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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Main Authors: Illner Sabine, Kohse Stefanie, Michaelis Claudia, Reske Thomas, Grabow Niels, Schmitz Klaus-Peter, Eickner Thomas
Format: Article
Language:English
Published: De Gruyter 2018-09-01
Series:Current Directions in Biomedical Engineering
Subjects:
Online Access:https://doi.org/10.1515/cdbme-2018-0142
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spelling 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 AT illnersabine invitrostudyofsirolimusreleasefromnonwovenpllamatrices
AT kohsestefanie invitrostudyofsirolimusreleasefromnonwovenpllamatrices
AT michaelisclaudia invitrostudyofsirolimusreleasefromnonwovenpllamatrices
AT reskethomas invitrostudyofsirolimusreleasefromnonwovenpllamatrices
AT grabowniels invitrostudyofsirolimusreleasefromnonwovenpllamatrices
AT schmitzklauspeter invitrostudyofsirolimusreleasefromnonwovenpllamatrices
AT eicknerthomas invitrostudyofsirolimusreleasefromnonwovenpllamatrices
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