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Thermal Gradient Mid- and Far-Infrared Spectroscopy as Tools for Characterization of Protein Carbohydrate Lyophilizates
[Image: see text] Protein drugs play an important role in modern day medicine. Typically, these proteins are formulated as liquids requiring cold chain processing. To circumvent the cold chain and achieve better storage stability, these proteins can be dried in the presence of carbohydrates. We demo...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5627341/ https://www.ncbi.nlm.nih.gov/pubmed/28874050 http://dx.doi.org/10.1021/acs.molpharmaceut.7b00568 |
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author | Mensink, M. A. Šibík, J. Frijlink, H. W. van der Voort Maarschalk, K. Hinrichs, W. L. J. Zeitler, J. A. |
author_facet | Mensink, M. A. Šibík, J. Frijlink, H. W. van der Voort Maarschalk, K. Hinrichs, W. L. J. Zeitler, J. A. |
author_sort | Mensink, M. A. |
collection | PubMed |
description | [Image: see text] Protein drugs play an important role in modern day medicine. Typically, these proteins are formulated as liquids requiring cold chain processing. To circumvent the cold chain and achieve better storage stability, these proteins can be dried in the presence of carbohydrates. We demonstrate that thermal gradient mid- and far-infrared spectroscopy (FTIR and THz-TDS, respectively) can provide useful information about solid-state protein carbohydrate formulations regarding mobility and intermolecular interactions. A model protein (BSA) was lyophilized in the presence of three carbohydrates with different size and protein stabilizing capacity. A gradual increase in mobility was observed with increasing temperature in formulations containing protein and/or larger carbohydrates (oligo- or polysaccharides), lacking a clear onset of fast mobility as was observed for smaller molecules. Furthermore, both techniques are able to identify the glass transition temperatures (T(g)) of the samples. FTIR provides additional information as it can independently monitor changes in protein and carbohydrate bands at the T(g). Lastly, THz-TDS confirms previous findings that protein–carbohydrate interactions decrease with increasing molecular weight of the carbohydrate, which results in decreased protein stabilization. |
format | Online Article Text |
id | pubmed-5627341 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-56273412017-10-05 Thermal Gradient Mid- and Far-Infrared Spectroscopy as Tools for Characterization of Protein Carbohydrate Lyophilizates Mensink, M. A. Šibík, J. Frijlink, H. W. van der Voort Maarschalk, K. Hinrichs, W. L. J. Zeitler, J. A. Mol Pharm [Image: see text] Protein drugs play an important role in modern day medicine. Typically, these proteins are formulated as liquids requiring cold chain processing. To circumvent the cold chain and achieve better storage stability, these proteins can be dried in the presence of carbohydrates. We demonstrate that thermal gradient mid- and far-infrared spectroscopy (FTIR and THz-TDS, respectively) can provide useful information about solid-state protein carbohydrate formulations regarding mobility and intermolecular interactions. A model protein (BSA) was lyophilized in the presence of three carbohydrates with different size and protein stabilizing capacity. A gradual increase in mobility was observed with increasing temperature in formulations containing protein and/or larger carbohydrates (oligo- or polysaccharides), lacking a clear onset of fast mobility as was observed for smaller molecules. Furthermore, both techniques are able to identify the glass transition temperatures (T(g)) of the samples. FTIR provides additional information as it can independently monitor changes in protein and carbohydrate bands at the T(g). Lastly, THz-TDS confirms previous findings that protein–carbohydrate interactions decrease with increasing molecular weight of the carbohydrate, which results in decreased protein stabilization. American Chemical Society 2017-09-05 2017-10-02 /pmc/articles/PMC5627341/ /pubmed/28874050 http://dx.doi.org/10.1021/acs.molpharmaceut.7b00568 Text en Copyright © 2017 American Chemical Society This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) , which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes. |
spellingShingle | Mensink, M. A. Šibík, J. Frijlink, H. W. van der Voort Maarschalk, K. Hinrichs, W. L. J. Zeitler, J. A. Thermal Gradient Mid- and Far-Infrared Spectroscopy as Tools for Characterization of Protein Carbohydrate Lyophilizates |
title | Thermal Gradient Mid- and Far-Infrared Spectroscopy
as Tools for Characterization of Protein Carbohydrate Lyophilizates |
title_full | Thermal Gradient Mid- and Far-Infrared Spectroscopy
as Tools for Characterization of Protein Carbohydrate Lyophilizates |
title_fullStr | Thermal Gradient Mid- and Far-Infrared Spectroscopy
as Tools for Characterization of Protein Carbohydrate Lyophilizates |
title_full_unstemmed | Thermal Gradient Mid- and Far-Infrared Spectroscopy
as Tools for Characterization of Protein Carbohydrate Lyophilizates |
title_short | Thermal Gradient Mid- and Far-Infrared Spectroscopy
as Tools for Characterization of Protein Carbohydrate Lyophilizates |
title_sort | thermal gradient mid- and far-infrared spectroscopy
as tools for characterization of protein carbohydrate lyophilizates |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5627341/ https://www.ncbi.nlm.nih.gov/pubmed/28874050 http://dx.doi.org/10.1021/acs.molpharmaceut.7b00568 |
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