Dissolving polyvinylpyrrolidone-based microneedle systems for in-vitro delivery of sumatriptan succinate
Document Type
Article
Publication Date
3-1-2018
Abstract
In-vitro permeation studies were conducted to assess the feasibility of fabricating dissolving-microneedle-array systems to release sumatriptan succinate. The formulations consisted mainly of the encapsulated active ingredient and a water-soluble biologically compatible polymer, polyvinylpyrrolidone (PVP), approved by the U.S. Food and Drug Administration (FDA). Tests with Franz-type diffusion cells and Göttingen minipig skins showed an increase of the transdermal flux compared to passive diffusion. A preparation, containing 30% by mass of PVP and 8.7 mg sumatriptan, produced a delivery rate of 395 ± 31 μg/cm2 h over a 7-hour period after a negligible lag time of approximately 39 min. Theoretically, a 10.7 cm2 microneedle-array patch loaded with 118.8 mg of the drug would provide the required plasma concentration, 72 ng/mL, for nearly 7 h.
Identifier
85038034791 (Scopus)
Publication Title
European Journal of Pharmaceutical Sciences
External Full Text Location
https://doi.org/10.1016/j.ejps.2017.11.031
e-ISSN
18790720
ISSN
09280987
PubMed ID
29203152
First Page
84
Last Page
92
Volume
114
Recommended Citation
Ronnander, P.; Simon, L.; Spilgies, H.; Koch, A.; and Scherr, S., "Dissolving polyvinylpyrrolidone-based microneedle systems for in-vitro delivery of sumatriptan succinate" (2018). Faculty Publications. 8813.
https://digitalcommons.njit.edu/fac_pubs/8813
