PRE-FORMULATION DESIGN OF SUSTAINED-RELEASE GnRHa-LOADED PLGA MICROSPHERES AND ASSOCIATED FORMULATIONS FOR CONTROLLING REPRODUCTION IN AQUACULTURE

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This publication doesn't include Faculty of Medicine. It includes Faculty of Pharmacy. Official publication website can be found on muni.cz.
Authors

HOLICKÁ Martina VYSLOUŽIL Jakub KUBOVÁ Kateřina MUSELÍK Jan RADINOVÁ Eva VETCHÝ David KOTOLOVÁ Hana HAMMER Tomáš MAŠEK J. PODHOREC P. KNOWLES J.

Year of publication 2021
Type Article in Periodical
Magazine / Source ACTA POLONIAE PHARMACEUTICA
MU Faculty or unit

Faculty of Pharmacy

Citation
Web https://www.ptfarm.pl/download/?file=File%2FActa_Poloniae%2F2021%2F6%2F801.pdf
Doi http://dx.doi.org/10.32383/appdr/146287
Keywords GnRH analogsmicroparticlessolvent evaporationgelatinesustained drug releasefish reproduction
Description Poly(lactide-co-glycolide) PLGA microparticles represent an efficient and modern tool to encapsulate peptide drugs, which enables their administration to live organisms with the benefit of prolongedrelease. One area that could make the best of this opportunity is fish breeding in aquaculture. The presented study was centered on the formulation of gonadotropin-releasing hormone (GnRH) analog loaded PLGA microparticles intended for fish breeding augmentation, using the double emulsion evaporation method. In this initial experiment, the influence of several input variables (drug, PLGA type, emulsifier concentration, gelatine concentration in internal phase) on observed parameters (morphology, particle size, drug content, drug release, resuspension index) was evaluated. It was found that at lower emulsifier concentration, the particle size is apparently lower (8.54 +/- 6.13-10.36 +/- 4.65 vs. 25.56 +/- 18.86), which is more advantageous in injection administration. Encapsulation efficiency ranged from 39.13 +/- 8.85 to 75.30 +/- 8.83, favoring lower emulsifier concentration, while resuspension index (70.99 +/- 6.47%) suggested the possibility of longer-term administration. Dissolution tests revealed prolonged release for ten days, with most of the drug released in 72-96 hrs. A follow-up study discerning polymer type/gelatine concentration was suggested. Accompanying studies of imaging agent coumarin-6 encapsulation for eventual distribution imaging and metoclopramide base drug release for potential adjuvant use were also successfully realized.
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