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Evaluation of Nonmodified Wireframe DNA Origami for Acute Toxicity and Biodistribution in Mice

[Image: see text] Wireframe DNA origami can be used to fabricate virus-like particles for a range of biomedical applications, including the delivery of nucleic acid therapeutics. However, the acute toxicity and biodistribution of these wireframe nucleic acid nanoparticles (NANPs) have not been previ...

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Autores principales: Wamhoff, Eike-Christian, Knappe, Grant A., Burds, Aurora A., Du, Rebecca R., Neun, Barry W., Difilippantonio, Simone, Sanders, Chelsea, Edmondson, Elijah F., Matta, Jennifer L., Dobrovolskaia, Marina A., Bathe, Mark
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10189729/
https://www.ncbi.nlm.nih.gov/pubmed/37040258
http://dx.doi.org/10.1021/acsabm.3c00155
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author Wamhoff, Eike-Christian
Knappe, Grant A.
Burds, Aurora A.
Du, Rebecca R.
Neun, Barry W.
Difilippantonio, Simone
Sanders, Chelsea
Edmondson, Elijah F.
Matta, Jennifer L.
Dobrovolskaia, Marina A.
Bathe, Mark
author_facet Wamhoff, Eike-Christian
Knappe, Grant A.
Burds, Aurora A.
Du, Rebecca R.
Neun, Barry W.
Difilippantonio, Simone
Sanders, Chelsea
Edmondson, Elijah F.
Matta, Jennifer L.
Dobrovolskaia, Marina A.
Bathe, Mark
author_sort Wamhoff, Eike-Christian
collection PubMed
description [Image: see text] Wireframe DNA origami can be used to fabricate virus-like particles for a range of biomedical applications, including the delivery of nucleic acid therapeutics. However, the acute toxicity and biodistribution of these wireframe nucleic acid nanoparticles (NANPs) have not been previously characterized in animal models. In the present study, we observed no indications of toxicity in BALB/c mice following a therapeutically relevant dosage of nonmodified DNA-based NANPs via intravenous administration, based on liver and kidney histology, liver and kidney biochemistry, and body weight. Further, the immunotoxicity of these NANPs was minimal, as indicated by blood cell counts and type-I interferon and pro-inflammatory cytokines. In an SJL/J model of autoimmunity, we observed no indications of NANP-mediated DNA-specific antibody response or immune-mediated kidney pathology following the intraperitoneal administration of NANPs. Finally, biodistribution studies revealed that these NANPs accumulate in the liver within one hour, concomitant with substantial renal clearance. Our observations support the continued development of wireframe DNA-based NANPs as next-generation nucleic acid therapeutic delivery platforms.
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spelling pubmed-101897292023-05-18 Evaluation of Nonmodified Wireframe DNA Origami for Acute Toxicity and Biodistribution in Mice Wamhoff, Eike-Christian Knappe, Grant A. Burds, Aurora A. Du, Rebecca R. Neun, Barry W. Difilippantonio, Simone Sanders, Chelsea Edmondson, Elijah F. Matta, Jennifer L. Dobrovolskaia, Marina A. Bathe, Mark ACS Appl Bio Mater [Image: see text] Wireframe DNA origami can be used to fabricate virus-like particles for a range of biomedical applications, including the delivery of nucleic acid therapeutics. However, the acute toxicity and biodistribution of these wireframe nucleic acid nanoparticles (NANPs) have not been previously characterized in animal models. In the present study, we observed no indications of toxicity in BALB/c mice following a therapeutically relevant dosage of nonmodified DNA-based NANPs via intravenous administration, based on liver and kidney histology, liver and kidney biochemistry, and body weight. Further, the immunotoxicity of these NANPs was minimal, as indicated by blood cell counts and type-I interferon and pro-inflammatory cytokines. In an SJL/J model of autoimmunity, we observed no indications of NANP-mediated DNA-specific antibody response or immune-mediated kidney pathology following the intraperitoneal administration of NANPs. Finally, biodistribution studies revealed that these NANPs accumulate in the liver within one hour, concomitant with substantial renal clearance. Our observations support the continued development of wireframe DNA-based NANPs as next-generation nucleic acid therapeutic delivery platforms. American Chemical Society 2023-04-11 /pmc/articles/PMC10189729/ /pubmed/37040258 http://dx.doi.org/10.1021/acsabm.3c00155 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Wamhoff, Eike-Christian
Knappe, Grant A.
Burds, Aurora A.
Du, Rebecca R.
Neun, Barry W.
Difilippantonio, Simone
Sanders, Chelsea
Edmondson, Elijah F.
Matta, Jennifer L.
Dobrovolskaia, Marina A.
Bathe, Mark
Evaluation of Nonmodified Wireframe DNA Origami for Acute Toxicity and Biodistribution in Mice
title Evaluation of Nonmodified Wireframe DNA Origami for Acute Toxicity and Biodistribution in Mice
title_full Evaluation of Nonmodified Wireframe DNA Origami for Acute Toxicity and Biodistribution in Mice
title_fullStr Evaluation of Nonmodified Wireframe DNA Origami for Acute Toxicity and Biodistribution in Mice
title_full_unstemmed Evaluation of Nonmodified Wireframe DNA Origami for Acute Toxicity and Biodistribution in Mice
title_short Evaluation of Nonmodified Wireframe DNA Origami for Acute Toxicity and Biodistribution in Mice
title_sort evaluation of nonmodified wireframe dna origami for acute toxicity and biodistribution in mice
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10189729/
https://www.ncbi.nlm.nih.gov/pubmed/37040258
http://dx.doi.org/10.1021/acsabm.3c00155
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