Influence of the molecular weight of polymer, solvents and operational condition in the electrospinning of polycaprolactone
DOI:
https://doi.org/10.17533/udea.redin.n84a05Keywords:
electrospinning, nanofiber, solvents, polymer solution, collector, polycaprolactoneAbstract
The objective of this study was to determine the influence of the molecular weight of polycaprolactone, solvents and operational conditions to obtain polymeric nanofibers by the electrospinning technique. In this study, an electrospinning equipment constructed at University was employed, in which you can control the process parameters such as voltage, deposition rate, collector distance, speed and direction of rotation of the collector. In this paper, polycaprolactone (PCL) of three different Molecular Weight (Mw=14,000 g·mol-1, Mw=45,000 g·mol-1, and Mw=80,000 g·mol-1) was used. Solvents used were Acetone and mixtures of Acetone with Acetic Acid in different ratios. The tests carried out showed that polycaprolactone of 14,000 g·mol-1did not allow getting fibers. While the tests carried out with polycaprolactone of 45,000 g·mol-1 and 80,000 g·mol-1 allowed getting fibers under the different conditions evaluated. The higher concentration of the polymer provokes the solution of the polymer does not flow through the tip of the syringe, while the low concentration of the polymer favors that the fibers break and defects appear in the film. In this study, it was found that using a voltage of 15 KV, an injection rate of 0.1 mL/h and a collector distance from 15 cm with PCL solution of 45,000 g·mol-1 at 20% in solution 1:1 of acetone and acetic acid, it was possible to obtain the highest percentage of nanofibers from all experiments (77%) with an average diameter of of 88 nm.
Downloads
References
N. Bhardwaj and S. C. Kundu, “Electrospinning: A fascinating fiber fabrication technique,” Biotechnol. Adv. , vol. 28, no. 3, pp. 325–347, 2010.
U. Paaver et al. , “Electrospun nanofibers as a potential controlled-release solid dispersion system for poorly water-soluble drugs,” Int. J. Pharm. , vol. 479, no. 1, pp. 252–260, 2015.
R. Sridhar et al. , “Electrospun nanofibers for pharmaceutical and medical applications,” J. Drug Deliv. Sci. Technol. , vol. 21, no. 6, pp. 451–468, 2011.
X. Hu et al. , “Electrospinning of polymeric nano fi bers for drug delivery applications,” J. Control. Release , vol. 185, pp. 12–21, 2014.
J. Zeng et al. , “Biodegradable electrospun fibers for drug delivery,” J. Control. Release , vol. 92, no. 3, pp. 227–231, 2003.
Z. Ershuai et al. , “Electrospun PDLLA / PLGA composite membranes for potential application in guided tissue regeneration,” Mater. Sci. Eng. C , vol. 58, pp. 278–285, 2016.
T. J. Sill and H. A. von Recum, “Electrospinning: Applications in drug delivery and tissue engineering,” Biomaterials , vol. 29, no. 13, pp. 1989–2006, 2008.
Q. P. Pham, U. Sharma, and A. G. Mikos, “Electrospinning of polymeric nanofibers for tissue engineering applications: a review,” Tissue Eng. , vol. 12, no. 5, pp. 1197–1211, 2006.
T. K. Dash and V. B. Konkimalla, “Poly-e-caprolactone based formulations for drug delivery and tissue engineering: A review,” J. Control. Release , vol. 158, no. 1, pp. 15–33, 2012.
Z. McEachin and K. Lozano, “Effects of expandable graphite and modified ammonium polyphosphate on the flame-retardant and mechanical properties of wood flour-polypropylene composites,” Polym. Polym. Compos. , vol. 21, no. 7, pp. 449–456, 2013.
K. K. Phua, E. R. Roberts, and K. W. Leong, “Degradable Polymers,” in Comprehensive biomaterials , P. Ducheyne, K. E. Healy, D. W. Hutmacher, D. W. Grainger, and C. J. Kirkpatrick (eds). Amsterdam, Netherlands: Elsevier Ltd., 2011, pp. 381-415.
N. Aditya, P. R. Ravi, U. S. Avula, and R. Vats, “Poly ( ε -caprolactone) nanocapsules for oral delivery of raloxifene: process optimization by hybrid design approach, in vitro and in vivo evaluation,” J. Microencapsul. , vol. 31, no. 5, pp. 508–18, 2014.
S. Agarwal, A. Greiner, and J. H. Wendorff, “Progress in Polymer Science Functional materials by electrospinning of polymers,” Prog. Polym. Sci. , vol. 38, no. 6, pp. 963–991, 2013.
P. Karuppuswamy and J. Reddy, “Polycaprolactone nano fi bers for the controlled release of tetracycline hydrochloride,” Mater. Lett. , vol. 141, pp. 180–186, 2015.
K. Madhaiyan, R. Sridhar, S. Sundarrajan, J. R. Venugopal, and S. Ramakrishna, “Vitamin B12 loaded polycaprolactone nanofibers: A novel transdermal route for the water soluble energy supplement delivery,” Int. J. Pharm. , vol. 444, no. 1–2, pp. 70–76, 2013.
J. López, L. F. Espinosa, A. Donohue, and S. Y. Reyes, “Antimicrobial activity of silver nanoparticles in polycaprolactone nanofibers against Gram-positive and negative bacteria,” Ind. Eng. Chem. Res. , vol. 55, pp. 12532–12538, 2016.
J. P. Chen, G. C. Lai, and Y. S. Chang, “Preparation of composite electrospun nanofibers of polycaprolactone and nanohydroxyapatite for osteogenic differentiation of stem cells,” in 3 rd Int. Nanoelectron. Conf. (INEC), Hong Kong, China, 2010, pp. 1395–1396.
Z. Sultanova, G. Kaleli, G. Kabay, and M. Mutlu, “Controlled release of a hydrophilic drug from coaxially electrospun polycaprolactone nanofibers,” Int. J. Pharm. , vol. 505, no. 1–2, pp. 133–138, 2016.
F. Liu, R. Guo, M. Shen, S. Wang, and X. Shi, “Effect of processing variables on the morphology of electrospun poly[(lactic acid)-co-(glycolic acid)] nanofibers,” Macromol. Mater. Eng. , vol. 294, no. 10, pp. 666–672, 2009.
L. Duque, L. Rodriguez, and M. López, “Electrospinning : La Era De Las Nanofibras,” Rev. Iberoam. Polímeros , vol. 14, no. 1, pp. 10–27, 2014.
S. Chakraborty, I. C. Liao, A. Adler, and K. W. Leong, “Electrohydrodynamics: A facile technique to fabricate drug delivery systems,” Adv. Drug Deliv. Rev. , vol. 61, no. 12, pp. 1043–1054, 2009.
Z. X. Meng, W. Zheng, L. Li, and Y. F. Zheng, “Fabrication, characterization and in vitro drug release behavior of electrospun PLGA/chitosan nanofibrous scaffold,” Mater. Chem. Phys. , vol. 125, no. 3, pp. 606–611, 2011.
D. Liang, B. S. Hsiao, and B. Chu, “Functional electrospun nanofibrous scaffolds for biomedical applications,” Adv. Drug Deliv. Rev. , vol. 59, no. 14, pp. 1392–1412, 2007.
A. Baji, Y. W. Mai, S. C. Wong, M. Abtahi, and P. Chen, “Electrospinning of polymer nanofibers: Effects on oriented morphology, structures and tensile properties,” Compos. Sci. Technol. , vol. 70, no. 5, pp. 703–718, 2010.
F. Croisier, A. Duwez, C. Jérôme, A. Léonard, K. Van Der Werf, P. Dijkstra, M. Bennink, “Mechanical testing of electrospun PCL fibers,” Acta Biomater., vol. 8, no. 1, pp. 218–224, 2012.
Downloads
Published
How to Cite
Issue
Section
License
Copyright (c) 2017 Revista Facultad de Ingeniería Universidad de Antioquia

This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License.
Revista Facultad de Ingeniería, Universidad de Antioquia is licensed under the Creative Commons Attribution BY-NC-SA 4.0 license. https://creativecommons.org/licenses/by-nc-sa/4.0/deed.en
You are free to:
Share — copy and redistribute the material in any medium or format
Adapt — remix, transform, and build upon the material
Under the following terms:
Attribution — You must give appropriate credit, provide a link to the license, and indicate if changes were made. You may do so in any reasonable manner, but not in any way that suggests the licensor endorses you or your use.
NonCommercial — You may not use the material for commercial purposes.
ShareAlike — If you remix, transform, or build upon the material, you must distribute your contributions under the same license as the original.
The material published in the journal can be distributed, copied and exhibited by third parties if the respective credits are given to the journal. No commercial benefit can be obtained and derivative works must be under the same license terms as the original work.