Compositions for Transfecting Resistant Cell Types

A transfection reagent composition comprising: 30-60 MOL % of an cationic lipid, or pharmaceutical acceptable salt thereof; 10-60 MOL % structural lipid; a sterol and 0.1 to about 10 MOL % of a stabilizing agent is provided. The reagent is particularly adapted for neuron and related cell types. A method of manufacturing LNP including nucleic acid for selective uptake into either neurons or astrocytes or neural progenitor cells is also provided.

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Description

This application claims the benefit of U.S. application No. 62/403,640 filed on Oct. 3, 2016.

BACKGROUND OF THE INVENTION Field of Invention

The field of the invention is the transfer of active nucleic acids into cells.

Related Art

Nucleic acids in the form of polynucleotides or oligonucleotides can be used to focus treatment on a particular genetic target, either by interfering with its expression, or by restoring or augmenting its expression, or by editing the gene.

Delivering nucleic acids into cells or tissues presents challenges because nucleic acids are relatively large, negatively charged, hydrophilic compounds which are not capable of passively diffusing across the cell membrane and are also vulnerable to nucleases. (Akhtar, Basu S Fau-Wickstrom et al. 1991)

Existing approaches for delivering these nucleic acids across the cell membrane include viruses such as adeno-associated viruses as vectors for gene restoration, but these can cause immune responses in treated individuals (Mingozzi and High 2013). Cationic lipids and polymers have also been used in experiments, but each has issues of transfection efficiency, stability and toxicity. (Lv, Zhang et al. 2006) To increase the therapeutic activity of the nucleic acids, significant efforts in the field have focused on lipid nanoparticles (LNP) that comprise cationic lipids, including ionizable cationic lipids (also known as “cationic lipids”) and PEGylated lipids, for the efficient encapsulation and delivery of nucleic acids to cells (Tam, Chen et al. 2013, Kauffman, Webber et al. 2015).

LNPs have been engineered to obtain different pharmacokinetics, different bio-distribution in tissues, biodegradability, or altered toxicity, to favor the therapeutic activity of the nucleic acid.

CNS tissue is notoriously difficult to transfect (O'Mahony, Godinho et al. 2013). The cells are sensitive to their conditions and are hard to maintain in vitro. A more effective method for effectively delivering nucleic acids into neurons is still required.

SUMMARY OF THE INVENTION

According to embodiments of the invention, there is provided a transfection reagent composition comprising: 30-60 MOL % of an cationic lipid, or pharmaceutical acceptable salt thereof; 10-60 MOL % structural lipid; a sterol and 0.1 to about 10 MOL % Stabilizing agent. In embodiments, the composition of Claim 1, wherein the cationic lipid is an amino lipid. In embodiments, The composition of Claim 1 or 2, wherein the cationic lipid is selected from the group consisting of 1,17-bis(2-octylcyclopropyl)heptadecan-9-yl-4-(dimethylamino)butanoate, DODAC, DOTMA, DDAB, DOTAP, DOTAP⋅Cl, DC-Chol, DOSPA, DOGS, DODAP, DODMA, DMRIE, C12-200, and pharmaceutically acceptable salts thereof. In embodiments, the cationic lipid has the formula:

or a pharmaceutically acceptable salt thereof, wherein:

R1 and R2 are each independently H, alkyl, alkenyl, alkynyl, cycloalkyl, aryl, heteroaryl, and heterocyclyl,

wherein each of alkyl, alkenyl, alkynyl, cycloalkyl, aryl, heteroaryl, and heterocyclyl is optionally substituted by H, halo, hydroxy, cyano, oxo, Ci-C6 alkyl optionally substituted by halo, hydroxy, or alkoxy;

or R1 and R2 are taken together with the N atom to which they are both attached to form a 3-8 member heteroaryl or heterocyclyl;

wherein each of the heteroaryl and heterocyclyl is optionally substituted by H, halo, hydroxy, cyano, oxo, nitro, C1-C6 alkyl optionally substituted by halo, hydroxyl, or alkoxy;

R3 is absent, H, alkyl, alkenyl, alkynyl, cycloalkyl, aryl, heteroaryl, or heterocyclyl;

R4 and R5 are each independently H, alkyl, alkenyl, alkynyl, cycloalkyl, aryl, heteroaryl, or heterocyclyl;

wherein each of alkyl, alkenyl, alkynyl, cycloalkyl, aryl, heteroaryl, and heterocyclyl is optionally substituted by H, halo, hydroxy; cyano; oxo; C1-C6 alkyl optionally substituted by halo, hydroxy, or alkoxy;

X is O, S, —NR4—, —S—S—, —OC(═O)—, —C(═O)O—, —OC(═O)O—, —NR4C(═O)—, —C(═O)NR4—, —NR4C(═O)O—, —OC(═O)NR4—, —NR4C NR4, —NR4C(═S)O—, —OC(═S)NR4—, —NR4C(═S)NR4—, or —CR4R5—;

Y and Z are independently C10 to C30 groups having the formula L1-(CR6R7)a-[L2-(CR6R7)P]y-L3-Re, wherein: L1 is a bond, —(CR6Ry)-, —O—, —CO—, —NR8—, —S—, or a combination thereof; each 5 and R7, independently, is H, halo, hydroxyl, cyano, C1-C6 alkyl optionally substituted by halo, hydroxyl, or alkoxy;

L2 is a bond, —(CR6R7)—, —O—, —CO—, —NR8—, —S—,

or a combination thereof, or has the formula

wherein b, c, and d are each independently 0, 1, 2, or 3, given the sum of b, c, and d is at least 1 and no greater than 8; and R9 and R10 are each independently R7, or adjacent R9 and R10, taken together, are optionally a bond;

L3 is a bond, —(CR6R7)—, —O—, —CO—, —NR8—, —S—,

or a combination thereof;

R8 is independently H, halo, hydroxy, cyano, alkoxy, aryl, heteroaryl, or C1-C6 alkyl optionally substituted by halo, hydroxy, or heterocyclyl, or R8 has the formula:

a is 0, 1, 2, 3, or 4; a is 0-6; each β, independently, is 0-6; and γ is 0-6.

In embodiments, the cationic lipid is 1,17-bis(2-octylcyclopropyl)heptadecan-9-yl-4-(dimethylamino)butanoate or a pharmaceutically acceptable salt thereof.

In embodiments, the structural lipid is selected from the group consisting of diacylphosphatidylcholines, diacylphosphatidylethanolamines, sterols, ceramides, sphingomyelins, dihydrosphingomyelins, cephalins, and cerebrosides. In embodiments, the stabilizing agent is selected from the group consisting of polyethylene glycol, polyethylene glycol-DMG, polyoxyethylene alkyl ethers, diblock polyoxyethylene ether co-polymers, triblock polyoxyethylene alkyl ethers co-polymers, and amphiphilic branched polymers. In embodiments, the sterol is cholesterol. In embodiments, the stabilizing agent is selected from the group consisting of polyoxyethylene (20) oleyl ether, polyoxyethylene (23) lauryl ether, polyoxyethylene (40) stearate, poly(propylene glycol)11-block-poly(ethylene glycol)16-block-poly(propylene glycol)11, poly(propylene glycol)12-block-poly(ethylene glycol)28-block-poly(propylene glycol)12. In embodiments, the stabilizing agent is PEG-conjugated lipid. In embodiments, the stabilizing agent is PEG-DMG. In embodiments, the cationic lipid comprises about 40 MOL %. In embodiments, the stabilizing agent comprises about 2.5 MOL % stabilizer.

According to embodiments of the invention, there is provided a transfection reagent composition comprising: 30-60 MOL % of an cationic lipid, or pharmaceutical acceptable salt thereof; 10-60 MOL % structural lipid; a sterol and 0.1 to about 10 MOL % Stabilizing agent. wherein: the cationic lipid is 1,17-bis(2-octylcyclopropyl)heptadecan-9-yl-4-(dimethylamino)butanoate or a pharmaceutically acceptable salt thereof; the structural lipid is 1,2-dioleoyl-sn-glycero-3-phosphoethanolamine (DOPE); the sterol is cholesterol, and the stabilizing agent is polyoxyethylene (40) stearate.

According to embodiments of the invention, there is provided a transfection reagent composition comprising: 30-60 MOL % of an cationic lipid, or pharmaceutical acceptable salt thereof; 10-60 MOL % structural lipid; a sterol and 0.1 to about 10 MOL % Stabilizing agent. wherein: the cationic lipid is 1,17-bis(2-octylcyclopropyl)heptadecan-9-yl-4-(dimethylamino)butanoate or a pharmaceutically acceptable salt thereof; the structural lipid is 1,2-dioleoyl-sn-glycero-3-phosphoethanolamine (DOPE); the sterol is cholesterol, and the stabilizing agent is polyethylene glycol conjugated lipid.

In embodiments, the structural lipid is from about 10 to about 40 MOL % 1,2-dioleoyl-sn-glycero-3-phosphoethanolamine (DOPE). In embodiments, the sterol is present at 10 to 20 MOL %.

In embodiments, the composition further includes a nucleic acid. In embodiments, the nucleic acid is a therapeutic nucleic acid. In other embodiments, it is a restorative nucleic acid replacing a missing or poorly functioning gene in a cell. In other embodiments, it is a modulating nucleic acid that reduces a genetic action in the cell. In other embodiments, it is a diagnostic nucleic acid, that identifies diseased cells.

In embodiments, the nucleic acid is a DNA, an RNA, a locked nucleic acid, a nucleic acid analog, or a plasmid capable of expressing an RNA.

In other embodiments, the nucleic acid is an antisense oligonucleotide, ribozyme, miRNA, rRNA, tRNA, siRNA, saRNA, snRNA, snoRNA, lncRNA, piRNA, tsRNA, srRNA, crRNA, tracrRNA, sgRNA, shRNA, ncRNA, miRNA, mRNA, pre-condensed DNA, pDNA, an aptamer, or a combination thereof.

In embodiments, the transfecting reagent is used to transfect a neuron, an astrocyte, and/or a progenitor cell. In embodiments, the composition exists in the form of nanoparticles having a diameter of from about 15 nm, 20 nm, 30 nm, 40 nm, 50 nm, 60 nm, 70 nm, 80 nm, 90 nm, 100 nm, 110 nm, 120 nm, 130 nm, 140 nm, 150 nm, 160 nm, 170 nm, 180 nm, 190 nm, 200 nm, to about 300 nm.

In embodiments of the invention, there is provided a method for introducing a nucleic acid into a cell, by contacting a cell with a transfecting reagent described above in combination with a nucleic acid, and wherein the activity of the nucleic acid, as well as the viability of the cell, are maintained. In embodiments, there is provided a method for modulating the expression of a target polynucleotide or polypeptide, comprising contacting a cell with the transfecting reagent in combination with a nucleic acid, wherein the nucleic acid is capable of modulating the expression of a target polynucleotide or polypeptide while the viability of the cell is preserved. In embodiments, the cell is a neuron. In embodiments, the cell is astrocyte. In embodiments, the cell is a progenitor cell.

According to embodiments of the invention, there is provided a method of manufacturing a lipid nanoparticle capable of targeting neurons, the method including increasing the ratio of cationic lipid to structural lipid in the lipid nanoparticle.

According to another embodiment of the invention, there is provided a method of manufacturing a lipid nanoparticle capable of targeting astrocytes, the method including decreasing the ratio of cationic lipid to structural lipid in the lipid nanoparticle. In embodiments, the cell is a mammalian cell. In embodiments, the cell is human.

Other aspects and features of the present invention will become apparent to those ordinarily skilled in the art upon review of the following description of specific embodiments of the invention in conjunction with the accompanying figures.

BRIEF DESCRIPTION OF THE DRAWINGS

In drawings which illustrate embodiments of the invention,

FIG. 1 is a photograph of neurons that have been treated with labelled Lipid Mix D formulated nanoparticles containing GFP mRNA. The top right is MAP2 (a neuronal marker) antibody staining, the bottom right is DiD labelling of the nanoparticle (a lipid label); the bottom left is GFP expression in the neurons, and the top left quadrant is a merged image showing DiD, MAP2, and GFP, establishing GFP expression in the live neurons;

FIG. 2 is a photograph showing staining perspectives to illustrate the ability of Lipid Mix B to transfect primary mixed neuronal culture. The top right is MAP2 (a neuronal marker) antibody staining, the bottom right is DiD labelling of the nanoparticle (a lipid label); the bottom left is GFP expression in the neurons, and the top left quadrant is a merged image showing DiD, DAPI, MAP2, and GFP, establishing GFP expression occurs in the glial cells. All images include DAPi, a nuclear stain;

FIG. 3 is a photograph showing staining perspectives to illustrate the ability of Lipid Mix C to transfect, and the viability of cells. The top right is MAP2 antibody staining, the bottom right is DID labelling of the nanoparticle; the bottom left is GFP expression in the neurons, and the top left quadrant is a merged image showing DiD, DAPI, MAP2, and GFP, establishing GFP expression in the live neurons. All images include DAPi, a nuclear stain;

FIG. 4 is a bar graph showing the level of GFP expression in neurons measured by ELISA following treatment with mRNA GFP Lipid Mix A and Lipid Mix D nanoparticles;

FIG. 5 is a bar graph showing the mean fluorescence intensity of GFP expression levels in neurons following treatment with mRNA GFP for Lipid Mix A and Lipid Mix D in comparison with Lipofectamine™ Messenger Max™ transfecting agent;

FIG. 6 is a bar graph showing viability of astrocytes 48 hours post treatment with mRNA loaded in Lipid Mix D versus MessengerMax™ transfecting reagent, as measured by Presto Blue assay;

FIG. 7 is a flow cytometry histogram showing Lipid Mix D GFP mRNA LNP-mediated mean fluorescence intensity in human neural progenitor cells (grey histogram) compared to untreated cells (black histogram)

FIG. 8 are two bar graphs showing Mean Fluorescent Intensity (MFI) levels and Percentage (%) of cells expressing GFP by flow cytometry of neural progenitor cells treated with GFP plasmid in LNPs comprised of Lipid Mix B (50 MOL % cationic lipid) and Lipid Mix C (40 MOL % cationic lipid);

FIG. 9 are two bar graphs showing percentage (%) of cells expressing GFP and Mean Fluorescent Intensity (MFI) levels via flow cytometry for neural progenitor cells treated with Lipid Mix A and Lipid Mix D GFP plasmid LNPs 48 hours post exposure; and

FIG. 10 is a bar graph showing Mean Fluorescence Intensity of GFP expression in human neural progenitor cells treated with GFP plasmid LNP formulations of Lipid Mix A, Lipid Mix B, Lipid Mix C, Lipid Mix D, Lipid Mix E and Lipid Mix F by flow cytometry.

 DETAILED DESCRIPTION

The present invention provides compositions, lipid particles containing a therapeutic agent, methods for making the lipid particles containing a therapeutic agent, methods for targeting specific cell types, and methods for delivering a therapeutic agent using the lipid particles.

In one aspect, the invention provides compositions of matter including one or more cationic lipid(s), one or more structural lipid(s), and one or more stabilizing agent(s).

In another aspect, the compositions of the invention are provided for mixing with nucleic acid therapeutics for delivery to target cells or tissues, or for treatment of mammals in need of such delivery for treatment of insufficiency or disease.

In another aspect, the invention provides compositions of matter including one or more cationic lipid(s), one or more structural lipid(s), one or more stabilizing agent(s), and one or more nucleic acid (NA).

In another aspect, the compositions according the invention are provided for formulating nucleic acid therapeutics for the treatment of diseases of the CNS. In another aspect, the invention provides a method for changing the target of a lipid nanoparticle from astrocytes to neurons.

“Lipid” refers to a group of organic compounds that are esters of fatty acids and are characterized by being insoluble in water but soluble in many organic solvents.

Lipid Particles. The invention provides lipid particles manufactured from the compositions described above. The lipid particles contain a therapeutic agent in some embodiments. The lipid particles include one or more cationic lipids, one or more structural lipid(s), one or more stabilizing agent(s), and one or more nucleic acids.

Cationic lipid. The lipid particles include a cationic lipid. As used herein, the term “cationic lipid” refers to a lipid that is cationic or becomes ionizable (protonated) as the pH is lowered below the pK of the cationic group of the lipid, but is progressively more neutral at higher pH values. At pH values below the pK, the lipid is then able to associate with negatively charged nucleic acids (e.g., oligonucleotides). As used herein, the term “cationic lipid” includes zwitterionic lipids that assume a positive charge on pH decrease, and any of a number of lipid species which carry a net positive charge at a selective pH, such as physiological pH. Such lipids include, but are not limited to, N,N-dioleyl-N,N-dimethylammonium chloride (DODAC); N-(2,3-dioleyloxy)propyl)-N,N,N-trimethylammonium chloride (DOTMA); N,N-distearyl-N,N-dimethylammonium bromide (DDAB); N-(2,3-dioleoyloxy)propyl)-N,N,N-trimethylammonium chloride (DOTAP); 3-(N—(N′,N′-dimethylaminoethane)-carbamoyl)cholesterol (DC-Chol), C12-200 and N-(1,2-dimyristyloxyprop-3-yl)-N,N-dimethyl-N-hydroxyethyl ammonium bromide (DMRIE).

In one embodiment, the cationic lipid is an amino lipid. Suitable amino lipids useful in the invention include those described in WO 2009/096558, incorporated herein by reference in its entirety. Representative amino lipids include 1,17-bis(2-octylcyclopropyl)heptadecan-9-yl 4-(dimethylamino)butanoate hydrochloride, I,2-dilinoleyoxy-3-(dimethylamino)acetoxypropane (DLin-DAC), 1,2-dilinoleyoxy-3-morpholinopropane (DLin-MA), I,2-dilinoleoyl-3-dimethylaminopropane (DLinDAP), I,2-dilinoleylthio-3-dimethylaminopropane (DLin-S-DMA), I-linoleoyl-2-linoleyloxy-3-dimethylaminopropane (DLin-2-DMAP), I,2-dilinoleyloxy-3-trimethylaminopropane chloride salt (DLin-TMA⋅Cl), I,2-dilinoleoyl-3-trimethylaminopropane chloride salt (DLin-TAP⋅Cl), I,2-dilinoleyloxy-3-(N-methylpiperazino)propane (DLin-MPZ), 3-(N,N-dilinoleylamino)-I,2-propanediol (DLinAP), 3-(N,N-dioleylamino)-I,2-propanedio (DOAP), I,2-dilinoleyloxo-3-(2-N,N-dimethylamino)ethoxypropane (DLin-EG-DMA), and 2,2-dilinoleyl-4-dimethylaminomethyl-[I,3]-dioxolane (DLin-K-DMA).

Suitable amino lipids include those having the general formula:

wherein R1 and R2 are either the same or different and independently optionally substituted C10-C24 alkyl, optionally substituted C10-C24 alkenyl, optionally substituted C10-C24 alkynyl, or optionally substituted C10-C24 acyl;

R3 and R4 are either the same or different and independently optionally substituted C1-C6 alkyl, optionally substituted C2-C6 alkenyl, or optionally substituted C2-C6 alkynyl or R3 and R4 may join to form an optionally substituted heterocyclic ring of 4 to 6 carbon atoms and 1 or 2 heteroatoms chosen from nitrogen and oxygen;

R5 is either absent or present and when present is hydrogen or C1-C6 alkyl;

m, n, and p are either the same or different and independently either 0 or 1 with the proviso that m, n, and p are not simultaneously 0;

q is 0, 1, 2, 3, or 4; and Y and Z are either the same or different and independently O, S, or NH.

In one embodiment, R1 and R2 are each linoleyl, and the amino lipid is a dilinoleyl amino lipid. In one embodiment, the amino lipid is a dilinoleyl amino lipid.

In embodiments of the invention, the cationic lipid is 1,17-bis(2-octylcyclopropyl)heptadecan-9-yl 4-(dimethylamino)butanoate hydrochloride. This compound is disclosed in United States Published Application 2013323269.

In other embodiments, the cationic lipid-like material is C12-200 as described by Kaufmann and his colleagues (Kaufmann k 2015)

The cationic lipid is present in embodiments of the composition and lipid particle of the invention comprise an amount from about 30 to about 60 mole percent (“MOL %”, or the percentage of the total moles that is of a particular component), preferably from 30 to 50 MOL %. In embodiments, the cationic lipid is present in 35 MOL %. In preferred embodiments, the cationic lipid is present in 40 MOL %.

Structural lipids. The composition and lipid particles of the invention include one or more structural lipids. Suitable structural lipids support the formation of particles during manufacture. Structural lipids refer to any one of a number of lipid species that exist in either in an anionic, uncharged or neutral zwitterionic form at physiological pH. Representative structural lipids include diacylphosphatidylcholines, diacylphosphatidylethanolamines, diacylphosphatidylglycerols, ceramides, sphingomyelins, dihydrosphingomyelins, cephalins, and cerebrosides.

Exemplary structural lipids include zwitterionic lipids, for example, distearoylphosphatidylcholine (DSPC), dioleoylphosphatidylcholine (DOPC), dipalmitoylphosphatidylcholine (DPPC), dioleoyl-phosphatidylethanolamine (DOPE), palmitoyloleoylphosphatidylcholine (POPC), palmitoyloleoyl-phosphatidylethanolamine (POPE) and dioleoyl-phosphatidylethanolamine 4-(N-maleimidomethyl)-cyclohexane-1-carboxylate (DOPE-mal), dipalmitoyl phosphatidyl ethanolamine (DPPE), dimyristoylphosphoethanolamine (DMPE), distearoyl-phosphatidylethanolamine (DSPE), 16-O-monomethyl PE, 16-O-dimethyl PE, 18-1-trans PE, 1-stearioyl-2-oleoyl-phosphatidyethanol amine (SOPE), and 1,2-dielaidoyl-sn-glycero-3-phosphoethanolamine (transDOPE).

In one embodiment, the structural lipid is 1,2-dioleoyl-sn-glycero-3-phosphoethanolamine (DOPE).

In one embodiment the structural lipid may be any lipid that is negatively charged at physiological pH. These lipids include phosphatidylglycerol such as dioleoylphosphatidylglycerol (DOPG), dipalmitoylphosphatidylglycerol (DPPG), palmitoyloleyolphosphatidylglycerol (POPG), cardiolipin, phosphatidylinositol, diacylphosphatidylserine, diacylphosphatidic acid, other anionic modifying groups joined to neutral lipids.

Stabilizing Agents are included in compositions and lipid nucleic acid embodiments to ensure integrity of the mixture. Stabilizing agents, in some embodiments of the invention, are polyethylene glycol-lipids. Suitable polyethylene glycol-lipids include PEG-modified phosphatidylethanolamine, PEG-modified phosphatidic acid, PEG-modified ceramides (e.g., PEG-CerC14 or PEG-CerC20), PEG-modified dialkylamines, PEG-modified diacylglycerols, PEG-modified dialkylglycerols. Representative polyethylene glycol-lipids include PEG-c-DOMG, PEG-c-DMA, and PEG-s-DMG. In one embodiment, the polyethylene glycol-lipid is N-[(methoxy poly(ethylene glycol)2000)carbamyl]-1,2-dimyristyloxlpropyl-3-amine (PEG-c-DMA).

In one embodiment, the polyethylene glycol-lipid is PEG-c-DOMG. In one embodiment, the polyethylene glycol-lipid is PEG-DMG (1,2-Dimyristoyl-sn-glycerol, methoxypolyethylene glycol). In embodiments, the polyethylene glycol lipid content is from 0 to 10%

Sterols are included in the preferred compositions, and lipid particles made therefrom include sterols, such as cholesterol.

Cholesterol was present 37 or 17 MOL % in some embodiments, and 0 MOL % in one formulation tested. Stabilizing agent was present at 1 to 2.5 MOL %.

In embodiments of the invention, the cationic lipid 1,17-bis(2-octylcyclopropyl)heptadecan-9-yl 4-(dimethylamino)butanoate hydrochloride, was varied from 35 MOL % to 50 MOL % while keeping the structural lipid (DSPC, DOPC, DOPE, POPC, for example) could be maintained at 10 to 40 MOL %.

Other suitable structural lipids include glycolipids (e.g., monosialoganglioside GM1).

In certain embodiments, the structural lipid is present in the lipid particle in an amount from about 10 to about 40 MOL %. In one embodiment, the structural lipid is present in the lipid particle in an amount from about 20 to about 30 MOL %. In one embodiment, the structural lipid is present in the lipid particle in about 17 MOL %. In one embodiment, the structural lipid is present in the lipid particle in about 20 MOL %, or in about 30 MOL %, or in about 40 MOL %.

Nucleic Acids. The compositions and lipid particles of the present invention are useful for the systemic or local delivery of nucleic acid therapeutics. As described herein, the nucleic acid therapeutic (NAT) is incorporated into the lipid particle during its formation.

As used herein, the term “nucleic acid therapeutic” (NAT) is meant to include any oligonucleotide or polynucleotide whose delivery into a cell causes a desirable effect Fragments containing up to 50 nucleotides are generally termed oligonucleotides, and longer fragments are called polynucleotides. In particular embodiments, oligonucleotides of the present invention are 20-50 nucleotides in length. Embodiments of the invention, oligonucleotides are 996 to 4500 nucleotides in length, as in the case of messenger RNA. In the context of this invention, the terms “polynucleotide” and “oligonucleotide” refer to a polymer or oligomer of nucleotide or nucleoside monomers consisting of naturally occurring bases, sugars and intersugar (backbone) linkages. The terms “polynucleotide” and “oligonucleotide” also includes polymers or oligomers comprising non-naturally occurring monomers, or portions thereof, which function similarly. Such modified or substituted oligonucleotides are often preferred over native forms because of properties such as, for example, enhanced cellular uptake and increased stability in the presence of nucleases. Oligonucleotides are classified as deoxyribooligonucleotides or ribooligonucleotides. A deoxyribooligonucleotide consists of a 5-carbon sugar called deoxyribose joined covalently to phosphate at the 5′ and 3′ carbons of this sugar to form an alternating, unbranched polymer. A ribooligonucleotide consists of a similar repeating structure where the 5-carbon sugar is ribose. The nucleic acid that is present in a lipid particle according to this invention includes any form of nucleic acid that is known. The nucleic acids used herein can be single-stranded DNA or RNA, or double-stranded DNA or RNA, or DNA-RNA hybrids. Examples of double-stranded DNA include structural genes, genes including control and termination regions, and self-replicating systems such as viral or plasmid DNA. Examples of double-stranded RNA include siRNA and other RNA interference reagents. Single-stranded nucleic acids include antisense oligonucleotides, ribozymes, microRNA, mRNA, and triplex-forming oligonucleotides.

In one embodiment, the polynucleic acid is an antisense oligonucleotide. In certain embodiments, the nucleic acid is a ribozyme, a non-coding nuclear or nucleolar RNA as explained in HUGO http://www.genenames.org/cgi-bin/genefamilies, miRNA, rRNA, tRNA, siRNA, saRNA, snRNA, snoRNA, lncRNA, piRNA, tsRNA, srRNA, crRNA, tracrRNA, sgRNA, shRNA, ncRNA, miRNA, mRNA, pre-condensed DNA, pDNA, an aptamer, or a combination thereof. In one embodiment, the nucleic acid therapeutic (NAT) is a plasmid or circular nucleic acid construct. In one embodiment, the NAT is a mRNA. In one embodiment, the NAT is a siRNA. In one embodiment, the NAT is a miRNA. In one embodiment, the NAT is a tracrRNA. In one embodiment, the NAT is a sgRNA.

The term “nucleic acids” also refers to ribonucleotides, deoxynucleotides, modified ribonucleotides, modified deoxyribonucleotides, modified phosphate-sugar-backbone oligonucleotides, other nucleotides, nucleotide analogs, and combinations thereof, and can be single stranded, double stranded, or contain portions of both double stranded and single stranded sequence, as appropriate.

The term “nucleotide,” as used herein, generically encompasses the following terms, which are defined below: nucleotide base, nucleoside, nucleotide analog, and universal nucleotide.

The term “nucleotide base,” as used herein, refers to a substituted or unsubstituted parent aromatic ring or rings. In some Embodiments, the aromatic ring or rings contain at least one nitrogen atom. In some embodiments, the nucleotide base is capable of forming Watson-Crick and/or Hoogsteen hydrogen bonds with an appropriately complementary nucleotide base. Exemplary nucleotide bases and analogs thereof include, but are not limited to, purines such as 2-aminopurine, 2,6-diaminopurine, adenine (A), ethenoadenine, N6-2-isopentenyladenine (6iA), N6-2-isopentenyl-2-methylthioadenine (2ms6iA), N6-methyladenine, guanine (G), isoguanine, N2-dimethylguanine (dmG), 7-methylguanine (7mG), 2-thiopyrimidine, 6-thioguanine (6sG) hypoxanthine and O6-methylguanine; 7-deaza-purines such as 7-deazaadenine (7-deaza-A) and 7-deazaguanine (7-deaza-G); pyrimidines such as cytosine (C), 5-propynylcytosine, isocytosine, thymine (T), 4-thiothymine (4sT), 5,6-dihydrothymine, O4-methylthymine, uracil (U), 4-thiouracil (4sU) and 5,6-dihydrouracil (dihydrouracil; D); indoles such as nitroindole and 4-methylindole; pyrroles such as nitropyrrole; nebularine; base (Y); In some Embodiments, nucleotide bases are universal nucleotide bases.

The term “nucleoside,” as used herein, refers to a compound having a nucleotide base covalently linked to the C-1′ carbon of a pentose sugar. In some Embodiments, the linkage is via a heteroaromatic ring nitrogen. Typical pentose sugars include, but are not limited to, those pentoses in which one or more of the carbon atoms are each independently substituted with one or more of the same or different —R, —OR, —NRR or halogen groups, where each R is independently hydrogen, (C1-C6) alkyl or (C5-C14) aryl. The pentose sugar may be saturated or unsaturated. Exemplary pentose sugars and analogs thereof include, but are not limited to, ribose, 2′-deoxyribose, 2′-(C1-C6)alkoxyribose, 2′-(C5-C14)aryloxyribose, 2′,3′-dideoxyribose, 2′,3′-didehydroribose, 2′-deoxy-3′-haloribose, 2′-deoxy-3′-fluororibose, 2′-deoxy-3′-chlororibose, 2′-deoxy-3′-aminoribose, 2′-deoxy-3′-(C1-C6)alkylribose, 2′-deoxy-3′-(C1-C6)alkoxyribose and 2′-deoxy-3′-(C5-C14)aryloxyribose. Also see, e.g., 2′-O-methyl, 4′-α-anomeric nucleotides, 1′-α-anomeric nucleotides (U.S. Pat. No. 4,835,263, Nguyen et al.), 2′-4′- and 3′-4′-linked and other “locked” or “LNA,” bicyclic sugar modifications (WO 98/22489; WO 98/39352; WO 99/14226). “LNA” or “locked nucleic acid” is a DNA analogue that is conformationally locked such that the ribose ring is constrained by a methylene linkage between the 2′-oxygen and the 3′- or 4′-carbon.

Sugars include modifications at the 2′- or 3′-position such as methoxy, ethoxy, allyloxy, isopropoxy, butoxy, isobutoxy, methoxyethyl, alkoxy, phenoxy, azido, amino, alkylamino, fluoro, chloro and bromo. Nucleosides and nucleotides include the natural D configurational isomer (D-form), as well as the L configurational isomer (L-form) (Beigelman, U.S. Pat. No. 6,251,666; Chu, U.S. Pat. No. 5,753,789; Shudo, EP0540742). When the nucleobase is purine, e.g., A or G, the ribose sugar is attached to the N9-position of the nucleobase. When the nucleobase is pyrimidine, e.g., C, T or U, the pentose sugar is attached to the N1-position of the nucleobase.

One or more of the pentose carbons of a nucleoside may be substituted with a phosphate ester. In some Embodiments, the phosphate ester is attached to the 3′- or 5′-carbon of the pentose. In some Embodiments, the nucleosides are those in which the nucleotide base is a purine, a 7-deazapurine, a pyrimidine, a universal nucleotide base, a specific nucleotide base, or an analog thereof.

The term “nucleotide analog,” as used herein, refers to embodiments in which the pentose sugar and/or the nucleotide base and/or one or more of the phosphate esters of a nucleoside may be replaced with its respective analog. In some embodiments, exemplary pentose sugar analogs are those described above. In some embodiments, the nucleotide analogs have a nucleotide base analog as described above. In some embodiments, exemplary phosphate ester analogs include, but are not limited to, alkylphosphonates, methylphosphonates, phosphoramidates, phosphotriesters, phosphorothioates, phosphorodithioates, phosphoroselenoates, phosphorodiselenoates, phosphoroanilothioates, phosphoroanilidates, phosphoroamidates, boronophosphates, and may include associated counterions. Other nucleic acid analogs and bases include for example intercalating nucleic acids (INAs, as described in Christensen and Pedersen, 2002), and AEGIS bases (Eragen, U.S. Pat. No. 5,432,272). Nucleic acids containing one or more carbocyclic sugars are also included within the definition of nucleic acids

The term “universal nucleotide base” or “universal base,” as used herein, refers to an aromatic ring moiety, which may or may not contain nitrogen atoms. In some Embodiments, a universal base may be covalently attached to the C-1′ carbon of a pentose sugar to make a universal nucleotide. In some Embodiments, a universal nucleotide base does not hydrogen bond specifically with another nucleotide base. In some Embodiments, a universal nucleotide base hydrogen bonds with nucleotide base, up to and including all nucleotide bases in a particular target polynucleotide. In some Embodiments, a nucleotide base may interact with adjacent nucleotide bases on the same nucleic acid strand by hydrophobic stacking. Universal nucleotides include, but are not limited to, deoxy-7-azaindole triphosphate (d7AITP), deoxyisocarbostyril triphosphate (dICSTP), deoxypropynylisocarbostyril triphosphate (dPICSTP), deoxymethyl-7-azaindole triphosphate (dM7AITP), deoxylmPy triphosphate (dlmPyTP), deoxyPP triphosphate (dPPTP), or deoxypropynyl-7-azaindole triphosphate (dP7AITP).

Further examples of such universal bases can be found, inter alia, in Published U.S. application Ser. No. 10/290,672, and U.S. Pat. No. 6,433,134.

As used herein, the terms “polynucleotide” and “oligonucleotide” are used interchangeably and mean single-stranded and double-stranded polymers of nucleotide monomers, including 2′-deoxyribonucleotides (DNA) and ribonucleotides (RNA) linked by internucleotide phosphodiester bond linkages, e.g., 3′-5′ and 2′-5′, inverted linkages, e.g., 3′-3′ and 5′-5′, branched structures, or internucleotide analogs. Polynucleotides have associated counter ions, such as H+, NH4+, trialkylammonium, Mg2+, Na+, and the like. A polynucleotide may be composed entirely of deoxyribonucleotides, entirely of ribonucleotides, or chimeric mixtures thereof. Polynucleotides may be comprised of internucleotide, nucleobase and/or sugar analogs. Polynucleotides typically range in size from a few monomeric units, e.g., 3-40 when they are more commonly frequently referred to in the art as oligonucleotides, to several thousands of monomeric nucleotide units. Unless denoted otherwise, whenever a polynucleotide sequence is represented, it will be understood that the nucleotides are in 5′ to 3′ order from left to right and that “A” denotes deoxyadenosine, “C” denotes deoxycytosine, “G” denotes deoxyguanosine, and “T” denotes thymidine, unless otherwise noted.

As used herein, “nucleobase” means those naturally occurring and those non-naturally occurring heterocyclic moieties commonly known to those who utilize nucleic acid technology or utilize peptide nucleic acid technology to thereby generate polymers that can sequence specifically bind to nucleic acids. Non-limiting examples of suitable nucleobases include: adenine, cytosine, guanine, thymine, uracil, 5-propynyl-uracil, 2-thio-5-propynyl-uracil, 5-methylcytosine, pseudoisocytosine, 2-thiouracil and 2-thiothymine, 2-aminopurine, N9-(2-amino-6-chloropurine), N9-(2,6-diaminopurine), hypoxanthine, N9-(7-deaza-guanine), N9-(7-deaza-8-aza-guanine) and N8-(7-deaza-8-aza-adenine).

As used herein, “nucleobase sequence” means any segment, or aggregate of two or more segments (e.g. the aggregate nucleobase sequence of two or more oligomer blocks), of a polymer that comprises nucleobase-containing subunits. Non-limiting examples of suitable polymers or polymers segments include oligodeoxynucleotides (e.g. DNA), oligoribonucleotides (e.g. RNA), peptide nucleic acids (PNA), PNA chimeras, PNA combination oligomers, nucleic acid analogs and/or nucleic acid mimics.

As used herein, “polynucleobase strand” means a complete single polymer strand comprising nucleobase subunits. For example, a single nucleic acid strand of a double stranded nucleic acid is a polynucleobase strand.

As used herein, “nucleic acid” is a nucleobase sequence-containing polymer, or polymer segment, having a backbone formed from nucleotides, or analogs thereof.

Preferred nucleic acids are DNA and RNA.

As used herein, nucleic acids may also refer to “peptide nucleic acid” or “PNA” means any oligomer or polymer segment (e.g., block oligomer) comprising two or more PNA subunits (residues), but not nucleic acid subunits (or analogs thereof), including, but not limited to, any of the oligomer or polymer segments referred to or claimed as peptide nucleic acids in U.S. Pat. Nos. 5,539,082; 5,527,675; 5,623,049; 5,714,331; 5,718,262; 5,736,336; 5,773,571; 5,766,855; 5,786,461; 5,837,459; 5,891,625; 5,972,610; 5,986,053; and 6,107,470; all of which are herein incorporated by reference. The term “peptide nucleic acid” or “PNA” shall also apply to any oligomer or polymer segment comprising two or more subunits of those nucleic acid mimics such as those described in Peptide-Based Nucleic Acid Mimics (PENAMS) of Shah et al. as disclosed in WO96/04000.

The lipid particles according to some embodiments of the invention can also be characterized by electron microscopy. The particles of the invention having a substantially solid core have an electron dense core as seen by electron microscopy. One such structure is disclosed in U.S. Pat. No. 9,758,795 by Cullis et al. Electron dense is defined such that area-averaged electron density of the interior 50% of the projected area of a solid core particle (as seen in a 2-D cryo EM image) is not less than x % (x=20%, 40%, 60%) of the maximum electron density at the periphery of the particle. Electron density is calculated as the absolute value of the difference in image intensity of the region of interest from the background intensity in a region containing no nanoparticle.

The lipid particles of the invention have a diameter (mean particle diameter) from about 15 to about 300 nm. In some embodiments, the mean particle diameter is greater than 300 nm. In some Embodiments, the lipid particle has a diameter of about 300 nm or less, 250 nm or less, 200 nm or less, 150 nm or less, 100 nm or less, or 50 nm or less. In one embodiment, the lipid particle has a diameter from about 50 to about 150 nm. These particles generally exhibit increased circulatory lifetime in vivo compared to large particles. In one embodiment, the lipid particle has a diameter from about 15 to about 50 nm.

These particles are capable of advantageously escaping the vascular system. In one embodiment, the lipid particle has a diameter from about 15 to about 20 nm. These particles near the limit size for particles that contain a nucleic acid; such particles may include a single polynucleotide (e.g., siRNA).

The lipid particles of the invention are substantially homogeneous in their size distribution. In certain embodiments, the lipid particles of the invention have a mean particle diameter standard deviation of from about 65 to about 25%. In one embodiment, the lipid particles of the invention have a mean particle diameter standard deviation of about 60, 50, 40, 35, or 30%. In some embodiments, the lipid nucleic acid particles of the invention have a PDI of about 0.01 to 0.3.

The lipid particles according to embodiments of the invention are prepared by a process by which nearly 100% of the nucleic acid used in the formation process is encapsulated in the particles. In one embodiment, the lipid particles are prepared by a process by which from about 90 to about 95% of the nucleic acid used in the formation process is encapsulated in the particles.

In one aspect, the invention provides a method for making lipid particles containing a therapeutic agent.

A variety of methods have been developed to formulate LNP systems containing genetic drugs. These methods include mixing preformed LNP with NAT in the presence of ethanol or mixing lipid dissolved in ethanol with an aqueous media containing NAT and result in LNP with NAT encapsulation efficiencies of 65-95%. Both of these methods rely on the presence of cationic lipid to achieve encapsulation of NAT and a stabilizing agent to inhibit aggregation and the formation of large structures. The properties of the LNP systems produced, including size and NAT encapsulation efficiency, are sensitive to a variety of formulation parameters such as ionic strength, lipid and ethanol concentration, pH, NAT concentration and mixing rates. In general, parameters such as the relative lipid and NAT concentrations at the time of mixing, as well as the mixing rates are difficult to control using current formulation procedures, resulting in variability in the characteristics of NAT produced, both within and between preparations.

Microfluidic devices enable controlled and rapid mixing of fluids on a nanoliter scale. Temperature, residence times, and solute concentrations are controlled during the process of rapid microfluidic mixing applied in the synthesis of inorganic nanoparticles and microparticles, and can outperform macroscale systems in large scale production of nanoparticles. Microfluidic two-phase droplet techniques have been applied to produce monodisperse polymeric microparticles for drug delivery or to produce large vesicles for the encapsulation of cells, proteins, or other biomolecules. The use of hydrodynamic flow focusing, a common microfluidic technique to provide rapid mixing of reagents, to create monodisperse liposomes of controlled size has been demonstrated. This technique has also proven useful in the production of polymeric nanoparticles where smaller, more monodisperse particles were obtained, with higher encapsulation of small molecules as compared to bulk production methods.

U.S. Application Pub. Nos. 20120276209 and 20140328759, by Cullis et al. describe methods of using small volume mixing technology and novel formulations derived thereby. U.S. Application Pub. No. 20160022580 by Ramsay et al. describes more advanced methods of using small volume mixing technology and products to formulate different materials. U.S. Application Pub. No. US2016235688 by Walsh, et al. discloses microfluidic mixers with different paths and wells to elements to be mixed. PCT Publication WO17117647 discloses microfluidic mixers with disposable sterile paths. PCT Publication No WO/2017/11764 by Wild, Leaver and Taylor discloses bifurcating toroidal micromixing geometries and their application to micromixing. U.S. Design patents D771834, D771833 and D772427 by Wild and Weaver disclose cartridges for microfluidic mixers.

In embodiments of the invention, devices for biological microfluidic mixing are used to prepare the lipid particles and therapeutic formulations of the invention. Precision NanoSystems Inc., in Vancouver, Canada, manufactures and sells such devices under the NanoAssemblr™ brand. The devices include a first and second stream of reagents, which feed into the microfluidic mixer, and lipid nanoparticles are collected from the outlet, or in other embodiments, emerge into a sterile environment.

The first stream includes a therapeutic agent in a first solvent. Suitable first solvents include solvents in which the therapeutic agents are soluble and that are miscible with the second solvent. Suitable first solvents include aqueous buffers. Representative first solvents include citrate and acetate buffers.

The second stream includes lipid particle-forming materials in a second solvent. Suitable second solvents include solvents in which the cationic lipids are soluble and that are miscible with the first solvent. Suitable second solvents include 1,4-dioxane, tetrahydrofuran, acetone, acetonitrile, dimethyl sulfoxide, dimethylformamide, acids, and alcohols. Representative second solvents include aqueous ethanol 90%, or anhydrous ethanol.

In one embodiment of the invention, a suitable device includes one or more microchannels (i.e., a channel having its greatest dimension less than 1 millimeter). In one example, the microchannel has a diameter from about 20 to about 300 μm. In examples, at least one region of the microchannel has a principal flow direction and one or more surfaces having at least one groove or protrusion defined therein, the groove or protrusion having an orientation that forms an angle with the principal direction (e.g., a staggered herringbone mixer), as described in U.S. Application Publication No. 2004/0262223, expressly incorporated herein by reference in its entirety. In examples, at least one region of the microchannel comprises bas-relief structures. To achieve maximal mixing rates, it is advantageous to avoid undue fluidic resistance prior to the mixing region. Thus, one example of a device has non-microfluidic channels having dimensions greater than 1000 microns, to deliver the fluids to a single mixing channel.

In other examples of mixing technology, the first and second streams are mixed with other micromixers. Suitable micromixers include droplet mixers, T-mixers, zigzag mixers, multilaminate mixers, or other active mixers.

The lipid particles of the present invention may be used to deliver a therapeutic agent to a cell, in vitro or in vivo. In particular embodiments, the therapeutic agent is a nucleic acid, which is delivered to a cell using nucleic acid-lipid particles of the present invention. The methods and compositions may be readily adapted for the delivery of any suitable therapeutic agent for the treatment of any disease or disorder that would benefit from such treatment.

In certain embodiments, the present invention provides methods for introducing a nucleic acid into a cell. Preferred nucleic acids for introduction into cells are siRNA, mRNA, immune-stimulating oligonucleotides, plasmids, antisense and ribozymes. These methods may be carried out by contacting the particles or compositions of the present invention with the cells for a period of time sufficient for intracellular delivery to occur.

Typical applications include using well known procedures to provide intracellular delivery of siRNA to knock down or silence specific cellular targets. Alternatively applications include delivery of DNA or mRNA sequences that code for therapeutically useful polypeptides. In this manner, therapy is provided for genetic diseases by supplying deficient or absent gene products. Methods of the present invention may be practiced in vitro, ex vivo, or in vivo. For example, the compositions of the present invention can also be used for delivery of nucleic acids to cells in vivo, using methods which are known to those of skill in the art.

The delivery of siRNA, mRNA and plasmid nucleic acid therapeutics by a lipid particle of the invention is described below.

For in vivo administration, the pharmaceutical compositions are preferably administered parenterally (e.g., intraarticularly, intravenously, intraperitoneally, subcutaneously, intradermally, intratracheally, intraosseous or intramuscularly). In particular embodiments, the pharmaceutical compositions are administered intravenously or intraperitoneally by a bolus injection. Other routes of administration include topical (skin, eyes, mucus membranes), oral, pulmonary, intranasal, sublingual, rectal, and vaginal.

In one embodiment, the present invention provides a method of modulating the expression of a target polynucleotide or polypeptide. These methods generally comprise contacting a cell with a lipid particle of the present invention that is associated with a nucleic acid capable of modulating the expression of a target polynucleotide or polypeptide. As used herein, the term “modulating” refers to altering the expression of a target polynucleotide or polypeptide. Modulating can mean increasing or enhancing, or it can mean decreasing or reducing.

In related embodiments, the present invention provides a method of treating a disease or disorder characterized by overexpression of a polypeptide in a subject, comprising providing to the subject a pharmaceutical composition of the present invention, wherein the therapeutic agent is selected from an siRNA, a microRNA, an antisense oligonucleotide, and a plasmid capable of expressing an siRNA, a microRNA, or an antisense oligonucleotide, and wherein the siRNA, microRNA, or antisense RNA comprises a polynucleotide that specifically binds to a polynucleotide that encodes the polypeptide, or a complement thereof.

In related embodiments, the present invention provides a method of treating a disease or disorder characterized by underexpression of a polypeptide in a subject, comprising providing to the subject a pharmaceutical composition of the present invention, wherein the therapeutic agent is selected from an mRNA, a self-replicating DNA, or a plasmid, comprises a nucleic acid therapeutic that specifically encodes or expresses the under-expressed polypeptide, or a complement thereof.

Exemplary mRNA encodes the protein or enzyme selected from human growth hormone, erythropoietin, a 1-antitrypsin, acid alpha glucosidase, arylsulfatase A, carboxypeptidase N, a-galactosidase A, alpha-L-iduronidase, iduronate-2-sulfatase, iduronate sulfatase, N-acetylglucosamine-1-phosphate transferase, N-acetylglucosaminidase, alpha-glucosaminide acetyltransferase, N-acetylglucosamine 6-sulfatase, N-acetylgalactosamine-4-sulfatase, beta-glucosidase, galactose-6-sulfate sulfatase, beta-galactosidase, beta-glucuronidase, glucocerebrosidase, heparan sulfamidase, heparin-N-sulfatase, lysosomal acid lipase, hyaluronidase, galactocerebrosidase, ornithine transcarbamylase (OTC), carbamoyl-phosphate synthetase 1 (CPS 1), argininosuccinate synthetase (ASS 1), argininosuccinate lyase (ASL), arginase 1 (ARGI), cystic fibrosis transmembrane conductance regulator (CFTR), survival motor neuron (SMN), Factor VIII, Factor IX, meganucleases like TALENS, Cas9 and self-replicating RNA's and low density lipoprotein receptors (LDLR).

In a further aspect, the invention provides a pharmaceutical composition comprising a lipid particle of the invention and a pharmaceutically acceptable carrier or diluent. Representative pharmaceutically acceptable carriers or diluents include solutions for intravenous injection (e.g., saline or dextrose). The composition can take the form of a cream, ointment, gel, suspension, or emulsion.

The following is a description of a representative lipid nucleic acid particle (LNP) system, device and method for making the LNP system, and method for using a LNP for delivering therapeutic agents.

Formulation of LNPs was performed by rapidly mixing a lipid-ethanol solution with an aqueous buffer inside a microfluidic mixer designed to induce chaotic advection and provide a controlled mixing environment at intermediate Reynolds number (24<Re<1000). The microfluidic channel have herringbone features or configured in a manner as shown in WO/2017/117647.

Particle sizes and “polydispersity index” (PDI) of the LNP were measured by dynamic light scattering (DLS). PDI indicates the width of the particle distribution. This is a parameter calculated from a cumulative analysis of the (DLS)-measured intensity autocorrelation function assuming a single particle size mode and a single exponential fit to the autocorrelation function. From a biophysical point of view, a PDI below 0.1 indicates that the sample is monodisperse. (As a reference, PDI of the NIST standards are below 0.05.) The particles produced are homogeneous in size.

The following embodiments are provided for the purpose of illustrating, not limiting, the claimed invention.

In certain embodiments, a stabilizing agent is present in the particle in an amount from about 0.1 to about 20 MOL %. In some embodiments, the stabilizing agent is a surfactant. In some embodiments, the stabilizing agent is a PEG Lipid.

In some embodiments, the stabilizing agent is present in the particle in an amount from about 0.5 to about 10 MOL %. In one embodiment, the stabilizing agent is present in the lipid nanoparticle at about 2 MOL %.

In a preferred embodiment, the stabilizing agent is polyoxyethylene (40) stearate. In another embodiment, the stabilizing agent is polyoxyethylene (20) oleyl ether. In yet another embodiment, the stabilizing agent is polyoxyethylene (44) stearate. “Myrj52™” is a tradename for polyoxyethylene (40) stearate. It is sold by Sigma-Aldrich Canada Co.

In certain embodiments, the stabilizing agent is a polyethylene glycol-lipid. Suitable polyethylene glycol-lipids include PEG-modified phosphatidylethanolamine, PEG-modified phosphatidic acid, PEG-modified ceramides (e.g., PEG-CerC14 or PEG-CerC20), PEG-modified dialkylamines, PEG-modified diacylglycerols, PEG-modified dialkylglycerols. Representative polyethylene glycol-lipids include PEG-c-DOMG, PEG-c-DMA, and PEG-s-DMG. Many of these are for sale from NOF America Corporation, White Plains, N.Y. under brand names such as SUNBRIGHT® GM-020 (DMG-PEG)

In some embodiments, stabilizing agent can be a non-ionic surfactant. In embodiments of the invention, the Stabilizing agent is a PEG-lipid is present at concentrations of 0 to 10 MOL %. In some embodiments, stabilizing agent can be vitamin E TPGS. In some embodiments the repeating PEG moiety has an average molecular weight of 1000-2000. In some embodiments molecular weight average of the PEG segment is 1700-2000 with n value (number of PEG repeating units) between 39-47.

In other preferred embodiments, the nucleic acid is a plasmid composed of double stranded deoxyribonucleic acid. A plasmid is a genetic structure that resides in a cell's cytoplasm (as opposed to the nucleic where the traditional cellular genetics reside) cell that can replicate independently of the chromosomes, typically a small circular DNA strand. This is not a normal mammalian genetic construct, but is used as a therapeutic option for replacing or restoring faulty genetic function in a cell. Plasmids can also be used to create novel cellular or animal models for medical research. An engineered plasmid will have, in addition to a replication origin (or not, depending on the intended use), restriction enzyme recognition sites, which allow breaking the circle to introduce new genetic material, and a selective marker such as an antibiotic resistance gene. A plasmid may be from 2,000 to about 1 million base pairs (bp). The larger the plasmid, the more susceptible it is to shearing forces.

Further Definitions

DiD means ‘DiD’; _DiIC18(5) oil (1,1′-Dioctadecyl-3,3,3′,3′-Tetramethylindodicarbocyanine Perchlorate) (Invitrogen D-307) and is a lipid label. It is useful for laboratory work but has not been tested for human use. It is not an intended component of the final product. Other such agents are dansyl DOPE and Fluorescein DHPE. These are non transferable, remaining with the lipid nanoparticles to indicate their location.

As used herein, the term “about” is defined as meaning 10% plus or minus the recited number. It is used to signify that the desired target concentration might be, for example, 40 MOL %, but that through mixing inconsistencies, the actual percentage might differ by +/−5 MOL %.

As used herein, the term “nucleic acid” is defined as a substance intended to have a direct effect in the diagnosis, cure, mitigation, treatment or prevention of disease, or to have direct effect in restoring, correcting or modifying physiological functions, or to act as a research reagent. In preferred embodiments, the nucleic acid is an oligonucleotide. In preferred embodiments, the therapeutic agent is a nucleic acid therapeutic, such as an RNA polynucleotide. In preferred embodiments, the therapeutic agent is double stranded circular DNA (plasmid).

As used herein, the term “research reagent” is defined by the fact that it has a direct influence on the biological effect of cells, tissues or organs. Research reagents include but are not limited polynucleotides, proteins, peptides, polysaccharides, inorganic ions and radionuclides. Examples of nucleic acid research reagents include but are not limited to antisense oligonucleotides, ribozymes, microRNA, mRNA, ribozyme, tRNA, tracrRNA, sgRNA, snRNA, siRNA, shRNA, ncRNA, miRNA, mRNA, pre-condensed DNA, pDNA or an aptamer. Nucleic acid Research Reagents are used to silence genes (with for example siRNA), express genes (with for example mRNA), edit genomes (with for example CRISPR/Cas9).

In this disclosure, the word “comprising” is used in a non-limiting sense to mean that items following the word are included, but items not specifically mentioned are not excluded. It will be understood that in embodiments which comprise or may comprise a specified feature or variable or parameter, alternative embodiments may consist, or consist essentially of such features, or variables or parameters. A reference to an element by the indefinite article “a” does not exclude the possibility that more than one of the elements is present, unless the context clearly requires that there be one and only one of the elements.

In this disclosure, “transfecting reagent” means a composition that enhances the transfer of nucleic acid into cells. It typically includes a cationic lipid to associate with nucleic acid, and structural lipids. LIPOFECTIN™ and LIPOFECTAMINE™ are legacy transfecting reagent. MESSENGER MAX™ LIPOFECTAMINE™ is a contemporary transfecting reagent.

In this disclosure the recitation of numerical ranges by endpoints includes all numbers subsumed within that range including all whole numbers, all integers and all fractional intermediates (e.g., 1 to 5 includes 1, 1.5, 2, 2.75, 3, 3.80, 4, and 5 etc.). In this disclosure the singular forms an “an”, and “the” include plural referents unless the content clearly dictates otherwise. Thus, for example, reference to a composition containing “a compound” includes a mixture of two or more compounds.

In this disclosure term “or” is generally employed in its sense including “and/or” unless the content clearly dictates otherwise.

The following examples are provided for the purpose of illustrating, not limiting, the invention.

Materials

1,17-bis(2-octylcyclopropyl)heptadecan-9-yl-4-(dimethylamino)butanoate hydrochloride 1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC), 1,2-distearoyl-sn-glycero-3-phosphocholine (DSPC) Ammonium acetate, sodium acetate and sodium chloride were obtained from Fisher Scientific (Fair Lawn, N.J.). RNase A was obtained from Applied Biosystems/Ambion (Austin, Tex.), 1,17-bis(2-octylcyclopropyl)heptadecan-9-yl 4-(dimethylamino) butanoate was synthesized by Avanti Polar Lipids (Alabaster, Ala., USA), and PEG (40) stearate was from Sigma St Louis, Mo., USA.

Methods

Oligonucleotide or polynucleotide (siRNA, mRNA or plasmid, hereinafter referred to as “nucleic acid”) solution was prepared in 25 mM-100 mM acetate buffer at pH 4.0. Depending on the desired oligonucleotide-to-lipid ratio and formulation concentration, solutions were prepared at a target concentration of 2.3 mg/ml to 4 mg/ml total lipid. A lipid solution containing 1,17-bis(2-octylcyclopropyl)heptadecan-9-yl 4-(dimethylamino)butanoate hydrochloride, a selection of one of DSPC, DOPC, DOPE, Myrj52 at 1 or 2.5 MOL % or PEG-lipid at 0-10%, DiD label was prepared in ethanol and mixed with the oligonucleotide or polynucleotide to achieve an ethanol concentration of 25% (v/v). Optionally, cholesterol, was present at about 20-40%. Later tests showed that cholesterol presence had no impact on cell toxicity or transfection.

LNP were prepared by standard processes described above. Mixing occurred by chaotic advection, causing the separation of laminate streams to become increasingly small, thereby promoting rapid diffusion. This mixing occurs on a millisecond time scale and results in the lipids being transferred to a progressively more aqueous environment, reducing their solubility and resulting in the spontaneous formation of lipid nanoparticles (LNP). By including cationic lipids in the lipid composition, entrapment of oligonucleotide or polynucleotide species is obtained through association of the positively charged lipid head group and negatively charged oligonucleotide.

Following mixing in the microfluidic device, the LNP mixture was generally diluted into RNAse free tubes containing three to forty volumes of stirred phosphate buffered saline (PBS) buffer, pH 7.4. Ethanol is finally removed through dialysis in PBS, pH 7 or using amicon centrifugal filters (Millipore, USA) at 3000 RPM. Once the required concentration is achieved, the particles were filter sterilized using 200 um filters in aseptic conditions. Empty vesicles were similarly produced, with the oligonucleotide absent from the buffer solution.

Particle size was determined by dynamic light scattering using a ZetaSizer Nano ZS™, Malvern Instruments, UK). Lipid concentrations were verified by measuring total cholesterol using the Cholesterol E enzymatic assay from Wako Chemicals USA (Richmond, Va.).

RNA concentration and Encapsulation Efficiency was measured by a modified RiboGreen assay (Quant-IT-Ribogreen® Assay kit, Invitrogen). Encapsulation efficiency is defined as the percentage of RNA protected with in the LNP. Briefly, Standards and samples were prepared in a 96 well plate with and without 1% Triton-X100. 96 well plate was incubated at 37° C. for 15 minutes to break open the RNA LNPs. On completion of incubation, Ribogreen® reagent was added to samples and standards, and fluorescence intensities of standards and samples with and without triton were measured (Exc. 485 nm/Em 520 nm). Percent Encapsulation or Encapsulation Efficiency is defined by the following equation.


Encapsulation Efficiency=[(Total RNA−Free RNA (un-encapsulated RNA)), Total RNA]%

For the culture of neurons, microsurgically dissected Cortex tissue from E18 Sprague Dawley rat was purchased from BrainBits, LLC, Springfield, Ill. This tissue was processed and the neuronal cells plated using the neuronal plating protocol from StemCell Technologies, Vancouver, BC. In short the E18 cortex tissues were removed from the shipping medium and digested for 20 minutes using 0.25% trypsin. Following this the trypsin was inactivated using DMEM media containing 10% FBS. The tissue was then pelleted and the FBS containing media was replaced with fresh DMEM. Following this the tissue was again pelleted and the pellet was triturated in Neuronal Culture Media supplemented with SM1, (StemCell Technologies). The cell suspension was then passed through a 40 μM cell strainer_to form a single cell suspension. The concentration of the cell suspension was assessed using trypan blue and a hemocytometer. The cell suspension was seeded at a density of 4.8×104 cells/cm2 on PDL coated plates or at a density of 3.2×104 cells/cm2 on PDL coated coverslips. The cells were incubated in a 37° C. incubator with 5% CO2 and half of the media was changed with fresh media every 3-4 days. Confirmation of neuronal cell type was done using visual inspection of the culture by microscope as well as positive MAP2 staining, a marker of neuronal cells.

For the culture of astrocytes, microsurgically dissected Cortex tissue from E18 Sprague Dawley rat was purchased from BrainBits, LLC, Springfield, Ill. This tissue was then processed by digestion with 0.25% trypsin for 20 minutes followed by inactivation of the trypsin by the addition of astrocyte medium (DMEM media containing 10% FBS and 2 mM of L-glutamine). Following centrifugation the tissue pellet was resuspended in astrocyte medium, triturated to form a cell suspension, and passed through a 40 μM cell strainer to form a single cell suspension. The concentration of the cell suspension was assessed using Trypan blue and a hemocytometer. The suspension was then seeded at a density of 1.33×104 cells/cm2 in PDL coated T150 flasks. The cells were incubated in a 37° C. incubator with 5% CO2 following seeding and the media was changed every 3-4 days. After 10 days in culture the flasks were fully confluent and the astrocyte morphology of the cells could clearly be seen. The astrocytes were harvested by tapping the flasks to remove any remaining microglia in the culture and then by washing the flask with PBS without calcium or magnesium. 0.25% trypsin was added to detach the astrocytes from the flask through incubation for 5 minutes at 37° C. DMEM media containing 10% FBS and 2 mM of L-glutamine was then added to inactivate the trypsin. A cell scraper was used to ensure that all the astrocytes were detached from the flask as well as a titration and washing of the flask with the media. The resulting cell suspension was then counted using Trypan blue and a hemocytometer and the astrocytes were then either plated directly for experiments or cryopreserved for later expansion and use. For experiments, the astrocytes were seeded on tissue culture plates at a density of 2×104 cells/cm2 in regular tissue culture treated plates or on Poly-D-lysine (PDL) coated coverslips. Confirmation of astrocyte cell type was done using visual inspection of the culture by microscope as well as positive GFAP staining, a marker of astrocyte cells.

Human iPSC-Derived Neural Progenitor Cells. Human neural progenitor cells derived from male human pluripotent stem cell line XCL-1, Size: 1×106 cells, purchased from StemCell Technologies, Vancouver, Canada. They were cultured in neural progenitor medium 2, also purchased from StemCell, according to vendor directions.

Cell Treatment

Neurons: After 7 days in culture, neurons were treated with 2.5 μg/mL of mRNA LNP and supplemented with 5 μg/mL of ApoE (neurons do not produce enough ApoE in enriched cultures to facilitate uptake of the LNP). 48H after treatment, the neurons were harvested for downstream assessment. Best results were obtained when both mRNA and plasmid were added to human NPCs when they were seeded. Thus when the cells are passaged, they were seeded in individual wells and then the APoE and LNP added immediately.

Astrocytes: 48H after being seeded, the astrocytes were treated with 2.5 μg/mL of mRNA LNP. 24H after treatment, the astrocytes were harvested for downstream assessment.

Human iPSC-Derived Neural Progenitor Cells (“NPC”)

NPC were treated with 100 ng/mL of mRNA or plasmid at the time of seeding, with 1 ug/ml ApoE. Samples were then assayed using flow cytometry at 48 h post seeding.

Immunocytochemistry

For either neurons or astrocytes, cells were seeded at the appropriate density on PDL coated coverslips. Following treatment and incubation, the cells were fixed by 4% paraformaldehyde. The cells were permeabilized using 0.1% Triton X-100 in PBS and then blocked using 10% normal donkey serum. Following blocking, the primary antibody was added, MAP2 for neuronal cells and GFAP for astrocytes, and incubated overnight at 4° C. The following day, the primary antibody was removed and secondary antibody was added as well as DAPI for staining the nucleus. The coverslips were then mounted on glass slides using ProLong Diamond™ fixative, ThermoScientific. Images were acquired using a confocal microscope.

Viability Assay

Neurons or astrocytes cells were seeded at the appropriate density in 96 well plates in a final media volume per well of 100 μl. Following treatment and treatment incubation time 10 μl of medium was removed and 10 μl of PrestoBlue® cell viability reagent, ThermoScientific, was added and the plate was incubated for_30 minutes at 37° C. before being read using a plate reader (Synergy H1 plate reader (BioTek) using the reader specifications in the PrestoBlue® cell viability reagent.

Flow Cytometry

Following treatment and treatment incubation of either neurons or astrocytes the media from each well was collected and the cells were harvested using 0.25% trypsin. The trypsin was inactivated using 3% FBS in PBS and the cells were pelleted in their corresponding media. Following centrifugation the cells were washed once with PBS and again pelleted. The cells were then resuspended in Binding Buffer, BD Biosciences, and Propidium Iodine was added to stain for cells with completely ruptured membranes, dead cells. The cells were then assessed using a BD Biosciences Canto II flow cytometer.

The comparison of Lipid Mix A and Lipid Mix D flow cytometry results for mRNA are shown in FIG. 6. Lipid Mix D is far superior.

GFP ELISA

Following treatment and treatment incubation of either neurons or astrocytes the cells were harvested following the protocol provided with SimpleStep™ GFP ELISA, AbCam. In short the cells were washed with PBS and then lysed using the provided lysis buffer. Following lysis and collection the lysate was incubated on ice and then centrifuged to remove any remaining undigested cell debris. Total protein concentration was assessed using the BCA Protein Quantification Kit (AbCam, Cambridge, UK). The total protein concentration for each sample was then normalized to 1 ng/μl for use in the SimpleStep™ GFP ELISA.

Example 1

LNP Characterization

Particle size (hydrodynamic diameter of the particles) was determined by Dynamic Light Scattering (DLS) using a ZetaSizer Nano ZS™, Malvern Instruments, UK). He/Ne laser of 633 nm wavelength was used as the light source. Data were measured from the scattered intensity data conducted in backscattering detection mode (measurement angle 173°). Measurements were an average of 10 runs of two cycles each per sample. Z-Average size was reported as the LNP size, and is defined as the harmonic intensity averaged particle diameter.

RNA encapsulated was measured using the Ribogreen® dye method. The RiboGreen® dye is a fluorescent nucleic acid stain for quantitating intact RNA. RiboGreen® assay provides RNA quantitation with minimal consumption of sample. A standard curve established using known concentrations of control RNA sample. Then the test solutions are run and their measurements translated using the standard curve.

TABLE 1 Physico-chemical parameters of GFP mRNA LNP Particles Size Formulation ID Encap. Efficiency (%) (nm) PDI Lipid Mix A 98  87 0.12 Lipid Mix B 89 113 0.15 Lipid Mix C 98 122 0.10 Lipid Mix D 98 127 0.18 Lipid Mix E 96 133 0.19 Lipid Mix F 90 140 0.16

Formulations Tested.

Formulations contained various ratios of the cationic lipid 1,17-bis(2-octylcyclopropyl)heptadecan-9-yl 4-(dimethylamino)butanoate hydrochloride, structural lipids selected from DSPC and DOPE, Myrj52 as a stabilizing agent, and 0.5 MOL % of DiD. In some formulations, cholesterol was present. All of the formulations shown in Table 1 had good encapsulation efficiency, size and PDI characteristics.

A list of components ratios for the Lipid Mixes is shown in Table 2.

TABLE 2 Components and Ratios of Lipid Mix A-F Lipid 50 MOL % cationic lipid/10 MOL % DSPC/37.5 MOL % mix A cholesterol/2.5 MOL % Myrj52 Lipid 50 MOL % cationic lipid/20 MOL % DOPE/27.5 MOL % mix B cholesterol/2.5 MOL % Myrj52 Lipid 40 MOL % cationic lipid/20 MOL % DOPE/37.5 MOL % mix C cholesterol/2.5 MOL % Myrj52 Lipid 40 MOL % cationic lipid/40 MOL % /DOPE/17.5 MOL % mix D cholesterol/2.5 Myj52 Lipid 50 MOL % cationic lipid/30 MOL % DOPE/17.5 MOL % mix E cholesterol/2.5 MOL % Myrj52 Lipid 60 MOL % cationic lipid/20 MOL % DOPE/17.5 MOL % mix F cholesterol/2.5 MOL % Myrj52

Example 2

mRNA Transfection and Expression in Neurons

Messenger RNAs reagents were purchased from Trilink Biotechnologies, San Diego, Calif. The mRNA was used to study the transfection ability of the nanoparticles.

EGFP mRNA (5meC, ψ)) Enhanced Green Fluorescent Protein mRNA (5-methylcytidine, pseudouridine), 1.0 mg/mL in 10 mM Tris-HCl, pH 7.5, Length: 996 nucleotides (Seq Id. No 1). Then unknown bases are a portion of alpha globin which the vendor would not reveal.

Encapsulation efficiency was established for formulations as set out supra in Table 1. Size of the nanoparticles, as well as homogeneity of the size of the nanoparticles (PDI) was measured.

LNP Formulations Lipid Mix A, B, C, and D containing messenger RNA (GFP) were tested on enriched neurons in order to identify those that are most promising for GFP expression. A table of the observed intensity of signals in photographs, ELISAS, and flow cytometry as shown in the columns below was prepared to aid comparing the Lipid Mixes. “Not interpreted” means that observations were not recorded in this manner.

TABLE 3 Qualitative Results for Different Formulations-mRNA Cell Types Astrocytes Neurons Neurons Neurons Neurons Astroctyes or Neurons MRNA siRNA Readouts Flow Flow cytometry- cytometry-% ELISA (GFP Mean of Neurons Formulation Immuno expression) Fluorescence expressing ELISA (GFP ID Individual scores Intensity GFP expression) Preference Overall Overall Lipid Mix − + + + Not A Poor or Good A interpreted Low Lipid Mix B − Not done + + Not A Poor Good interpreted Lipid Mix C + Not done ++ ++ Not N Med Good interpreted Lipid Mix ++ ++ +++ +++ +++ Both Good Good D Lipid Mix E Not Not + + Not done Not done Low Good interpreted interpreted Lipid Mix F Not Not + − Not done Not done Low Good interpreted interpreted

The formulations contained structural lipids in the form of DSPC or DOPE at ratios ranging from 10 to 40 MOL %. Cationic lipid was present in the ratio of 35 to 50 MOL %. Cholesterol was present at 17 or 37 or 38.5 MOL %. Stabilizing agent was present from 1 or 2.5 MOL %. DiD was present in all of the formulations at 0.5 MOL %, as it was a necessary label.

The goal was to transfect and have expressed mRNA in neurons. Lipid Mix A and Lipid Mix B gave poor expression of mRNA. Lipid Mix A had provided good transfection for siRNA in an earlier baseline experiment, so it was surprising that it did not work for mRNA. Lipid Mix A contained 50/10/37/2.5 cationic lipid/Structural Lipid/Cholesterol/Stabilizing agent, with structural lipid being DSPC in Lipid Mix A.

FIGS. 1 through 3 are photographic images rendered into grayscale for the purposes of the present application. All images include DAPi, a nuclear stain. FIG. 1 is a photograph of live neurons that have been treated with labelled Lipid Mix D formulated nanoparticles containing GFP mRNA. The top right quadrant shows MAP2 (a neuronal marker) antibody staining, the bottom right is DiD lipid labelling of the nanoparticle; the bottom left is GFP expression in the neurons, and the top left quadrant is a merged image showing DiD, MAP2, and GFP, establishing GFP expression in the live neurons. FIG. 2 shows staining perspectives to illustrate the ability of Lipid Mix B organized as for FIG. 1. FIG. 3 is a photograph showing the same staining perspectives for Lipid Mix C.

Lipid Mix A and Lipid mix D mRNA nanoparticles were compared to the same mRNA in MessengerMax™ transfection reagent. In FIG. 5, the translated mRNA is visualized by mean fluorescence intensity of GFP expression levels in neurons for the three test nanoparticles.

ELISA results are shown comparing Lipid Mix A and Lipid Mix D formulations for GFP mRNA are shown in FIG. 4, which is a bar graph showing the translated mRNA expression levels in neurons by ELISA for Lipid Mix A and Lipid Mix D nanoparticles. The Lipid Mix D efficiency of transfection is much better than that of Lipid Mix A, B, C, with not all results shown.

FIG. 10 is a bar graph showing Mean Fluorescence Intensity of GFP expression in human neural progenitor cells treated with plasmid LNP formulations of Lipid Mix A, Lipid Mix B, Lipid Mix C, Lipid Mix D, Lipid Mix E and Lipid Mix F by flow cytometry.

This data suggests that by lowering the cationic lipid composition to 40 MOL %, surprising activity can be achieved [Lipid Mix A, Lipid Mix B and Lipid Mix E contained 50 MOL % cationic lipid, Lipid Mix F contained 60 MOL % cationic lipid and Lipid Mix C and Lipid Mix D contained 40 MOL % cationic lipid.] All Formulations had stabilizing agent present at 2.5%. The mole ratios of structural lipids were adjusted such that total MOL % was 100.

Human neural progenitor cells were used as model for mRNA expression using Lipid Mix D mRNA LNP. A flow cytometry histogram showing showing mean fluorescence intensity of GFP expression in human neural progenitor cells (grey histogram) compared to untreated cells (black histogram) is shown in FIG. 7. Percentage (%) of cells expressing GFP and Mean Fluorescent Intensity (MFI) levels via flow cytometry for neural progenitor cells treated with Lipid Mix A and Lipid Mix D plasmid LNPs 48 hours post exposure is shown in the bar graph of FIG. 9.

Lipid Mix C LNPs showed moderate levels of activity and preferential expression in neurons compared to Lipid Mix B, whereas Lipid Mix B showed better levels of expression in astrocytes than in neurons

Example 3

siRNA Transfection Procedures

mRNA silencing by RNA interference is induced by double stranded oligoribonucleotides with a length of about 22 base pairs with 2-nucleotide long 3′ overhangs. This type of small dsRNA is called “small interfering RNA” or “siRNA”. For experimental purposes, siRNA can be produced synthetically and then transfected into the target cells, or it can be expressed in vitro or in vivo using a specially designed expression plasmid.

Enriched neurons were treated with Lipid Nanoparticles containing an off-the-shelf dicer-substrate siRNA (DsiRNA) HPRT (SEQ ID NO 2, sense, SEQ ID NO 3, antisense)) or control siRNA DS NC1, a nonsilencing, negative control DsiRNA that does not recognize any sequences in human, mouse, or rat transcriptomes (SEQ ID NO 4, sense, SEQ ID NO 5, antisense). Both DsiRNA and DsNC1 were purchased from Integrated DNA Technologies, Inc., Coralville, Iowa, U.S.)

HPRT is an acronym for hypoxanthine phosphoribosyltransferase 1, a transferase that catalyzes conversion of hypoxanthine to inosine monophosphate and guanine to guanosine monophosphate. Uptake of HPRT siRNA was measured of Day 0, Day 2, Day 14 and Day 28. Knockdown of HPRT by said siRNA was measured at the same timepoints. Cell viability across LNP concentrations (0-5000 ng/ml) showed no toxicity at these concentrations. Stability data of siRNA LNP generated up to 28 days indicated that the siRNA LNP was stable and that there was no change in its activity/potency over this period. SiRNA LNP (1000, 100 and 10 ng/ml) along with a non-coding control siRNA formulation was used as a control when collecting the gene knockdown data.

Cell lysates were collected and the HPRT mRNA levels were measured by qPCR. Data was normalized against the house keeping gene β-actin. All tested formulations were capable of delivering siRNA successfully to the neurons. Data is not shown.

Example 4

Plasmid Transfection

Plasmid preparation pCX-EGFP Plasmid size 5514 nt, SEQ ID NO 6, custom made by GenScript USA Inc, Piscataway, N.J., including ampicillin resistance, restriction enzyme HINDIII, in ddH2O. The plasmid included a GFP expressing component which produces target protein only when the plasmid is expressed within a cell.

Lipid Mix A and Lipid Mix D with plasmid encapsulated was added to cell cultures of neurons and astrocytes as described above. Excellent expression was noted in the cell culture treated with Lipid Mix D encapsulated plasmid.

The results of the plasmid encapsulation for Lipid Mix A, and Lipid Mix D are shown in Table 4. There was good encapsulation in the two formulations shown in Table 3, with excellent polydispersity.

TABLE 4 Plasmid LNP Particles: Physico-chemical parameters Encapsulation Formulation Efficiency ID (%) Size PDI Lipid Mix A 99 94 0.223 Lipid Mix D 99 88 0.149

Plasmid LNPs comprised of Lipid Mix B (50 MOL % cationic lipid) and Lipid Mix C (40 MOL % cationic lipid) were tested in neural progentor cells. Human neural progenitor cells derived from male human pluripotent stem cell line XCL-1, Size: 1×106 cells more purchased from StemCell Technologies, Vancouver, Canada. They were cultured in Neural Progenitor Medium 2 also purchased from StemCell. Flow cytometry results are shown in FIG. 8, and were measured for Mean Fluorescent Intensity (MFI) levels (bar graph on the left), and Percentage (%) of cells expressing GFP (bar graph on the right).

Example 5

Improvement over Commercial Standard

The viability of astrocytes 48 h post treatment with the mRNA LNP formulation Lipid Mix D and a commercial formulation MessengerMax™ Lipofectamine™ transfecting agent (ThermoFisher Scientific, USA, web order) as measured by the intensity of the cells on treatment with PrestoBlue® is shown in FIG. 6. Lipofectamine™ MessengerMAX™ Transfection Reagent is a transfection reagent marketed for the delivery of mRNA, small RNA, and short dsDNA or HDR templates. PrestoBlue® is a cell viability indicator.

The provided example shows that MessengerMax™ is somewhat toxic in this setting to astrocytes at the concentrations of 1000-2500 ng/mL. Similar results were seen in neurons treated with MessengerMax™ and Lipid Mix D. Lipid Mix D lipid nanoparticles did not show any signs of toxicity below doses of 5 ug/mL. These results are not shown.

While specific embodiments of the invention have been described and illustrated, such embodiments should be considered illustrative of the invention only and not as limiting the invention as construed in accordance with the accompanying claims.

BIBLIOGRAPHY

  • Akhtar, S., E. Basu S Fau-Wickstrom, R. L. Wickstrom E Fau-Juliano and R. L. Juliano (1991). “Interactions of antisense DNA oligonucleotide analogs with phospholipid membranes (liposomes).” (0305-1048 (Print)).
  • Kauffman, K. J., M. J. Webber and D. G. Anderson (2015). “Materials for non-viral intracellular delivery of messenger RNA therapeutics.” J Control Release.
  • Kaufmann k, Dorkin Robert J; Yang, Jung H; Heartlein, Michael W; De Rosa, Frank; Mir, Faryal F; Fenton, Owen S; Anderson, Daniel G (2015). “Optimization of Lipid Nanoparticle Formulations for mRNA Delivery in Vivo with Fractional Factorial and Definitive Screening Designs.” Nano Letters 15: 7300-7306.
  • Lv, H., S. Zhang, B. Wang, S. Cui and J. Yan (2006). “Toxicity of cationic lipids and cationic polymers in gene delivery.” Journal of Controlled Release 114(1): 100-109.
  • Mingozzi, F. and K. A. High (2013). “Immune responses to AAV vectors: overcoming barriers to successful gene therapy.” Blood 122(1): 23-36.
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Claims

1. A transfection reagent composition comprising:

(a) 30-60 MOL % of a cationic lipid, or a pharmaceutically acceptable salt thereof;
(b) 10-60 MOL % structural lipid;
(c) a sterol
(d) 0.1 to about 10 MOL % stabilizing agent.

2. The composition of claim 1, wherein the cationic lipid is an amino lipid or a pharmaceutically acceptable salt thereof.

3. The composition of claim 1 or 2, wherein the cationic lipid is selected from the group consisting of 1,17-bis(2-octylcyclopropyl)heptadecan-9-yl-4-(dimethylamino)butanoate, DODAC, DOTMA, DDAB, DOTAP, DOTAP⋅Cl, DC-Chol, DOSPA, DOGS, DODAP, DODMA, DMRIE, C12-200, and pharmaceutically acceptable salts thereof.

4. The composition of claim 1, wherein the cationic lipid has the formula:

or a pharmaceutically acceptable salt thereof, wherein:
R1 and R2 are each independently H, alkyl, akenyl, alkynyl, cycloalkyl, aryl, heteroaryl, and heterocyclyl,
wherein each of alkyl, alkenyl, alkynyl, cycloalkyl, aryl, heteroaryl, and heterocyclyl is optionally substituted by H, halo, hydroxy, cyano, oxo, C1-C6 alkyl optionally substituted by halo, hydroxy, or alkoxy;
or R1 and R2 are taken together with the N atom to which they are both attached to form a 3-8 member heteroaryl or heterocyclyl;
wherein each of the heteroaryl and heterocyclyl is optionally substituted by H, halo, hydroxy, cyano, oxo, nitro, C1-C6 alkyl optionally substituted by halo, hydroxyl, or alkoxy;
R3 is absent, H, alkyl, alkenyl, alkynyl, cycloalkyl, aryl, heteroaryl, or heterocyclyl;
R4 and R5 are each independently H, alkyl, alkenyl, alkynyl, cycloalkyl, aryl, heteroaryl, or heterocyclyl;
wherein each of alkyl, alkenyl, alkynyl, cycloalkyl, aryl, heteroaryl, and heterocyclyl is optionally substituted by H, halo, hydroxy; cyano; oxo; C1-C6 alkyl optionally substituted by halo, hydroxy, or alkoxy;
X is O, S, —NR4—, —S—S—, —OC(═O)—, —C(═O)O—, —OC(═O)O—, —NR4C(═O)—, —C(═O)NR4—, —NR4C(═O)O—, —OC(═O)NR4—, —NR4C NR4, —NR4C(═S)O—, —OC(═S)NR4—, —NR4C(═S)NR4—, or —CR4R5—;
Y and Z are independently C10 to C30 groups having the formula L1-(CR6R7)a-[L2-(CR6R7)P]y-L3-Re, wherein:
L1 is a bond, —(CR6Ry)-, —O—, —CO—, —NR8—, —S—, or a combination thereof; each R5 and R7, independently, is H, halo, hydroxyl, cyano, C1-C6 alkyl optionally substituted by halo, hydroxyl, or alkoxy;
L2 is a bond, —(CR6R7)—, —O—, —CO—, —NR8—, —S—,
or a combination thereof, or has the formula
wherein b, c, and d are each independently 0, 1, 2, or 3, given the sum of b, c, and d is at least 1 and no greater than 8; and R9 and R10 are each independently R7, or adjacent R9 and R10, taken together, are optionally a bond;
L3 is a bond, —(CR6R7)—, —O—, —CO—, —NR8—, —S—,
or a combination thereof;
R8 is independently H, halo, hydroxy, cyano, alkoxy, aryl, heteroaryl, or C1-C6 alkyl optionally substituted by halo, hydroxy, or heterocyclyl, or R8 has the formula:
a is 0, 1, 2, 3, or 4;
a is 0-6;
each β, independently, is 0-6; and
γ is 0-6.

5. The composition of any one of claims 1-4, wherein the cationic lipid is 1,17-bis(2-octylcyclopropyl)heptadecan-9-yl-4-(dimethylamino)butanoate or a pharmaceutically acceptable salt thereof.

6. The composition of any one of claims 1-5, wherein the structural lipid is selected from the group consisting of diacylphosphatidylcholines, diacylphosphatidylethanolamines, sterols, ceramides, sphingomyelins, dihydrosphingomyelins, cephalins, and cerebrosides.

7. The composition of any one of claims 1-6, wherein the stabilizing agent is selected from the group consisting of polyethylene glycol, polyethylene glycol-DMG, polyoxyethylene alkyl ethers, diblock polyoxyethylene ether co-polymers, triblock polyoxyethylene alkyl ethers co-polymers, and amphiphilic branched polymers.

8. The composition of any one of claims 1-7 wherein the sterol is cholesterol.

9. The composition of any one of claims 1-8, wherein the stabilizing agent is selected from the group consisting of polyoxyethylene (20) oleyl ether, polyoxyethylene (23) lauryl ether, polyoxyethylene (40) stearate, poly(propylene glycol)11-block-poly(ethylene glycol)16-block-poly(propylene glycol)11, poly(propylene glycol)12-block-poly(ethylene glycol)28-block-poly(propylene glycol)12.

10. The composition of any one of claims 1-9 wherein the stabilizing agent is PEG-conjugated lipid.

11. The composition of claim 10 wherein the stabilizing agent is PEG-DMG

12. The composition of any one of claims 1-11, wherein the cationic lipid comprises about 40 MOL %.

13. The composition of any one of claims 1-12, wherein the stabilizing agent comprises about 2.5 MOL % stabilizer.

14. The composition of claim 1, wherein:

(a) the cationic lipid is 1,17-bis(2-octylcyclopropyl)heptadecan-9-yl-4-(dimethylamino)butanoate or a pharmaceutically acceptable salt thereof;
(b) the structural lipid is 1,2-dioleoyl-sn-glycero-3-phosphoethanolamine (DOPE);
(c) the sterol is cholesterol, and
(d) the stabilizing agent is polyoxyethylene (40) stearate.

15. The composition of claim 1, wherein:

(a) the cationic lipid is 1,17-bis(2-octylcyclopropyl)heptadecan-9-yl-4-(dimethylamino)butanoate or a pharmaceutically acceptable salt thereof;
(b) the structural lipid is 1,2-dioleoyl-sn-glycero-3-phosphoethanolamine (DOPE); and
(c) the sterol is cholesterol, and
(d) the stabilizing agent is polyethylene glycol conjugated lipid.

16. The composition claim 1, wherein the structural lipid comprises about 10 to about 40 MOL % 1,2-dioleoyl-sn-glycero-3-phosphoethanolamine (DOPE).

17. The composition of of any one of claims 1-16 wherein the sterol is present from 10 to 20 MOL %.

18. The composition of any one of claims 1-17, further comprising a nucleic acid.

19. The composition of claim 18, wherein the nucleic acid is a DNA, an RNA, a locked nucleic acid, a nucleic acid analog, or a plasmid capable of expressing an RNA.

20. The composition of claim 18, wherein the nucleic acid is an antisense oligonucleotide, ribozyme, miRNA, rRNA, tRNA, siRNA, saRNA, snRNA, snoRNA, lncRNA, piRNA, tsRNA, srRNA, crRNA, tracrRNA, sgRNA, shRNA, ncRNA, miRNA, mRNA, pre-condensed DNA, pDNA, an aptamer, or a combination thereof.

21. The composition of any one of claims 1-20, wherein the cell is a neuron.

22. The composition of any one of claims 1-20, wherein the cell is astrocyte.

23. The composition of any one of claims 1-20, wherein the cell is a progenitor cell.

24. The composition of any one of claims 1-20, wherein the composition exists in the form of nanoparticles having a diameter of from about 15 nm to about 300 nm.

25. The composition of any one of claims 1-20 wherein the composition exists in the form of nanoparticles having a diameter of from about 80 nm to 150 nm.

26. A method for introducing a nucleic acid into a cell, while maintaining activity of the nucleic acid and viability of the cell, comprising contacting the cell with the composition of any one of claims 18-20.

27. A method for modulating the expression of a target polynucleotide or polypeptide in a cell, while maintaining cell viability, comprising contacting a cell with the composition of any one of claims 18-20, wherein the nucleic acid is capable of modulating the expression of a target polynucleotide or polypeptide.

28. The method of claim 26 or 27, wherein the cell is a neuron.

29. The method of claim 26 or 27, wherein the cell is astrocyte.

30. The method of claim 26 or 27, wherein the cell is a progenitor cell.

31. The method of claims 26-30 wherein the cell is a mammalian cell.

32. A method of manufacturing a lipid nanoparticle capable of targeting neurons, the method including increasing the ratio of cationic lipid to structural lipid in the lipid nanoparticle.

33. A method of manufacturing a lipid nanoparticle capable of targeting astrocytes, the method including decreasing the ratio of cationic lipid to structural lipid in the lipid nanoparticle.

Patent History
Publication number: 20210284998
Type: Application
Filed: Oct 2, 2017
Publication Date: Sep 16, 2021
Applicant: Precision NanoSystems Inc. (Vancouver, BC)
Inventors: Anitha Thomas (New Westminster), Rebecca Anne Grace De Souza (Vancouver), Eric Ouellet (New Westminster), Grace Tharmini Tharmarajah (Toronto), Jagbir Singh (Vancouver), Shyam Madhusudan Garg (Richmond)
Application Number: 16/334,351
Classifications
International Classification: C12N 15/113 (20060101);