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We are analyzing https://www.nature.com/articles/nbt1402.

Title:
A combinatorial library of lipid-like materials for delivery of RNAi therapeutics | Nature Biotechnology
Description:
The safe and effective delivery of RNA interference (RNAi) therapeutics remains an important challenge for clinical development. The diversity of current delivery materials remains limited, in part because of their slow, multi-step syntheses. Here we describe a new class of lipid-like delivery molecules, termed lipidoids, as delivery agents for RNAi therapeutics. Chemical methods were developed to allow the rapid synthesis of a large library of over 1,200 structurally diverse lipidoids. From this library, we identified lipidoids that facilitate high levels of specific silencing of endogenous gene transcripts when formulated with either double-stranded small interfering RNA (siRNA) or single-stranded antisense 2′-O-methyl (2′-OMe) oligoribonucleotides targeting microRNA (miRNA). The safety and efficacy of lipidoids were evaluated in three animal models: mice, rats and nonhuman primates. The studies reported here suggest that these materials may have broad utility for both local and systemic delivery of RNA therapeutics.
Website Age:
30 years and 10 months (reg. 1994-08-11).

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🌆 Monumental Traffic: 20M - 50M visitors per month


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$531,700 per month
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Keywords {🔍}

article, google, scholar, cas, nature, delivery, therapeutics, gene, sirna, rna, access, vivo, nat, usa, content, systemic, massachusetts, cookies, library, materials, lipidoids, silencing, interfering, mrna, cationic, privacy, rnai, akinc, robert, john, interference, small, sirnas, biotechnol, mol, ther, research, data, information, combinatorial, lipidlike, zumbuehl, constien, anderson, synthesis, mice, nucleic, degradable, res, growth,

Topics {✒️}

nature portfolio permissions reprints jürgen soutschek & hans-peter vornlocher privacy policy integrative cancer research nanoparticle research inhibits tumor growth single-stranded antisense 2′-o-methyl advertising social media clinical development ethanol-destabilized cationic liposomes nature 430 nature 432 nature 438 nature 441 nature 439 nature chitosan/sirna nanoparticle system bone marrow-derived macrophages amidine-incorporated degradable lipids rna-based medicines john rnai-mediated gene-targeting author correspondence vivo anti-hbv activity personal data cell type-specific delivery springerlink instant access data protection permissions small interfering rnas rnai-mediated gene silencing oligoribonucleotides targeting microrna antonin de fougerolles short interfering rna sirna-based therapeutics privacy aptamer-sirna chimeras robert langer & daniel nanoparticles identifies cationic influenza virus production nasally administered sirna dicer substrate sirna cell-surface receptors egfp reporter mouse monitor cre recombination encapsulated nucleic acids biomembrane-derived nanoplexes explore content subscription content

Schema {🗺️}

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         description:The safe and effective delivery of RNA interference (RNAi) therapeutics remains an important challenge for clinical development. The diversity of current delivery materials remains limited, in part because of their slow, multi-step syntheses. Here we describe a new class of lipid-like delivery molecules, termed lipidoids, as delivery agents for RNAi therapeutics. Chemical methods were developed to allow the rapid synthesis of a large library of over 1,200 structurally diverse lipidoids. From this library, we identified lipidoids that facilitate high levels of specific silencing of endogenous gene transcripts when formulated with either double-stranded small interfering RNA (siRNA) or single-stranded antisense 2′-O-methyl (2′-OMe) oligoribonucleotides targeting microRNA (miRNA). The safety and efficacy of lipidoids were evaluated in three animal models: mice, rats and nonhuman primates. The studies reported here suggest that these materials may have broad utility for both local and systemic delivery of RNA therapeutics.
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      headline:A combinatorial library of lipid-like materials for delivery of RNAi therapeutics
      description:The safe and effective delivery of RNA interference (RNAi) therapeutics remains an important challenge for clinical development. The diversity of current delivery materials remains limited, in part because of their slow, multi-step syntheses. Here we describe a new class of lipid-like delivery molecules, termed lipidoids, as delivery agents for RNAi therapeutics. Chemical methods were developed to allow the rapid synthesis of a large library of over 1,200 structurally diverse lipidoids. From this library, we identified lipidoids that facilitate high levels of specific silencing of endogenous gene transcripts when formulated with either double-stranded small interfering RNA (siRNA) or single-stranded antisense 2′-O-methyl (2′-OMe) oligoribonucleotides targeting microRNA (miRNA). The safety and efficacy of lipidoids were evaluated in three animal models: mice, rats and nonhuman primates. The studies reported here suggest that these materials may have broad utility for both local and systemic delivery of RNA therapeutics.
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                  address:
                     name:Present addresses: Roche Kulmbach GmbH, Fritz-Hornschuch-Str. 9, 95326 Kulmbach, Germany (R.C., M.J. and H.-P.V.) and Regulus Therapeutics, 1896 Rutherford Road, Carlsbad, California 92008, USA (J.S.).,
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         1546-1696
         1087-0156
      volumeNumber:26
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            name:Alnylam Europe AG
            address:
               name:Alnylam Europe AG, Kulmbach, Germany
               type:PostalAddress
            type:Organization
            name:Present addresses: Roche Kulmbach GmbH, Fritz-Hornschuch-Str. 9, 95326 Kulmbach, Germany (R.C., M.J. and H.-P.V.) and Regulus Therapeutics, 1896 Rutherford Road, Carlsbad, California 92008, USA (J.S.).
            address:
               name:Present addresses: Roche Kulmbach GmbH, Fritz-Hornschuch-Str. 9, 95326 Kulmbach, Germany (R.C., M.J. and H.-P.V.) and Regulus Therapeutics, 1896 Rutherford Road, Carlsbad, California 92008, USA (J.S.).,
               type:PostalAddress
            type:Organization
      name:Ivanka Toudjarska
      affiliation:
            name:Alnylam Pharmaceuticals, Inc.
            address:
               name:Alnylam Pharmaceuticals, Inc., Cambridge, USA
               type:PostalAddress
            type:Organization
      name:Hans-Peter Vornlocher
      affiliation:
            name:Alnylam Europe AG
            address:
               name:Alnylam Europe AG, Kulmbach, Germany
               type:PostalAddress
            type:Organization
            name:Present addresses: Roche Kulmbach GmbH, Fritz-Hornschuch-Str. 9, 95326 Kulmbach, Germany (R.C., M.J. and H.-P.V.) and Regulus Therapeutics, 1896 Rutherford Road, Carlsbad, California 92008, USA (J.S.).
            address:
               name:Present addresses: Roche Kulmbach GmbH, Fritz-Hornschuch-Str. 9, 95326 Kulmbach, Germany (R.C., M.J. and H.-P.V.) and Regulus Therapeutics, 1896 Rutherford Road, Carlsbad, California 92008, USA (J.S.).,
               type:PostalAddress
            type:Organization
      name:Tracy S Zimmermann
      affiliation:
            name:Alnylam Pharmaceuticals, Inc.
            address:
               name:Alnylam Pharmaceuticals, Inc., Cambridge, USA
               type:PostalAddress
            type:Organization
      name:Robert Langer
      affiliation:
            name:David H. Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology
            address:
               name:David H. Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, USA
               type:PostalAddress
            type:Organization
            name:Massachusetts Institute of Technology
            address:
               name:Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, USA
               type:PostalAddress
            type:Organization
            name:Massachusetts Institute of Technology
            address:
               name:Department of Chemistry, Massachusetts Institute of Technology, Cambridge, USA
               type:PostalAddress
            type:Organization
      name:Daniel G Anderson
      affiliation:
            name:David H. Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology
            address:
               name:David H. Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, USA
               type:PostalAddress
            type:Organization
      email:[email protected]
PostalAddress:
      name:David H. Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, USA
      name:Alnylam Pharmaceuticals, Inc., Cambridge, USA
      name:Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, USA
      name:Department of Organic Chemistry, University of Geneva, Switzerland
      name:Department of Chemistry, Massachusetts Institute of Technology, Cambridge, USA
      name:Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, USA
      name:Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, USA
      name:Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, USA
      name:Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, USA
      name:Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, USA
      name:Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, USA
      name:Alnylam Pharmaceuticals, Inc., Cambridge, USA
      name:Alnylam Pharmaceuticals, Inc., Cambridge, USA
      name:Alnylam Pharmaceuticals, Inc., Cambridge, USA
      name:Alnylam Europe AG, Kulmbach, Germany
      name:Present addresses: Roche Kulmbach GmbH, Fritz-Hornschuch-Str. 9, 95326 Kulmbach, Germany (R.C., M.J. and H.-P.V.) and Regulus Therapeutics, 1896 Rutherford Road, Carlsbad, California 92008, USA (J.S.).,
      name:Alnylam Pharmaceuticals, Inc., Cambridge, USA
      name:Alnylam Pharmaceuticals, Inc., Cambridge, USA
      name:Alnylam Pharmaceuticals, Inc., Cambridge, USA
      name:Alnylam Pharmaceuticals, Inc., Cambridge, USA
      name:Alnylam Europe AG, Kulmbach, Germany
      name:Present addresses: Roche Kulmbach GmbH, Fritz-Hornschuch-Str. 9, 95326 Kulmbach, Germany (R.C., M.J. and H.-P.V.) and Regulus Therapeutics, 1896 Rutherford Road, Carlsbad, California 92008, USA (J.S.).,
      name:Alnylam Pharmaceuticals, Inc., Cambridge, USA
      name:Alnylam Pharmaceuticals, Inc., Cambridge, USA
      name:Alnylam Pharmaceuticals, Inc., Cambridge, USA
      name:Alnylam Pharmaceuticals, Inc., Cambridge, USA
      name:Alnylam Pharmaceuticals, Inc., Cambridge, USA
      name:Alnylam Pharmaceuticals, Inc., Cambridge, USA
      name:Alnylam Pharmaceuticals, Inc., Cambridge, USA
      name:Alnylam Pharmaceuticals, Inc., Cambridge, USA
      name:Alnylam Europe AG, Kulmbach, Germany
      name:Present addresses: Roche Kulmbach GmbH, Fritz-Hornschuch-Str. 9, 95326 Kulmbach, Germany (R.C., M.J. and H.-P.V.) and Regulus Therapeutics, 1896 Rutherford Road, Carlsbad, California 92008, USA (J.S.).,
      name:Alnylam Pharmaceuticals, Inc., Cambridge, USA
      name:Alnylam Europe AG, Kulmbach, Germany
      name:Present addresses: Roche Kulmbach GmbH, Fritz-Hornschuch-Str. 9, 95326 Kulmbach, Germany (R.C., M.J. and H.-P.V.) and Regulus Therapeutics, 1896 Rutherford Road, Carlsbad, California 92008, USA (J.S.).,
      name:Alnylam Pharmaceuticals, Inc., Cambridge, USA
      name:David H. Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, USA
      name:Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, USA
      name:Department of Chemistry, Massachusetts Institute of Technology, Cambridge, USA
      name:David H. Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, USA
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