WO2020077007A1 - Compositions and systems comprising transfection-competent vesicles free of organic-solvents and detergents and methods related thereto - Google Patents

Compositions and systems comprising transfection-competent vesicles free of organic-solvents and detergents and methods related thereto Download PDF

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Publication number
WO2020077007A1
WO2020077007A1 PCT/US2019/055472 US2019055472W WO2020077007A1 WO 2020077007 A1 WO2020077007 A1 WO 2020077007A1 US 2019055472 W US2019055472 W US 2019055472W WO 2020077007 A1 WO2020077007 A1 WO 2020077007A1
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Prior art keywords
lipid
tcv
composition
selected cargo
mol
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PCT/US2019/055472
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English (en)
French (fr)
Inventor
Blair Leavitt
Pieter Cullis
Terri PETKAU
Austin Hill
Pamela WAGNER
Jayesh KULKAMI
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University of British Columbia
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University of British Columbia
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Priority to DK19871608.6T priority Critical patent/DK3864163T3/da
Priority to FIEP19871608.6T priority patent/FI3864163T3/fi
Priority to BR112021006539A priority patent/BR112021006539A2/pt
Priority to KR1020217009987A priority patent/KR20210093232A/ko
Priority to RS20240470A priority patent/RS65449B1/sr
Priority to CA3114699A priority patent/CA3114699A1/en
Priority to AU2019359299A priority patent/AU2019359299B2/en
Priority to HRP20240586TT priority patent/HRP20240586T1/hr
Priority to EA202190688A priority patent/EA202190688A1/ru
Priority to JP2021517982A priority patent/JP7555123B2/ja
Priority to CN201980065376.1A priority patent/CN113166783B/zh
Priority to EP19871608.6A priority patent/EP3864163B1/en
Priority to US17/281,678 priority patent/US11980673B2/en
Priority to ES19871608T priority patent/ES2982542T3/es
Priority to PL19871608.6T priority patent/PL3864163T3/pl
Application filed by University of British Columbia filed Critical University of British Columbia
Priority to EP24156927.6A priority patent/EP4379053A3/en
Priority to CN202411356247.7A priority patent/CN119320803A/zh
Publication of WO2020077007A1 publication Critical patent/WO2020077007A1/en
Priority to PH12021550626A priority patent/PH12021550626A1/en
Priority to ZA2021/02238A priority patent/ZA202102238B/en
Priority to IL282063A priority patent/IL282063A/en
Anticipated expiration legal-status Critical
Priority to AU2022203149A priority patent/AU2022203149B2/en
Priority to US17/941,669 priority patent/US11865190B2/en
Priority to JP2023204608A priority patent/JP7840578B2/ja
Priority to US18/392,143 priority patent/US20240342315A1/en
Priority to US18/660,467 priority patent/US20240350676A1/en
Priority to AU2025202803A priority patent/AU2025202803A1/en
Priority to JP2025099115A priority patent/JP2025143306A/ja
Ceased legal-status Critical Current

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    • C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09—Recombinant DNA-technology
    • C12N15/11—DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
    • C12N15/111—General methods applicable to biologically active non-coding nucleic acids
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    • C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09—Recombinant DNA-technology
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    • A61K47/24—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing atoms other than carbon, hydrogen, oxygen, halogen, nitrogen or sulfur, e.g. cyclomethicone or phospholipids
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    • A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
    • A61K47/28—Steroids, e.g. cholesterol, bile acids or glycyrrhetinic acid
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    • A61K9/0012—Galenical forms characterised by the site of application
    • A61K9/0019—Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
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    • A61K9/10—Dispersions; Emulsions
    • A61K9/127—Synthetic bilayered vehicles, e.g. liposomes or liposomes with cholesterol as the only non-phosphatidyl surfactant
    • A61K9/1271—Non-conventional liposomes, e.g. PEGylated liposomes or liposomes coated or grafted with polymers
    • A61K9/1272—Non-conventional liposomes, e.g. PEGylated liposomes or liposomes coated or grafted with polymers comprising non-phosphatidyl surfactants as bilayer-forming substances, e.g. cationic lipids or non-phosphatidyl liposomes coated or grafted with polymers
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Definitions

  • LNPs lipid nanoparticles
  • liposomes are lipid-based structures with a single bilayer and an aqueous core.
  • Typical established processes of LNP formation load the vesicle with specific cargo at time of initial vesicle formation. These processes further use specialized instrumentation, organic solvents and/or detergents, require large amounts of material, and constitute processing times on the order of days, all of which severely hamper utility, accessibility and therapeutic usability.
  • LNPs and other lipid particles typically comprise an ionizable cationic lipid, one or more phospholipid(s), cholesterol (Chol), and polyethyleneglycol-lipid (PEG-lipid)
  • PEG-lipid polyethyleneglycol-lipid
  • the lipid-based TCV can comprise a cationic lipid, such as an ionizable cationic lipid.
  • the lipid-based TCV can comprise about 20 mol % to 50 mol % cationic lipid.
  • the ionizable cationic lipid can comprise l,2-Dioleyloxy-3-dimethylamino-propane (DODMA).
  • FIGS 1A-1D Transfection-competent vesicles (TCVs) produced according to the methods herein display knockdown in immortalized cells and primary neurons.
  • TCVs Transfection-competent vesicles
  • A Relative luciferase expression in HEK-Luc cells after transfection with organic solvent-free, detergent-free TCVs composed of 50% ionizable cationic lipid.
  • B Cell viability from the same set of transfections presented in (A) as % of control (cells only) wells.
  • C Relative expression of hdh mRNA in primary cortical neurons after organic solvent-free, detergent- free TCV-mediated transfection of an siRNA selected cargo into the neurons. The siRNA targeted hdh.
  • FIG. 3A-3D Organic solvent- free, detergent-free empty TCVs containing a reduced amount of ionizable lipid facilitate potent siRNA delivery with decreased toxicity.
  • DODMA Relative luciferase expression in HEK-Luc cells after transfection with TCVs composed of either 20% or 50% of the ionizable lipid l,2-Dioleyloxy-3-dimethylamino-propane
  • Cryo-TEM was performed as described previously (Kulkami, Darjuan et al. 2018). Briefly, TCVs were concentrated to a total lipid concentration of approximately 20 mg/mL using an Amicon centrifugal concentration unit (lOkDa NWCO). A small volume (3-5 uL) of material was applied to a glow-discharged copper grid and plunge-frozen using an FEI Mark IV Vitrobot (Hillsboro, OR). The grids were stored under liquid nitrogen until imaged. All imaging was performed using an FEI Tecnai G2 instrument operating at 200 kV in low-dose mode. Images were captured using an FEI Eagle 4k CCD bottom-mount detector. All sample preparation and imaging was performed at the UBC Bioimaging Facility (Vancouver, BC).
  • An established lipid composition currently used in clinical formulations (see Patisiran ), includes a significant amount of ionizable cationic lipid (50 mol%) (Jayaraman, Ansell et al. 2012; Suhr, Coelho et al. 2015). While such high amounts allow for improvements in the effective dose to achieve 50% gene silencing (ED50) in vivo (Jayaraman, Ansell et al. 2012), the persistence of lipid metabolites following administration (Maier, Jayaraman et al. 2013; Sabnis, Kumarasinghe et al. 2018) and the toxicity associated with those molecules renders the formulation toxic in high- dose regimens and repeat administration (or to sensitive cell types).
  • the current compositions, TCVs, etc. can be comprised of materials that are biodegradable or facilitate elimination. Here, the current compositions, TCVs, etc., decrease the amount of toxic ingredients maintaining transfection potency.
  • Figure 6 provides a photomicrograph of Cas9 located within a primary neuron.
  • RNP delivered via organic solvent-free, detergent-free TCV as discussed herein can be seen within a primary neuron as fluorescent signals; the untreated control has no such fluorescent signals.
  • immunocytochemistry of primary neuronal cells showed localization of Cas9 protein (red) within the nucleus (blue) of cortical neurons derived from mice. Cells were also stained for phalloidin (green) to show cellular morphology.

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PCT/US2019/055472 2018-10-09 2019-10-09 Compositions and systems comprising transfection-competent vesicles free of organic-solvents and detergents and methods related thereto Ceased WO2020077007A1 (en)

Priority Applications (27)

Application Number Priority Date Filing Date Title
PL19871608.6T PL3864163T3 (pl) 2018-10-09 2019-10-09 Kompozycje i układy zawierające pęcherzyki zdolne do transfekcji wolne od rozpuszczalników organicznych i detergentów oraz związane z nimi sposoby postępowania
BR112021006539A BR112021006539A2 (pt) 2018-10-09 2019-10-09 composições e sistemas competentes de vesículas competentes para transfecção isentas de solventes e detergentes orgânicos e métodos relacionados às mesmas
KR1020217009987A KR20210093232A (ko) 2018-10-09 2019-10-09 유기용매와 세제가 없는 형질감염 적격 소포를 포함하는 조성물과 시스템 및 관련 방법
RS20240470A RS65449B1 (sr) 2018-10-09 2019-10-09 Supstance i sistemi koji obuhvataju vezikule kompetentne za transfekciju bez organskih rastvarača i deterdženata i metode za to
CA3114699A CA3114699A1 (en) 2018-10-09 2019-10-09 Compositions and systems comprising transfection-competent vesicles free of organic-solvents and detergents and methods related thereto
AU2019359299A AU2019359299B2 (en) 2018-10-09 2019-10-09 Compositions and systems comprising transfection-competent vesicles free of organic-solvents and detergents and methods related thereto
HRP20240586TT HRP20240586T1 (hr) 2018-10-09 2019-10-09 Sastavi i sustavi koji sadrže transfekcijske sposobne vezikle bez organskih otapala i deterdženta i s njim povezanim postupcima
EA202190688A EA202190688A1 (ru) 2018-10-09 2019-10-09 Композиции и системы, содержащие трансфекционно-компетентные везикулы, не содержащие органических растворителей и детергентов, и связанные с ними способы
JP2021517982A JP7555123B2 (ja) 2018-10-09 2019-10-09 有機溶媒不含かつ劣化剤不含のトランスフェクション・コンピテント・ベシクルを含む組成物及びシステム並びにそれらに関連する方法
CN201980065376.1A CN113166783B (zh) 2018-10-09 2019-10-09 包含无有机溶剂和去污剂的转染活性囊泡的组合物和系统以及与之相关的方法
EP19871608.6A EP3864163B1 (en) 2018-10-09 2019-10-09 Compositions and systems comprising transfection-competent vesicles free of organic-solvents and detergents and methods related thereto
US17/281,678 US11980673B2 (en) 2018-10-09 2019-10-09 Compositions and systems comprising transfection-competent vesicles free of organic-solvents and detergents and methods related thereto
ES19871608T ES2982542T3 (es) 2018-10-09 2019-10-09 Composiciones y sistemas que comprenden vesículas competentes para la transfección sin solventes orgánicos ni detergentes y métodos relacionados con los mismos
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CN202411356247.7A CN119320803A (zh) 2018-10-09 2019-10-09 包含无有机溶剂和去污剂的转染活性囊泡的组合物和系统以及与之相关的方法
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US12064479B2 (en) 2022-05-25 2024-08-20 Akagera Medicines, Inc. Lipid nanoparticles for delivery of nucleic acids and methods of use thereof
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US11865190B2 (en) 2024-01-09
AU2019359299A1 (en) 2021-05-13
RS65449B1 (sr) 2024-05-31
CN113166783B (zh) 2024-10-11
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JP7555123B2 (ja) 2024-09-24
CN113166783A (zh) 2021-07-23
EP3864163B1 (en) 2024-03-20
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DK3864163T3 (da) 2024-05-06
JP2024028838A (ja) 2024-03-05
HUE066181T2 (hu) 2024-07-28
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EA202190688A1 (ru) 2021-06-07
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US20220118112A1 (en) 2022-04-21
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