In vitro study of sirolimus release from nonwoven PLLA matrices
Sirolimus incorporated nonwoven polymer matrices were fabricated via electrospinning. Release kinetics considering different fiber diameters and layer thicknesses were investigated. In vitro drug release profiles were evaluated by measuring the drug concentration in an established drug release mediu...
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2018-09-01
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Online Access: | https://doi.org/10.1515/cdbme-2018-0142 |
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doaj-3aece2b2e38745d196dbbb5467f1044f2021-09-06T19:19:26ZengDe GruyterCurrent Directions in Biomedical Engineering2364-55042018-09-014159159410.1515/cdbme-2018-0142cdbme-2018-0142In vitro study of sirolimus release from nonwoven PLLA matricesIllner Sabine0Kohse Stefanie1Michaelis Claudia2Reske Thomas3Grabow Niels4Schmitz Klaus-Peter5Eickner Thomas6Institute for Biomedical Engineering, University Medical Center Rostock, Rostock-Warnemünde, GermanyInstitute for Biomedical Engineering, University Medical Center Rostock, Rostock-Warnemünde, GermanyInstitute for Biomedical Engineering, University Medical Center Rostock, Rostock-Warnemünde, GermanyInstitute for Biomedical Engineering, University Medical Center Rostock, Rostock-Warnemünde, GermanyInstitute for Biomedical Engineering, University Medical Center Rostock, Rostock-Warnemünde, GermanyInstitute for ImplantTechnology and Biomaterials e.V.,Rostock, GermanyInstitute for Biomedical Engineering, University Medical Center Rostock, Rostock-Warnemünde, GermanySirolimus incorporated nonwoven polymer matrices were fabricated via electrospinning. Release kinetics considering different fiber diameters and layer thicknesses were investigated. In vitro drug release profiles were evaluated by measuring the drug concentration in an established drug release medium (0.9% saline solution with additives, not buffered) at predetermined time points. Furthermore, an NH3-plasma pretreatment was examined to ensure complete wetting from the beginning of the study. In comparison to thin drug-loaded PLLA spray coatings it was shown that the release of sirolimus is diffusion- and degradation-controlled regardless of the surface-to-volume ratio, though fiber diameters or a hydrophilization can affect its release kinetics.https://doi.org/10.1515/cdbme-2018-0142drug releasefibrous materialnonwovenfilm layersurface modificationhydrophilization |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Illner Sabine Kohse Stefanie Michaelis Claudia Reske Thomas Grabow Niels Schmitz Klaus-Peter Eickner Thomas |
spellingShingle |
Illner Sabine Kohse Stefanie Michaelis Claudia Reske Thomas Grabow Niels Schmitz Klaus-Peter Eickner Thomas In vitro study of sirolimus release from nonwoven PLLA matrices Current Directions in Biomedical Engineering drug release fibrous material nonwoven film layer surface modification hydrophilization |
author_facet |
Illner Sabine Kohse Stefanie Michaelis Claudia Reske Thomas Grabow Niels Schmitz Klaus-Peter Eickner Thomas |
author_sort |
Illner Sabine |
title |
In vitro study of sirolimus release from nonwoven PLLA matrices |
title_short |
In vitro study of sirolimus release from nonwoven PLLA matrices |
title_full |
In vitro study of sirolimus release from nonwoven PLLA matrices |
title_fullStr |
In vitro study of sirolimus release from nonwoven PLLA matrices |
title_full_unstemmed |
In vitro study of sirolimus release from nonwoven PLLA matrices |
title_sort |
in vitro study of sirolimus release from nonwoven plla matrices |
publisher |
De Gruyter |
series |
Current Directions in Biomedical Engineering |
issn |
2364-5504 |
publishDate |
2018-09-01 |
description |
Sirolimus incorporated nonwoven polymer matrices were fabricated via electrospinning. Release kinetics considering different fiber diameters and layer thicknesses were investigated. In vitro drug release profiles were evaluated by measuring the drug concentration in an established drug release medium (0.9% saline solution with additives, not buffered) at predetermined time points. Furthermore, an NH3-plasma pretreatment was examined to ensure complete wetting from the beginning of the study. In comparison to thin drug-loaded PLLA spray coatings it was shown that the release of sirolimus is diffusion- and degradation-controlled regardless of the surface-to-volume ratio, though fiber diameters or a hydrophilization can affect its release kinetics. |
topic |
drug release fibrous material nonwoven film layer surface modification hydrophilization |
url |
https://doi.org/10.1515/cdbme-2018-0142 |
work_keys_str_mv |
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1717778583679664128 |