WO2022191567A1 - Covid-19를 포함하는 호흡기 바이러스 감염증, 바이러스 감염에 의한 폐섬유증, 또는 호흡기 질환 예방 또는 치료를 위한 초음파 방식 연무식 흡입기를 이용한 이중가닥 올리고뉴클레오티드 구조체 투여용 조성물 - Google Patents

Covid-19를 포함하는 호흡기 바이러스 감염증, 바이러스 감염에 의한 폐섬유증, 또는 호흡기 질환 예방 또는 치료를 위한 초음파 방식 연무식 흡입기를 이용한 이중가닥 올리고뉴클레오티드 구조체 투여용 조성물 Download PDF

Info

Publication number
WO2022191567A1
WO2022191567A1 PCT/KR2022/003245 KR2022003245W WO2022191567A1 WO 2022191567 A1 WO2022191567 A1 WO 2022191567A1 KR 2022003245 W KR2022003245 W KR 2022003245W WO 2022191567 A1 WO2022191567 A1 WO 2022191567A1
Authority
WO
WIPO (PCT)
Prior art keywords
pharmaceutical composition
group
bond
double
composition according
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/KR2022/003245
Other languages
English (en)
French (fr)
Korean (ko)
Inventor
박한오
이상규
윤성일
권오승
고은아
고영호
박준홍
송강
김장선
이미선
최순자
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Sirnagen Therapeutics Corp
Bioneer Corp
Original Assignee
Sirnagen Therapeutics Corp
Bioneer Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Sirnagen Therapeutics Corp, Bioneer Corp filed Critical Sirnagen Therapeutics Corp
Priority to US18/281,251 priority Critical patent/US20250066787A1/en
Priority to CN202280030335.0A priority patent/CN117677402A/zh
Priority to EP22767463.7A priority patent/EP4306133A4/en
Priority to JP2023555188A priority patent/JP2024509906A/ja
Priority to CA3210813A priority patent/CA3210813A1/en
Publication of WO2022191567A1 publication Critical patent/WO2022191567A1/ko
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Images

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K48/00—Medicinal preparations containing genetic material which is inserted into cells of the living body to treat genetic diseases; Gene therapy
    • A61K48/0075—Medicinal preparations containing genetic material which is inserted into cells of the living body to treat genetic diseases; Gene therapy characterised by an aspect of the delivery route, e.g. oral, subcutaneous
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/70—Carbohydrates; Sugars; Derivatives thereof
    • A61K31/7088—Compounds having three or more nucleosides or nucleotides
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/70—Carbohydrates; Sugars; Derivatives thereof
    • A61K31/7088—Compounds having three or more nucleosides or nucleotides
    • A61K31/713—Double-stranded nucleic acids or oligonucleotides
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
    • A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
    • A61K47/54—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic compound
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
    • A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
    • A61K47/54—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic compound
    • A61K47/543—Lipids, e.g. triglycerides; Polyamines, e.g. spermine or spermidine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
    • A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
    • A61K47/54—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic compound
    • A61K47/554—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic compound the modifying agent being a steroid plant sterol, glycyrrhetic acid, enoxolone or bile acid
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
    • A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
    • A61K47/56—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic macromolecular compound, e.g. an oligomeric, polymeric or dendrimeric molecule
    • A61K47/58—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic macromolecular compound, e.g. an oligomeric, polymeric or dendrimeric molecule obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. poly[meth]acrylate, polyacrylamide, polystyrene, polyvinylpyrrolidone, polyvinylalcohol or polystyrene sulfonic acid resin
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
    • A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
    • A61K47/56—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic macromolecular compound, e.g. an oligomeric, polymeric or dendrimeric molecule
    • A61K47/59—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic macromolecular compound, e.g. an oligomeric, polymeric or dendrimeric molecule obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyureas or polyurethanes
    • A61K47/60—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic macromolecular compound, e.g. an oligomeric, polymeric or dendrimeric molecule obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyureas or polyurethanes the organic macromolecular compound being a polyoxyalkylene oligomer, polymer or dendrimer, e.g. PEG, PPG, PEO or polyglycerol
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
    • A61K47/69—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit
    • A61K47/6921—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit the form being a particulate, a powder, an adsorbate, a bead or a sphere
    • A61K47/6927—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit the form being a particulate, a powder, an adsorbate, a bead or a sphere the form being a solid microparticle having no hollow or gas-filled cores
    • A61K47/6929—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit the form being a particulate, a powder, an adsorbate, a bead or a sphere the form being a solid microparticle having no hollow or gas-filled cores the form being a nanoparticle, e.g. an immuno-nanoparticle
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K48/00—Medicinal preparations containing genetic material which is inserted into cells of the living body to treat genetic diseases; Gene therapy
    • A61K48/0008—Medicinal preparations containing genetic material which is inserted into cells of the living body to treat genetic diseases; Gene therapy characterised by an aspect of the 'non-active' part of the composition delivered, e.g. wherein such 'non-active' part is not delivered simultaneously with the 'active' part of the composition
    • A61K48/0025—Medicinal preparations containing genetic material which is inserted into cells of the living body to treat genetic diseases; Gene therapy characterised by an aspect of the 'non-active' part of the composition delivered, e.g. wherein such 'non-active' part is not delivered simultaneously with the 'active' part of the composition wherein the non-active part clearly interacts with the delivered nucleic acid
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/0012—Galenical forms characterised by the site of application
    • A61K9/007—Pulmonary tract; Aromatherapy
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/0012—Galenical forms characterised by the site of application
    • A61K9/007—Pulmonary tract; Aromatherapy
    • A61K9/0073—Sprays or powders for inhalation; Aerolised or nebulised preparations generated by other means than thermal energy
    • A61K9/0078—Sprays or powders for inhalation; Aerolised or nebulised preparations generated by other means than thermal energy for inhalation via a nebulizer such as a jet nebulizer, ultrasonic nebulizer, e.g. in the form of aqueous drug solutions or dispersions
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12—Antivirals
    • A61P31/14—Antivirals for RNA viruses
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • 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
    • C12N15/113—Non-coding nucleic acids modulating the expression of genes, e.g. antisense oligonucleotides; Antisense DNA or RNA; Triplex- forming oligonucleotides; Catalytic nucleic acids, e.g. ribozymes; Nucleic acids used in co-suppression or gene silencing
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • 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
    • C12N15/113—Non-coding nucleic acids modulating the expression of genes, e.g. antisense oligonucleotides; Antisense DNA or RNA; Triplex- forming oligonucleotides; Catalytic nucleic acids, e.g. ribozymes; Nucleic acids used in co-suppression or gene silencing
    • C12N15/1131—Non-coding nucleic acids modulating the expression of genes, e.g. antisense oligonucleotides; Antisense DNA or RNA; Triplex- forming oligonucleotides; Catalytic nucleic acids, e.g. ribozymes; Nucleic acids used in co-suppression or gene silencing against viruses
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • 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
    • C12N15/87—Introduction of foreign genetic material using processes not otherwise provided for, e.g. co-transformation
    • C12N15/88—Introduction of foreign genetic material using processes not otherwise provided for, e.g. co-transformation using microencapsulation, e.g. using amphiphile liposome vesicle
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N2310/00—Structure or type of the nucleic acid
    • C12N2310/10—Type of nucleic acid
    • C12N2310/14—Type of nucleic acid interfering nucleic acids [NA]
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N2310/00—Structure or type of the nucleic acid
    • C12N2310/10—Type of nucleic acid
    • C12N2310/14—Type of nucleic acid interfering nucleic acids [NA]
    • C12N2310/141—MicroRNAs, miRNAs
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N2310/00—Structure or type of the nucleic acid
    • C12N2310/30—Chemical structure
    • C12N2310/35—Nature of the modification
    • C12N2310/351—Conjugate
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N2310/00—Structure or type of the nucleic acid
    • C12N2310/30—Chemical structure
    • C12N2310/35—Nature of the modification
    • C12N2310/351—Conjugate
    • C12N2310/3515—Lipophilic moiety, e.g. cholesterol
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N2310/00—Structure or type of the nucleic acid
    • C12N2310/50—Physical structure
    • C12N2310/53—Physical structure partially self-complementary or closed
    • C12N2310/531—Stem-loop; Hairpin
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N2320/00—Applications; Uses
    • C12N2320/30—Special therapeutic applications
    • C12N2320/32—Special delivery means, e.g. tissue-specific

Definitions

  • the present invention relates to a composition for administering a double-stranded oligonucleotide structure using an ultrasonic nebulizer, particularly for preventing or treating respiratory viral infections including COVID-19, pulmonary fibrosis caused by viral infections, or respiratory diseases.
  • a composition for administering a double-stranded oligonucleotide structure using an ultrasonic nebulizer inhaler particularly for preventing or treating respiratory viral infections including COVID-19, pulmonary fibrosis caused by viral infections, or respiratory diseases.
  • it relates to a composition for administering a double-stranded oligonucleotide structure using an ultrasonic nebulizer inhaler.
  • Inhalation drug delivery is not only easy to use, but it can also show the necessary effect with a small dose, and it can avoid or minimize systemic side effects by reaching the target organ, especially the bronchi or lungs directly, and delivering drugs that show rapid drug effect. way.
  • Inhalers are classified into metered dose inhaler (MDI), dry powder inhaler (DPI), and nebulizer according to drug properties.
  • MDI metered dose inhaler
  • DPI dry powder inhaler
  • nebulizer nebulizer according to drug properties.
  • gas is filled in the drug container, and a certain amount of drug is released by the pressure of the gas when used.
  • the mist-type inhaler uses mechanical vibration to make the drug into small liquid particles that can be sprayed, and then uses air pressure to deliver it to the patient using an inhalation tube. Because it is delivered, it has the advantage of being usable for respiratory viral infections, interstitial pulmonary fibrosis, chronic obstructive pulmonary disease, asthma, bronchiectasis, bronchitis, pneumonia, and emphysema.
  • the mist inhaler can be divided into a compressor type and an ultrasonic type according to a method of spraying.
  • the compressor creates atomized particles as air passes through the nebulizer drug chamber, and an aerosol is generated through the micropores of the vibrating mesh.
  • the ultrasonic nebulizer vibrates the drug and creates an aerosol as the ultrasonic waves pass through the drug chamber.
  • an aerosol with a certain size is generated by passing through the micropores of the mesh.
  • siRNA-based drugs as inhalants, but mainly as dry powder formulations, hyaluronic acid-coated liposome spray (lyophilized form), albumin and PLGA (poly-lactic-co-glycolic acid)
  • hyaluronic acid-coated liposome spray lyophilized form
  • albumin and PLGA (poly-lactic-co-glycolic acid)
  • MPG cell-penetrating proteins
  • RNAi RNA interference
  • target genes such as cancer and genetic diseases that are the cause of overexpression of specific genes can be removed from the mRNA level, thereby developing therapeutic agents for disease treatment And it can be utilized as an important tool for target verification.
  • a technique for suppressing the expression of a target gene a technique for introducing a transgene for a target gene has been disclosed. There is a method of introducing a transgene into
  • RNA therapy targeting such RNA is a method that removes the function of the gene by using an oligonucleotide for the target RNA.
  • ASOs antisense oligonucleotides
  • Antisense oligonucleotide is a short-length synthetic DNA designed to bind to a target gene according to the Watson-Crick base reaction, and can specifically inhibit the expression of a specific nucleotide sequence of a gene. It has been used to study the function of genes and to develop therapeutics that can treat diseases such as cancer at the molecular level.
  • ASO has the advantage that it can be easily manufactured by setting various targets for suppressing gene expression, and there have been studies to utilize it to suppress the expression of oncogenic genes and the growth of cancer cells.
  • ASO suppresses the expression of a specific gene is achieved by binding to a complementary mRNA sequence and inducing RNase H activity to remove mRNA or to interfere with the formation and progression of a ribosome complex for protein translation. It was also reported that ASO binds to genomic DNA and inhibits gene transcription by forming a triple-helix structure. ASO has the above potential, but in order to be used in clinical practice, it must be efficiently delivered into a target tissue or cell to improve stability to nucleases and specifically bind to the nucleotide sequence of a target gene.
  • the secondary and tertiary structure of gene mRNA is an important factor for specific binding of ASO, and since the part with less secondary structure of mRNA is very advantageous for ASO to access, less secondary structure of mRNA is generated before synthesizing ASO Efforts have been made to effectively achieve gene-specific inhibition not only in vitro but also in vivo by systematically analyzing the target region.
  • These ASOs are very stable than siRNA, a kind of RNA, and have the advantage of being well soluble in water and physiological saline.
  • FDA Federal Drug Administration
  • RNA interference (hereinafter referred to as 'RNAi') has been found to act on sequence-specific mRNA in various types of mammalian cells (Barik, S., J Mol. Med. (2005) 83: 764-773).
  • 'RNAi' RNA interference
  • the transferred RNA double-strand is processed into 21 to 23 double-stranded (base pair, bp) by an endonuclease called Dicer (small interfering RNA).
  • siRNA binds to RISC (RNA-induced silencing complex) and the guide (antisense) strand recognizes and degrades the target mRNA to sequence-specifically to hinder
  • RISC RNA-induced silencing complex
  • antisense RNA-induced silencing complex
  • siRNA binds to RISC (RNA-induced silencing complex) and the guide (antisense) strand recognizes and degrades the target mRNA to sequence-specifically to hinder
  • RISC RNA-induced silencing complex
  • the gene expression suppression technology using siRNA suppresses the expression of the target gene in the target cell and observes the change resulting therefrom, and is useful in research to identify the function of the target gene in the target cell. Suppressing the function of a target gene in the back will be useful for developing a treatment method for the disease, and the results of in vitro studies and in vivo studies using experimental animals , it has been reported that it is possible to suppress the expression of a target gene by siRNA.
  • siRNA for the same target gene has a superior effect on the inhibitory effect of mRNA expression in vitro and in vivo compared to ASO, and has a long-lasting effect.
  • the mechanism of action of siRNA binds complementary to the target mRNA and regulates the expression of the target gene in a sequence-specific manner. It has the advantage that it can be expanded to (MA Behlke, MOLECULAR THERAPY. 2006 13(4):664-670).
  • siRNA In spite of the excellent effect and wide range of use of siRNA, for siRNA to be developed as a therapeutic agent, siRNA needs to be effectively delivered to target cells by improving the stability of siRNA in the body and improving cell delivery efficiency.
  • some nucleotides or backbone of siRNA are modified to have nuclease resistance or a viral vector, Research on this is being actively attempted, such as using a carrier such as liposomes or nanoparticles.
  • a delivery system using a viral vector such as an adenovirus or a retrovirus has high transfection efficacy, but high immunogenicity and oncogenicity.
  • a non-viral delivery system including nanoparticles has a low cell delivery efficiency compared to a viral delivery system, but has high in vivo stability, is capable of target-specific delivery, and contains It has the advantage of uptake and internalization of RNAi oligonucleotides into cells or tissues, and almost no cytotoxicity and innate immune stimulation. (Akhtar S, J Clin Invest. 2007 December 3; 117(12): 3623-3632).
  • the method of using a nanocarrier is a method of forming nanoparticles by using various polymers such as liposomes and cationic polymer complexes, and carrying siRNA on these nanoparticles, that is, a nanocarrier, and delivering it to cells.
  • the methods using nanocarriers include polymeric nanoparticles, polymer micelles, and lipoplexes.
  • the method using lipoplex is composed of cationic lipids It interacts with the anionic lipids of the endosome to induce a destabilizing effect of the endosome and deliver it into the cell.
  • siRNA passenger (sense) strand it is known that high efficiency can be induced in vivo by linking chemicals to the end of the siRNA passenger (sense) strand to have enhanced pharmacokinetics (J Soutschek, Nature 11;432(7014):173-8, 2004).
  • the stability of the siRNA varies depending on the nature of the chemical compound bound to the end of the siRNA sense (passenger) or antisense (guide) strand.
  • siRNA conjugated with a high molecular compound such as polyethylene glycol (PEG) interacts with the anionic phosphate group of siRNA in the presence of a cationic material to form a complex, resulting in improved siRNA stability.
  • PEG polyethylene glycol
  • micelles composed of polymer complexes are extremely small in size compared to other systems used as drug delivery vehicles, such as microspheres or nanoparticles, but their distribution is very uniform and spontaneously formed. It has the advantage of being easy to manage and secure reproducibility.
  • siRNA conjugates in which a biocompatible polymer, a hydrophilic substance (eg, polyethylene glycol) is conjugated to siRNA by a simple covalent bond or a linker-mediated covalent bond, siRNA A technology has been developed for securing the stability and efficient cell membrane permeability of siRNA (Korean Patent No.
  • oligo RNA structure in which hydrophilic and hydrophobic substances are bound to oligonucleotides, particularly double-stranded oligo RNA such as siRNA, has been developed, and the structure is made of a hydrophobic material.
  • SAMiRNA self-assembled micelle inhibitory RNA
  • PEG or HEG Hexaethylenglycol
  • PEG is a synthetic polymer and is often used in pharmaceuticals, especially for increasing the solubility of proteins and controlling pharmacokinetics.
  • used PEG is a polydisperse material, and one batch of polymer is composed of the sum of different numbers of monomers, so the molecular weight is in the form of a Gaussian curve, and the polydisperse value (Mw/Mn) is It expresses the degree of homogeneity of a substance.
  • PEG has a low molecular weight (3 to 5 kDa), it shows a polydispersity index of about 1.01, and when it has a high molecular weight (20 kDa), it shows a high polydispersity index of about 1.2. looks like Therefore, when PEG is combined with pharmaceuticals, the polydispersity of PEG is reflected in the conjugate, making it difficult to verify a single substance.
  • the hydrophilic material of the double-stranded oligonucleotide structure constituting SAMiRNA is combined with uniform 1 to 15 monomers having a constant molecular weight and, if necessary, a linker.
  • a new type of carrier technology with a smaller size and remarkably improved polydispersity compared to the existing SAMiRNA has been developed. was developed (Korean Patent No. 18162349).
  • siRNA when siRNA is injected into the body, siRNA is rapidly degraded by various enzymes present in the blood, resulting in poor delivery efficiency to target cells or tissues. There was a variation in expression inhibition rate. Therefore, in order to more stably and effectively inhibit the expression of a target gene using the improved self-assembled nanoparticle SAMiRNA, the present inventors used a DNA sequence of ASO as a guide and an RNA sequence as an antisense strand as a passenger. By applying the double-stranded oligonucleotide of the -RNA hybrid type, it was possible to enhance the expression inhibitory effect and stability of the target gene.
  • the conventional RNAi drug delivery method is mainly in the form of powder, which, as described above, has limitations in drug delivery and drug efficacy along with the toxicity of the particles themselves and the risk of non-specific immune responses.
  • an attempt was made to develop a drug delivery method particularly suitable for SAMiRNA that can overcome this limitation.
  • the present invention was completed by confirming that the SAMiRNA was effectively delivered to the lungs without cytotoxicity while maintaining the concentration, molecular weight, purity, nanoparticle size, and osmolality, and maintaining target gene suppression ability.
  • the present invention provides a pharmaceutical composition for preventing or treating respiratory viral infection, viral pulmonary fibrosis, or respiratory disease comprising a double-stranded oligonucleotide structure having the structure of the following structural formula (1), the pharmaceutical composition provides a pharmaceutical composition characterized in that it is administered using an nebulizer inhaler:
  • A is a hydrophilic material
  • B is a hydrophobic material
  • X and Y are each independently a simple covalent bond or a linker-mediated covalent bond
  • R is a double-stranded oligonucleotide.
  • FIG. 5a shows the results of analyzing the weight of each organ by administering SAMiRNA-Cy5 nanoparticles to a hamster using an ultrasonic mist inhaler and extracting the lungs, spleen, liver, kidneys, etc. 24 hours later.
  • Figure 5b shows SAMiRNA-Cy5 nanoparticles were administered to a hamster using an ultrasonic mist inhaler and the lungs, spleen, liver, kidneys, etc. were extracted 24 hours later, and optical images (left), fluorescence images (center) and fluorescence values ( Right) The analysis result is shown.
  • FIG. 6 shows the results of confocal image analysis showing that SAMiRNA-Cy5 nanoparticles are effectively delivered and distributed in lung tissue extracted 24 hours after administration of SAMiRNA-Cy5 nanoparticles to hamsters using an ultrasonic mist inhaler.
  • FIG. 7a shows a schematic diagram of an experiment in which the SAMiRNA-Cy5 nanoparticles were administered to mice using an ultrasonic nebulizer inhaler and then tissue harvested at each hour (1, 24, 48, 96, 168 hr).
  • FIG. 7b shows that after administration of SAMiRNA-Cy5 nanoparticles to mice using an ultrasonic mist inhaler, the lungs, spleen, liver, kidneys, heart, etc. are extracted by time (1, 24, 48, 96, 168 hr), and optical It is the result of analyzing the image and the fluorescence image.
  • Figure 8a shows the results of analyzing the fluorescence quantification of nasal and lung tissues extracted by time (1, 24, 48, 96, 168 hr) after administering SAMiRNA-Cy5 nanoparticles to mice using an ultrasonic mist inhaler. .
  • 8B shows the results of PK analysis of lung tissue extracted by time (1, 24, 48, 96, 168 hr) after administering SAMiRNA-Cy5 nanoparticles to mice using an ultrasonic mist inhaler.
  • 9a is a confocal image analysis of the delivery and distribution of lung tissue extracted by time (1, 24, 48, 96, 168 hr) after administering SAMiRNA-Cy5 nanoparticles to mice using an ultrasonic nebulizer inhaler. show the results.
  • Figure 9b shows the results of confocal image analysis of the delivery and distribution of lung tissue extracted 1 hour after administering SAMiRNA-Cy5 nanoparticles to mice using an ultrasonic nebulizer inhaler.
  • the ultrasonic nebulizer inhaler is an optimized inhalation drug delivery method that does not affect the physical/chemical properties of the construct.
  • the concentration, molecular weight, purity, nanoparticle size, and osmolarity could be maintained as the stock solution.
  • the compressor method of the aerosol atomizer it was confirmed that the nanoparticle size, molecular weight, and purity were the same as the raw material, but the material concentration and osmolality were significantly reduced compared to the raw material.
  • the present invention provides a pharmaceutical composition for preventing or treating respiratory viral infection, viral pulmonary fibrosis, or respiratory disease comprising a double-stranded oligonucleotide structure comprising the structure of Structural Formula 1, the pharmaceutical composition comprising: It relates to a pharmaceutical composition, characterized in that it is administered using an aerosol inhaler:
  • A is a hydrophilic material
  • B is a hydrophobic material
  • X and Y are each independently a simple covalent bond or a linker-mediated covalent bond
  • R is a double-stranded oligonucleotide.
  • the mist-type inhaler may be characterized as an ultrasonic-type inhaler.
  • the double-stranded oligonucleotide may include a sense strand and an anti-sense strand comprising a complementary sequence thereto.
  • the sense strand or antisense strand may be characterized in that it consists of 19 to 31 nucleotides, but is not limited thereto.
  • the sense or antisense strand may be independently characterized in that it is DNA or RNA, for example, it may include a sequence in the form of RNA/RNA, DNA/DNA, or DNA/RNA hybrid. have.
  • the sense strand or the antisense strand may include chemical modification
  • the chemical modification is a methyl group (-CH3), a methoxy group (-OCH3), an amine group (-NH2), a fluorine (-F), O -2-methoxyethyl group, O-propyl group, O-2-methylthioethyl group, O-3-aminopropyl group, O-3-dimethylaminopropyl group, O-N-methylacetamido group and O-dimethylamidooxy group a modification substituted with any one selected from the group consisting of ethyl;
  • nucleotide bond is any one bond selected from the group consisting of a phosphorothioate bond, a boranophosphate bond, and a methyl phosphonate bond;
  • PNA peptide nucleic acid
  • LNA locked nucleic acid
  • UAA unlocked nucleic acid
  • the chemical modification may contribute to improving in vivo stability, or conferring nuclease resistance and reducing non-specific immune responses.
  • the present invention may be characterized in that one or more phosphate groups are bonded to the 5' end of the antisense strand, preferably 1 to 3 phosphate groups are bonded,
  • the present invention is not limited thereto.
  • the double-stranded oligonucleotide according to the present invention is a concept that includes all substances having a general RNAi action. It is self-evident to those who have the knowledge of That is, the oligonucleotide may be characterized in that it is siRNA, shRNA or miRNA.
  • the double-stranded oligonucleotide according to the present invention may include an overhang, which is a structure comprising one or more unpaired nucleotides at the 3' end of one or both strands.
  • the form of the double-stranded oligonucleotide according to the present invention is preferably a DNA-RNA hybrid, siRNA (short interfering RNA), shRNA (short hairpin RNA), and miRNA (microRNA), but is not limited thereto, and an antagonist for miRNA Single-stranded miRNA inhibitors that can act as antagonists are also included.
  • the pharmaceutical composition according to the present invention may comprise a structure of the following Structural Formula 2:
  • S and AS refer to the sense strand and the antisense strand of the double-stranded oligonucleotide, and A, B, X and Y are the same as defined in Structural Formula 1.
  • the pharmaceutical composition according to the present invention comprises a structure of formula 3:
  • a pharmaceutical composition according to the present invention comprises a structure of formula 3':
  • Structural Formulas 3 and 3' A, B, X, Y, S and AS have the same definitions as in Structural Formula 2, and 5' and 3' refer to the 5' and 3' ends of the sense strand.
  • the molecular weight of the hydrophilic material may be characterized in that 200 to 10,000, but is not limited thereto.
  • the hydrophilic material may be selected from the group consisting of polyethylene glycol (PEG), polyvinylpyrrolidone and polyoxazoline, but is not limited thereto.
  • the hydrophilic material may be characterized in that it has a structure of the following Structural Formula 4 or Structural Formula 5:
  • A' is a hydrophilic material monomer (monomer)
  • J is a linker connecting between m hydrophilic material monomers or m hydrophilic material monomers and siRNA
  • m is an integer of 1 to 15
  • n is 1 to 10 means the integer of
  • the hydrophilic material monomer A' is any one compound selected from the following compounds (1) to (3), and the linker (J) is selected from the group consisting of PO 3 ⁇ , SO 3 and CO 2 ;
  • G is selected from the group consisting of CH 2 , O, S and NH;
  • the double-stranded oligonucleotide structure according to the present invention may have a structure as shown in Structural Formula 6 or 7 below.
  • Structural Formulas 6 and 7 X, R, Y and B have the same definitions as in Structural Formula 1, and A', J, m and n are the same as in Structural Formulas 4 and 5.
  • the hydrophilic material monomer (A') can be used without limitation as long as it meets the purpose of the present invention among the monomers of the nonionic hydrophilic polymer, preferably compounds (1) to compounds described in Table 1
  • the monomer represented by compound (1) can introduce various functional groups, has good in vivo compatibility and has excellent bio-compatibility, such as inducing less immune response, It has the advantage of increasing the in vivo stability of the double-stranded oligonucleotide included in the construct according to Structural Formula 6 or 7 and increasing the delivery efficiency, and thus is very suitable for the preparation of the construct according to the present invention.
  • the hydrophilic material in Structural Formulas 4 to 7 has a total molecular weight in the range of 1,000 to 2,000.
  • the amount of hexaethylene glycol spacer Since the magnetic weight is 344, the number of repetitions n is preferably 3 to 5.
  • the repeating unit of the hydrophilic group represented by (A' m -J) n or (J-A' m ) n in Structural Formulas 4 and 5, that is, the hydrophilic material block is represented by n, if necessary.
  • a different hydrophilic material monomer may be used for every hydrophilic material block, such as the hydrophilic material monomer according to compound (3) is used, and any hydrophilic material monomer selected from compounds (1) to (3) according to the compound (1) to (3) may be used in all the hydrophilic material blocks.
  • hydrophilic material monomer may be used identically.
  • the same linker may be used for each block of the hydrophilic material, or a different linker may be used for each block of the hydrophilic material as a linker for mediating the binding of the hydrophilic material monomer.
  • m the number of hydrophilic material monomers, may be the same or different between blocks of the hydrophilic material.
  • the linker (J) is -PO 3 - -, -SO 3 - And -CO 2 - is preferably selected from the group consisting of, but is not limited thereto, and it is obvious to those skilled in the art that any linker may be used as long as it meets the purpose of the present invention depending on the monomer of the hydrophilic material used. will be.
  • the hydrophobic material (B) in Structural Formulas to Structural Formulas 3' and Structural Formulas 6 and 7 serves to form nanoparticles composed of a double-stranded oligonucleotide structure through hydrophobic interactions.
  • the hydrophobic material preferably has a molecular weight of 250 to 1,000, steroid derivatives, glyceride derivatives, glycerol ether, polypropylene glycol, C12 to C50 unsaturated or saturated hydrocarbons, diacylphosphatidylcholine, fatty acids, phospholipids, lipopolyamines (lipopolyamine), lipid (lipid), any one selected from the group consisting of tocopherol (tocopherol) and tocotrienol (tocotrienol) may be used, but is not limited thereto, and any hydrophobic material that meets the purpose of the present invention It is also apparent to those of ordinary skill in the art to which the present invention pertains.
  • the steroid derivative may be selected from the group consisting of cholesterol, colistanol, cholic acid, cholesteryl formate, cotestanyl formate and colistanylamine, and the glyceride derivative is mono-, di - and tri-glyceride, etc., wherein the fatty acid of the glyceride is preferably a C 12 to C 50 unsaturated or saturated fatty acid.
  • saturated or unsaturated hydrocarbons or cholesterol are preferable in that they have the advantage that they can be easily combined in the synthesis step of the double-stranded oligonucleotide structure according to the present invention, and include C 24 hydrocarbons, particularly disulfide bonds. form is most preferable.
  • the hydrophobic material is bound to the distal end of the hydrophilic material, and may be bound to any position of the sense strand or the antisense strand.
  • the hydrophilic or hydrophobic material in Structural Formulas 1 to 3', Structural Formulas 6 and 7 according to the present invention and the double-stranded oligonucleotide are bonded by a simple covalent bond or a linker-mediated covalent bond (X or Y).
  • the linker mediating the covalent bond is not particularly limited as long as it provides a bond capable of covalently bonding with a hydrophilic material or a hydrophobic material and a double-stranded oligonucleotide at the end of the double-stranded oligonucleotide, if necessary.
  • any compound that binds to the linker to activate the double-stranded oligonucleotide and/or the hydrophilic material (or the hydrophobic material) may be used as the linker during the preparation of the double-stranded oligonucleotide construct according to the present invention.
  • the covalent bond may be either a non-degradable bond or a degradable bond.
  • the non-degradable bond includes an amide bond or a phosphorylation bond
  • the degradable bond includes a disulfide bond, an acid-decomposable bond, an ester bond, an anhydride bond, a biodegradable bond, or an enzyme-degradable bond, but is not limited thereto. .
  • the present invention also provides that, in the construct including the double-stranded oligonucleotide according to the present invention, an amine group or a polyhistidine group may be additionally introduced at the opposite end site of the hydrophilic material in the construct, which is bonded to the oligonucleotide.
  • This is for facilitating the intracellular introduction and endosomal escape of the transporter of the construct containing the double-stranded oligonucleotide according to the present invention, and has already facilitated the intracellular introduction and endosomal escape of transporters such as Quantum dot, Dendrimer, and liposome. It has been reported that the introduction of an amine group and the use of a polyhistidine group to make it work and its effects have been reported.
  • the primary amine group modified at the end or the outside of the carrier forms a conjugate by electrostatic interaction with the negatively charged gene while protonated at the pH in vivo, and has a buffering effect at low pH of endosomes after influx into the cell. It is known that the transporter can be protected from degradation of lysosomes by facilitating the escape of endosomes due to the internal tertiary amine with Vol. 23, No. 3, pp254-259),
  • histidine Since histidine, one of the non-essential amino acids, has imidazoling (pKa3 6.04) at the residue (-R), it has the effect of increasing the buffering capacity in endosomes and lysosomes, and non-viral genes including liposomes It is known that histidine modification can be used to increase the endosomal escape efficiency in non-viral gene carriers (Novel histidine-conjugated galactosylated cationic liposomes for efficient hepatocyte selective gene transfer in human hepatoma HepG2 cells. J. Controlled Release 118, pp262-270).
  • the amine group or polyhistidine group may be connected to the hydrophilic material or the hydrophilic material block through one or more linkers.
  • an amine group or a polyhistidine group is introduced into the hydrophilic material of the double-stranded oligonucleotide structure according to Structural Formula 1 of the present invention, it may have a structure as shown in Structural Formula 8.
  • J 1 and J 2 are linkers, J 1 and J 2 are independently a simple covalent bond, PO 3 - , SO 3 , CO 2 , C 2-12 alkyl, It may be selected from alkenyl and alkynyl, but is not limited thereto, and it is obvious to those skilled in the art that any linker may be used as J 1 and J 2 meeting the purpose of the present invention depending on the hydrophilic material used. .
  • J 2 is a simple covalent bond or PO 3 -
  • J 1 is preferably C 6 alkyl, but is not limited thereto.
  • J 2 is a simple covalent bond or PO 3 -
  • J 1 is preferably compound (4), but is not limited thereto.
  • hydrophilic material of the double-stranded oligonucleotide structure according to Structural Formula 8 is a hydrophilic material block according to Structural Formula 5 or 6, and an amine group or polyhistidine group is introduced thereto, it may have a structure such as Structural Formula 9 or 10 have.
  • Structural Formulas 9 and 10 X, R, Y, B, A', J, m and n are the same as defined in Structural Formula 4 or 5, and P, J 1 and J 2 are defined in Structural Formula 8 same as
  • Structural Formulas 9 and 10 the hydrophilic material is preferably bound to the 3' end of the double-stranded oligonucleotide sense strand, and in this case, Structural Formulas 8 to 10 are the following Structural Formulas 11 to 13 can have
  • X, R, Y, B, A, A' J, m, n. P, J 1 and J 2 are the same as defined in Structural Formulas 8 to 10, and 5' and 3' refer to the 5' end and 3' end of the target gene-specific double-stranded oligonucleotide sense strand.
  • amine group that can be introduced in the present invention primary to tertiary amine groups may be used, and it is particularly preferable that primary amine groups are used.
  • the introduced amine group may exist as an amine salt, for example, the salt of the primary amine group may exist in the form of NH 3 + .
  • polyhistidine group that may be introduced in the present invention preferably includes 3 to 10 histidines, particularly preferably 5 to 8, and most preferably 6 histidines. Additionally, one or more cysteines may be included in addition to histidine.
  • the target cell can be efficiently transferred to, and a relatively low concentration It can be delivered to target cells even at a dose of
  • the present invention provides a target cell internalization through a ligand (L), particularly receptor-mediated endocytosis (RME), in the structures according to Structural Formulas 1 to 3', Structural Formulas 6 and 7 It provides a double-stranded oligo RNA, a structure additionally bound to a ligand having a specific binding property with a receptor that promotes it, for example, a form in which a ligand is bound to a double-stranded oligo RNA construct according to Structural Formula 1 is It has the same structure as the following Structural Formula 14.
  • A, B, X and Y are the same as defined in Structural Formula 1, and L promotes target cell internalization through receptor-mediated end ocytosis (RME) denotes a ligand having a property of specifically binding to a receptor, and i is an integer of 1 to 5, preferably an integer of 1 to 3.
  • RME receptor-mediated end ocytosis
  • the ligand in Structural Formula 14 is preferably a target receptor-specific antibody, aptamer, or peptide having RME properties for enhancing target cell-specific cell internalization;
  • folate generally folate and folic acid are used interchangeably, and folic acid in the present invention refers to folate in a natural state or an activated state in the human body
  • N-acetyl galactosamine NAG
  • hydrophilic material A in Structural Formula 14 may be used in the form of a hydrophilic material block according to Structural Formulas 4 and 5.
  • the double-stranded oligonucleotides represented by R (or S and AS) in Structural Formulas 1 to 3', Structural Formulas 6 and 7 are Amphiregulin, RelA/p65 and SARS-CoV- Any one that specifically inhibits the expression of a gene selected from the group consisting of 2 may be used without limitation.
  • the double-stranded oligonucleotide represented by R (or S and AS) may specifically inhibit the expression of amphiregulin gene and may include a sequence targeting amphiregulin.
  • the amphiregulin target sequence may include, for example, the sequences of SEQ ID NOs: 5 and/or 6. Specifically, it may include a sense sequence of SEQ ID NO: 5 and an antisense sequence of SEQ ID NO: 6.
  • the double-stranded oligonucleotide represented by R may include a sequence targeting SARS-CoV-2.
  • the SARS-CoV-2 target sequence may include, for example, a sequence selected from the group consisting of SEQ ID NOs: 11 to 30.
  • the present invention is suitable for the prevention or treatment of various respiratory diseases, and in particular, a composition for the prevention or treatment of respiratory viral infections, pulmonary fibrosis caused by viral infections, or respiratory diseases is particularly suitable as a dosing method.
  • the respiratory virus may be characterized as COVID-19, but is not limited thereto.
  • the pulmonary fibrosis caused by the viral infection is an example of the sequelae caused by the viral infection.
  • the respiratory disease is from the group consisting of interstitial lung disease, chronic obstructive disease (COPD), pneumonia, asthma, acute and chronic bronchitis, allergic rhinitis, bronchitis, bronchiolitis, pharyngitis, tonsillitis and laryngitis. It may be characterized by being selected, but is not limited thereto
  • the double-stranded oligonucleotide structure may be characterized in that it forms self-assembled nanoparticles having a neutral charge with a size of 10-100 nm in an aqueous solution for administration.
  • the nanoparticles may be characterized in that the double-stranded oligonucleotide structure comprising the double-stranded oligonucleotides having different sequences is mixed.
  • composition of the present invention may be prepared by including one or more pharmaceutically acceptable carriers in addition to the active ingredients described above for administration.
  • a pharmaceutically acceptable carrier must be compatible with the active ingredient of the present invention, and contains saline, sterile water, Ringer's solution, buffered saline, dextrose solution, maltodextrin solution, glycerol, ethanol, and one or two or more of these components. They can be mixed and used, and other conventional additives such as antioxidants, buffers, and bacteriostats can be added as needed.
  • diluents, dispersants, surfactants, binders and lubricants may be additionally added to form an injectable formulation such as an aqueous solution, suspension, emulsion, and the like.
  • an injectable formulation such as an aqueous solution, suspension, emulsion, and the like.
  • a method commonly known in the art to which the present invention pertains may be used, and a stabilizer for freeze-drying may be added.
  • it can be preferably formulated according to each disease or component using a method disclosed in Remington's Pharmaceutical Science (Remington's Pharmaceutical Science, Mack Publishing company, Easton PA) by an appropriate method in the art.
  • Parenteral administration of the pharmaceutical composition of the present invention is preferable, and in particular, administration to the lungs through endobronchial inhalation is preferable.
  • the dosage of the composition according to the present invention varies depending on the patient's weight, age, sex, health status, diet, administration time, method, excretion rate or severity of disease, etc. can be easily determined.
  • the double-stranded oligonucleotide construct SAMiRNA prepared in the present invention has a structure as shown in the following structural formula.
  • the sense strand of the monoSAMiRNA double-stranded oligo structure is 3,4,6-triacetyl-1-hexa(ethylene glycol)-CPG (1-Hexa(Ethylene Glycol) CPG as a support, and DMT hexaethylene glycol as a hydrophilic material monomer.
  • the DNA single-stranded and DNA-polymer structure synthesized by treating 28% (v/v) ammonia in a hot water heater at 60° C. is separated from the CPG, and then protected through a deprotection reaction. The residue was removed.
  • a single strand of DNA, a DNA-polymer structure, and a DNA-polymer structure bound to a ligand are separated by high performance liquid chromatography (HPLC), and the result is a MALDI-TOF mass spectrometer (MALDI TOF-MS, SHIMADZU, Japan) was used to measure the molecular weight, and it was confirmed that the nucleotide sequence to be synthesized and the DNA-polymer structure were consistent with each other.
  • HPLC high performance liquid chromatography
  • RNA synthesis of a sequence complementary to the sense strand was performed using a linker (UnyLinkerTM) as a support, and then an antisense strand having a phosphate group (PO4) bonded to the 5' end was made.
  • linker UnyLinkerTM
  • PO4 phosphate group
  • RNA single-stranded and RNA-polymer structure synthesized by treating 28% (v/v) ammonia in a hot water heater at 60° C. is separated from the CPG, and then protected through a deprotection reaction The residue was removed.
  • RNA single-stranded and RNA-polymer structures from which protective residues have been removed were prepared by mixing N-methylpyrolidon, triethylamine and triethylaminetrihydrofluoride in an oven at 70° C. in a volume ratio. 2'TBDMS (tert-butyldimethylsilyl) was removed by treatment in a ratio of 10:3:4.
  • RNA single-stranded, RNA-polymer structures and ligand-bound RNA-polymer structures were separated from the reactants by High Performance Liquid Chromatography (HPLC), and then analyzed by MALDI-TOF mass spectrometry (MALDI TOF-MS, SHIMADZU, Japan) was used to measure the molecular weight, and it was confirmed whether the nucleotide sequence and RNA-polymer structure to be synthesized matched.
  • HPLC High Performance Liquid Chromatography
  • MALDI TOF-MS MALDI TOF-MS, SHIMADZU, Japan
  • each double-stranded oligo structure the sense strand and the antisense strand were mixed in equal amounts, put into (1X)PBS (Phosphate buffer saline, 30mg/1ml(1x)PBS), and placed in a water bath at 90° C. for 5 minutes. After the reaction, the desired SAMiRNA was prepared by slowly lowering the temperature to room temperature. The prepared double-stranded oligo structures were annealed through high performance liquid chromatography (HPLC, non denaturation). The sequence information of the SAMiRNA-AREG synthesized for efficacy evaluation is shown in Table 2 below.
  • SAMiRNA was collected using an ultrasonic method and a compressor type aerosol inhaler, respectively.
  • the captured SAMiRNA is separated by high-performance liquid chromatography to separate RNA single-stranded, RNA-polymer structures, and ligand-bound RNA-polymer structures, and the presence of the intended sequence is determined and confirmed using MALDI-TOF mass spectrometry. did.
  • the osmolarity of the collected SAMiRNA was measured with an Osmomat 3000 (gonotec, Germany) device to confirm the osmolarity, such as that of physiological saline, which does not cause a change in osmotic pressure even when directly entering the blood vessel.
  • the particle size of the captured SAMiRNA was determined using the Zetasizer NANO-ZS (Malvern, UK), a dynamic light scattering (DLS) device, and The qNano Gold (IZON, New Zealand) equipment using tunable resistive pulse detection (TRPS) according to the manufacturer's protocol. were used and analyzed accordingly.
  • the SAMiRNA nanoparticles collected using the ultrasonic aerosol inhaler were able to confirm the same concentration, molecular weight, purity, nanoparticle size, and osmotic molarity as the material before using the aerosol inhaler, whereas the In the case of SAMiRNA collected using a foodless inhaler, the nanoparticle size, molecular weight, and purity were the same, but the concentration was reduced 3.6 times to 8.3 mg/ml, and the osmolality was also significantly lower than that of physiological saline (Fig. One).
  • a human lung cancer cell line A549 (CCL-185, ATCC, US) and a human nasal epithelial cell line RPMI2650 (Korea Cell Line Bank, KR) were used to evaluate the cytotoxicity of SAMiRNA nanoparticles collected using an ultrasonic mist inhaler.
  • the A549 cell line was cultured at 37 ° C., 5% CO 2 condition using F12K medium (Gibco, US) containing 10% Fetal Bovine Serum (Hyclone, US) and 1% Penicillin-Streptomycin (Hyclone, US).
  • RPMI2650 cells were cultured at 37 ° C., 5% CO 2 condition using RPMI1640 medium (Hyclone, US) containing 10% Fetal Bovine Serum (Hyclone, US) and 1% Penicillin-Streptomycin (Hyclone, US).
  • A549 cells were dispensed in a 96-well plate (Falcon, US) at 3X10 3 cells/well, RPMI2650 cells were dispensed at 1X10 4 cells/well, and the next day, SAMiRNA collected using an ultrasonic aerosol inhaler was administered by concentration ( 0, 1, 5, 10, 20, 50 ⁇ M).
  • the WST assay kit DOGEN, KR was used to measure cytotoxicity, and the experiment was performed according to the manufacturer's protocol and analyzed.
  • Example 5 Evaluation of target gene expression inhibition ability of SAMiRNA nanoparticles collected using an ultrasonic nebulizer inhaler
  • A549 (CCL-185, ATCC, US) and RPMI2650 (Korea Cell Line Bank, KR) cell lines were used to analyze whether SAMiRNA nanoparticles collected using an ultrasonic mist inhaler effectively inhibit target gene expression.
  • the A549 cell line was cultured at 37° C., 5% CO 2 condition using F12K medium (Gibco, US) containing 10% Fetal Bovine Serum (Hyclone, US) and 1% Penicillin-Streptomycin (Hyclone, US).
  • RPMI2650 cells were cultured at 37° C., 5% CO 2 condition using RPMI1640 medium (Hyclone, US) containing 10% Fetal Bovine Serum (Hyclone, US) and 1% Penicillin-Streptomycin (Hyclone, US).
  • A549 cells were dispensed in a 12-well plate (Falcon, US) at the condition of 5X10 4 cells/well, and RPMI2650 cells were dispensed at the condition of 1.2X10 5 cells/well. 0, 0.1, 0.5, 1, 5, 10 ⁇ M).
  • RNA expression levels of human AREG and RPL13A were analyzed by qRT-PCR using GreenStar TM RT-qPCR Master Mix (Bioneer, KR) according to the manufacturer's protocol.
  • the Ct values of the two genes derived after qPCR array were calculated as 2(- Delta Delta C(T)) Method [Livak KJ, Schmittgen TD. 2001. Analys is of relative gene expression data using real-time quantitativ e PCR and the 2(-Delta Delta C(T)) Method. Methods. Dec;25(4):4 02-8], the relative amount (fold change) of AREG mRNA in the experimental group compared to the control group was calculated by relative quantitative analysis.
  • the primer sequences for each gene are as follows (Table 3).
  • Example 6 Evaluation of delivery efficacy of SAMiRNA nanoparticles administered using an ultrasonic nebulizer inhaler in an animal model
  • SAMiRNA-Cy5 nanoparticles collected by the method of Example 2 using an ultrasonic nebulizer inhaler were analyzed by the method of Example 3.
  • the SAMiRNA-Cy5 nanoparticles collected using the ultrasonic aerosol inhaler had the same fluorescence value, concentration, molecular weight, purity, nanoparticle size, and osmolality as the material before using the aerosol inhaler (Fig. 4). ).
  • a hamster was used as the experimental animal, and a hamster (5 weeks old, male) was purchased from the central laboratory animal, and the experiment was performed after a one-week acclimatization period.
  • 1 ml of SAMiRNA-Cy5 (5 mg/ml) or PBS was put into the drug chamber, and the ultrasonic aerosol inhaler was operated for 2 minutes and 30 seconds to expose to the hamster.
  • the lungs, liver, spleen, and kidneys were excised and weighed.
  • Davinch-InvivoTM imaging system Davinch-InvivoTM imaging system (Davinch-K, KR) was used.
  • Lung tissue extracted from hamsters exposed to PBS and SAMiRNA-Cy5 of Example 6-2 through an ultrasonic nebulizer inhaler was subjected to immunofluorescence. After storing for one day in 10% neutral buffered formalin (Sigma, US) for tissue fixation, dehydration was carried out by sequentially putting them in 10%, 20%, and 30% sucrose (Sigma, US) solutions. Each lung tissue sample was placed in a base mold (Thermo Scientific, US) containing OCT compound (Sakura Finetek, US), a stainless plate was placed in a container containing liquid nitrogen, and placed on top to completely freeze the OCT compound.
  • a base mold Thermo Scientific, US
  • OCT compound Sakura Finetek, US
  • Frozen tissue was stored at -70 °C, and placed at -20 °C for 30 minutes to facilitate tissue sectioning before cutting with a tissue sectioner.
  • the tissue sections were placed on a slide with a thickness of 14 ⁇ m and dried for 1 hour. After incubation for 10 minutes in 0.1% Triton-X100 (Sigma, US) solution for cell permeation, it was placed in a solution containing 5% normal goat serum (Abcam, GB) and 1% BSA (Sigma, US) for 1 hour. After blocking, the alpha-actin-2 antibody (Sigma, US) was reacted at 4 °C for one day.
  • the secondary antibody was reacted with anti-mouse-Alexa Fluor 488 (Invitrogen, US) for 1 hour, followed by washing. After washing in 1 ⁇ M DAPI (Sigma, US) solution for 10 minutes, the mounting solution (Thermo Scientific, US) was dropped and covered with a cover glass (VWR, US) to proceed with the mounting process. For fluorescence analysis of the stained tissue, it was analyzed using a spinning disk confocal (Dragonfly high-speed confocal image platform, Andor, GB).
  • mice C57BL/6 mice were used as experimental animals, and mice (6 weeks old, male) were purchased from Daehan Biolink, and the experiment was performed after a one-week acclimatization period.
  • SAMiRNA-Cy5 the material analyzed in Example 6-1 was used.
  • SAMiRNA-Cy5 2 mg or PBS in the drug chamber and operate the ultrasonic mist inhaler for 30 seconds (15 seconds exposure-15 rest-15 seconds exposure condition) and was administered (Fig. 7a). After administration, each time (0, 1, 24, 48, 96, 168 hours), the nasal cavity, lung, liver, spleen, kidney, heart, etc.
  • Davinch-InvivoTM imaging system (Davinch-K, KR) is used. Fluorescence image analysis was performed using Fluorescence image analysis was performed under the same conditions (fluorescence intensity, exposure time, etc.) for all tissues extracted by time.
  • Fluorescence quantification and PK analysis were performed using nasal and lung tissues extracted from mice exposed to PBS and SAMiRNA-Cy5 through an ultrasonic nebulizer in Example 6-4.
  • the weight of each extracted tissue was measured, the whole tissue was put in a round bottom tube (SPL, KR), 1ml of tissue lysis buffer (Bioneer, KR) was added, and the tissue was crushed using a homogenizer (IKA, DE). After incubation on ice for 15 minutes, centrifugation was performed at 14,000 rpm and 4°C for 15 minutes, and the supernatant was transferred to a 1.5 ml amber micro-centrifuge tube (Axigen, US) and stored.
  • SPL, KR tissue lysis buffer
  • IKA homogenizer
  • a standard sample for fluorescence quantitative analysis was prepared by spiking SAMiRNA-Cy5 at each concentration (0.1, 0.5, 0.25, 0.125 ug/ml) in the PBS-treated tissue lysate. After dispensing 100ul of standard and sample in a black 96 well microplate (Corning Costar, US), fluorescence intensity (Excitation Wavelength 645nm, Emission Wavelength 675nm) was measured with a microplate reader (TECAN, CH) and substituted into the calculated standard curve. The residual amount of SAMiRNA-Cy5 in the tissue was analyzed. For SAMiRNA PK analysis, the lysed tissue samples were ground once more using a QIAshredder (QIAGEN).
  • Ago2 immunoprecipitation was performed from the tissue lysate using the MagListoTM Protein G Kit (Bioneer, KR) attached with an anti-mouse AGO2 antibody (Sigma, US).
  • the obtained RISC-loaded siRNA was subjected to absolute quantitative analysis by stem-loop RT-qPCR.
  • SAMiRNA containing the SARS-CoV-2 target is delivered to the nasal cavity and lung tissue using the same method as above, and the SARS-CoV-2 target sequence is shown in Table 5 below.
  • Example 6-4 SAMiRNA distribution analysis was performed using lung tissue extracted from mice exposed to PBS and SAMiRNA-Cy5 through an ultrasonic nebulizer. After storing for one day in 10% neutral buffered formalin (Sigma, US) for tissue fixation, dehydration was carried out by sequentially putting them in 10%, 20%, and 30% sucrose (Sigma, US) solutions. After separating each lung tissue sample into left and right lobes, put it in a base mold (Thermo Scientific, US) containing OCT compound (Sakura Finetek, US), put a stainless plate in a container containing liquid nitrogen, and put it on the OCT The compound was completely frozen.
  • 10% neutral buffered formalin Sigma, US
  • OCT compound Sakura Finetek, US
  • Frozen tissue was stored at -70 °C, and placed at -20 °C for 30 minutes to facilitate tissue sectioning before cutting with a tissue sectioner.
  • the tissue sections were placed on a slide with a thickness of 8 ⁇ m and dried for 1 hour. After incubation for 10 minutes in 0.1% Triton-X100 (Sigma, US) solution for cell permeation, it was placed in a solution containing 5% normal goat serum (Abcam, GB) and 1% BSA (Sigma, US) for 1 hour. blocking was performed. After washing by reacting with 1 ⁇ M DAPI (Sigma, US) solution for 10 minutes, a mounting solution (Thermo Scientific, US) was dropped and covered with a cover glass (VWR, US) to proceed with the mounting process.
  • confocal microscope analysis was performed under the same conditions (fluorescence intensity, exposure time, etc.) for all lung tissue samples.
  • the double-stranded oligonucleotide structure according to the present invention forms self-assembled nanoparticles having a neutral charge of 90 nm in size in aqueous solution, it is an siRNA platform optimized for a nebulizer that is sprayed in the form of fine particles of 5 ⁇ m or less.
  • a nebulizer that is sprayed in the form of fine particles of 5 ⁇ m or less.
  • an ultrasonic aerosol inhaler when used, it maintains the same concentration, molecular weight, purity, nanoparticle size, and osmolality as well as the target gene suppression ability of the stock solution to be administered, which may occur during the administration process.
  • the pharmaceutical composition according to the present invention can be efficiently delivered to the nasal cavity and to the lungs (alveoli).
  • the present invention is suitable for the treatment of respiratory viral infections, pulmonary fibrosis or pneumonia caused by viral infections, or other respiratory diseases, and in particular, SARS-CoV-2, a novel respiratory virus that is currently causing explosive infections and deaths worldwide.
  • SARS-CoV-2 a novel respiratory virus that is currently causing explosive infections and deaths worldwide.

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • Genetics & Genomics (AREA)
  • Epidemiology (AREA)
  • Molecular Biology (AREA)
  • Biomedical Technology (AREA)
  • Organic Chemistry (AREA)
  • Biotechnology (AREA)
  • Zoology (AREA)
  • Wood Science & Technology (AREA)
  • General Engineering & Computer Science (AREA)
  • Virology (AREA)
  • Biochemistry (AREA)
  • Biophysics (AREA)
  • Pulmonology (AREA)
  • Microbiology (AREA)
  • Plant Pathology (AREA)
  • Physics & Mathematics (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Immunology (AREA)
  • Nanotechnology (AREA)
  • Communicable Diseases (AREA)
  • Dispersion Chemistry (AREA)
  • Otolaryngology (AREA)
  • Oncology (AREA)
  • Botany (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Medicinal Preparation (AREA)
PCT/KR2022/003245 2021-03-08 2022-03-08 Covid-19를 포함하는 호흡기 바이러스 감염증, 바이러스 감염에 의한 폐섬유증, 또는 호흡기 질환 예방 또는 치료를 위한 초음파 방식 연무식 흡입기를 이용한 이중가닥 올리고뉴클레오티드 구조체 투여용 조성물 Ceased WO2022191567A1 (ko)

Priority Applications (5)

Application Number Priority Date Filing Date Title
US18/281,251 US20250066787A1 (en) 2021-03-08 2022-03-08 Composition for Administration of Double-Stranded Oligonucleotide Structures Using Ultrasonic Nebulizer for Prevention or Treatment of Respiratory Viral Infection Including COVID-19, Pulmonary Fibrosis Caused by Viral Infection, or Respiratory Diseases
CN202280030335.0A CN117677402A (zh) 2021-03-08 2022-03-08 用于使用超声雾化器施用用于预防或治疗包括covid-19的呼吸道病毒感染、由病毒感染引起的肺纤维化或呼吸道疾病的双链寡核苷酸结构的组合物
EP22767463.7A EP4306133A4 (en) 2021-03-08 2022-03-08 Composition for administration of double-stranded oligonucleotide structures using ultrasonic nebulizer for prevention or treatment of respiratory viral infection including covid-19, pulmonary fibrosis caused by viral infection, or respiratory diseases
JP2023555188A JP2024509906A (ja) 2021-03-08 2022-03-08 Ｃｏｖｉｄ‐１９を含む呼吸器系ウイルス感染症、ウイルス感染を原因とする肺線維症、又は呼吸器疾患の予防又は治療のために超音波ネブライザを使用して二本鎖オリゴヌクレオチド構造物を投与するための組成物
CA3210813A CA3210813A1 (en) 2021-03-08 2022-03-08 Composition for administration of double-stranded oligonucleotide structures using ultrasonic nebulizer for prevention or treatment of respiratory viral infection including covid-19, pulmonary fibrosis caused by viral infection, or respiratory disease

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
KR20210029927 2021-03-08
KR10-2021-0029927 2021-03-08

Publications (1)

Publication Number Publication Date
WO2022191567A1 true WO2022191567A1 (ko) 2022-09-15

Family

ID=83227995

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/KR2022/003245 Ceased WO2022191567A1 (ko) 2021-03-08 2022-03-08 Covid-19를 포함하는 호흡기 바이러스 감염증, 바이러스 감염에 의한 폐섬유증, 또는 호흡기 질환 예방 또는 치료를 위한 초음파 방식 연무식 흡입기를 이용한 이중가닥 올리고뉴클레오티드 구조체 투여용 조성물

Country Status (7)

Country Link
US (1) US20250066787A1 (https=)
EP (1) EP4306133A4 (https=)
JP (1) JP2024509906A (https=)
KR (1) KR102570826B1 (https=)
CN (1) CN117677402A (https=)
CA (1) CA3210813A1 (https=)
WO (1) WO2022191567A1 (https=)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP4183879A4 (en) * 2020-05-22 2024-11-06 Bioneer Corporation DOUBLE-STRANDED OLIGONUCLEOTIDE AND COMPOSITION FOR TREATING COVID-19 CONTAINING SAME

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100883471B1 (ko) 2005-08-17 2009-02-16 (주)바이오니아 siRNA의 세포내 전달을 위한 siRNA와 친수성 고분자 간의접합체 및 그의 제조방법
US20090131360A1 (en) * 2007-10-02 2009-05-21 Rxi Pharmaceuticals, Corp. Tripartite RNAi constructs
KR101224828B1 (ko) 2009-05-14 2013-01-22 (주)바이오니아 ｓｉＲＮＡ 접합체 및 그 제조방법
KR20160039607A (ko) * 2013-07-05 2016-04-11 (주)바이오니아 개선된 고효율 나노입자형 올리고뉴클레오타이드 구조체 및 그의 제조방법
CN108162349A (zh) 2017-12-25 2018-06-15 江苏君华特种工程塑料制品有限公司 一种适用于齿科牙盘的peek改性材料的制备方法
KR20200064233A (ko) * 2018-11-28 2020-06-08 (주)바이오니아 안드로젠 수용체 특이적 서열을 포함하는 이중나선 올리고뉴클레오티드 구조체, 및 이를 포함하는 탈모 예방 및 발모용 조성물

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NZ585784A (en) * 2007-12-13 2012-09-28 Alnylam Pharmaceuticals Inc siRNAs for the treatment and prevention of respiratory syncytial virus (RSV) infection
WO2012024526A2 (en) * 2010-08-20 2012-02-23 Cerulean Pharma Inc. Conjugates, particles, compositions, and related methods
CN110592082A (zh) * 2013-07-05 2019-12-20 柏业公司 呼吸疾病相关基因特异性siRNA、含有siRNA的双螺旋寡RNA结构及其用途
EP3128008B1 (en) * 2014-04-04 2024-05-29 Bioneer Corporation Double-stranded oligo rna and pharmaceutical composition comprising same for preventing or treating fibrosis or respiratory diseases
KR102746742B1 (ko) * 2018-05-25 2024-12-26 (주)바이오니아 엠피레귤린 유전자 특이적 이중가닥 올리고뉴클레오티드 및 이를 포함하는 섬유증 관련 질환 및 호흡기 관련 질환 예방 및 치료용 조성물

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100883471B1 (ko) 2005-08-17 2009-02-16 (주)바이오니아 siRNA의 세포내 전달을 위한 siRNA와 친수성 고분자 간의접합체 및 그의 제조방법
US20090131360A1 (en) * 2007-10-02 2009-05-21 Rxi Pharmaceuticals, Corp. Tripartite RNAi constructs
KR101224828B1 (ko) 2009-05-14 2013-01-22 (주)바이오니아 ｓｉＲＮＡ 접합체 및 그 제조방법
KR20160039607A (ko) * 2013-07-05 2016-04-11 (주)바이오니아 개선된 고효율 나노입자형 올리고뉴클레오타이드 구조체 및 그의 제조방법
KR101862349B1 (ko) 2013-07-05 2018-05-31 (주)바이오니아 개선된 고효율 나노입자형 올리고뉴클레오타이드 구조체 및 그의 제조방법
CN108162349A (zh) 2017-12-25 2018-06-15 江苏君华特种工程塑料制品有限公司 一种适用于齿科牙盘的peek改性材料的制备方法
KR20200064233A (ko) * 2018-11-28 2020-06-08 (주)바이오니아 안드로젠 수용체 특이적 서열을 포함하는 이중나선 올리고뉴클레오티드 구조체, 및 이를 포함하는 탈모 예방 및 발모용 조성물

Non-Patent Citations (17)

* Cited by examiner, † Cited by third party
Title
"Gene Delivery and Expression Inhibition Using Polymer-Based Hybrid Material", POLYMER SCI. TECHNOL., vol. 23, no. 3, pages 254 - 259
"Novel histidine-conjugated galactosylated cationic liposomes for efficient hepatocyte selective gene transfer in human hepatoma HepG2 cells", J. CONTROLLED RELEASE, vol. 118, pages 262 - 270
AKHTAR S, J CLIN INVEST, vol. 117, no. 12, 3 December 2007 (2007-12-03), pages 3623 - 3632
BARIK, S., J MOL. MED, vol. 83, 2005, pages 764 - 773
FRANCESCO M.V., DRUG DISCOVERY TODAY, vol. 10, no. 21, 2005, pages 1451 - 1458
HASAN ULUDAG, FRONT. BIOENG. BIOTECHNOL, vol. 8, July 2020 (2020-07-01), pages 916
HASAN ULUDAG, FRONT. BIOENG. BIOTECHNOL., vol. 8, July 2020 (2020-07-01), pages 916
J. SOUTSCHEK, NATURE, vol. 11, 2004, pages 73 - 8
JESSICA, C., J POSTDOC RES, vol. 4, 2016, pages 35 - 50
JESSICA, C., J POSTDOC RES., vol. 4, 2016, pages 35 - 50
LAM JENNY KA-WING; LIANG WANLING; CHAN HAK-KIM: "Pulmonary delivery of therapeutic siRNA", ADVANCED DRUG DELIVERY REVIEWS, ELSEVIER, AMSTERDAM , NL, vol. 64, no. 1, 1 January 1900 (1900-01-01), Amsterdam , NL , pages 1 - 15, XP028908210, ISSN: 0169-409X, DOI: 10.1016/j.addr.2011.02.006 *
MA BEHLKE, MOLECULAR THERAPY, vol. 13, no. 4, 2006, pages 664 - 670
MEHTA ADITI, MICHLER THOMAS, MERKEL OLIVIA M.: "siRNA Therapeutics against Respiratory Viral Infections—What Have We Learned for Potential COVID‐19 Therapies?", ADVANCED HEALTHCARE MATERIALS, WILEY - V C H VERLAG GMBH & CO. KGAA, DE, vol. 10, no. 7, 1 April 2021 (2021-04-01), DE , pages 2001650, XP055964903, ISSN: 2192-2640, DOI: 10.1002/adhm.202001650 *
MINDAUGAS RUDOKAS, MED. PRINC. PRACT, vol. 25, March 2016 (2016-03-01), pages 60
MINDAUGAS RUDOKAS, MED. PRINC. PRACT., vol. 25, March 2016 (2016-03-01), pages 60
See also references of EP4306133A4
SH KIM, J CONTROL RELEASE, vol. 129, no. 2, 2008, pages 107 - 16

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP4183879A4 (en) * 2020-05-22 2024-11-06 Bioneer Corporation DOUBLE-STRANDED OLIGONUCLEOTIDE AND COMPOSITION FOR TREATING COVID-19 CONTAINING SAME

Also Published As

Publication number Publication date
KR20220126659A (ko) 2022-09-16
KR102570826B1 (ko) 2023-08-29
EP4306133A1 (en) 2024-01-17
CA3210813A1 (en) 2022-09-15
JP2024509906A (ja) 2024-03-05
CN117677402A (zh) 2024-03-08
EP4306133A4 (en) 2025-04-30
US20250066787A1 (en) 2025-02-27

Similar Documents

Publication Publication Date Title
WO2021145595A1 (ko) 생체 내 약물 전달을 위한 지질 나노입자 및 이의 용도
RU2175337C2 (ru) Полинуклеотидные композиции
WO2013109057A1 (ko) 자성나노입자-samirna 복합체 및 그 제조방법
JP5401323B2 (ja) オリゴヌクレオチド、タンパク、および／またはペプチド・ポリマー接合体
WO2019156365A1 (ko) 엔도좀 탈출능을 갖는 펩티드 핵산 복합체 및 이의 용도
JP2021533800A (ja) 核酸、当該核酸を含む薬物組成物及び複合体ならびにその使用
WO2013103249A1 (ko) 고효율 나노입자형 이중나선 올리고 rna 구조체 및 그의 제조방법
JP7154403B2 (ja) アンフィレグリン遺伝子特異的二重鎖オリゴヌクレオチド及びこれを含む線維症関連疾患及び呼吸器関連疾患の予防及び治療用組成物
WO2018030789A1 (ko) 세포투과성이 향상된 펩티드 핵산 복합체 및 이를 포함하는 약학적 조성물
WO2013089522A1 (ko) 신규한 올리고뉴클레오티드 접합체 및 그 용도
WO2022139528A1 (ko) 만노스를 포함하는 지질 나노입자 또는 이의 용도
WO2014169264A2 (en) Nanoparticle mediated delivery of sirna
WO2020111614A1 (ko) 안드로젠 수용체 특이적 서열을 포함하는 이중나선 올리고뉴클레오티드 구조체, 및 이를 포함하는 탈모 예방 및 발모용 조성물
WO2022191567A1 (ko) Covid-19를 포함하는 호흡기 바이러스 감염증, 바이러스 감염에 의한 폐섬유증, 또는 호흡기 질환 예방 또는 치료를 위한 초음파 방식 연무식 흡입기를 이용한 이중가닥 올리고뉴클레오티드 구조체 투여용 조성물
CN116157521A (zh) 双链寡核苷酸和用于治疗covid-19的含有其的组合物
WO2020149644A1 (ko) Dkk1 유전자를 표적으로 하는 이중나선 올리고뉴클레오티드, 이를 포함하는 구조체 및 이를 포함하는 탈모 예방 또는 발모용 조성물
US20260015614A1 (en) BRANCHED LIPID CONJUGATES OF siRNA FOR SPECIFIC TISSUE DELIVERY
WO2015002512A1 (ko) 뎅기 바이러스 특이적 siRNA, 그러한 siRNA를 포함하는 이중나선 올리고 RNA 구조체 및 이를 포함하는 뎅기 바이러스 증식 억제용 조성물
WO2021141368A2 (ko) 세포 투과성 핵산 복합체를 유효성분으로 함유하는 황반변성의 예방 또는 치료용 조성물
WO2021101113A1 (ko) Ctgf 유전자 특이적 이중가닥 올리고뉴클레오티드 및 이를 포함하는 섬유증 관련 질환 및 호흡기 관련 질환 예방 및 치료용 조성물
WO2016068617A1 (ko) 폴리올계 삼투압적 폴리디자일리톨 폴리머 유전자 전달체 및 이의 용도
WO2021075880A1 (ko) 혈뇌장벽 투과능을 가지는 펩티드 핵산 복합체 및 이를 포함하는 조성물
WO2022045763A1 (ko) 세포 투과성 핵산 복합체를 유효성분으로 함유하는 류마티스 관절염의 예방 또는 치료용 조성물
HK40105394A (en) Composition for administration of double-stranded oligonucleotide structures using ultrasonic nebulizer for prevention or treatment of respiratory viral infection including covid-19, pulmonary fibrosis caused by viral infection, or respiratory diseases
WO2012133997A1 (ko) 폴리소르비톨계 삼투압적 활성 전달체 및 이를 이용한 유전자 치료

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 22767463

Country of ref document: EP

Kind code of ref document: A1

WWE Wipo information: entry into national phase

Ref document number: 3210813

Country of ref document: CA

WWE Wipo information: entry into national phase

Ref document number: 2023555188

Country of ref document: JP

REG Reference to national code

Ref country code: BR

Ref legal event code: B01A

Ref document number: 112023018186

Country of ref document: BR

WWE Wipo information: entry into national phase

Ref document number: 202347066424

Country of ref document: IN

WWE Wipo information: entry into national phase

Ref document number: 2022767463

Country of ref document: EP

NENP Non-entry into the national phase

Ref country code: DE

ENP Entry into the national phase

Ref document number: 2022767463

Country of ref document: EP

Effective date: 20231009

WWE Wipo information: entry into national phase

Ref document number: 202280030335.0

Country of ref document: CN

ENP Entry into the national phase

Ref document number: 112023018186

Country of ref document: BR

Kind code of ref document: A2

Effective date: 20230907

WWE Wipo information: entry into national phase

Ref document number: 523450603

Country of ref document: SA

WWE Wipo information: entry into national phase

Ref document number: 523450603

Country of ref document: SA

WWP Wipo information: published in national office

Ref document number: 18281251

Country of ref document: US

WWE Wipo information: entry into national phase

Ref document number: 523450603

Country of ref document: SA