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A comparison of inverted and upright laser-activated titanium nitride micropyramids for intracellular delivery

The delivery of biomolecules into cells relies on porating the plasma membrane to allow exterior molecules to enter the cell via diffusion. Various established delivery methods, including electroporation and viral techniques, come with drawbacks such as low viability or immunotoxicity, respectively....

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Autores principales: Raun, Alexander, Saklayen, Nabiha, Zgrabik, Christine, Shen, Weilu, Madrid, Marinna, Huber, Marinus, Hu, Evelyn, Mazur, Eric
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6197185/
https://www.ncbi.nlm.nih.gov/pubmed/30349063
http://dx.doi.org/10.1038/s41598-018-33885-y
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author Raun, Alexander
Saklayen, Nabiha
Zgrabik, Christine
Shen, Weilu
Madrid, Marinna
Huber, Marinus
Hu, Evelyn
Mazur, Eric
author_facet Raun, Alexander
Saklayen, Nabiha
Zgrabik, Christine
Shen, Weilu
Madrid, Marinna
Huber, Marinus
Hu, Evelyn
Mazur, Eric
author_sort Raun, Alexander
collection PubMed
description The delivery of biomolecules into cells relies on porating the plasma membrane to allow exterior molecules to enter the cell via diffusion. Various established delivery methods, including electroporation and viral techniques, come with drawbacks such as low viability or immunotoxicity, respectively. An optics-based delivery method that uses laser pulses to excite plasmonic titanium nitride (TiN) micropyramids presents an opportunity to overcome these shortcomings. This laser excitation generates localized nano-scale heating effects and bubbles, which produce transient pores in the cell membrane for payload entry. TiN is a promising plasmonic material due to its high hardness and thermal stability. In this study, two designs of TiN micropyramid arrays are constructed and tested. These designs include inverted and upright pyramid structures, each coated with a 50-nm layer of TiN. Simulation software shows that the inverted and upright designs reach temperatures of 875 °C and 307 °C, respectively, upon laser irradiation. Collectively, experimental results show that these reusable designs achieve maximum cell poration efficiency greater than 80% and viability greater than 90% when delivering calcein dye to target cells. Overall, we demonstrate that TiN microstructures are strong candidates for future use in biomedical devices for intracellular delivery and regenerative medicine.
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spelling pubmed-61971852018-10-24 A comparison of inverted and upright laser-activated titanium nitride micropyramids for intracellular delivery Raun, Alexander Saklayen, Nabiha Zgrabik, Christine Shen, Weilu Madrid, Marinna Huber, Marinus Hu, Evelyn Mazur, Eric Sci Rep Article The delivery of biomolecules into cells relies on porating the plasma membrane to allow exterior molecules to enter the cell via diffusion. Various established delivery methods, including electroporation and viral techniques, come with drawbacks such as low viability or immunotoxicity, respectively. An optics-based delivery method that uses laser pulses to excite plasmonic titanium nitride (TiN) micropyramids presents an opportunity to overcome these shortcomings. This laser excitation generates localized nano-scale heating effects and bubbles, which produce transient pores in the cell membrane for payload entry. TiN is a promising plasmonic material due to its high hardness and thermal stability. In this study, two designs of TiN micropyramid arrays are constructed and tested. These designs include inverted and upright pyramid structures, each coated with a 50-nm layer of TiN. Simulation software shows that the inverted and upright designs reach temperatures of 875 °C and 307 °C, respectively, upon laser irradiation. Collectively, experimental results show that these reusable designs achieve maximum cell poration efficiency greater than 80% and viability greater than 90% when delivering calcein dye to target cells. Overall, we demonstrate that TiN microstructures are strong candidates for future use in biomedical devices for intracellular delivery and regenerative medicine. Nature Publishing Group UK 2018-10-22 /pmc/articles/PMC6197185/ /pubmed/30349063 http://dx.doi.org/10.1038/s41598-018-33885-y Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Raun, Alexander
Saklayen, Nabiha
Zgrabik, Christine
Shen, Weilu
Madrid, Marinna
Huber, Marinus
Hu, Evelyn
Mazur, Eric
A comparison of inverted and upright laser-activated titanium nitride micropyramids for intracellular delivery
title A comparison of inverted and upright laser-activated titanium nitride micropyramids for intracellular delivery
title_full A comparison of inverted and upright laser-activated titanium nitride micropyramids for intracellular delivery
title_fullStr A comparison of inverted and upright laser-activated titanium nitride micropyramids for intracellular delivery
title_full_unstemmed A comparison of inverted and upright laser-activated titanium nitride micropyramids for intracellular delivery
title_short A comparison of inverted and upright laser-activated titanium nitride micropyramids for intracellular delivery
title_sort comparison of inverted and upright laser-activated titanium nitride micropyramids for intracellular delivery
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6197185/
https://www.ncbi.nlm.nih.gov/pubmed/30349063
http://dx.doi.org/10.1038/s41598-018-33885-y
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