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A method to rapidly analyze the simultaneous release of multiple pharmaceuticals from electrospun fibers. | LitMetric

A method to rapidly analyze the simultaneous release of multiple pharmaceuticals from electrospun fibers.

Int J Pharm

Department of Neurology, University of Michigan, Ann Arbor, Michigan, United States; Geriatrics Research, Education, and Clinical Center, Veterans Administration Ann Arbor Healthcare Center, Ann Arbor, Michigan, United States; Department of Biomedical Engineering, University of Michigan,Ann Arbor, M

Published: January 2020


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Article Abstract

Electrospun fibers are a commonly used cell scaffold and have also been used as pharmaceutical delivery devices. In this study, we developed a method to analyze the release of multiple pharmaceuticals from a single electrospun fiber scaffold and determine how each pharmaceutical's loading concentration affects the release rate of each pharmaceutical. Our analysis methods were tested on electrospun fibers loaded with two pharmaceuticals: 6-aminonicotinamide (6AN) and ibuprofen. Pharmaceutical concentration in electrospun fibers ranged from 1.5% to 8.5% by weight. We found that 6AN release was dependent on the concentration of 6AN and ibuprofen loaded into the fibers, while ibuprofen release was only dependent on the loading concentration of ibuprofen but not 6AN. Unexpectedly, ibuprofen release became dependent on both 6AN and ibuprofen loading concentrations when fibers were aged for 1-month post-fabrication at room temperature in the laboratory followed by a 4-hour incubation inside the cell culture incubator at 37 °C and 5% CO. One additional discovery was an unknown signal that was attributed to the medical grade syringes used for electrospinning, which was easily removed using our method. These results demonstrate the utility of the methods developed here and indicate multiple agents can be released concomitantly from electrospun fibers to meet the demands of more complex tissue engineering approaches. Future work will focus on analysis of pharmaceutical release profiles to exploit the dependencies on pharmaceutical loading concentrations.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7733704PMC
http://dx.doi.org/10.1016/j.ijpharm.2019.118871DOI Listing

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