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Screening of Oligomeric (Meth)acrylate Vaccine Adjuvants Synthesized via Catalytic Chain Transfer Polymerization
This report details the first systematic screening of free-radical-produced methacrylate oligomer reaction mixtures as alternative vaccine adjuvant components to replace the current benchmark compound squalene, which is unsustainably sourced from shark livers. Homo-/co-oligomer mixtures of methyl, b...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10538096/ https://www.ncbi.nlm.nih.gov/pubmed/37765685 http://dx.doi.org/10.3390/polym15183831 |
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author | Hege, Cordula S. Stimpson, Amy Sefton, Joseph Summers, James Henke, Helena Dundas, Adam A. Phan, Tony Kinsey, Robert Guderian, Jeffrey A. Sivananthan, Sandra J. Mohamath, Raodoh Lykins, William R. Ramer-Denisoff, Gabi Lin, Susan Fox, Christopher B. Irvine, Derek J. |
author_facet | Hege, Cordula S. Stimpson, Amy Sefton, Joseph Summers, James Henke, Helena Dundas, Adam A. Phan, Tony Kinsey, Robert Guderian, Jeffrey A. Sivananthan, Sandra J. Mohamath, Raodoh Lykins, William R. Ramer-Denisoff, Gabi Lin, Susan Fox, Christopher B. Irvine, Derek J. |
author_sort | Hege, Cordula S. |
collection | PubMed |
description | This report details the first systematic screening of free-radical-produced methacrylate oligomer reaction mixtures as alternative vaccine adjuvant components to replace the current benchmark compound squalene, which is unsustainably sourced from shark livers. Homo-/co-oligomer mixtures of methyl, butyl, lauryl, and stearyl methacrylate were successfully synthesized using catalytic chain transfer control, where the use of microwave heating was shown to promote propagation over chain transfer. Controlling the mixture material properties allowed the correct viscosity to be achieved, enabling the mixtures to be effectively used in vaccine formulations. Emulsions of selected oligomers stimulated comparable cytokine levels to squalene emulsion when incubated with human whole blood and elicited an antigen-specific cellular immune response when administered with an inactivated influenza vaccine, indicating the potential utility of the compounds as vaccine adjuvant components. Furthermore, the oligomers’ molecular sizes were demonstrated to be large enough to enable greater emulsion stability than squalene, especially at high temperatures, but are predicted to be small enough to allow for rapid clearance from the body. |
format | Online Article Text |
id | pubmed-10538096 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-105380962023-09-29 Screening of Oligomeric (Meth)acrylate Vaccine Adjuvants Synthesized via Catalytic Chain Transfer Polymerization Hege, Cordula S. Stimpson, Amy Sefton, Joseph Summers, James Henke, Helena Dundas, Adam A. Phan, Tony Kinsey, Robert Guderian, Jeffrey A. Sivananthan, Sandra J. Mohamath, Raodoh Lykins, William R. Ramer-Denisoff, Gabi Lin, Susan Fox, Christopher B. Irvine, Derek J. Polymers (Basel) Article This report details the first systematic screening of free-radical-produced methacrylate oligomer reaction mixtures as alternative vaccine adjuvant components to replace the current benchmark compound squalene, which is unsustainably sourced from shark livers. Homo-/co-oligomer mixtures of methyl, butyl, lauryl, and stearyl methacrylate were successfully synthesized using catalytic chain transfer control, where the use of microwave heating was shown to promote propagation over chain transfer. Controlling the mixture material properties allowed the correct viscosity to be achieved, enabling the mixtures to be effectively used in vaccine formulations. Emulsions of selected oligomers stimulated comparable cytokine levels to squalene emulsion when incubated with human whole blood and elicited an antigen-specific cellular immune response when administered with an inactivated influenza vaccine, indicating the potential utility of the compounds as vaccine adjuvant components. Furthermore, the oligomers’ molecular sizes were demonstrated to be large enough to enable greater emulsion stability than squalene, especially at high temperatures, but are predicted to be small enough to allow for rapid clearance from the body. MDPI 2023-09-20 /pmc/articles/PMC10538096/ /pubmed/37765685 http://dx.doi.org/10.3390/polym15183831 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Hege, Cordula S. Stimpson, Amy Sefton, Joseph Summers, James Henke, Helena Dundas, Adam A. Phan, Tony Kinsey, Robert Guderian, Jeffrey A. Sivananthan, Sandra J. Mohamath, Raodoh Lykins, William R. Ramer-Denisoff, Gabi Lin, Susan Fox, Christopher B. Irvine, Derek J. Screening of Oligomeric (Meth)acrylate Vaccine Adjuvants Synthesized via Catalytic Chain Transfer Polymerization |
title | Screening of Oligomeric (Meth)acrylate Vaccine Adjuvants Synthesized via Catalytic Chain Transfer Polymerization |
title_full | Screening of Oligomeric (Meth)acrylate Vaccine Adjuvants Synthesized via Catalytic Chain Transfer Polymerization |
title_fullStr | Screening of Oligomeric (Meth)acrylate Vaccine Adjuvants Synthesized via Catalytic Chain Transfer Polymerization |
title_full_unstemmed | Screening of Oligomeric (Meth)acrylate Vaccine Adjuvants Synthesized via Catalytic Chain Transfer Polymerization |
title_short | Screening of Oligomeric (Meth)acrylate Vaccine Adjuvants Synthesized via Catalytic Chain Transfer Polymerization |
title_sort | screening of oligomeric (meth)acrylate vaccine adjuvants synthesized via catalytic chain transfer polymerization |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10538096/ https://www.ncbi.nlm.nih.gov/pubmed/37765685 http://dx.doi.org/10.3390/polym15183831 |
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