid molecules through and/or to the skin of a mammal, depends on several factors which are discussed below, including transfection efficiency and the composition of the formulated nucleic acid molecule.
I. DNA Infection Variables The intensity of an immune response and the level of gene delivery and expression achieved with the present invention can be optimized (>5-fold effect over controls) by altering the following variables. The variables are: the formulation (composition, plasmid topology), the technique and protocol for injection (angle of injection, state of muscle), and, the pretreatment of the muscle with myotoxic agents. An immune response can be measured by, but is not limited to, the amount of antibodies produced for a protein encoded and expressed by the injected nucleic acid molecule.
Other injection variables that can be used to significantly effect the levels of antibodies and/or cytotoxic T-lymphocytes produced in response to the protein encoded by the formulated nucleic acid molecule provided by the needle-free injection method of the present invention are the state of the muscle being injected and injection technique.
Examples of the variables include muscle stimulation, muscle contraction, muscle massage, delivery angle, and apparatus manipulation. Massaging the muscle may force plasmid out of the muscle either directly or via lymphatic drainage. By altering the depth of penetration and/or the angle at which the needle-flee device is placed in relation to muscle fibers the present invention improves the plasmid distribution throughout the injection area which subsequently increases the antibody response to the protein which is encoded and expressed by the plasmid.
Needle flee injection systems pmvide an attractive method for administration of plasmid DNA for the purpose of intramuscular immunization. Not only do they provide the general benefit of avoiding needle-stick injury, but they may produce better distribution of injected substances in the muscle. Direct gene transfer was first demonstrated on mammary tissue using the Ped-O jet system, but this apparatus was designed largely for intradennal or subcutaneous injections (Forth et al., Anal. bioclrem.
205:365-368., 1992).
We have found that needle-free injection of formulated nucleic acids can be superior to classical needle injection in a dog model. We injected a plasmid, suspended in saline, containing the gene for Human Growth Hormone by needle-free and needle injection to dog muscle and measured antibody production. We found that with needle free injection at 14 and 28 days and prior to boost resulted in a measurable antibody titer versus needle injection which resulted in an almost undetectable titer.

II. Nucleic acid based vaccines The present invention can be used to deliver nucleic acid vaccines in a more efficient manner than is conventionally done at the present time. Nucleic acid vaccines, or the use of plasmid encoding antigens or therapeutic molecules such as Human Growth Hormone, has become an area of intensive research and development in the last half decade. Comprehensive reviews on nucleic acid based vaccines have been published [M.A. Liu, et al.(Eds.), 1995, DNA Vaccines: A new era in vaccinology, Vol.
772, Ann.
NY. Acad. Sci., New York; Kumar, V., and Sercarz, E., 1996, Nat. Med. 2:857-859;
Ulmer, J.B., et al., (Fds.) Current Opinion in Immunology; 8:531-536. Vol.
772, Ann. NY.
Acad. Sci., New York]. Pmtective immunity in an animal model using plasmid encoding a viral protein was first observed in 1993 by Ulmer et al. [Ulmer, J.B., et al., 1993, Science 259:1745-1749]. Since then, several studies have demonstrated protective immunity for several disease targets and human clinical trials have been started. Many disease targets have been investigated. Examples include antigens of Borrelia burgdorferi, the tick-borne infectious agent for Lyme disease (Luke et al., J. Infect. Dis. 175:91-97, 1997), human immunodeficiency virus-1, (Letvin et al., Proc. Nat. Acod Sci. USA 94:9378-9383, 1997), B cell lymphoma (Syrengelas et al., Nature Medicine. 2:1038-41, 199, Herpes simplex virus (Bourne et al., J. Infectious dis. 173:800-807, 1996), hepatitis C virus (Tedeschi et al., Hepatology 25:459-462, 1997), rabies virus (Xiang et al., virology, 209:569-579, 1995), Mycobacterium tuberculosis (Lowrie in Genetic Vaccines and Immunotherapeutic Strategies CA Thibeault, ed. Intl Bus Comm, Inc., southbomugh, MA 01772 pp. 87-122, 1996), and Plasmodium falciparum (Hoffman et al., Vaccine 15:842-845, 1997).
An important goal of gene therapy is to effect the uptake of nucleic acid by cells, thereby causing an immune response to the pmtein encoded by the injected nucleic acid.
Uptake of nucleic acid by cells is dependent on a number of factors, one of which is the length of time during which a nucleic acid is in proximity to a cellular surface. The present invention provides formulations which increase the length of time during which a nucleic acid is in proximity to a cellular surface, and penetrate the cell thereby delivering nucleic acid molecules into the cell.
Nucleic acid based vaccines are an attractive alternative vaccination strategy to subunit vaccines, purified viral protein vaccines, or viral vector vaccines.
Each of the WO 99/31262 PCTNS98/2b823 traditional approaches has limitations that are overcome if the antigens) is expressed directly in cells of the body. Furthermore, these traditional vaccines are only protective in a strain-specific fashion. Thus, it is very difficult, and even impossible using traditional vaccine approaches to obtain long lasting immunity to viruses that have several sera types~r 5 or viruses that are prone to mutation.
Nucleic acid based vaccines offer the potential to produce long lasting immunity against viral epitopes that are highly conserved, such as with the nucleoprotein of viruses.
Injecting plasmids encoding specific proteins by the present invention results.in increased immune responses, as measured by antibody production. Thus, the present invention 10 includes new methods of providing nucleic acid vaccines by delivering a formulated nucleic acid molecule with a needle-free device as described herein.
The efficacy of nucleic acid vaccines is enhanced by one of at least three methods:
(1) the use of delivery systems to increase the stability and distribution of plasmid within the muscle, (2) by the expression (or delivery) of molecules to stimulate antigen 15 presentation/tcansfer, or (3) by the use of adjuvants that may modulate the immune response.
Polvmeric and non- ,pQlvmeric formulations for ~asmid del~verv to muscle The present invention provides polymeric and non-polymeric formulations which address problems associated with injection of nucleic acids suspended in saline. Plasmids suspended in saline have poor bioavailability in muscle due to rapid degradation of plasmid by extracellular nucleases. One possible approach to overcome the poor bioavailability is to protect plasmid from rapid nuclease degradation by condensing the plasmid with commonly used cationic complexing agents. However, due to the physiology of the muscle, the use of rigid condensed particles containing plasmid for efficient transfection of a larger number of muscle cells has not been successful to date.
Cationic lipid and polylysine plasmid complexes do not cross the external lamina to gain access to the caveolae and T tubules [Wolff, J.A., et al., 1992, J. Cell. Sci.
103:1249-1259].
Thus, the strategy identified for increasing the bioavailability of plasmid in muscle was to: protect plasmid from rapid extracellular nuclease degradation, disperse and retain intact plasmid in the muscle, and facilitate the uptake of plasmid by muscle cells. Two specific methods of accomplishing this, which preferably are used in conjunction with needle-free delivery, are (a) the use of protective, interactive, non-condensing systems (b) the use of modified gold particles.
Delivery and expression of nucleic adds is limited due to degradation of the nucleic acids by components of organisms, such as nucleases. Thus, protection of the nucleic acids when delivered in vivo can greatly enhance the resulting expression, thereby enhancing a desired pharmacological or then~peutic effect. It was found that certain types of compounds which interact with a nucleic acid (e.g., DNA) in solution but do not condense the nucleic acid provide ~n vivo protection to the nucleic acid, and correspondingly enhance the expression of an encoded gene product. A detailed description of the formulations that can be used in the present invention can be found in PCT Application No. PCT/US96/05679 which is hereby incorporated as a reference in its entirety including any drawings. As noted above, preferably such formulations are delivered by using a needle free device as described herein.
Inert particles coated with DNA have been used to deliver genes to cells. An advantage of coating inert particles, for instance gold beads, with nucleic acids is that the particle carrier actually penetrates the cell. Hence, the nucleic acid is delivered to the interior of the cell and should become incorporated and expressed in a more efficient manner. However, the conventional procedure for preparation of DNA-coated gold particles results in heterogeneous distribution of DNA from particle to particle, which produces variable expression from cell to cell (Butow et al., Meth Enzymol.
264:265-278, 1996).
It is undesirable to create nucleic acid vaccines which pmduce variable results from sample to sample. Thus, the present invention provides gold particles uniformly coated with DNA by covalently attaching cysteine terminated DNA binding peptides to the gold surface. Furthermore, the invention enhances the intracellular transport of DNA released from the gold particles by non-covalent association of high affinity DNA
binding peptides, which contain nuclear localization sequences, with the plasmid. The formulation provides the most reproducible amount of plasmid on gold particles, independent of the diameter of WO 99/31262 PCT/US9$/26823 the particle. Preferably such modified gold particle formulations are delivered by using a needle-free device as described herein.
VI Diseases and Conditions for Intramuscutar p,~ De]ivg~y The present invention described herein can be utilized for the delivery and expression of many different coding sequences. In particular, the demonstrated effectiveness for the PINC systems (PCT Application No. PCT/US96/05679) for delivery to muscle indicate that such formulations are effective for delivery of a large variety of coding sequences to muscle by needle free injection. Specific suggestions for delivery of coding sequences to muscle with the needle free device of the present invention include those summarized in Table 1 below.
Table 1: Applications for Plaamid-Based Gene Therapy by Intramnscalar Injection Muscle and nerve dborden References are numbered as they are cited in U.S.
Application No. PCT/US96N5679, which hu beeo incorporated by reference in its entirety.
Duehonne's muscular dystrophy Acsadi 1991 [5], Karpati 1993 [6J, Miller 1993 [7j Myotrophic disorders (IGF-I) Coleman 1997 [8], Alila 1997 [9]
Neumtrophic disorders (IGF-I) Alila 1997 [9], Rabinovsky 1997 [10]
2S Secretion of a:preaod protein into the systemic circulation Hemophiliac A and B Anwer 1996 [I1], Kuwahara-Rundell 1994 [12], Miller 1994 [131 30 l.rythropoictin-responsive Tripathy 1996 [14]

Pituitary dwarfism Anwer 1996 [l l], Dahler 1994 [!5]

1-Antittypsin defiaency Levy 1996 [I6]

Autoimmune and Inflammatory Raz 1993 [17]
diseases Hypercholesterolema Fazio 1994 [18J

35 Hypotension Ma 1995 [191 Hypertension Xiong 1995 [20]

WO 99/31262 PCT/US98/2b823 Nncleieweid vaccines Herpes Simplex Virus Manickan 1995 [21], Ghiasi 1995 [22], McClements 1996 [23], Kriesel 1996 [24]

S Hepatitis B Virus Davis 1993 [25], Davis 1994 [2b], Davis 1996 [27]

Influenza Virus Donnelly 1995 [28], Ulmer 1993 [29], Uhner 1994 [30]

Tuberculosis Ld~vtie 1994 [31], Tascon, 1996 [32]

Human immunodeflciency Virus Shiver 1995 [33], Coney 1994 [34], Wang 1993 [35]

Cancer Raz 1993 [I7], Russell 1994 [36]

1 U Maleria Hoffman 1995 [37j, Sedegah 1994 [38]

Hepatitis C virus Major 1995 [39], Lagging 1995 [40]

Flavivirus Phillpotts ! 996 [41 ]

C:ytom~alovirus Parade 1995 [42]

Salmonella typhi Lopez-Macias 1995 [43]

1$ Mycoplasma puhnonis Lai 1995 [44]

Rabies virus Xiang 1995 [45]

]~~CS
20 The following examples are offered by way of illustration and are not intended to limit the scope of the invention in any manner. One of ordinary skill in the art would recognize that the various molecules and/ or amounts disclosed in the examples could be adjusted or substituted by larger amounts (for larger scaled experiments) or by inclusion of a different Transfection Facilitating Agent.
Ezample 1 Demonstration of Transfection Facilitatinsz Agent Plasmid DNA Complex Formation ~paration of PyP Formulated Nucleic Acid Molecules Concentrated pDNA stock solutions were made by lyophilizing and rehydrating pDNA with water to a final pDNA concentration of 3-Smg/ml. Formulations were made by aliquoting appropriate volumes of sterile stock solutions of pDNA, SM NaCL, and polymer to obtain a final pDNA concentration in an isotonic polymer salution.
Stock solutions were added in the following order: water, plasmid, polymer, and SM
NaCI. The plasmid and polymers were allowed to incubate at room temperature for 15 minutes prior to adding salt or lactose for ionicity adjustments. Likewise, Na-citrate buffers in 0.9%
NaCI were added after incubating the plasmid and polymers for 15 minutes at room temperature. The osmotic pressure of selected formulations was measured (n=3) using a Fiske One-Ten Micro-Sample Osmometer. The pH of all formulations was measured using, an Accumet Model 15 pH Meter and the viscosity of all formulations was musing a Progrannmable Rheometer Model DV-III.
Dynamic dialysis was used with various interactive polymer formulations to measure binding between PVP and plasmid DNA. One ml of formulations and corresponding controls were place in prewashed dialysis sacs. The dialysis sacs were closed and suspended in stsrred saline solutions (100 ml) at 25°C. One ml aliquots were taken from the acceptor compartment over time and replaced with fresh media.
The concentration of PVP in the diffused samples collected over time was measured spectroscopically at 220 nm.
In all cases, the rate of PVP diffusion through the dialysis membrane was d in the presence of plasmid DNA, indicating complex formation between PVP and plasmid DNA. The reduction in the diffusion rate for PVP in the presence of plasmid DNA was directly proportional to the initial amount of PVP in the dialysis sac. It was also determined that the sac volume remained constant during the duration of the experiment and that adherence of PVP to the membrane was negligible.
~~xration of Nucleic Acid Molecules Formulated With Modified Gold Particles 100 mg of 2.3 m gold particles were place in fuming nitric acid overnight at 23°C.
The particles were then washed exhaustively with 18 S2 deionized water, which had been degassed under vacuum. A solution of Cys-Tyr-Lys-Ala- (Lys)8-Trp-Lys (CK8) was treated for 1 hr with l OmM dithiothreitol and then passed over a desalting column prepared in degassed water. Su~cient peptide to make the final solution 1mM
CK8 was added to the cleaned gold particles and allowed to sit under N2 overnight at 23°C. The particles were then washed with degassed water until there was no absorbance at 280 nm and then lyophilized. One pg of CMV-luciferase was added in water to 0.45 mg of modified gold particles, and then dried in a desiccator. Binding of the DNA to the CK8 modified particles was shown by eluting with 1.5 mM phosphate, and visualizing the eluted relaxed and supercoiled plasmid on an agarose gel with ethidium bromide. As a control, DNA was precipitated with Cap''', dried and added to the center of the Kapton cagier membrane in 100% ethanol. DNA formulated with modified gold particle was transferred to the Kapton membrane in water and in 100% ethanol. (Fig. 3) 5 Significant iuciferase expression in vivq.was observed with DNA formulated with modified gold particles when the formulation was transferred to the Kapton membrane in both 100~/o ethanol and, more importantly, in water (fig 3). Although the average expression was lower using water as the transfer solvent, this result suggests that it will be possible to include proteins such as transcription factors with the DNA.
Ezample 2 N 1' Device.
Formulated plasnuds were prepared as follows in a sterile manner in 2m1 single dose vials.
Plesmid/iriposomes (DOTMA:DOPE 1:1 m/m) 1:3 -/+ 20 g DNAImI
Plasmid/K8/TTS-1 1:3:1 -/+/- 20 g DNA/ml pVP 5% w/v 20 g DNA/ml PEG 10% w/v 20 g DNA/ml Control:
DNA suspended in Saline 20 g DNAImI
DNA formulations were injected by needle-free device into SOmI polypropylene tubes indicative of a "high impact" worst case scenario. Additionally the needle free device was set at maximum penetration as described in the product instruction manual.
DNA stability was determined by agarose gel electrophoresis of the samples before and after injection. Measurement of stability was determined by the amount of visible degradation, i.e. smearing, and by quantitating supercoiled and open circular DNA. Our data indicates that even in this extreme example the formulated DNA samples only exhibit slight degradation.

Eznmple 3 Demono~ of Formulated Nucleic Acid Stabili~,y Upgn_Ir~iection Through Variops Needle Free Device Deliverv Nozzles Formulated nucleic acid molecules were prepared as follows in a sterile manner.
0.1 mg pCT0129/mL in DOTMA:Chol (1:1 ~m) 1:3 (-/+); 10%lactose 3.0 mg pCT0129/mL in S% PVP (50 kDa); 150 mM NaCI
Non-formulated samples:
0.1 mg pCT0129/mL in 150 mM NaCL
3.0 mg pCT0129/mL in 150 mM NaCL
Each of these formulations were injected through different size needle-free injection nozzles. A non-injected formulation was used as a control for each experiment.
The formulation was injected into a 50mL conical tube. Each sample was agarose gel electrophoresed after injection.
Measurement of stability was determined by the amount of visible degradation, i.e., smearing, and by quantitating supercoiled and open circular DNA. Our data indicates that even in this example which uses the most extreme injection parameters the nozzle size did not effect the state of the formulated DNA.
Example 4 Elicitation of Immune Res~~onse Following~tramuscular Iniection~f plasmid.
In this study, a Human Growth Hormone {hGH) expression plasmid is injected into the muscle of dogs and pigs to examine the production of anti-hGH
antibodies.(figs 1,2).
The expression plasmid was injected via a needle free device or by a needle to examine if the magnitude of the immune response is affected by the injection method or formulation.
For elicitation of immune response, pCMV-hGH plasmid was suspended in saline or formulated with PVP and injected into biceps femoris and semitendinosus muscles of dogs using a needle free device or 22 gauge needle. Blood was collected before plasmid injection and once a week after the injection. Blood samples were kept overnight at 4° C, centrifuged at 2000 g for 15 min and serum was collected for detection of anti-hGH
antibodies by ELISA.

Significant levels of hGH antibodies were detectable in jet (aerosol) injected animals 14 days after a single i.m. dose of hGH plasmid. The levels of hGH
antibodies increased over time reaching a plateau by 21 days and remained elevated throughout the 112 day pre-boost periods. Repeating the plasmid dose on day 112 augmented the antibody response by 100 fold.
In comparison, the needle injection of hGH plasmid formulated with PVP did not pmduce significantly detectable levels of hGH antibodies. A booster dose was required to achieve significant antibody response from needle injection. Peak antibody levels from aerosol injections were about 20 times higher than from needle injections.
Control animals received CMV-CAT plasmid formulated with PVP without the hGH gene, and the animals did not produce anti-hGH antibodies.
Needle-free injection of hGH plasmid suspended in saline also leads to the production of anti-hGH antibodies. A single dose of naked DNA was su~cient to achieve significant levels of hGH antibodies when administered via the needle-free device.
I S In comparison, multiple doses were required to elicit antibody response with needle injection. The antibody response from needle-free injection was 5 times higher compared to needle injection.
In the same experiment, needle-fi~ee injection gave 15-20 times better immune response compared to needle injection when the plasmid was formulated with PVP.
One skilled in the art would readily appreciate that the present invention is well adapted to carry out the objects and obtain the ends and advantages mentioned, as well as those inherent therein. The molecular complexes and the methods, procedures, treatments, molecules, specific compounds described herein are presently representative of preferred embodiments are exemplary and are not intended as limitations on the scope of the invention. Changes therein and other uses will occur to those skilled in the art which are encompassed within the spirit of the invention are defined by the scope of the claims.
It will be readily apparent to one skilled in the art that varying substitutions and modifications may be made to the invention disclosed herein without departing from the scope and spirit of the invention.

All patents and publications mentioned in the specification are indicative of the levels of those skilled in the art to which the invention pertains. All patents and publications are herein incorporated by reference to the same extent as if each individual publication was specifically and individually indicated to be incorporated by reference.
The invention illustratively described h'grein suitably may be practiced in the absence of any element or elcments, limitation or limitations which is not specifically disclosed herein. Thus, for example, in each instance herein any of the teens "comprising", "consisting essentially of and "consisting of may be replaced with either of the other two teens. The terms and expressions which have been employed are used as terms of description and not of limitation, and there is no intention that in the use of such terms and expressions of excluding any equivalents of the features shown and described or portions thereof, but it is recognized that various modifications are possible within the scope of the invention claimed. Thus, it should be understood that although the present invention has been specifically disclosed by prefen~ed embodiments and optional features, modification and variation of the concepts herein disclosed may be resorted to by those skilled in the art, and that such modifications and variations are considered to be within the scope of this invention as defined by the appended claims.
In addition, where features or aspects of the invention are described in teens of Markush groups, those skilled in the art will recognize that the invention is also thereby described in terms of any individual member or subgroup of members of the Markush group. For example, if X is described as selected from the group consisting of bromine, chlorine, and iodine, claims for X being bromine and claims for X being bmmine and chlorine are fully described.
Those references not previously incorporated herein by reference, including both patent and non-patent references, are expressly incorporated herein by reference for all purposes. Other embodiments are within the following claims.

Claims

CLAIMS:

1. A method for delivering a nucleic acid molecule to a mammal comprising the step of providing said nucleic acid molecule formulated with a transfection facilitating agent through and/or to the skin of said mammal by use of a needle-free device configured and arranged to cause aerosol delivery of said nucleic acid molecule through and/or to the skin of said mammal.

2. The method of claim 1, wherein said nucleic acid molecule is DNA.

3. The method of claim 1, wherein said nucleic acid molecule is a plasmid with a eukaryotic promoter which expresses a therapeutic molecule.

4. The method of claim 3, wherein said therapeutic molecule is for human growth hormone.

5. The method of claim 1, wherein said nucleic acid molecule is RNA.

6. The method of claim 1, wherein said transfection facilitating agent is a protective, interactive and non-condensing compound.

7. The method of claim 1, wherein said transfection facilitating agent is selected from the group consisting of one or more polyvinyl-pyrrolidones, one or more cationic lipids, one or more liposomes, one or more peptides, one or more modified gold particles, and one or more lipopepddes.

8. The method of claim 1, wherein said method results in an antibody response.

9. The method of claim 8, wherein said antibody response is at least 3 times greater than the antibody response caused by needle injection of the nucleic acid molecule suspended in saline.

10. The method of claim 9, wherein said antibody response is at least 10 times greater than the antibody response caused by needle injection of the nucleic acid molecule formulated with polyvinyl-pyrrolidone.

11. The method of claim 1, wherein said method induces an immune response.

12. The method of claim 11, wherein said immune response is a humoral immune response.

13. The method of claim 11, wherein said immune response is a T-cell mediated immune response.

14. The method of claim 11, wherein said immune response is a prophylactic immune response.

15 The method of claim 11, wherein said immune response is a therapeutic immune response.

16. The method of claim 1, wherein said maximal is a human.

17. The method of claim 1, wherein said needle-free means for delivering is a needle-free device that injects said nucleic acid molecule by aerosol delivery through and/or to the skin of a mammal.

18. The method of claim 1, wherein said needle-free means for delivering is a gas pressure device.

19. The method of claim 1, wherein said needle-free means for delivering is a mechanical spring device.

20. The method of claim 1, wherein said needle-free means for delivering is a multi-port device.

21. A kit comprising a provider for providing a nucleic acid molecule formulated with a transfection facilitating agent and a needle-free device for delivering said nucleic acid molecule through and/or to the skin of a mammal.

22. The kit of claim 21, wherein said nucleic acid molecule is DNA.

23. The kit of claim 21, wherein said nucleic acid molecule is a plasmid with a eukaryotic promoter which expresses a gene.

24. The kit of claim 23, wherein said gene is human growth hormone.

25. The kit of claim 21, wherein said nucleic acid molecule is RNA.

26. The kit of claim 21, wherein said tranfection facilitating agent is a protective, interactive and non-condensing compound.

27. The kit of claim 21, wherein said transfection facilitating agent is selected from the group consisting of one or more polyvinyl-pyrrolidones, one or more cationic lipids, one or more liposomes, one or more modified gold particles, one or more peptides, and one or more lipopeptides.

28. The kit of claim 21, wherein said needle-free device for delivering is a needle-free device that injects said nucleic acid molecule by aerosol delivery through and/or to the skin of a mammal.

29. The kit of claim 21, wherein said needle-free device for delivering is a gas pressure device.

30. The kit of claim 21, wherein said needle-free device for delivering is a mechanical spring device.

31. The kit of claim 21, wherein said needle-free device for delivering is a multi-port device.

32. A method for making a kit comprising the steps of combining (i) a provider for providing a formulated nucleic acid molecule formulated with a transfection facilitating agent with (ii) a needle-free device for delivering said nucleic acid molecule through and/or to the skin of a mammal.

33. The method of claim 32, wherein said nucleic acid molecule is DNA.

34. The method of claim 32, wherein said nucleic acid molecule is a plasmid with a eukaryotic promoter which expresses a gene.

35. The method of claim 34, wherein said gene is for human growth hormone.

36. The method of claim 32, wherein said nucleic acid molecule is RNA.

37. The method of claim 32, wherein said tranfection facilitating agent is a protective, interactive and non-condensing compound.

38. The method of claim 32, wherein said transfection facilitating agent is selected from the group consisting of: one or more polyvinyl-pyrrolidones, one or more cationic lipids, one or more liposomes, one or more modified gold particles, one or more peptides, and one or more lipopeptides.

39. The method of claim 32, wherein said needle-free device for delivering is a needle-free device that injects said nucleic acid molecule by aerosol delivery through and/or to the skin of a mannmal.

40. The method of claim 32, wherein said needle-free device for delivering is a gas pressure device.

41. The method of claim 32, wherein said needle-free device for delivering is a mechanical spring device.

42. The method of claim 32, wherein said needle-free device for delivering is a multi-port device.

43. A method of treating a mammal suffering from a disorder conventionally treated by administering human growth hormone, comprising the step of providing a nucleic acid molecule formulated with a transfection facilitating agent encoding human growth hormone through and/or to the skin of said mammal by use of a needle-free device configured and awanged to cause aerosol delivery of said nucleic acid molecule through and/or to the skin of said mammal.

44. The method of claim 43, wherein said mammal is a human.

45. The method of claim 43, wherein said tranfection facilitating agent is a protective, interactive and non-condensing compound.

46. The method of claim 43, wherein said transfection facilitating agent is selected from the group consisting of: one or more polyvinyl-pyrrolidones, one or more cationic lipids, one or more liposomes, one or more modified gold particles, one or more peptides, and one or more lipopeptides.

47. The method of claim 43, wherein said needle-free device for delivering is a needle-free device that injects said nucleic acid molecule by aerosol delivery through and/or to the skin of a mammal.

48. The method of claim 43, wherein said needle-free device for delivering is a gas pressure device.

49. The method of claim 43, wherein said needle-free device for delivering is a mechanical spring device.

50. The method of claim 43, wherein said needle-free device for delivering is a multi-port device.

51. A method of treating a mammal suffering from cancer, comprising the step of providing a nucleic acid molecule formulated with a transfection facilitating agent through and/or to the skin of said mammal by use of a needle-free device configured and arranged to cause aerosol delivery of said nucleic acid molecule through and/or to the skin of said mammal, wherein said molecule encodes a cancer antigen.

52. The method of claim 51, wherein said mammal is a human.

53. The method of claim 51, wherein said cancer antigen is MAGE 1, and said cancer is melanoma.

54. The method of claim 51, wherein said tranfection facilitating agent is a protective, interactive and non-condensing compound.

55. The method of claim 51, wherein said transfection facilitating agent is selected from the group consisting of: one or more polyvinyl-pyrrolidones, one or more cationic lipids, one or more liposomes, one or more modified gold particles, one or more peptides, and one or more lipopeptides.

56. The method of claim 51, wherein said needle-free device for delivering is a needle-free device that injects said nucleic acid molecule by aerosol delivery through and/or to the skin of a mammal.

57. The method of claim 51, wherein said needle-free device for delivering is a gas pressure device.

58. The method of claim 51, wherein said needle-free device for delivering is a mechanical spring device.

59. The method of claim 51, wherein said needle-free device for delivering is a multi-port device.

60. A method of treating a mammal suffering from an infectious disease, comprising the step of providing a nucleic acid molecule formulated with a transfection facilitating agent through and/or to the skin of said mammal by use of a needle-free device configured and arranged to cause aerosol delivery of said nucleic acid molecule through and/or to the skin of said mammal, wherein said molecule encodes an antigen for said infectious disease.

61. The method of claim 60, wherein said mammal is a human.

62. The method of claim 60, wherein said infectious disease antigen is HBV
core antigen, and said infectious disease is chronic hepatitis.

63. The method of claim 60, wherein said transfection facilitating agent is a protective, interactive and non-condensing compound.

64. The method of claim 60, wherein said transfection facilitating agent is selected from the group consisting of: one or more polyvinyl-pyrrolidones, one or more cationic lipids, one or more liposomes, one or more modified gold particles, one or more peptides, and one or more lipopeptides.

65. The method of claim 60, wherein said needle-free device for delivering is a needle-free device that injects said nucleic acid molecule by aerosol delivery through and/or to the skin of a mammal.

66. The method of claim 60, wherein said needle-free device for delivering is a gas pressure device.

67. The method of claim 60, wherein said needle-free device for delivering is a mechanical spring device.

68. The method of claim 60, wherein said needle-free device for delivering is a mufti-port device.

69. A method of formulating nucleic acid molecules with modified inert particles comprising the steps of combining said nucleic acid molecules with said modified inert particles in an aqueous environment.

70. The method of claim 69, wherein said modified inert particles are modified gold particles.

71. A method of modifying gold particles comprising the steps of washing said gold particles in fuming or mixed acid solutions, and combining said gold particles with cationic DNA binding peptides to form a monolayer coating.

72. The method of claim 71, wherein said cationic DNA binding peptides have cysteine as the terminal residue.

73. The method of claim 71, wherein said fuming acid is nitric acid.

74. The method claim 71, wherein said mixed acid comprises nitric acid and sulfuric acid.

75. A method for delivering a nucleic acid molecule to a mammal comprising the step of providing said nucleic acid molecule formulated with modified gold particles through and/or to the skin of said mammal by use of a needle-free device configured and arranged to cause aerosol delivery through and/or to the skin of said mammal.

76. The method of claim 74, wherein said needle-free device for delivering is a needle-free device that injects said nucleic acid molecule by aerosol delivery through and/or to the skin of a mammal.

77. The method of claim 74, wherein said needle-free device for delivering is a gas pressure device.

78. The method of claim 74, wherein said needle-free device for delivering is a mechanical spring device.

79. The method of claim 74, wherein said needle-flee device for delivering is a multi-port device.