Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Mensink, M. A., Šibík, J., Frijlink, H. W., van der Voort Maarschalk, K., Hinrichs, W. L. J., Zeitler, J. A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2017
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
_version_ 1783268700226322432
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
work_keys_str_mv AT mensinkma thermalgradientmidandfarinfraredspectroscopyastoolsforcharacterizationofproteincarbohydratelyophilizates
AT sibikj thermalgradientmidandfarinfraredspectroscopyastoolsforcharacterizationofproteincarbohydratelyophilizates
AT frijlinkhw thermalgradientmidandfarinfraredspectroscopyastoolsforcharacterizationofproteincarbohydratelyophilizates
AT vandervoortmaarschalkk thermalgradientmidandfarinfraredspectroscopyastoolsforcharacterizationofproteincarbohydratelyophilizates
AT hinrichswlj thermalgradientmidandfarinfraredspectroscopyastoolsforcharacterizationofproteincarbohydratelyophilizates
AT zeitlerja thermalgradientmidandfarinfraredspectroscopyastoolsforcharacterizationofproteincarbohydratelyophilizates