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Cationic lipids and methods of use

a cationic lipid and lipid technology, applied in the field of cationic lipids and methods of use, can solve the problems of large complex, large potential for reversion, and varied limitations, and achieve the effects of increasing the fluidity of the membrane of the liposome or splp, enhancing the properties of liposomes, and increasing flexibility

Inactive Publication Date: 2011-10-27
ARBUTUS BIOPHARMA CORPORAT ION
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0006]The present invention provides novel cationic lipids that have increased flexibility over commonly used cationic lipids (such as DODAC and DODMA). More particularly, it has surprisingly been found that the cationic lipids of the present invention enhance the properties of liposomes as well as nucleic acid-lipid particles (SPLPs) by increasing the membrane fluidity of the liposome or SPLP, thus increasing the efficiency of delivery of bioactive agents in the liposomes and SPLP. In particular, the present invention provides compounds of Formula I having the following structure:

Problems solved by technology

Viral vectors are relatively efficient gene delivery systems, but suffer from a variety of limitations, such as the potential for reversion to the wild type as well as immune response concerns.
However, complexes are large, poorly defined systems that are not suited for systemic applications and can elicit considerable toxic side effects (Harrison, et al., Biotechniques 19:816-823 (1995); Huang, et al., Nature Biotechnology 15:620-621 (1997); Templeton, et al., Nature Biotechnology 15:647-652 (1997); Hofland, et al., Pharmaceutical Research 14:742-749 (1997)).
Unfortunately, cationic lipids with only a single site of unsaturation can lack flexibility.
Liposomes or SPLP comprising these cationic lipids can lack sufficient membrane fluidity, thus impacting the efficiency of delivery of a bioactive agent to a cell or to a patient.

Method used

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  • Cationic lipids and methods of use
  • Cationic lipids and methods of use
  • Cationic lipids and methods of use

Examples

Experimental program
Comparison scheme
Effect test

example 1

Materials and Methods

[0225]Materials: DPPS, 1,2-Distearoyl-sn-glycero-3-phosphocholine (DSPC) and cholesterol were purchased from Avanti Polar Lipids (Alabaster, Ala.). TNS was obtained from Sigma-Aldrich Canada (Oakville, ON). RiboGreen was obtained from Molecular Probes (Eugene, Oreg.). The alkyl mesylates were purchased from Nu-Chek Prep, Inc. (Elysian, Minn., USA). siRNA (anti-luciferase and mismatch control) was purchased from Dharmacon (Lafayette, Colo., USA). The anti-luciferase sense sequence was 5′-G.A.U.U.A.U.G.U.C.C.G.G.U.U.A.U.G.U.A.U.U-3′. The anti-luciferase antisense sequence was 5′-U.A.C.A.U.A.A.C.C.G.G.A.C.A.U.A.A.U.C.U.U-3′. All other chemicals were purchased from Sigma-Aldrich (Oakville, ON, Canada).

[0226]Synthesis of DSDMA and DODMA: DSDMA and DODMA were synthesized using the respective alkyl bromides with methodology derived from that of a DOTMA precursor (Felgner et al, PNAS USA, 84, 7413-7417 (1987)). 3-(Dimethylamino)-1,2-propanediol (714 mg, 6 mmol) and 95% ...

example 2

Assays for Serum Stability

[0236]Lipid / nucleic acid particles formulated according to the above noted techniques can be assayed for serum stability by a variety of methods.

[0237]For instance, in a typical DNase 1 digestion, 1 μg of DNA encapsulated in the particle of interest is incubated in a total volume of 100 μL of 5 mM HEPES, 150 mM NaCl, 10.0 mM MgCl2 pH 7.4. DNase treated samples are treated with either 100 or 10 U of DNase I (Gibco—BRL). 1.0% Triton X-100 can be added in control experiments to ensure that lipid formulations are not directly inactivating the enzyme. Samples are incubated at 37° C. for 30 min after which time the DNA is isolated by addition of 500 μL of DNAZOL followed by 1.0 mL of ethanol. The samples are centrifuged for 30 min at 15,000 rpm in a tabletop microfuge. The supernatant is decanted and the resulting DNA pellet is washed twice with 80% ethanol and dried. This DNA is resuspended in 30 μL of TE buffer. 20 μL of this sample is loaded on a 1.0% agarose ...

example 3

Synthesis of 1,2-DiLinoleyloxy-N,N-dimethylaminopropane (DLinDMA) and 1,2-Dilinolenyloxy-N,N-dimethylaminopropane (DLenDMA)

[0240]3-(Dimethylamino)-1,2-propanediol (714 mg, 6 mmol) and 95% sodium hydride (NaH, 1.26 g, 50 mmol) are stirred in benzene (30 mL) under nitrogen for 30 minutes. Linoleyl mesylate (5.0 g, 15 mmol) is added and the reaction refluxed under nitrogen for 3 hours. The reaction mixture is then cooled in an ice bath while quenching via the slow addition of ethanol. Following dilution with a further 150 mL of benzene, the mixture is washed with distilled water (2×150 mL) and brine (150 mL). The organic phase is dried over magnesium sulphate and evaporated to give the crude product.

[0241]The crude product is purified on a silica gel (Kiesel Gel 60) column eluted with 0-5% methanol in chloroform. Column fractions are analyzed by thin layer chromatography (TLC) (silica gel, chloroform / methanol 9:1 v / v, visualized with molybdate dip) and fractions containing purified pro...

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Abstract

The present invention provides compositions comprising cationic lipids, liposomes and nucleic acid-lipid particles comprising the cationic lipids, and methods of using such compositions, liposomes, and nucleic acid-lipid particles.

Description

CROSS-REFERENCES TO RELATED APPLICATIONS[0001]This application is a Continuation of U.S. patent application Ser. No. 11 / 148,430 filed Jun. 7, 2005 and claims the benefit of U.S. Provisional Patent Application Nos. 60 / 578,075 filed Jun. 7, 2004, 60 / 610,746, filed Sep. 17, 2004, and 60 / 679,427, filed May 9, 2005, the disclosures of each of which is incorporated by reference in its entirety for all purposes.BACKGROUND OF THE INVENTION[0002]An effective and safe gene delivery system is required for gene therapy to be clinically useful. Viral vectors are relatively efficient gene delivery systems, but suffer from a variety of limitations, such as the potential for reversion to the wild type as well as immune response concerns. As a result, nonviral gene delivery systems are receiving increasing attention (Worgall, et al., Human Gene Therapy 8:37-44 (1997); Peeters, et al., Human Gene Therapy 7:1693-1699 (1996); Yei, et al., Gene Therapy 1:192-200 (1994); Hope, et al., Molecular Membrane...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): A61K9/127C12N5/071C07C217/28A61K38/02A61K31/7088A61P31/00A61K31/7105A61P37/02A61P29/00A61P25/00A61P35/00C12N15/88A61K31/713A61K9/16A61K47/26A61K48/00C07C217/40
CPCA61K9/0019A61K9/1271A61K9/1617A61K47/26C12N15/88A61K48/00A61K48/0025C07C217/28C07C217/40A61K47/48815A61K47/6911A61P25/00A61P29/00A61P31/00A61P35/00A61P37/02A61P43/00
Inventor HEYES, JAMESMACLACHLAN, IANPALMER, LORNE R.
Owner ARBUTUS BIOPHARMA CORPORAT ION
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