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  1. AU=Midoux Patrick AU=Midoux Patrick
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  1. Artikel ; Online: Reversible stabilization of DNA/PEI complexes by reducible click-linkage between DNA and polymer. A new polyplex concept for lowering polymer quantity.

    Maze, Delphine / Pichon, Chantal / Midoux, Patrick

    Gene therapy

    2023  Band 30, Heft 12, Seite(n) 783–791

    Abstract: Nonviral transfection of mammalian cells can be performed with electrostatic complexes (polyplexes) between a plasmid DNA (pDNA) encoding a foreign gene and a cationic polymer. However, an excess of the cationic polymer is required for pDNA condensation ... ...

    Abstract Nonviral transfection of mammalian cells can be performed with electrostatic complexes (polyplexes) between a plasmid DNA (pDNA) encoding a foreign gene and a cationic polymer. However, an excess of the cationic polymer is required for pDNA condensation and polyplexes formation, which generate in vivo toxicity. Here, we present a new concept of polyplexes preparation aiming to reduce the polymer quantity. pDNA was functionalized with 3,6,9-trioxaundecan-1- {4 - [(2-chloroethyl) ethylamino)] - benzylamino}, 11-azide, and polyethyleneimine (lPEI) with reducible dibenzocyclooctyl (SS-DBCO) groups allowing azide-alkyne cycloaddition between pDNA and lPEI after condensation. The size of polyplexes with DBCO-SS-lPEI was smaller than with lPEI due to a stronger DNA condensation thanks to linkages between polymer and pDNA preventing dissociation until disulfide bridges reduction. In vitro transfection showed that the amount of DBCO-SS-lPEI leading to the most efficient polyplexes was three times lower than lPEI. As expected, toxicity in mice was significantly reduced upon intravenous injection of DBCO-SS-lPEI polyplexes at doses where the lPEI polyplexes killed mice. This is probably due to the high stability of the DBCO-SS-lPEI polyplexes which prevented their aggregation in the pulmonary capillaries. Overall, this new concept of polyplexes with DBCO-SS-lPEI offering the possibility of administering higher doses of polyplexes than lPEI and their ability to pass the pulmonary barrier could be favorably exploited for transfection of distant organs or tissues, such as tumors.
    Mesh-Begriff(e) Animals ; Mice ; Polymers ; Azides ; DNA/genetics ; Plasmids/genetics ; Transfection ; Polyethyleneimine ; Mammals/genetics
    Chemische Substanzen Polymers ; Azides ; DNA (9007-49-2) ; Polyethyleneimine (9002-98-6)
    Sprache Englisch
    Erscheinungsdatum 2023-02-09
    Erscheinungsland England
    Dokumenttyp Journal Article
    ZDB-ID 1191036-7
    ISSN 1476-5462 ; 0969-7128
    ISSN (online) 1476-5462
    ISSN 0969-7128
    DOI 10.1038/s41434-023-00386-1
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  2. Artikel ; Online: CFTR and dystrophin encoding plasmids carrying both luciferase reporter gene, nuclear import specific sequences and triple helix sites.

    Maze, Delphine / Girardin, Caroline / Benz, Nathalie / Montier, Tristan / Pichon, Chantal / Midoux, Patrick

    Plasmid

    2023  Band 127, Seite(n) 102686

    Abstract: Duchenne Muscular Dystrophy and Cystic Fibrosis are two major monogenetic diseases which could be treated by non-viral gene therapy. For this purpose, plasmid DNA (pDNA) coding for the functional genes requires its equipment with signal molecules ... ...

    Abstract Duchenne Muscular Dystrophy and Cystic Fibrosis are two major monogenetic diseases which could be treated by non-viral gene therapy. For this purpose, plasmid DNA (pDNA) coding for the functional genes requires its equipment with signal molecules favouring its intracellular trafficking and delivery in the nucleus of the target cells. Here, two novel constructions of large pDNAs encoding the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) and full-length dystrophin (DYS) genes are reported. The expression of CFTR and DYS genes are driven respectively by the hCEF1 airway epithelial cells and spc5-12 muscle cells specific promoter. Those pDNAs encode also the luciferase reporter gene driven by the CMV promoter to evaluate gene delivery in animals by bioluminescence. In addition, oligopurine • oligopyrimidine sequences are inserted to enable equipment of pDNAs with peptides conjugated with a triple helix forming oligonucleotide (TFO). Furthermore, specific κB sequences are also inserted to promote their NFκB-mediated nuclear import. pDNA constructions are reported; transfection efficiency, tissue specific expression of CFTR and dystrophin in target cells, and triple helix formation are demonstrated. These plasmids are tools of interest to develop non-viral gene therapy of Cystic Fibrosis and Duchenne Muscular Dystrophy.
    Mesh-Begriff(e) Animals ; Active Transport, Cell Nucleus ; Cystic Fibrosis/genetics ; Cystic Fibrosis/therapy ; Cystic Fibrosis/metabolism ; Cystic Fibrosis Transmembrane Conductance Regulator/genetics ; Cystic Fibrosis Transmembrane Conductance Regulator/metabolism ; DNA ; Dystrophin/genetics ; Dystrophin/metabolism ; Genes, Reporter ; Muscular Dystrophy, Duchenne/genetics ; Muscular Dystrophy, Duchenne/therapy ; Plasmids/genetics
    Chemische Substanzen Cystic Fibrosis Transmembrane Conductance Regulator (126880-72-6) ; DNA (9007-49-2) ; Dystrophin
    Sprache Englisch
    Erscheinungsdatum 2023-05-18
    Erscheinungsland United States
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 282384-6
    ISSN 1095-9890 ; 0147-619X
    ISSN (online) 1095-9890
    ISSN 0147-619X
    DOI 10.1016/j.plasmid.2023.102686
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  3. Artikel: mRNA Lipoplexes with Cationic and Ionizable α-Amino-lipophosphonates: Membrane Fusion, Transfection, mRNA Translation and Conformation.

    Akhter, Sohail / Berchel, Mathieu / Jaffrès, Paul-Alain / Midoux, Patrick / Pichon, Chantal

    Pharmaceutics

    2022  Band 14, Heft 3

    Abstract: Cationic liposomes are attractive carriers for mRNA delivery. Here, mRNA lipoplexes (LX) were prepared with the cationic lipids α-aminolipophosphonate ( ...

    Abstract Cationic liposomes are attractive carriers for mRNA delivery. Here, mRNA lipoplexes (LX) were prepared with the cationic lipids α-aminolipophosphonate (
    Sprache Englisch
    Erscheinungsdatum 2022-03-07
    Erscheinungsland Switzerland
    Dokumenttyp Journal Article
    ZDB-ID 2527217-2
    ISSN 1999-4923
    ISSN 1999-4923
    DOI 10.3390/pharmaceutics14030581
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  4. Artikel: DNA minicircles as novel STAT3 decoy oligodeoxynucleotides endowed with anticancer activity in triple-negative breast cancer.

    Casas, Geoffrey / Perche, Federico / Midoux, Patrick / Pichon, Chantal / Malinge, Jean-Marc

    Molecular therapy. Nucleic acids

    2022  Band 29, Seite(n) 162–175

    Abstract: Decoy technology is a versatile and specific DNA oligonucleotide-based targeting strategy of pathogenic transcription factors (TFs). Chemical modifications of linear decoy oligonucleotides have been made to decrease nuclease sensitivity because of the ... ...

    Abstract Decoy technology is a versatile and specific DNA oligonucleotide-based targeting strategy of pathogenic transcription factors (TFs). Chemical modifications of linear decoy oligonucleotides have been made to decrease nuclease sensitivity because of the presence of free ends but at the cost of new limitations that affect their use as therapeutic drugs. Although a short DNA minicircle is a phosphodiester nucleic acid without free ends, its potential therapeutic activity as a TF decoy oligonucleotide has not yet been investigated. Here we describe the
    Sprache Englisch
    Erscheinungsdatum 2022-06-22
    Erscheinungsland United States
    Dokumenttyp Journal Article
    ZDB-ID 2662631-7
    ISSN 2162-2531
    ISSN 2162-2531
    DOI 10.1016/j.omtn.2022.06.012
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  5. Artikel: Intracellular Routing and Recognition of Lipid-Based mRNA Nanoparticles.

    Delehedde, Christophe / Even, Luc / Midoux, Patrick / Pichon, Chantal / Perche, Federico

    Pharmaceutics

    2021  Band 13, Heft 7

    Abstract: Messenger RNA (mRNA) is being extensively used in gene therapy and vaccination due to its safety over DNA, in the following ways: its lack of integration risk, cytoplasmic expression, and transient expression compatible with fine regulations. However, ... ...

    Abstract Messenger RNA (mRNA) is being extensively used in gene therapy and vaccination due to its safety over DNA, in the following ways: its lack of integration risk, cytoplasmic expression, and transient expression compatible with fine regulations. However, clinical applications of mRNA are limited by its fast degradation by nucleases, and the activation of detrimental immune responses. Advances in mRNA applications, with the recent approval of COVID-19 vaccines, were fueled by optimization of the mRNA sequence and the development of mRNA delivery systems. Although delivery systems and mRNA sequence optimization have been abundantly reviewed, understanding of the intracellular processing of mRNA is mandatory to improve its applications. We will focus on lipid nanoparticles (LNPs) as they are the most advanced nanocarriers for the delivery of mRNA. Here, we will review how mRNA therapeutic potency can be affected by its interactions with cellular proteins and intracellular distribution.
    Sprache Englisch
    Erscheinungsdatum 2021-06-24
    Erscheinungsland Switzerland
    Dokumenttyp Journal Article ; Review
    ZDB-ID 2527217-2
    ISSN 1999-4923
    ISSN 1999-4923
    DOI 10.3390/pharmaceutics13070945
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  6. Artikel ; Online: CEBA: A new heterobifunctional reagent for plasmid DNA functionalization by click chemistry.

    Gao, Haifei / Gonçalves, Cristine / Maze, Delphine / Pichon, Chantal / Midoux, Patrick

    International journal of pharmaceutics

    2021  Band 601, Seite(n) 120566

    Abstract: Here, we report the synthesis of 3,6,9-trioxaundecan-1-{4-[(2-Chloroethyl)Ethylamino)]-Benzylamino},11-Azide (CEBA). CEBA alkylates the N7 of guanine of DNA thanks its chloroethyl group and can be coupled by a strain-promoted azide-alkyne cycloaddition ... ...

    Abstract Here, we report the synthesis of 3,6,9-trioxaundecan-1-{4-[(2-Chloroethyl)Ethylamino)]-Benzylamino},11-Azide (CEBA). CEBA alkylates the N7 of guanine of DNA thanks its chloroethyl group and can be coupled by a strain-promoted azide-alkyne cycloaddition to an alkynylated molecule. The optimization of the alkylation level of pDNA reveals that the expression of the encoded gene is preserved when it is randomly modified with at most 1 CEBA molecule per 150 bp. We show that the azido group of CEBA allows the linkage via click chemistry of CEBA-pDNA with a fluorophore or a peptide containing a dibenzocyclooctyne (DBCO) function. This new heterobifunctional reagent opens new ways to equip pDNA easily with signal molecules including peptides and nucleic acids without side products providing great interest for non-viral gene therapy.
    Mesh-Begriff(e) Alkynes ; Azides ; Click Chemistry ; DNA ; Plasmids/genetics
    Chemische Substanzen Alkynes ; Azides ; DNA (9007-49-2)
    Sprache Englisch
    Erscheinungsdatum 2021-04-02
    Erscheinungsland Netherlands
    Dokumenttyp Journal Article
    ZDB-ID 428962-6
    ISSN 1873-3476 ; 0378-5173
    ISSN (online) 1873-3476
    ISSN 0378-5173
    DOI 10.1016/j.ijpharm.2021.120566
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  7. Artikel ; Online: CFTR and dystrophin encoding plasmids carrying both luciferase reporter gene, nuclear import specific sequences and triple helix sites

    Maze, Delphine / Girardin, Caroline / Benz, Nathalie / Montier, Tristan / Pichon, Chantal / Midoux, Patrick

    Plasmid. 2023 July, v. 127 p.102686-

    2023  

    Abstract: Duchenne Muscular Dystrophy and Cystic Fibrosis are two major monogenetic diseases which could be treated by non-viral gene therapy. For this purpose, plasmid DNA (pDNA) coding for the functional genes requires its equipment with signal molecules ... ...

    Abstract Duchenne Muscular Dystrophy and Cystic Fibrosis are two major monogenetic diseases which could be treated by non-viral gene therapy. For this purpose, plasmid DNA (pDNA) coding for the functional genes requires its equipment with signal molecules favouring its intracellular trafficking and delivery in the nucleus of the target cells. Here, two novel constructions of large pDNAs encoding the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) and full-length dystrophin (DYS) genes are reported. The expression of CFTR and DYS genes are driven respectively by the hCEF1 airway epithelial cells and spc5–12 muscle cells specific promoter. Those pDNAs encode also the luciferase reporter gene driven by the CMV promoter to evaluate gene delivery in animals by bioluminescence. In addition, oligopurine • oligopyrimidine sequences are inserted to enable equipment of pDNAs with peptides conjugated with a triple helix forming oligonucleotide (TFO). Furthermore, specific κB sequences are also inserted to promote their NFκB-mediated nuclear import. pDNA constructions are reported; transfection efficiency, tissue specific expression of CFTR and dystrophin in target cells, and triple helix formation are demonstrated. These plasmids are tools of interest to develop non-viral gene therapy of Cystic Fibrosis and Duchenne Muscular Dystrophy.
    Schlagwörter bioluminescence ; cystic fibrosis ; cystic fibrosis transmembrane conductance regulator ; dystrophin ; epithelium ; equipment ; gene therapy ; luciferase ; muscles ; muscular dystrophy ; oligonucleotides ; peptides ; physiological transport ; plasmids ; reporter genes ; transfection ; CFTR ; DNA constructs ; Triple helix ; Tissue specific promoter
    Sprache Englisch
    Erscheinungsverlauf 2023-07
    Erscheinungsort Elsevier Inc.
    Dokumenttyp Artikel ; Online
    ZDB-ID 282384-6
    ISSN 1095-9890 ; 0147-619X
    ISSN (online) 1095-9890
    ISSN 0147-619X
    DOI 10.1016/j.plasmid.2023.102686
    Datenquelle NAL Katalog (AGRICOLA)

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  8. Artikel ; Online: Impact of net charge, targeting ligand amount and mRNA modification on the uptake, intracellular routing and the transfection efficiency of mRNA lipopolyplexes in dendritic cells.

    Delehedde, Christophe / Ciganek, Ivan / Rameix, Nathalie / Laroui, Nabila / Gonçalves, Cristine / Even, Luc / Midoux, Patrick / Pichon, Chantal

    International journal of pharmaceutics

    2023  Band 647, Seite(n) 123531

    Abstract: Targeting mRNA formulations to achieve cell specificity is one of the challenges that must be tackled to mettle their therapeutic potential. Here, lipopolyplexes (LPR) bearing tri-mannose-lipid (TM) are used to target mannose receptor on dendritic cells. ...

    Abstract Targeting mRNA formulations to achieve cell specificity is one of the challenges that must be tackled to mettle their therapeutic potential. Here, lipopolyplexes (LPR) bearing tri-mannose-lipid (TM) are used to target mannose receptor on dendritic cells. We investigated the impact of the net charge and percentage of TM units on the binding, uptake, transfection efficiency (TE) and RNA sensors activation. Binding and uptake capacities of naked and targeted LPR increase with the percent of cationic lipid, but the latter are 2-fold more up taken by the cells. Cationic LPR bearing 5 % and 10 % TM were localized in acidic compartments in contrast to naked LPR and 2.5 % TM-LPR. The drawback is the dramatic decrease of TE as the number of TM-units increases. Cationic LPR bearing 5 % and 10 % TM strongly induced NF-κB and PKR phosphorylation at 6 h. Conversely, mTOR is less activated in line with their low TE. Those side effects are overcome by using 5-methoxyuridine mRNA resulting in an improved TE due to non-phosphorylation of NF-κB and PKR and mTOR activation. Our results point out that targeting DC via mannose receptor triggers a higher uptake of cationic LPRs and fast routing to acidic compartments, and that efficient TE requires low number of TM units use or modified mRNA to escape RNA sensors activation to enhance the translation.
    Mesh-Begriff(e) Ligands ; RNA, Messenger/genetics ; RNA, Messenger/metabolism ; Mannose Receptor ; NF-kappa B/genetics ; Transfection ; Lipids ; TOR Serine-Threonine Kinases/metabolism ; Dendritic Cells/metabolism ; Liposomes
    Chemische Substanzen Ligands ; RNA, Messenger ; Mannose Receptor ; NF-kappa B ; Lipids ; TOR Serine-Threonine Kinases (EC 2.7.11.1) ; Liposomes
    Sprache Englisch
    Erscheinungsdatum 2023-10-18
    Erscheinungsland Netherlands
    Dokumenttyp Journal Article
    ZDB-ID 428962-6
    ISSN 1873-3476 ; 0378-5173
    ISSN (online) 1873-3476
    ISSN 0378-5173
    DOI 10.1016/j.ijpharm.2023.123531
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  9. Artikel ; Online: Neutral Block Copolymer Assisted Gene Delivery using Hydrodynamic Limb Vein Injection.

    Guen, Yann Le / Delecourt, Gwendoline / Gall, Tony Le / Du, Haiqin / Illy, Nicolas / Huin, Cécile / Bennevault, Véronique / Midoux, Patrick / Montier, Tristan / Guégan, Philippe

    Macromolecular bioscience

    2024  , Seite(n) e2300568

    Abstract: Three different amphiphilic block copolymer families are synthesized to investigate new opportunities to enhance gene delivery via Hydrodynamic Limb Vein (HLV) injections. First a polyoxazoline-based family containing mostly one poly(2-methyl-2-oxazoline) ...

    Abstract Three different amphiphilic block copolymer families are synthesized to investigate new opportunities to enhance gene delivery via Hydrodynamic Limb Vein (HLV) injections. First a polyoxazoline-based family containing mostly one poly(2-methyl-2-oxazoline) (PMeOx) block and a second block POx with an ethyl (EtOx), isopropyl (iPrOx) or phenyl substituent (PhOx) is synthesized. Then an ABC poly(2-ethyl-2-oxazoline)-b-poly(2-n-propyl-2-oxazoline)-b-poly(2-methyl-2-oxazoline) triblock copolymer is synthesized, with a thermosensitive middle block. Finally, polyglycidol-b-polybutylenoxide-b-polyglycidol copolymers with various molar masses and amphiphilic balance are produced. The simple architecture of neutral amphiphilic triblock copolymer is not sufficient to obtain enhanced in vivo gene transfection. Double or triple amphiphilic neutral block copolymers are improving the in vivo transfection performances through HLV administration as far as a block having an lower critical solution temperature is incorporated in the vector. The molar mass of the copolymer does not seem to affect the vector performances in a significant manner.
    Sprache Englisch
    Erscheinungsdatum 2024-03-21
    Erscheinungsland Germany
    Dokumenttyp Journal Article
    ZDB-ID 2039130-4
    ISSN 1616-5195 ; 1616-5187
    ISSN (online) 1616-5195
    ISSN 1616-5187
    DOI 10.1002/mabi.202300568
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  10. Artikel ; Online: Selective attachment of a microtubule interacting peptide to plasmid DNA via a triplex forming oligonucleotide for transfection improvement.

    Girardin, Caroline / Maze, Delphine / Gonçalves, Cristine / Le Guen, Yann Thierry / Pluchon, Kevin / Pichon, Chantal / Montier, Tristan / Midoux, Patrick

    Gene therapy

    2022  Band 30, Heft 3-4, Seite(n) 271–277

    Abstract: In nonviral gene therapy approaches, the linkage of signal molecules to plasmid DNA (pDNA) is of interest for guiding its delivery to the nucleus. Here, we report its linkage to a peptide ( ... ...

    Abstract In nonviral gene therapy approaches, the linkage of signal molecules to plasmid DNA (pDNA) is of interest for guiding its delivery to the nucleus. Here, we report its linkage to a peptide (P
    Mesh-Begriff(e) Mice ; Animals ; Oligonucleotides/genetics ; Oligonucleotides/chemistry ; DNA/genetics ; Plasmids/genetics ; Transfection ; Microtubules/metabolism ; Peptides/genetics
    Chemische Substanzen Oligonucleotides ; DNA (9007-49-2) ; Peptides
    Sprache Englisch
    Erscheinungsdatum 2022-07-07
    Erscheinungsland England
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1191036-7
    ISSN 1476-5462 ; 0969-7128
    ISSN (online) 1476-5462
    ISSN 0969-7128
    DOI 10.1038/s41434-022-00354-1
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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