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Acerola exosome-like nanovesicles to systemically deliver nucleic acid medicine via oral administration.
Umezu, Tomohiro; Takanashi, Masakatsu; Murakami, Yoshiki; Ohno, Shin-Ichiro; Kanekura, Kohsuke; Sudo, Katsuko; Nagamine, Kenichi; Takeuchi, Shin; Ochiya, Takahiro; Kuroda, Masahiko.
Affiliation
  • Umezu T; Department of Molecular Pathology, Tokyo Medical University, Tokyo, Japan.
  • Takanashi M; Department of Molecular Pathology, Tokyo Medical University, Tokyo, Japan.
  • Murakami Y; Department of Molecular Pathology, Tokyo Medical University, Tokyo, Japan.
  • Ohno SI; Department of Molecular Pathology, Tokyo Medical University, Tokyo, Japan.
  • Kanekura K; Department of Molecular Pathology, Tokyo Medical University, Tokyo, Japan.
  • Sudo K; Preclinical Research Center, Tokyo Medical University, Tokyo, Japan.
  • Nagamine K; Research and Development, Global Innovation Center, Nichirei Biosciences inc, Tokyo, Japan.
  • Takeuchi S; Research and Development, Global Innovation Center, Nichirei Biosciences inc, Tokyo, Japan.
  • Ochiya T; Department of Molecular and Cellular Medicine, Institute of Medical Science, Tokyo Medical University, Tokyo, Japan.
  • Kuroda M; Department of Molecular Pathology, Tokyo Medical University, Tokyo, Japan.
Mol Ther Methods Clin Dev ; 21: 199-208, 2021 Jun 11.
Article in En | MEDLINE | ID: mdl-33850951
ABSTRACT
Extracellular vesicles derived from mammalian cells could be useful carriers for drug delivery systems (DDSs); however, with regard to clinical application, there are several issues to be overcome. Acerola (Malpighia emarginata DC.) is a popular health food. In this study, the feasibility of orally administered nucleic acid drug delivery by acerola exosome-like nanoparticles (AELNs) was examined. AELNs were recovered from acerola juice using an affinity column instead of ultracentrifugation. MicroRNA (miRNA) was sufficiently encapsulated in AELNs by 30-min incubation on ice and was protected against RNase, strong acid, and base treatments. The administration of an AELN/miRNA mixture in cells achieved downregulation of the miRNA's target gene, and this mixture showed cytoplasmic localization. AELNs orally delivered small RNA to the digestive system in vivo. The target gene-suppressing effect in the small intestine and liver peaked 1 day after administration, indicating potential for use as an oral DDS for nucleic acid in the digestive system.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Mol Ther Methods Clin Dev Year: 2021 Document type: Article Affiliation country: Japan

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Mol Ther Methods Clin Dev Year: 2021 Document type: Article Affiliation country: Japan
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