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Development of the iLiNP Device: Fine Tuning the Lipid Nanoparticle Size within 10 nm for Drug Delivery
[Image: see text] The precise size control of the lipid nanoparticle (LNP)-based nanodrug delivery system (DDS) carriers, such as 10 nm size tuning of LNPs, is one major challenge for the development of next-generation nanomedicines. Size-controlled LNPs would realize size-selective tumor targeting...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6641893/ https://www.ncbi.nlm.nih.gov/pubmed/31458718 http://dx.doi.org/10.1021/acsomega.8b00341 |
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author | Kimura, Niko Maeki, Masatoshi Sato, Yusuke Note, Yusuke Ishida, Akihiko Tani, Hirofumi Harashima, Hideyoshi Tokeshi, Manabu |
author_facet | Kimura, Niko Maeki, Masatoshi Sato, Yusuke Note, Yusuke Ishida, Akihiko Tani, Hirofumi Harashima, Hideyoshi Tokeshi, Manabu |
author_sort | Kimura, Niko |
collection | PubMed |
description | [Image: see text] The precise size control of the lipid nanoparticle (LNP)-based nanodrug delivery system (DDS) carriers, such as 10 nm size tuning of LNPs, is one major challenge for the development of next-generation nanomedicines. Size-controlled LNPs would realize size-selective tumor targeting and deliver DNA and RNA to target tumor tissues effectively by passing through the stromal cells. Herein, we developed a baffle mixer device named the invasive lipid nanoparticle production device, or iLiNP device for short, which has a simple two-dimensional microchannel and mixer structure, and we achieved the first reported LNP size tuning at 10 nm intervals in the size range from 20 to 100 nm. In comparison with the conventional LNP preparation methods and reported micromixer devices, our iLiNP device showed better LNP size controllability, robustness of device design, and LNP productivity. Furthermore, we prepared 80 nm sized LNPs with encapsulated small interfering RNA (siRNA) using the iLiNP device; these LNPs effectively performed as nano-DDS carriers in an in vivo experiment. We expect iLiNP devices will become novel apparatuses for LNP production in nano-DDS applications. |
format | Online Article Text |
id | pubmed-6641893 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-66418932019-08-27 Development of the iLiNP Device: Fine Tuning the Lipid Nanoparticle Size within 10 nm for Drug Delivery Kimura, Niko Maeki, Masatoshi Sato, Yusuke Note, Yusuke Ishida, Akihiko Tani, Hirofumi Harashima, Hideyoshi Tokeshi, Manabu ACS Omega [Image: see text] The precise size control of the lipid nanoparticle (LNP)-based nanodrug delivery system (DDS) carriers, such as 10 nm size tuning of LNPs, is one major challenge for the development of next-generation nanomedicines. Size-controlled LNPs would realize size-selective tumor targeting and deliver DNA and RNA to target tumor tissues effectively by passing through the stromal cells. Herein, we developed a baffle mixer device named the invasive lipid nanoparticle production device, or iLiNP device for short, which has a simple two-dimensional microchannel and mixer structure, and we achieved the first reported LNP size tuning at 10 nm intervals in the size range from 20 to 100 nm. In comparison with the conventional LNP preparation methods and reported micromixer devices, our iLiNP device showed better LNP size controllability, robustness of device design, and LNP productivity. Furthermore, we prepared 80 nm sized LNPs with encapsulated small interfering RNA (siRNA) using the iLiNP device; these LNPs effectively performed as nano-DDS carriers in an in vivo experiment. We expect iLiNP devices will become novel apparatuses for LNP production in nano-DDS applications. American Chemical Society 2018-05-09 /pmc/articles/PMC6641893/ /pubmed/31458718 http://dx.doi.org/10.1021/acsomega.8b00341 Text en Copyright © 2018 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Kimura, Niko Maeki, Masatoshi Sato, Yusuke Note, Yusuke Ishida, Akihiko Tani, Hirofumi Harashima, Hideyoshi Tokeshi, Manabu Development of the iLiNP Device: Fine Tuning the Lipid Nanoparticle Size within 10 nm for Drug Delivery |
title | Development of the iLiNP Device: Fine Tuning the Lipid
Nanoparticle Size within 10 nm for Drug Delivery |
title_full | Development of the iLiNP Device: Fine Tuning the Lipid
Nanoparticle Size within 10 nm for Drug Delivery |
title_fullStr | Development of the iLiNP Device: Fine Tuning the Lipid
Nanoparticle Size within 10 nm for Drug Delivery |
title_full_unstemmed | Development of the iLiNP Device: Fine Tuning the Lipid
Nanoparticle Size within 10 nm for Drug Delivery |
title_short | Development of the iLiNP Device: Fine Tuning the Lipid
Nanoparticle Size within 10 nm for Drug Delivery |
title_sort | development of the ilinp device: fine tuning the lipid
nanoparticle size within 10 nm for drug delivery |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6641893/ https://www.ncbi.nlm.nih.gov/pubmed/31458718 http://dx.doi.org/10.1021/acsomega.8b00341 |
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