Coaxial electrospinning as a process to engineer biodegradable polymeric scaffolds as drug delivery systems for anti-inflammatory and anti- thrombotic pharmaceutical agents
posted on 2019-03-01, 14:28authored byAlexandros Repanas, Willem F. Wolkers, Oleksandr Gryshkov, P. Kalozoumis, Marc Mueller, Holger Zernetsch, Sotiris KorossisSotiris Korossis, B. Glasmacher
Objective: Blend electrospinning has been acknowledged as a cost-effective technique for the production of
fibrous scaffolds, suitable for various biomedical applications. Coaxial electrospinning is a method variant that results
in core-shell structures with advantages, such as delayed diffusion and protection of sensitive biomolecules. The aim of
this work was to evaluate how different process and solution parameters affect the structural, mechanical and physical
properties of the fibers, created by polycaprolactone (PCL). In addition, acetylsalicylic acid (ASA) that was used as a
model anti-inflammatory and anti-thrombotic agent, was loaded within the fiber meshes in order to compare release
kinetics between fibers produced by conventional blend and coaxial electrospinning.
Methods: Scanning electron microscopy (SEM) was used to investigate the structural and morphological
characteristics of the fibers. The fibers’ hydrophilicity was investigated using contact angle measurements while
the electrical conductivity of the polymeric solutions and the thermal properties of the fibers were also evaluated.
Differential scanning calorimetry (DSC) was used to determine the fibers’ melting point and mechanical tensile tests
were performed in order to study the mechanical properties of the fibers. Moreover, UV-vis spectroscopy was used to
determine the release kinetics of ASA.
Results: The results indicated that increasing the concentration of PCL led to thicker and less aligned fibers.
Furthermore, the physicochemical characterization did not reveal significant changes during the process. Coaxially
electrospun fibers that were loaded with ASA exhibited a slower and sustained, biphasic release profile compared to
blend electrospun fibers with 34% of ASA released during the first 8h and 97% in total after 3 months.
Conclusion: Taken together, fibrous meshes created by coaxial electrospinning using PCL, can be tailor-made by
a careful optimization of all the process and solution parameters, in order to fit the scope of specific applications in the
fields of biomedical engineering and drug delivery.
Funding
This research was granted by the German Research Foundation (DFG) by
the Cluster of Excellence REBIRTH (From Regenerative Biology to Reconstructive
Therapy, DFG EXC 62/1).T
History
School
Mechanical, Electrical and Manufacturing Engineering
Published in
Clinical & Experimental Pharmacology
Volume
05
Issue
05
Citation
REPANAS, A. ... et al., 2015. Coaxial electrospinning as a process to engineer biodegradable polymeric scaffolds as drug delivery systems for anti-inflammatory and anti- thrombotic pharmaceutical agents. Clinical & Experimental Pharmacology, 05: 192.
This work is made available according to the conditions of the Creative Commons Attribution 4.0 International (CC BY 4.0) licence. Full details of this licence are available at: http://creativecommons.org/licenses/ by/4.0/
Publication date
2015
Notes
This is an Open Access Article. It is published by Omics under the Creative Commons Attribution 4.0 Unported Licence (CC BY). Full details of this licence are available at: http://creativecommons.org/licenses/by/4.0/