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Single-Administration Long-Acting Microarray Patch with Ultrahigh Loading Capacity and Multiple Releases of Thermally Stable Antibodies
[Image: see text] Current antibody (Ab) therapies require development of stable formulations and an optimal delivery system. Here, we present a new strategy to create a single-administration long-lasting Ab-delivery microarray (MA) patch, which can carry high doses of thermally stabilized Abs. The M...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10155177/ https://www.ncbi.nlm.nih.gov/pubmed/37014806 http://dx.doi.org/10.1021/acs.molpharmaceut.2c00919 |
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author | Tran, Khanh T. M. Le, Thinh T. Agrahari, Vivek Peet, M. Melissa Ouattara, Louise A. Anderson, Sharon M. Le-Kim, Trang Huyen Singh, Onkar N. Doncel, Gustavo F. Nguyen, Thanh D. |
author_facet | Tran, Khanh T. M. Le, Thinh T. Agrahari, Vivek Peet, M. Melissa Ouattara, Louise A. Anderson, Sharon M. Le-Kim, Trang Huyen Singh, Onkar N. Doncel, Gustavo F. Nguyen, Thanh D. |
author_sort | Tran, Khanh T. M. |
collection | PubMed |
description | [Image: see text] Current antibody (Ab) therapies require development of stable formulations and an optimal delivery system. Here, we present a new strategy to create a single-administration long-lasting Ab-delivery microarray (MA) patch, which can carry high doses of thermally stabilized Abs. The MA fabricated by an additive three-dimensional manufacturing technology can be fully embedded into the skin via a single application to deliver doses of Abs at multiple programmable time points, thus sustaining Ab concentrations in systemic circulation. We developed an MA formulation that stabilized and delivered human immunoglobulins (hIg) in a time-controlled manner while maintaining their structure and functionality. As an example, the b12 Ab—a broadly neutralizing Ab against HIV-1—maintained antiviral activity in vitro after MA manufacturing and heat exposure. Pharmacokinetic studies of MA patch-delivered hIg in rats successfully provided a proof of concept for concurrent and time-delayed Ab delivery. These MA patches codeliver different Abs, providing a tool for expanded protection against viral infections or combination HIV therapy and prevention. |
format | Online Article Text |
id | pubmed-10155177 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-101551772023-05-04 Single-Administration Long-Acting Microarray Patch with Ultrahigh Loading Capacity and Multiple Releases of Thermally Stable Antibodies Tran, Khanh T. M. Le, Thinh T. Agrahari, Vivek Peet, M. Melissa Ouattara, Louise A. Anderson, Sharon M. Le-Kim, Trang Huyen Singh, Onkar N. Doncel, Gustavo F. Nguyen, Thanh D. Mol Pharm [Image: see text] Current antibody (Ab) therapies require development of stable formulations and an optimal delivery system. Here, we present a new strategy to create a single-administration long-lasting Ab-delivery microarray (MA) patch, which can carry high doses of thermally stabilized Abs. The MA fabricated by an additive three-dimensional manufacturing technology can be fully embedded into the skin via a single application to deliver doses of Abs at multiple programmable time points, thus sustaining Ab concentrations in systemic circulation. We developed an MA formulation that stabilized and delivered human immunoglobulins (hIg) in a time-controlled manner while maintaining their structure and functionality. As an example, the b12 Ab—a broadly neutralizing Ab against HIV-1—maintained antiviral activity in vitro after MA manufacturing and heat exposure. Pharmacokinetic studies of MA patch-delivered hIg in rats successfully provided a proof of concept for concurrent and time-delayed Ab delivery. These MA patches codeliver different Abs, providing a tool for expanded protection against viral infections or combination HIV therapy and prevention. American Chemical Society 2023-04-04 /pmc/articles/PMC10155177/ /pubmed/37014806 http://dx.doi.org/10.1021/acs.molpharmaceut.2c00919 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 | Tran, Khanh T. M. Le, Thinh T. Agrahari, Vivek Peet, M. Melissa Ouattara, Louise A. Anderson, Sharon M. Le-Kim, Trang Huyen Singh, Onkar N. Doncel, Gustavo F. Nguyen, Thanh D. Single-Administration Long-Acting Microarray Patch with Ultrahigh Loading Capacity and Multiple Releases of Thermally Stable Antibodies |
title | Single-Administration
Long-Acting Microarray Patch
with Ultrahigh Loading Capacity and Multiple Releases of Thermally
Stable Antibodies |
title_full | Single-Administration
Long-Acting Microarray Patch
with Ultrahigh Loading Capacity and Multiple Releases of Thermally
Stable Antibodies |
title_fullStr | Single-Administration
Long-Acting Microarray Patch
with Ultrahigh Loading Capacity and Multiple Releases of Thermally
Stable Antibodies |
title_full_unstemmed | Single-Administration
Long-Acting Microarray Patch
with Ultrahigh Loading Capacity and Multiple Releases of Thermally
Stable Antibodies |
title_short | Single-Administration
Long-Acting Microarray Patch
with Ultrahigh Loading Capacity and Multiple Releases of Thermally
Stable Antibodies |
title_sort | single-administration
long-acting microarray patch
with ultrahigh loading capacity and multiple releases of thermally
stable antibodies |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10155177/ https://www.ncbi.nlm.nih.gov/pubmed/37014806 http://dx.doi.org/10.1021/acs.molpharmaceut.2c00919 |
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