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Laser-Induced Forward Transfer Printing on Microneedles for Transdermal Delivery of Gemcitabine
Cancer treatment with chemotherapeutic drugs remains to be challenging to the physician due to limitations associated with lack of efficacy or high toxicities. Typically, chemotherapeutic drugs are administered intravenously, leading to high drug concentrations that drive efficacy but also lead to k...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Whioce Publishing Pte. Ltd.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9159537/ https://www.ncbi.nlm.nih.gov/pubmed/35669329 http://dx.doi.org/10.18063/ijb.v8i2.554 |
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author | Kanaki, Zoi Chandrinou, Chrysoula Orfanou, Ioanna-Maria Kryou, Christina Ziesmer, Jill Sotiriou, Georgios A. Klinakis, Apostolos Tamvakopoulos, Constantin Zergioti, Ioanna |
author_facet | Kanaki, Zoi Chandrinou, Chrysoula Orfanou, Ioanna-Maria Kryou, Christina Ziesmer, Jill Sotiriou, Georgios A. Klinakis, Apostolos Tamvakopoulos, Constantin Zergioti, Ioanna |
author_sort | Kanaki, Zoi |
collection | PubMed |
description | Cancer treatment with chemotherapeutic drugs remains to be challenging to the physician due to limitations associated with lack of efficacy or high toxicities. Typically, chemotherapeutic drugs are administered intravenously, leading to high drug concentrations that drive efficacy but also lead to known side effects. Delivery of drugs through transdermal microneedles (MNs) has become an important alternative treatment approach. Such delivery options are well suited for chemotherapeutic drugs in which sustained levels would be desirable. In the context of developing a novel approach, laser-induced forward transfer (LIFT) was applied for bioprinting of gemcitabine (Gem) to coat polymethylmethacrylate MNs. Gem, a chemotherapeutic agent used to treat various types of cancer, is a good candidate for MN-assisted transdermal delivery to improve the pharmacokinetics of Gem while reducing efficiency limitations. LIFT bioprinting of Gem for coating of MNs with different drug amounts and successful transdermal delivery in mice is presented in this study. Our approach produced reproducible, accurate, and uniform coatings of the drug on MN arrays, and on in vivo transdermal application of the coated MNs in mice, dose-proportional concentrations of Gem in the plasma of mice was achieved. The developed approach may be extended to several chemotherapeutics and provide advantages for metronomic drug dosing. |
format | Online Article Text |
id | pubmed-9159537 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Whioce Publishing Pte. Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-91595372022-06-05 Laser-Induced Forward Transfer Printing on Microneedles for Transdermal Delivery of Gemcitabine Kanaki, Zoi Chandrinou, Chrysoula Orfanou, Ioanna-Maria Kryou, Christina Ziesmer, Jill Sotiriou, Georgios A. Klinakis, Apostolos Tamvakopoulos, Constantin Zergioti, Ioanna Int J Bioprint Research Article Cancer treatment with chemotherapeutic drugs remains to be challenging to the physician due to limitations associated with lack of efficacy or high toxicities. Typically, chemotherapeutic drugs are administered intravenously, leading to high drug concentrations that drive efficacy but also lead to known side effects. Delivery of drugs through transdermal microneedles (MNs) has become an important alternative treatment approach. Such delivery options are well suited for chemotherapeutic drugs in which sustained levels would be desirable. In the context of developing a novel approach, laser-induced forward transfer (LIFT) was applied for bioprinting of gemcitabine (Gem) to coat polymethylmethacrylate MNs. Gem, a chemotherapeutic agent used to treat various types of cancer, is a good candidate for MN-assisted transdermal delivery to improve the pharmacokinetics of Gem while reducing efficiency limitations. LIFT bioprinting of Gem for coating of MNs with different drug amounts and successful transdermal delivery in mice is presented in this study. Our approach produced reproducible, accurate, and uniform coatings of the drug on MN arrays, and on in vivo transdermal application of the coated MNs in mice, dose-proportional concentrations of Gem in the plasma of mice was achieved. The developed approach may be extended to several chemotherapeutics and provide advantages for metronomic drug dosing. Whioce Publishing Pte. Ltd. 2022-02-08 /pmc/articles/PMC9159537/ /pubmed/35669329 http://dx.doi.org/10.18063/ijb.v8i2.554 Text en Copyright: © 2022 Kanaki, et al. https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Attribution-NonCommercial 4.0 International 4.0 (CC BY-NC 4.0), which permits all non-commercial use, distribution, and reproduction in any medium provided the original work is properly cited. |
spellingShingle | Research Article Kanaki, Zoi Chandrinou, Chrysoula Orfanou, Ioanna-Maria Kryou, Christina Ziesmer, Jill Sotiriou, Georgios A. Klinakis, Apostolos Tamvakopoulos, Constantin Zergioti, Ioanna Laser-Induced Forward Transfer Printing on Microneedles for Transdermal Delivery of Gemcitabine |
title | Laser-Induced Forward Transfer Printing on Microneedles for Transdermal Delivery of Gemcitabine |
title_full | Laser-Induced Forward Transfer Printing on Microneedles for Transdermal Delivery of Gemcitabine |
title_fullStr | Laser-Induced Forward Transfer Printing on Microneedles for Transdermal Delivery of Gemcitabine |
title_full_unstemmed | Laser-Induced Forward Transfer Printing on Microneedles for Transdermal Delivery of Gemcitabine |
title_short | Laser-Induced Forward Transfer Printing on Microneedles for Transdermal Delivery of Gemcitabine |
title_sort | laser-induced forward transfer printing on microneedles for transdermal delivery of gemcitabine |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9159537/ https://www.ncbi.nlm.nih.gov/pubmed/35669329 http://dx.doi.org/10.18063/ijb.v8i2.554 |
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